{
    "batchid": 13,
    "recordid": "P98161-1",
    "recordtype": "protein",
    "sections": {
        "snv": [
            {
                "evidence": [
                    {
                        "id": "rs2092034761",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs2092034761"
                    },
                    {
                        "id": "rs2092034761",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs2092034761#frequency_tab"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3232,
                "end_pos": 3232,
                "sequence_org": "K",
                "sequence_mut": "E",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2100184",
                "ref_nt": "C",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "K3232",
                "disease": [
                    {
                        "disease_id": "DOID:0080322",
                        "recommended_name": {
                            "id": "DOID:0080322",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0080322",
                            "name": "polycystic kidney disease",
                            "description": "A cystic kidney disease that is characterized by the growth of fluid-filled cysts in the kidneys that reduces kidney function and may lead to kidney failure."
                        },
                        "synonyms": [
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0080322",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0080322"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0110858",
                        "recommended_name": {
                            "id": "DOID:0110858",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0110858",
                            "name": "polycystic kidney disease 1",
                            "description": "A autosomal dominant polycystic kidney disease that has_material_basis_in autosomal dominant inheritance of mutation in the PKD1 gene on chromosome 16p13.3."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "Polycystic Kidney Disease, Adult, Type I",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            },
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            }
                        ]
                    }
                ],
                "keywords": [
                    "ebi",
                    "germline",
                    "disease"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs988225678",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs988225678"
                    },
                    {
                        "id": "rs988225678",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs988225678#frequency_tab"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3232,
                "end_pos": 3232,
                "sequence_org": "K",
                "sequence_mut": "R",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2100183",
                "ref_nt": "C",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "K3232",
                "keywords": [
                    "ebi",
                    "germline",
                    "disease"
                ],
                "disease": [
                    {
                        "disease_id": "DOID:0080322",
                        "recommended_name": {
                            "id": "DOID:0080322",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0080322",
                            "name": "polycystic kidney disease",
                            "description": "A cystic kidney disease that is characterized by the growth of fluid-filled cysts in the kidneys that reduces kidney function and may lead to kidney failure."
                        },
                        "synonyms": [
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0080322",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0080322"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0110858",
                        "recommended_name": {
                            "id": "DOID:0110858",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0110858",
                            "name": "polycystic kidney disease 1",
                            "description": "A autosomal dominant polycystic kidney disease that has_material_basis_in autosomal dominant inheritance of mutation in the PKD1 gene on chromosome 16p13.3."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "Polycystic Kidney Disease, Adult, Type I",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            },
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            }
                        ]
                    }
                ]
            },
            {
                "evidence": [
                    {
                        "id": "P98161",
                        "database": "BioMuta",
                        "url": "https://hivelab.biochemistry.gwu.edu/biomuta/proteinview/P98161"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3233,
                "end_pos": 3233,
                "subjects_tested": "2670",
                "subjects_positive": "1",
                "frequency": "0.0",
                "sequence_org": "E",
                "sequence_mut": "*",
                "comment": "Somatic mutation passed 0 out of 6 filters: .",
                "chr_id": "16",
                "chr_pos": "2100181",
                "ref_nt": "C",
                "alt_nt": "A",
                "minor_allelic_frequency": "",
                "site_lbl": "E3233",
                "disease": [
                    {
                        "disease_id": "DOID:1319",
                        "recommended_name": {
                            "id": "DOID:1319",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:1319",
                            "name": "brain cancer",
                            "description": "A central nervous system cancer that is characterized by the growth of abnormal cells in the tissues of the brain."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:1319",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:1319",
                                "name": "BT - Brain tumour",
                                "description": ""
                            },
                            {
                                "id": "DOID:1319",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:1319",
                                "name": "adult brain tumor",
                                "description": ""
                            },
                            {
                                "id": "DOID:1319",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:1319",
                                "name": "adult malignant brain neoplasm",
                                "description": ""
                            },
                            {
                                "id": "DOID:1319",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:1319",
                                "name": "brain neoplasm",
                                "description": ""
                            },
                            {
                                "id": "DOID:1319",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:1319",
                                "name": "brain neoplasm, adult",
                                "description": ""
                            },
                            {
                                "id": "DOID:1319",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:1319",
                                "name": "malignant brain tumour",
                                "description": ""
                            },
                            {
                                "id": "DOID:1319",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:1319",
                                "name": "malignant primary brain neoplasm",
                                "description": ""
                            },
                            {
                                "id": "DOID:1319",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:1319",
                                "name": "malignant primary brain tumor",
                                "description": ""
                            },
                            {
                                "id": "DOID:1319",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:1319",
                                "name": "malignant tumor of Brain",
                                "description": ""
                            },
                            {
                                "id": "DOID:1319",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:1319",
                                "name": "malignant tumor of adult brain",
                                "description": ""
                            },
                            {
                                "id": "DOID:1319",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:1319",
                                "name": "neoplasm of brain",
                                "description": ""
                            },
                            {
                                "id": "DOID:1319",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:1319",
                                "name": "primary brain neoplasm",
                                "description": ""
                            },
                            {
                                "id": "DOID:1319",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:1319",
                                "name": "primary brain tumor",
                                "description": ""
                            },
                            {
                                "id": "DOID:1319",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:1319",
                                "name": "primary malignant neoplasm of brain",
                                "description": ""
                            },
                            {
                                "id": "DOID:1319",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:1319",
                                "name": "tumor of the Brain",
                                "description": ""
                            }
                        ],
                        "unlinked_id_list": [
                            "DOID:4203",
                            "DOID:3541",
                            "DOID:4706",
                            "DOID:1659",
                            "DOID:368"
                        ],
                        "evidence": [
                            {
                                "id": "1319",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:1319"
                            }
                        ]
                    }
                ],
                "keywords": [
                    "biomuta",
                    "somatic",
                    "cancer",
                    "disease"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs2092034590",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs2092034590"
                    },
                    {
                        "id": "rs2092034590",
                        "database": "ENSEMBL",
                        "url": "https://www.ensembl.org/id/rs2092034590"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3233,
                "end_pos": 3233,
                "sequence_org": "E",
                "sequence_mut": "D",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2100179",
                "ref_nt": "G",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "E3233",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs2092034641",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs2092034641"
                    },
                    {
                        "id": "rs2092034641",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs2092034641#frequency_tab"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3233,
                "end_pos": 3233,
                "sequence_org": "E",
                "sequence_mut": "V",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2100180",
                "ref_nt": "A",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "E3233",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs2544715201",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs2544715201"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3233,
                "end_pos": 3233,
                "sequence_org": "E",
                "sequence_mut": "null",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2100182",
                "ref_nt": "p",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "E3233",
                "disease": [
                    {
                        "disease_id": "DOID:0080322",
                        "recommended_name": {
                            "id": "DOID:0080322",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0080322",
                            "name": "polycystic kidney disease",
                            "description": "A cystic kidney disease that is characterized by the growth of fluid-filled cysts in the kidneys that reduces kidney function and may lead to kidney failure."
                        },
                        "synonyms": [
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0080322",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0080322"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0110858",
                        "recommended_name": {
                            "id": "DOID:0110858",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0110858",
                            "name": "polycystic kidney disease 1",
                            "description": "A autosomal dominant polycystic kidney disease that has_material_basis_in autosomal dominant inheritance of mutation in the PKD1 gene on chromosome 16p13.3."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "Polycystic Kidney Disease, Adult, Type I",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            },
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            }
                        ]
                    }
                ],
                "keywords": [
                    "ebi",
                    "germline",
                    "disease"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs2092034492",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs2092034492"
                    },
                    {
                        "id": "rs2092034492",
                        "database": "ENSEMBL",
                        "url": "https://www.ensembl.org/id/rs2092034492"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3234,
                "end_pos": 3234,
                "sequence_org": "V",
                "sequence_mut": "A",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2100177",
                "ref_nt": "G",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "V3234",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs2092034438",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs2092034438"
                    },
                    {
                        "id": "rs2092034438",
                        "database": "ENSEMBL",
                        "url": "https://www.ensembl.org/id/rs2092034438"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3235,
                "end_pos": 3235,
                "sequence_org": "L",
                "sequence_mut": "V",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2100175",
                "ref_nt": "C",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "L3235",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs748442072",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs748442072"
                    },
                    {
                        "id": "rs748442072",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs748442072"
                    },
                    {
                        "id": "rs748442072",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs748442072#frequency_tab"
                    },
                    {
                        "id": "rs748442072",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs748442072"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3236,
                "end_pos": 3236,
                "sequence_org": "A",
                "sequence_mut": "T",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2100172",
                "ref_nt": "T",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "A3236",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs779137772",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs779137772"
                    },
                    {
                        "id": "rs779137772",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs779137772"
                    },
                    {
                        "id": "rs779137772",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs779137772#frequency_tab"
                    },
                    {
                        "id": "rs779137772",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs779137772"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3236,
                "end_pos": 3236,
                "sequence_org": "A",
                "sequence_mut": "V",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2100171",
                "ref_nt": "A",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "A3236",
                "keywords": [
                    "ebi",
                    "germline",
                    "disease"
                ],
                "disease": [
                    {
                        "disease_id": "DOID:0080322",
                        "recommended_name": {
                            "id": "DOID:0080322",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0080322",
                            "name": "polycystic kidney disease",
                            "description": "A cystic kidney disease that is characterized by the growth of fluid-filled cysts in the kidneys that reduces kidney function and may lead to kidney failure."
                        },
                        "synonyms": [
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0080322",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0080322"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0110858",
                        "recommended_name": {
                            "id": "DOID:0110858",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0110858",
                            "name": "polycystic kidney disease 1",
                            "description": "A autosomal dominant polycystic kidney disease that has_material_basis_in autosomal dominant inheritance of mutation in the PKD1 gene on chromosome 16p13.3."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "Polycystic Kidney Disease, Adult, Type I",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            },
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            }
                        ]
                    }
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs754218771",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs754218771"
                    },
                    {
                        "id": "rs754218771",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs754218771"
                    },
                    {
                        "id": "rs754218771",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs754218771#frequency_tab"
                    },
                    {
                        "id": "rs754218771",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs754218771"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3237,
                "end_pos": 3237,
                "sequence_org": "A",
                "sequence_mut": "S",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2100169",
                "ref_nt": "A",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "A3237",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs754218771",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs754218771"
                    },
                    {
                        "id": "rs754218771",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs754218771"
                    },
                    {
                        "id": "rs754218771",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs754218771#frequency_tab"
                    },
                    {
                        "id": "rs754218771",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs754218771"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3237,
                "end_pos": 3237,
                "sequence_org": "A",
                "sequence_mut": "T",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2100169",
                "ref_nt": "T",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "A3237",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs780474965",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs780474965"
                    },
                    {
                        "id": "rs780474965",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs780474965"
                    },
                    {
                        "id": "rs780474965",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs780474965#frequency_tab"
                    },
                    {
                        "id": "rs780474965",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs780474965"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3237,
                "end_pos": 3237,
                "sequence_org": "A",
                "sequence_mut": "V",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2100168",
                "ref_nt": "A",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "A3237",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs761888631",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs761888631"
                    }
                ],
                "glycoeffect": [
                    "o-glyco-site-loss"
                ],
                "start_pos": 3238,
                "end_pos": 3238,
                "sequence_org": "S",
                "sequence_mut": "=",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2100070",
                "ref_nt": "A",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "S3238",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs1349251807",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1349251807"
                    },
                    {
                        "id": "rs1349251807",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs1349251807#frequency_tab"
                    },
                    {
                        "id": "rs1349251807",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs1349251807"
                    }
                ],
                "glycoeffect": [
                    "o-glyco-site-loss"
                ],
                "start_pos": 3238,
                "end_pos": 3238,
                "sequence_org": "S",
                "sequence_mut": "R",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2100166",
                "ref_nt": "G",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "S3238",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs774484157",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs774484157"
                    },
                    {
                        "id": "rs774484157",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs774484157"
                    },
                    {
                        "id": "rs774484157",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs774484157#frequency_tab"
                    },
                    {
                        "id": "rs774484157",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs774484157"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3239,
                "end_pos": 3239,
                "sequence_org": "D",
                "sequence_mut": "H",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2100069",
                "ref_nt": "G",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "D3239",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs774484157",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs774484157"
                    },
                    {
                        "id": "rs774484157",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs774484157"
                    },
                    {
                        "id": "rs774484157",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs774484157#frequency_tab"
                    },
                    {
                        "id": "rs774484157",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs774484157"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3239,
                "end_pos": 3239,
                "sequence_org": "D",
                "sequence_mut": "N",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2100069",
                "ref_nt": "T",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "D3239",
                "keywords": [
                    "ebi",
                    "germline",
                    "disease"
                ],
                "disease": [
                    {
                        "disease_id": "DOID:0080322",
                        "recommended_name": {
                            "id": "DOID:0080322",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0080322",
                            "name": "polycystic kidney disease",
                            "description": "A cystic kidney disease that is characterized by the growth of fluid-filled cysts in the kidneys that reduces kidney function and may lead to kidney failure."
                        },
                        "synonyms": [
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0080322",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0080322"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0110858",
                        "recommended_name": {
                            "id": "DOID:0110858",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0110858",
                            "name": "polycystic kidney disease 1",
                            "description": "A autosomal dominant polycystic kidney disease that has_material_basis_in autosomal dominant inheritance of mutation in the PKD1 gene on chromosome 16p13.3."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "Polycystic Kidney Disease, Adult, Type I",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            },
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            }
                        ]
                    }
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs751148776",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs751148776"
                    },
                    {
                        "id": "rs751148776",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs751148776"
                    },
                    {
                        "id": "rs751148776",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs751148776#frequency_tab"
                    },
                    {
                        "id": "rs751148776",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs751148776"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 323,
                "end_pos": 323,
                "sequence_org": "H",
                "sequence_mut": "R",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2118024",
                "ref_nt": "C",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "H323",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs1567217428",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1567217428"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 323,
                "end_pos": 323,
                "sequence_org": "H",
                "sequence_mut": "null",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2118028_2118029",
                "ref_nt": "p",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "H323",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "P98161",
                        "database": "BioMuta",
                        "url": "https://hivelab.biochemistry.gwu.edu/biomuta/proteinview/P98161"
                    },
                    {
                        "id": "rs143312683",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs143312683"
                    },
                    {
                        "id": "rs143312683",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs143312683"
                    },
                    {
                        "id": "rs143312683",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs143312683#frequency_tab"
                    },
                    {
                        "id": "rs143312683",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs143312683"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3240,
                "end_pos": 3240,
                "subjects_tested": "3601",
                "subjects_positive": "1",
                "frequency": "0.0",
                "sequence_org": "A",
                "sequence_mut": "T",
                "comment": "Somatic mutation passed 0 out of 6 filters: .",
                "chr_id": "16",
                "chr_pos": "2100066",
                "ref_nt": "C",
                "alt_nt": "T",
                "minor_allelic_frequency": "",
                "site_lbl": "A3240",
                "disease": [
                    {
                        "disease_id": "DOID:9256",
                        "recommended_name": {
                            "id": "DOID:9256",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:9256",
                            "name": "colorectal cancer",
                            "description": "A large intestine cancer that is located_in the colon and/or located_in the rectum."
                        },
                        "synonyms": [
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectal cancer",
                                "description": "A primary or metastatic malignant neoplasm that affects the colon or rectum. Representative examples include carcinoma, lymphoma, and sarcoma."
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "cancer of colorectum",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "cancer of large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "cancer of large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "cancer of the large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colon cancer, advanced, somatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colon cancer, somatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectal cancer",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectal cancer with chromosomal instability, somatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectal cancer, autosomal dominant, somatic mutation",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectal cancer, somatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectal cancer, susceptibility to, autosomal dominant, somatic mutation",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectum cancer",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant colorectal neoplasm",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant colorectal tumor",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant colorectal tumour",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant colorectum neoplasm",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant large bowel neoplasm",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant large bowel tumor",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant large bowel tumour",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant large intestine neoplasm",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant large intestine tumor",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant large intestine tumour",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant neoplasm of colorectum",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant neoplasm of large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant neoplasm of large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant neoplasm of the large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant neoplasm of the large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumor of large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumor of large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumor of the large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumor of the large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumour of large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumour of large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumour of the large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumour of the large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "CRC",
                                "description": ""
                            },
                            {
                                "id": "MIM:114500",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/114500",
                                "name": "Colorectal cancer",
                                "description": "Colorectal cancer"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "9256",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:9256"
                            }
                        ]
                    }
                ],
                "keywords": [
                    "biomuta",
                    "somatic",
                    "cancer",
                    "disease",
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs919605814",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs919605814"
                    },
                    {
                        "id": "rs919605814",
                        "database": "ENSEMBL",
                        "url": "https://www.ensembl.org/id/rs919605814"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3241,
                "end_pos": 3241,
                "sequence_org": "A",
                "sequence_mut": "S",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2100063",
                "ref_nt": "A",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "A3241",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs780284563",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs780284563"
                    },
                    {
                        "id": "rs780284563",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs780284563"
                    },
                    {
                        "id": "rs780284563",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs780284563#frequency_tab"
                    },
                    {
                        "id": "rs780284563",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs780284563"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3242,
                "end_pos": 3242,
                "sequence_org": "L",
                "sequence_mut": "V",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2100060",
                "ref_nt": "C",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "L3242",
                "keywords": [
                    "ebi",
                    "germline",
                    "disease"
                ],
                "disease": [
                    {
                        "disease_id": "DOID:0080322",
                        "recommended_name": {
                            "id": "DOID:0080322",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0080322",
                            "name": "polycystic kidney disease",
                            "description": "A cystic kidney disease that is characterized by the growth of fluid-filled cysts in the kidneys that reduces kidney function and may lead to kidney failure."
                        },
                        "synonyms": [
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0080322",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0080322"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0110858",
                        "recommended_name": {
                            "id": "DOID:0110858",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0110858",
                            "name": "polycystic kidney disease 1",
                            "description": "A autosomal dominant polycystic kidney disease that has_material_basis_in autosomal dominant inheritance of mutation in the PKD1 gene on chromosome 16p13.3."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "Polycystic Kidney Disease, Adult, Type I",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            },
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            }
                        ]
                    }
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs2151739862",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs2151739862"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3243,
                "end_pos": 3243,
                "sequence_org": "L",
                "sequence_mut": "null",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2100057_2100058i",
                "ref_nt": "T",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "L3243",
                "disease": [
                    {
                        "disease_id": "DOID:0080322",
                        "recommended_name": {
                            "id": "DOID:0080322",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0080322",
                            "name": "polycystic kidney disease",
                            "description": "A cystic kidney disease that is characterized by the growth of fluid-filled cysts in the kidneys that reduces kidney function and may lead to kidney failure."
                        },
                        "synonyms": [
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0080322",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0080322"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0110858",
                        "recommended_name": {
                            "id": "DOID:0110858",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0110858",
                            "name": "polycystic kidney disease 1",
                            "description": "A autosomal dominant polycystic kidney disease that has_material_basis_in autosomal dominant inheritance of mutation in the PKD1 gene on chromosome 16p13.3."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "Polycystic Kidney Disease, Adult, Type I",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            },
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            }
                        ]
                    }
                ],
                "keywords": [
                    "ebi",
                    "germline",
                    "disease"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "P98161",
                        "database": "BioMuta",
                        "url": "https://hivelab.biochemistry.gwu.edu/biomuta/proteinview/P98161"
                    },
                    {
                        "id": "rs146732153",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs146732153"
                    },
                    {
                        "id": "rs146732153",
                        "database": "1000Genomes",
                        "url": "https://www.ensembl.org/homo_sapiens/Variation/Explore?v=rs146732153"
                    },
                    {
                        "id": "rs146732153",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs146732153"
                    },
                    {
                        "id": "rs146732153",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs146732153#frequency_tab"
                    },
                    {
                        "id": "rs146732153",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs146732153"
                    },
                    {
                        "id": "rs146732153",
                        "database": "COSMIC",
                        "url": "https://www.ensembl.org/homo_sapiens/Variation/Explore?v=rs146732153"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3244,
                "end_pos": 3244,
                "subjects_tested": "3601",
                "subjects_positive": "2",
                "frequency": "0.1",
                "sequence_org": "R",
                "sequence_mut": "C",
                "comment": "Somatic mutation passed 0 out of 6 filters: .",
                "chr_id": "16",
                "chr_pos": "2100054",
                "ref_nt": "G",
                "alt_nt": "A",
                "minor_allelic_frequency": "",
                "site_lbl": "R3244",
                "disease": [
                    {
                        "disease_id": "DOID:9256",
                        "recommended_name": {
                            "id": "DOID:9256",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:9256",
                            "name": "colorectal cancer",
                            "description": "A large intestine cancer that is located_in the colon and/or located_in the rectum."
                        },
                        "synonyms": [
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectal cancer",
                                "description": "A primary or metastatic malignant neoplasm that affects the colon or rectum. Representative examples include carcinoma, lymphoma, and sarcoma."
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "cancer of colorectum",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "cancer of large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "cancer of large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "cancer of the large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colon cancer, advanced, somatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colon cancer, somatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectal cancer",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectal cancer with chromosomal instability, somatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectal cancer, autosomal dominant, somatic mutation",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectal cancer, somatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectal cancer, susceptibility to, autosomal dominant, somatic mutation",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectum cancer",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant colorectal neoplasm",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant colorectal tumor",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant colorectal tumour",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant colorectum neoplasm",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant large bowel neoplasm",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant large bowel tumor",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant large bowel tumour",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant large intestine neoplasm",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant large intestine tumor",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant large intestine tumour",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant neoplasm of colorectum",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant neoplasm of large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant neoplasm of large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant neoplasm of the large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant neoplasm of the large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumor of large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumor of large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumor of the large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumor of the large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumour of large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumour of large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumour of the large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumour of the large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "CRC",
                                "description": ""
                            },
                            {
                                "id": "MIM:114500",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/114500",
                                "name": "Colorectal cancer",
                                "description": "Colorectal cancer"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "9256",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:9256"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:363",
                        "recommended_name": {
                            "id": "DOID:363",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:363",
                            "name": "uterine cancer",
                            "description": "A female reproductive organ cancer that is located_in the uterus."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:363",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:363",
                                "name": "CA - cancer of uterus",
                                "description": ""
                            },
                            {
                                "id": "DOID:363",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:363",
                                "name": "Tumour of uterus",
                                "description": ""
                            },
                            {
                                "id": "DOID:363",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:363",
                                "name": "malignant neoplasm of uterus",
                                "description": ""
                            },
                            {
                                "id": "DOID:363",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:363",
                                "name": "malignant uterine tumor",
                                "description": ""
                            },
                            {
                                "id": "DOID:363",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:363",
                                "name": "neoplasm of uterus",
                                "description": ""
                            },
                            {
                                "id": "DOID:363",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:363",
                                "name": "uterine tumor",
                                "description": ""
                            },
                            {
                                "id": "DOID:363",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:363",
                                "name": "uterus neoplasm",
                                "description": ""
                            }
                        ],
                        "unlinked_id_list": [
                            "DOID:9460",
                            "DOID:5166",
                            "DOID:2021",
                            "DOID:4114"
                        ],
                        "evidence": [
                            {
                                "id": "363",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:363"
                            }
                        ]
                    }
                ],
                "keywords": [
                    "biomuta",
                    "somatic",
                    "cancer",
                    "disease",
                    "ebi"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs1041239286",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1041239286"
                    },
                    {
                        "id": "rs1041239286",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs1041239286#frequency_tab"
                    },
                    {
                        "id": "rs1041239286",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs1041239286"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3244,
                "end_pos": 3244,
                "sequence_org": "R",
                "sequence_mut": "H",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2100053",
                "ref_nt": "T",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "R3244",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs146732153",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs146732153"
                    },
                    {
                        "id": "rs146732153",
                        "database": "1000Genomes",
                        "url": "https://www.ensembl.org/homo_sapiens/Variation/Explore?v=rs146732153"
                    },
                    {
                        "id": "rs146732153",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs146732153"
                    },
                    {
                        "id": "rs146732153",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs146732153#frequency_tab"
                    },
                    {
                        "id": "rs146732153",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs146732153"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3244,
                "end_pos": 3244,
                "sequence_org": "R",
                "sequence_mut": "S",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2100054",
                "ref_nt": "T",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "R3244",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs2092027387",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs2092027387"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3244,
                "end_pos": 3244,
                "sequence_org": "R",
                "sequence_mut": "null",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2100055",
                "ref_nt": "p",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "R3244",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs1487596694",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1487596694"
                    },
                    {
                        "id": "rs1487596694",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs1487596694#frequency_tab"
                    },
                    {
                        "id": "rs1487596694",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs1487596694"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3245,
                "end_pos": 3245,
                "sequence_org": "F",
                "sequence_mut": "V",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2100051",
                "ref_nt": "C",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "F3245",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs781673852",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs781673852"
                    },
                    {
                        "id": "rs781673852",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs781673852"
                    },
                    {
                        "id": "rs781673852",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs781673852#frequency_tab"
                    },
                    {
                        "id": "rs781673852",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs781673852"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3246,
                "end_pos": 3246,
                "sequence_org": "R",
                "sequence_mut": "P",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2100047",
                "ref_nt": "G",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "R3246",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs781673852",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs781673852"
                    },
                    {
                        "id": "rs781673852",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs781673852"
                    },
                    {
                        "id": "rs781673852",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs781673852#frequency_tab"
                    },
                    {
                        "id": "rs781673852",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs781673852"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3246,
                "end_pos": 3246,
                "sequence_org": "R",
                "sequence_mut": "Q",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2100047",
                "ref_nt": "T",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "R3246",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs746231158",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs746231158"
                    },
                    {
                        "id": "rs746231158",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs746231158"
                    },
                    {
                        "id": "rs746231158",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs746231158#frequency_tab"
                    },
                    {
                        "id": "rs746231158",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs746231158"
                    },
                    {
                        "id": "rs746231158",
                        "database": "COSMIC",
                        "url": "https://www.ensembl.org/homo_sapiens/Variation/Explore?v=rs746231158"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3246,
                "end_pos": 3246,
                "sequence_org": "R",
                "sequence_mut": "W",
                "comment": "Somatic mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2100048",
                "ref_nt": "A",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "R3246",
                "keywords": [
                    "ebi",
                    "somatic",
                    "disease"
                ],
                "disease": [
                    {
                        "disease_id": "DOID:0080322",
                        "recommended_name": {
                            "id": "DOID:0080322",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0080322",
                            "name": "polycystic kidney disease",
                            "description": "A cystic kidney disease that is characterized by the growth of fluid-filled cysts in the kidneys that reduces kidney function and may lead to kidney failure."
                        },
                        "synonyms": [
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0080322",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0080322"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0110858",
                        "recommended_name": {
                            "id": "DOID:0110858",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0110858",
                            "name": "polycystic kidney disease 1",
                            "description": "A autosomal dominant polycystic kidney disease that has_material_basis_in autosomal dominant inheritance of mutation in the PKD1 gene on chromosome 16p13.3."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "Polycystic Kidney Disease, Adult, Type I",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            },
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            }
                        ]
                    }
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs2092026801",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs2092026801"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3246,
                "end_pos": 3246,
                "sequence_org": "R",
                "sequence_mut": "null",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2100049",
                "ref_nt": "l",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "R3246",
                "disease": [
                    {
                        "disease_id": "DOID:0080322",
                        "recommended_name": {
                            "id": "DOID:0080322",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0080322",
                            "name": "polycystic kidney disease",
                            "description": "A cystic kidney disease that is characterized by the growth of fluid-filled cysts in the kidneys that reduces kidney function and may lead to kidney failure."
                        },
                        "synonyms": [
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0080322",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0080322"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0110858",
                        "recommended_name": {
                            "id": "DOID:0110858",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0110858",
                            "name": "polycystic kidney disease 1",
                            "description": "A autosomal dominant polycystic kidney disease that has_material_basis_in autosomal dominant inheritance of mutation in the PKD1 gene on chromosome 16p13.3."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "Polycystic Kidney Disease, Adult, Type I",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            },
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            }
                        ]
                    }
                ],
                "keywords": [
                    "ebi",
                    "germline",
                    "disease"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs757771138",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs757771138"
                    },
                    {
                        "id": "rs757771138",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs757771138"
                    },
                    {
                        "id": "rs757771138",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs757771138#frequency_tab"
                    },
                    {
                        "id": "rs757771138",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs757771138"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3247,
                "end_pos": 3247,
                "sequence_org": "R",
                "sequence_mut": "C",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2100045",
                "ref_nt": "A",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "R3247",
                "disease": [
                    {
                        "disease_id": "DOID:0080322",
                        "recommended_name": {
                            "id": "DOID:0080322",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0080322",
                            "name": "polycystic kidney disease",
                            "description": "A cystic kidney disease that is characterized by the growth of fluid-filled cysts in the kidneys that reduces kidney function and may lead to kidney failure."
                        },
                        "synonyms": [
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0080322",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0080322"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0110858",
                        "recommended_name": {
                            "id": "DOID:0110858",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0110858",
                            "name": "polycystic kidney disease 1",
                            "description": "A autosomal dominant polycystic kidney disease that has_material_basis_in autosomal dominant inheritance of mutation in the PKD1 gene on chromosome 16p13.3."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "Polycystic Kidney Disease, Adult, Type I",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            },
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            }
                        ]
                    }
                ],
                "keywords": [
                    "ebi",
                    "germline",
                    "disease"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs140791671",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs140791671"
                    },
                    {
                        "id": "rs140791671",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs140791671"
                    },
                    {
                        "id": "rs140791671",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs140791671#frequency_tab"
                    },
                    {
                        "id": "rs140791671",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs140791671"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3247,
                "end_pos": 3247,
                "sequence_org": "R",
                "sequence_mut": "H",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2100044",
                "ref_nt": "T",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "R3247",
                "keywords": [
                    "ebi",
                    "germline",
                    "disease"
                ],
                "disease": [
                    {
                        "disease_id": "DOID:0080322",
                        "recommended_name": {
                            "id": "DOID:0080322",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0080322",
                            "name": "polycystic kidney disease",
                            "description": "A cystic kidney disease that is characterized by the growth of fluid-filled cysts in the kidneys that reduces kidney function and may lead to kidney failure."
                        },
                        "synonyms": [
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0080322",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0080322"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0110858",
                        "recommended_name": {
                            "id": "DOID:0110858",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0110858",
                            "name": "polycystic kidney disease 1",
                            "description": "A autosomal dominant polycystic kidney disease that has_material_basis_in autosomal dominant inheritance of mutation in the PKD1 gene on chromosome 16p13.3."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "Polycystic Kidney Disease, Adult, Type I",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            },
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            }
                        ]
                    }
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs1278316500",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1278316500"
                    },
                    {
                        "id": "rs1278316500",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs1278316500#frequency_tab"
                    },
                    {
                        "id": "rs1278316500",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs1278316500"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3248,
                "end_pos": 3248,
                "sequence_org": "L",
                "sequence_mut": "M",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2100042",
                "ref_nt": "T",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "L3248",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs1278316500",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1278316500"
                    },
                    {
                        "id": "rs1278316500",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs1278316500#frequency_tab"
                    },
                    {
                        "id": "rs1278316500",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs1278316500"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3248,
                "end_pos": 3248,
                "sequence_org": "L",
                "sequence_mut": "V",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2100042",
                "ref_nt": "C",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "L3248",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "P98161",
                        "database": "BioMuta",
                        "url": "https://hivelab.biochemistry.gwu.edu/biomuta/proteinview/P98161"
                    },
                    {
                        "id": "rs763834774",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs763834774"
                    },
                    {
                        "id": "rs763834774",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs763834774"
                    },
                    {
                        "id": "rs763834774",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs763834774#frequency_tab"
                    },
                    {
                        "id": "rs763834774",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs763834774"
                    },
                    {
                        "id": "rs763834774",
                        "database": "COSMIC",
                        "url": "https://www.ensembl.org/homo_sapiens/Variation/Explore?v=rs763834774"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 324,
                "end_pos": 324,
                "subjects_tested": "2053",
                "subjects_positive": "1",
                "frequency": "0.0",
                "sequence_org": "R",
                "sequence_mut": "C",
                "comment": "Somatic mutation passed 0 out of 6 filters: .",
                "chr_id": "16",
                "chr_pos": "2118022",
                "ref_nt": "G",
                "alt_nt": "A",
                "minor_allelic_frequency": "",
                "site_lbl": "R324",
                "disease": [
                    {
                        "disease_id": "DOID:4159",
                        "recommended_name": {
                            "id": "DOID:4159",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:4159",
                            "name": "skin cancer",
                            "description": "An integumentary system cancer located_in the skin that is the uncontrolled growth of abnormal skin cells."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:4159",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:4159",
                                "name": "CA - skin cancer",
                                "description": ""
                            },
                            {
                                "id": "DOID:4159",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:4159",
                                "name": "malignant neoplasm of skin",
                                "description": ""
                            },
                            {
                                "id": "DOID:4159",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:4159",
                                "name": "melanoma and Non-melanoma skin cancer",
                                "description": ""
                            }
                        ],
                        "unlinked_id_list": [
                            "DOID:3149",
                            "DOID:3451"
                        ],
                        "evidence": [
                            {
                                "id": "4159",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:4159"
                            }
                        ]
                    }
                ],
                "keywords": [
                    "biomuta",
                    "somatic",
                    "cancer",
                    "disease",
                    "ebi"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "P98161",
                        "database": "BioMuta",
                        "url": "https://hivelab.biochemistry.gwu.edu/biomuta/proteinview/P98161"
                    },
                    {
                        "id": "rs199476099",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs199476099"
                    },
                    {
                        "id": "rs199476099",
                        "database": "1000Genomes",
                        "url": "https://www.ensembl.org/homo_sapiens/Variation/Explore?v=rs199476099"
                    },
                    {
                        "id": "rs199476099",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs199476099"
                    },
                    {
                        "id": "rs199476099",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs199476099#frequency_tab"
                    },
                    {
                        "id": "rs199476099",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs199476099"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 324,
                "end_pos": 324,
                "subjects_tested": "719",
                "subjects_positive": "1",
                "frequency": "0.1",
                "sequence_org": "R",
                "sequence_mut": "H",
                "comment": "Somatic mutation passed 0 out of 6 filters: .",
                "chr_id": "16",
                "chr_pos": "2118021",
                "ref_nt": "C",
                "alt_nt": "T",
                "minor_allelic_frequency": "",
                "site_lbl": "R324",
                "disease": [
                    {
                        "disease_id": "DOID:11934",
                        "recommended_name": {
                            "id": "DOID:11934",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:11934",
                            "name": "head and neck cancer",
                            "description": "An organ system cancer that arises in the head or neck region. This region includes the nasal cavity, sinuses, lips, mouth, salivary glands, throat, or larynx."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:11934",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:11934",
                                "name": "head and neck neoplasm",
                                "description": ""
                            },
                            {
                                "id": "DOID:11934",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:11934",
                                "name": "head and neck tumours",
                                "description": ""
                            },
                            {
                                "id": "DOID:11934",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:11934",
                                "name": "head/neck neoplasm",
                                "description": ""
                            },
                            {
                                "id": "DOID:11934",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:11934",
                                "name": "tumor of head and neck",
                                "description": ""
                            }
                        ],
                        "unlinked_id_list": [
                            "DOID:1542"
                        ],
                        "evidence": [
                            {
                                "id": "11934",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:11934"
                            }
                        ]
                    }
                ],
                "keywords": [
                    "biomuta",
                    "somatic",
                    "cancer",
                    "disease",
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs199476099",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs199476099"
                    },
                    {
                        "id": "rs199476099",
                        "database": "1000Genomes",
                        "url": "https://www.ensembl.org/homo_sapiens/Variation/Explore?v=rs199476099"
                    },
                    {
                        "id": "rs199476099",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs199476099"
                    },
                    {
                        "id": "rs199476099",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs199476099#frequency_tab"
                    },
                    {
                        "id": "rs199476099",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs199476099"
                    },
                    {
                        "id": "10364515",
                        "database": "PubMed",
                        "url": "https://glygen.org/publication/PubMed/10364515"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 324,
                "end_pos": 324,
                "sequence_org": "R",
                "sequence_mut": "L",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2118021",
                "ref_nt": "A",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "R324",
                "keywords": [
                    "ebi",
                    "germline",
                    "disease"
                ],
                "disease": [
                    {
                        "disease_id": "DOID:0080322",
                        "recommended_name": {
                            "id": "DOID:0080322",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0080322",
                            "name": "polycystic kidney disease",
                            "description": "A cystic kidney disease that is characterized by the growth of fluid-filled cysts in the kidneys that reduces kidney function and may lead to kidney failure."
                        },
                        "synonyms": [
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0080322",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0080322"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0110858",
                        "recommended_name": {
                            "id": "DOID:0110858",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0110858",
                            "name": "polycystic kidney disease 1",
                            "description": "A autosomal dominant polycystic kidney disease that has_material_basis_in autosomal dominant inheritance of mutation in the PKD1 gene on chromosome 16p13.3."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "Polycystic Kidney Disease, Adult, Type I",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            },
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            }
                        ]
                    }
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs778615597",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs778615597"
                    },
                    {
                        "id": "rs778615597",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs778615597"
                    },
                    {
                        "id": "rs778615597",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs778615597"
                    },
                    {
                        "id": "rs778615597",
                        "database": "COSMIC",
                        "url": "https://www.ensembl.org/homo_sapiens/Variation/Explore?v=rs778615597"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3250,
                "end_pos": 3250,
                "sequence_org": "V",
                "sequence_mut": "M",
                "comment": "Somatic mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2100036",
                "ref_nt": "T",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "V3250",
                "keywords": [
                    "ebi",
                    "somatic"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs1338408672",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1338408672"
                    },
                    {
                        "id": "rs1338408672",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs1338408672"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3251,
                "end_pos": 3251,
                "sequence_org": "A",
                "sequence_mut": "S",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2100033",
                "ref_nt": "A",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "A3251",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs2092025764",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs2092025764"
                    },
                    {
                        "id": "rs2092025764",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs2092025764"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3251,
                "end_pos": 3251,
                "sequence_org": "A",
                "sequence_mut": "V",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2100032",
                "ref_nt": "A",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "A3251",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs1317364403",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1317364403"
                    },
                    {
                        "id": "rs1317364403",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs1317364403"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3252,
                "end_pos": 3252,
                "sequence_org": "E",
                "sequence_mut": "D",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2100028",
                "ref_nt": "G",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "E3252",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs2544713808",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs2544713808"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3252,
                "end_pos": 3252,
                "sequence_org": "E",
                "sequence_mut": "K",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2100030",
                "ref_nt": "T",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "E3252",
                "disease": [
                    {
                        "disease_id": "DOID:0080322",
                        "recommended_name": {
                            "id": "DOID:0080322",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0080322",
                            "name": "polycystic kidney disease",
                            "description": "A cystic kidney disease that is characterized by the growth of fluid-filled cysts in the kidneys that reduces kidney function and may lead to kidney failure."
                        },
                        "synonyms": [
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0080322",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0080322"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0110858",
                        "recommended_name": {
                            "id": "DOID:0110858",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0110858",
                            "name": "polycystic kidney disease 1",
                            "description": "A autosomal dominant polycystic kidney disease that has_material_basis_in autosomal dominant inheritance of mutation in the PKD1 gene on chromosome 16p13.3."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "Polycystic Kidney Disease, Adult, Type I",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            },
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            }
                        ]
                    }
                ],
                "keywords": [
                    "ebi",
                    "germline",
                    "disease"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs2092025452",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs2092025452"
                    },
                    {
                        "id": "rs2092025452",
                        "database": "ENSEMBL",
                        "url": "https://www.ensembl.org/id/rs2092025452"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3253,
                "end_pos": 3253,
                "sequence_org": "L",
                "sequence_mut": "Q",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2100026",
                "ref_nt": "T",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "L3253",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs2544713742",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs2544713742"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3254,
                "end_pos": 3254,
                "sequence_org": "Q",
                "sequence_mut": "*",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2100024",
                "ref_nt": "A",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "Q3254",
                "disease": [
                    {
                        "disease_id": "DOID:0080322",
                        "recommended_name": {
                            "id": "DOID:0080322",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0080322",
                            "name": "polycystic kidney disease",
                            "description": "A cystic kidney disease that is characterized by the growth of fluid-filled cysts in the kidneys that reduces kidney function and may lead to kidney failure."
                        },
                        "synonyms": [
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0080322",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0080322"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0110858",
                        "recommended_name": {
                            "id": "DOID:0110858",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0110858",
                            "name": "polycystic kidney disease 1",
                            "description": "A autosomal dominant polycystic kidney disease that has_material_basis_in autosomal dominant inheritance of mutation in the PKD1 gene on chromosome 16p13.3."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "Polycystic Kidney Disease, Adult, Type I",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            },
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            }
                        ]
                    }
                ],
                "keywords": [
                    "ebi",
                    "germline",
                    "disease"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs1313285288",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1313285288"
                    },
                    {
                        "id": "rs1313285288",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs1313285288#frequency_tab"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3254,
                "end_pos": 3254,
                "sequence_org": "Q",
                "sequence_mut": "L",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2100023",
                "ref_nt": "A",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "Q3254",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs1313285288",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1313285288"
                    },
                    {
                        "id": "rs1313285288",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs1313285288#frequency_tab"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3254,
                "end_pos": 3254,
                "sequence_org": "Q",
                "sequence_mut": "R",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2100023",
                "ref_nt": "C",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "Q3254",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs753504044",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs753504044"
                    },
                    {
                        "id": "rs753504044",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs753504044"
                    },
                    {
                        "id": "rs753504044",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs753504044#frequency_tab"
                    },
                    {
                        "id": "rs753504044",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs753504044"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3255,
                "end_pos": 3255,
                "sequence_org": "R",
                "sequence_mut": "C",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2100021",
                "ref_nt": "A",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "R3255",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs1052458360",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1052458360"
                    },
                    {
                        "id": "rs1052458360",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs1052458360#frequency_tab"
                    },
                    {
                        "id": "rs1052458360",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs1052458360"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3255,
                "end_pos": 3255,
                "sequence_org": "R",
                "sequence_mut": "H",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2100020",
                "ref_nt": "T",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "R3255",
                "keywords": [
                    "ebi",
                    "germline",
                    "disease"
                ],
                "disease": [
                    {
                        "disease_id": "DOID:0080322",
                        "recommended_name": {
                            "id": "DOID:0080322",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0080322",
                            "name": "polycystic kidney disease",
                            "description": "A cystic kidney disease that is characterized by the growth of fluid-filled cysts in the kidneys that reduces kidney function and may lead to kidney failure."
                        },
                        "synonyms": [
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0080322",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0080322"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0110858",
                        "recommended_name": {
                            "id": "DOID:0110858",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0110858",
                            "name": "polycystic kidney disease 1",
                            "description": "A autosomal dominant polycystic kidney disease that has_material_basis_in autosomal dominant inheritance of mutation in the PKD1 gene on chromosome 16p13.3."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "Polycystic Kidney Disease, Adult, Type I",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            },
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            }
                        ]
                    }
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs1596512954",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1596512954"
                    },
                    {
                        "id": "rs1596512954",
                        "database": "ENSEMBL",
                        "url": "https://www.ensembl.org/id/rs1596512954"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3256,
                "end_pos": 3256,
                "sequence_org": "G",
                "sequence_mut": "V",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2100017",
                "ref_nt": "A",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "G3256",
                "disease": [
                    {
                        "disease_id": "DOID:0080322",
                        "recommended_name": {
                            "id": "DOID:0080322",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0080322",
                            "name": "polycystic kidney disease",
                            "description": "A cystic kidney disease that is characterized by the growth of fluid-filled cysts in the kidneys that reduces kidney function and may lead to kidney failure."
                        },
                        "synonyms": [
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0080322",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0080322"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0110858",
                        "recommended_name": {
                            "id": "DOID:0110858",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0110858",
                            "name": "polycystic kidney disease 1",
                            "description": "A autosomal dominant polycystic kidney disease that has_material_basis_in autosomal dominant inheritance of mutation in the PKD1 gene on chromosome 16p13.3."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "Polycystic Kidney Disease, Adult, Type I",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            },
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            }
                        ]
                    }
                ],
                "keywords": [
                    "ebi",
                    "germline",
                    "disease"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs1424341066",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1424341066"
                    },
                    {
                        "id": "rs1424341066",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs1424341066"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3259,
                "end_pos": 3259,
                "sequence_org": "D",
                "sequence_mut": "E",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2100007",
                "ref_nt": "C",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "D3259",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs1232180956",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1232180956"
                    },
                    {
                        "id": "rs1232180956",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs1232180956#frequency_tab"
                    },
                    {
                        "id": "rs1232180956",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs1232180956"
                    }
                ],
                "glycoeffect": [
                    "o-glyco-site-loss"
                ],
                "start_pos": 325,
                "end_pos": 325,
                "sequence_org": "Y",
                "sequence_mut": "C",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2118018",
                "ref_nt": "C",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "Y325",
                "keywords": [
                    "ebi",
                    "germline",
                    "disease"
                ],
                "disease": [
                    {
                        "disease_id": "DOID:0080322",
                        "recommended_name": {
                            "id": "DOID:0080322",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0080322",
                            "name": "polycystic kidney disease",
                            "description": "A cystic kidney disease that is characterized by the growth of fluid-filled cysts in the kidneys that reduces kidney function and may lead to kidney failure."
                        },
                        "synonyms": [
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0080322",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0080322"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0110858",
                        "recommended_name": {
                            "id": "DOID:0110858",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0110858",
                            "name": "polycystic kidney disease 1",
                            "description": "A autosomal dominant polycystic kidney disease that has_material_basis_in autosomal dominant inheritance of mutation in the PKD1 gene on chromosome 16p13.3."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "Polycystic Kidney Disease, Adult, Type I",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            },
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            }
                        ]
                    }
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs1232180956",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1232180956"
                    },
                    {
                        "id": "rs1232180956",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs1232180956#frequency_tab"
                    },
                    {
                        "id": "rs1232180956",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs1232180956"
                    }
                ],
                "glycoeffect": [
                    "o-glyco-site-loss"
                ],
                "start_pos": 325,
                "end_pos": 325,
                "sequence_org": "Y",
                "sequence_mut": "F",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2118018",
                "ref_nt": "A",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "Y325",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs2092024973",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs2092024973"
                    },
                    {
                        "id": "rs2092024973",
                        "database": "ENSEMBL",
                        "url": "https://www.ensembl.org/id/rs2092024973"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3260,
                "end_pos": 3260,
                "sequence_org": "K",
                "sequence_mut": "N",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2100004",
                "ref_nt": "G",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "K3260",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs2092024766",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs2092024766"
                    },
                    {
                        "id": "rs2092024766",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs2092024766#frequency_tab"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3262,
                "end_pos": 3262,
                "sequence_org": "I",
                "sequence_mut": "L",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2100000",
                "ref_nt": "G",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "I3262",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs2092024766",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs2092024766"
                    },
                    {
                        "id": "rs2092024766",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs2092024766#frequency_tab"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3262,
                "end_pos": 3262,
                "sequence_org": "I",
                "sequence_mut": "V",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2100000",
                "ref_nt": "C",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "I3262",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs1555449378",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1555449378"
                    },
                    {
                        "id": "rs1555449378",
                        "database": "ENSEMBL",
                        "url": "https://www.ensembl.org/id/rs1555449378"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3263,
                "end_pos": 3263,
                "sequence_org": "W",
                "sequence_mut": "S",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2099996",
                "ref_nt": "G",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "W3263",
                "disease": [
                    {
                        "disease_id": "DOID:0080322",
                        "recommended_name": {
                            "id": "DOID:0080322",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0080322",
                            "name": "polycystic kidney disease",
                            "description": "A cystic kidney disease that is characterized by the growth of fluid-filled cysts in the kidneys that reduces kidney function and may lead to kidney failure."
                        },
                        "synonyms": [
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0080322",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0080322"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0110858",
                        "recommended_name": {
                            "id": "DOID:0110858",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0110858",
                            "name": "polycystic kidney disease 1",
                            "description": "A autosomal dominant polycystic kidney disease that has_material_basis_in autosomal dominant inheritance of mutation in the PKD1 gene on chromosome 16p13.3."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "Polycystic Kidney Disease, Adult, Type I",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            },
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            }
                        ]
                    }
                ],
                "keywords": [
                    "ebi",
                    "germline",
                    "disease"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs1423631782",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1423631782"
                    },
                    {
                        "id": "rs1423631782",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs1423631782"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3264,
                "end_pos": 3264,
                "sequence_org": "L",
                "sequence_mut": "F",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2099994",
                "ref_nt": "A",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "L3264",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs2151739605",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs2151739605"
                    },
                    {
                        "id": "rs2151739605",
                        "database": "ENSEMBL",
                        "url": "https://www.ensembl.org/id/rs2151739605"
                    }
                ],
                "glycoeffect": [
                    "o-glyco-site-loss"
                ],
                "start_pos": 3265,
                "end_pos": 3265,
                "sequence_org": "S",
                "sequence_mut": "A",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2099991",
                "ref_nt": "C",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "S3265",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs1188643869",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1188643869"
                    },
                    {
                        "id": "rs1188643869",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs1188643869#frequency_tab"
                    },
                    {
                        "id": "rs1188643869",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs1188643869"
                    }
                ],
                "glycoeffect": [
                    "o-glyco-site-loss"
                ],
                "start_pos": 3265,
                "end_pos": 3265,
                "sequence_org": "S",
                "sequence_mut": "C",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2099990",
                "ref_nt": "C",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "S3265",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs1188643869",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1188643869"
                    },
                    {
                        "id": "rs1188643869",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs1188643869#frequency_tab"
                    },
                    {
                        "id": "rs1188643869",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs1188643869"
                    }
                ],
                "glycoeffect": [
                    "o-glyco-site-loss"
                ],
                "start_pos": 3265,
                "end_pos": 3265,
                "sequence_org": "S",
                "sequence_mut": "Y",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2099990",
                "ref_nt": "T",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "S3265",
                "keywords": [
                    "ebi",
                    "germline",
                    "disease"
                ],
                "disease": [
                    {
                        "disease_id": "DOID:0080322",
                        "recommended_name": {
                            "id": "DOID:0080322",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0080322",
                            "name": "polycystic kidney disease",
                            "description": "A cystic kidney disease that is characterized by the growth of fluid-filled cysts in the kidneys that reduces kidney function and may lead to kidney failure."
                        },
                        "synonyms": [
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0080322",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0080322"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0110858",
                        "recommended_name": {
                            "id": "DOID:0110858",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0110858",
                            "name": "polycystic kidney disease 1",
                            "description": "A autosomal dominant polycystic kidney disease that has_material_basis_in autosomal dominant inheritance of mutation in the PKD1 gene on chromosome 16p13.3."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "Polycystic Kidney Disease, Adult, Type I",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            },
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            }
                        ]
                    }
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs1198334760",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1198334760"
                    },
                    {
                        "id": "rs1198334760",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs1198334760"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3266,
                "end_pos": 3266,
                "sequence_org": "I",
                "sequence_mut": "M",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2099986",
                "ref_nt": "C",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "I3266",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs761800438",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs761800438"
                    },
                    {
                        "id": "rs761800438",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs761800438"
                    },
                    {
                        "id": "rs761800438",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs761800438#frequency_tab"
                    },
                    {
                        "id": "rs761800438",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs761800438"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3266,
                "end_pos": 3266,
                "sequence_org": "I",
                "sequence_mut": "T",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2099987",
                "ref_nt": "G",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "I3266",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs1460604173",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1460604173"
                    },
                    {
                        "id": "rs1460604173",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs1460604173"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3267,
                "end_pos": 3267,
                "sequence_org": "W",
                "sequence_mut": "*",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2099984",
                "ref_nt": "T",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "W3267",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs1460604173",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1460604173"
                    },
                    {
                        "id": "rs1460604173",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs1460604173"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3267,
                "end_pos": 3267,
                "sequence_org": "W",
                "sequence_mut": "L",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2099984",
                "ref_nt": "A",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "W3267",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "P98161",
                        "database": "BioMuta",
                        "url": "https://hivelab.biochemistry.gwu.edu/biomuta/proteinview/P98161"
                    },
                    {
                        "id": "rs550467690",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs550467690"
                    },
                    {
                        "id": "rs550467690",
                        "database": "1000Genomes",
                        "url": "https://www.ensembl.org/homo_sapiens/Variation/Explore?v=rs550467690"
                    },
                    {
                        "id": "rs550467690",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs550467690"
                    },
                    {
                        "id": "rs550467690",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs550467690#frequency_tab"
                    },
                    {
                        "id": "rs550467690",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs550467690"
                    },
                    {
                        "id": "rs550467690",
                        "database": "COSMIC",
                        "url": "https://www.ensembl.org/homo_sapiens/Variation/Explore?v=rs550467690"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3269,
                "end_pos": 3269,
                "subjects_tested": "2003",
                "subjects_positive": "1",
                "frequency": "0.0",
                "sequence_org": "R",
                "sequence_mut": "L",
                "comment": "Somatic mutation passed 0 out of 6 filters: .",
                "chr_id": "16",
                "chr_pos": "2099978",
                "ref_nt": "C",
                "alt_nt": "A",
                "minor_allelic_frequency": "",
                "site_lbl": "R3269",
                "disease": [
                    {
                        "disease_id": "DOID:3571",
                        "recommended_name": {
                            "id": "DOID:3571",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:3571",
                            "name": "liver cancer",
                            "description": "A hepatobiliary system cancer that is located_in the liver."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:3571",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:3571",
                                "name": "Ca liver - primary",
                                "description": ""
                            },
                            {
                                "id": "DOID:3571",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:3571",
                                "name": "Resectable malignant neoplasm of Liver",
                                "description": ""
                            },
                            {
                                "id": "DOID:3571",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:3571",
                                "name": "hepatic cancer",
                                "description": ""
                            },
                            {
                                "id": "DOID:3571",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:3571",
                                "name": "hepatic neoplasm",
                                "description": ""
                            },
                            {
                                "id": "DOID:3571",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:3571",
                                "name": "malignant hepato-biliary neoplasm",
                                "description": ""
                            },
                            {
                                "id": "DOID:3571",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:3571",
                                "name": "malignant neoplasm of liver",
                                "description": ""
                            },
                            {
                                "id": "DOID:3571",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:3571",
                                "name": "malignant neoplasm of liver, primary",
                                "description": ""
                            },
                            {
                                "id": "DOID:3571",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:3571",
                                "name": "malignant tumor of liver",
                                "description": ""
                            },
                            {
                                "id": "DOID:3571",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:3571",
                                "name": "neoplasm of liver",
                                "description": ""
                            },
                            {
                                "id": "DOID:3571",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:3571",
                                "name": "non-resectable primary hepatic malignant neoplasm",
                                "description": ""
                            },
                            {
                                "id": "DOID:3571",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:3571",
                                "name": "primary liver cancer",
                                "description": ""
                            },
                            {
                                "id": "DOID:3571",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:3571",
                                "name": "primary malignant neoplasm of liver",
                                "description": ""
                            },
                            {
                                "id": "DOID:3571",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:3571",
                                "name": "resectable malignant neoplasm of the liver",
                                "description": ""
                            },
                            {
                                "id": "DOID:3571",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:3571",
                                "name": "malignant neoplasm of liver, not specified as primary or secondary",
                                "description": ""
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "3571",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:3571"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:1324",
                        "recommended_name": {
                            "id": "DOID:1324",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:1324",
                            "name": "lung cancer",
                            "description": "A respiratory system cancer that is located_in the lung."
                        },
                        "synonyms": [
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "lung cancer",
                                "description": "A malignant neoplasm involving the lung."
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "adenocarcinoma of lung, response to tyrosine kinase inhibitor in, autosomal dominant, somatic mutation",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "adenocarcinoma of lung, somatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "cancer of lung",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "lung cancer",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "lung cancer, protection against, autosomal dominant, somatic mutation",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "lung cancer, resistance to, autosomal dominant, somatic mutation",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "lung cancer, somatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "lung cancer, susceptibility to, autosomal dominant, somatic mutation",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "malignant lung neoplasm",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "malignant lung tumor",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "malignant lung tumour",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "malignant neoplasm of lung",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "malignant neoplasm of the lung",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "malignant tumor of lung",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "malignant tumor of the lung",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "malignant tumour of lung",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "malignant tumour of the lung",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "nonsmall cell lung cancer, response to tyrosine kinase inhibitor in, autosomal dominant, somatic mutation",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "nonsmall cell lung cancer, somatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "nonsmall cell lung cancer, susceptibility to, autosomal dominant, somatic mutation",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012159",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012159",
                                "name": "lung cancer susceptibility 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012159",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012159",
                                "name": "LNCR1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012159",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012159",
                                "name": "lung cancer susceptibility",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012159",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012159",
                                "name": "lung cancer susceptibility 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012942",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012942",
                                "name": "lung cancer susceptibility 3",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012942",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012942",
                                "name": "LNCR3",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012942",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012942",
                                "name": "lung cancer susceptibility 3",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012955",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012955",
                                "name": "lung cancer susceptibility 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012955",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012955",
                                "name": "LNCR4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012955",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012955",
                                "name": "lung cancer susceptibility 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0013631",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0013631",
                                "name": "lung cancer susceptibility 5",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0013631",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0013631",
                                "name": "LNCR5",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0013631",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0013631",
                                "name": "lung cancer susceptibility 5",
                                "description": ""
                            },
                            {
                                "id": "MIM:211980",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/211980",
                                "name": "Lung cancer",
                                "description": "Lung cancer"
                            }
                        ],
                        "unlinked_id_list": [
                            "DOID:4765"
                        ],
                        "evidence": [
                            {
                                "id": "1324",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:1324"
                            }
                        ]
                    }
                ],
                "keywords": [
                    "biomuta",
                    "somatic",
                    "cancer",
                    "disease",
                    "ebi"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs550467690",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs550467690"
                    },
                    {
                        "id": "rs550467690",
                        "database": "1000Genomes",
                        "url": "https://www.ensembl.org/homo_sapiens/Variation/Explore?v=rs550467690"
                    },
                    {
                        "id": "rs550467690",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs550467690"
                    },
                    {
                        "id": "rs550467690",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs550467690#frequency_tab"
                    },
                    {
                        "id": "rs550467690",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs550467690"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3269,
                "end_pos": 3269,
                "sequence_org": "R",
                "sequence_mut": "Q",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2099978",
                "ref_nt": "T",
                "alt_nt": "null",
                "minor_allelic_frequency": "0.0002",
                "site_lbl": "R3269",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs980803513",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs980803513"
                    },
                    {
                        "id": "rs980803513",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs980803513#frequency_tab"
                    },
                    {
                        "id": "rs980803513",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs980803513"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3269,
                "end_pos": 3269,
                "sequence_org": "R",
                "sequence_mut": "W",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2099979",
                "ref_nt": "A",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "R3269",
                "disease": [
                    {
                        "disease_id": "DOID:0080322",
                        "recommended_name": {
                            "id": "DOID:0080322",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0080322",
                            "name": "polycystic kidney disease",
                            "description": "A cystic kidney disease that is characterized by the growth of fluid-filled cysts in the kidneys that reduces kidney function and may lead to kidney failure."
                        },
                        "synonyms": [
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0080322",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0080322"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0110858",
                        "recommended_name": {
                            "id": "DOID:0110858",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0110858",
                            "name": "polycystic kidney disease 1",
                            "description": "A autosomal dominant polycystic kidney disease that has_material_basis_in autosomal dominant inheritance of mutation in the PKD1 gene on chromosome 16p13.3."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "Polycystic Kidney Disease, Adult, Type I",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            },
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            }
                        ]
                    }
                ],
                "keywords": [
                    "ebi",
                    "germline",
                    "disease"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs763040931",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs763040931"
                    },
                    {
                        "id": "rs763040931",
                        "database": "1000Genomes",
                        "url": "https://www.ensembl.org/homo_sapiens/Variation/Explore?v=rs763040931"
                    },
                    {
                        "id": "rs763040931",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs763040931"
                    },
                    {
                        "id": "rs763040931",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs763040931#frequency_tab"
                    },
                    {
                        "id": "rs763040931",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs763040931"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3270,
                "end_pos": 3270,
                "sequence_org": "P",
                "sequence_mut": "L",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2099975",
                "ref_nt": "A",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "P3270",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs2092023462",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs2092023462"
                    },
                    {
                        "id": "rs2092023462",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs2092023462#frequency_tab"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3270,
                "end_pos": 3270,
                "sequence_org": "P",
                "sequence_mut": "S",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2099976",
                "ref_nt": "A",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "P3270",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs143453080",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs143453080"
                    },
                    {
                        "id": "rs143453080",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs143453080"
                    },
                    {
                        "id": "rs143453080",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs143453080#frequency_tab"
                    },
                    {
                        "id": "rs143453080",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs143453080"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3272,
                "end_pos": 3272,
                "sequence_org": "R",
                "sequence_mut": "C",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2099970",
                "ref_nt": "A",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "R3272",
                "disease": [
                    {
                        "disease_id": "DOID:0080322",
                        "recommended_name": {
                            "id": "DOID:0080322",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0080322",
                            "name": "polycystic kidney disease",
                            "description": "A cystic kidney disease that is characterized by the growth of fluid-filled cysts in the kidneys that reduces kidney function and may lead to kidney failure."
                        },
                        "synonyms": [
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0080322",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0080322"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0110858",
                        "recommended_name": {
                            "id": "DOID:0110858",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0110858",
                            "name": "polycystic kidney disease 1",
                            "description": "A autosomal dominant polycystic kidney disease that has_material_basis_in autosomal dominant inheritance of mutation in the PKD1 gene on chromosome 16p13.3."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "Polycystic Kidney Disease, Adult, Type I",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            },
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            }
                        ]
                    }
                ],
                "keywords": [
                    "ebi",
                    "germline",
                    "disease"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "P98161",
                        "database": "BioMuta",
                        "url": "https://hivelab.biochemistry.gwu.edu/biomuta/proteinview/P98161"
                    },
                    {
                        "id": "rs1452116333",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1452116333"
                    },
                    {
                        "id": "rs1452116333",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs1452116333#frequency_tab"
                    },
                    {
                        "id": "rs1452116333",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs1452116333"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3272,
                "end_pos": 3272,
                "subjects_tested": "2670",
                "subjects_positive": "1",
                "frequency": "0.0",
                "sequence_org": "R",
                "sequence_mut": "H",
                "comment": "Somatic mutation passed 0 out of 6 filters: .",
                "chr_id": "16",
                "chr_pos": "2099969",
                "ref_nt": "C",
                "alt_nt": "T",
                "minor_allelic_frequency": "",
                "site_lbl": "R3272",
                "disease": [
                    {
                        "disease_id": "DOID:1319",
                        "recommended_name": {
                            "id": "DOID:1319",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:1319",
                            "name": "brain cancer",
                            "description": "A central nervous system cancer that is characterized by the growth of abnormal cells in the tissues of the brain."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:1319",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:1319",
                                "name": "BT - Brain tumour",
                                "description": ""
                            },
                            {
                                "id": "DOID:1319",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:1319",
                                "name": "adult brain tumor",
                                "description": ""
                            },
                            {
                                "id": "DOID:1319",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:1319",
                                "name": "adult malignant brain neoplasm",
                                "description": ""
                            },
                            {
                                "id": "DOID:1319",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:1319",
                                "name": "brain neoplasm",
                                "description": ""
                            },
                            {
                                "id": "DOID:1319",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:1319",
                                "name": "brain neoplasm, adult",
                                "description": ""
                            },
                            {
                                "id": "DOID:1319",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:1319",
                                "name": "malignant brain tumour",
                                "description": ""
                            },
                            {
                                "id": "DOID:1319",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:1319",
                                "name": "malignant primary brain neoplasm",
                                "description": ""
                            },
                            {
                                "id": "DOID:1319",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:1319",
                                "name": "malignant primary brain tumor",
                                "description": ""
                            },
                            {
                                "id": "DOID:1319",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:1319",
                                "name": "malignant tumor of Brain",
                                "description": ""
                            },
                            {
                                "id": "DOID:1319",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:1319",
                                "name": "malignant tumor of adult brain",
                                "description": ""
                            },
                            {
                                "id": "DOID:1319",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:1319",
                                "name": "neoplasm of brain",
                                "description": ""
                            },
                            {
                                "id": "DOID:1319",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:1319",
                                "name": "primary brain neoplasm",
                                "description": ""
                            },
                            {
                                "id": "DOID:1319",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:1319",
                                "name": "primary brain tumor",
                                "description": ""
                            },
                            {
                                "id": "DOID:1319",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:1319",
                                "name": "primary malignant neoplasm of brain",
                                "description": ""
                            },
                            {
                                "id": "DOID:1319",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:1319",
                                "name": "tumor of the Brain",
                                "description": ""
                            }
                        ],
                        "unlinked_id_list": [
                            "DOID:4203",
                            "DOID:3541",
                            "DOID:4706",
                            "DOID:1659",
                            "DOID:368"
                        ],
                        "evidence": [
                            {
                                "id": "1319",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:1319"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0080322",
                        "recommended_name": {
                            "id": "DOID:0080322",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0080322",
                            "name": "polycystic kidney disease",
                            "description": "A cystic kidney disease that is characterized by the growth of fluid-filled cysts in the kidneys that reduces kidney function and may lead to kidney failure."
                        },
                        "synonyms": [
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0080322",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0080322"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0110858",
                        "recommended_name": {
                            "id": "DOID:0110858",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0110858",
                            "name": "polycystic kidney disease 1",
                            "description": "A autosomal dominant polycystic kidney disease that has_material_basis_in autosomal dominant inheritance of mutation in the PKD1 gene on chromosome 16p13.3."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "Polycystic Kidney Disease, Adult, Type I",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            },
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            }
                        ]
                    }
                ],
                "keywords": [
                    "biomuta",
                    "somatic",
                    "cancer",
                    "disease",
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs1333442702",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1333442702"
                    },
                    {
                        "id": "rs1333442702",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs1333442702"
                    }
                ],
                "glycoeffect": [
                    "o-glyco-site-loss"
                ],
                "start_pos": 3273,
                "end_pos": 3273,
                "sequence_org": "S",
                "sequence_mut": "C",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2099967",
                "ref_nt": "A",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "S3273",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs1464171367",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1464171367"
                    },
                    {
                        "id": "rs1464171367",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs1464171367"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3273,
                "end_pos": 3273,
                "sequence_org": "S",
                "sequence_mut": "T",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2099966",
                "ref_nt": "G",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "S3273",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "P98161",
                        "database": "BioMuta",
                        "url": "https://hivelab.biochemistry.gwu.edu/biomuta/proteinview/P98161"
                    },
                    {
                        "id": "rs531854741",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs531854741"
                    },
                    {
                        "id": "rs531854741",
                        "database": "1000Genomes",
                        "url": "https://www.ensembl.org/homo_sapiens/Variation/Explore?v=rs531854741"
                    },
                    {
                        "id": "rs531854741",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs531854741"
                    },
                    {
                        "id": "rs531854741",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs531854741#frequency_tab"
                    },
                    {
                        "id": "rs531854741",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs531854741"
                    },
                    {
                        "id": "rs531854741",
                        "database": "COSMIC",
                        "url": "https://www.ensembl.org/homo_sapiens/Variation/Explore?v=rs531854741"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3274,
                "end_pos": 3274,
                "subjects_tested": "2053",
                "subjects_positive": "1",
                "frequency": "0.0",
                "sequence_org": "R",
                "sequence_mut": "C",
                "comment": "Somatic mutation passed 0 out of 6 filters: .",
                "chr_id": "16",
                "chr_pos": "2099964",
                "ref_nt": "G",
                "alt_nt": "A",
                "minor_allelic_frequency": "",
                "site_lbl": "R3274",
                "disease": [
                    {
                        "disease_id": "DOID:4159",
                        "recommended_name": {
                            "id": "DOID:4159",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:4159",
                            "name": "skin cancer",
                            "description": "An integumentary system cancer located_in the skin that is the uncontrolled growth of abnormal skin cells."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:4159",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:4159",
                                "name": "CA - skin cancer",
                                "description": ""
                            },
                            {
                                "id": "DOID:4159",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:4159",
                                "name": "malignant neoplasm of skin",
                                "description": ""
                            },
                            {
                                "id": "DOID:4159",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:4159",
                                "name": "melanoma and Non-melanoma skin cancer",
                                "description": ""
                            }
                        ],
                        "unlinked_id_list": [
                            "DOID:3149",
                            "DOID:3451"
                        ],
                        "evidence": [
                            {
                                "id": "4159",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:4159"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0080322",
                        "recommended_name": {
                            "id": "DOID:0080322",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0080322",
                            "name": "polycystic kidney disease",
                            "description": "A cystic kidney disease that is characterized by the growth of fluid-filled cysts in the kidneys that reduces kidney function and may lead to kidney failure."
                        },
                        "synonyms": [
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0080322",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0080322"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0110858",
                        "recommended_name": {
                            "id": "DOID:0110858",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0110858",
                            "name": "polycystic kidney disease 1",
                            "description": "A autosomal dominant polycystic kidney disease that has_material_basis_in autosomal dominant inheritance of mutation in the PKD1 gene on chromosome 16p13.3."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "Polycystic Kidney Disease, Adult, Type I",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            },
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            }
                        ]
                    }
                ],
                "keywords": [
                    "biomuta",
                    "somatic",
                    "cancer",
                    "disease",
                    "ebi"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs771445965",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs771445965"
                    },
                    {
                        "id": "rs771445965",
                        "database": "1000Genomes",
                        "url": "https://www.ensembl.org/homo_sapiens/Variation/Explore?v=rs771445965"
                    },
                    {
                        "id": "rs771445965",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs771445965"
                    },
                    {
                        "id": "rs771445965",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs771445965#frequency_tab"
                    },
                    {
                        "id": "rs771445965",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs771445965"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3274,
                "end_pos": 3274,
                "sequence_org": "R",
                "sequence_mut": "H",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2099963",
                "ref_nt": "T",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "R3274",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs771445965",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs771445965"
                    },
                    {
                        "id": "rs771445965",
                        "database": "1000Genomes",
                        "url": "https://www.ensembl.org/homo_sapiens/Variation/Explore?v=rs771445965"
                    },
                    {
                        "id": "rs771445965",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs771445965"
                    },
                    {
                        "id": "rs771445965",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs771445965#frequency_tab"
                    },
                    {
                        "id": "rs771445965",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs771445965"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3274,
                "end_pos": 3274,
                "sequence_org": "R",
                "sequence_mut": "L",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2099963",
                "ref_nt": "A",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "R3274",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs1172286668",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1172286668"
                    },
                    {
                        "id": "rs1172286668",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs1172286668#frequency_tab"
                    },
                    {
                        "id": "rs1172286668",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs1172286668"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3275,
                "end_pos": 3275,
                "sequence_org": "F",
                "sequence_mut": "Y",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2099960",
                "ref_nt": "T",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "F3275",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs1474079108",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1474079108"
                    },
                    {
                        "id": "rs1474079108",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs1474079108#frequency_tab"
                    },
                    {
                        "id": "rs1474079108",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs1474079108"
                    }
                ],
                "glycoeffect": [
                    "o-glyco-site-loss"
                ],
                "start_pos": 3276,
                "end_pos": 3276,
                "sequence_org": "T",
                "sequence_mut": "A",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2099958",
                "ref_nt": "C",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "T3276",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs1367020335",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1367020335"
                    }
                ],
                "glycoeffect": [
                    "o-glyco-site-loss"
                ],
                "start_pos": 3276,
                "end_pos": 3276,
                "sequence_org": "T",
                "sequence_mut": "I",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2099957",
                "ref_nt": "A",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "T3276",
                "disease": [
                    {
                        "disease_id": "DOID:0080322",
                        "recommended_name": {
                            "id": "DOID:0080322",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0080322",
                            "name": "polycystic kidney disease",
                            "description": "A cystic kidney disease that is characterized by the growth of fluid-filled cysts in the kidneys that reduces kidney function and may lead to kidney failure."
                        },
                        "synonyms": [
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0080322",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0080322"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0110858",
                        "recommended_name": {
                            "id": "DOID:0110858",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0110858",
                            "name": "polycystic kidney disease 1",
                            "description": "A autosomal dominant polycystic kidney disease that has_material_basis_in autosomal dominant inheritance of mutation in the PKD1 gene on chromosome 16p13.3."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "Polycystic Kidney Disease, Adult, Type I",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            },
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            }
                        ]
                    }
                ],
                "keywords": [
                    "ebi",
                    "germline",
                    "disease"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs1367020335",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1367020335"
                    },
                    {
                        "id": "rs1367020335",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs1367020335#frequency_tab"
                    },
                    {
                        "id": "rs1367020335",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs1367020335"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3276,
                "end_pos": 3276,
                "sequence_org": "T",
                "sequence_mut": "S",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2099957",
                "ref_nt": "C",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "T3276",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs1596512729",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1596512729"
                    }
                ],
                "glycoeffect": [
                    "o-glyco-site-loss"
                ],
                "start_pos": 3276,
                "end_pos": 3276,
                "sequence_org": "T",
                "sequence_mut": "null",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2099957_2099960",
                "ref_nt": "l",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "T3276",
                "disease": [
                    {
                        "disease_id": "DOID:0080322",
                        "recommended_name": {
                            "id": "DOID:0080322",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0080322",
                            "name": "polycystic kidney disease",
                            "description": "A cystic kidney disease that is characterized by the growth of fluid-filled cysts in the kidneys that reduces kidney function and may lead to kidney failure."
                        },
                        "synonyms": [
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0080322",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0080322"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0110858",
                        "recommended_name": {
                            "id": "DOID:0110858",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0110858",
                            "name": "polycystic kidney disease 1",
                            "description": "A autosomal dominant polycystic kidney disease that has_material_basis_in autosomal dominant inheritance of mutation in the PKD1 gene on chromosome 16p13.3."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "Polycystic Kidney Disease, Adult, Type I",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            },
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            }
                        ]
                    }
                ],
                "keywords": [
                    "ebi",
                    "germline",
                    "disease"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs148812376",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs148812376"
                    },
                    {
                        "id": "rs148812376",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs148812376"
                    },
                    {
                        "id": "rs148812376",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs148812376#frequency_tab"
                    },
                    {
                        "id": "rs148812376",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs148812376"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3277,
                "end_pos": 3277,
                "sequence_org": "R",
                "sequence_mut": "C",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2099955",
                "ref_nt": "A",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "R3277",
                "keywords": [
                    "ebi",
                    "germline",
                    "disease"
                ],
                "disease": [
                    {
                        "disease_id": "DOID:0080322",
                        "recommended_name": {
                            "id": "DOID:0080322",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0080322",
                            "name": "polycystic kidney disease",
                            "description": "A cystic kidney disease that is characterized by the growth of fluid-filled cysts in the kidneys that reduces kidney function and may lead to kidney failure."
                        },
                        "synonyms": [
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0080322",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0080322"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0110858",
                        "recommended_name": {
                            "id": "DOID:0110858",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0110858",
                            "name": "polycystic kidney disease 1",
                            "description": "A autosomal dominant polycystic kidney disease that has_material_basis_in autosomal dominant inheritance of mutation in the PKD1 gene on chromosome 16p13.3."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "Polycystic Kidney Disease, Adult, Type I",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            },
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            }
                        ]
                    }
                ]
            },
            {
                "evidence": [
                    {
                        "id": "P98161",
                        "database": "BioMuta",
                        "url": "https://hivelab.biochemistry.gwu.edu/biomuta/proteinview/P98161"
                    },
                    {
                        "id": "rs1238446180",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1238446180"
                    },
                    {
                        "id": "rs1238446180",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs1238446180"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3277,
                "end_pos": 3277,
                "subjects_tested": "1704",
                "subjects_positive": "1",
                "frequency": "0.1",
                "sequence_org": "R",
                "sequence_mut": "H",
                "comment": "Somatic mutation passed 0 out of 6 filters: .",
                "chr_id": "16",
                "chr_pos": "2099954",
                "ref_nt": "C",
                "alt_nt": "T",
                "minor_allelic_frequency": "",
                "site_lbl": "R3277",
                "disease": [
                    {
                        "disease_id": "DOID:363",
                        "recommended_name": {
                            "id": "DOID:363",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:363",
                            "name": "uterine cancer",
                            "description": "A female reproductive organ cancer that is located_in the uterus."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:363",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:363",
                                "name": "CA - cancer of uterus",
                                "description": ""
                            },
                            {
                                "id": "DOID:363",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:363",
                                "name": "Tumour of uterus",
                                "description": ""
                            },
                            {
                                "id": "DOID:363",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:363",
                                "name": "malignant neoplasm of uterus",
                                "description": ""
                            },
                            {
                                "id": "DOID:363",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:363",
                                "name": "malignant uterine tumor",
                                "description": ""
                            },
                            {
                                "id": "DOID:363",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:363",
                                "name": "neoplasm of uterus",
                                "description": ""
                            },
                            {
                                "id": "DOID:363",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:363",
                                "name": "uterine tumor",
                                "description": ""
                            },
                            {
                                "id": "DOID:363",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:363",
                                "name": "uterus neoplasm",
                                "description": ""
                            }
                        ],
                        "unlinked_id_list": [
                            "DOID:9460",
                            "DOID:5166",
                            "DOID:2021",
                            "DOID:4114"
                        ],
                        "evidence": [
                            {
                                "id": "363",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:363"
                            }
                        ]
                    }
                ],
                "keywords": [
                    "biomuta",
                    "somatic",
                    "cancer",
                    "disease",
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs1271687787",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1271687787"
                    },
                    {
                        "id": "rs1271687787",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs1271687787"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3279,
                "end_pos": 3279,
                "sequence_org": "Q",
                "sequence_mut": "R",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2099948",
                "ref_nt": "C",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "Q3279",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs778455860",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs778455860"
                    },
                    {
                        "id": "rs778455860",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs778455860"
                    },
                    {
                        "id": "rs778455860",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs778455860#frequency_tab"
                    },
                    {
                        "id": "rs778455860",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs778455860"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3281,
                "end_pos": 3281,
                "sequence_org": "A",
                "sequence_mut": "G",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2099942",
                "ref_nt": "C",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "A3281",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs1210319842",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1210319842"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3281,
                "end_pos": 3281,
                "sequence_org": "A",
                "sequence_mut": "P",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2099943",
                "ref_nt": "G",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "A3281",
                "disease": [
                    {
                        "disease_id": "DOID:0080322",
                        "recommended_name": {
                            "id": "DOID:0080322",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0080322",
                            "name": "polycystic kidney disease",
                            "description": "A cystic kidney disease that is characterized by the growth of fluid-filled cysts in the kidneys that reduces kidney function and may lead to kidney failure."
                        },
                        "synonyms": [
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0080322",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0080322"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0110858",
                        "recommended_name": {
                            "id": "DOID:0110858",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0110858",
                            "name": "polycystic kidney disease 1",
                            "description": "A autosomal dominant polycystic kidney disease that has_material_basis_in autosomal dominant inheritance of mutation in the PKD1 gene on chromosome 16p13.3."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "Polycystic Kidney Disease, Adult, Type I",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            },
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            }
                        ]
                    }
                ],
                "keywords": [
                    "ebi",
                    "germline",
                    "disease"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs1210319842",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1210319842"
                    },
                    {
                        "id": "rs1210319842",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs1210319842"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3281,
                "end_pos": 3281,
                "sequence_org": "A",
                "sequence_mut": "T",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2099943",
                "ref_nt": "T",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "A3281",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs2092021706",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs2092021706"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3281,
                "end_pos": 3281,
                "sequence_org": "A",
                "sequence_mut": "null",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2099945",
                "ref_nt": "l",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "A3281",
                "disease": [
                    {
                        "disease_id": "DOID:0080322",
                        "recommended_name": {
                            "id": "DOID:0080322",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0080322",
                            "name": "polycystic kidney disease",
                            "description": "A cystic kidney disease that is characterized by the growth of fluid-filled cysts in the kidneys that reduces kidney function and may lead to kidney failure."
                        },
                        "synonyms": [
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0080322",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0080322"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0110858",
                        "recommended_name": {
                            "id": "DOID:0110858",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0110858",
                            "name": "polycystic kidney disease 1",
                            "description": "A autosomal dominant polycystic kidney disease that has_material_basis_in autosomal dominant inheritance of mutation in the PKD1 gene on chromosome 16p13.3."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "Polycystic Kidney Disease, Adult, Type I",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            },
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            }
                        ]
                    }
                ],
                "keywords": [
                    "ebi",
                    "germline",
                    "disease"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "P98161",
                        "database": "BioMuta",
                        "url": "https://hivelab.biochemistry.gwu.edu/biomuta/proteinview/P98161"
                    }
                ],
                "glycoeffect": [
                    "n-glyco-sequon-gain",
                    "o-glyco-site-loss"
                ],
                "start_pos": 3282,
                "end_pos": 3282,
                "subjects_tested": "2003",
                "subjects_positive": "1",
                "frequency": "0.0",
                "sequence_org": "T",
                "sequence_mut": "N",
                "comment": "Somatic mutation passed 1 out of 6 filters: n-glyco-sequon-gain (TCC->NCC).",
                "chr_id": "16",
                "chr_pos": "2099939",
                "ref_nt": "G",
                "alt_nt": "T",
                "minor_allelic_frequency": "",
                "site_lbl": "T3282",
                "disease": [
                    {
                        "disease_id": "DOID:3571",
                        "recommended_name": {
                            "id": "DOID:3571",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:3571",
                            "name": "liver cancer",
                            "description": "A hepatobiliary system cancer that is located_in the liver."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:3571",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:3571",
                                "name": "Ca liver - primary",
                                "description": ""
                            },
                            {
                                "id": "DOID:3571",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:3571",
                                "name": "Resectable malignant neoplasm of Liver",
                                "description": ""
                            },
                            {
                                "id": "DOID:3571",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:3571",
                                "name": "hepatic cancer",
                                "description": ""
                            },
                            {
                                "id": "DOID:3571",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:3571",
                                "name": "hepatic neoplasm",
                                "description": ""
                            },
                            {
                                "id": "DOID:3571",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:3571",
                                "name": "malignant hepato-biliary neoplasm",
                                "description": ""
                            },
                            {
                                "id": "DOID:3571",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:3571",
                                "name": "malignant neoplasm of liver",
                                "description": ""
                            },
                            {
                                "id": "DOID:3571",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:3571",
                                "name": "malignant neoplasm of liver, primary",
                                "description": ""
                            },
                            {
                                "id": "DOID:3571",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:3571",
                                "name": "malignant tumor of liver",
                                "description": ""
                            },
                            {
                                "id": "DOID:3571",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:3571",
                                "name": "neoplasm of liver",
                                "description": ""
                            },
                            {
                                "id": "DOID:3571",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:3571",
                                "name": "non-resectable primary hepatic malignant neoplasm",
                                "description": ""
                            },
                            {
                                "id": "DOID:3571",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:3571",
                                "name": "primary liver cancer",
                                "description": ""
                            },
                            {
                                "id": "DOID:3571",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:3571",
                                "name": "primary malignant neoplasm of liver",
                                "description": ""
                            },
                            {
                                "id": "DOID:3571",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:3571",
                                "name": "resectable malignant neoplasm of the liver",
                                "description": ""
                            },
                            {
                                "id": "DOID:3571",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:3571",
                                "name": "malignant neoplasm of liver, not specified as primary or secondary",
                                "description": ""
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "3571",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:3571"
                            }
                        ]
                    }
                ],
                "keywords": [
                    "biomuta",
                    "somatic",
                    "cancer",
                    "disease"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs2092021242",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs2092021242"
                    },
                    {
                        "id": "rs2092021242",
                        "database": "ENSEMBL",
                        "url": "https://www.ensembl.org/id/rs2092021242"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3283,
                "end_pos": 3283,
                "sequence_org": "C",
                "sequence_mut": "R",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2099937",
                "ref_nt": "G",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "C3283",
                "disease": [
                    {
                        "disease_id": "DOID:0080322",
                        "recommended_name": {
                            "id": "DOID:0080322",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0080322",
                            "name": "polycystic kidney disease",
                            "description": "A cystic kidney disease that is characterized by the growth of fluid-filled cysts in the kidneys that reduces kidney function and may lead to kidney failure."
                        },
                        "synonyms": [
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0080322",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0080322"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0110858",
                        "recommended_name": {
                            "id": "DOID:0110858",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0110858",
                            "name": "polycystic kidney disease 1",
                            "description": "A autosomal dominant polycystic kidney disease that has_material_basis_in autosomal dominant inheritance of mutation in the PKD1 gene on chromosome 16p13.3."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "Polycystic Kidney Disease, Adult, Type I",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            },
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            }
                        ]
                    }
                ],
                "keywords": [
                    "ebi",
                    "germline",
                    "disease"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs2544712917",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs2544712917"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3284,
                "end_pos": 3284,
                "sequence_org": "C",
                "sequence_mut": "R",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2099934",
                "ref_nt": "G",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "C3284",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "P98161",
                        "database": "BioMuta",
                        "url": "https://hivelab.biochemistry.gwu.edu/biomuta/proteinview/P98161"
                    },
                    {
                        "id": "rs2544712909",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs2544712909"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3284,
                "end_pos": 3284,
                "subjects_tested": "3601",
                "subjects_positive": "1",
                "frequency": "0.0",
                "sequence_org": "C",
                "sequence_mut": "Y",
                "comment": "Somatic mutation passed 0 out of 6 filters: .",
                "chr_id": "16",
                "chr_pos": "2099933",
                "ref_nt": "C",
                "alt_nt": "T",
                "minor_allelic_frequency": "",
                "site_lbl": "C3284",
                "disease": [
                    {
                        "disease_id": "DOID:9256",
                        "recommended_name": {
                            "id": "DOID:9256",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:9256",
                            "name": "colorectal cancer",
                            "description": "A large intestine cancer that is located_in the colon and/or located_in the rectum."
                        },
                        "synonyms": [
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectal cancer",
                                "description": "A primary or metastatic malignant neoplasm that affects the colon or rectum. Representative examples include carcinoma, lymphoma, and sarcoma."
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "cancer of colorectum",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "cancer of large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "cancer of large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "cancer of the large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colon cancer, advanced, somatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colon cancer, somatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectal cancer",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectal cancer with chromosomal instability, somatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectal cancer, autosomal dominant, somatic mutation",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectal cancer, somatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectal cancer, susceptibility to, autosomal dominant, somatic mutation",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectum cancer",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant colorectal neoplasm",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant colorectal tumor",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant colorectal tumour",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant colorectum neoplasm",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant large bowel neoplasm",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant large bowel tumor",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant large bowel tumour",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant large intestine neoplasm",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant large intestine tumor",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant large intestine tumour",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant neoplasm of colorectum",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant neoplasm of large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant neoplasm of large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant neoplasm of the large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant neoplasm of the large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumor of large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumor of large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumor of the large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumor of the large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumour of large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumour of large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumour of the large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumour of the large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "CRC",
                                "description": ""
                            },
                            {
                                "id": "MIM:114500",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/114500",
                                "name": "Colorectal cancer",
                                "description": "Colorectal cancer"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "9256",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:9256"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0080322",
                        "recommended_name": {
                            "id": "DOID:0080322",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0080322",
                            "name": "polycystic kidney disease",
                            "description": "A cystic kidney disease that is characterized by the growth of fluid-filled cysts in the kidneys that reduces kidney function and may lead to kidney failure."
                        },
                        "synonyms": [
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0080322",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0080322"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0110858",
                        "recommended_name": {
                            "id": "DOID:0110858",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0110858",
                            "name": "polycystic kidney disease 1",
                            "description": "A autosomal dominant polycystic kidney disease that has_material_basis_in autosomal dominant inheritance of mutation in the PKD1 gene on chromosome 16p13.3."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "Polycystic Kidney Disease, Adult, Type I",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            },
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            }
                        ]
                    }
                ],
                "keywords": [
                    "biomuta",
                    "somatic",
                    "cancer",
                    "disease",
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "P98161",
                        "database": "BioMuta",
                        "url": "https://hivelab.biochemistry.gwu.edu/biomuta/proteinview/P98161"
                    },
                    {
                        "id": "rs201780393",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs201780393"
                    },
                    {
                        "id": "rs201780393",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs201780393#frequency_tab"
                    },
                    {
                        "id": "rs201780393",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs201780393"
                    },
                    {
                        "id": "rs201780393",
                        "database": "COSMIC",
                        "url": "https://www.ensembl.org/homo_sapiens/Variation/Explore?v=rs201780393"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3285,
                "end_pos": 3285,
                "subjects_tested": "2003",
                "subjects_positive": "1",
                "frequency": "0.0",
                "sequence_org": "V",
                "sequence_mut": "I",
                "comment": "Somatic mutation passed 0 out of 6 filters: .",
                "chr_id": "16",
                "chr_pos": "2099931",
                "ref_nt": "C",
                "alt_nt": "T",
                "minor_allelic_frequency": "",
                "site_lbl": "V3285",
                "disease": [
                    {
                        "disease_id": "DOID:3571",
                        "recommended_name": {
                            "id": "DOID:3571",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:3571",
                            "name": "liver cancer",
                            "description": "A hepatobiliary system cancer that is located_in the liver."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:3571",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:3571",
                                "name": "Ca liver - primary",
                                "description": ""
                            },
                            {
                                "id": "DOID:3571",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:3571",
                                "name": "Resectable malignant neoplasm of Liver",
                                "description": ""
                            },
                            {
                                "id": "DOID:3571",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:3571",
                                "name": "hepatic cancer",
                                "description": ""
                            },
                            {
                                "id": "DOID:3571",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:3571",
                                "name": "hepatic neoplasm",
                                "description": ""
                            },
                            {
                                "id": "DOID:3571",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:3571",
                                "name": "malignant hepato-biliary neoplasm",
                                "description": ""
                            },
                            {
                                "id": "DOID:3571",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:3571",
                                "name": "malignant neoplasm of liver",
                                "description": ""
                            },
                            {
                                "id": "DOID:3571",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:3571",
                                "name": "malignant neoplasm of liver, primary",
                                "description": ""
                            },
                            {
                                "id": "DOID:3571",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:3571",
                                "name": "malignant tumor of liver",
                                "description": ""
                            },
                            {
                                "id": "DOID:3571",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:3571",
                                "name": "neoplasm of liver",
                                "description": ""
                            },
                            {
                                "id": "DOID:3571",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:3571",
                                "name": "non-resectable primary hepatic malignant neoplasm",
                                "description": ""
                            },
                            {
                                "id": "DOID:3571",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:3571",
                                "name": "primary liver cancer",
                                "description": ""
                            },
                            {
                                "id": "DOID:3571",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:3571",
                                "name": "primary malignant neoplasm of liver",
                                "description": ""
                            },
                            {
                                "id": "DOID:3571",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:3571",
                                "name": "resectable malignant neoplasm of the liver",
                                "description": ""
                            },
                            {
                                "id": "DOID:3571",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:3571",
                                "name": "malignant neoplasm of liver, not specified as primary or secondary",
                                "description": ""
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "3571",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:3571"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:9256",
                        "recommended_name": {
                            "id": "DOID:9256",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:9256",
                            "name": "colorectal cancer",
                            "description": "A large intestine cancer that is located_in the colon and/or located_in the rectum."
                        },
                        "synonyms": [
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectal cancer",
                                "description": "A primary or metastatic malignant neoplasm that affects the colon or rectum. Representative examples include carcinoma, lymphoma, and sarcoma."
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "cancer of colorectum",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "cancer of large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "cancer of large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "cancer of the large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colon cancer, advanced, somatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colon cancer, somatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectal cancer",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectal cancer with chromosomal instability, somatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectal cancer, autosomal dominant, somatic mutation",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectal cancer, somatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectal cancer, susceptibility to, autosomal dominant, somatic mutation",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectum cancer",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant colorectal neoplasm",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant colorectal tumor",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant colorectal tumour",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant colorectum neoplasm",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant large bowel neoplasm",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant large bowel tumor",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant large bowel tumour",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant large intestine neoplasm",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant large intestine tumor",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant large intestine tumour",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant neoplasm of colorectum",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant neoplasm of large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant neoplasm of large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant neoplasm of the large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant neoplasm of the large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumor of large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumor of large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumor of the large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumor of the large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumour of large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumour of large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumour of the large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumour of the large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "CRC",
                                "description": ""
                            },
                            {
                                "id": "MIM:114500",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/114500",
                                "name": "Colorectal cancer",
                                "description": "Colorectal cancer"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "9256",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:9256"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0080322",
                        "recommended_name": {
                            "id": "DOID:0080322",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0080322",
                            "name": "polycystic kidney disease",
                            "description": "A cystic kidney disease that is characterized by the growth of fluid-filled cysts in the kidneys that reduces kidney function and may lead to kidney failure."
                        },
                        "synonyms": [
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0080322",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0080322"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0110858",
                        "recommended_name": {
                            "id": "DOID:0110858",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0110858",
                            "name": "polycystic kidney disease 1",
                            "description": "A autosomal dominant polycystic kidney disease that has_material_basis_in autosomal dominant inheritance of mutation in the PKD1 gene on chromosome 16p13.3."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "Polycystic Kidney Disease, Adult, Type I",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            },
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            }
                        ]
                    }
                ],
                "keywords": [
                    "biomuta",
                    "somatic",
                    "cancer",
                    "disease",
                    "ebi"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs1324313309",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1324313309"
                    },
                    {
                        "id": "rs1324313309",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs1324313309#frequency_tab"
                    },
                    {
                        "id": "rs1324313309",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs1324313309"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3286,
                "end_pos": 3286,
                "sequence_org": "L",
                "sequence_mut": "H",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2099927",
                "ref_nt": "T",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "L3286",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs866033786",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs866033786"
                    },
                    {
                        "id": "rs866033786",
                        "database": "ENSEMBL",
                        "url": "https://www.ensembl.org/id/rs866033786"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3287,
                "end_pos": 3287,
                "sequence_org": "L",
                "sequence_mut": "V",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2099925",
                "ref_nt": "C",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "L3287",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs2092020811",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs2092020811"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3287,
                "end_pos": 3287,
                "sequence_org": "L",
                "sequence_mut": "null",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2099923_2099925GAG",
                "ref_nt": "]",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "L3287",
                "keywords": [
                    "ebi",
                    "germline",
                    "disease"
                ],
                "disease": [
                    {
                        "disease_id": "DOID:0080322",
                        "recommended_name": {
                            "id": "DOID:0080322",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0080322",
                            "name": "polycystic kidney disease",
                            "description": "A cystic kidney disease that is characterized by the growth of fluid-filled cysts in the kidneys that reduces kidney function and may lead to kidney failure."
                        },
                        "synonyms": [
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0080322",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0080322"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0110858",
                        "recommended_name": {
                            "id": "DOID:0110858",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0110858",
                            "name": "polycystic kidney disease 1",
                            "description": "A autosomal dominant polycystic kidney disease that has_material_basis_in autosomal dominant inheritance of mutation in the PKD1 gene on chromosome 16p13.3."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "Polycystic Kidney Disease, Adult, Type I",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            },
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            }
                        ]
                    }
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs569228781",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs569228781"
                    },
                    {
                        "id": "rs569228781",
                        "database": "1000Genomes",
                        "url": "https://www.ensembl.org/homo_sapiens/Variation/Explore?v=rs569228781"
                    },
                    {
                        "id": "rs569228781",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs569228781"
                    },
                    {
                        "id": "rs569228781",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs569228781#frequency_tab"
                    },
                    {
                        "id": "rs569228781",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs569228781"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3288,
                "end_pos": 3288,
                "sequence_org": "I",
                "sequence_mut": "M",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2099920",
                "ref_nt": "C",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "I3288",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs1389263500",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1389263500"
                    },
                    {
                        "id": "rs1389263500",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs1389263500#frequency_tab"
                    },
                    {
                        "id": "rs1389263500",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs1389263500"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3288,
                "end_pos": 3288,
                "sequence_org": "I",
                "sequence_mut": "T",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2099921",
                "ref_nt": "G",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "I3288",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs146756469",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs146756469"
                    },
                    {
                        "id": "rs146756469",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs146756469"
                    },
                    {
                        "id": "rs146756469",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs146756469#frequency_tab"
                    },
                    {
                        "id": "rs146756469",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs146756469"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3288,
                "end_pos": 3288,
                "sequence_org": "I",
                "sequence_mut": "V",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2099922",
                "ref_nt": "C",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "I3288",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs2544712802",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs2544712802"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3288,
                "end_pos": 3288,
                "sequence_org": "I",
                "sequence_mut": "null",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2099921",
                "ref_nt": "l",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "I3288",
                "disease": [
                    {
                        "disease_id": "DOID:0080322",
                        "recommended_name": {
                            "id": "DOID:0080322",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0080322",
                            "name": "polycystic kidney disease",
                            "description": "A cystic kidney disease that is characterized by the growth of fluid-filled cysts in the kidneys that reduces kidney function and may lead to kidney failure."
                        },
                        "synonyms": [
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0080322",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0080322"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0110858",
                        "recommended_name": {
                            "id": "DOID:0110858",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0110858",
                            "name": "polycystic kidney disease 1",
                            "description": "A autosomal dominant polycystic kidney disease that has_material_basis_in autosomal dominant inheritance of mutation in the PKD1 gene on chromosome 16p13.3."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "Polycystic Kidney Disease, Adult, Type I",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            },
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            }
                        ]
                    }
                ],
                "keywords": [
                    "ebi",
                    "germline",
                    "disease"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs1420757773",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1420757773"
                    },
                    {
                        "id": "rs1420757773",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs1420757773#frequency_tab"
                    },
                    {
                        "id": "rs1420757773",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs1420757773"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3289,
                "end_pos": 3289,
                "sequence_org": "C",
                "sequence_mut": "*",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2099917",
                "ref_nt": "T",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "C3289",
                "disease": [
                    {
                        "disease_id": "DOID:0080322",
                        "recommended_name": {
                            "id": "DOID:0080322",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0080322",
                            "name": "polycystic kidney disease",
                            "description": "A cystic kidney disease that is characterized by the growth of fluid-filled cysts in the kidneys that reduces kidney function and may lead to kidney failure."
                        },
                        "synonyms": [
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0080322",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0080322"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0110858",
                        "recommended_name": {
                            "id": "DOID:0110858",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0110858",
                            "name": "polycystic kidney disease 1",
                            "description": "A autosomal dominant polycystic kidney disease that has_material_basis_in autosomal dominant inheritance of mutation in the PKD1 gene on chromosome 16p13.3."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "Polycystic Kidney Disease, Adult, Type I",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            },
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            }
                        ]
                    }
                ],
                "keywords": [
                    "ebi",
                    "germline",
                    "disease"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs1287460547",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1287460547"
                    },
                    {
                        "id": "rs1287460547",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs1287460547"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 328,
                "end_pos": 328,
                "sequence_org": "P",
                "sequence_mut": "L",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2118009",
                "ref_nt": "A",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "P328",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs2092020440",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs2092020440"
                    },
                    {
                        "id": "rs2092020440",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs2092020440"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3290,
                "end_pos": 3290,
                "sequence_org": "L",
                "sequence_mut": "V",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2099916",
                "ref_nt": "C",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "L3290",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs767268955",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs767268955"
                    },
                    {
                        "id": "rs767268955",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs767268955"
                    },
                    {
                        "id": "rs767268955",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs767268955#frequency_tab"
                    },
                    {
                        "id": "rs767268955",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs767268955"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3291,
                "end_pos": 3291,
                "sequence_org": "F",
                "sequence_mut": "L",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2099911",
                "ref_nt": "C",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "F3291",
                "keywords": [
                    "ebi",
                    "germline",
                    "disease"
                ],
                "disease": [
                    {
                        "disease_id": "DOID:0080322",
                        "recommended_name": {
                            "id": "DOID:0080322",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0080322",
                            "name": "polycystic kidney disease",
                            "description": "A cystic kidney disease that is characterized by the growth of fluid-filled cysts in the kidneys that reduces kidney function and may lead to kidney failure."
                        },
                        "synonyms": [
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0080322",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0080322"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0110858",
                        "recommended_name": {
                            "id": "DOID:0110858",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0110858",
                            "name": "polycystic kidney disease 1",
                            "description": "A autosomal dominant polycystic kidney disease that has_material_basis_in autosomal dominant inheritance of mutation in the PKD1 gene on chromosome 16p13.3."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "Polycystic Kidney Disease, Adult, Type I",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            },
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            }
                        ]
                    }
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs1468310382",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1468310382"
                    },
                    {
                        "id": "rs1468310382",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs1468310382#frequency_tab"
                    },
                    {
                        "id": "rs1468310382",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs1468310382"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3292,
                "end_pos": 3292,
                "sequence_org": "L",
                "sequence_mut": "V",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2099910",
                "ref_nt": "C",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "L3292",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs2544712716",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs2544712716"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3292,
                "end_pos": 3292,
                "sequence_org": "L",
                "sequence_mut": "null",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2099911",
                "ref_nt": "l",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "L3292",
                "keywords": [
                    "ebi",
                    "germline",
                    "disease"
                ],
                "disease": [
                    {
                        "disease_id": "DOID:0080322",
                        "recommended_name": {
                            "id": "DOID:0080322",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0080322",
                            "name": "polycystic kidney disease",
                            "description": "A cystic kidney disease that is characterized by the growth of fluid-filled cysts in the kidneys that reduces kidney function and may lead to kidney failure."
                        },
                        "synonyms": [
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0080322",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0080322"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0110858",
                        "recommended_name": {
                            "id": "DOID:0110858",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0110858",
                            "name": "polycystic kidney disease 1",
                            "description": "A autosomal dominant polycystic kidney disease that has_material_basis_in autosomal dominant inheritance of mutation in the PKD1 gene on chromosome 16p13.3."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "Polycystic Kidney Disease, Adult, Type I",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            },
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            }
                        ]
                    }
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs1231769968",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1231769968"
                    },
                    {
                        "id": "rs1231769968",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs1231769968"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3293,
                "end_pos": 3293,
                "sequence_org": "G",
                "sequence_mut": "S",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2099907",
                "ref_nt": "T",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "G3293",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs1199015395",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1199015395"
                    },
                    {
                        "id": "rs1199015395",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs1199015395"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3293,
                "end_pos": 3293,
                "sequence_org": "G",
                "sequence_mut": "V",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2099906",
                "ref_nt": "A",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "G3293",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs1596512512",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1596512512"
                    },
                    {
                        "id": "rs1596512512",
                        "database": "ENSEMBL",
                        "url": "https://www.ensembl.org/id/rs1596512512"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3294,
                "end_pos": 3294,
                "sequence_org": "A",
                "sequence_mut": "D",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2099903",
                "ref_nt": "T",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "A3294",
                "disease": [
                    {
                        "disease_id": "DOID:0080322",
                        "recommended_name": {
                            "id": "DOID:0080322",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0080322",
                            "name": "polycystic kidney disease",
                            "description": "A cystic kidney disease that is characterized by the growth of fluid-filled cysts in the kidneys that reduces kidney function and may lead to kidney failure."
                        },
                        "synonyms": [
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0080322",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0080322"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0110858",
                        "recommended_name": {
                            "id": "DOID:0110858",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0110858",
                            "name": "polycystic kidney disease 1",
                            "description": "A autosomal dominant polycystic kidney disease that has_material_basis_in autosomal dominant inheritance of mutation in the PKD1 gene on chromosome 16p13.3."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "Polycystic Kidney Disease, Adult, Type I",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            },
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            }
                        ]
                    }
                ],
                "keywords": [
                    "ebi",
                    "germline",
                    "disease"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs1265262304",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1265262304"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3294,
                "end_pos": 3294,
                "sequence_org": "A",
                "sequence_mut": "S",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2099904",
                "ref_nt": "A",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "A3294",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "P98161",
                        "database": "BioMuta",
                        "url": "https://hivelab.biochemistry.gwu.edu/biomuta/proteinview/P98161"
                    },
                    {
                        "id": "rs1265262304",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1265262304"
                    },
                    {
                        "id": "rs1265262304",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs1265262304"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3294,
                "end_pos": 3294,
                "subjects_tested": "1704",
                "subjects_positive": "1",
                "frequency": "0.1",
                "sequence_org": "A",
                "sequence_mut": "T",
                "comment": "Somatic mutation passed 0 out of 6 filters: .",
                "chr_id": "16",
                "chr_pos": "2099904",
                "ref_nt": "C",
                "alt_nt": "T",
                "minor_allelic_frequency": "",
                "site_lbl": "A3294",
                "disease": [
                    {
                        "disease_id": "DOID:363",
                        "recommended_name": {
                            "id": "DOID:363",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:363",
                            "name": "uterine cancer",
                            "description": "A female reproductive organ cancer that is located_in the uterus."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:363",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:363",
                                "name": "CA - cancer of uterus",
                                "description": ""
                            },
                            {
                                "id": "DOID:363",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:363",
                                "name": "Tumour of uterus",
                                "description": ""
                            },
                            {
                                "id": "DOID:363",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:363",
                                "name": "malignant neoplasm of uterus",
                                "description": ""
                            },
                            {
                                "id": "DOID:363",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:363",
                                "name": "malignant uterine tumor",
                                "description": ""
                            },
                            {
                                "id": "DOID:363",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:363",
                                "name": "neoplasm of uterus",
                                "description": ""
                            },
                            {
                                "id": "DOID:363",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:363",
                                "name": "uterine tumor",
                                "description": ""
                            },
                            {
                                "id": "DOID:363",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:363",
                                "name": "uterus neoplasm",
                                "description": ""
                            }
                        ],
                        "unlinked_id_list": [
                            "DOID:9460",
                            "DOID:5166",
                            "DOID:2021",
                            "DOID:4114"
                        ],
                        "evidence": [
                            {
                                "id": "363",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:363"
                            }
                        ]
                    }
                ],
                "keywords": [
                    "biomuta",
                    "somatic",
                    "cancer",
                    "disease",
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "P98161",
                        "database": "BioMuta",
                        "url": "https://hivelab.biochemistry.gwu.edu/biomuta/proteinview/P98161"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3294,
                "end_pos": 3294,
                "subjects_tested": "1704",
                "subjects_positive": "1",
                "frequency": "0.1",
                "sequence_org": "A",
                "sequence_mut": "V",
                "comment": "Somatic mutation passed 0 out of 6 filters: .",
                "chr_id": "16",
                "chr_pos": "2099903",
                "ref_nt": "G",
                "alt_nt": "A",
                "minor_allelic_frequency": "",
                "site_lbl": "A3294",
                "disease": [
                    {
                        "disease_id": "DOID:363",
                        "recommended_name": {
                            "id": "DOID:363",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:363",
                            "name": "uterine cancer",
                            "description": "A female reproductive organ cancer that is located_in the uterus."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:363",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:363",
                                "name": "CA - cancer of uterus",
                                "description": ""
                            },
                            {
                                "id": "DOID:363",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:363",
                                "name": "Tumour of uterus",
                                "description": ""
                            },
                            {
                                "id": "DOID:363",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:363",
                                "name": "malignant neoplasm of uterus",
                                "description": ""
                            },
                            {
                                "id": "DOID:363",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:363",
                                "name": "malignant uterine tumor",
                                "description": ""
                            },
                            {
                                "id": "DOID:363",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:363",
                                "name": "neoplasm of uterus",
                                "description": ""
                            },
                            {
                                "id": "DOID:363",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:363",
                                "name": "uterine tumor",
                                "description": ""
                            },
                            {
                                "id": "DOID:363",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:363",
                                "name": "uterus neoplasm",
                                "description": ""
                            }
                        ],
                        "unlinked_id_list": [
                            "DOID:9460",
                            "DOID:5166",
                            "DOID:2021",
                            "DOID:4114"
                        ],
                        "evidence": [
                            {
                                "id": "363",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:363"
                            }
                        ]
                    }
                ],
                "keywords": [
                    "biomuta",
                    "somatic",
                    "cancer",
                    "disease"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs751447044",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs751447044"
                    },
                    {
                        "id": "rs751447044",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs751447044"
                    },
                    {
                        "id": "rs751447044",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs751447044#frequency_tab"
                    },
                    {
                        "id": "rs751447044",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs751447044"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3295,
                "end_pos": 3295,
                "sequence_org": "N",
                "sequence_mut": "S",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2099900",
                "ref_nt": "C",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "N3295",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs751447044",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs751447044"
                    },
                    {
                        "id": "rs751447044",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs751447044"
                    },
                    {
                        "id": "rs751447044",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs751447044#frequency_tab"
                    },
                    {
                        "id": "rs751447044",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs751447044"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3295,
                "end_pos": 3295,
                "sequence_org": "N",
                "sequence_mut": "T",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2099900",
                "ref_nt": "G",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "N3295",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs1596512492",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1596512492"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3295,
                "end_pos": 3295,
                "sequence_org": "N",
                "sequence_mut": "null",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2099899",
                "ref_nt": "l",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "N3295",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs1287896776",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1287896776"
                    },
                    {
                        "id": "rs1287896776",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs1287896776"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3296,
                "end_pos": 3296,
                "sequence_org": "A",
                "sequence_mut": "S",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2099898",
                "ref_nt": "A",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "A3296",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs1287896776",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1287896776"
                    },
                    {
                        "id": "rs1287896776",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs1287896776"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3296,
                "end_pos": 3296,
                "sequence_org": "A",
                "sequence_mut": "T",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2099898",
                "ref_nt": "T",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "A3296",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs1238190746",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1238190746"
                    },
                    {
                        "id": "rs1238190746",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs1238190746"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3296,
                "end_pos": 3296,
                "sequence_org": "A",
                "sequence_mut": "V",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2099897",
                "ref_nt": "A",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "A3296",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs775497330",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs775497330"
                    },
                    {
                        "id": "rs775497330",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs775497330"
                    },
                    {
                        "id": "rs775497330",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs775497330#frequency_tab"
                    },
                    {
                        "id": "rs775497330",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs775497330"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3297,
                "end_pos": 3297,
                "sequence_org": "V",
                "sequence_mut": "L",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2099895",
                "ref_nt": "A",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "V3297",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "P98161",
                        "database": "BioMuta",
                        "url": "https://hivelab.biochemistry.gwu.edu/biomuta/proteinview/P98161"
                    },
                    {
                        "id": "rs775497330",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs775497330"
                    },
                    {
                        "id": "rs775497330",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs775497330"
                    },
                    {
                        "id": "rs775497330",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs775497330#frequency_tab"
                    },
                    {
                        "id": "rs775497330",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs775497330"
                    },
                    {
                        "id": "rs775497330",
                        "database": "COSMIC",
                        "url": "https://www.ensembl.org/homo_sapiens/Variation/Explore?v=rs775497330"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3297,
                "end_pos": 3297,
                "subjects_tested": "1704",
                "subjects_positive": "1",
                "frequency": "0.1",
                "sequence_org": "V",
                "sequence_mut": "M",
                "comment": "Somatic mutation passed 0 out of 6 filters: .",
                "chr_id": "16",
                "chr_pos": "2099895",
                "ref_nt": "C",
                "alt_nt": "T",
                "minor_allelic_frequency": "",
                "site_lbl": "V3297",
                "disease": [
                    {
                        "disease_id": "DOID:363",
                        "recommended_name": {
                            "id": "DOID:363",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:363",
                            "name": "uterine cancer",
                            "description": "A female reproductive organ cancer that is located_in the uterus."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:363",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:363",
                                "name": "CA - cancer of uterus",
                                "description": ""
                            },
                            {
                                "id": "DOID:363",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:363",
                                "name": "Tumour of uterus",
                                "description": ""
                            },
                            {
                                "id": "DOID:363",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:363",
                                "name": "malignant neoplasm of uterus",
                                "description": ""
                            },
                            {
                                "id": "DOID:363",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:363",
                                "name": "malignant uterine tumor",
                                "description": ""
                            },
                            {
                                "id": "DOID:363",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:363",
                                "name": "neoplasm of uterus",
                                "description": ""
                            },
                            {
                                "id": "DOID:363",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:363",
                                "name": "uterine tumor",
                                "description": ""
                            },
                            {
                                "id": "DOID:363",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:363",
                                "name": "uterus neoplasm",
                                "description": ""
                            }
                        ],
                        "unlinked_id_list": [
                            "DOID:9460",
                            "DOID:5166",
                            "DOID:2021",
                            "DOID:4114"
                        ],
                        "evidence": [
                            {
                                "id": "363",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:363"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0080322",
                        "recommended_name": {
                            "id": "DOID:0080322",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0080322",
                            "name": "polycystic kidney disease",
                            "description": "A cystic kidney disease that is characterized by the growth of fluid-filled cysts in the kidneys that reduces kidney function and may lead to kidney failure."
                        },
                        "synonyms": [
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0080322",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0080322"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0110858",
                        "recommended_name": {
                            "id": "DOID:0110858",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0110858",
                            "name": "polycystic kidney disease 1",
                            "description": "A autosomal dominant polycystic kidney disease that has_material_basis_in autosomal dominant inheritance of mutation in the PKD1 gene on chromosome 16p13.3."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "Polycystic Kidney Disease, Adult, Type I",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            },
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            }
                        ]
                    }
                ],
                "keywords": [
                    "biomuta",
                    "somatic",
                    "cancer",
                    "disease",
                    "ebi"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs1415277933",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1415277933"
                    },
                    {
                        "id": "rs1415277933",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs1415277933#frequency_tab"
                    },
                    {
                        "id": "rs1415277933",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs1415277933"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3298,
                "end_pos": 3298,
                "sequence_org": "W",
                "sequence_mut": "*",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2099890",
                "ref_nt": "T",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "W3298",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs1415277933",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1415277933"
                    },
                    {
                        "id": "rs1415277933",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs1415277933#frequency_tab"
                    },
                    {
                        "id": "rs1415277933",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs1415277933"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3298,
                "end_pos": 3298,
                "sequence_org": "W",
                "sequence_mut": "C",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2099890",
                "ref_nt": "A",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "W3298",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs1329847323",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1329847323"
                    },
                    {
                        "id": "rs1329847323",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs1329847323"
                    }
                ],
                "glycoeffect": [
                    "o-glyco-site-loss"
                ],
                "start_pos": 3299,
                "end_pos": 3299,
                "sequence_org": "Y",
                "sequence_mut": "C",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2099888",
                "ref_nt": "C",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "Y3299",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs2151823406",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs2151823406"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 329,
                "end_pos": 329,
                "sequence_org": "G",
                "sequence_mut": "null",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2118015_2118034",
                "ref_nt": "p",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "G329",
                "keywords": [
                    "ebi",
                    "germline",
                    "disease"
                ],
                "disease": [
                    {
                        "disease_id": "DOID:0080322",
                        "recommended_name": {
                            "id": "DOID:0080322",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0080322",
                            "name": "polycystic kidney disease",
                            "description": "A cystic kidney disease that is characterized by the growth of fluid-filled cysts in the kidneys that reduces kidney function and may lead to kidney failure."
                        },
                        "synonyms": [
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0080322",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0080322"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0110858",
                        "recommended_name": {
                            "id": "DOID:0110858",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0110858",
                            "name": "polycystic kidney disease 1",
                            "description": "A autosomal dominant polycystic kidney disease that has_material_basis_in autosomal dominant inheritance of mutation in the PKD1 gene on chromosome 16p13.3."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "Polycystic Kidney Disease, Adult, Type I",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            },
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            }
                        ]
                    }
                ]
            },
            {
                "evidence": [
                    {
                        "id": "P98161",
                        "database": "BioMuta",
                        "url": "https://hivelab.biochemistry.gwu.edu/biomuta/proteinview/P98161"
                    },
                    {
                        "id": "rs777024498",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs777024498"
                    },
                    {
                        "id": "rs777024498",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs777024498"
                    },
                    {
                        "id": "rs777024498",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs777024498#frequency_tab"
                    },
                    {
                        "id": "rs777024498",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs777024498"
                    },
                    {
                        "id": "rs777024498",
                        "database": "COSMIC",
                        "url": "https://www.ensembl.org/homo_sapiens/Variation/Explore?v=rs777024498"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3300,
                "end_pos": 3300,
                "subjects_tested": "3601",
                "subjects_positive": "1",
                "frequency": "0.0",
                "sequence_org": "G",
                "sequence_mut": "R",
                "comment": "Somatic mutation passed 0 out of 6 filters: .",
                "chr_id": "16",
                "chr_pos": "2099886",
                "ref_nt": "C",
                "alt_nt": "T",
                "minor_allelic_frequency": "",
                "site_lbl": "G3300",
                "disease": [
                    {
                        "disease_id": "DOID:9256",
                        "recommended_name": {
                            "id": "DOID:9256",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:9256",
                            "name": "colorectal cancer",
                            "description": "A large intestine cancer that is located_in the colon and/or located_in the rectum."
                        },
                        "synonyms": [
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectal cancer",
                                "description": "A primary or metastatic malignant neoplasm that affects the colon or rectum. Representative examples include carcinoma, lymphoma, and sarcoma."
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "cancer of colorectum",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "cancer of large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "cancer of large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "cancer of the large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colon cancer, advanced, somatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colon cancer, somatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectal cancer",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectal cancer with chromosomal instability, somatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectal cancer, autosomal dominant, somatic mutation",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectal cancer, somatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectal cancer, susceptibility to, autosomal dominant, somatic mutation",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectum cancer",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant colorectal neoplasm",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant colorectal tumor",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant colorectal tumour",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant colorectum neoplasm",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant large bowel neoplasm",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant large bowel tumor",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant large bowel tumour",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant large intestine neoplasm",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant large intestine tumor",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant large intestine tumour",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant neoplasm of colorectum",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant neoplasm of large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant neoplasm of large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant neoplasm of the large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant neoplasm of the large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumor of large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumor of large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumor of the large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumor of the large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumour of large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumour of large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumour of the large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumour of the large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "CRC",
                                "description": ""
                            },
                            {
                                "id": "MIM:114500",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/114500",
                                "name": "Colorectal cancer",
                                "description": "Colorectal cancer"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "9256",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:9256"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0080322",
                        "recommended_name": {
                            "id": "DOID:0080322",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0080322",
                            "name": "polycystic kidney disease",
                            "description": "A cystic kidney disease that is characterized by the growth of fluid-filled cysts in the kidneys that reduces kidney function and may lead to kidney failure."
                        },
                        "synonyms": [
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0080322",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0080322"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0110858",
                        "recommended_name": {
                            "id": "DOID:0110858",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0110858",
                            "name": "polycystic kidney disease 1",
                            "description": "A autosomal dominant polycystic kidney disease that has_material_basis_in autosomal dominant inheritance of mutation in the PKD1 gene on chromosome 16p13.3."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "Polycystic Kidney Disease, Adult, Type I",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            },
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            }
                        ]
                    }
                ],
                "keywords": [
                    "biomuta",
                    "somatic",
                    "cancer",
                    "disease",
                    "ebi"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "P98161",
                        "database": "BioMuta",
                        "url": "https://hivelab.biochemistry.gwu.edu/biomuta/proteinview/P98161"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3301,
                "end_pos": 3301,
                "subjects_tested": "2670",
                "subjects_positive": "1",
                "frequency": "0.0",
                "sequence_org": "A",
                "sequence_mut": "V",
                "comment": "Somatic mutation passed 0 out of 6 filters: .",
                "chr_id": "16",
                "chr_pos": "2099882",
                "ref_nt": "G",
                "alt_nt": "A",
                "minor_allelic_frequency": "",
                "site_lbl": "A3301",
                "disease": [
                    {
                        "disease_id": "DOID:1319",
                        "recommended_name": {
                            "id": "DOID:1319",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:1319",
                            "name": "brain cancer",
                            "description": "A central nervous system cancer that is characterized by the growth of abnormal cells in the tissues of the brain."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:1319",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:1319",
                                "name": "BT - Brain tumour",
                                "description": ""
                            },
                            {
                                "id": "DOID:1319",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:1319",
                                "name": "adult brain tumor",
                                "description": ""
                            },
                            {
                                "id": "DOID:1319",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:1319",
                                "name": "adult malignant brain neoplasm",
                                "description": ""
                            },
                            {
                                "id": "DOID:1319",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:1319",
                                "name": "brain neoplasm",
                                "description": ""
                            },
                            {
                                "id": "DOID:1319",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:1319",
                                "name": "brain neoplasm, adult",
                                "description": ""
                            },
                            {
                                "id": "DOID:1319",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:1319",
                                "name": "malignant brain tumour",
                                "description": ""
                            },
                            {
                                "id": "DOID:1319",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:1319",
                                "name": "malignant primary brain neoplasm",
                                "description": ""
                            },
                            {
                                "id": "DOID:1319",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:1319",
                                "name": "malignant primary brain tumor",
                                "description": ""
                            },
                            {
                                "id": "DOID:1319",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:1319",
                                "name": "malignant tumor of Brain",
                                "description": ""
                            },
                            {
                                "id": "DOID:1319",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:1319",
                                "name": "malignant tumor of adult brain",
                                "description": ""
                            },
                            {
                                "id": "DOID:1319",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:1319",
                                "name": "neoplasm of brain",
                                "description": ""
                            },
                            {
                                "id": "DOID:1319",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:1319",
                                "name": "primary brain neoplasm",
                                "description": ""
                            },
                            {
                                "id": "DOID:1319",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:1319",
                                "name": "primary brain tumor",
                                "description": ""
                            },
                            {
                                "id": "DOID:1319",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:1319",
                                "name": "primary malignant neoplasm of brain",
                                "description": ""
                            },
                            {
                                "id": "DOID:1319",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:1319",
                                "name": "tumor of the Brain",
                                "description": ""
                            }
                        ],
                        "unlinked_id_list": [
                            "DOID:4203",
                            "DOID:3541",
                            "DOID:4706",
                            "DOID:1659",
                            "DOID:368"
                        ],
                        "evidence": [
                            {
                                "id": "1319",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:1319"
                            }
                        ]
                    }
                ],
                "keywords": [
                    "biomuta",
                    "somatic",
                    "cancer",
                    "disease"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs2092019152",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs2092019152"
                    },
                    {
                        "id": "rs2092019152",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs2092019152"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3302,
                "end_pos": 3302,
                "sequence_org": "V",
                "sequence_mut": "A",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2099879",
                "ref_nt": "G",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "V3302",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs771383072",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs771383072"
                    },
                    {
                        "id": "rs771383072",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs771383072"
                    },
                    {
                        "id": "rs771383072",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs771383072#frequency_tab"
                    },
                    {
                        "id": "rs771383072",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs771383072"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3302,
                "end_pos": 3302,
                "sequence_org": "V",
                "sequence_mut": "F",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2099880",
                "ref_nt": "A",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "V3302",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs771383072",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs771383072"
                    },
                    {
                        "id": "rs771383072",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs771383072"
                    },
                    {
                        "id": "rs771383072",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs771383072#frequency_tab"
                    },
                    {
                        "id": "rs771383072",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs771383072"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3302,
                "end_pos": 3302,
                "sequence_org": "V",
                "sequence_mut": "I",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2099880",
                "ref_nt": "T",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "V3302",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs771383072",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs771383072"
                    },
                    {
                        "id": "rs771383072",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs771383072"
                    },
                    {
                        "id": "rs771383072",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs771383072#frequency_tab"
                    },
                    {
                        "id": "rs771383072",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs771383072"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3302,
                "end_pos": 3302,
                "sequence_org": "V",
                "sequence_mut": "L",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2099880",
                "ref_nt": "G",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "V3302",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs773798664",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs773798664"
                    },
                    {
                        "id": "rs773798664",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs773798664"
                    },
                    {
                        "id": "rs773798664",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs773798664#frequency_tab"
                    },
                    {
                        "id": "rs773798664",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs773798664"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3304,
                "end_pos": 3304,
                "sequence_org": "D",
                "sequence_mut": "N",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2099874",
                "ref_nt": "T",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "D3304",
                "keywords": [
                    "ebi",
                    "germline",
                    "disease"
                ],
                "disease": [
                    {
                        "disease_id": "DOID:0080322",
                        "recommended_name": {
                            "id": "DOID:0080322",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0080322",
                            "name": "polycystic kidney disease",
                            "description": "A cystic kidney disease that is characterized by the growth of fluid-filled cysts in the kidneys that reduces kidney function and may lead to kidney failure."
                        },
                        "synonyms": [
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0080322",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0080322"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0110858",
                        "recommended_name": {
                            "id": "DOID:0110858",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0110858",
                            "name": "polycystic kidney disease 1",
                            "description": "A autosomal dominant polycystic kidney disease that has_material_basis_in autosomal dominant inheritance of mutation in the PKD1 gene on chromosome 16p13.3."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "Polycystic Kidney Disease, Adult, Type I",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            },
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            }
                        ]
                    }
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs2092018909",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs2092018909"
                    },
                    {
                        "id": "rs2092018909",
                        "database": "ENSEMBL",
                        "url": "https://www.ensembl.org/id/rs2092018909"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3305,
                "end_pos": 3305,
                "sequence_org": "S",
                "sequence_mut": "T",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2099871",
                "ref_nt": "T",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "S3305",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs1567169638",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1567169638"
                    }
                ],
                "glycoeffect": [
                    "o-glyco-site-loss"
                ],
                "start_pos": 3305,
                "end_pos": 3305,
                "sequence_org": "S",
                "sequence_mut": "null",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2099869AG",
                "ref_nt": "]",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "S3305",
                "disease": [
                    {
                        "disease_id": "DOID:0080322",
                        "recommended_name": {
                            "id": "DOID:0080322",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0080322",
                            "name": "polycystic kidney disease",
                            "description": "A cystic kidney disease that is characterized by the growth of fluid-filled cysts in the kidneys that reduces kidney function and may lead to kidney failure."
                        },
                        "synonyms": [
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0080322",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0080322"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0110858",
                        "recommended_name": {
                            "id": "DOID:0110858",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0110858",
                            "name": "polycystic kidney disease 1",
                            "description": "A autosomal dominant polycystic kidney disease that has_material_basis_in autosomal dominant inheritance of mutation in the PKD1 gene on chromosome 16p13.3."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "Polycystic Kidney Disease, Adult, Type I",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            },
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            }
                        ]
                    }
                ],
                "keywords": [
                    "ebi",
                    "germline",
                    "disease"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs903949574",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs903949574"
                    },
                    {
                        "id": "rs903949574",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs903949574#frequency_tab"
                    },
                    {
                        "id": "rs903949574",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs903949574"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3306,
                "end_pos": 3306,
                "sequence_org": "A",
                "sequence_mut": "P",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2099868",
                "ref_nt": "G",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "A3306",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs903949574",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs903949574"
                    },
                    {
                        "id": "rs903949574",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs903949574#frequency_tab"
                    },
                    {
                        "id": "rs903949574",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs903949574"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3306,
                "end_pos": 3306,
                "sequence_org": "A",
                "sequence_mut": "S",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2099868",
                "ref_nt": "A",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "A3306",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs903949574",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs903949574"
                    },
                    {
                        "id": "rs903949574",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs903949574#frequency_tab"
                    },
                    {
                        "id": "rs903949574",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs903949574"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3306,
                "end_pos": 3306,
                "sequence_org": "A",
                "sequence_mut": "T",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2099868",
                "ref_nt": "T",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "A3306",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs772714161",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs772714161"
                    },
                    {
                        "id": "rs772714161",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs772714161"
                    },
                    {
                        "id": "rs772714161",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs772714161"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3306,
                "end_pos": 3306,
                "sequence_org": "A",
                "sequence_mut": "V",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2099867",
                "ref_nt": "A",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "A3306",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs551648618",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs551648618"
                    },
                    {
                        "id": "rs551648618",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs551648618#frequency_tab"
                    },
                    {
                        "id": "rs551648618",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs551648618"
                    }
                ],
                "glycoeffect": [
                    "o-glyco-site-loss"
                ],
                "start_pos": 3307,
                "end_pos": 3307,
                "sequence_org": "Y",
                "sequence_mut": "C",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2099864",
                "ref_nt": "C",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "Y3307",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs551648618",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs551648618"
                    },
                    {
                        "id": "rs551648618",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs551648618#frequency_tab"
                    },
                    {
                        "id": "rs551648618",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs551648618"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3307,
                "end_pos": 3307,
                "sequence_org": "Y",
                "sequence_mut": "S",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2099864",
                "ref_nt": "G",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "Y3307",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs779492205",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs779492205"
                    },
                    {
                        "id": "rs779492205",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs779492205"
                    },
                    {
                        "id": "rs779492205",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs779492205#frequency_tab"
                    },
                    {
                        "id": "rs779492205",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs779492205"
                    }
                ],
                "glycoeffect": [
                    "o-glyco-site-loss"
                ],
                "start_pos": 3308,
                "end_pos": 3308,
                "sequence_org": "S",
                "sequence_mut": "C",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2099862",
                "ref_nt": "A",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "S3308",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs779492205",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs779492205"
                    },
                    {
                        "id": "rs779492205",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs779492205"
                    },
                    {
                        "id": "rs779492205",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs779492205#frequency_tab"
                    },
                    {
                        "id": "rs779492205",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs779492205"
                    }
                ],
                "glycoeffect": [
                    "o-glyco-site-loss"
                ],
                "start_pos": 3308,
                "end_pos": 3308,
                "sequence_org": "S",
                "sequence_mut": "G",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2099862",
                "ref_nt": "C",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "S3308",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "P98161",
                        "database": "BioMuta",
                        "url": "https://hivelab.biochemistry.gwu.edu/biomuta/proteinview/P98161"
                    },
                    {
                        "id": "rs1313548057",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1313548057"
                    },
                    {
                        "id": "rs1313548057",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs1313548057#frequency_tab"
                    },
                    {
                        "id": "rs1313548057",
                        "database": "COSMIC",
                        "url": "https://www.ensembl.org/homo_sapiens/Variation/Explore?v=rs1313548057"
                    }
                ],
                "glycoeffect": [
                    "o-glyco-site-loss"
                ],
                "start_pos": 3308,
                "end_pos": 3308,
                "subjects_tested": "3601",
                "subjects_positive": "1",
                "frequency": "0.0",
                "sequence_org": "S",
                "sequence_mut": "N",
                "comment": "Somatic mutation passed 0 out of 6 filters: .",
                "chr_id": "16",
                "chr_pos": "2099861",
                "ref_nt": "C",
                "alt_nt": "T",
                "minor_allelic_frequency": "",
                "site_lbl": "S3308",
                "disease": [
                    {
                        "disease_id": "DOID:9256",
                        "recommended_name": {
                            "id": "DOID:9256",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:9256",
                            "name": "colorectal cancer",
                            "description": "A large intestine cancer that is located_in the colon and/or located_in the rectum."
                        },
                        "synonyms": [
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectal cancer",
                                "description": "A primary or metastatic malignant neoplasm that affects the colon or rectum. Representative examples include carcinoma, lymphoma, and sarcoma."
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "cancer of colorectum",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "cancer of large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "cancer of large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "cancer of the large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colon cancer, advanced, somatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colon cancer, somatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectal cancer",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectal cancer with chromosomal instability, somatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectal cancer, autosomal dominant, somatic mutation",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectal cancer, somatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectal cancer, susceptibility to, autosomal dominant, somatic mutation",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectum cancer",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant colorectal neoplasm",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant colorectal tumor",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant colorectal tumour",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant colorectum neoplasm",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant large bowel neoplasm",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant large bowel tumor",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant large bowel tumour",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant large intestine neoplasm",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant large intestine tumor",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant large intestine tumour",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant neoplasm of colorectum",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant neoplasm of large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant neoplasm of large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant neoplasm of the large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant neoplasm of the large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumor of large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumor of large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumor of the large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumor of the large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumour of large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumour of large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumour of the large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumour of the large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "CRC",
                                "description": ""
                            },
                            {
                                "id": "MIM:114500",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/114500",
                                "name": "Colorectal cancer",
                                "description": "Colorectal cancer"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "9256",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:9256"
                            }
                        ]
                    }
                ],
                "keywords": [
                    "biomuta",
                    "somatic",
                    "cancer",
                    "disease",
                    "ebi"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs779492205",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs779492205"
                    },
                    {
                        "id": "rs779492205",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs779492205"
                    },
                    {
                        "id": "rs779492205",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs779492205#frequency_tab"
                    },
                    {
                        "id": "rs779492205",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs779492205"
                    }
                ],
                "glycoeffect": [
                    "o-glyco-site-loss"
                ],
                "start_pos": 3308,
                "end_pos": 3308,
                "sequence_org": "S",
                "sequence_mut": "R",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2099862",
                "ref_nt": "G",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "S3308",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs1596511656",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1596511656"
                    },
                    {
                        "id": "rs1596511656",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs1596511656#frequency_tab"
                    }
                ],
                "glycoeffect": [
                    "o-glyco-site-loss"
                ],
                "start_pos": 3309,
                "end_pos": 3309,
                "sequence_org": "T",
                "sequence_mut": "A",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2099769",
                "ref_nt": "C",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "T3309",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs761055827",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs761055827"
                    },
                    {
                        "id": "rs761055827",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs761055827"
                    },
                    {
                        "id": "rs761055827",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs761055827#frequency_tab"
                    },
                    {
                        "id": "rs761055827",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs761055827"
                    },
                    {
                        "id": "rs761055827",
                        "database": "COSMIC",
                        "url": "https://www.ensembl.org/homo_sapiens/Variation/Explore?v=rs761055827"
                    }
                ],
                "glycoeffect": [
                    "o-glyco-site-loss"
                ],
                "start_pos": 3309,
                "end_pos": 3309,
                "sequence_org": "T",
                "sequence_mut": "M",
                "comment": "Somatic mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2099768",
                "ref_nt": "A",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "T3309",
                "keywords": [
                    "ebi",
                    "somatic"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs1596511656",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1596511656"
                    },
                    {
                        "id": "rs1596511656",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs1596511656#frequency_tab"
                    }
                ],
                "glycoeffect": [
                    "o-glyco-site-loss"
                ],
                "start_pos": 3309,
                "end_pos": 3309,
                "sequence_org": "T",
                "sequence_mut": "P",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2099769",
                "ref_nt": "G",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "T3309",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs761055827",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs761055827"
                    },
                    {
                        "id": "rs761055827",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs761055827"
                    },
                    {
                        "id": "rs761055827",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs761055827#frequency_tab"
                    },
                    {
                        "id": "rs761055827",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs761055827"
                    }
                ],
                "glycoeffect": [
                    "o-glyco-site-loss"
                ],
                "start_pos": 3309,
                "end_pos": 3309,
                "sequence_org": "T",
                "sequence_mut": "R",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2099768",
                "ref_nt": "C",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "T3309",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs2151738483",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs2151738483"
                    }
                ],
                "glycoeffect": [
                    "o-glyco-site-loss"
                ],
                "start_pos": 3309,
                "end_pos": 3309,
                "sequence_org": "T",
                "sequence_mut": "null",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2099769",
                "ref_nt": "p",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "T3309",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs776765857",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs776765857"
                    },
                    {
                        "id": "rs776765857",
                        "database": "1000Genomes",
                        "url": "https://www.ensembl.org/homo_sapiens/Variation/Explore?v=rs776765857"
                    },
                    {
                        "id": "rs776765857",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs776765857"
                    },
                    {
                        "id": "rs776765857",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs776765857#frequency_tab"
                    },
                    {
                        "id": "rs776765857",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs776765857"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 330,
                "end_pos": 330,
                "sequence_org": "R",
                "sequence_mut": "C",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2118004",
                "ref_nt": "A",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "R330",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs776765857",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs776765857"
                    },
                    {
                        "id": "rs776765857",
                        "database": "1000Genomes",
                        "url": "https://www.ensembl.org/homo_sapiens/Variation/Explore?v=rs776765857"
                    },
                    {
                        "id": "rs776765857",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs776765857"
                    },
                    {
                        "id": "rs776765857",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs776765857#frequency_tab"
                    },
                    {
                        "id": "rs776765857",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs776765857"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 330,
                "end_pos": 330,
                "sequence_org": "R",
                "sequence_mut": "G",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2118004",
                "ref_nt": "C",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "R330",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs771076473",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs771076473"
                    },
                    {
                        "id": "rs771076473",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs771076473"
                    },
                    {
                        "id": "rs771076473",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs771076473"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 330,
                "end_pos": 330,
                "sequence_org": "R",
                "sequence_mut": "H",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2118003",
                "ref_nt": "T",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "R330",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs771076473",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs771076473"
                    },
                    {
                        "id": "rs771076473",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs771076473"
                    },
                    {
                        "id": "rs771076473",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs771076473"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 330,
                "end_pos": 330,
                "sequence_org": "R",
                "sequence_mut": "L",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2118003",
                "ref_nt": "A",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "R330",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs1242837732",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1242837732"
                    },
                    {
                        "id": "rs1242837732",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs1242837732#frequency_tab"
                    },
                    {
                        "id": "rs1242837732",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs1242837732"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3311,
                "end_pos": 3311,
                "sequence_org": "H",
                "sequence_mut": "R",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2099762",
                "ref_nt": "C",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "H3311",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs1442974903",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1442974903"
                    },
                    {
                        "id": "rs1442974903",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs1442974903#frequency_tab"
                    },
                    {
                        "id": "rs1442974903",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs1442974903"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3311,
                "end_pos": 3311,
                "sequence_org": "H",
                "sequence_mut": "Y",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2099763",
                "ref_nt": "A",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "H3311",
                "keywords": [
                    "ebi",
                    "germline",
                    "disease"
                ],
                "disease": [
                    {
                        "disease_id": "DOID:0080322",
                        "recommended_name": {
                            "id": "DOID:0080322",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0080322",
                            "name": "polycystic kidney disease",
                            "description": "A cystic kidney disease that is characterized by the growth of fluid-filled cysts in the kidneys that reduces kidney function and may lead to kidney failure."
                        },
                        "synonyms": [
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0080322",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0080322"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0110858",
                        "recommended_name": {
                            "id": "DOID:0110858",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0110858",
                            "name": "polycystic kidney disease 1",
                            "description": "A autosomal dominant polycystic kidney disease that has_material_basis_in autosomal dominant inheritance of mutation in the PKD1 gene on chromosome 16p13.3."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "Polycystic Kidney Disease, Adult, Type I",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            },
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            }
                        ]
                    }
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs1459100196",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1459100196"
                    },
                    {
                        "id": "rs1459100196",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs1459100196#frequency_tab"
                    },
                    {
                        "id": "rs1459100196",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs1459100196"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3312,
                "end_pos": 3312,
                "sequence_org": "V",
                "sequence_mut": "M",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2099760",
                "ref_nt": "T",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "V3312",
                "disease": [
                    {
                        "disease_id": "DOID:0080322",
                        "recommended_name": {
                            "id": "DOID:0080322",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0080322",
                            "name": "polycystic kidney disease",
                            "description": "A cystic kidney disease that is characterized by the growth of fluid-filled cysts in the kidneys that reduces kidney function and may lead to kidney failure."
                        },
                        "synonyms": [
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0080322",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0080322"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0110858",
                        "recommended_name": {
                            "id": "DOID:0110858",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0110858",
                            "name": "polycystic kidney disease 1",
                            "description": "A autosomal dominant polycystic kidney disease that has_material_basis_in autosomal dominant inheritance of mutation in the PKD1 gene on chromosome 16p13.3."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "Polycystic Kidney Disease, Adult, Type I",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            },
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            }
                        ]
                    }
                ],
                "keywords": [
                    "ebi",
                    "germline",
                    "disease"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs2092011416",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs2092011416"
                    },
                    {
                        "id": "rs2092011416",
                        "database": "ENSEMBL",
                        "url": "https://www.ensembl.org/id/rs2092011416"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3314,
                "end_pos": 3314,
                "sequence_org": "R",
                "sequence_mut": "S",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2099752",
                "ref_nt": "A",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "R3314",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs772695904",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs772695904"
                    },
                    {
                        "id": "rs772695904",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs772695904"
                    },
                    {
                        "id": "rs772695904",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs772695904#frequency_tab"
                    },
                    {
                        "id": "rs772695904",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs772695904"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3317,
                "end_pos": 3317,
                "sequence_org": "P",
                "sequence_mut": "L",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2099744",
                "ref_nt": "A",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "P3317",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs1322874650",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1322874650"
                    },
                    {
                        "id": "rs1322874650",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs1322874650"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3317,
                "end_pos": 3317,
                "sequence_org": "P",
                "sequence_mut": "S",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2099745",
                "ref_nt": "A",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "P3317",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs2092010863",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs2092010863"
                    },
                    {
                        "id": "rs2092010863",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs2092010863"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3318,
                "end_pos": 3318,
                "sequence_org": "L",
                "sequence_mut": "M",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2099742",
                "ref_nt": "T",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "L3318",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs1380112705",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1380112705"
                    },
                    {
                        "id": "rs1380112705",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs1380112705#frequency_tab"
                    },
                    {
                        "id": "rs1380112705",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs1380112705"
                    }
                ],
                "glycoeffect": [
                    "o-glyco-site-loss"
                ],
                "start_pos": 3319,
                "end_pos": 3319,
                "sequence_org": "S",
                "sequence_mut": "N",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2099738",
                "ref_nt": "T",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "S3319",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs1378427626",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1378427626"
                    },
                    {
                        "id": "rs1378427626",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs1378427626"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3320,
                "end_pos": 3320,
                "sequence_org": "V",
                "sequence_mut": "G",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2099735",
                "ref_nt": "C",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "V3320",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs575333098",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs575333098"
                    },
                    {
                        "id": "rs575333098",
                        "database": "1000Genomes",
                        "url": "https://www.ensembl.org/homo_sapiens/Variation/Explore?v=rs575333098"
                    },
                    {
                        "id": "rs575333098",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs575333098"
                    },
                    {
                        "id": "rs575333098",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs575333098#frequency_tab"
                    },
                    {
                        "id": "rs575333098",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs575333098"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3320,
                "end_pos": 3320,
                "sequence_org": "V",
                "sequence_mut": "I",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2099736",
                "ref_nt": "T",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "V3320",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs2092010200",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs2092010200"
                    },
                    {
                        "id": "rs2092010200",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs2092010200#frequency_tab"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3321,
                "end_pos": 3321,
                "sequence_org": "D",
                "sequence_mut": "G",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2099732",
                "ref_nt": "C",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "D3321",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "P98161",
                        "database": "BioMuta",
                        "url": "https://hivelab.biochemistry.gwu.edu/biomuta/proteinview/P98161"
                    },
                    {
                        "id": "rs948156316",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs948156316"
                    },
                    {
                        "id": "rs948156316",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs948156316#frequency_tab"
                    },
                    {
                        "id": "rs948156316",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs948156316"
                    },
                    {
                        "id": "rs948156316",
                        "database": "COSMIC",
                        "url": "https://www.ensembl.org/homo_sapiens/Variation/Explore?v=rs948156316"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3321,
                "end_pos": 3321,
                "subjects_tested": "3601",
                "subjects_positive": "1",
                "frequency": "0.0",
                "sequence_org": "D",
                "sequence_mut": "N",
                "comment": "Somatic mutation passed 0 out of 6 filters: .",
                "chr_id": "16",
                "chr_pos": "2099733",
                "ref_nt": "C",
                "alt_nt": "T",
                "minor_allelic_frequency": "",
                "site_lbl": "D3321",
                "disease": [
                    {
                        "disease_id": "DOID:9256",
                        "recommended_name": {
                            "id": "DOID:9256",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:9256",
                            "name": "colorectal cancer",
                            "description": "A large intestine cancer that is located_in the colon and/or located_in the rectum."
                        },
                        "synonyms": [
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectal cancer",
                                "description": "A primary or metastatic malignant neoplasm that affects the colon or rectum. Representative examples include carcinoma, lymphoma, and sarcoma."
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "cancer of colorectum",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "cancer of large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "cancer of large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "cancer of the large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colon cancer, advanced, somatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colon cancer, somatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectal cancer",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectal cancer with chromosomal instability, somatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectal cancer, autosomal dominant, somatic mutation",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectal cancer, somatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectal cancer, susceptibility to, autosomal dominant, somatic mutation",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectum cancer",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant colorectal neoplasm",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant colorectal tumor",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant colorectal tumour",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant colorectum neoplasm",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant large bowel neoplasm",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant large bowel tumor",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant large bowel tumour",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant large intestine neoplasm",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant large intestine tumor",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant large intestine tumour",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant neoplasm of colorectum",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant neoplasm of large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant neoplasm of large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant neoplasm of the large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant neoplasm of the large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumor of large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumor of large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumor of the large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumor of the large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumour of large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumour of large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumour of the large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumour of the large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "CRC",
                                "description": ""
                            },
                            {
                                "id": "MIM:114500",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/114500",
                                "name": "Colorectal cancer",
                                "description": "Colorectal cancer"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "9256",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:9256"
                            }
                        ]
                    }
                ],
                "keywords": [
                    "biomuta",
                    "somatic",
                    "cancer",
                    "disease",
                    "ebi"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs1211897255",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1211897255"
                    },
                    {
                        "id": "rs1211897255",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs1211897255"
                    }
                ],
                "glycoeffect": [
                    "o-glyco-site-loss"
                ],
                "start_pos": 3322,
                "end_pos": 3322,
                "sequence_org": "T",
                "sequence_mut": "A",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2099730",
                "ref_nt": "C",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "T3322",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs1350441991",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1350441991"
                    },
                    {
                        "id": "rs1350441991",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs1350441991#frequency_tab"
                    },
                    {
                        "id": "rs1350441991",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs1350441991"
                    }
                ],
                "glycoeffect": [
                    "o-glyco-site-loss"
                ],
                "start_pos": 3322,
                "end_pos": 3322,
                "sequence_org": "T",
                "sequence_mut": "I",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2099729",
                "ref_nt": "A",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "T3322",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs1350441991",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1350441991"
                    },
                    {
                        "id": "rs1350441991",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs1350441991#frequency_tab"
                    },
                    {
                        "id": "rs1350441991",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs1350441991"
                    }
                ],
                "glycoeffect": [
                    "o-glyco-site-loss"
                ],
                "start_pos": 3322,
                "end_pos": 3322,
                "sequence_org": "T",
                "sequence_mut": "K",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2099729",
                "ref_nt": "T",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "T3322",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs1350441991",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1350441991"
                    },
                    {
                        "id": "rs1350441991",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs1350441991#frequency_tab"
                    },
                    {
                        "id": "rs1350441991",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs1350441991"
                    }
                ],
                "glycoeffect": [
                    "o-glyco-site-loss"
                ],
                "start_pos": 3322,
                "end_pos": 3322,
                "sequence_org": "T",
                "sequence_mut": "R",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2099729",
                "ref_nt": "C",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "T3322",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs2544711045",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs2544711045"
                    }
                ],
                "glycoeffect": [
                    "o-glyco-site-loss"
                ],
                "start_pos": 3322,
                "end_pos": 3322,
                "sequence_org": "T",
                "sequence_mut": "null",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2099729GT",
                "ref_nt": "]",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "T3322",
                "disease": [
                    {
                        "disease_id": "DOID:0080322",
                        "recommended_name": {
                            "id": "DOID:0080322",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0080322",
                            "name": "polycystic kidney disease",
                            "description": "A cystic kidney disease that is characterized by the growth of fluid-filled cysts in the kidneys that reduces kidney function and may lead to kidney failure."
                        },
                        "synonyms": [
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0080322",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0080322"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0110858",
                        "recommended_name": {
                            "id": "DOID:0110858",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0110858",
                            "name": "polycystic kidney disease 1",
                            "description": "A autosomal dominant polycystic kidney disease that has_material_basis_in autosomal dominant inheritance of mutation in the PKD1 gene on chromosome 16p13.3."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "Polycystic Kidney Disease, Adult, Type I",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            },
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            }
                        ]
                    }
                ],
                "keywords": [
                    "ebi",
                    "germline",
                    "disease"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs2092009642",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs2092009642"
                    },
                    {
                        "id": "rs2092009642",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs2092009642#frequency_tab"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3324,
                "end_pos": 3324,
                "sequence_org": "A",
                "sequence_mut": "G",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2099723",
                "ref_nt": "C",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "A3324",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs1422578175",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1422578175"
                    },
                    {
                        "id": "rs1422578175",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs1422578175#frequency_tab"
                    },
                    {
                        "id": "rs1422578175",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs1422578175"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3324,
                "end_pos": 3324,
                "sequence_org": "A",
                "sequence_mut": "S",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2099724",
                "ref_nt": "A",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "A3324",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs1422578175",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1422578175"
                    },
                    {
                        "id": "rs1422578175",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs1422578175#frequency_tab"
                    },
                    {
                        "id": "rs1422578175",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs1422578175"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3324,
                "end_pos": 3324,
                "sequence_org": "A",
                "sequence_mut": "T",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2099724",
                "ref_nt": "T",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "A3324",
                "disease": [
                    {
                        "disease_id": "DOID:0080322",
                        "recommended_name": {
                            "id": "DOID:0080322",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0080322",
                            "name": "polycystic kidney disease",
                            "description": "A cystic kidney disease that is characterized by the growth of fluid-filled cysts in the kidneys that reduces kidney function and may lead to kidney failure."
                        },
                        "synonyms": [
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0080322",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0080322"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0110858",
                        "recommended_name": {
                            "id": "DOID:0110858",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0110858",
                            "name": "polycystic kidney disease 1",
                            "description": "A autosomal dominant polycystic kidney disease that has_material_basis_in autosomal dominant inheritance of mutation in the PKD1 gene on chromosome 16p13.3."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "Polycystic Kidney Disease, Adult, Type I",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            },
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            }
                        ]
                    }
                ],
                "keywords": [
                    "ebi",
                    "germline",
                    "disease"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs745392733",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs745392733"
                    },
                    {
                        "id": "rs745392733",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs745392733"
                    },
                    {
                        "id": "rs745392733",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs745392733#frequency_tab"
                    },
                    {
                        "id": "rs745392733",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs745392733"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3325,
                "end_pos": 3325,
                "sequence_org": "V",
                "sequence_mut": "A",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2099720",
                "ref_nt": "G",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "V3325",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs1384393685",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1384393685"
                    },
                    {
                        "id": "rs1384393685",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs1384393685#frequency_tab"
                    },
                    {
                        "id": "rs1384393685",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs1384393685"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3325,
                "end_pos": 3325,
                "sequence_org": "V",
                "sequence_mut": "F",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2099721",
                "ref_nt": "A",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "V3325",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs1384393685",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1384393685"
                    },
                    {
                        "id": "rs1384393685",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs1384393685#frequency_tab"
                    },
                    {
                        "id": "rs1384393685",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs1384393685"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3325,
                "end_pos": 3325,
                "sequence_org": "V",
                "sequence_mut": "I",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2099721",
                "ref_nt": "T",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "V3325",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs1347045052",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1347045052"
                    },
                    {
                        "id": "rs1347045052",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs1347045052#frequency_tab"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3326,
                "end_pos": 3326,
                "sequence_org": "G",
                "sequence_mut": "A",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2099717",
                "ref_nt": "G",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "G3326",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs780752957",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs780752957"
                    },
                    {
                        "id": "rs780752957",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs780752957"
                    },
                    {
                        "id": "rs780752957",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs780752957#frequency_tab"
                    },
                    {
                        "id": "rs780752957",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs780752957"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3328,
                "end_pos": 3328,
                "sequence_org": "V",
                "sequence_mut": "L",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2099712",
                "ref_nt": "A",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "V3328",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs1203304646",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1203304646"
                    },
                    {
                        "id": "rs1203304646",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs1203304646#frequency_tab"
                    },
                    {
                        "id": "rs1203304646",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs1203304646"
                    }
                ],
                "glycoeffect": [
                    "o-glyco-site-loss"
                ],
                "start_pos": 3329,
                "end_pos": 3329,
                "sequence_org": "S",
                "sequence_mut": "F",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2099708",
                "ref_nt": "A",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "S3329",
                "disease": [
                    {
                        "disease_id": "DOID:0080322",
                        "recommended_name": {
                            "id": "DOID:0080322",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0080322",
                            "name": "polycystic kidney disease",
                            "description": "A cystic kidney disease that is characterized by the growth of fluid-filled cysts in the kidneys that reduces kidney function and may lead to kidney failure."
                        },
                        "synonyms": [
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0080322",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0080322"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0110858",
                        "recommended_name": {
                            "id": "DOID:0110858",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0110858",
                            "name": "polycystic kidney disease 1",
                            "description": "A autosomal dominant polycystic kidney disease that has_material_basis_in autosomal dominant inheritance of mutation in the PKD1 gene on chromosome 16p13.3."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "Polycystic Kidney Disease, Adult, Type I",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            },
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            }
                        ]
                    }
                ],
                "keywords": [
                    "ebi",
                    "germline",
                    "disease"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs773259284",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs773259284"
                    },
                    {
                        "id": "rs773259284",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs773259284"
                    },
                    {
                        "id": "rs773259284",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs773259284#frequency_tab"
                    },
                    {
                        "id": "rs773259284",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs773259284"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 332,
                "end_pos": 332,
                "sequence_org": "H",
                "sequence_mut": "Q",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2117996",
                "ref_nt": "C",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "H332",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs747089979",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs747089979"
                    },
                    {
                        "id": "rs747089979",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs747089979"
                    },
                    {
                        "id": "rs747089979",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs747089979"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 332,
                "end_pos": 332,
                "sequence_org": "H",
                "sequence_mut": "Y",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2117998",
                "ref_nt": "A",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "H332",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs2092008791",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs2092008791"
                    },
                    {
                        "id": "rs2092008791",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs2092008791#frequency_tab"
                    }
                ],
                "glycoeffect": [
                    "o-glyco-site-loss"
                ],
                "start_pos": 3330,
                "end_pos": 3330,
                "sequence_org": "S",
                "sequence_mut": "G",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2099706",
                "ref_nt": "C",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "S3330",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs1176736427",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1176736427"
                    },
                    {
                        "id": "rs1176736427",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs1176736427"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3330,
                "end_pos": 3330,
                "sequence_org": "S",
                "sequence_mut": "T",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2099705",
                "ref_nt": "G",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "S3330",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs796053523",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs796053523"
                    }
                ],
                "glycoeffect": [
                    "o-glyco-site-loss"
                ],
                "start_pos": 3330,
                "end_pos": 3330,
                "sequence_org": "S",
                "sequence_mut": "null",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2099706",
                "ref_nt": "p",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "S3330",
                "disease": [
                    {
                        "disease_id": "DOID:0080322",
                        "recommended_name": {
                            "id": "DOID:0080322",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0080322",
                            "name": "polycystic kidney disease",
                            "description": "A cystic kidney disease that is characterized by the growth of fluid-filled cysts in the kidneys that reduces kidney function and may lead to kidney failure."
                        },
                        "synonyms": [
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0080322",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0080322"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0110858",
                        "recommended_name": {
                            "id": "DOID:0110858",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0110858",
                            "name": "polycystic kidney disease 1",
                            "description": "A autosomal dominant polycystic kidney disease that has_material_basis_in autosomal dominant inheritance of mutation in the PKD1 gene on chromosome 16p13.3."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "Polycystic Kidney Disease, Adult, Type I",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            },
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            }
                        ]
                    }
                ],
                "keywords": [
                    "ebi",
                    "germline",
                    "disease"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs541894980",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs541894980"
                    },
                    {
                        "id": "rs541894980",
                        "database": "1000Genomes",
                        "url": "https://www.ensembl.org/homo_sapiens/Variation/Explore?v=rs541894980"
                    },
                    {
                        "id": "rs541894980",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs541894980"
                    },
                    {
                        "id": "rs541894980",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs541894980#frequency_tab"
                    },
                    {
                        "id": "rs541894980",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs541894980"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3331,
                "end_pos": 3331,
                "sequence_org": "V",
                "sequence_mut": "L",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2099703",
                "ref_nt": "G",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "V3331",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs541894980",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs541894980"
                    },
                    {
                        "id": "rs541894980",
                        "database": "1000Genomes",
                        "url": "https://www.ensembl.org/homo_sapiens/Variation/Explore?v=rs541894980"
                    },
                    {
                        "id": "rs541894980",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs541894980"
                    },
                    {
                        "id": "rs541894980",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs541894980#frequency_tab"
                    },
                    {
                        "id": "rs541894980",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs541894980"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3331,
                "end_pos": 3331,
                "sequence_org": "V",
                "sequence_mut": "M",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2099703",
                "ref_nt": "T",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "V3331",
                "keywords": [
                    "ebi",
                    "germline",
                    "disease"
                ],
                "disease": [
                    {
                        "disease_id": "DOID:0080322",
                        "recommended_name": {
                            "id": "DOID:0080322",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0080322",
                            "name": "polycystic kidney disease",
                            "description": "A cystic kidney disease that is characterized by the growth of fluid-filled cysts in the kidneys that reduces kidney function and may lead to kidney failure."
                        },
                        "synonyms": [
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0080322",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0080322"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0110858",
                        "recommended_name": {
                            "id": "DOID:0110858",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0110858",
                            "name": "polycystic kidney disease 1",
                            "description": "A autosomal dominant polycystic kidney disease that has_material_basis_in autosomal dominant inheritance of mutation in the PKD1 gene on chromosome 16p13.3."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "Polycystic Kidney Disease, Adult, Type I",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            },
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            }
                        ]
                    }
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs1272713748",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1272713748"
                    },
                    {
                        "id": "rs1272713748",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs1272713748#frequency_tab"
                    },
                    {
                        "id": "rs1272713748",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs1272713748"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3332,
                "end_pos": 3332,
                "sequence_org": "V",
                "sequence_mut": "F",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2099700",
                "ref_nt": "A",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "V3332",
                "keywords": [
                    "ebi",
                    "germline",
                    "disease"
                ],
                "disease": [
                    {
                        "disease_id": "DOID:0080322",
                        "recommended_name": {
                            "id": "DOID:0080322",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0080322",
                            "name": "polycystic kidney disease",
                            "description": "A cystic kidney disease that is characterized by the growth of fluid-filled cysts in the kidneys that reduces kidney function and may lead to kidney failure."
                        },
                        "synonyms": [
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0080322",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0080322"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0110858",
                        "recommended_name": {
                            "id": "DOID:0110858",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0110858",
                            "name": "polycystic kidney disease 1",
                            "description": "A autosomal dominant polycystic kidney disease that has_material_basis_in autosomal dominant inheritance of mutation in the PKD1 gene on chromosome 16p13.3."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "Polycystic Kidney Disease, Adult, Type I",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            },
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            }
                        ]
                    }
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs1555449235",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1555449235"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3332,
                "end_pos": 3332,
                "sequence_org": "V",
                "sequence_mut": "null",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2099701",
                "ref_nt": "l",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "V3332",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs2092008224",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs2092008224"
                    },
                    {
                        "id": "rs2092008224",
                        "database": "ENSEMBL",
                        "url": "https://www.ensembl.org/id/rs2092008224"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3333,
                "end_pos": 3333,
                "sequence_org": "V",
                "sequence_mut": "L",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2099697",
                "ref_nt": "G",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "V3333",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs1287231217",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1287231217"
                    },
                    {
                        "id": "rs1287231217",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs1287231217#frequency_tab"
                    },
                    {
                        "id": "rs1287231217",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs1287231217"
                    }
                ],
                "glycoeffect": [
                    "o-glyco-site-loss"
                ],
                "start_pos": 3334,
                "end_pos": 3334,
                "sequence_org": "Y",
                "sequence_mut": "C",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2099693",
                "ref_nt": "C",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "Y3334",
                "keywords": [
                    "ebi",
                    "germline",
                    "disease"
                ],
                "disease": [
                    {
                        "disease_id": "DOID:0080322",
                        "recommended_name": {
                            "id": "DOID:0080322",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0080322",
                            "name": "polycystic kidney disease",
                            "description": "A cystic kidney disease that is characterized by the growth of fluid-filled cysts in the kidneys that reduces kidney function and may lead to kidney failure."
                        },
                        "synonyms": [
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0080322",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0080322"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0110858",
                        "recommended_name": {
                            "id": "DOID:0110858",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0110858",
                            "name": "polycystic kidney disease 1",
                            "description": "A autosomal dominant polycystic kidney disease that has_material_basis_in autosomal dominant inheritance of mutation in the PKD1 gene on chromosome 16p13.3."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "Polycystic Kidney Disease, Adult, Type I",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            },
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            }
                        ]
                    }
                ]
            },
            {
                "evidence": [
                    {
                        "id": "P98161",
                        "database": "BioMuta",
                        "url": "https://hivelab.biochemistry.gwu.edu/biomuta/proteinview/P98161"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3335,
                "end_pos": 3335,
                "subjects_tested": "2670",
                "subjects_positive": "1",
                "frequency": "0.0",
                "sequence_org": "P",
                "sequence_mut": "L",
                "comment": "Somatic mutation passed 0 out of 6 filters: .",
                "chr_id": "16",
                "chr_pos": "2099690",
                "ref_nt": "G",
                "alt_nt": "A",
                "minor_allelic_frequency": "",
                "site_lbl": "P3335",
                "disease": [
                    {
                        "disease_id": "DOID:1319",
                        "recommended_name": {
                            "id": "DOID:1319",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:1319",
                            "name": "brain cancer",
                            "description": "A central nervous system cancer that is characterized by the growth of abnormal cells in the tissues of the brain."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:1319",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:1319",
                                "name": "BT - Brain tumour",
                                "description": ""
                            },
                            {
                                "id": "DOID:1319",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:1319",
                                "name": "adult brain tumor",
                                "description": ""
                            },
                            {
                                "id": "DOID:1319",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:1319",
                                "name": "adult malignant brain neoplasm",
                                "description": ""
                            },
                            {
                                "id": "DOID:1319",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:1319",
                                "name": "brain neoplasm",
                                "description": ""
                            },
                            {
                                "id": "DOID:1319",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:1319",
                                "name": "brain neoplasm, adult",
                                "description": ""
                            },
                            {
                                "id": "DOID:1319",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:1319",
                                "name": "malignant brain tumour",
                                "description": ""
                            },
                            {
                                "id": "DOID:1319",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:1319",
                                "name": "malignant primary brain neoplasm",
                                "description": ""
                            },
                            {
                                "id": "DOID:1319",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:1319",
                                "name": "malignant primary brain tumor",
                                "description": ""
                            },
                            {
                                "id": "DOID:1319",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:1319",
                                "name": "malignant tumor of Brain",
                                "description": ""
                            },
                            {
                                "id": "DOID:1319",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:1319",
                                "name": "malignant tumor of adult brain",
                                "description": ""
                            },
                            {
                                "id": "DOID:1319",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:1319",
                                "name": "neoplasm of brain",
                                "description": ""
                            },
                            {
                                "id": "DOID:1319",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:1319",
                                "name": "primary brain neoplasm",
                                "description": ""
                            },
                            {
                                "id": "DOID:1319",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:1319",
                                "name": "primary brain tumor",
                                "description": ""
                            },
                            {
                                "id": "DOID:1319",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:1319",
                                "name": "primary malignant neoplasm of brain",
                                "description": ""
                            },
                            {
                                "id": "DOID:1319",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:1319",
                                "name": "tumor of the Brain",
                                "description": ""
                            }
                        ],
                        "unlinked_id_list": [
                            "DOID:4203",
                            "DOID:3541",
                            "DOID:4706",
                            "DOID:1659",
                            "DOID:368"
                        ],
                        "evidence": [
                            {
                                "id": "1319",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:1319"
                            }
                        ]
                    }
                ],
                "keywords": [
                    "biomuta",
                    "somatic",
                    "cancer",
                    "disease"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs753957271",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs753957271"
                    },
                    {
                        "id": "rs753957271",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs753957271"
                    },
                    {
                        "id": "rs753957271",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs753957271"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3336,
                "end_pos": 3336,
                "sequence_org": "V",
                "sequence_mut": "A",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2099687",
                "ref_nt": "G",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "V3336",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs754956606",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs754956606"
                    },
                    {
                        "id": "rs754956606",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs754956606"
                    },
                    {
                        "id": "rs754956606",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs754956606#frequency_tab"
                    },
                    {
                        "id": "rs754956606",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs754956606"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3336,
                "end_pos": 3336,
                "sequence_org": "V",
                "sequence_mut": "F",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2099688",
                "ref_nt": "A",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "V3336",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs754956606",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs754956606"
                    },
                    {
                        "id": "rs754956606",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs754956606"
                    },
                    {
                        "id": "rs754956606",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs754956606#frequency_tab"
                    },
                    {
                        "id": "rs754956606",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs754956606"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3336,
                "end_pos": 3336,
                "sequence_org": "V",
                "sequence_mut": "I",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2099688",
                "ref_nt": "T",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "V3336",
                "keywords": [
                    "ebi",
                    "germline",
                    "disease"
                ],
                "disease": [
                    {
                        "disease_id": "DOID:0080322",
                        "recommended_name": {
                            "id": "DOID:0080322",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0080322",
                            "name": "polycystic kidney disease",
                            "description": "A cystic kidney disease that is characterized by the growth of fluid-filled cysts in the kidneys that reduces kidney function and may lead to kidney failure."
                        },
                        "synonyms": [
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0080322",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0080322"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0110858",
                        "recommended_name": {
                            "id": "DOID:0110858",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0110858",
                            "name": "polycystic kidney disease 1",
                            "description": "A autosomal dominant polycystic kidney disease that has_material_basis_in autosomal dominant inheritance of mutation in the PKD1 gene on chromosome 16p13.3."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "Polycystic Kidney Disease, Adult, Type I",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            },
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            }
                        ]
                    }
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs761039266",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs761039266"
                    },
                    {
                        "id": "rs761039266",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs761039266"
                    },
                    {
                        "id": "rs761039266",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs761039266"
                    }
                ],
                "glycoeffect": [
                    "o-glyco-site-loss"
                ],
                "start_pos": 3337,
                "end_pos": 3337,
                "sequence_org": "Y",
                "sequence_mut": "C",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2099684",
                "ref_nt": "C",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "Y3337",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs2544710685",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs2544710685"
                    }
                ],
                "glycoeffect": [
                    "o-glyco-site-loss"
                ],
                "start_pos": 3337,
                "end_pos": 3337,
                "sequence_org": "Y",
                "sequence_mut": "null",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2099686_2099687",
                "ref_nt": "p",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "Y3337",
                "disease": [
                    {
                        "disease_id": "DOID:0080322",
                        "recommended_name": {
                            "id": "DOID:0080322",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0080322",
                            "name": "polycystic kidney disease",
                            "description": "A cystic kidney disease that is characterized by the growth of fluid-filled cysts in the kidneys that reduces kidney function and may lead to kidney failure."
                        },
                        "synonyms": [
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0080322",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0080322"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0110858",
                        "recommended_name": {
                            "id": "DOID:0110858",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0110858",
                            "name": "polycystic kidney disease 1",
                            "description": "A autosomal dominant polycystic kidney disease that has_material_basis_in autosomal dominant inheritance of mutation in the PKD1 gene on chromosome 16p13.3."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "Polycystic Kidney Disease, Adult, Type I",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            },
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            }
                        ]
                    }
                ],
                "keywords": [
                    "ebi",
                    "germline",
                    "disease"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs2092007148",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs2092007148"
                    },
                    {
                        "id": "rs2092007148",
                        "database": "ENSEMBL",
                        "url": "https://www.ensembl.org/id/rs2092007148"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3339,
                "end_pos": 3339,
                "sequence_org": "A",
                "sequence_mut": "G",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2099678",
                "ref_nt": "C",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "A3339",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs1364686083",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1364686083"
                    },
                    {
                        "id": "rs1364686083",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs1364686083"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3339,
                "end_pos": 3339,
                "sequence_org": "A",
                "sequence_mut": "T",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2099679",
                "ref_nt": "T",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "A3339",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs772316684",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs772316684"
                    },
                    {
                        "id": "rs772316684",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs772316684"
                    },
                    {
                        "id": "rs772316684",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs772316684#frequency_tab"
                    },
                    {
                        "id": "rs772316684",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs772316684"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 333,
                "end_pos": 333,
                "sequence_org": "V",
                "sequence_mut": "M",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2117995",
                "ref_nt": "T",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "V333",
                "keywords": [
                    "ebi",
                    "germline",
                    "disease"
                ],
                "disease": [
                    {
                        "disease_id": "DOID:0080322",
                        "recommended_name": {
                            "id": "DOID:0080322",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0080322",
                            "name": "polycystic kidney disease",
                            "description": "A cystic kidney disease that is characterized by the growth of fluid-filled cysts in the kidneys that reduces kidney function and may lead to kidney failure."
                        },
                        "synonyms": [
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0080322",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0080322"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0110858",
                        "recommended_name": {
                            "id": "DOID:0110858",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0110858",
                            "name": "polycystic kidney disease 1",
                            "description": "A autosomal dominant polycystic kidney disease that has_material_basis_in autosomal dominant inheritance of mutation in the PKD1 gene on chromosome 16p13.3."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "Polycystic Kidney Disease, Adult, Type I",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            },
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            }
                        ]
                    }
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs1298604442",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1298604442"
                    },
                    {
                        "id": "rs1298604442",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs1298604442"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3340,
                "end_pos": 3340,
                "sequence_org": "I",
                "sequence_mut": "M",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2099674",
                "ref_nt": "C",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "I3340",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "P98161",
                        "database": "BioMuta",
                        "url": "https://hivelab.biochemistry.gwu.edu/biomuta/proteinview/P98161"
                    },
                    {
                        "id": "rs1421726664",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1421726664"
                    },
                    {
                        "id": "rs1421726664",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs1421726664"
                    },
                    {
                        "id": "rs1421726664",
                        "database": "COSMIC",
                        "url": "https://www.ensembl.org/homo_sapiens/Variation/Explore?v=rs1421726664"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3341,
                "end_pos": 3341,
                "subjects_tested": "2053",
                "subjects_positive": "1",
                "frequency": "0.0",
                "sequence_org": "L",
                "sequence_mut": "F",
                "comment": "Somatic mutation passed 0 out of 6 filters: .",
                "chr_id": "16",
                "chr_pos": "2099673",
                "ref_nt": "G",
                "alt_nt": "A",
                "minor_allelic_frequency": "",
                "site_lbl": "L3341",
                "disease": [
                    {
                        "disease_id": "DOID:4159",
                        "recommended_name": {
                            "id": "DOID:4159",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:4159",
                            "name": "skin cancer",
                            "description": "An integumentary system cancer located_in the skin that is the uncontrolled growth of abnormal skin cells."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:4159",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:4159",
                                "name": "CA - skin cancer",
                                "description": ""
                            },
                            {
                                "id": "DOID:4159",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:4159",
                                "name": "malignant neoplasm of skin",
                                "description": ""
                            },
                            {
                                "id": "DOID:4159",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:4159",
                                "name": "melanoma and Non-melanoma skin cancer",
                                "description": ""
                            }
                        ],
                        "unlinked_id_list": [
                            "DOID:3149",
                            "DOID:3451"
                        ],
                        "evidence": [
                            {
                                "id": "4159",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:4159"
                            }
                        ]
                    }
                ],
                "keywords": [
                    "biomuta",
                    "somatic",
                    "cancer",
                    "disease",
                    "ebi"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "P98161",
                        "database": "BioMuta",
                        "url": "https://hivelab.biochemistry.gwu.edu/biomuta/proteinview/P98161"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3341,
                "end_pos": 3341,
                "subjects_tested": "4177",
                "subjects_positive": "1",
                "frequency": "0.0",
                "sequence_org": "L",
                "sequence_mut": "P",
                "comment": "Somatic mutation passed 0 out of 6 filters: .",
                "chr_id": "16",
                "chr_pos": "2099672",
                "ref_nt": "A",
                "alt_nt": "G",
                "minor_allelic_frequency": "",
                "site_lbl": "L3341",
                "disease": [
                    {
                        "disease_id": "DOID:10283",
                        "recommended_name": {
                            "id": "DOID:10283",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:10283",
                            "name": "prostate cancer",
                            "description": "A male reproductive organ cancer that is located_in the prostate."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:10283",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:10283",
                                "name": "NGP - new growth of prostate",
                                "description": ""
                            },
                            {
                                "id": "DOID:10283",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:10283",
                                "name": "hereditary prostate cancer",
                                "description": ""
                            },
                            {
                                "id": "DOID:10283",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:10283",
                                "name": "malignant tumor of the prostate",
                                "description": ""
                            },
                            {
                                "id": "DOID:10283",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:10283",
                                "name": "prostate cancer, familial",
                                "description": ""
                            },
                            {
                                "id": "DOID:10283",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:10283",
                                "name": "prostate neoplasm",
                                "description": ""
                            },
                            {
                                "id": "DOID:10283",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:10283",
                                "name": "prostatic cancer",
                                "description": ""
                            },
                            {
                                "id": "DOID:10283",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:10283",
                                "name": "prostatic neoplasm",
                                "description": ""
                            },
                            {
                                "id": "DOID:10283",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:10283",
                                "name": "tumor of the prostate",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0010257",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0010257",
                                "name": "prostate cancer, hereditary, X-linked 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0010257",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0010257",
                                "name": "HPCX1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0010257",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0010257",
                                "name": "prostate cancer, hereditary, X-linked 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0010405",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0010405",
                                "name": "prostate cancer, hereditary, X-linked 2",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0010405",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0010405",
                                "name": "HPCX2",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0010405",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0010405",
                                "name": "prostate cancer, hereditary, X-linked 2",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011098",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011098",
                                "name": "prostate cancer, hereditary, 1",
                                "description": "Any familial prostate cancer in which the cause of the disease is a mutation in the RNASEL gene."
                            },
                            {
                                "id": "MONDO:0011098",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011098",
                                "name": "RNASEL familial prostate cancer",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011098",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011098",
                                "name": "familial prostate cancer caused by mutation in RNASEL",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011098",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011098",
                                "name": "prostate cancer 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011098",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011098",
                                "name": "prostate cancer, hereditary, 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011098",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011098",
                                "name": "prostate cancer, hereditary, type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011098",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011098",
                                "name": "HPC1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011270",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011270",
                                "name": "prostate cancer, hereditary, 8",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011270",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011270",
                                "name": "prostate cancer, hereditary, 8",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011270",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011270",
                                "name": "prostate cancer, hereditary, type 8",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011270",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011270",
                                "name": "HPC8",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012093",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012093",
                                "name": "prostate cancer, hereditary, 3",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012093",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012093",
                                "name": "prostate cancer, hereditary, 3",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012093",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012093",
                                "name": "prostate cancer, hereditary, type 3",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012093",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012093",
                                "name": "prostate cancer, susceptibility to, 3",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012093",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012093",
                                "name": "HPC3",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012094",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012094",
                                "name": "prostate cancer, hereditary, 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012094",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012094",
                                "name": "prostate cancer, hereditary, 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012094",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012094",
                                "name": "prostate cancer, hereditary, type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012094",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012094",
                                "name": "prostate cancer, susceptibility to, 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012094",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012094",
                                "name": "HPC4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012244",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012244",
                                "name": "prostate cancer, hereditary, 5",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012244",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012244",
                                "name": "prostate cancer, hereditary, 5",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012244",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012244",
                                "name": "prostate cancer, hereditary, type 5",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012244",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012244",
                                "name": "HPC5",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012300",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012300",
                                "name": "prostate cancer, hereditary, 6",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012300",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012300",
                                "name": "prostate cancer, hereditary, 6",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012300",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012300",
                                "name": "prostate cancer, hereditary, type 6",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012300",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012300",
                                "name": "HPC6",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012470",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012470",
                                "name": "prostate cancer, hereditary, 7",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012470",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012470",
                                "name": "HPC7",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012470",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012470",
                                "name": "prostate cancer, hereditary, 7",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012597",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012597",
                                "name": "prostate cancer, hereditary, 9",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012597",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012597",
                                "name": "prostate cancer, hereditary, 9",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012597",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012597",
                                "name": "prostate cancer, hereditary, type 9",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012597",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012597",
                                "name": "HPC9",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012620",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012620",
                                "name": "prostate cancer, hereditary, 10",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012620",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012620",
                                "name": "HPC10",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012620",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012620",
                                "name": "prostate cancer, hereditary, 10",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012741",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012741",
                                "name": "prostate cancer, hereditary, 12",
                                "description": "Any familial prostate cancer in which the cause of the disease is a mutation in the EHBP1 gene."
                            },
                            {
                                "id": "MONDO:0012741",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012741",
                                "name": "EHBP1 familial prostate cancer",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012741",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012741",
                                "name": "familial prostate cancer caused by mutation in EHBP1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012741",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012741",
                                "name": "prostate cancer, hereditary, 12",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012741",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012741",
                                "name": "prostate cancer, hereditary, type 12",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012741",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012741",
                                "name": "HPC12",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012758",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012758",
                                "name": "prostate cancer, hereditary, 13",
                                "description": "Any familial prostate cancer in which the cause of the disease is a mutation in the MSMB gene."
                            },
                            {
                                "id": "MONDO:0012758",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012758",
                                "name": "MSMB familial prostate cancer",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012758",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012758",
                                "name": "familial prostate cancer caused by mutation in MSMB",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012758",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012758",
                                "name": "prostate cancer, hereditary, 13",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012758",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012758",
                                "name": "prostate cancer, hereditary, type 13",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012758",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012758",
                                "name": "HPC13",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012768",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012768",
                                "name": "prostate cancer, hereditary, 11",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012768",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012768",
                                "name": "HPC11",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012768",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012768",
                                "name": "prostate cancer, hereditary, 11",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012769",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012769",
                                "name": "prostate cancer, hereditary, 14",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012769",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012769",
                                "name": "HPC14",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012769",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012769",
                                "name": "prostate cancer, hereditary, 14",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012770",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012770",
                                "name": "prostate cancer, hereditary, 15",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012770",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012770",
                                "name": "HPC15",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012770",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012770",
                                "name": "prostate cancer, hereditary, 15",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0700275",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0700275",
                                "name": "prostate cancer, hereditary",
                                "description": "An instance of prostate cancer that is caused by an inherited genomic modification in an individual. Familial prostate cancer (FPC) is a malignant tumor of the prostate with an early onset. FPC is either asymptomatic or causes mictionary symptoms, erectile dysfunction, bone pain, venous compression and infectious or inflammatory syndrome (for the metastatic forms). It is also characterized by familial antecedents."
                            },
                            {
                                "id": "MIM:601518",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/601518",
                                "name": "Prostate cancer, hereditary, 1",
                                "description": "Prostate cancer, hereditary, 1"
                            },
                            {
                                "id": "MIM:610997",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/610997",
                                "name": "Prostate cancer, hereditary, 9",
                                "description": "Prostate cancer, hereditary, 9"
                            },
                            {
                                "id": "MIM:611868",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/611868",
                                "name": "Prostate cancer, hereditary, 12",
                                "description": "Prostate cancer, hereditary, 12"
                            },
                            {
                                "id": "MIM:611928",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/611928",
                                "name": "Prostate cancer, hereditary, 13",
                                "description": "Prostate cancer, hereditary, 13"
                            },
                            {
                                "id": "MIM:611955",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/611955",
                                "name": "Prostate cancer, hereditary, 11",
                                "description": "Prostate cancer, hereditary, 11"
                            },
                            {
                                "id": "MIM:176807",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/176807",
                                "name": "Prostate cancer",
                                "description": "Prostate cancer"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "10283",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:10283"
                            }
                        ]
                    }
                ],
                "keywords": [
                    "biomuta",
                    "somatic",
                    "cancer",
                    "disease"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs1158465434",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1158465434"
                    },
                    {
                        "id": "rs1158465434",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs1158465434#frequency_tab"
                    },
                    {
                        "id": "rs1158465434",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs1158465434"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3343,
                "end_pos": 3343,
                "sequence_org": "L",
                "sequence_mut": "F",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2099667",
                "ref_nt": "A",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "L3343",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs1158465434",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1158465434"
                    },
                    {
                        "id": "rs1158465434",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs1158465434#frequency_tab"
                    },
                    {
                        "id": "rs1158465434",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs1158465434"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3343,
                "end_pos": 3343,
                "sequence_org": "L",
                "sequence_mut": "V",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2099667",
                "ref_nt": "C",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "L3343",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs1567169118",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1567169118"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3343,
                "end_pos": 3343,
                "sequence_org": "L",
                "sequence_mut": "null",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2099672",
                "ref_nt": "p",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "L3343",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs2092006545",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs2092006545"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3344,
                "end_pos": 3344,
                "sequence_org": "F",
                "sequence_mut": "null",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2099664",
                "ref_nt": "l",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "F3344",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs956410708",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs956410708"
                    },
                    {
                        "id": "rs956410708",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs956410708#frequency_tab"
                    },
                    {
                        "id": "rs956410708",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs956410708"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3345,
                "end_pos": 3345,
                "sequence_org": "R",
                "sequence_mut": "Q",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2099660",
                "ref_nt": "T",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "R3345",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs986431548",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs986431548"
                    },
                    {
                        "id": "rs986431548",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs986431548#frequency_tab"
                    },
                    {
                        "id": "rs986431548",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs986431548"
                    },
                    {
                        "id": "rs986431548",
                        "database": "COSMIC",
                        "url": "https://www.ensembl.org/homo_sapiens/Variation/Explore?v=rs986431548"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3345,
                "end_pos": 3345,
                "sequence_org": "R",
                "sequence_mut": "W",
                "comment": "Somatic mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2099661",
                "ref_nt": "A",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "R3345",
                "keywords": [
                    "ebi",
                    "somatic"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs2092006341",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs2092006341"
                    },
                    {
                        "id": "rs2092006341",
                        "database": "ENSEMBL",
                        "url": "https://www.ensembl.org/id/rs2092006341"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3346,
                "end_pos": 3346,
                "sequence_org": "M",
                "sequence_mut": "L",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2099658",
                "ref_nt": "A",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "M3346",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs762256401",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs762256401"
                    },
                    {
                        "id": "rs762256401",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs762256401"
                    },
                    {
                        "id": "rs762256401",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs762256401#frequency_tab"
                    },
                    {
                        "id": "rs762256401",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs762256401"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3346,
                "end_pos": 3346,
                "sequence_org": "M",
                "sequence_mut": "R",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2099657",
                "ref_nt": "C",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "M3346",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs774658731",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs774658731"
                    },
                    {
                        "id": "rs774658731",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs774658731"
                    },
                    {
                        "id": "rs774658731",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs774658731"
                    }
                ],
                "glycoeffect": [
                    "o-glyco-site-loss"
                ],
                "start_pos": 3347,
                "end_pos": 3347,
                "sequence_org": "S",
                "sequence_mut": "A",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2099655",
                "ref_nt": "C",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "S3347",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "P98161",
                        "database": "BioMuta",
                        "url": "https://hivelab.biochemistry.gwu.edu/biomuta/proteinview/P98161"
                    },
                    {
                        "id": "rs774658731",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs774658731"
                    },
                    {
                        "id": "rs774658731",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs774658731"
                    },
                    {
                        "id": "rs774658731",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs774658731"
                    },
                    {
                        "id": "rs774658731",
                        "database": "COSMIC",
                        "url": "https://www.ensembl.org/homo_sapiens/Variation/Explore?v=rs774658731"
                    }
                ],
                "glycoeffect": [
                    "o-glyco-site-loss"
                ],
                "start_pos": 3347,
                "end_pos": 3347,
                "subjects_tested": "3601",
                "subjects_positive": "1",
                "frequency": "0.0",
                "sequence_org": "S",
                "sequence_mut": "P",
                "comment": "Somatic mutation passed 0 out of 6 filters: .",
                "chr_id": "16",
                "chr_pos": "2099655",
                "ref_nt": "A",
                "alt_nt": "G",
                "minor_allelic_frequency": "",
                "site_lbl": "S3347",
                "disease": [
                    {
                        "disease_id": "DOID:9256",
                        "recommended_name": {
                            "id": "DOID:9256",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:9256",
                            "name": "colorectal cancer",
                            "description": "A large intestine cancer that is located_in the colon and/or located_in the rectum."
                        },
                        "synonyms": [
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectal cancer",
                                "description": "A primary or metastatic malignant neoplasm that affects the colon or rectum. Representative examples include carcinoma, lymphoma, and sarcoma."
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "cancer of colorectum",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "cancer of large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "cancer of large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "cancer of the large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colon cancer, advanced, somatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colon cancer, somatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectal cancer",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectal cancer with chromosomal instability, somatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectal cancer, autosomal dominant, somatic mutation",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectal cancer, somatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectal cancer, susceptibility to, autosomal dominant, somatic mutation",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectum cancer",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant colorectal neoplasm",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant colorectal tumor",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant colorectal tumour",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant colorectum neoplasm",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant large bowel neoplasm",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant large bowel tumor",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant large bowel tumour",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant large intestine neoplasm",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant large intestine tumor",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant large intestine tumour",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant neoplasm of colorectum",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant neoplasm of large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant neoplasm of large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant neoplasm of the large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant neoplasm of the large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumor of large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumor of large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumor of the large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumor of the large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumour of large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumour of large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumour of the large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumour of the large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "CRC",
                                "description": ""
                            },
                            {
                                "id": "MIM:114500",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/114500",
                                "name": "Colorectal cancer",
                                "description": "Colorectal cancer"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "9256",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:9256"
                            }
                        ]
                    }
                ],
                "keywords": [
                    "biomuta",
                    "somatic",
                    "cancer",
                    "disease",
                    "ebi"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs146494724",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs146494724"
                    },
                    {
                        "id": "rs146494724",
                        "database": "1000Genomes",
                        "url": "https://www.ensembl.org/homo_sapiens/Variation/Explore?v=rs146494724"
                    },
                    {
                        "id": "rs146494724",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs146494724"
                    },
                    {
                        "id": "rs146494724",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs146494724#frequency_tab"
                    },
                    {
                        "id": "rs146494724",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs146494724"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3348,
                "end_pos": 3348,
                "sequence_org": "R",
                "sequence_mut": "P",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2099651",
                "ref_nt": "G",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "R3348",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs146494724",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs146494724"
                    },
                    {
                        "id": "rs146494724",
                        "database": "1000Genomes",
                        "url": "https://www.ensembl.org/homo_sapiens/Variation/Explore?v=rs146494724"
                    },
                    {
                        "id": "rs146494724",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs146494724"
                    },
                    {
                        "id": "rs146494724",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs146494724#frequency_tab"
                    },
                    {
                        "id": "rs146494724",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs146494724"
                    },
                    {
                        "id": "rs146494724",
                        "database": "COSMIC",
                        "url": "https://www.ensembl.org/homo_sapiens/Variation/Explore?v=rs146494724"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3348,
                "end_pos": 3348,
                "sequence_org": "R",
                "sequence_mut": "Q",
                "comment": "Somatic mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2099651",
                "ref_nt": "T",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "R3348",
                "keywords": [
                    "ebi",
                    "somatic",
                    "disease"
                ],
                "disease": [
                    {
                        "disease_id": "DOID:0080322",
                        "recommended_name": {
                            "id": "DOID:0080322",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0080322",
                            "name": "polycystic kidney disease",
                            "description": "A cystic kidney disease that is characterized by the growth of fluid-filled cysts in the kidneys that reduces kidney function and may lead to kidney failure."
                        },
                        "synonyms": [
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0080322",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0080322"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0110858",
                        "recommended_name": {
                            "id": "DOID:0110858",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0110858",
                            "name": "polycystic kidney disease 1",
                            "description": "A autosomal dominant polycystic kidney disease that has_material_basis_in autosomal dominant inheritance of mutation in the PKD1 gene on chromosome 16p13.3."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "Polycystic Kidney Disease, Adult, Type I",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            },
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            }
                        ]
                    }
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs769208706",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs769208706"
                    },
                    {
                        "id": "rs769208706",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs769208706"
                    },
                    {
                        "id": "rs769208706",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs769208706#frequency_tab"
                    },
                    {
                        "id": "rs769208706",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs769208706"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3348,
                "end_pos": 3348,
                "sequence_org": "R",
                "sequence_mut": "W",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2099652",
                "ref_nt": "A",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "R3348",
                "disease": [
                    {
                        "disease_id": "DOID:0080322",
                        "recommended_name": {
                            "id": "DOID:0080322",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0080322",
                            "name": "polycystic kidney disease",
                            "description": "A cystic kidney disease that is characterized by the growth of fluid-filled cysts in the kidneys that reduces kidney function and may lead to kidney failure."
                        },
                        "synonyms": [
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0080322",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0080322"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0110858",
                        "recommended_name": {
                            "id": "DOID:0110858",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0110858",
                            "name": "polycystic kidney disease 1",
                            "description": "A autosomal dominant polycystic kidney disease that has_material_basis_in autosomal dominant inheritance of mutation in the PKD1 gene on chromosome 16p13.3."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "Polycystic Kidney Disease, Adult, Type I",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            },
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            }
                        ]
                    }
                ],
                "keywords": [
                    "ebi",
                    "germline",
                    "disease"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs967886730",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs967886730"
                    },
                    {
                        "id": "rs967886730",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs967886730#frequency_tab"
                    }
                ],
                "glycoeffect": [
                    "o-glyco-site-loss"
                ],
                "start_pos": 3349,
                "end_pos": 3349,
                "sequence_org": "S",
                "sequence_mut": "N",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2099648",
                "ref_nt": "T",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "S3349",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs967886730",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs967886730"
                    },
                    {
                        "id": "rs967886730",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs967886730#frequency_tab"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3349,
                "end_pos": 3349,
                "sequence_org": "S",
                "sequence_mut": "T",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2099648",
                "ref_nt": "G",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "S3349",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs4018169",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs4018169"
                    },
                    {
                        "id": "rs4018169",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs4018169"
                    },
                    {
                        "id": "rs4018169",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs4018169#frequency_tab"
                    },
                    {
                        "id": "rs4018169",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs4018169"
                    }
                ],
                "glycoeffect": [
                    "o-glyco-site-loss"
                ],
                "start_pos": 334,
                "end_pos": 334,
                "sequence_org": "T",
                "sequence_mut": "M",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2117991",
                "ref_nt": "A",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "T334",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "P98161",
                        "database": "BioMuta",
                        "url": "https://hivelab.biochemistry.gwu.edu/biomuta/proteinview/P98161"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3350,
                "end_pos": 3350,
                "subjects_tested": "1704",
                "subjects_positive": "1",
                "frequency": "0.1",
                "sequence_org": "K",
                "sequence_mut": "E",
                "comment": "Somatic mutation passed 0 out of 6 filters: .",
                "chr_id": "16",
                "chr_pos": "2099646",
                "ref_nt": "T",
                "alt_nt": "C",
                "minor_allelic_frequency": "",
                "site_lbl": "K3350",
                "disease": [
                    {
                        "disease_id": "DOID:363",
                        "recommended_name": {
                            "id": "DOID:363",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:363",
                            "name": "uterine cancer",
                            "description": "A female reproductive organ cancer that is located_in the uterus."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:363",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:363",
                                "name": "CA - cancer of uterus",
                                "description": ""
                            },
                            {
                                "id": "DOID:363",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:363",
                                "name": "Tumour of uterus",
                                "description": ""
                            },
                            {
                                "id": "DOID:363",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:363",
                                "name": "malignant neoplasm of uterus",
                                "description": ""
                            },
                            {
                                "id": "DOID:363",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:363",
                                "name": "malignant uterine tumor",
                                "description": ""
                            },
                            {
                                "id": "DOID:363",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:363",
                                "name": "neoplasm of uterus",
                                "description": ""
                            },
                            {
                                "id": "DOID:363",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:363",
                                "name": "uterine tumor",
                                "description": ""
                            },
                            {
                                "id": "DOID:363",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:363",
                                "name": "uterus neoplasm",
                                "description": ""
                            }
                        ],
                        "unlinked_id_list": [
                            "DOID:9460",
                            "DOID:5166",
                            "DOID:2021",
                            "DOID:4114"
                        ],
                        "evidence": [
                            {
                                "id": "363",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:363"
                            }
                        ]
                    }
                ],
                "keywords": [
                    "biomuta",
                    "somatic",
                    "cancer",
                    "disease"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs780176792",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs780176792"
                    },
                    {
                        "id": "rs780176792",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs780176792"
                    },
                    {
                        "id": "rs780176792",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs780176792#frequency_tab"
                    },
                    {
                        "id": "rs780176792",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs780176792"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3351,
                "end_pos": 3351,
                "sequence_org": "V",
                "sequence_mut": "G",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2097983",
                "ref_nt": "C",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "V3351",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs1024272951",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1024272951"
                    },
                    {
                        "id": "rs1024272951",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs1024272951#frequency_tab"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3352,
                "end_pos": 3352,
                "sequence_org": "A",
                "sequence_mut": "P",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2097981",
                "ref_nt": "G",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "A3352",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs1024272951",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1024272951"
                    },
                    {
                        "id": "rs1024272951",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs1024272951#frequency_tab"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3352,
                "end_pos": 3352,
                "sequence_org": "A",
                "sequence_mut": "T",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2097981",
                "ref_nt": "T",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "A3352",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs756201243",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs756201243"
                    },
                    {
                        "id": "rs756201243",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs756201243"
                    },
                    {
                        "id": "rs756201243",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs756201243#frequency_tab"
                    },
                    {
                        "id": "rs756201243",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs756201243"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3352,
                "end_pos": 3352,
                "sequence_org": "A",
                "sequence_mut": "V",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2097980",
                "ref_nt": "A",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "A3352",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs1451091699",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1451091699"
                    },
                    {
                        "id": "rs1451091699",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs1451091699#frequency_tab"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3353,
                "end_pos": 3353,
                "sequence_org": "G",
                "sequence_mut": "R",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2097978",
                "ref_nt": "T",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "G3353",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs1452197858",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1452197858"
                    },
                    {
                        "id": "rs1452197858",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs1452197858#frequency_tab"
                    },
                    {
                        "id": "rs1452197858",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs1452197858"
                    }
                ],
                "glycoeffect": [
                    "o-glyco-site-loss"
                ],
                "start_pos": 3354,
                "end_pos": 3354,
                "sequence_org": "S",
                "sequence_mut": "I",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2097974",
                "ref_nt": "A",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "S3354",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs1452197858",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1452197858"
                    },
                    {
                        "id": "rs1452197858",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs1452197858#frequency_tab"
                    },
                    {
                        "id": "rs1452197858",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs1452197858"
                    }
                ],
                "glycoeffect": [
                    "o-glyco-site-loss"
                ],
                "start_pos": 3354,
                "end_pos": 3354,
                "sequence_org": "S",
                "sequence_mut": "N",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2097974",
                "ref_nt": "T",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "S3354",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs745944405",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs745944405"
                    },
                    {
                        "id": "rs745944405",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs745944405"
                    },
                    {
                        "id": "rs745944405",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs745944405#frequency_tab"
                    },
                    {
                        "id": "rs745944405",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs745944405"
                    }
                ],
                "glycoeffect": [
                    "o-glyco-site-loss"
                ],
                "start_pos": 3354,
                "end_pos": 3354,
                "sequence_org": "S",
                "sequence_mut": "R",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2097973",
                "ref_nt": "C",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "S3354",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs1452197858",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1452197858"
                    },
                    {
                        "id": "rs1452197858",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs1452197858#frequency_tab"
                    },
                    {
                        "id": "rs1452197858",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs1452197858"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3354,
                "end_pos": 3354,
                "sequence_org": "S",
                "sequence_mut": "T",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2097974",
                "ref_nt": "G",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "S3354",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs781263445",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs781263445"
                    },
                    {
                        "id": "rs781263445",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs781263445"
                    },
                    {
                        "id": "rs781263445",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs781263445#frequency_tab"
                    },
                    {
                        "id": "rs781263445",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs781263445"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3355,
                "end_pos": 3355,
                "sequence_org": "P",
                "sequence_mut": "L",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2097971",
                "ref_nt": "A",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "P3355",
                "keywords": [
                    "ebi",
                    "germline",
                    "disease"
                ],
                "disease": [
                    {
                        "disease_id": "DOID:0080322",
                        "recommended_name": {
                            "id": "DOID:0080322",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0080322",
                            "name": "polycystic kidney disease",
                            "description": "A cystic kidney disease that is characterized by the growth of fluid-filled cysts in the kidneys that reduces kidney function and may lead to kidney failure."
                        },
                        "synonyms": [
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0080322",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0080322"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0110858",
                        "recommended_name": {
                            "id": "DOID:0110858",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0110858",
                            "name": "polycystic kidney disease 1",
                            "description": "A autosomal dominant polycystic kidney disease that has_material_basis_in autosomal dominant inheritance of mutation in the PKD1 gene on chromosome 16p13.3."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "Polycystic Kidney Disease, Adult, Type I",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            },
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            }
                        ]
                    }
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs764557478",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs764557478"
                    },
                    {
                        "id": "rs764557478",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs764557478"
                    },
                    {
                        "id": "rs764557478",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs764557478#frequency_tab"
                    },
                    {
                        "id": "rs764557478",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs764557478"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3357,
                "end_pos": 3357,
                "sequence_org": "P",
                "sequence_mut": "L",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2097965",
                "ref_nt": "A",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "P3357",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs751845305",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs751845305"
                    },
                    {
                        "id": "rs751845305",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs751845305"
                    },
                    {
                        "id": "rs751845305",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs751845305"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3357,
                "end_pos": 3357,
                "sequence_org": "P",
                "sequence_mut": "T",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2097966",
                "ref_nt": "T",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "P3357",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs1161207926",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1161207926"
                    },
                    {
                        "id": "rs1161207926",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs1161207926"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3359,
                "end_pos": 3359,
                "sequence_org": "P",
                "sequence_mut": "A",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2097960",
                "ref_nt": "C",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "P3359",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs1443656752",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1443656752"
                    },
                    {
                        "id": "rs1443656752",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs1443656752"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3359,
                "end_pos": 3359,
                "sequence_org": "P",
                "sequence_mut": "L",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2097959",
                "ref_nt": "A",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "P3359",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs1161207926",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1161207926"
                    },
                    {
                        "id": "rs1161207926",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs1161207926"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3359,
                "end_pos": 3359,
                "sequence_org": "P",
                "sequence_mut": "S",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2097960",
                "ref_nt": "A",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "P3359",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs1458099402",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1458099402"
                    },
                    {
                        "id": "rs1458099402",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs1458099402#frequency_tab"
                    },
                    {
                        "id": "rs1458099402",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs1458099402"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 335,
                "end_pos": 335,
                "sequence_org": "A",
                "sequence_mut": "V",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2117988",
                "ref_nt": "A",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "A335",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs2092667308",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs2092667308"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 335,
                "end_pos": 335,
                "sequence_org": "A",
                "sequence_mut": "null",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2117975_2117990",
                "ref_nt": "l",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "A335",
                "disease": [
                    {
                        "disease_id": "DOID:0080322",
                        "recommended_name": {
                            "id": "DOID:0080322",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0080322",
                            "name": "polycystic kidney disease",
                            "description": "A cystic kidney disease that is characterized by the growth of fluid-filled cysts in the kidneys that reduces kidney function and may lead to kidney failure."
                        },
                        "synonyms": [
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0080322",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0080322"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0110858",
                        "recommended_name": {
                            "id": "DOID:0110858",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0110858",
                            "name": "polycystic kidney disease 1",
                            "description": "A autosomal dominant polycystic kidney disease that has_material_basis_in autosomal dominant inheritance of mutation in the PKD1 gene on chromosome 16p13.3."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "Polycystic Kidney Disease, Adult, Type I",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            },
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            }
                        ]
                    }
                ],
                "keywords": [
                    "ebi",
                    "germline",
                    "disease"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs765747211",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs765747211"
                    },
                    {
                        "id": "rs765747211",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs765747211"
                    },
                    {
                        "id": "rs765747211",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs765747211#frequency_tab"
                    },
                    {
                        "id": "rs765747211",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs765747211"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3360,
                "end_pos": 3360,
                "sequence_org": "A",
                "sequence_mut": "G",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2097956",
                "ref_nt": "C",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "A3360",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs753152916",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs753152916"
                    },
                    {
                        "id": "rs753152916",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs753152916"
                    },
                    {
                        "id": "rs753152916",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs753152916"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3360,
                "end_pos": 3360,
                "sequence_org": "A",
                "sequence_mut": "T",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2097957",
                "ref_nt": "T",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "A3360",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs765747211",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs765747211"
                    },
                    {
                        "id": "rs765747211",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs765747211"
                    },
                    {
                        "id": "rs765747211",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs765747211#frequency_tab"
                    },
                    {
                        "id": "rs765747211",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs765747211"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3360,
                "end_pos": 3360,
                "sequence_org": "A",
                "sequence_mut": "V",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2097956",
                "ref_nt": "A",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "A3360",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs1210372765",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1210372765"
                    },
                    {
                        "id": "rs1210372765",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs1210372765"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3361,
                "end_pos": 3361,
                "sequence_org": "G",
                "sequence_mut": "E",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2097953",
                "ref_nt": "T",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "G3361",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "P98161",
                        "database": "BioMuta",
                        "url": "https://hivelab.biochemistry.gwu.edu/biomuta/proteinview/P98161"
                    },
                    {
                        "id": "rs556305710",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs556305710"
                    },
                    {
                        "id": "rs556305710",
                        "database": "1000Genomes",
                        "url": "https://www.ensembl.org/homo_sapiens/Variation/Explore?v=rs556305710"
                    },
                    {
                        "id": "rs556305710",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs556305710"
                    },
                    {
                        "id": "rs556305710",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs556305710#frequency_tab"
                    },
                    {
                        "id": "rs556305710",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs556305710"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3361,
                "end_pos": 3361,
                "subjects_tested": "2617",
                "subjects_positive": "1",
                "frequency": "0.0",
                "sequence_org": "G",
                "sequence_mut": "R",
                "comment": "Somatic mutation passed 0 out of 6 filters: .",
                "chr_id": "16",
                "chr_pos": "2097954",
                "ref_nt": "C",
                "alt_nt": "T",
                "minor_allelic_frequency": "",
                "site_lbl": "G3361",
                "disease": [
                    {
                        "disease_id": "DOID:1793",
                        "recommended_name": {
                            "id": "DOID:1793",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:1793",
                            "name": "pancreatic cancer",
                            "description": "An endocrine gland cancer located_in the pancreas."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:1793",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:1793",
                                "name": "Ca body of pancreas",
                                "description": ""
                            },
                            {
                                "id": "DOID:1793",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:1793",
                                "name": "Ca head of pancreas",
                                "description": ""
                            },
                            {
                                "id": "DOID:1793",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:1793",
                                "name": "Ca tail of pancreas",
                                "description": ""
                            },
                            {
                                "id": "DOID:1793",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:1793",
                                "name": "malignant neoplasm of body of pancreas",
                                "description": ""
                            },
                            {
                                "id": "DOID:1793",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:1793",
                                "name": "malignant neoplasm of head of pancreas",
                                "description": ""
                            },
                            {
                                "id": "DOID:1793",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:1793",
                                "name": "malignant neoplasm of tail of pancreas",
                                "description": ""
                            },
                            {
                                "id": "DOID:1793",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:1793",
                                "name": "pancreas neoplasm",
                                "description": ""
                            },
                            {
                                "id": "DOID:1793",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:1793",
                                "name": "pancreatic neoplasm",
                                "description": ""
                            },
                            {
                                "id": "DOID:1793",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:1793",
                                "name": "pancreatic tumor",
                                "description": ""
                            }
                        ],
                        "unlinked_id_list": [
                            "DOID:1795"
                        ],
                        "evidence": [
                            {
                                "id": "1793",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:1793"
                            }
                        ]
                    }
                ],
                "keywords": [
                    "biomuta",
                    "somatic",
                    "cancer",
                    "disease",
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs1567166045",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1567166045"
                    },
                    {
                        "id": "rs1567166045",
                        "database": "ENSEMBL",
                        "url": "https://www.ensembl.org/id/rs1567166045"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3362,
                "end_pos": 3362,
                "sequence_org": "Q",
                "sequence_mut": "*",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2097951",
                "ref_nt": "A",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "Q3362",
                "keywords": [
                    "ebi",
                    "germline",
                    "disease"
                ],
                "disease": [
                    {
                        "disease_id": "DOID:0080322",
                        "recommended_name": {
                            "id": "DOID:0080322",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0080322",
                            "name": "polycystic kidney disease",
                            "description": "A cystic kidney disease that is characterized by the growth of fluid-filled cysts in the kidneys that reduces kidney function and may lead to kidney failure."
                        },
                        "synonyms": [
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0080322",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0080322"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0110858",
                        "recommended_name": {
                            "id": "DOID:0110858",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0110858",
                            "name": "polycystic kidney disease 1",
                            "description": "A autosomal dominant polycystic kidney disease that has_material_basis_in autosomal dominant inheritance of mutation in the PKD1 gene on chromosome 16p13.3."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "Polycystic Kidney Disease, Adult, Type I",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            },
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            }
                        ]
                    }
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs767064899",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs767064899"
                    },
                    {
                        "id": "rs767064899",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs767064899"
                    },
                    {
                        "id": "rs767064899",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs767064899#frequency_tab"
                    },
                    {
                        "id": "rs767064899",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs767064899"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3362,
                "end_pos": 3362,
                "sequence_org": "Q",
                "sequence_mut": "H",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2097949",
                "ref_nt": "A",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "Q3362",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs1490760670",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1490760670"
                    },
                    {
                        "id": "rs1490760670",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs1490760670"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3362,
                "end_pos": 3362,
                "sequence_org": "Q",
                "sequence_mut": "L",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2097950",
                "ref_nt": "A",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "Q3362",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs1490760670",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1490760670"
                    },
                    {
                        "id": "rs1490760670",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs1490760670"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3362,
                "end_pos": 3362,
                "sequence_org": "Q",
                "sequence_mut": "R",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2097950",
                "ref_nt": "C",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "Q3362",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs2151729320",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs2151729320"
                    },
                    {
                        "id": "rs2151729320",
                        "database": "ENSEMBL",
                        "url": "https://www.ensembl.org/id/rs2151729320"
                    },
                    {
                        "id": "rs2151729320",
                        "database": "COSMIC",
                        "url": "https://www.ensembl.org/homo_sapiens/Variation/Explore?v=rs2151729320"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3363,
                "end_pos": 3363,
                "sequence_org": "Q",
                "sequence_mut": "*",
                "comment": "Somatic mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2097948",
                "ref_nt": "A",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "Q3363",
                "disease": [
                    {
                        "disease_id": "DOID:0080322",
                        "recommended_name": {
                            "id": "DOID:0080322",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0080322",
                            "name": "polycystic kidney disease",
                            "description": "A cystic kidney disease that is characterized by the growth of fluid-filled cysts in the kidneys that reduces kidney function and may lead to kidney failure."
                        },
                        "synonyms": [
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0080322",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0080322"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0110858",
                        "recommended_name": {
                            "id": "DOID:0110858",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0110858",
                            "name": "polycystic kidney disease 1",
                            "description": "A autosomal dominant polycystic kidney disease that has_material_basis_in autosomal dominant inheritance of mutation in the PKD1 gene on chromosome 16p13.3."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "Polycystic Kidney Disease, Adult, Type I",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            },
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            }
                        ]
                    }
                ],
                "keywords": [
                    "ebi",
                    "somatic",
                    "disease"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs761578129",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs761578129"
                    },
                    {
                        "id": "rs761578129",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs761578129"
                    },
                    {
                        "id": "rs761578129",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs761578129"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3364,
                "end_pos": 3364,
                "sequence_org": "V",
                "sequence_mut": "L",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2097945",
                "ref_nt": "A",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "V3364",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs1354750094",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1354750094"
                    },
                    {
                        "id": "rs1354750094",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs1354750094#frequency_tab"
                    },
                    {
                        "id": "rs1354750094",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs1354750094"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3365,
                "end_pos": 3365,
                "sequence_org": "L",
                "sequence_mut": "M",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2097942",
                "ref_nt": "T",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "L3365",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs1596503620",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1596503620"
                    },
                    {
                        "id": "rs1596503620",
                        "database": "ENSEMBL",
                        "url": "https://www.ensembl.org/id/rs1596503620"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3365,
                "end_pos": 3365,
                "sequence_org": "L",
                "sequence_mut": "P",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2097941",
                "ref_nt": "G",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "L3365",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs1567165997",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1567165997"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3365,
                "end_pos": 3365,
                "sequence_org": "L",
                "sequence_mut": "null",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2097943",
                "ref_nt": "p",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "L3365",
                "disease": [
                    {
                        "disease_id": "DOID:0080322",
                        "recommended_name": {
                            "id": "DOID:0080322",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0080322",
                            "name": "polycystic kidney disease",
                            "description": "A cystic kidney disease that is characterized by the growth of fluid-filled cysts in the kidneys that reduces kidney function and may lead to kidney failure."
                        },
                        "synonyms": [
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0080322",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0080322"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0110858",
                        "recommended_name": {
                            "id": "DOID:0110858",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0110858",
                            "name": "polycystic kidney disease 1",
                            "description": "A autosomal dominant polycystic kidney disease that has_material_basis_in autosomal dominant inheritance of mutation in the PKD1 gene on chromosome 16p13.3."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "Polycystic Kidney Disease, Adult, Type I",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            },
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            }
                        ]
                    }
                ],
                "keywords": [
                    "ebi",
                    "germline",
                    "disease"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs889929339",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs889929339"
                    },
                    {
                        "id": "rs889929339",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs889929339#frequency_tab"
                    },
                    {
                        "id": "rs889929339",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs889929339"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3366,
                "end_pos": 3366,
                "sequence_org": "D",
                "sequence_mut": "E",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2097937",
                "ref_nt": "C",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "D3366",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs773989174",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs773989174"
                    },
                    {
                        "id": "rs773989174",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs773989174"
                    },
                    {
                        "id": "rs773989174",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs773989174#frequency_tab"
                    },
                    {
                        "id": "rs773989174",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs773989174"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3367,
                "end_pos": 3367,
                "sequence_org": "I",
                "sequence_mut": "V",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2097936",
                "ref_nt": "C",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "I3367",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "P98161",
                        "database": "BioMuta",
                        "url": "https://hivelab.biochemistry.gwu.edu/biomuta/proteinview/P98161"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3368,
                "end_pos": 3368,
                "subjects_tested": "1704",
                "subjects_positive": "1",
                "frequency": "0.1",
                "sequence_org": "D",
                "sequence_mut": "G",
                "comment": "Somatic mutation passed 0 out of 6 filters: .",
                "chr_id": "16",
                "chr_pos": "2097932",
                "ref_nt": "T",
                "alt_nt": "C",
                "minor_allelic_frequency": "",
                "site_lbl": "D3368",
                "disease": [
                    {
                        "disease_id": "DOID:363",
                        "recommended_name": {
                            "id": "DOID:363",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:363",
                            "name": "uterine cancer",
                            "description": "A female reproductive organ cancer that is located_in the uterus."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:363",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:363",
                                "name": "CA - cancer of uterus",
                                "description": ""
                            },
                            {
                                "id": "DOID:363",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:363",
                                "name": "Tumour of uterus",
                                "description": ""
                            },
                            {
                                "id": "DOID:363",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:363",
                                "name": "malignant neoplasm of uterus",
                                "description": ""
                            },
                            {
                                "id": "DOID:363",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:363",
                                "name": "malignant uterine tumor",
                                "description": ""
                            },
                            {
                                "id": "DOID:363",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:363",
                                "name": "neoplasm of uterus",
                                "description": ""
                            },
                            {
                                "id": "DOID:363",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:363",
                                "name": "uterine tumor",
                                "description": ""
                            },
                            {
                                "id": "DOID:363",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:363",
                                "name": "uterus neoplasm",
                                "description": ""
                            }
                        ],
                        "unlinked_id_list": [
                            "DOID:9460",
                            "DOID:5166",
                            "DOID:2021",
                            "DOID:4114"
                        ],
                        "evidence": [
                            {
                                "id": "363",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:363"
                            }
                        ]
                    }
                ],
                "keywords": [
                    "biomuta",
                    "somatic",
                    "cancer",
                    "disease"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "P98161",
                        "database": "BioMuta",
                        "url": "https://hivelab.biochemistry.gwu.edu/biomuta/proteinview/P98161"
                    },
                    {
                        "id": "rs762866943",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs762866943"
                    },
                    {
                        "id": "rs762866943",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs762866943"
                    },
                    {
                        "id": "rs762866943",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs762866943#frequency_tab"
                    },
                    {
                        "id": "rs762866943",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs762866943"
                    },
                    {
                        "id": "rs762866943",
                        "database": "COSMIC",
                        "url": "https://www.ensembl.org/homo_sapiens/Variation/Explore?v=rs762866943"
                    }
                ],
                "glycoeffect": [
                    "n-glyco-sequon-gain"
                ],
                "start_pos": 3368,
                "end_pos": 3368,
                "subjects_tested": "1773",
                "subjects_positive": "1",
                "frequency": "0.1",
                "sequence_org": "D",
                "sequence_mut": "N",
                "comment": "Somatic mutation passed 1 out of 6 filters: n-glyco-sequon-gain (DSC->NSC).",
                "chr_id": "16",
                "chr_pos": "2097933",
                "ref_nt": "C",
                "alt_nt": "T",
                "minor_allelic_frequency": "",
                "site_lbl": "D3368",
                "disease": [
                    {
                        "disease_id": "DOID:10534",
                        "recommended_name": {
                            "id": "DOID:10534",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:10534",
                            "name": "stomach cancer",
                            "description": "A gastrointestinal system cancer that is located_in the stomach."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:10534",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:10534",
                                "name": "gastric cancer",
                                "description": ""
                            },
                            {
                                "id": "DOID:10534",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:10534",
                                "name": "gastric neoplasm",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001056",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001056",
                                "name": "gastric cancer",
                                "description": "A primary or metastatic malignant neoplasm involving the stomach."
                            },
                            {
                                "id": "MONDO:0001056",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001056",
                                "name": "gastric neoplasm",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001056",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001056",
                                "name": "Ca lesser curvature - stomach",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001056",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001056",
                                "name": "GC",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001056",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001056",
                                "name": "cancer of stomach",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001056",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001056",
                                "name": "gastric cancer",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001056",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001056",
                                "name": "gastric cancer risk after h. pylori infection",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001056",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001056",
                                "name": "gastric cancer, somatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001056",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001056",
                                "name": "malignant gastric neoplasm",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001056",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001056",
                                "name": "malignant gastric tumor",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001056",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001056",
                                "name": "malignant gastric tumour",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001056",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001056",
                                "name": "malignant neoplasm of lesser curve of stomach",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001056",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001056",
                                "name": "malignant neoplasm of stomach",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001056",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001056",
                                "name": "malignant neoplasm of the stomach",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001056",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001056",
                                "name": "malignant stomach neoplasm",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001056",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001056",
                                "name": "malignant tumor of body of stomach",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001056",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001056",
                                "name": "malignant tumor of greater curve of stomach",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001056",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001056",
                                "name": "malignant tumor of lesser curve of stomach",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001056",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001056",
                                "name": "malignant tumor of stomach",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001056",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001056",
                                "name": "malignant tumor of the stomach",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001056",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001056",
                                "name": "malignant tumour of body of stomach",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001056",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001056",
                                "name": "malignant tumour of greater curve of stomach",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001056",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001056",
                                "name": "malignant tumour of lesser curve of stomach",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001056",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001056",
                                "name": "malignant tumour of stomach",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001056",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001056",
                                "name": "malignant tumour of the stomach",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001056",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001056",
                                "name": "stomach cancer",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001056",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001056",
                                "name": "Ca body - stomach",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001056",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001056",
                                "name": "ca greater curvature of stomach",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001056",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001056",
                                "name": "malignant neoplasm of body of stomach",
                                "description": ""
                            },
                            {
                                "id": "MIM:613659",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/613659",
                                "name": "Gastric cancer",
                                "description": "Gastric cancer"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "10534",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:10534"
                            },
                            {
                                "id": "10534",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:10534"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:5041",
                        "recommended_name": {
                            "id": "DOID:5041",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:5041",
                            "name": "esophageal cancer",
                            "description": "A gastrointestinal system cancer that is located_in the esophagus."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:5041",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:5041",
                                "name": "Ca lower third oesophagus",
                                "description": ""
                            },
                            {
                                "id": "DOID:5041",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:5041",
                                "name": "Ca middle third oesophagus",
                                "description": ""
                            },
                            {
                                "id": "DOID:5041",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:5041",
                                "name": "esophagus cancer",
                                "description": ""
                            },
                            {
                                "id": "DOID:5041",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:5041",
                                "name": "malignant neoplasm of distal third of esophagus",
                                "description": ""
                            },
                            {
                                "id": "DOID:5041",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:5041",
                                "name": "malignant neoplasm of lower third of oesophagus",
                                "description": ""
                            },
                            {
                                "id": "DOID:5041",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:5041",
                                "name": "malignant neoplasm of middle third of oesophagus",
                                "description": ""
                            },
                            {
                                "id": "DOID:5041",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:5041",
                                "name": "malignant neoplasm of proximal third of esophagus",
                                "description": ""
                            },
                            {
                                "id": "DOID:5041",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:5041",
                                "name": "malignant neoplasm of upper third esophagus",
                                "description": ""
                            },
                            {
                                "id": "DOID:5041",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:5041",
                                "name": "malignant tumor of Distal Third of esophagus",
                                "description": ""
                            },
                            {
                                "id": "DOID:5041",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:5041",
                                "name": "malignant tumor of Proximal Third of esophagus",
                                "description": ""
                            },
                            {
                                "id": "DOID:5041",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:5041",
                                "name": "malignant tumor of abdominal esophagus",
                                "description": ""
                            },
                            {
                                "id": "DOID:5041",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:5041",
                                "name": "malignant tumor of the middle Third of the esophagus",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007576",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007576",
                                "name": "esophageal cancer",
                                "description": "A primary or metastatic malignant neoplasm involving the esophagus."
                            },
                            {
                                "id": "MONDO:0007576",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007576",
                                "name": "cancer of esophagus",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007576",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007576",
                                "name": "cancer of oesophagus",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007576",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007576",
                                "name": "esophageal cancer",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007576",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007576",
                                "name": "esophageal cancer, somatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007576",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007576",
                                "name": "esophageal carcinoma, somatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007576",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007576",
                                "name": "esophageal squamous cell carcinoma, somatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007576",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007576",
                                "name": "esophagus cancer",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007576",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007576",
                                "name": "malignant esophageal neoplasm",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007576",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007576",
                                "name": "malignant esophageal tumor",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007576",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007576",
                                "name": "malignant esophageal tumour",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007576",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007576",
                                "name": "malignant esophagus neoplasm",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007576",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007576",
                                "name": "malignant esophagus tumor",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007576",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007576",
                                "name": "malignant neoplasm of esophagus",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007576",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007576",
                                "name": "malignant neoplasm of oesophagus",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007576",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007576",
                                "name": "malignant neoplasm of the esophagus",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007576",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007576",
                                "name": "malignant neoplasm of the oesophagus",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007576",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007576",
                                "name": "malignant oesophagus neoplasm",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007576",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007576",
                                "name": "malignant oesophagus tumour",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007576",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007576",
                                "name": "malignant tumor of esophagus",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007576",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007576",
                                "name": "malignant tumor of the esophagus",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007576",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007576",
                                "name": "malignant tumour of oesophagus",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007576",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007576",
                                "name": "malignant tumour of the oesophagus",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007576",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007576",
                                "name": "oesophagus cancer",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007576",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007576",
                                "name": "Ca lower third esophagus",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007576",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007576",
                                "name": "Ca lower third oesophagus",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007576",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007576",
                                "name": "Ca middle third esophagus",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007576",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007576",
                                "name": "Ca middle third oesophagus",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007576",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007576",
                                "name": "malignant neoplasm of distal third of esophagus",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007576",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007576",
                                "name": "malignant neoplasm of distal third of oesophagus",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007576",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007576",
                                "name": "malignant neoplasm of lower third of esophagus",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007576",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007576",
                                "name": "malignant neoplasm of lower third of oesophagus",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007576",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007576",
                                "name": "malignant neoplasm of middle third of esophagus",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007576",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007576",
                                "name": "malignant neoplasm of middle third of oesophagus",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007576",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007576",
                                "name": "malignant neoplasm of proximal third of esophagus",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007576",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007576",
                                "name": "malignant neoplasm of proximal third of oesophagus",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007576",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007576",
                                "name": "malignant neoplasm of upper third esophagus",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007576",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007576",
                                "name": "malignant neoplasm of upper third oesophagus",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007576",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007576",
                                "name": "malignant tumor of abdominal esophagus",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007576",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007576",
                                "name": "malignant tumor of distal third of esophagus",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007576",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007576",
                                "name": "malignant tumor of proximal third of esophagus",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007576",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007576",
                                "name": "malignant tumor of the middle third of the esophagus",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007576",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007576",
                                "name": "malignant tumour of abdominal oesophagus",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007576",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007576",
                                "name": "malignant tumour of distal third of oesophagus",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007576",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007576",
                                "name": "malignant tumour of proximal third of oesophagus",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007576",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007576",
                                "name": "malignant tumour of the middle third of the oesophagus",
                                "description": ""
                            },
                            {
                                "id": "MIM:133239",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/133239",
                                "name": "Esophageal cancer",
                                "description": "Esophageal cancer"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "5041",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:5041"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0080322",
                        "recommended_name": {
                            "id": "DOID:0080322",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0080322",
                            "name": "polycystic kidney disease",
                            "description": "A cystic kidney disease that is characterized by the growth of fluid-filled cysts in the kidneys that reduces kidney function and may lead to kidney failure."
                        },
                        "synonyms": [
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0080322",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0080322"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0110858",
                        "recommended_name": {
                            "id": "DOID:0110858",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0110858",
                            "name": "polycystic kidney disease 1",
                            "description": "A autosomal dominant polycystic kidney disease that has_material_basis_in autosomal dominant inheritance of mutation in the PKD1 gene on chromosome 16p13.3."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "Polycystic Kidney Disease, Adult, Type I",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            },
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            }
                        ]
                    }
                ],
                "keywords": [
                    "biomuta",
                    "somatic",
                    "cancer",
                    "disease",
                    "ebi"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs775497716",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs775497716"
                    },
                    {
                        "id": "rs775497716",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs775497716"
                    },
                    {
                        "id": "rs775497716",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs775497716#frequency_tab"
                    },
                    {
                        "id": "rs775497716",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs775497716"
                    }
                ],
                "glycoeffect": [
                    "o-glyco-site-loss"
                ],
                "start_pos": 3369,
                "end_pos": 3369,
                "sequence_org": "S",
                "sequence_mut": "G",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2097930",
                "ref_nt": "C",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "S3369",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs769914779",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs769914779"
                    },
                    {
                        "id": "rs769914779",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs769914779"
                    },
                    {
                        "id": "rs769914779",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs769914779"
                    }
                ],
                "glycoeffect": [
                    "o-glyco-site-loss"
                ],
                "start_pos": 3369,
                "end_pos": 3369,
                "sequence_org": "S",
                "sequence_mut": "N",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2097929",
                "ref_nt": "T",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "S3369",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs745926227",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs745926227"
                    },
                    {
                        "id": "rs745926227",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs745926227"
                    },
                    {
                        "id": "rs745926227",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs745926227#frequency_tab"
                    },
                    {
                        "id": "rs745926227",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs745926227"
                    }
                ],
                "glycoeffect": [
                    "o-glyco-site-loss"
                ],
                "start_pos": 3369,
                "end_pos": 3369,
                "sequence_org": "S",
                "sequence_mut": "R",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2097928",
                "ref_nt": "T",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "S3369",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs769914779",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs769914779"
                    },
                    {
                        "id": "rs769914779",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs769914779"
                    },
                    {
                        "id": "rs769914779",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs769914779"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3369,
                "end_pos": 3369,
                "sequence_org": "S",
                "sequence_mut": "T",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2097929",
                "ref_nt": "G",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "S3369",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs749740622",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs749740622"
                    },
                    {
                        "id": "rs749740622",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs749740622"
                    },
                    {
                        "id": "rs749740622",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs749740622#frequency_tab"
                    },
                    {
                        "id": "rs749740622",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs749740622"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 336,
                "end_pos": 336,
                "sequence_org": "V",
                "sequence_mut": "L",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2117986",
                "ref_nt": "G",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "V336",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "P98161",
                        "database": "BioMuta",
                        "url": "https://hivelab.biochemistry.gwu.edu/biomuta/proteinview/P98161"
                    },
                    {
                        "id": "rs749740622",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs749740622"
                    },
                    {
                        "id": "rs749740622",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs749740622"
                    },
                    {
                        "id": "rs749740622",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs749740622#frequency_tab"
                    },
                    {
                        "id": "rs749740622",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs749740622"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 336,
                "end_pos": 336,
                "subjects_tested": "2617",
                "subjects_positive": "1",
                "frequency": "0.0",
                "sequence_org": "V",
                "sequence_mut": "M",
                "comment": "Somatic mutation passed 0 out of 6 filters: .",
                "chr_id": "16",
                "chr_pos": "2117986",
                "ref_nt": "C",
                "alt_nt": "T",
                "minor_allelic_frequency": "",
                "site_lbl": "V336",
                "disease": [
                    {
                        "disease_id": "DOID:1793",
                        "recommended_name": {
                            "id": "DOID:1793",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:1793",
                            "name": "pancreatic cancer",
                            "description": "An endocrine gland cancer located_in the pancreas."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:1793",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:1793",
                                "name": "Ca body of pancreas",
                                "description": ""
                            },
                            {
                                "id": "DOID:1793",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:1793",
                                "name": "Ca head of pancreas",
                                "description": ""
                            },
                            {
                                "id": "DOID:1793",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:1793",
                                "name": "Ca tail of pancreas",
                                "description": ""
                            },
                            {
                                "id": "DOID:1793",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:1793",
                                "name": "malignant neoplasm of body of pancreas",
                                "description": ""
                            },
                            {
                                "id": "DOID:1793",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:1793",
                                "name": "malignant neoplasm of head of pancreas",
                                "description": ""
                            },
                            {
                                "id": "DOID:1793",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:1793",
                                "name": "malignant neoplasm of tail of pancreas",
                                "description": ""
                            },
                            {
                                "id": "DOID:1793",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:1793",
                                "name": "pancreas neoplasm",
                                "description": ""
                            },
                            {
                                "id": "DOID:1793",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:1793",
                                "name": "pancreatic neoplasm",
                                "description": ""
                            },
                            {
                                "id": "DOID:1793",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:1793",
                                "name": "pancreatic tumor",
                                "description": ""
                            }
                        ],
                        "unlinked_id_list": [
                            "DOID:1795"
                        ],
                        "evidence": [
                            {
                                "id": "1793",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:1793"
                            }
                        ]
                    }
                ],
                "keywords": [
                    "biomuta",
                    "somatic",
                    "cancer",
                    "disease",
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs781379310",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs781379310"
                    },
                    {
                        "id": "rs781379310",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs781379310"
                    },
                    {
                        "id": "rs781379310",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs781379310#frequency_tab"
                    },
                    {
                        "id": "rs781379310",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs781379310"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3370,
                "end_pos": 3370,
                "sequence_org": "C",
                "sequence_mut": "S",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2097926",
                "ref_nt": "G",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "C3370",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs781379310",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs781379310"
                    },
                    {
                        "id": "rs781379310",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs781379310"
                    },
                    {
                        "id": "rs781379310",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs781379310#frequency_tab"
                    },
                    {
                        "id": "rs781379310",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs781379310"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3370,
                "end_pos": 3370,
                "sequence_org": "C",
                "sequence_mut": "Y",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2097926",
                "ref_nt": "T",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "C3370",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs747213853",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs747213853"
                    },
                    {
                        "id": "rs747213853",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs747213853"
                    },
                    {
                        "id": "rs747213853",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs747213853"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3372,
                "end_pos": 3372,
                "sequence_org": "D",
                "sequence_mut": "G",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2097920",
                "ref_nt": "C",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "D3372",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs373222937",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs373222937"
                    }
                ],
                "glycoeffect": [
                    "o-glyco-site-loss"
                ],
                "start_pos": 3373,
                "end_pos": 3373,
                "sequence_org": "S",
                "sequence_mut": "*",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2097917",
                "ref_nt": "T",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "S3373",
                "keywords": [
                    "ebi",
                    "germline",
                    "disease"
                ],
                "disease": [
                    {
                        "disease_id": "DOID:0080322",
                        "recommended_name": {
                            "id": "DOID:0080322",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0080322",
                            "name": "polycystic kidney disease",
                            "description": "A cystic kidney disease that is characterized by the growth of fluid-filled cysts in the kidneys that reduces kidney function and may lead to kidney failure."
                        },
                        "synonyms": [
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0080322",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0080322"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0110858",
                        "recommended_name": {
                            "id": "DOID:0110858",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0110858",
                            "name": "polycystic kidney disease 1",
                            "description": "A autosomal dominant polycystic kidney disease that has_material_basis_in autosomal dominant inheritance of mutation in the PKD1 gene on chromosome 16p13.3."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "Polycystic Kidney Disease, Adult, Type I",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            },
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            }
                        ]
                    }
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs373222937",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs373222937"
                    },
                    {
                        "id": "rs373222937",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs373222937"
                    },
                    {
                        "id": "rs373222937",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs373222937#frequency_tab"
                    },
                    {
                        "id": "rs373222937",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs373222937"
                    }
                ],
                "glycoeffect": [
                    "o-glyco-site-loss"
                ],
                "start_pos": 3373,
                "end_pos": 3373,
                "sequence_org": "S",
                "sequence_mut": "L",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2097917",
                "ref_nt": "A",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "S3373",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs777879712",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs777879712"
                    },
                    {
                        "id": "rs777879712",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs777879712"
                    },
                    {
                        "id": "rs777879712",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs777879712"
                    }
                ],
                "glycoeffect": [
                    "o-glyco-site-loss"
                ],
                "start_pos": 3373,
                "end_pos": 3373,
                "sequence_org": "S",
                "sequence_mut": "P",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2097918",
                "ref_nt": "G",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "S3373",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "P98161",
                        "database": "BioMuta",
                        "url": "https://hivelab.biochemistry.gwu.edu/biomuta/proteinview/P98161"
                    }
                ],
                "glycoeffect": [
                    "o-glyco-site-loss"
                ],
                "start_pos": 3374,
                "end_pos": 3374,
                "subjects_tested": "2053",
                "subjects_positive": "1",
                "frequency": "0.0",
                "sequence_org": "S",
                "sequence_mut": "F",
                "comment": "Somatic mutation passed 0 out of 6 filters: .",
                "chr_id": "16",
                "chr_pos": "2097914",
                "ref_nt": "G",
                "alt_nt": "A",
                "minor_allelic_frequency": "",
                "site_lbl": "S3374",
                "disease": [
                    {
                        "disease_id": "DOID:4159",
                        "recommended_name": {
                            "id": "DOID:4159",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:4159",
                            "name": "skin cancer",
                            "description": "An integumentary system cancer located_in the skin that is the uncontrolled growth of abnormal skin cells."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:4159",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:4159",
                                "name": "CA - skin cancer",
                                "description": ""
                            },
                            {
                                "id": "DOID:4159",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:4159",
                                "name": "malignant neoplasm of skin",
                                "description": ""
                            },
                            {
                                "id": "DOID:4159",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:4159",
                                "name": "melanoma and Non-melanoma skin cancer",
                                "description": ""
                            }
                        ],
                        "unlinked_id_list": [
                            "DOID:3149",
                            "DOID:3451"
                        ],
                        "evidence": [
                            {
                                "id": "4159",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:4159"
                            }
                        ]
                    }
                ],
                "keywords": [
                    "biomuta",
                    "somatic",
                    "cancer",
                    "disease"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs371283948",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs371283948"
                    },
                    {
                        "id": "rs371283948",
                        "database": "1000Genomes",
                        "url": "https://www.ensembl.org/homo_sapiens/Variation/Explore?v=rs371283948"
                    },
                    {
                        "id": "rs371283948",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs371283948"
                    },
                    {
                        "id": "rs371283948",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs371283948#frequency_tab"
                    },
                    {
                        "id": "rs371283948",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs371283948"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3375,
                "end_pos": 3375,
                "sequence_org": "V",
                "sequence_mut": "M",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2097912",
                "ref_nt": "T",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "V3375",
                "disease": [
                    {
                        "disease_id": "DOID:0080322",
                        "recommended_name": {
                            "id": "DOID:0080322",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0080322",
                            "name": "polycystic kidney disease",
                            "description": "A cystic kidney disease that is characterized by the growth of fluid-filled cysts in the kidneys that reduces kidney function and may lead to kidney failure."
                        },
                        "synonyms": [
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0080322",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0080322"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0110858",
                        "recommended_name": {
                            "id": "DOID:0110858",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0110858",
                            "name": "polycystic kidney disease 1",
                            "description": "A autosomal dominant polycystic kidney disease that has_material_basis_in autosomal dominant inheritance of mutation in the PKD1 gene on chromosome 16p13.3."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "Polycystic Kidney Disease, Adult, Type I",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            },
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            }
                        ]
                    }
                ],
                "keywords": [
                    "ebi",
                    "germline",
                    "disease"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs139792535",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs139792535"
                    },
                    {
                        "id": "rs139792535",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs139792535"
                    },
                    {
                        "id": "rs139792535",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs139792535#frequency_tab"
                    },
                    {
                        "id": "rs139792535",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs139792535"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3376,
                "end_pos": 3376,
                "sequence_org": "L",
                "sequence_mut": "P",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2097908",
                "ref_nt": "G",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "L3376",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs751179613",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs751179613"
                    },
                    {
                        "id": "rs751179613",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs751179613"
                    },
                    {
                        "id": "rs751179613",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs751179613#frequency_tab"
                    },
                    {
                        "id": "rs751179613",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs751179613"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3377,
                "end_pos": 3377,
                "sequence_org": "D",
                "sequence_mut": "H",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2097906",
                "ref_nt": "G",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "D3377",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs1307120106",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1307120106"
                    },
                    {
                        "id": "rs1307120106",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs1307120106#frequency_tab"
                    },
                    {
                        "id": "rs1307120106",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs1307120106"
                    }
                ],
                "glycoeffect": [
                    "o-glyco-site-loss"
                ],
                "start_pos": 3378,
                "end_pos": 3378,
                "sequence_org": "S",
                "sequence_mut": "G",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2097903",
                "ref_nt": "C",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "S3378",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs2091911255",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs2091911255"
                    },
                    {
                        "id": "rs2091911255",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs2091911255#frequency_tab"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3378,
                "end_pos": 3378,
                "sequence_org": "S",
                "sequence_mut": "T",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2097902",
                "ref_nt": "G",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "S3378",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs763653467",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs763653467"
                    },
                    {
                        "id": "rs763653467",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs763653467"
                    },
                    {
                        "id": "rs763653467",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs763653467#frequency_tab"
                    },
                    {
                        "id": "rs763653467",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs763653467"
                    }
                ],
                "glycoeffect": [
                    "o-glyco-site-loss"
                ],
                "start_pos": 3379,
                "end_pos": 3379,
                "sequence_org": "S",
                "sequence_mut": "C",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2097899",
                "ref_nt": "C",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "S3379",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "P98161",
                        "database": "BioMuta",
                        "url": "https://hivelab.biochemistry.gwu.edu/biomuta/proteinview/P98161"
                    },
                    {
                        "id": "rs763653467",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs763653467"
                    },
                    {
                        "id": "rs763653467",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs763653467"
                    },
                    {
                        "id": "rs763653467",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs763653467#frequency_tab"
                    },
                    {
                        "id": "rs763653467",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs763653467"
                    },
                    {
                        "id": "rs763653467",
                        "database": "COSMIC",
                        "url": "https://www.ensembl.org/homo_sapiens/Variation/Explore?v=rs763653467"
                    }
                ],
                "glycoeffect": [
                    "o-glyco-site-loss"
                ],
                "start_pos": 3379,
                "end_pos": 3379,
                "subjects_tested": "2053",
                "subjects_positive": "1",
                "frequency": "0.0",
                "sequence_org": "S",
                "sequence_mut": "F",
                "comment": "Somatic mutation passed 0 out of 6 filters: .",
                "chr_id": "16",
                "chr_pos": "2097899",
                "ref_nt": "G",
                "alt_nt": "A",
                "minor_allelic_frequency": "",
                "site_lbl": "S3379",
                "disease": [
                    {
                        "disease_id": "DOID:4159",
                        "recommended_name": {
                            "id": "DOID:4159",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:4159",
                            "name": "skin cancer",
                            "description": "An integumentary system cancer located_in the skin that is the uncontrolled growth of abnormal skin cells."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:4159",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:4159",
                                "name": "CA - skin cancer",
                                "description": ""
                            },
                            {
                                "id": "DOID:4159",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:4159",
                                "name": "malignant neoplasm of skin",
                                "description": ""
                            },
                            {
                                "id": "DOID:4159",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:4159",
                                "name": "melanoma and Non-melanoma skin cancer",
                                "description": ""
                            }
                        ],
                        "unlinked_id_list": [
                            "DOID:3149",
                            "DOID:3451"
                        ],
                        "evidence": [
                            {
                                "id": "4159",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:4159"
                            }
                        ]
                    }
                ],
                "keywords": [
                    "biomuta",
                    "somatic",
                    "cancer",
                    "disease",
                    "ebi"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs1389602268",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1389602268"
                    },
                    {
                        "id": "rs1389602268",
                        "database": "ENSEMBL",
                        "url": "https://www.ensembl.org/id/rs1389602268"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 337,
                "end_pos": 337,
                "sequence_org": "L",
                "sequence_mut": "Q",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2117982",
                "ref_nt": "T",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "L337",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "P98161",
                        "database": "BioMuta",
                        "url": "https://hivelab.biochemistry.gwu.edu/biomuta/proteinview/P98161"
                    },
                    {
                        "id": "rs1344216597",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1344216597"
                    },
                    {
                        "id": "rs1344216597",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs1344216597#frequency_tab"
                    },
                    {
                        "id": "rs1344216597",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs1344216597"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3380,
                "end_pos": 3380,
                "subjects_tested": "3601",
                "subjects_positive": "1",
                "frequency": "0.0",
                "sequence_org": "F",
                "sequence_mut": "L",
                "comment": "Somatic mutation passed 0 out of 6 filters: .",
                "chr_id": "16",
                "chr_pos": "2097897",
                "ref_nt": "A",
                "alt_nt": "G",
                "minor_allelic_frequency": "",
                "site_lbl": "F3380",
                "disease": [
                    {
                        "disease_id": "DOID:9256",
                        "recommended_name": {
                            "id": "DOID:9256",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:9256",
                            "name": "colorectal cancer",
                            "description": "A large intestine cancer that is located_in the colon and/or located_in the rectum."
                        },
                        "synonyms": [
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectal cancer",
                                "description": "A primary or metastatic malignant neoplasm that affects the colon or rectum. Representative examples include carcinoma, lymphoma, and sarcoma."
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "cancer of colorectum",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "cancer of large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "cancer of large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "cancer of the large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colon cancer, advanced, somatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colon cancer, somatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectal cancer",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectal cancer with chromosomal instability, somatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectal cancer, autosomal dominant, somatic mutation",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectal cancer, somatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectal cancer, susceptibility to, autosomal dominant, somatic mutation",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectum cancer",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant colorectal neoplasm",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant colorectal tumor",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant colorectal tumour",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant colorectum neoplasm",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant large bowel neoplasm",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant large bowel tumor",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant large bowel tumour",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant large intestine neoplasm",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant large intestine tumor",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant large intestine tumour",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant neoplasm of colorectum",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant neoplasm of large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant neoplasm of large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant neoplasm of the large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant neoplasm of the large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumor of large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumor of large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumor of the large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumor of the large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumour of large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumour of large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumour of the large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumour of the large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "CRC",
                                "description": ""
                            },
                            {
                                "id": "MIM:114500",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/114500",
                                "name": "Colorectal cancer",
                                "description": "Colorectal cancer"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "9256",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:9256"
                            }
                        ]
                    }
                ],
                "keywords": [
                    "biomuta",
                    "somatic",
                    "cancer",
                    "disease",
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs2544693381",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs2544693381"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3380,
                "end_pos": 3380,
                "sequence_org": "F",
                "sequence_mut": "null",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2097892_2097895",
                "ref_nt": "l",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "F3380",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs142799331",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs142799331"
                    },
                    {
                        "id": "rs142799331",
                        "database": "1000Genomes",
                        "url": "https://www.ensembl.org/homo_sapiens/Variation/Explore?v=rs142799331"
                    },
                    {
                        "id": "rs142799331",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs142799331"
                    },
                    {
                        "id": "rs142799331",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs142799331#frequency_tab"
                    },
                    {
                        "id": "rs142799331",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs142799331"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3381,
                "end_pos": 3381,
                "sequence_org": "L",
                "sequence_mut": "F",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2097894",
                "ref_nt": "A",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "L3381",
                "disease": [
                    {
                        "disease_id": "DOID:0080322",
                        "recommended_name": {
                            "id": "DOID:0080322",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0080322",
                            "name": "polycystic kidney disease",
                            "description": "A cystic kidney disease that is characterized by the growth of fluid-filled cysts in the kidneys that reduces kidney function and may lead to kidney failure."
                        },
                        "synonyms": [
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0080322",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0080322"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0110858",
                        "recommended_name": {
                            "id": "DOID:0110858",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0110858",
                            "name": "polycystic kidney disease 1",
                            "description": "A autosomal dominant polycystic kidney disease that has_material_basis_in autosomal dominant inheritance of mutation in the PKD1 gene on chromosome 16p13.3."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "Polycystic Kidney Disease, Adult, Type I",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            },
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            }
                        ]
                    }
                ],
                "keywords": [
                    "ebi",
                    "germline",
                    "disease"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs776463508",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs776463508"
                    },
                    {
                        "id": "rs776463508",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs776463508"
                    },
                    {
                        "id": "rs776463508",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs776463508#frequency_tab"
                    },
                    {
                        "id": "rs776463508",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs776463508"
                    }
                ],
                "glycoeffect": [
                    "o-glyco-site-loss"
                ],
                "start_pos": 3382,
                "end_pos": 3382,
                "sequence_org": "T",
                "sequence_mut": "K",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2097890",
                "ref_nt": "T",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "T3382",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs776463508",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs776463508"
                    },
                    {
                        "id": "rs776463508",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs776463508"
                    },
                    {
                        "id": "rs776463508",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs776463508#frequency_tab"
                    },
                    {
                        "id": "rs776463508",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs776463508"
                    }
                ],
                "glycoeffect": [
                    "o-glyco-site-loss"
                ],
                "start_pos": 3382,
                "end_pos": 3382,
                "sequence_org": "T",
                "sequence_mut": "M",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2097890",
                "ref_nt": "A",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "T3382",
                "disease": [
                    {
                        "disease_id": "DOID:0080322",
                        "recommended_name": {
                            "id": "DOID:0080322",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0080322",
                            "name": "polycystic kidney disease",
                            "description": "A cystic kidney disease that is characterized by the growth of fluid-filled cysts in the kidneys that reduces kidney function and may lead to kidney failure."
                        },
                        "synonyms": [
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0080322",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0080322"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0110858",
                        "recommended_name": {
                            "id": "DOID:0110858",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0110858",
                            "name": "polycystic kidney disease 1",
                            "description": "A autosomal dominant polycystic kidney disease that has_material_basis_in autosomal dominant inheritance of mutation in the PKD1 gene on chromosome 16p13.3."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "Polycystic Kidney Disease, Adult, Type I",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            },
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            }
                        ]
                    }
                ],
                "keywords": [
                    "ebi",
                    "germline",
                    "disease"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs776463508",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs776463508"
                    },
                    {
                        "id": "rs776463508",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs776463508"
                    },
                    {
                        "id": "rs776463508",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs776463508#frequency_tab"
                    },
                    {
                        "id": "rs776463508",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs776463508"
                    }
                ],
                "glycoeffect": [
                    "o-glyco-site-loss"
                ],
                "start_pos": 3382,
                "end_pos": 3382,
                "sequence_org": "T",
                "sequence_mut": "R",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2097890",
                "ref_nt": "C",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "T3382",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs777985330",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs777985330"
                    },
                    {
                        "id": "rs777985330",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs777985330"
                    },
                    {
                        "id": "rs777985330",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs777985330#frequency_tab"
                    },
                    {
                        "id": "rs777985330",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs777985330"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3383,
                "end_pos": 3383,
                "sequence_org": "F",
                "sequence_mut": "L",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2097886",
                "ref_nt": "C",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "F3383",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs1383556063",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1383556063"
                    },
                    {
                        "id": "rs1383556063",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs1383556063#frequency_tab"
                    },
                    {
                        "id": "rs1383556063",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs1383556063"
                    }
                ],
                "glycoeffect": [
                    "o-glyco-site-loss"
                ],
                "start_pos": 3384,
                "end_pos": 3384,
                "sequence_org": "S",
                "sequence_mut": "*",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2097884",
                "ref_nt": "C",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "S3384",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs1383556063",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1383556063"
                    },
                    {
                        "id": "rs1383556063",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs1383556063#frequency_tab"
                    },
                    {
                        "id": "rs1383556063",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs1383556063"
                    }
                ],
                "glycoeffect": [
                    "o-glyco-site-loss"
                ],
                "start_pos": 3384,
                "end_pos": 3384,
                "sequence_org": "S",
                "sequence_mut": "L",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2097884",
                "ref_nt": "A",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "S3384",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs1481358141",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1481358141"
                    },
                    {
                        "id": "rs1481358141",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs1481358141"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3386,
                "end_pos": 3386,
                "sequence_org": "L",
                "sequence_mut": "F",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2097879",
                "ref_nt": "A",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "L3386",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs780451430",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs780451430"
                    },
                    {
                        "id": "rs780451430",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs780451430"
                    },
                    {
                        "id": "rs780451430",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs780451430#frequency_tab"
                    },
                    {
                        "id": "rs780451430",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs780451430"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3388,
                "end_pos": 3388,
                "sequence_org": "A",
                "sequence_mut": "G",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2097872",
                "ref_nt": "C",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "A3388",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "P98161",
                        "database": "BioMuta",
                        "url": "https://hivelab.biochemistry.gwu.edu/biomuta/proteinview/P98161"
                    },
                    {
                        "id": "rs369548825",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs369548825"
                    },
                    {
                        "id": "rs369548825",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs369548825"
                    },
                    {
                        "id": "rs369548825",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs369548825#frequency_tab"
                    },
                    {
                        "id": "rs369548825",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs369548825"
                    },
                    {
                        "id": "rs369548825",
                        "database": "COSMIC",
                        "url": "https://www.ensembl.org/homo_sapiens/Variation/Explore?v=rs369548825"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3388,
                "end_pos": 3388,
                "subjects_tested": "4484",
                "subjects_positive": "1",
                "frequency": "0.0",
                "sequence_org": "A",
                "sequence_mut": "T",
                "comment": "Somatic mutation passed 0 out of 6 filters: .",
                "chr_id": "16",
                "chr_pos": "2097873",
                "ref_nt": "C",
                "alt_nt": "T",
                "minor_allelic_frequency": "",
                "site_lbl": "A3388",
                "disease": [
                    {
                        "disease_id": "DOID:1612",
                        "recommended_name": {
                            "id": "DOID:1612",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:1612",
                            "name": "breast cancer",
                            "description": "An organ system cancer that originates in the mammary gland."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:1612",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:1612",
                                "name": "breast tumor",
                                "description": ""
                            },
                            {
                                "id": "DOID:1612",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:1612",
                                "name": "malignant neoplasm of breast",
                                "description": ""
                            },
                            {
                                "id": "DOID:1612",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:1612",
                                "name": "malignant tumor of the breast",
                                "description": ""
                            },
                            {
                                "id": "DOID:1612",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:1612",
                                "name": "mammary cancer",
                                "description": ""
                            },
                            {
                                "id": "DOID:1612",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:1612",
                                "name": "mammary tumor",
                                "description": ""
                            },
                            {
                                "id": "DOID:1612",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:1612",
                                "name": "primary breast cancer",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0016419",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0016419",
                                "name": "hereditary breast carcinoma",
                                "description": "Breast carcinoma that has developed in relatives of patients with history of breast carcinoma."
                            },
                            {
                                "id": "MONDO:0016419",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0016419",
                                "name": "breast cancer susceptibility, autosomal dominant, somatic mutation",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0016419",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0016419",
                                "name": "breast cancer, early-onset, susceptibility to, autosomal dominant, somatic mutation",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0016419",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0016419",
                                "name": "breast cancer, invasive ductal, autosomal dominant, somatic mutation",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0016419",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0016419",
                                "name": "breast cancer, lobular, somatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0016419",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0016419",
                                "name": "breast cancer, male, susceptibility to, autosomal dominant, somatic mutation",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0016419",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0016419",
                                "name": "breast cancer, protection against, autosomal dominant, somatic mutation",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0016419",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0016419",
                                "name": "breast cancer, somatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0016419",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0016419",
                                "name": "breast cancer, susceptibility to, autosomal dominant, somatic mutation",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0016419",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0016419",
                                "name": "familial breast cancer",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0016419",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0016419",
                                "name": "familial breast carcinoma",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0016419",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0016419",
                                "name": "familial cancer of breast",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0016419",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0016419",
                                "name": "familial cancer of the breast",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0016419",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0016419",
                                "name": "hereditary breast cancer",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0016419",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0016419",
                                "name": "hereditary breast carcinoma",
                                "description": ""
                            },
                            {
                                "id": "MIM:114480",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/114480",
                                "name": "Breast cancer",
                                "description": "Breast cancer"
                            }
                        ],
                        "unlinked_id_list": [
                            "DOID:3017",
                            "DOID:0050938"
                        ],
                        "evidence": [
                            {
                                "id": "1612",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:1612"
                            }
                        ]
                    }
                ],
                "keywords": [
                    "biomuta",
                    "somatic",
                    "cancer",
                    "disease",
                    "ebi"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs1596503384",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1596503384"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3388,
                "end_pos": 3388,
                "sequence_org": "A",
                "sequence_mut": "null",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2097872",
                "ref_nt": "l",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "A3388",
                "disease": [
                    {
                        "disease_id": "DOID:0080322",
                        "recommended_name": {
                            "id": "DOID:0080322",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0080322",
                            "name": "polycystic kidney disease",
                            "description": "A cystic kidney disease that is characterized by the growth of fluid-filled cysts in the kidneys that reduces kidney function and may lead to kidney failure."
                        },
                        "synonyms": [
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0080322",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0080322"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0110858",
                        "recommended_name": {
                            "id": "DOID:0110858",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0110858",
                            "name": "polycystic kidney disease 1",
                            "description": "A autosomal dominant polycystic kidney disease that has_material_basis_in autosomal dominant inheritance of mutation in the PKD1 gene on chromosome 16p13.3."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "Polycystic Kidney Disease, Adult, Type I",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            },
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            }
                        ]
                    }
                ],
                "keywords": [
                    "ebi",
                    "germline",
                    "disease"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs756738297",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs756738297"
                    },
                    {
                        "id": "rs756738297",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs756738297"
                    },
                    {
                        "id": "rs756738297",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs756738297#frequency_tab"
                    },
                    {
                        "id": "rs756738297",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs756738297"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3389,
                "end_pos": 3389,
                "sequence_org": "E",
                "sequence_mut": "K",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2097870",
                "ref_nt": "T",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "E3389",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs756738297",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs756738297"
                    },
                    {
                        "id": "rs756738297",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs756738297"
                    },
                    {
                        "id": "rs756738297",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs756738297#frequency_tab"
                    },
                    {
                        "id": "rs756738297",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs756738297"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3389,
                "end_pos": 3389,
                "sequence_org": "E",
                "sequence_mut": "Q",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2097870",
                "ref_nt": "G",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "E3389",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs2151728536",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs2151728536"
                    },
                    {
                        "id": "rs2151728536",
                        "database": "ENSEMBL",
                        "url": "https://www.ensembl.org/id/rs2151728536"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3390,
                "end_pos": 3390,
                "sequence_org": "Q",
                "sequence_mut": "*",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2097780",
                "ref_nt": "A",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "Q3390",
                "disease": [
                    {
                        "disease_id": "DOID:0080322",
                        "recommended_name": {
                            "id": "DOID:0080322",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0080322",
                            "name": "polycystic kidney disease",
                            "description": "A cystic kidney disease that is characterized by the growth of fluid-filled cysts in the kidneys that reduces kidney function and may lead to kidney failure."
                        },
                        "synonyms": [
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0080322",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0080322"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0110858",
                        "recommended_name": {
                            "id": "DOID:0110858",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0110858",
                            "name": "polycystic kidney disease 1",
                            "description": "A autosomal dominant polycystic kidney disease that has_material_basis_in autosomal dominant inheritance of mutation in the PKD1 gene on chromosome 16p13.3."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "Polycystic Kidney Disease, Adult, Type I",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            },
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            }
                        ]
                    }
                ],
                "keywords": [
                    "ebi",
                    "germline",
                    "disease"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs139324800",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs139324800"
                    },
                    {
                        "id": "rs139324800",
                        "database": "1000Genomes",
                        "url": "https://www.ensembl.org/homo_sapiens/Variation/Explore?v=rs139324800"
                    },
                    {
                        "id": "rs139324800",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs139324800"
                    },
                    {
                        "id": "rs139324800",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs139324800#frequency_tab"
                    },
                    {
                        "id": "rs139324800",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs139324800"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3391,
                "end_pos": 3391,
                "sequence_org": "A",
                "sequence_mut": "D",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2097776",
                "ref_nt": "T",
                "alt_nt": "null",
                "minor_allelic_frequency": "0.000588697",
                "site_lbl": "A3391",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "P98161",
                        "database": "BioMuta",
                        "url": "https://hivelab.biochemistry.gwu.edu/biomuta/proteinview/P98161"
                    },
                    {
                        "id": "rs2091906125",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs2091906125"
                    },
                    {
                        "id": "rs2091906125",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs2091906125#frequency_tab"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3391,
                "end_pos": 3391,
                "subjects_tested": "2670",
                "subjects_positive": "1",
                "frequency": "0.0",
                "sequence_org": "A",
                "sequence_mut": "T",
                "comment": "Somatic mutation passed 0 out of 6 filters: .",
                "chr_id": "16",
                "chr_pos": "2097777",
                "ref_nt": "C",
                "alt_nt": "T",
                "minor_allelic_frequency": "",
                "site_lbl": "A3391",
                "disease": [
                    {
                        "disease_id": "DOID:1319",
                        "recommended_name": {
                            "id": "DOID:1319",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:1319",
                            "name": "brain cancer",
                            "description": "A central nervous system cancer that is characterized by the growth of abnormal cells in the tissues of the brain."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:1319",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:1319",
                                "name": "BT - Brain tumour",
                                "description": ""
                            },
                            {
                                "id": "DOID:1319",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:1319",
                                "name": "adult brain tumor",
                                "description": ""
                            },
                            {
                                "id": "DOID:1319",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:1319",
                                "name": "adult malignant brain neoplasm",
                                "description": ""
                            },
                            {
                                "id": "DOID:1319",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:1319",
                                "name": "brain neoplasm",
                                "description": ""
                            },
                            {
                                "id": "DOID:1319",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:1319",
                                "name": "brain neoplasm, adult",
                                "description": ""
                            },
                            {
                                "id": "DOID:1319",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:1319",
                                "name": "malignant brain tumour",
                                "description": ""
                            },
                            {
                                "id": "DOID:1319",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:1319",
                                "name": "malignant primary brain neoplasm",
                                "description": ""
                            },
                            {
                                "id": "DOID:1319",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:1319",
                                "name": "malignant primary brain tumor",
                                "description": ""
                            },
                            {
                                "id": "DOID:1319",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:1319",
                                "name": "malignant tumor of Brain",
                                "description": ""
                            },
                            {
                                "id": "DOID:1319",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:1319",
                                "name": "malignant tumor of adult brain",
                                "description": ""
                            },
                            {
                                "id": "DOID:1319",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:1319",
                                "name": "neoplasm of brain",
                                "description": ""
                            },
                            {
                                "id": "DOID:1319",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:1319",
                                "name": "primary brain neoplasm",
                                "description": ""
                            },
                            {
                                "id": "DOID:1319",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:1319",
                                "name": "primary brain tumor",
                                "description": ""
                            },
                            {
                                "id": "DOID:1319",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:1319",
                                "name": "primary malignant neoplasm of brain",
                                "description": ""
                            },
                            {
                                "id": "DOID:1319",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:1319",
                                "name": "tumor of the Brain",
                                "description": ""
                            }
                        ],
                        "unlinked_id_list": [
                            "DOID:4203",
                            "DOID:3541",
                            "DOID:4706",
                            "DOID:1659",
                            "DOID:368"
                        ],
                        "evidence": [
                            {
                                "id": "1319",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:1319"
                            }
                        ]
                    }
                ],
                "keywords": [
                    "biomuta",
                    "somatic",
                    "cancer",
                    "disease",
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs139324800",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs139324800"
                    },
                    {
                        "id": "rs139324800",
                        "database": "1000Genomes",
                        "url": "https://www.ensembl.org/homo_sapiens/Variation/Explore?v=rs139324800"
                    },
                    {
                        "id": "rs139324800",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs139324800"
                    },
                    {
                        "id": "rs139324800",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs139324800#frequency_tab"
                    },
                    {
                        "id": "rs139324800",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs139324800"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3391,
                "end_pos": 3391,
                "sequence_org": "A",
                "sequence_mut": "V",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2097776",
                "ref_nt": "A",
                "alt_nt": "null",
                "minor_allelic_frequency": "0.000588697",
                "site_lbl": "A3391",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs3865207",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs3865207"
                    },
                    {
                        "id": "rs3865207",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs3865207"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3393,
                "end_pos": 3393,
                "sequence_org": "V",
                "sequence_mut": "A",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2097770",
                "ref_nt": "G",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "V3393",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "P98161",
                        "database": "BioMuta",
                        "url": "https://hivelab.biochemistry.gwu.edu/biomuta/proteinview/P98161"
                    },
                    {
                        "id": "rs2544692167",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs2544692167"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3393,
                "end_pos": 3393,
                "subjects_tested": "2617",
                "subjects_positive": "1",
                "frequency": "0.0",
                "sequence_org": "V",
                "sequence_mut": "I",
                "comment": "Somatic mutation passed 0 out of 6 filters: .",
                "chr_id": "16",
                "chr_pos": "2097771",
                "ref_nt": "C",
                "alt_nt": "T",
                "minor_allelic_frequency": "",
                "site_lbl": "V3393",
                "disease": [
                    {
                        "disease_id": "DOID:1793",
                        "recommended_name": {
                            "id": "DOID:1793",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:1793",
                            "name": "pancreatic cancer",
                            "description": "An endocrine gland cancer located_in the pancreas."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:1793",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:1793",
                                "name": "Ca body of pancreas",
                                "description": ""
                            },
                            {
                                "id": "DOID:1793",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:1793",
                                "name": "Ca head of pancreas",
                                "description": ""
                            },
                            {
                                "id": "DOID:1793",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:1793",
                                "name": "Ca tail of pancreas",
                                "description": ""
                            },
                            {
                                "id": "DOID:1793",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:1793",
                                "name": "malignant neoplasm of body of pancreas",
                                "description": ""
                            },
                            {
                                "id": "DOID:1793",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:1793",
                                "name": "malignant neoplasm of head of pancreas",
                                "description": ""
                            },
                            {
                                "id": "DOID:1793",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:1793",
                                "name": "malignant neoplasm of tail of pancreas",
                                "description": ""
                            },
                            {
                                "id": "DOID:1793",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:1793",
                                "name": "pancreas neoplasm",
                                "description": ""
                            },
                            {
                                "id": "DOID:1793",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:1793",
                                "name": "pancreatic neoplasm",
                                "description": ""
                            },
                            {
                                "id": "DOID:1793",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:1793",
                                "name": "pancreatic tumor",
                                "description": ""
                            }
                        ],
                        "unlinked_id_list": [
                            "DOID:1795"
                        ],
                        "evidence": [
                            {
                                "id": "1793",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:1793"
                            }
                        ]
                    }
                ],
                "keywords": [
                    "biomuta",
                    "somatic",
                    "cancer",
                    "disease",
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "P98161",
                        "database": "BioMuta",
                        "url": "https://hivelab.biochemistry.gwu.edu/biomuta/proteinview/P98161"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3394,
                "end_pos": 3394,
                "subjects_tested": "4799",
                "subjects_positive": "1",
                "frequency": "0.0",
                "sequence_org": "G",
                "sequence_mut": "V",
                "comment": "Somatic mutation passed 0 out of 6 filters: .",
                "chr_id": "16",
                "chr_pos": "2097767",
                "ref_nt": "C",
                "alt_nt": "A",
                "minor_allelic_frequency": "",
                "site_lbl": "G3394",
                "disease": [
                    {
                        "disease_id": "DOID:1324",
                        "recommended_name": {
                            "id": "DOID:1324",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:1324",
                            "name": "lung cancer",
                            "description": "A respiratory system cancer that is located_in the lung."
                        },
                        "synonyms": [
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "lung cancer",
                                "description": "A malignant neoplasm involving the lung."
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "adenocarcinoma of lung, response to tyrosine kinase inhibitor in, autosomal dominant, somatic mutation",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "adenocarcinoma of lung, somatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "cancer of lung",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "lung cancer",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "lung cancer, protection against, autosomal dominant, somatic mutation",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "lung cancer, resistance to, autosomal dominant, somatic mutation",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "lung cancer, somatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "lung cancer, susceptibility to, autosomal dominant, somatic mutation",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "malignant lung neoplasm",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "malignant lung tumor",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "malignant lung tumour",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "malignant neoplasm of lung",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "malignant neoplasm of the lung",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "malignant tumor of lung",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "malignant tumor of the lung",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "malignant tumour of lung",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "malignant tumour of the lung",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "nonsmall cell lung cancer, response to tyrosine kinase inhibitor in, autosomal dominant, somatic mutation",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "nonsmall cell lung cancer, somatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "nonsmall cell lung cancer, susceptibility to, autosomal dominant, somatic mutation",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012159",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012159",
                                "name": "lung cancer susceptibility 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012159",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012159",
                                "name": "LNCR1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012159",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012159",
                                "name": "lung cancer susceptibility",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012159",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012159",
                                "name": "lung cancer susceptibility 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012942",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012942",
                                "name": "lung cancer susceptibility 3",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012942",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012942",
                                "name": "LNCR3",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012942",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012942",
                                "name": "lung cancer susceptibility 3",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012955",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012955",
                                "name": "lung cancer susceptibility 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012955",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012955",
                                "name": "LNCR4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012955",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012955",
                                "name": "lung cancer susceptibility 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0013631",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0013631",
                                "name": "lung cancer susceptibility 5",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0013631",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0013631",
                                "name": "LNCR5",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0013631",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0013631",
                                "name": "lung cancer susceptibility 5",
                                "description": ""
                            },
                            {
                                "id": "MIM:211980",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/211980",
                                "name": "Lung cancer",
                                "description": "Lung cancer"
                            }
                        ],
                        "unlinked_id_list": [
                            "DOID:4765"
                        ],
                        "evidence": [
                            {
                                "id": "1324",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:1324"
                            }
                        ]
                    }
                ],
                "keywords": [
                    "biomuta",
                    "somatic",
                    "cancer",
                    "disease"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs1294437050",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1294437050"
                    },
                    {
                        "id": "rs1294437050",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs1294437050"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3395,
                "end_pos": 3395,
                "sequence_org": "Q",
                "sequence_mut": "*",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2097765",
                "ref_nt": "A",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "Q3395",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs1247651403",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1247651403"
                    },
                    {
                        "id": "rs1247651403",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs1247651403"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3395,
                "end_pos": 3395,
                "sequence_org": "Q",
                "sequence_mut": "R",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2097764",
                "ref_nt": "C",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "Q3395",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs2091905645",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs2091905645"
                    },
                    {
                        "id": "rs2091905645",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs2091905645#frequency_tab"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3396,
                "end_pos": 3396,
                "sequence_org": "M",
                "sequence_mut": "T",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2097761",
                "ref_nt": "G",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "M3396",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs1040082776",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1040082776"
                    },
                    {
                        "id": "rs1040082776",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs1040082776"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3396,
                "end_pos": 3396,
                "sequence_org": "M",
                "sequence_mut": "V",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2097762",
                "ref_nt": "C",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "M3396",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs2544692049",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs2544692049"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3397,
                "end_pos": 3397,
                "sequence_org": "K",
                "sequence_mut": "null",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2097760",
                "ref_nt": "p",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "K3397",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs1452634111",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1452634111"
                    },
                    {
                        "id": "rs1452634111",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs1452634111#frequency_tab"
                    },
                    {
                        "id": "rs1452634111",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs1452634111"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3399,
                "end_pos": 3399,
                "sequence_org": "D",
                "sequence_mut": "V",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2097752",
                "ref_nt": "A",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "D3399",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs2092941253",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs2092941253"
                    },
                    {
                        "id": "rs2092941253",
                        "database": "ENSEMBL",
                        "url": "https://www.ensembl.org/id/rs2092941253"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 33,
                "end_pos": 33,
                "sequence_org": "C",
                "sequence_mut": "*",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2135591",
                "ref_nt": "T",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "C33",
                "disease": [
                    {
                        "disease_id": "DOID:0080322",
                        "recommended_name": {
                            "id": "DOID:0080322",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0080322",
                            "name": "polycystic kidney disease",
                            "description": "A cystic kidney disease that is characterized by the growth of fluid-filled cysts in the kidneys that reduces kidney function and may lead to kidney failure."
                        },
                        "synonyms": [
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0080322",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0080322"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0110858",
                        "recommended_name": {
                            "id": "DOID:0110858",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0110858",
                            "name": "polycystic kidney disease 1",
                            "description": "A autosomal dominant polycystic kidney disease that has_material_basis_in autosomal dominant inheritance of mutation in the PKD1 gene on chromosome 16p13.3."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "Polycystic Kidney Disease, Adult, Type I",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            },
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            }
                        ]
                    }
                ],
                "keywords": [
                    "ebi",
                    "germline",
                    "disease"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs2544960532",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs2544960532"
                    },
                    {
                        "id": "rs2544960516",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs2544960516"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 33,
                "end_pos": 33,
                "sequence_org": "C",
                "sequence_mut": "null",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2135600_2135618",
                "ref_nt": "p",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "C33",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "P98161",
                        "database": "BioMuta",
                        "url": "https://hivelab.biochemistry.gwu.edu/biomuta/proteinview/P98161"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3402,
                "end_pos": 3402,
                "subjects_tested": "1704",
                "subjects_positive": "1",
                "frequency": "0.1",
                "sequence_org": "L",
                "sequence_mut": "M",
                "comment": "Somatic mutation passed 0 out of 6 filters: .",
                "chr_id": "16",
                "chr_pos": "2097744",
                "ref_nt": "G",
                "alt_nt": "T",
                "minor_allelic_frequency": "",
                "site_lbl": "L3402",
                "disease": [
                    {
                        "disease_id": "DOID:363",
                        "recommended_name": {
                            "id": "DOID:363",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:363",
                            "name": "uterine cancer",
                            "description": "A female reproductive organ cancer that is located_in the uterus."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:363",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:363",
                                "name": "CA - cancer of uterus",
                                "description": ""
                            },
                            {
                                "id": "DOID:363",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:363",
                                "name": "Tumour of uterus",
                                "description": ""
                            },
                            {
                                "id": "DOID:363",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:363",
                                "name": "malignant neoplasm of uterus",
                                "description": ""
                            },
                            {
                                "id": "DOID:363",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:363",
                                "name": "malignant uterine tumor",
                                "description": ""
                            },
                            {
                                "id": "DOID:363",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:363",
                                "name": "neoplasm of uterus",
                                "description": ""
                            },
                            {
                                "id": "DOID:363",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:363",
                                "name": "uterine tumor",
                                "description": ""
                            },
                            {
                                "id": "DOID:363",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:363",
                                "name": "uterus neoplasm",
                                "description": ""
                            }
                        ],
                        "unlinked_id_list": [
                            "DOID:9460",
                            "DOID:5166",
                            "DOID:2021",
                            "DOID:4114"
                        ],
                        "evidence": [
                            {
                                "id": "363",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:363"
                            }
                        ]
                    }
                ],
                "keywords": [
                    "biomuta",
                    "somatic",
                    "cancer",
                    "disease"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs2544691950",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs2544691950"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3402,
                "end_pos": 3402,
                "sequence_org": "L",
                "sequence_mut": "null",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2097747",
                "ref_nt": "p",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "L3402",
                "disease": [
                    {
                        "disease_id": "DOID:0080322",
                        "recommended_name": {
                            "id": "DOID:0080322",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0080322",
                            "name": "polycystic kidney disease",
                            "description": "A cystic kidney disease that is characterized by the growth of fluid-filled cysts in the kidneys that reduces kidney function and may lead to kidney failure."
                        },
                        "synonyms": [
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0080322",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0080322"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0110858",
                        "recommended_name": {
                            "id": "DOID:0110858",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0110858",
                            "name": "polycystic kidney disease 1",
                            "description": "A autosomal dominant polycystic kidney disease that has_material_basis_in autosomal dominant inheritance of mutation in the PKD1 gene on chromosome 16p13.3."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "Polycystic Kidney Disease, Adult, Type I",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            },
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            }
                        ]
                    }
                ],
                "keywords": [
                    "ebi",
                    "germline",
                    "disease"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs774485992",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs774485992"
                    },
                    {
                        "id": "rs774485992",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs774485992"
                    },
                    {
                        "id": "rs774485992",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs774485992#frequency_tab"
                    },
                    {
                        "id": "rs774485992",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs774485992"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3403,
                "end_pos": 3403,
                "sequence_org": "D",
                "sequence_mut": "G",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2097740",
                "ref_nt": "C",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "D3403",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs761908925",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs761908925"
                    },
                    {
                        "id": "rs761908925",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs761908925"
                    },
                    {
                        "id": "rs761908925",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs761908925#frequency_tab"
                    },
                    {
                        "id": "rs761908925",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs761908925"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3403,
                "end_pos": 3403,
                "sequence_org": "D",
                "sequence_mut": "H",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2097741",
                "ref_nt": "G",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "D3403",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs2091905133",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs2091905133"
                    },
                    {
                        "id": "rs2091905133",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs2091905133#frequency_tab"
                    },
                    {
                        "id": "rs2091905133",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs2091905133"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3404,
                "end_pos": 3404,
                "sequence_org": "D",
                "sequence_mut": "N",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2097738",
                "ref_nt": "T",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "D3404",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs1304784564",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1304784564"
                    },
                    {
                        "id": "rs1304784564",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs1304784564"
                    }
                ],
                "glycoeffect": [
                    "o-glyco-site-loss"
                ],
                "start_pos": 3405,
                "end_pos": 3405,
                "sequence_org": "S",
                "sequence_mut": "F",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2097734",
                "ref_nt": "A",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "S3405",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs1246648220",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1246648220"
                    },
                    {
                        "id": "rs1246648220",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs1246648220#frequency_tab"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3406,
                "end_pos": 3406,
                "sequence_org": "K",
                "sequence_mut": "E",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2097732",
                "ref_nt": "C",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "K3406",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "P98161",
                        "database": "BioMuta",
                        "url": "https://hivelab.biochemistry.gwu.edu/biomuta/proteinview/P98161"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3406,
                "end_pos": 3406,
                "subjects_tested": "4799",
                "subjects_positive": "1",
                "frequency": "0.0",
                "sequence_org": "K",
                "sequence_mut": "N",
                "comment": "Somatic mutation passed 0 out of 6 filters: .",
                "chr_id": "16",
                "chr_pos": "2097730",
                "ref_nt": "C",
                "alt_nt": "G",
                "minor_allelic_frequency": "",
                "site_lbl": "K3406",
                "disease": [
                    {
                        "disease_id": "DOID:1324",
                        "recommended_name": {
                            "id": "DOID:1324",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:1324",
                            "name": "lung cancer",
                            "description": "A respiratory system cancer that is located_in the lung."
                        },
                        "synonyms": [
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "lung cancer",
                                "description": "A malignant neoplasm involving the lung."
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "adenocarcinoma of lung, response to tyrosine kinase inhibitor in, autosomal dominant, somatic mutation",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "adenocarcinoma of lung, somatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "cancer of lung",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "lung cancer",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "lung cancer, protection against, autosomal dominant, somatic mutation",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "lung cancer, resistance to, autosomal dominant, somatic mutation",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "lung cancer, somatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "lung cancer, susceptibility to, autosomal dominant, somatic mutation",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "malignant lung neoplasm",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "malignant lung tumor",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "malignant lung tumour",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "malignant neoplasm of lung",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "malignant neoplasm of the lung",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "malignant tumor of lung",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "malignant tumor of the lung",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "malignant tumour of lung",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "malignant tumour of the lung",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "nonsmall cell lung cancer, response to tyrosine kinase inhibitor in, autosomal dominant, somatic mutation",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "nonsmall cell lung cancer, somatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "nonsmall cell lung cancer, susceptibility to, autosomal dominant, somatic mutation",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012159",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012159",
                                "name": "lung cancer susceptibility 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012159",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012159",
                                "name": "LNCR1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012159",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012159",
                                "name": "lung cancer susceptibility",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012159",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012159",
                                "name": "lung cancer susceptibility 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012942",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012942",
                                "name": "lung cancer susceptibility 3",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012942",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012942",
                                "name": "LNCR3",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012942",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012942",
                                "name": "lung cancer susceptibility 3",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012955",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012955",
                                "name": "lung cancer susceptibility 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012955",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012955",
                                "name": "LNCR4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012955",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012955",
                                "name": "lung cancer susceptibility 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0013631",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0013631",
                                "name": "lung cancer susceptibility 5",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0013631",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0013631",
                                "name": "LNCR5",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0013631",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0013631",
                                "name": "lung cancer susceptibility 5",
                                "description": ""
                            },
                            {
                                "id": "MIM:211980",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/211980",
                                "name": "Lung cancer",
                                "description": "Lung cancer"
                            }
                        ],
                        "unlinked_id_list": [
                            "DOID:4765"
                        ],
                        "evidence": [
                            {
                                "id": "1324",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:1324"
                            }
                        ]
                    }
                ],
                "keywords": [
                    "biomuta",
                    "somatic",
                    "cancer",
                    "disease"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs2151728391",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs2151728391"
                    }
                ],
                "glycoeffect": [
                    "o-glyco-site-loss"
                ],
                "start_pos": 3407,
                "end_pos": 3407,
                "sequence_org": "S",
                "sequence_mut": "null",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2097729",
                "ref_nt": "l",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "S3407",
                "disease": [
                    {
                        "disease_id": "DOID:0080322",
                        "recommended_name": {
                            "id": "DOID:0080322",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0080322",
                            "name": "polycystic kidney disease",
                            "description": "A cystic kidney disease that is characterized by the growth of fluid-filled cysts in the kidneys that reduces kidney function and may lead to kidney failure."
                        },
                        "synonyms": [
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0080322",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0080322"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0110858",
                        "recommended_name": {
                            "id": "DOID:0110858",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0110858",
                            "name": "polycystic kidney disease 1",
                            "description": "A autosomal dominant polycystic kidney disease that has_material_basis_in autosomal dominant inheritance of mutation in the PKD1 gene on chromosome 16p13.3."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "Polycystic Kidney Disease, Adult, Type I",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            },
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            }
                        ]
                    }
                ],
                "keywords": [
                    "ebi",
                    "germline",
                    "disease"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs1297060661",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1297060661"
                    },
                    {
                        "id": "rs1297060661",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs1297060661"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3408,
                "end_pos": 3408,
                "sequence_org": "L",
                "sequence_mut": "P",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2097501",
                "ref_nt": "G",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "L3408",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs1296638609",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1296638609"
                    },
                    {
                        "id": "rs1296638609",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs1296638609"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3408,
                "end_pos": 3408,
                "sequence_org": "L",
                "sequence_mut": "V",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2097502",
                "ref_nt": "C",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "L3408",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs779510789",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs779510789"
                    },
                    {
                        "id": "rs779510789",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs779510789"
                    },
                    {
                        "id": "rs779510789",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs779510789#frequency_tab"
                    },
                    {
                        "id": "rs779510789",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs779510789"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3409,
                "end_pos": 3409,
                "sequence_org": "V",
                "sequence_mut": "A",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2097498",
                "ref_nt": "G",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "V3409",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs779510789",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs779510789"
                    },
                    {
                        "id": "rs779510789",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs779510789"
                    },
                    {
                        "id": "rs779510789",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs779510789#frequency_tab"
                    },
                    {
                        "id": "rs779510789",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs779510789"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3409,
                "end_pos": 3409,
                "sequence_org": "V",
                "sequence_mut": "G",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2097498",
                "ref_nt": "C",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "V3409",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "P98161",
                        "database": "BioMuta",
                        "url": "https://hivelab.biochemistry.gwu.edu/biomuta/proteinview/P98161"
                    },
                    {
                        "id": "rs61747420",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs61747420"
                    },
                    {
                        "id": "rs61747420",
                        "database": "1000Genomes",
                        "url": "https://www.ensembl.org/homo_sapiens/Variation/Explore?v=rs61747420"
                    },
                    {
                        "id": "rs61747420",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs61747420"
                    },
                    {
                        "id": "rs61747420",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs61747420#frequency_tab"
                    },
                    {
                        "id": "rs61747420",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs61747420"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3409,
                "end_pos": 3409,
                "subjects_tested": "4799",
                "subjects_positive": "4",
                "frequency": "0.1",
                "sequence_org": "V",
                "sequence_mut": "L",
                "comment": "Somatic mutation passed 0 out of 6 filters: .",
                "chr_id": "16",
                "chr_pos": "2097499",
                "ref_nt": "C",
                "alt_nt": "G",
                "minor_allelic_frequency": "",
                "site_lbl": "V3409",
                "disease": [
                    {
                        "disease_id": "DOID:1324",
                        "recommended_name": {
                            "id": "DOID:1324",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:1324",
                            "name": "lung cancer",
                            "description": "A respiratory system cancer that is located_in the lung."
                        },
                        "synonyms": [
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "lung cancer",
                                "description": "A malignant neoplasm involving the lung."
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "adenocarcinoma of lung, response to tyrosine kinase inhibitor in, autosomal dominant, somatic mutation",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "adenocarcinoma of lung, somatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "cancer of lung",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "lung cancer",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "lung cancer, protection against, autosomal dominant, somatic mutation",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "lung cancer, resistance to, autosomal dominant, somatic mutation",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "lung cancer, somatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "lung cancer, susceptibility to, autosomal dominant, somatic mutation",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "malignant lung neoplasm",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "malignant lung tumor",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "malignant lung tumour",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "malignant neoplasm of lung",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "malignant neoplasm of the lung",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "malignant tumor of lung",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "malignant tumor of the lung",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "malignant tumour of lung",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "malignant tumour of the lung",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "nonsmall cell lung cancer, response to tyrosine kinase inhibitor in, autosomal dominant, somatic mutation",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "nonsmall cell lung cancer, somatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "nonsmall cell lung cancer, susceptibility to, autosomal dominant, somatic mutation",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012159",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012159",
                                "name": "lung cancer susceptibility 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012159",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012159",
                                "name": "LNCR1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012159",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012159",
                                "name": "lung cancer susceptibility",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012159",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012159",
                                "name": "lung cancer susceptibility 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012942",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012942",
                                "name": "lung cancer susceptibility 3",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012942",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012942",
                                "name": "LNCR3",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012942",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012942",
                                "name": "lung cancer susceptibility 3",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012955",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012955",
                                "name": "lung cancer susceptibility 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012955",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012955",
                                "name": "LNCR4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012955",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012955",
                                "name": "lung cancer susceptibility 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0013631",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0013631",
                                "name": "lung cancer susceptibility 5",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0013631",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0013631",
                                "name": "LNCR5",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0013631",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0013631",
                                "name": "lung cancer susceptibility 5",
                                "description": ""
                            },
                            {
                                "id": "MIM:211980",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/211980",
                                "name": "Lung cancer",
                                "description": "Lung cancer"
                            }
                        ],
                        "unlinked_id_list": [
                            "DOID:4765"
                        ],
                        "evidence": [
                            {
                                "id": "1324",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:1324"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0080322",
                        "recommended_name": {
                            "id": "DOID:0080322",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0080322",
                            "name": "polycystic kidney disease",
                            "description": "A cystic kidney disease that is characterized by the growth of fluid-filled cysts in the kidneys that reduces kidney function and may lead to kidney failure."
                        },
                        "synonyms": [
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0080322",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0080322"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0110858",
                        "recommended_name": {
                            "id": "DOID:0110858",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0110858",
                            "name": "polycystic kidney disease 1",
                            "description": "A autosomal dominant polycystic kidney disease that has_material_basis_in autosomal dominant inheritance of mutation in the PKD1 gene on chromosome 16p13.3."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "Polycystic Kidney Disease, Adult, Type I",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            },
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            }
                        ]
                    }
                ],
                "keywords": [
                    "biomuta",
                    "somatic",
                    "cancer",
                    "disease",
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs1406565745",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1406565745"
                    },
                    {
                        "id": "rs1406565745",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs1406565745"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 340,
                "end_pos": 340,
                "sequence_org": "G",
                "sequence_mut": "E",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2117973",
                "ref_nt": "T",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "G340",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs769539998",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs769539998"
                    },
                    {
                        "id": "rs769539998",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs769539998"
                    },
                    {
                        "id": "rs769539998",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs769539998#frequency_tab"
                    },
                    {
                        "id": "rs769539998",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs769539998"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3410,
                "end_pos": 3410,
                "sequence_org": "C",
                "sequence_mut": "S",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2097495",
                "ref_nt": "G",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "C3410",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs1395927794",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1395927794"
                    },
                    {
                        "id": "rs1395927794",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs1395927794#frequency_tab"
                    },
                    {
                        "id": "rs1395927794",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs1395927794"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3410,
                "end_pos": 3410,
                "sequence_org": "C",
                "sequence_mut": "W",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2097494",
                "ref_nt": "C",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "C3410",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "P98161",
                        "database": "BioMuta",
                        "url": "https://hivelab.biochemistry.gwu.edu/biomuta/proteinview/P98161"
                    },
                    {
                        "id": "rs769539998",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs769539998"
                    },
                    {
                        "id": "rs769539998",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs769539998"
                    },
                    {
                        "id": "rs769539998",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs769539998#frequency_tab"
                    },
                    {
                        "id": "rs769539998",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs769539998"
                    },
                    {
                        "id": "rs769539998",
                        "database": "COSMIC",
                        "url": "https://www.ensembl.org/homo_sapiens/Variation/Explore?v=rs769539998"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3410,
                "end_pos": 3410,
                "subjects_tested": "3601",
                "subjects_positive": "1",
                "frequency": "0.0",
                "sequence_org": "C",
                "sequence_mut": "Y",
                "comment": "Somatic mutation passed 0 out of 6 filters: .",
                "chr_id": "16",
                "chr_pos": "2097495",
                "ref_nt": "C",
                "alt_nt": "T",
                "minor_allelic_frequency": "",
                "site_lbl": "C3410",
                "disease": [
                    {
                        "disease_id": "DOID:9256",
                        "recommended_name": {
                            "id": "DOID:9256",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:9256",
                            "name": "colorectal cancer",
                            "description": "A large intestine cancer that is located_in the colon and/or located_in the rectum."
                        },
                        "synonyms": [
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectal cancer",
                                "description": "A primary or metastatic malignant neoplasm that affects the colon or rectum. Representative examples include carcinoma, lymphoma, and sarcoma."
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "cancer of colorectum",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "cancer of large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "cancer of large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "cancer of the large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colon cancer, advanced, somatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colon cancer, somatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectal cancer",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectal cancer with chromosomal instability, somatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectal cancer, autosomal dominant, somatic mutation",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectal cancer, somatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectal cancer, susceptibility to, autosomal dominant, somatic mutation",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectum cancer",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant colorectal neoplasm",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant colorectal tumor",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant colorectal tumour",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant colorectum neoplasm",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant large bowel neoplasm",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant large bowel tumor",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant large bowel tumour",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant large intestine neoplasm",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant large intestine tumor",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant large intestine tumour",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant neoplasm of colorectum",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant neoplasm of large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant neoplasm of large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant neoplasm of the large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant neoplasm of the large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumor of large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumor of large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumor of the large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumor of the large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumour of large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumour of large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumour of the large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumour of the large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "CRC",
                                "description": ""
                            },
                            {
                                "id": "MIM:114500",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/114500",
                                "name": "Colorectal cancer",
                                "description": "Colorectal cancer"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "9256",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:9256"
                            }
                        ]
                    }
                ],
                "keywords": [
                    "biomuta",
                    "somatic",
                    "cancer",
                    "disease",
                    "ebi"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs1300254603",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1300254603"
                    },
                    {
                        "id": "rs1300254603",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs1300254603"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3411,
                "end_pos": 3411,
                "sequence_org": "W",
                "sequence_mut": "*",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2097491",
                "ref_nt": "T",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "W3411",
                "disease": [
                    {
                        "disease_id": "DOID:0080322",
                        "recommended_name": {
                            "id": "DOID:0080322",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0080322",
                            "name": "polycystic kidney disease",
                            "description": "A cystic kidney disease that is characterized by the growth of fluid-filled cysts in the kidneys that reduces kidney function and may lead to kidney failure."
                        },
                        "synonyms": [
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0080322",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0080322"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0110858",
                        "recommended_name": {
                            "id": "DOID:0110858",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0110858",
                            "name": "polycystic kidney disease 1",
                            "description": "A autosomal dominant polycystic kidney disease that has_material_basis_in autosomal dominant inheritance of mutation in the PKD1 gene on chromosome 16p13.3."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "Polycystic Kidney Disease, Adult, Type I",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            },
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            }
                        ]
                    }
                ],
                "keywords": [
                    "ebi",
                    "germline",
                    "disease"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs1300254603",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1300254603"
                    },
                    {
                        "id": "rs1300254603",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs1300254603"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3411,
                "end_pos": 3411,
                "sequence_org": "W",
                "sequence_mut": "C",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2097491",
                "ref_nt": "A",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "W3411",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs549326097",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs549326097"
                    },
                    {
                        "id": "rs549326097",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs549326097"
                    },
                    {
                        "id": "rs549326097",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs549326097#frequency_tab"
                    },
                    {
                        "id": "rs549326097",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs549326097"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3411,
                "end_pos": 3411,
                "sequence_org": "W",
                "sequence_mut": "S",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2097492",
                "ref_nt": "G",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "W3411",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs1596501760",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1596501760"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3411,
                "end_pos": 3411,
                "sequence_org": "W",
                "sequence_mut": "null",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2097492",
                "ref_nt": "l",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "W3411",
                "disease": [
                    {
                        "disease_id": "DOID:0080322",
                        "recommended_name": {
                            "id": "DOID:0080322",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0080322",
                            "name": "polycystic kidney disease",
                            "description": "A cystic kidney disease that is characterized by the growth of fluid-filled cysts in the kidneys that reduces kidney function and may lead to kidney failure."
                        },
                        "synonyms": [
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0080322",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0080322"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0110858",
                        "recommended_name": {
                            "id": "DOID:0110858",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0110858",
                            "name": "polycystic kidney disease 1",
                            "description": "A autosomal dominant polycystic kidney disease that has_material_basis_in autosomal dominant inheritance of mutation in the PKD1 gene on chromosome 16p13.3."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "Polycystic Kidney Disease, Adult, Type I",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            },
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            }
                        ]
                    }
                ],
                "keywords": [
                    "ebi",
                    "germline",
                    "disease"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs1389951508",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1389951508"
                    },
                    {
                        "id": "rs1389951508",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs1389951508"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3412,
                "end_pos": 3412,
                "sequence_org": "P",
                "sequence_mut": "L",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2097489",
                "ref_nt": "A",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "P3412",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "P98161",
                        "database": "BioMuta",
                        "url": "https://hivelab.biochemistry.gwu.edu/biomuta/proteinview/P98161"
                    },
                    {
                        "id": "rs149605181",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs149605181"
                    },
                    {
                        "id": "rs149605181",
                        "database": "1000Genomes",
                        "url": "https://www.ensembl.org/homo_sapiens/Variation/Explore?v=rs149605181"
                    },
                    {
                        "id": "rs149605181",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs149605181"
                    },
                    {
                        "id": "rs149605181",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs149605181#frequency_tab"
                    },
                    {
                        "id": "rs149605181",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs149605181"
                    },
                    {
                        "id": "rs149605181",
                        "database": "COSMIC",
                        "url": "https://www.ensembl.org/homo_sapiens/Variation/Explore?v=rs149605181"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3412,
                "end_pos": 3412,
                "subjects_tested": "4177",
                "subjects_positive": "1",
                "frequency": "0.0",
                "sequence_org": "P",
                "sequence_mut": "S",
                "comment": "Somatic mutation passed 0 out of 6 filters: .",
                "chr_id": "16",
                "chr_pos": "2097490",
                "ref_nt": "G",
                "alt_nt": "A",
                "minor_allelic_frequency": "",
                "site_lbl": "P3412",
                "disease": [
                    {
                        "disease_id": "DOID:10283",
                        "recommended_name": {
                            "id": "DOID:10283",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:10283",
                            "name": "prostate cancer",
                            "description": "A male reproductive organ cancer that is located_in the prostate."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:10283",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:10283",
                                "name": "NGP - new growth of prostate",
                                "description": ""
                            },
                            {
                                "id": "DOID:10283",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:10283",
                                "name": "hereditary prostate cancer",
                                "description": ""
                            },
                            {
                                "id": "DOID:10283",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:10283",
                                "name": "malignant tumor of the prostate",
                                "description": ""
                            },
                            {
                                "id": "DOID:10283",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:10283",
                                "name": "prostate cancer, familial",
                                "description": ""
                            },
                            {
                                "id": "DOID:10283",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:10283",
                                "name": "prostate neoplasm",
                                "description": ""
                            },
                            {
                                "id": "DOID:10283",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:10283",
                                "name": "prostatic cancer",
                                "description": ""
                            },
                            {
                                "id": "DOID:10283",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:10283",
                                "name": "prostatic neoplasm",
                                "description": ""
                            },
                            {
                                "id": "DOID:10283",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:10283",
                                "name": "tumor of the prostate",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0010257",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0010257",
                                "name": "prostate cancer, hereditary, X-linked 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0010257",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0010257",
                                "name": "HPCX1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0010257",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0010257",
                                "name": "prostate cancer, hereditary, X-linked 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0010405",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0010405",
                                "name": "prostate cancer, hereditary, X-linked 2",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0010405",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0010405",
                                "name": "HPCX2",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0010405",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0010405",
                                "name": "prostate cancer, hereditary, X-linked 2",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011098",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011098",
                                "name": "prostate cancer, hereditary, 1",
                                "description": "Any familial prostate cancer in which the cause of the disease is a mutation in the RNASEL gene."
                            },
                            {
                                "id": "MONDO:0011098",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011098",
                                "name": "RNASEL familial prostate cancer",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011098",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011098",
                                "name": "familial prostate cancer caused by mutation in RNASEL",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011098",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011098",
                                "name": "prostate cancer 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011098",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011098",
                                "name": "prostate cancer, hereditary, 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011098",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011098",
                                "name": "prostate cancer, hereditary, type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011098",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011098",
                                "name": "HPC1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011270",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011270",
                                "name": "prostate cancer, hereditary, 8",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011270",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011270",
                                "name": "prostate cancer, hereditary, 8",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011270",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011270",
                                "name": "prostate cancer, hereditary, type 8",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011270",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011270",
                                "name": "HPC8",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012093",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012093",
                                "name": "prostate cancer, hereditary, 3",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012093",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012093",
                                "name": "prostate cancer, hereditary, 3",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012093",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012093",
                                "name": "prostate cancer, hereditary, type 3",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012093",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012093",
                                "name": "prostate cancer, susceptibility to, 3",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012093",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012093",
                                "name": "HPC3",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012094",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012094",
                                "name": "prostate cancer, hereditary, 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012094",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012094",
                                "name": "prostate cancer, hereditary, 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012094",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012094",
                                "name": "prostate cancer, hereditary, type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012094",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012094",
                                "name": "prostate cancer, susceptibility to, 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012094",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012094",
                                "name": "HPC4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012244",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012244",
                                "name": "prostate cancer, hereditary, 5",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012244",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012244",
                                "name": "prostate cancer, hereditary, 5",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012244",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012244",
                                "name": "prostate cancer, hereditary, type 5",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012244",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012244",
                                "name": "HPC5",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012300",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012300",
                                "name": "prostate cancer, hereditary, 6",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012300",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012300",
                                "name": "prostate cancer, hereditary, 6",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012300",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012300",
                                "name": "prostate cancer, hereditary, type 6",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012300",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012300",
                                "name": "HPC6",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012470",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012470",
                                "name": "prostate cancer, hereditary, 7",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012470",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012470",
                                "name": "HPC7",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012470",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012470",
                                "name": "prostate cancer, hereditary, 7",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012597",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012597",
                                "name": "prostate cancer, hereditary, 9",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012597",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012597",
                                "name": "prostate cancer, hereditary, 9",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012597",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012597",
                                "name": "prostate cancer, hereditary, type 9",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012597",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012597",
                                "name": "HPC9",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012620",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012620",
                                "name": "prostate cancer, hereditary, 10",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012620",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012620",
                                "name": "HPC10",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012620",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012620",
                                "name": "prostate cancer, hereditary, 10",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012741",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012741",
                                "name": "prostate cancer, hereditary, 12",
                                "description": "Any familial prostate cancer in which the cause of the disease is a mutation in the EHBP1 gene."
                            },
                            {
                                "id": "MONDO:0012741",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012741",
                                "name": "EHBP1 familial prostate cancer",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012741",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012741",
                                "name": "familial prostate cancer caused by mutation in EHBP1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012741",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012741",
                                "name": "prostate cancer, hereditary, 12",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012741",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012741",
                                "name": "prostate cancer, hereditary, type 12",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012741",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012741",
                                "name": "HPC12",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012758",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012758",
                                "name": "prostate cancer, hereditary, 13",
                                "description": "Any familial prostate cancer in which the cause of the disease is a mutation in the MSMB gene."
                            },
                            {
                                "id": "MONDO:0012758",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012758",
                                "name": "MSMB familial prostate cancer",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012758",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012758",
                                "name": "familial prostate cancer caused by mutation in MSMB",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012758",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012758",
                                "name": "prostate cancer, hereditary, 13",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012758",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012758",
                                "name": "prostate cancer, hereditary, type 13",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012758",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012758",
                                "name": "HPC13",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012768",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012768",
                                "name": "prostate cancer, hereditary, 11",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012768",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012768",
                                "name": "HPC11",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012768",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012768",
                                "name": "prostate cancer, hereditary, 11",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012769",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012769",
                                "name": "prostate cancer, hereditary, 14",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012769",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012769",
                                "name": "HPC14",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012769",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012769",
                                "name": "prostate cancer, hereditary, 14",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012770",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012770",
                                "name": "prostate cancer, hereditary, 15",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012770",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012770",
                                "name": "HPC15",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012770",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012770",
                                "name": "prostate cancer, hereditary, 15",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0700275",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0700275",
                                "name": "prostate cancer, hereditary",
                                "description": "An instance of prostate cancer that is caused by an inherited genomic modification in an individual. Familial prostate cancer (FPC) is a malignant tumor of the prostate with an early onset. FPC is either asymptomatic or causes mictionary symptoms, erectile dysfunction, bone pain, venous compression and infectious or inflammatory syndrome (for the metastatic forms). It is also characterized by familial antecedents."
                            },
                            {
                                "id": "MIM:601518",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/601518",
                                "name": "Prostate cancer, hereditary, 1",
                                "description": "Prostate cancer, hereditary, 1"
                            },
                            {
                                "id": "MIM:610997",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/610997",
                                "name": "Prostate cancer, hereditary, 9",
                                "description": "Prostate cancer, hereditary, 9"
                            },
                            {
                                "id": "MIM:611868",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/611868",
                                "name": "Prostate cancer, hereditary, 12",
                                "description": "Prostate cancer, hereditary, 12"
                            },
                            {
                                "id": "MIM:611928",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/611928",
                                "name": "Prostate cancer, hereditary, 13",
                                "description": "Prostate cancer, hereditary, 13"
                            },
                            {
                                "id": "MIM:611955",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/611955",
                                "name": "Prostate cancer, hereditary, 11",
                                "description": "Prostate cancer, hereditary, 11"
                            },
                            {
                                "id": "MIM:176807",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/176807",
                                "name": "Prostate cancer",
                                "description": "Prostate cancer"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "10283",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:10283"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:1324",
                        "recommended_name": {
                            "id": "DOID:1324",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:1324",
                            "name": "lung cancer",
                            "description": "A respiratory system cancer that is located_in the lung."
                        },
                        "synonyms": [
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "lung cancer",
                                "description": "A malignant neoplasm involving the lung."
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "adenocarcinoma of lung, response to tyrosine kinase inhibitor in, autosomal dominant, somatic mutation",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "adenocarcinoma of lung, somatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "cancer of lung",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "lung cancer",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "lung cancer, protection against, autosomal dominant, somatic mutation",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "lung cancer, resistance to, autosomal dominant, somatic mutation",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "lung cancer, somatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "lung cancer, susceptibility to, autosomal dominant, somatic mutation",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "malignant lung neoplasm",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "malignant lung tumor",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "malignant lung tumour",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "malignant neoplasm of lung",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "malignant neoplasm of the lung",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "malignant tumor of lung",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "malignant tumor of the lung",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "malignant tumour of lung",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "malignant tumour of the lung",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "nonsmall cell lung cancer, response to tyrosine kinase inhibitor in, autosomal dominant, somatic mutation",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "nonsmall cell lung cancer, somatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "nonsmall cell lung cancer, susceptibility to, autosomal dominant, somatic mutation",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012159",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012159",
                                "name": "lung cancer susceptibility 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012159",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012159",
                                "name": "LNCR1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012159",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012159",
                                "name": "lung cancer susceptibility",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012159",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012159",
                                "name": "lung cancer susceptibility 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012942",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012942",
                                "name": "lung cancer susceptibility 3",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012942",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012942",
                                "name": "LNCR3",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012942",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012942",
                                "name": "lung cancer susceptibility 3",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012955",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012955",
                                "name": "lung cancer susceptibility 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012955",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012955",
                                "name": "LNCR4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012955",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012955",
                                "name": "lung cancer susceptibility 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0013631",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0013631",
                                "name": "lung cancer susceptibility 5",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0013631",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0013631",
                                "name": "LNCR5",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0013631",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0013631",
                                "name": "lung cancer susceptibility 5",
                                "description": ""
                            },
                            {
                                "id": "MIM:211980",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/211980",
                                "name": "Lung cancer",
                                "description": "Lung cancer"
                            }
                        ],
                        "unlinked_id_list": [
                            "DOID:4765"
                        ],
                        "evidence": [
                            {
                                "id": "1324",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:1324"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0080322",
                        "recommended_name": {
                            "id": "DOID:0080322",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0080322",
                            "name": "polycystic kidney disease",
                            "description": "A cystic kidney disease that is characterized by the growth of fluid-filled cysts in the kidneys that reduces kidney function and may lead to kidney failure."
                        },
                        "synonyms": [
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0080322",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0080322"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0110858",
                        "recommended_name": {
                            "id": "DOID:0110858",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0110858",
                            "name": "polycystic kidney disease 1",
                            "description": "A autosomal dominant polycystic kidney disease that has_material_basis_in autosomal dominant inheritance of mutation in the PKD1 gene on chromosome 16p13.3."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "Polycystic Kidney Disease, Adult, Type I",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            },
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            }
                        ]
                    }
                ],
                "keywords": [
                    "biomuta",
                    "somatic",
                    "cancer",
                    "disease",
                    "ebi"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs137986581",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs137986581"
                    },
                    {
                        "id": "rs137986581",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs137986581"
                    },
                    {
                        "id": "rs137986581",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs137986581#frequency_tab"
                    },
                    {
                        "id": "rs137986581",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs137986581"
                    }
                ],
                "glycoeffect": [
                    "o-glyco-site-loss"
                ],
                "start_pos": 3413,
                "end_pos": 3413,
                "sequence_org": "S",
                "sequence_mut": "F",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2097486",
                "ref_nt": "A",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "S3413",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs2544689115",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs2544689115"
                    }
                ],
                "glycoeffect": [
                    "o-glyco-site-loss"
                ],
                "start_pos": 3413,
                "end_pos": 3413,
                "sequence_org": "S",
                "sequence_mut": "null",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2097490",
                "ref_nt": "l",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "S3413",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs371762181",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs371762181"
                    },
                    {
                        "id": "rs371762181",
                        "database": "1000Genomes",
                        "url": "https://www.ensembl.org/homo_sapiens/Variation/Explore?v=rs371762181"
                    },
                    {
                        "id": "rs371762181",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs371762181"
                    },
                    {
                        "id": "rs371762181",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs371762181#frequency_tab"
                    },
                    {
                        "id": "rs371762181",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs371762181"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3414,
                "end_pos": 3414,
                "sequence_org": "G",
                "sequence_mut": "S",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2097484",
                "ref_nt": "T",
                "alt_nt": "null",
                "minor_allelic_frequency": "0.000196232",
                "site_lbl": "G3414",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs752880451",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs752880451"
                    },
                    {
                        "id": "rs752880451",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs752880451"
                    },
                    {
                        "id": "rs752880451",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs752880451#frequency_tab"
                    },
                    {
                        "id": "rs752880451",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs752880451"
                    },
                    {
                        "id": "rs752880451",
                        "database": "COSMIC",
                        "url": "https://www.ensembl.org/homo_sapiens/Variation/Explore?v=rs752880451"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3415,
                "end_pos": 3415,
                "sequence_org": "E",
                "sequence_mut": "K",
                "comment": "Somatic mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2097481",
                "ref_nt": "T",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "E3415",
                "keywords": [
                    "ebi",
                    "somatic"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs1197492524",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1197492524"
                    },
                    {
                        "id": "rs1197492524",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs1197492524"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3416,
                "end_pos": 3416,
                "sequence_org": "G",
                "sequence_mut": "R",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2097478",
                "ref_nt": "T",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "G3416",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs1596501702",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1596501702"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3416,
                "end_pos": 3416,
                "sequence_org": "G",
                "sequence_mut": "null",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2097479",
                "ref_nt": "l",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "G3416",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs765373300",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs765373300"
                    },
                    {
                        "id": "rs765373300",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs765373300"
                    },
                    {
                        "id": "rs765373300",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs765373300#frequency_tab"
                    },
                    {
                        "id": "rs765373300",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs765373300"
                    }
                ],
                "glycoeffect": [
                    "o-glyco-site-loss"
                ],
                "start_pos": 3417,
                "end_pos": 3417,
                "sequence_org": "T",
                "sequence_mut": "A",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2097475",
                "ref_nt": "C",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "T3417",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs377052445",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs377052445"
                    },
                    {
                        "id": "rs377052445",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs377052445"
                    },
                    {
                        "id": "rs377052445",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs377052445#frequency_tab"
                    },
                    {
                        "id": "rs377052445",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs377052445"
                    },
                    {
                        "id": "rs377052445",
                        "database": "COSMIC",
                        "url": "https://www.ensembl.org/homo_sapiens/Variation/Explore?v=rs377052445"
                    }
                ],
                "glycoeffect": [
                    "o-glyco-site-loss"
                ],
                "start_pos": 3417,
                "end_pos": 3417,
                "sequence_org": "T",
                "sequence_mut": "M",
                "comment": "Somatic mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2097474",
                "ref_nt": "A",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "T3417",
                "keywords": [
                    "ebi",
                    "somatic"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs377052445",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs377052445"
                    },
                    {
                        "id": "rs377052445",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs377052445"
                    },
                    {
                        "id": "rs377052445",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs377052445#frequency_tab"
                    },
                    {
                        "id": "rs377052445",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs377052445"
                    }
                ],
                "glycoeffect": [
                    "o-glyco-site-loss"
                ],
                "start_pos": 3417,
                "end_pos": 3417,
                "sequence_org": "T",
                "sequence_mut": "R",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2097474",
                "ref_nt": "C",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "T3417",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs1361916151",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1361916151"
                    },
                    {
                        "id": "rs1361916151",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs1361916151"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3418,
                "end_pos": 3418,
                "sequence_org": "L",
                "sequence_mut": "P",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2097471",
                "ref_nt": "G",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "L3418",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs914151219",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs914151219"
                    },
                    {
                        "id": "rs914151219",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs914151219#frequency_tab"
                    },
                    {
                        "id": "rs914151219",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs914151219"
                    }
                ],
                "glycoeffect": [
                    "o-glyco-site-loss"
                ],
                "start_pos": 3419,
                "end_pos": 3419,
                "sequence_org": "S",
                "sequence_mut": "C",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2097469",
                "ref_nt": "A",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "S3419",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs914151219",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs914151219"
                    },
                    {
                        "id": "rs914151219",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs914151219#frequency_tab"
                    },
                    {
                        "id": "rs914151219",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs914151219"
                    }
                ],
                "glycoeffect": [
                    "o-glyco-site-loss"
                ],
                "start_pos": 3419,
                "end_pos": 3419,
                "sequence_org": "S",
                "sequence_mut": "G",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2097469",
                "ref_nt": "C",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "S3419",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs773523147",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs773523147"
                    },
                    {
                        "id": "rs773523147",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs773523147"
                    },
                    {
                        "id": "rs773523147",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs773523147"
                    }
                ],
                "glycoeffect": [
                    "o-glyco-site-loss"
                ],
                "start_pos": 3419,
                "end_pos": 3419,
                "sequence_org": "S",
                "sequence_mut": "N",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2097468",
                "ref_nt": "T",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "S3419",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs2855337",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs2855337"
                    },
                    {
                        "id": "rs2855337",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs2855337#frequency_tab"
                    },
                    {
                        "id": "rs2855337",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs2855337"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 341,
                "end_pos": 341,
                "sequence_org": "A",
                "sequence_mut": "T",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2117971",
                "ref_nt": "T",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "A341",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs2544878096",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs2544878096"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 341,
                "end_pos": 341,
                "sequence_org": "A",
                "sequence_mut": "null",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2117975",
                "ref_nt": "p",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "A341",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "P98161",
                        "database": "BioMuta",
                        "url": "https://hivelab.biochemistry.gwu.edu/biomuta/proteinview/P98161"
                    },
                    {
                        "id": "rs2151727019",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs2151727019"
                    },
                    {
                        "id": "rs2151727019",
                        "database": "ENSEMBL",
                        "url": "https://www.ensembl.org/id/rs2151727019"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3420,
                "end_pos": 3420,
                "subjects_tested": "3601",
                "subjects_positive": "2",
                "frequency": "0.1",
                "sequence_org": "W",
                "sequence_mut": "*",
                "comment": "Somatic mutation passed 0 out of 6 filters: .",
                "chr_id": "16",
                "chr_pos": "2097464",
                "ref_nt": "C",
                "alt_nt": "T",
                "minor_allelic_frequency": "",
                "site_lbl": "W3420",
                "disease": [
                    {
                        "disease_id": "DOID:9256",
                        "recommended_name": {
                            "id": "DOID:9256",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:9256",
                            "name": "colorectal cancer",
                            "description": "A large intestine cancer that is located_in the colon and/or located_in the rectum."
                        },
                        "synonyms": [
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectal cancer",
                                "description": "A primary or metastatic malignant neoplasm that affects the colon or rectum. Representative examples include carcinoma, lymphoma, and sarcoma."
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "cancer of colorectum",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "cancer of large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "cancer of large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "cancer of the large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colon cancer, advanced, somatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colon cancer, somatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectal cancer",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectal cancer with chromosomal instability, somatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectal cancer, autosomal dominant, somatic mutation",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectal cancer, somatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectal cancer, susceptibility to, autosomal dominant, somatic mutation",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectum cancer",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant colorectal neoplasm",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant colorectal tumor",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant colorectal tumour",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant colorectum neoplasm",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant large bowel neoplasm",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant large bowel tumor",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant large bowel tumour",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant large intestine neoplasm",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant large intestine tumor",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant large intestine tumour",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant neoplasm of colorectum",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant neoplasm of large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant neoplasm of large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant neoplasm of the large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant neoplasm of the large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumor of large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumor of large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumor of the large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumor of the large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumour of large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumour of large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumour of the large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumour of the large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "CRC",
                                "description": ""
                            },
                            {
                                "id": "MIM:114500",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/114500",
                                "name": "Colorectal cancer",
                                "description": "Colorectal cancer"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "9256",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:9256"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0080322",
                        "recommended_name": {
                            "id": "DOID:0080322",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0080322",
                            "name": "polycystic kidney disease",
                            "description": "A cystic kidney disease that is characterized by the growth of fluid-filled cysts in the kidneys that reduces kidney function and may lead to kidney failure."
                        },
                        "synonyms": [
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0080322",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0080322"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0110858",
                        "recommended_name": {
                            "id": "DOID:0110858",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0110858",
                            "name": "polycystic kidney disease 1",
                            "description": "A autosomal dominant polycystic kidney disease that has_material_basis_in autosomal dominant inheritance of mutation in the PKD1 gene on chromosome 16p13.3."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "Polycystic Kidney Disease, Adult, Type I",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            },
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            }
                        ]
                    }
                ],
                "keywords": [
                    "biomuta",
                    "somatic",
                    "cancer",
                    "disease",
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs2091893602",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs2091893602"
                    },
                    {
                        "id": "rs2091893602",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs2091893602#frequency_tab"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3420,
                "end_pos": 3420,
                "sequence_org": "W",
                "sequence_mut": "C",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2097464",
                "ref_nt": "G",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "W3420",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "P98161",
                        "database": "BioMuta",
                        "url": "https://hivelab.biochemistry.gwu.edu/biomuta/proteinview/P98161"
                    },
                    {
                        "id": "rs545053536",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs545053536"
                    },
                    {
                        "id": "rs545053536",
                        "database": "1000Genomes",
                        "url": "https://www.ensembl.org/homo_sapiens/Variation/Explore?v=rs545053536"
                    },
                    {
                        "id": "rs545053536",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs545053536"
                    },
                    {
                        "id": "rs545053536",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs545053536#frequency_tab"
                    },
                    {
                        "id": "rs545053536",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs545053536"
                    },
                    {
                        "id": "rs545053536",
                        "database": "COSMIC",
                        "url": "https://www.ensembl.org/homo_sapiens/Variation/Explore?v=rs545053536"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3421,
                "end_pos": 3421,
                "subjects_tested": "1704",
                "subjects_positive": "1",
                "frequency": "0.1",
                "sequence_org": "P",
                "sequence_mut": "L",
                "comment": "Somatic mutation passed 0 out of 6 filters: .",
                "chr_id": "16",
                "chr_pos": "2097462",
                "ref_nt": "G",
                "alt_nt": "A",
                "minor_allelic_frequency": "",
                "site_lbl": "P3421",
                "disease": [
                    {
                        "disease_id": "DOID:363",
                        "recommended_name": {
                            "id": "DOID:363",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:363",
                            "name": "uterine cancer",
                            "description": "A female reproductive organ cancer that is located_in the uterus."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:363",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:363",
                                "name": "CA - cancer of uterus",
                                "description": ""
                            },
                            {
                                "id": "DOID:363",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:363",
                                "name": "Tumour of uterus",
                                "description": ""
                            },
                            {
                                "id": "DOID:363",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:363",
                                "name": "malignant neoplasm of uterus",
                                "description": ""
                            },
                            {
                                "id": "DOID:363",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:363",
                                "name": "malignant uterine tumor",
                                "description": ""
                            },
                            {
                                "id": "DOID:363",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:363",
                                "name": "neoplasm of uterus",
                                "description": ""
                            },
                            {
                                "id": "DOID:363",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:363",
                                "name": "uterine tumor",
                                "description": ""
                            },
                            {
                                "id": "DOID:363",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:363",
                                "name": "uterus neoplasm",
                                "description": ""
                            }
                        ],
                        "unlinked_id_list": [
                            "DOID:9460",
                            "DOID:5166",
                            "DOID:2021",
                            "DOID:4114"
                        ],
                        "evidence": [
                            {
                                "id": "363",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:363"
                            }
                        ]
                    }
                ],
                "keywords": [
                    "biomuta",
                    "somatic",
                    "cancer",
                    "disease",
                    "ebi"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs545053536",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs545053536"
                    },
                    {
                        "id": "rs545053536",
                        "database": "1000Genomes",
                        "url": "https://www.ensembl.org/homo_sapiens/Variation/Explore?v=rs545053536"
                    },
                    {
                        "id": "rs545053536",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs545053536"
                    },
                    {
                        "id": "rs545053536",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs545053536#frequency_tab"
                    },
                    {
                        "id": "rs545053536",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs545053536"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3421,
                "end_pos": 3421,
                "sequence_org": "P",
                "sequence_mut": "R",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2097462",
                "ref_nt": "C",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "P3421",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs1309699863",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1309699863"
                    },
                    {
                        "id": "rs1309699863",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs1309699863"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3421,
                "end_pos": 3421,
                "sequence_org": "P",
                "sequence_mut": "S",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2097463",
                "ref_nt": "A",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "P3421",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs2544688790",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs2544688790"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3421,
                "end_pos": 3421,
                "sequence_org": "P",
                "sequence_mut": "null",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2097462_2097465",
                "ref_nt": "l",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "P3421",
                "disease": [
                    {
                        "disease_id": "DOID:0080322",
                        "recommended_name": {
                            "id": "DOID:0080322",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0080322",
                            "name": "polycystic kidney disease",
                            "description": "A cystic kidney disease that is characterized by the growth of fluid-filled cysts in the kidneys that reduces kidney function and may lead to kidney failure."
                        },
                        "synonyms": [
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0080322",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0080322"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0110858",
                        "recommended_name": {
                            "id": "DOID:0110858",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0110858",
                            "name": "polycystic kidney disease 1",
                            "description": "A autosomal dominant polycystic kidney disease that has_material_basis_in autosomal dominant inheritance of mutation in the PKD1 gene on chromosome 16p13.3."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "Polycystic Kidney Disease, Adult, Type I",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            },
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            }
                        ]
                    }
                ],
                "keywords": [
                    "ebi",
                    "germline",
                    "disease"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs769418821",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs769418821"
                    },
                    {
                        "id": "rs769418821",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs769418821"
                    },
                    {
                        "id": "rs769418821",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs769418821"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3422,
                "end_pos": 3422,
                "sequence_org": "D",
                "sequence_mut": "N",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2097460",
                "ref_nt": "T",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "D3422",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs1282609791",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1282609791"
                    },
                    {
                        "id": "rs1282609791",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs1282609791#frequency_tab"
                    },
                    {
                        "id": "rs1282609791",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs1282609791"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3423,
                "end_pos": 3423,
                "sequence_org": "L",
                "sequence_mut": "V",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2097457",
                "ref_nt": "C",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "L3423",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "P98161",
                        "database": "BioMuta",
                        "url": "https://hivelab.biochemistry.gwu.edu/biomuta/proteinview/P98161"
                    },
                    {
                        "id": "rs776300382",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs776300382"
                    },
                    {
                        "id": "rs776300382",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs776300382"
                    },
                    {
                        "id": "rs776300382",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs776300382#frequency_tab"
                    },
                    {
                        "id": "rs776300382",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs776300382"
                    },
                    {
                        "id": "rs776300382",
                        "database": "COSMIC",
                        "url": "https://www.ensembl.org/homo_sapiens/Variation/Explore?v=rs776300382"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3424,
                "end_pos": 3424,
                "subjects_tested": "1704",
                "subjects_positive": "1",
                "frequency": "0.1",
                "sequence_org": "L",
                "sequence_mut": "F",
                "comment": "Somatic mutation passed 0 out of 6 filters: .",
                "chr_id": "16",
                "chr_pos": "2097454",
                "ref_nt": "G",
                "alt_nt": "A",
                "minor_allelic_frequency": "",
                "site_lbl": "L3424",
                "disease": [
                    {
                        "disease_id": "DOID:363",
                        "recommended_name": {
                            "id": "DOID:363",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:363",
                            "name": "uterine cancer",
                            "description": "A female reproductive organ cancer that is located_in the uterus."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:363",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:363",
                                "name": "CA - cancer of uterus",
                                "description": ""
                            },
                            {
                                "id": "DOID:363",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:363",
                                "name": "Tumour of uterus",
                                "description": ""
                            },
                            {
                                "id": "DOID:363",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:363",
                                "name": "malignant neoplasm of uterus",
                                "description": ""
                            },
                            {
                                "id": "DOID:363",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:363",
                                "name": "malignant uterine tumor",
                                "description": ""
                            },
                            {
                                "id": "DOID:363",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:363",
                                "name": "neoplasm of uterus",
                                "description": ""
                            },
                            {
                                "id": "DOID:363",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:363",
                                "name": "uterine tumor",
                                "description": ""
                            },
                            {
                                "id": "DOID:363",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:363",
                                "name": "uterus neoplasm",
                                "description": ""
                            }
                        ],
                        "unlinked_id_list": [
                            "DOID:9460",
                            "DOID:5166",
                            "DOID:2021",
                            "DOID:4114"
                        ],
                        "evidence": [
                            {
                                "id": "363",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:363"
                            }
                        ]
                    }
                ],
                "keywords": [
                    "biomuta",
                    "somatic",
                    "cancer",
                    "disease",
                    "ebi"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs2091893171",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs2091893171"
                    },
                    {
                        "id": "rs2091893171",
                        "database": "ENSEMBL",
                        "url": "https://www.ensembl.org/id/rs2091893171"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3424,
                "end_pos": 3424,
                "sequence_org": "L",
                "sequence_mut": "P",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2097453",
                "ref_nt": "G",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "L3424",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs776300382",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs776300382"
                    },
                    {
                        "id": "rs776300382",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs776300382"
                    },
                    {
                        "id": "rs776300382",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs776300382#frequency_tab"
                    },
                    {
                        "id": "rs776300382",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs776300382"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3424,
                "end_pos": 3424,
                "sequence_org": "L",
                "sequence_mut": "V",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2097454",
                "ref_nt": "C",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "L3424",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs978481700",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs978481700"
                    },
                    {
                        "id": "rs978481700",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs978481700#frequency_tab"
                    },
                    {
                        "id": "rs978481700",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs978481700"
                    }
                ],
                "glycoeffect": [
                    "o-glyco-site-loss"
                ],
                "start_pos": 3425,
                "end_pos": 3425,
                "sequence_org": "S",
                "sequence_mut": "G",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2097451",
                "ref_nt": "C",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "S3425",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs978481700",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs978481700"
                    },
                    {
                        "id": "rs978481700",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs978481700#frequency_tab"
                    },
                    {
                        "id": "rs978481700",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs978481700"
                    }
                ],
                "glycoeffect": [
                    "o-glyco-site-loss"
                ],
                "start_pos": 3425,
                "end_pos": 3425,
                "sequence_org": "S",
                "sequence_mut": "R",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2097451",
                "ref_nt": "G",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "S3425",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs746835479",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs746835479"
                    },
                    {
                        "id": "rs746835479",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs746835479"
                    },
                    {
                        "id": "rs746835479",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs746835479"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3426,
                "end_pos": 3426,
                "sequence_org": "D",
                "sequence_mut": "E",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2097446",
                "ref_nt": "T",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "D3426",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs373894977",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs373894977"
                    },
                    {
                        "id": "rs373894977",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs373894977"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3427,
                "end_pos": 3427,
                "sequence_org": "P",
                "sequence_mut": "A",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2097445",
                "ref_nt": "C",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "P3427",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs531914267",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs531914267"
                    },
                    {
                        "id": "rs531914267",
                        "database": "1000Genomes",
                        "url": "https://www.ensembl.org/homo_sapiens/Variation/Explore?v=rs531914267"
                    },
                    {
                        "id": "rs531914267",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs531914267"
                    },
                    {
                        "id": "rs531914267",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs531914267"
                    },
                    {
                        "id": "rs531914267",
                        "database": "COSMIC",
                        "url": "https://www.ensembl.org/homo_sapiens/Variation/Explore?v=rs531914267"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3427,
                "end_pos": 3427,
                "sequence_org": "P",
                "sequence_mut": "L",
                "comment": "Somatic mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2097444",
                "ref_nt": "A",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "P3427",
                "keywords": [
                    "ebi",
                    "somatic"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs531914267",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs531914267"
                    },
                    {
                        "id": "rs531914267",
                        "database": "1000Genomes",
                        "url": "https://www.ensembl.org/homo_sapiens/Variation/Explore?v=rs531914267"
                    },
                    {
                        "id": "rs531914267",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs531914267"
                    },
                    {
                        "id": "rs531914267",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs531914267"
                    },
                    {
                        "id": "rs531914267",
                        "database": "COSMIC",
                        "url": "https://www.ensembl.org/homo_sapiens/Variation/Explore?v=rs531914267"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3427,
                "end_pos": 3427,
                "sequence_org": "P",
                "sequence_mut": "Q",
                "comment": "Somatic mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2097444",
                "ref_nt": "T",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "P3427",
                "keywords": [
                    "ebi",
                    "somatic"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs373894977",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs373894977"
                    },
                    {
                        "id": "rs373894977",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs373894977"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3427,
                "end_pos": 3427,
                "sequence_org": "P",
                "sequence_mut": "S",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2097445",
                "ref_nt": "A",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "P3427",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs1223040043",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1223040043"
                    },
                    {
                        "id": "rs1223040043",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs1223040043"
                    }
                ],
                "glycoeffect": [
                    "o-glyco-site-loss"
                ],
                "start_pos": 3428,
                "end_pos": 3428,
                "sequence_org": "S",
                "sequence_mut": "F",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2097441",
                "ref_nt": "A",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "S3428",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs2151726918",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs2151726918"
                    }
                ],
                "glycoeffect": [
                    "o-glyco-site-loss"
                ],
                "start_pos": 3428,
                "end_pos": 3428,
                "sequence_org": "S",
                "sequence_mut": "null",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2097446",
                "ref_nt": "p",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "S3428",
                "disease": [
                    {
                        "disease_id": "DOID:0080322",
                        "recommended_name": {
                            "id": "DOID:0080322",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0080322",
                            "name": "polycystic kidney disease",
                            "description": "A cystic kidney disease that is characterized by the growth of fluid-filled cysts in the kidneys that reduces kidney function and may lead to kidney failure."
                        },
                        "synonyms": [
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0080322",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0080322"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0110858",
                        "recommended_name": {
                            "id": "DOID:0110858",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0110858",
                            "name": "polycystic kidney disease 1",
                            "description": "A autosomal dominant polycystic kidney disease that has_material_basis_in autosomal dominant inheritance of mutation in the PKD1 gene on chromosome 16p13.3."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "Polycystic Kidney Disease, Adult, Type I",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            },
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            }
                        ]
                    }
                ],
                "keywords": [
                    "ebi",
                    "germline",
                    "disease"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs371881043",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs371881043"
                    },
                    {
                        "id": "rs371881043",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs371881043"
                    },
                    {
                        "id": "rs371881043",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs371881043#frequency_tab"
                    },
                    {
                        "id": "rs371881043",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs371881043"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3429,
                "end_pos": 3429,
                "sequence_org": "I",
                "sequence_mut": "L",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2097439",
                "ref_nt": "G",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "I3429",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs371881043",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs371881043"
                    },
                    {
                        "id": "rs371881043",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs371881043"
                    },
                    {
                        "id": "rs371881043",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs371881043#frequency_tab"
                    },
                    {
                        "id": "rs371881043",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs371881043"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3429,
                "end_pos": 3429,
                "sequence_org": "I",
                "sequence_mut": "V",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2097439",
                "ref_nt": "C",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "I3429",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs1244926793",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1244926793"
                    },
                    {
                        "id": "rs1244926793",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs1244926793#frequency_tab"
                    },
                    {
                        "id": "rs1244926793",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs1244926793"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 342,
                "end_pos": 342,
                "sequence_org": "G",
                "sequence_mut": "S",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2117968",
                "ref_nt": "T",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "G342",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs1289793709",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1289793709"
                    },
                    {
                        "id": "rs1289793709",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs1289793709#frequency_tab"
                    },
                    {
                        "id": "rs1289793709",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs1289793709"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3431,
                "end_pos": 3431,
                "sequence_org": "G",
                "sequence_mut": "C",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2097433",
                "ref_nt": "A",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "G3431",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs1289793709",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1289793709"
                    },
                    {
                        "id": "rs1289793709",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs1289793709#frequency_tab"
                    },
                    {
                        "id": "rs1289793709",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs1289793709"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3431,
                "end_pos": 3431,
                "sequence_org": "G",
                "sequence_mut": "S",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2097433",
                "ref_nt": "T",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "G3431",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "P98161",
                        "database": "BioMuta",
                        "url": "https://hivelab.biochemistry.gwu.edu/biomuta/proteinview/P98161"
                    }
                ],
                "glycoeffect": [
                    "o-glyco-site-loss"
                ],
                "start_pos": 3432,
                "end_pos": 3432,
                "subjects_tested": "1704",
                "subjects_positive": "2",
                "frequency": "0.1",
                "sequence_org": "S",
                "sequence_mut": "G",
                "comment": "Somatic mutation passed 0 out of 6 filters: .",
                "chr_id": "16",
                "chr_pos": "2097430",
                "ref_nt": "T",
                "alt_nt": "C",
                "minor_allelic_frequency": "",
                "site_lbl": "S3432",
                "disease": [
                    {
                        "disease_id": "DOID:363",
                        "recommended_name": {
                            "id": "DOID:363",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:363",
                            "name": "uterine cancer",
                            "description": "A female reproductive organ cancer that is located_in the uterus."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:363",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:363",
                                "name": "CA - cancer of uterus",
                                "description": ""
                            },
                            {
                                "id": "DOID:363",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:363",
                                "name": "Tumour of uterus",
                                "description": ""
                            },
                            {
                                "id": "DOID:363",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:363",
                                "name": "malignant neoplasm of uterus",
                                "description": ""
                            },
                            {
                                "id": "DOID:363",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:363",
                                "name": "malignant uterine tumor",
                                "description": ""
                            },
                            {
                                "id": "DOID:363",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:363",
                                "name": "neoplasm of uterus",
                                "description": ""
                            },
                            {
                                "id": "DOID:363",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:363",
                                "name": "uterine tumor",
                                "description": ""
                            },
                            {
                                "id": "DOID:363",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:363",
                                "name": "uterus neoplasm",
                                "description": ""
                            }
                        ],
                        "unlinked_id_list": [
                            "DOID:9460",
                            "DOID:5166",
                            "DOID:2021",
                            "DOID:4114"
                        ],
                        "evidence": [
                            {
                                "id": "363",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:363"
                            }
                        ]
                    }
                ],
                "keywords": [
                    "biomuta",
                    "somatic",
                    "cancer",
                    "disease"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "P98161",
                        "database": "BioMuta",
                        "url": "https://hivelab.biochemistry.gwu.edu/biomuta/proteinview/P98161"
                    }
                ],
                "glycoeffect": [
                    "o-glyco-site-loss"
                ],
                "start_pos": 3432,
                "end_pos": 3432,
                "subjects_tested": "1704",
                "subjects_positive": "1",
                "frequency": "0.1",
                "sequence_org": "S",
                "sequence_mut": "N",
                "comment": "Somatic mutation passed 0 out of 6 filters: .",
                "chr_id": "16",
                "chr_pos": "2097429",
                "ref_nt": "C",
                "alt_nt": "T",
                "minor_allelic_frequency": "",
                "site_lbl": "S3432",
                "disease": [
                    {
                        "disease_id": "DOID:363",
                        "recommended_name": {
                            "id": "DOID:363",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:363",
                            "name": "uterine cancer",
                            "description": "A female reproductive organ cancer that is located_in the uterus."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:363",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:363",
                                "name": "CA - cancer of uterus",
                                "description": ""
                            },
                            {
                                "id": "DOID:363",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:363",
                                "name": "Tumour of uterus",
                                "description": ""
                            },
                            {
                                "id": "DOID:363",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:363",
                                "name": "malignant neoplasm of uterus",
                                "description": ""
                            },
                            {
                                "id": "DOID:363",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:363",
                                "name": "malignant uterine tumor",
                                "description": ""
                            },
                            {
                                "id": "DOID:363",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:363",
                                "name": "neoplasm of uterus",
                                "description": ""
                            },
                            {
                                "id": "DOID:363",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:363",
                                "name": "uterine tumor",
                                "description": ""
                            },
                            {
                                "id": "DOID:363",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:363",
                                "name": "uterus neoplasm",
                                "description": ""
                            }
                        ],
                        "unlinked_id_list": [
                            "DOID:9460",
                            "DOID:5166",
                            "DOID:2021",
                            "DOID:4114"
                        ],
                        "evidence": [
                            {
                                "id": "363",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:363"
                            }
                        ]
                    }
                ],
                "keywords": [
                    "biomuta",
                    "somatic",
                    "cancer",
                    "disease"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs2091892492",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs2091892492"
                    },
                    {
                        "id": "rs2091892492",
                        "database": "ENSEMBL",
                        "url": "https://www.ensembl.org/id/rs2091892492"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3433,
                "end_pos": 3433,
                "sequence_org": "N",
                "sequence_mut": "S",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2097426",
                "ref_nt": "C",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "N3433",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs779097316",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs779097316"
                    },
                    {
                        "id": "rs779097316",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs779097316"
                    },
                    {
                        "id": "rs779097316",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs779097316#frequency_tab"
                    },
                    {
                        "id": "rs779097316",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs779097316"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3433,
                "end_pos": 3433,
                "sequence_org": "N",
                "sequence_mut": "Y",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2097427",
                "ref_nt": "A",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "N3433",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "P98161",
                        "database": "BioMuta",
                        "url": "https://hivelab.biochemistry.gwu.edu/biomuta/proteinview/P98161"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3435,
                "end_pos": 3435,
                "subjects_tested": "1704",
                "subjects_positive": "1",
                "frequency": "0.1",
                "sequence_org": "R",
                "sequence_mut": "G",
                "comment": "Somatic mutation passed 0 out of 6 filters: .",
                "chr_id": "16",
                "chr_pos": "2097421",
                "ref_nt": "G",
                "alt_nt": "C",
                "minor_allelic_frequency": "",
                "site_lbl": "R3435",
                "disease": [
                    {
                        "disease_id": "DOID:363",
                        "recommended_name": {
                            "id": "DOID:363",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:363",
                            "name": "uterine cancer",
                            "description": "A female reproductive organ cancer that is located_in the uterus."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:363",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:363",
                                "name": "CA - cancer of uterus",
                                "description": ""
                            },
                            {
                                "id": "DOID:363",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:363",
                                "name": "Tumour of uterus",
                                "description": ""
                            },
                            {
                                "id": "DOID:363",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:363",
                                "name": "malignant neoplasm of uterus",
                                "description": ""
                            },
                            {
                                "id": "DOID:363",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:363",
                                "name": "malignant uterine tumor",
                                "description": ""
                            },
                            {
                                "id": "DOID:363",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:363",
                                "name": "neoplasm of uterus",
                                "description": ""
                            },
                            {
                                "id": "DOID:363",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:363",
                                "name": "uterine tumor",
                                "description": ""
                            },
                            {
                                "id": "DOID:363",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:363",
                                "name": "uterus neoplasm",
                                "description": ""
                            }
                        ],
                        "unlinked_id_list": [
                            "DOID:9460",
                            "DOID:5166",
                            "DOID:2021",
                            "DOID:4114"
                        ],
                        "evidence": [
                            {
                                "id": "363",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:363"
                            }
                        ]
                    }
                ],
                "keywords": [
                    "biomuta",
                    "somatic",
                    "cancer",
                    "disease"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs140189010",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs140189010"
                    },
                    {
                        "id": "rs140189010",
                        "database": "1000Genomes",
                        "url": "https://www.ensembl.org/homo_sapiens/Variation/Explore?v=rs140189010"
                    },
                    {
                        "id": "rs140189010",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs140189010"
                    },
                    {
                        "id": "rs140189010",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs140189010#frequency_tab"
                    },
                    {
                        "id": "rs140189010",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs140189010"
                    },
                    {
                        "id": "rs140189010",
                        "database": "COSMIC",
                        "url": "https://www.ensembl.org/homo_sapiens/Variation/Explore?v=rs140189010"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3435,
                "end_pos": 3435,
                "sequence_org": "R",
                "sequence_mut": "Q",
                "comment": "Somatic mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2097420",
                "ref_nt": "T",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "R3435",
                "keywords": [
                    "ebi",
                    "somatic",
                    "disease"
                ],
                "disease": [
                    {
                        "disease_id": "DOID:0080322",
                        "recommended_name": {
                            "id": "DOID:0080322",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0080322",
                            "name": "polycystic kidney disease",
                            "description": "A cystic kidney disease that is characterized by the growth of fluid-filled cysts in the kidneys that reduces kidney function and may lead to kidney failure."
                        },
                        "synonyms": [
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0080322",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0080322"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0110858",
                        "recommended_name": {
                            "id": "DOID:0110858",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0110858",
                            "name": "polycystic kidney disease 1",
                            "description": "A autosomal dominant polycystic kidney disease that has_material_basis_in autosomal dominant inheritance of mutation in the PKD1 gene on chromosome 16p13.3."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "Polycystic Kidney Disease, Adult, Type I",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            },
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            }
                        ]
                    }
                ]
            },
            {
                "evidence": [
                    {
                        "id": "P98161",
                        "database": "BioMuta",
                        "url": "https://hivelab.biochemistry.gwu.edu/biomuta/proteinview/P98161"
                    },
                    {
                        "id": "rs562831339",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs562831339"
                    },
                    {
                        "id": "rs562831339",
                        "database": "1000Genomes",
                        "url": "https://www.ensembl.org/homo_sapiens/Variation/Explore?v=rs562831339"
                    },
                    {
                        "id": "rs562831339",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs562831339"
                    },
                    {
                        "id": "rs562831339",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs562831339#frequency_tab"
                    },
                    {
                        "id": "rs562831339",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs562831339"
                    },
                    {
                        "id": "rs562831339",
                        "database": "COSMIC",
                        "url": "https://www.ensembl.org/homo_sapiens/Variation/Explore?v=rs562831339"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3435,
                "end_pos": 3435,
                "subjects_tested": "3601",
                "subjects_positive": "1",
                "frequency": "0.0",
                "sequence_org": "R",
                "sequence_mut": "W",
                "comment": "Somatic mutation passed 0 out of 6 filters: .",
                "chr_id": "16",
                "chr_pos": "2097421",
                "ref_nt": "G",
                "alt_nt": "A",
                "minor_allelic_frequency": "",
                "site_lbl": "R3435",
                "disease": [
                    {
                        "disease_id": "DOID:9256",
                        "recommended_name": {
                            "id": "DOID:9256",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:9256",
                            "name": "colorectal cancer",
                            "description": "A large intestine cancer that is located_in the colon and/or located_in the rectum."
                        },
                        "synonyms": [
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectal cancer",
                                "description": "A primary or metastatic malignant neoplasm that affects the colon or rectum. Representative examples include carcinoma, lymphoma, and sarcoma."
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "cancer of colorectum",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "cancer of large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "cancer of large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "cancer of the large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colon cancer, advanced, somatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colon cancer, somatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectal cancer",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectal cancer with chromosomal instability, somatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectal cancer, autosomal dominant, somatic mutation",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectal cancer, somatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectal cancer, susceptibility to, autosomal dominant, somatic mutation",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectum cancer",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant colorectal neoplasm",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant colorectal tumor",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant colorectal tumour",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant colorectum neoplasm",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant large bowel neoplasm",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant large bowel tumor",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant large bowel tumour",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant large intestine neoplasm",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant large intestine tumor",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant large intestine tumour",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant neoplasm of colorectum",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant neoplasm of large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant neoplasm of large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant neoplasm of the large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant neoplasm of the large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumor of large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumor of large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumor of the large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumor of the large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumour of large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumour of large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumour of the large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumour of the large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "CRC",
                                "description": ""
                            },
                            {
                                "id": "MIM:114500",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/114500",
                                "name": "Colorectal cancer",
                                "description": "Colorectal cancer"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "9256",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:9256"
                            }
                        ]
                    }
                ],
                "keywords": [
                    "biomuta",
                    "somatic",
                    "cancer",
                    "disease",
                    "ebi"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs2151726823",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs2151726823"
                    },
                    {
                        "id": "rs2151726823",
                        "database": "ENSEMBL",
                        "url": "https://www.ensembl.org/id/rs2151726823"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3436,
                "end_pos": 3436,
                "sequence_org": "Q",
                "sequence_mut": "*",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2097418",
                "ref_nt": "A",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "Q3436",
                "keywords": [
                    "ebi",
                    "germline",
                    "disease"
                ],
                "disease": [
                    {
                        "disease_id": "DOID:0080322",
                        "recommended_name": {
                            "id": "DOID:0080322",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0080322",
                            "name": "polycystic kidney disease",
                            "description": "A cystic kidney disease that is characterized by the growth of fluid-filled cysts in the kidneys that reduces kidney function and may lead to kidney failure."
                        },
                        "synonyms": [
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0080322",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0080322"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0110858",
                        "recommended_name": {
                            "id": "DOID:0110858",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0110858",
                            "name": "polycystic kidney disease 1",
                            "description": "A autosomal dominant polycystic kidney disease that has_material_basis_in autosomal dominant inheritance of mutation in the PKD1 gene on chromosome 16p13.3."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "Polycystic Kidney Disease, Adult, Type I",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            },
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            }
                        ]
                    }
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs2544688079",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs2544688079"
                    },
                    {
                        "id": "rs2544688348",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs2544688348"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3436,
                "end_pos": 3436,
                "sequence_org": "Q",
                "sequence_mut": "null",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2097398_2097420",
                "ref_nt": "l",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "Q3436",
                "disease": [
                    {
                        "disease_id": "DOID:0080322",
                        "recommended_name": {
                            "id": "DOID:0080322",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0080322",
                            "name": "polycystic kidney disease",
                            "description": "A cystic kidney disease that is characterized by the growth of fluid-filled cysts in the kidneys that reduces kidney function and may lead to kidney failure."
                        },
                        "synonyms": [
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0080322",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0080322"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0110858",
                        "recommended_name": {
                            "id": "DOID:0110858",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0110858",
                            "name": "polycystic kidney disease 1",
                            "description": "A autosomal dominant polycystic kidney disease that has_material_basis_in autosomal dominant inheritance of mutation in the PKD1 gene on chromosome 16p13.3."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "Polycystic Kidney Disease, Adult, Type I",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            },
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            }
                        ]
                    }
                ],
                "keywords": [
                    "ebi",
                    "germline",
                    "disease"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs756485613",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs756485613"
                    },
                    {
                        "id": "rs756485613",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs756485613"
                    },
                    {
                        "id": "rs756485613",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs756485613#frequency_tab"
                    },
                    {
                        "id": "rs756485613",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs756485613"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3437,
                "end_pos": 3437,
                "sequence_org": "L",
                "sequence_mut": "M",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2097415",
                "ref_nt": "T",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "L3437",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs1407203916",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1407203916"
                    },
                    {
                        "id": "rs1407203916",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs1407203916"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3437,
                "end_pos": 3437,
                "sequence_org": "L",
                "sequence_mut": "Q",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2097414",
                "ref_nt": "T",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "L3437",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "P98161",
                        "database": "BioMuta",
                        "url": "https://hivelab.biochemistry.gwu.edu/biomuta/proteinview/P98161"
                    },
                    {
                        "id": "rs1344032673",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1344032673"
                    },
                    {
                        "id": "rs1344032673",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs1344032673"
                    },
                    {
                        "id": "rs1344032673",
                        "database": "COSMIC",
                        "url": "https://www.ensembl.org/homo_sapiens/Variation/Explore?v=rs1344032673"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3438,
                "end_pos": 3438,
                "subjects_tested": "1704",
                "subjects_positive": "1",
                "frequency": "0.1",
                "sequence_org": "A",
                "sequence_mut": "T",
                "comment": "Somatic mutation passed 0 out of 6 filters: .",
                "chr_id": "16",
                "chr_pos": "2097412",
                "ref_nt": "C",
                "alt_nt": "T",
                "minor_allelic_frequency": "",
                "site_lbl": "A3438",
                "disease": [
                    {
                        "disease_id": "DOID:363",
                        "recommended_name": {
                            "id": "DOID:363",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:363",
                            "name": "uterine cancer",
                            "description": "A female reproductive organ cancer that is located_in the uterus."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:363",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:363",
                                "name": "CA - cancer of uterus",
                                "description": ""
                            },
                            {
                                "id": "DOID:363",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:363",
                                "name": "Tumour of uterus",
                                "description": ""
                            },
                            {
                                "id": "DOID:363",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:363",
                                "name": "malignant neoplasm of uterus",
                                "description": ""
                            },
                            {
                                "id": "DOID:363",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:363",
                                "name": "malignant uterine tumor",
                                "description": ""
                            },
                            {
                                "id": "DOID:363",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:363",
                                "name": "neoplasm of uterus",
                                "description": ""
                            },
                            {
                                "id": "DOID:363",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:363",
                                "name": "uterine tumor",
                                "description": ""
                            },
                            {
                                "id": "DOID:363",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:363",
                                "name": "uterus neoplasm",
                                "description": ""
                            }
                        ],
                        "unlinked_id_list": [
                            "DOID:9460",
                            "DOID:5166",
                            "DOID:2021",
                            "DOID:4114"
                        ],
                        "evidence": [
                            {
                                "id": "363",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:363"
                            }
                        ]
                    }
                ],
                "keywords": [
                    "biomuta",
                    "somatic",
                    "cancer",
                    "disease",
                    "ebi"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs138546384",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs138546384"
                    },
                    {
                        "id": "rs138546384",
                        "database": "1000Genomes",
                        "url": "https://www.ensembl.org/homo_sapiens/Variation/Explore?v=rs138546384"
                    },
                    {
                        "id": "rs138546384",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs138546384"
                    },
                    {
                        "id": "rs138546384",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs138546384#frequency_tab"
                    },
                    {
                        "id": "rs138546384",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs138546384"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3439,
                "end_pos": 3439,
                "sequence_org": "R",
                "sequence_mut": "P",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2097408",
                "ref_nt": "G",
                "alt_nt": "null",
                "minor_allelic_frequency": "0.000196232",
                "site_lbl": "R3439",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs138546384",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs138546384"
                    },
                    {
                        "id": "rs138546384",
                        "database": "1000Genomes",
                        "url": "https://www.ensembl.org/homo_sapiens/Variation/Explore?v=rs138546384"
                    },
                    {
                        "id": "rs138546384",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs138546384"
                    },
                    {
                        "id": "rs138546384",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs138546384#frequency_tab"
                    },
                    {
                        "id": "rs138546384",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs138546384"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3439,
                "end_pos": 3439,
                "sequence_org": "R",
                "sequence_mut": "Q",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2097408",
                "ref_nt": "T",
                "alt_nt": "null",
                "minor_allelic_frequency": "0.000196232",
                "site_lbl": "R3439",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "P98161",
                        "database": "BioMuta",
                        "url": "https://hivelab.biochemistry.gwu.edu/biomuta/proteinview/P98161"
                    },
                    {
                        "id": "rs374486955",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs374486955"
                    },
                    {
                        "id": "rs374486955",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs374486955"
                    },
                    {
                        "id": "rs374486955",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs374486955#frequency_tab"
                    },
                    {
                        "id": "rs374486955",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs374486955"
                    },
                    {
                        "id": "rs374486955",
                        "database": "COSMIC",
                        "url": "https://www.ensembl.org/homo_sapiens/Variation/Explore?v=rs374486955"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3439,
                "end_pos": 3439,
                "subjects_tested": "3601",
                "subjects_positive": "1",
                "frequency": "0.0",
                "sequence_org": "R",
                "sequence_mut": "W",
                "comment": "Somatic mutation passed 0 out of 6 filters: .",
                "chr_id": "16",
                "chr_pos": "2097409",
                "ref_nt": "G",
                "alt_nt": "A",
                "minor_allelic_frequency": "",
                "site_lbl": "R3439",
                "disease": [
                    {
                        "disease_id": "DOID:9256",
                        "recommended_name": {
                            "id": "DOID:9256",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:9256",
                            "name": "colorectal cancer",
                            "description": "A large intestine cancer that is located_in the colon and/or located_in the rectum."
                        },
                        "synonyms": [
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectal cancer",
                                "description": "A primary or metastatic malignant neoplasm that affects the colon or rectum. Representative examples include carcinoma, lymphoma, and sarcoma."
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "cancer of colorectum",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "cancer of large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "cancer of large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "cancer of the large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colon cancer, advanced, somatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colon cancer, somatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectal cancer",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectal cancer with chromosomal instability, somatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectal cancer, autosomal dominant, somatic mutation",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectal cancer, somatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectal cancer, susceptibility to, autosomal dominant, somatic mutation",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectum cancer",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant colorectal neoplasm",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant colorectal tumor",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant colorectal tumour",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant colorectum neoplasm",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant large bowel neoplasm",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant large bowel tumor",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant large bowel tumour",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant large intestine neoplasm",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant large intestine tumor",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant large intestine tumour",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant neoplasm of colorectum",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant neoplasm of large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant neoplasm of large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant neoplasm of the large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant neoplasm of the large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumor of large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumor of large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumor of the large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumor of the large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumour of large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumour of large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumour of the large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumour of the large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "CRC",
                                "description": ""
                            },
                            {
                                "id": "MIM:114500",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/114500",
                                "name": "Colorectal cancer",
                                "description": "Colorectal cancer"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "9256",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:9256"
                            }
                        ]
                    }
                ],
                "keywords": [
                    "biomuta",
                    "somatic",
                    "cancer",
                    "disease",
                    "ebi"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs2151823309",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs2151823309"
                    },
                    {
                        "id": "rs2151823309",
                        "database": "ENSEMBL",
                        "url": "https://www.ensembl.org/id/rs2151823309"
                    }
                ],
                "glycoeffect": [
                    "o-glyco-site-loss"
                ],
                "start_pos": 343,
                "end_pos": 343,
                "sequence_org": "S",
                "sequence_mut": "A",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2117965",
                "ref_nt": "C",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "S343",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs756720009",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs756720009"
                    },
                    {
                        "id": "rs756720009",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs756720009"
                    },
                    {
                        "id": "rs756720009",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs756720009"
                    }
                ],
                "glycoeffect": [
                    "o-glyco-site-loss"
                ],
                "start_pos": 343,
                "end_pos": 343,
                "sequence_org": "S",
                "sequence_mut": "L",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2117964",
                "ref_nt": "A",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "S343",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs2091891993",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs2091891993"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3440,
                "end_pos": 3440,
                "sequence_org": "G",
                "sequence_mut": "null",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2097408",
                "ref_nt": "l",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "G3440",
                "disease": [
                    {
                        "disease_id": "DOID:0080322",
                        "recommended_name": {
                            "id": "DOID:0080322",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0080322",
                            "name": "polycystic kidney disease",
                            "description": "A cystic kidney disease that is characterized by the growth of fluid-filled cysts in the kidneys that reduces kidney function and may lead to kidney failure."
                        },
                        "synonyms": [
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0080322",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0080322"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0110858",
                        "recommended_name": {
                            "id": "DOID:0110858",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0110858",
                            "name": "polycystic kidney disease 1",
                            "description": "A autosomal dominant polycystic kidney disease that has_material_basis_in autosomal dominant inheritance of mutation in the PKD1 gene on chromosome 16p13.3."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "Polycystic Kidney Disease, Adult, Type I",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            },
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            }
                        ]
                    }
                ],
                "keywords": [
                    "ebi",
                    "germline",
                    "disease"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs918228674",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs918228674"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3441,
                "end_pos": 3441,
                "sequence_org": "Q",
                "sequence_mut": "*",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2097403",
                "ref_nt": "A",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "Q3441",
                "disease": [
                    {
                        "disease_id": "DOID:0080322",
                        "recommended_name": {
                            "id": "DOID:0080322",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0080322",
                            "name": "polycystic kidney disease",
                            "description": "A cystic kidney disease that is characterized by the growth of fluid-filled cysts in the kidneys that reduces kidney function and may lead to kidney failure."
                        },
                        "synonyms": [
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0080322",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0080322"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0110858",
                        "recommended_name": {
                            "id": "DOID:0110858",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0110858",
                            "name": "polycystic kidney disease 1",
                            "description": "A autosomal dominant polycystic kidney disease that has_material_basis_in autosomal dominant inheritance of mutation in the PKD1 gene on chromosome 16p13.3."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "Polycystic Kidney Disease, Adult, Type I",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            },
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            }
                        ]
                    }
                ],
                "keywords": [
                    "ebi",
                    "germline",
                    "disease"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs918228674",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs918228674"
                    },
                    {
                        "id": "rs918228674",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs918228674#frequency_tab"
                    },
                    {
                        "id": "rs918228674",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs918228674"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3441,
                "end_pos": 3441,
                "sequence_org": "Q",
                "sequence_mut": "E",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2097403",
                "ref_nt": "C",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "Q3441",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs1346048514",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1346048514"
                    },
                    {
                        "id": "rs1346048514",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs1346048514"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3441,
                "end_pos": 3441,
                "sequence_org": "Q",
                "sequence_mut": "R",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2097402",
                "ref_nt": "C",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "Q3441",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs2544688140",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs2544688140"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3441,
                "end_pos": 3441,
                "sequence_org": "Q",
                "sequence_mut": "null",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2097402_2097406",
                "ref_nt": "l",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "Q3441",
                "disease": [
                    {
                        "disease_id": "DOID:0080322",
                        "recommended_name": {
                            "id": "DOID:0080322",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0080322",
                            "name": "polycystic kidney disease",
                            "description": "A cystic kidney disease that is characterized by the growth of fluid-filled cysts in the kidneys that reduces kidney function and may lead to kidney failure."
                        },
                        "synonyms": [
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0080322",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0080322"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0110858",
                        "recommended_name": {
                            "id": "DOID:0110858",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0110858",
                            "name": "polycystic kidney disease 1",
                            "description": "A autosomal dominant polycystic kidney disease that has_material_basis_in autosomal dominant inheritance of mutation in the PKD1 gene on chromosome 16p13.3."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "Polycystic Kidney Disease, Adult, Type I",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            },
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            }
                        ]
                    }
                ],
                "keywords": [
                    "ebi",
                    "germline",
                    "disease"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "rs144593342",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs144593342"
                    },
                    {
                        "id": "rs144593342",
                        "database": "1000Genomes",
                        "url": "https://www.ensembl.org/homo_sapiens/Variation/Explore?v=rs144593342"
                    },
                    {
                        "id": "rs144593342",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs144593342"
                    },
                    {
                        "id": "rs144593342",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs144593342#frequency_tab"
                    },
                    {
                        "id": "rs144593342",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs144593342"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3442,
                "end_pos": 3442,
                "sequence_org": "A",
                "sequence_mut": "E",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, lectin/c-type/polycystin.",
                "chr_id": "16",
                "chr_pos": "2097399",
                "ref_nt": "T",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "A3442",
                "keywords": [
                    "ebi",
                    "germline"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "P98161",
                        "database": "BioMuta",
                        "url": "https://hivelab.biochemistry.gwu.edu/biomuta/proteinview/P98161"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3442,
                "end_pos": 3442,
                "subjects_tested": "4177",
                "subjects_positive": "2",
                "frequency": "0.0",
                "sequence_org": "A",
                "sequence_mut": "T",
                "comment": "Somatic mutation passed 0 out of 6 filters: .",
                "chr_id": "16",
                "chr_pos": "2097400",
                "ref_nt": "C",
                "alt_nt": "T",
                "minor_allelic_frequency": "",
                "site_lbl": "A3442",
                "disease": [
                    {
                        "disease_id": "DOID:10283",
                        "recommended_name": {
                            "id": "DOID:10283",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:10283",
                            "name": "prostate cancer",
                            "description": "A male reproductive organ cancer that is located_in the prostate."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:10283",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:10283",
                                "name": "NGP - new growth of prostate",
                                "description": ""
                            },
                            {
                                "id": "DOID:10283",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:10283",
                                "name": "hereditary prostate cancer",
                                "description": ""
                            },
                            {
                                "id": "DOID:10283",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:10283",
                                "name": "malignant tumor of the prostate",
                                "description": ""
                            },
                            {
                                "id": "DOID:10283",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:10283",
                                "name": "prostate cancer, familial",
                                "description": ""
                            },
                            {
                                "id": "DOID:10283",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:10283",
                                "name": "prostate neoplasm",
                                "description": ""
                            },
                            {
                                "id": "DOID:10283",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:10283",
                                "name": "prostatic cancer",
                                "description": ""
                            },
                            {
                                "id": "DOID:10283",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:10283",
                                "name": "prostatic neoplasm",
                                "description": ""
                            },
                            {
                                "id": "DOID:10283",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:10283",
                                "name": "tumor of the prostate",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0010257",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0010257",
                                "name": "prostate cancer, hereditary, X-linked 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0010257",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0010257",
                                "name": "HPCX1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0010257",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0010257",
                                "name": "prostate cancer, hereditary, X-linked 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0010405",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0010405",
                                "name": "prostate cancer, hereditary, X-linked 2",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0010405",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0010405",
                                "name": "HPCX2",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0010405",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0010405",
                                "name": "prostate cancer, hereditary, X-linked 2",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011098",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011098",
                                "name": "prostate cancer, hereditary, 1",
                                "description": "Any familial prostate cancer in which the cause of the disease is a mutation in the RNASEL gene."
                            },
                            {
                                "id": "MONDO:0011098",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011098",
                                "name": "RNASEL familial prostate cancer",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011098",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011098",
                                "name": "familial prostate cancer caused by mutation in RNASEL",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011098",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011098",
                                "name": "prostate cancer 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011098",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011098",
                                "name": "prostate cancer, hereditary, 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011098",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011098",
                                "name": "prostate cancer, hereditary, type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011098",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011098",
                                "name": "HPC1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011270",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011270",
                                "name": "prostate cancer, hereditary, 8",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011270",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011270",
                                "name": "prostate cancer, hereditary, 8",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011270",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011270",
                                "name": "prostate cancer, hereditary, type 8",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011270",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011270",
                                "name": "HPC8",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012093",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012093",
                                "name": "prostate cancer, hereditary, 3",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012093",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012093",
                                "name": "prostate cancer, hereditary, 3",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012093",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012093",
                                "name": "prostate cancer, hereditary, type 3",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012093",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012093",
                                "name": "prostate cancer, susceptibility to, 3",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012093",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012093",
                                "name": "HPC3",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012094",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012094",
                                "name": "prostate cancer, hereditary, 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012094",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012094",
                                "name": "prostate cancer, hereditary, 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012094",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012094",
                                "name": "prostate cancer, hereditary, type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012094",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012094",
                                "name": "prostate cancer, susceptibility to, 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012094",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012094",
                                "name": "HPC4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012244",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012244",
                                "name": "prostate cancer, hereditary, 5",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012244",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012244",
                                "name": "prostate cancer, hereditary, 5",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012244",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012244",
                                "name": "prostate cancer, hereditary, type 5",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012244",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012244",
                                "name": "HPC5",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012300",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012300",
                                "name": "prostate cancer, hereditary, 6",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012300",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012300",
                                "name": "prostate cancer, hereditary, 6",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012300",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012300",
                                "name": "prostate cancer, hereditary, type 6",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012300",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012300",
                                "name": "HPC6",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012470",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012470",
                                "name": "prostate cancer, hereditary, 7",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012470",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012470",
                                "name": "HPC7",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012470",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012470",
                                "name": "prostate cancer, hereditary, 7",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012597",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012597",
                                "name": "prostate cancer, hereditary, 9",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012597",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012597",
                                "name": "prostate cancer, hereditary, 9",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012597",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012597",
                                "name": "prostate cancer, hereditary, type 9",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012597",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012597",
                                "name": "HPC9",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012620",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012620",
                                "name": "prostate cancer, hereditary, 10",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012620",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012620",
                                "name": "HPC10",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012620",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012620",
                                "name": "prostate cancer, hereditary, 10",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012741",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012741",
                                "name": "prostate cancer, hereditary, 12",
                                "description": "Any familial prostate cancer in which the cause of the disease is a mutation in the EHBP1 gene."
                            },
                            {
                                "id": "MONDO:0012741",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012741",
                                "name": "EHBP1 familial prostate cancer",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012741",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012741",
                                "name": "familial prostate cancer caused by mutation in EHBP1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012741",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012741",
                                "name": "prostate cancer, hereditary, 12",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012741",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012741",
                                "name": "prostate cancer, hereditary, type 12",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012741",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012741",
                                "name": "HPC12",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012758",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012758",
                                "name": "prostate cancer, hereditary, 13",
                                "description": "Any familial prostate cancer in which the cause of the disease is a mutation in the MSMB gene."
                            },
                            {
                                "id": "MONDO:0012758",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012758",
                                "name": "MSMB familial prostate cancer",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012758",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012758",
                                "name": "familial prostate cancer caused by mutation in MSMB",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012758",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012758",
                                "name": "prostate cancer, hereditary, 13",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012758",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012758",
                                "name": "prostate cancer, hereditary, type 13",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012758",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012758",
                                "name": "HPC13",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012768",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012768",
                                "name": "prostate cancer, hereditary, 11",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012768",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012768",
                                "name": "HPC11",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012768",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012768",
                                "name": "prostate cancer, hereditary, 11",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012769",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012769",
                                "name": "prostate cancer, hereditary, 14",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012769",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012769",
                                "name": "HPC14",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012769",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012769",
                                "name": "prostate cancer, hereditary, 14",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012770",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012770",
                                "name": "prostate cancer, hereditary, 15",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012770",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012770",
                                "name": "HPC15",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012770",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012770",
                                "name": "prostate cancer, hereditary, 15",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0700275",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0700275",
                                "name": "prostate cancer, hereditary",
                                "description": "An instance of prostate cancer that is caused by an inherited genomic modification in an individual. Familial prostate cancer (FPC) is a malignant tumor of the prostate with an early onset. FPC is either asymptomatic or causes mictionary symptoms, erectile dysfunction, bone pain, venous compression and infectious or inflammatory syndrome (for the metastatic forms). It is also characterized by familial antecedents."
                            },
                            {
                                "id": "MIM:601518",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/601518",
                                "name": "Prostate cancer, hereditary, 1",
                                "description": "Prostate cancer, hereditary, 1"
                            },
                            {
                                "id": "MIM:610997",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/610997",
                                "name": "Prostate cancer, hereditary, 9",
                                "description": "Prostate cancer, hereditary, 9"
                            },
                            {
                                "id": "MIM:611868",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/611868",
                                "name": "Prostate cancer, hereditary, 12",
                                "description": "Prostate cancer, hereditary, 12"
                            },
                            {
                                "id": "MIM:611928",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/611928",
                                "name": "Prostate cancer, hereditary, 13",
                                "description": "Prostate cancer, hereditary, 13"
                            },
                            {
                                "id": "MIM:611955",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/611955",
                                "name": "Prostate cancer, hereditary, 11",
                                "description": "Prostate cancer, hereditary, 11"
                            },
                            {
                                "id": "MIM:176807",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/176807",
                                "name": "Prostate cancer",
                                "description": "Prostate cancer"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "10283",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:10283"
                            }
                        ]
                    }
                ],
                "keywords": [
                    "biomuta",
                    "somatic",
                    "cancer",
                    "disease"
                ]
            },
            {
                "evidence": [
                    {
                        "id": "P98161",
                        "database": "BioMuta",
                        "url": "https://hivelab.biochemistry.gwu.edu/biomuta/proteinview/P98161"
                    },
                    {
                        "id": "rs144593342",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs144593342"
                    },
                    {
                        "id": "rs144593342",
                        "database": "1000Genomes",
                        "url": "https://www.ensembl.org/homo_sapiens/Variation/Explore?v=rs144593342"
                    },
                    {
                        "id": "rs144593342",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs144593342"
                    },
                    {
                        "id": "rs144593342",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs144593342#frequency_tab"
                    },
                    {
                        "id": "rs144593342",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs144593342"
                    },
                    {
                        "id": "rs144593342",
                        "database": "COSMIC",
                        "url": "https://www.ensembl.org/homo_sapiens/Variation/Explore?v=rs144593342"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 3442,
                "end_pos": 3442,
                "subjects_tested": "2003",
                "subjects_positive": "1",
                "frequency": "0.0",
                "sequence_org": "A",
                "sequence_mut": "V",
                "comment": "Somatic mutation passed 1 out of 6 filters: num. of cancers (4).",
                "chr_id": "16",
                "chr_pos": "2097399",
                "ref_nt": "G",
                "alt_nt": "A",
                "minor_allelic_frequency": "",
                "site_lbl": "A3442",
                "disease": [
                    {
                        "disease_id": "DOID:3571",
                        "recommended_name": {
                            "id": "DOID:3571",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:3571",
                            "name": "liver cancer",
                            "description": "A hepatobiliary system cancer that is located_in the liver."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:3571",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:3571",
                                "name": "Ca liver - primary",
                                "description": ""
                            },
                            {
                                "id": "DOID:3571",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:3571",
                                "name": "Resectable malignant neoplasm of Liver",
                                "description": ""
                            },
                            {
                                "id": "DOID:3571",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:3571",
                                "name": "hepatic cancer",
                                "description": ""
                            },
                            {
                                "id": "DOID:3571",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:3571",
                                "name": "hepatic neoplasm",
                                "description": ""
                            },
                            {
                                "id": "DOID:3571",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:3571",
                                "name": "malignant hepato-biliary neoplasm",
                                "description": ""
                            },
                            {
                                "id": "DOID:3571",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:3571",
                                "name": "malignant neoplasm of liver",
                                "description": ""
                            },
                            {
                                "id": "DOID:3571",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:3571",
                                "name": "malignant neoplasm of liver, primary",
                                "description": ""
                            },
                            {
                                "id": "DOID:3571",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:3571",
                                "name": "malignant tumor of liver",
                                "description": ""
                            },
                            {
                                "id": "DOID:3571",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:3571",
                                "name": "neoplasm of liver",
                                "description": ""
                            },
                            {
                                "id": "DOID:3571",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:3571",
                                "name": "non-resectable primary hepatic malignant neoplasm",
                                "description": ""
                            },
                            {
                                "id": "DOID:3571",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:3571",
                                "name": "primary liver cancer",
                                "description": ""
                            },
                            {
                                "id": "DOID:3571",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:3571",
                                "name": "primary malignant neoplasm of liver",
                                "description": ""
                            },
                            {
                                "id": "DOID:3571",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:3571",
                                "name": "resectable malignant neoplasm of the liver",
                                "description": ""
                            },
                            {
                                "id": "DOID:3571",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:3571",
                                "name": "malignant neoplasm of liver, not specified as primary or secondary",
                                "description": ""
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "3571",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:3571"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:10283",
                        "recommended_name": {
                            "id": "DOID:10283",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:10283",
                            "name": "prostate cancer",
                            "description": "A male reproductive organ cancer that is located_in the prostate."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:10283",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:10283",
                                "name": "NGP - new growth of prostate",
                                "description": ""
                            },
                            {
                                "id": "DOID:10283",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:10283",
                                "name": "hereditary prostate cancer",
                                "description": ""
                            },
                            {
                                "id": "DOID:10283",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:10283",
                                "name": "malignant tumor of the prostate",
                                "description": ""
                            },
                            {
                                "id": "DOID:10283",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:10283",
                                "name": "prostate cancer, familial",
                                "description": ""
                            },
                            {
                                "id": "DOID:10283",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:10283",
                                "name": "prostate neoplasm",
                                "description": ""
                            },
                            {
                                "id": "DOID:10283",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:10283",
                                "name": "prostatic cancer",
                                "description": ""
                            },
                            {
                                "id": "DOID:10283",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:10283",
                                "name": "prostatic neoplasm",
                                "description": ""
                            },
                            {
                                "id": "DOID:10283",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:10283",
                                "name": "tumor of the prostate",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0010257",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0010257",
                                "name": "prostate cancer, hereditary, X-linked 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0010257",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0010257",
                                "name": "HPCX1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0010257",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0010257",
                                "name": "prostate cancer, hereditary, X-linked 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0010405",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0010405",
                                "name": "prostate cancer, hereditary, X-linked 2",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0010405",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0010405",
                                "name": "HPCX2",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0010405",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0010405",
                                "name": "prostate cancer, hereditary, X-linked 2",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011098",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011098",
                                "name": "prostate cancer, hereditary, 1",
                                "description": "Any familial prostate cancer in which the cause of the disease is a mutation in the RNASEL gene."
                            },
                            {
                                "id": "MONDO:0011098",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011098",
                                "name": "RNASEL familial prostate cancer",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011098",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011098",
                                "name": "familial prostate cancer caused by mutation in RNASEL",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011098",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011098",
                                "name": "prostate cancer 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011098",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011098",
                                "name": "prostate cancer, hereditary, 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011098",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011098",
                                "name": "prostate cancer, hereditary, type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011098",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011098",
                                "name": "HPC1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011270",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011270",
                                "name": "prostate cancer, hereditary, 8",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011270",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011270",
                                "name": "prostate cancer, hereditary, 8",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011270",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011270",
                                "name": "prostate cancer, hereditary, type 8",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011270",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011270",
                                "name": "HPC8",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012093",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012093",
                                "name": "prostate cancer, hereditary, 3",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012093",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012093",
                                "name": "prostate cancer, hereditary, 3",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012093",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012093",
                                "name": "prostate cancer, hereditary, type 3",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012093",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012093",
                                "name": "prostate cancer, susceptibility to, 3",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012093",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012093",
                                "name": "HPC3",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012094",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012094",
                                "name": "prostate cancer, hereditary, 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012094",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012094",
                                "name": "prostate cancer, hereditary, 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012094",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012094",
                                "name": "prostate cancer, hereditary, type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012094",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012094",
                                "name": "prostate cancer, susceptibility to, 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012094",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012094",
                                "name": "HPC4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012244",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012244",
                                "name": "prostate cancer, hereditary, 5",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012244",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012244",
                                "name": "prostate cancer, hereditary, 5",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012244",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012244",
                                "name": "prostate cancer, hereditary, type 5",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012244",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012244",
                                "name": "HPC5",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012300",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012300",
                                "name": "prostate cancer, hereditary, 6",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012300",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012300",
                                "name": "prostate cancer, hereditary, 6",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012300",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012300",
                                "name": "prostate cancer, hereditary, type 6",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012300",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012300",
                                "name": "HPC6",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012470",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012470",
                                "name": "prostate cancer, hereditary, 7",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012470",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012470",
                                "name": "HPC7",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012470",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012470",
                                "name": "prostate cancer, hereditary, 7",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012597",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012597",
                                "name": "prostate cancer, hereditary, 9",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012597",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012597",
                                "name": "prostate cancer, hereditary, 9",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012597",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012597",
                                "name": "prostate cancer, hereditary, type 9",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012597",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012597",
                                "name": "HPC9",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012620",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012620",
                                "name": "prostate cancer, hereditary, 10",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012620",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012620",
                                "name": "HPC10",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012620",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012620",
                                "name": "prostate cancer, hereditary, 10",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012741",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012741",
                                "name": "prostate cancer, hereditary, 12",
                                "description": "Any familial prostate cancer in which the cause of the disease is a mutation in the EHBP1 gene."
                            },
                            {
                                "id": "MONDO:0012741",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012741",
                                "name": "EHBP1 familial prostate cancer",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012741",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012741",
                                "name": "familial prostate cancer caused by mutation in EHBP1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012741",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012741",
                                "name": "prostate cancer, hereditary, 12",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012741",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012741",
                                "name": "prostate cancer, hereditary, type 12",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012741",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012741",
                                "name": "HPC12",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012758",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012758",
                                "name": "prostate cancer, hereditary, 13",
                                "description": "Any familial prostate cancer in which the cause of the disease is a mutation in the MSMB gene."
                            },
                            {
                                "id": "MONDO:0012758",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012758",
                                "name": "MSMB familial prostate cancer",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012758",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012758",
                                "name": "familial prostate cancer caused by mutation in MSMB",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012758",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012758",
                                "name": "prostate cancer, hereditary, 13",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012758",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012758",
                                "name": "prostate cancer, hereditary, type 13",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012758",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012758",
                                "name": "HPC13",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012768",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012768",
                                "name": "prostate cancer, hereditary, 11",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012768",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012768",
                                "name": "HPC11",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012768",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012768",
                                "name": "prostate cancer, hereditary, 11",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012769",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012769",
                                "name": "prostate cancer, hereditary, 14",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012769",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012769",
                                "name": "HPC14",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012769",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012769",
                                "name": "prostate cancer, hereditary, 14",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012770",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012770",
                                "name": "prostate cancer, hereditary, 15",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012770",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012770",
                                "name": "HPC15",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012770",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012770",
                                "name": "prostate cancer, hereditary, 15",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0700275",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0700275",
                                "name": "prostate cancer, hereditary",
                                "description": "An instance of prostate cancer that is caused by an inherited genomic modification in an individual. Familial prostate cancer (FPC) is a malignant tumor of the prostate with an early onset. FPC is either asymptomatic or causes mictionary symptoms, erectile dysfunction, bone pain, venous compression and infectious or inflammatory syndrome (for the metastatic forms). It is also characterized by familial antecedents."
                            },
                            {
                                "id": "MIM:601518",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/601518",
                                "name": "Prostate cancer, hereditary, 1",
                                "description": "Prostate cancer, hereditary, 1"
                            },
                            {
                                "id": "MIM:610997",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/610997",
                                "name": "Prostate cancer, hereditary, 9",
                                "description": "Prostate cancer, hereditary, 9"
                            },
                            {
                                "id": "MIM:611868",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/611868",
                                "name": "Prostate cancer, hereditary, 12",
                                "description": "Prostate cancer, hereditary, 12"
                            },
                            {
                                "id": "MIM:611928",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/611928",
                                "name": "Prostate cancer, hereditary, 13",
                                "description": "Prostate cancer, hereditary, 13"
                            },
                            {
                                "id": "MIM:611955",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/611955",
                                "name": "Prostate cancer, hereditary, 11",
                                "description": "Prostate cancer, hereditary, 11"
                            },
                            {
                                "id": "MIM:176807",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/176807",
                                "name": "Prostate cancer",
                                "description": "Prostate cancer"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "10283",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:10283"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:1319",
                        "recommended_name": {
                            "id": "DOID:1319",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:1319",
                            "name": "brain cancer",
                            "description": "A central nervous system cancer that is characterized by the growth of abnormal cells in the tissues of the brain."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:1319",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:1319",
                                "name": "BT - Brain tumour",
                                "description": ""
                            },
                            {
                                "id": "DOID:1319",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:1319",
                                "name": "adult brain tumor",
                                "description": ""
                            },
                            {
                                "id": "DOID:1319",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:1319",
                                "name": "adult malignant brain neoplasm",
                                "description": ""
                            },
                            {
                                "id": "DOID:1319",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:1319",
                                "name": "brain neoplasm",
                                "description": ""
                            },
                            {
                                "id": "DOID:1319",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:1319",
                                "name": "brain neoplasm, adult",
                                "description": ""
                            },
                            {
                                "id": "DOID:1319",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:1319",
                                "name": "malignant brain tumour",
                                "description": ""
                            },
                            {
                                "id": "DOID:1319",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:1319",
                                "name": "malignant primary brain neoplasm",
                                "description": ""
                            },
                            {
                                "id": "DOID:1319",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:1319",
                                "name": "malignant primary brain tumor",
                                "description": ""
                            },
                            {
                                "id": "DOID:1319",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:1319",
                                "name": "malignant tumor of Brain",
                                "description": ""
                            },
                            {
                                "id": "DOID:1319",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:1319",
                                "name": "malignant tumor of adult brain",
                                "description": ""
                            },
                            {
                                "id": "DOID:1319",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:1319",
                                "name": "neoplasm of brain",
                                "description": ""
                            },
                            {
                                "id": "DOID:1319",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:1319",
                                "name": "primary brain neoplasm",
                                "description": ""
                            },
                            {
                                "id": "DOID:1319",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:1319",
                                "name": "primary brain tumor",
                                "description": ""
                            },
                            {
                                "id": "DOID:1319",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:1319",
                                "name": "primary malignant neoplasm of brain",
                                "description": ""
                            },
                            {
                                "id": "DOID:1319",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:1319",
                                "name": "tumor of the Brain",
                                "description": ""
                            }
                        ],
                        "unlinked_id_list": [
                            "DOID:4203",
                            "DOID:3541",
                            "DOID:4706",
                            "DOID:1659",
                            "DOID:368"
                        ],
                        "evidence": [
                            {
                                "id": "1319",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:1319"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:9256",
                        "recommended_name": {
                            "id": "DOID:9256",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:9256",
                            "name": "colorectal cancer",
                            "description": "A large intestine cancer that is located_in the colon and/or located_in the rectum."
                        },
                        "synonyms": [
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectal cancer",
                                "description": "A primary or metastatic malignant neoplasm that affects the colon or rectum. Representative examples include carcinoma, lymphoma, and sarcoma."
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "cancer of colorectum",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "cancer of large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "cancer of large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "cancer of the large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colon cancer, advanced, somatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colon cancer, somatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectal cancer",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectal cancer with chromosomal instability, somatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectal cancer, autosomal dominant, somatic mutation",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectal cancer, somatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectal cancer, susceptibility to, autosomal dominant, somatic mutation",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectum cancer",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant colorectal neoplasm",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant colorectal tumor",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant colorectal tumour",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant colorectum neoplasm",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant large bowel neoplasm",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant large bowel tumor",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant large bowel tumour",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant large intestine neoplasm",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant large intestine tumor",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant large intestine tumour",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant neoplasm of colorectum",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant neoplasm of large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant neoplasm of large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant neoplasm of the large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant neoplasm of the large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumor of large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumor of large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumor of the large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumor of the large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumour of large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumour of large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumour of the large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumour of the large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "CRC",
                                "description": ""
                            },
                            {
                                "id": "MIM:114500",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/114500",
                                "name": "Colorectal cancer",
                                "description": "Colorectal cancer"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "9256",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:9256"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0080322",
                        "recommended_name": {
                            "id": "DOID:0080322",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0080322",
                            "name": "polycystic kidney disease",
                            "description": "A cystic kidney disease that is characterized by the growth of fluid-filled cysts in the kidneys that reduces kidney function and may lead to kidney failure."
                        },
                        "synonyms": [
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0080322",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0080322"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0110858",
                        "recommended_name": {
                            "id": "DOID:0110858",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0110858",
                            "name": "polycystic kidney disease 1",
                            "description": "A autosomal dominant polycystic kidney disease that has_material_basis_in autosomal dominant inheritance of mutation in the PKD1 gene on chromosome 16p13.3."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "Polycystic Kidney Disease, Adult, Type I",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110858",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110858",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": "Any autosomal dominant polycystic kidney disease in which the cause of the disease is a mutation in the PKD1 gene."
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "APKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "PKD1 autosomal dominant polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "autosomal dominant polycystic kidney disease caused by mutation in PKD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "polycystic kidney disease type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008263",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008263",
                                "name": "Potter type 3 polycystic kidney disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:173900",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/173900",
                                "name": "Polycystic kidney disease 1 with or without polycystic liver disease",
                                "description": "Polycystic kidney disease 1 with or without polycystic liver disease"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            },
                            {
                                "id": "0110858",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110858"
                            }
                        ]
                    }
                ],
                "keywords": [
                    "biomuta",
                    "somatic",
                    "cancer",
                    "disease",
                    "ebi"
                ]
            }
        ]
    }
}
