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                        {
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                {
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                                {
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                                {
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                                {
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                        },
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                                {
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                                {
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            ]
        },
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                    "length": 750,
                    "chemical_mass": 85514.0
                }
            ]
        },
        {
            "start_pos": "285",
            "site_seq": "N",
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            "glycoprotein": [
                {
                    "uniprot_canonical_ac": "P08473-1",
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                        {
                            "database": "PubMed",
                            "id": "37074911",
                            "url": "https://glygen.org/publication/PubMed/37074911"
                        },
                        {
                            "database": "PDC",
                            "id": "PDC000471",
                            "url": "https://proteomic.datacommons.cancer.gov/pdc/study/PDC000471"
                        }
                    ],
                    "protein_name": "Neprilysin",
                    "gene_name": "MME",
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                    "tax_name": "Homo sapiens",
                    "tax_common_name": "Human",
                    "length": 750,
                    "chemical_mass": 85514.0
                }
            ]
        },
        {
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            "glycoprotein": [
                {
                    "uniprot_canonical_ac": "P08473-1",
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                    "end_pos": 145,
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                    "evidence": [
                        {
                            "database": "PubMed",
                            "id": "37074911",
                            "url": "https://glygen.org/publication/PubMed/37074911"
                        },
                        {
                            "database": "PDC",
                            "id": "PDC000471",
                            "url": "https://proteomic.datacommons.cancer.gov/pdc/study/PDC000471"
                        }
                    ],
                    "protein_name": "Neprilysin",
                    "gene_name": "MME",
                    "tax_id": 9606,
                    "tax_name": "Homo sapiens",
                    "tax_common_name": "Human",
                    "length": 750,
                    "chemical_mass": 85514.0
                }
            ]
        },
        {
            "start_pos": "145",
            "site_seq": "N",
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            "residue": "Asn",
            "glycoprotein": [
                {
                    "uniprot_canonical_ac": "P08473-1",
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                    "end_pos": 145,
                    "residue": "Asn",
                    "evidence": [
                        {
                            "database": "PubMed",
                            "id": "37074911",
                            "url": "https://glygen.org/publication/PubMed/37074911"
                        },
                        {
                            "database": "PDC",
                            "id": "PDC000471",
                            "url": "https://proteomic.datacommons.cancer.gov/pdc/study/PDC000471"
                        }
                    ],
                    "protein_name": "Neprilysin",
                    "gene_name": "MME",
                    "tax_id": 9606,
                    "tax_name": "Homo sapiens",
                    "tax_common_name": "Human",
                    "length": 750,
                    "chemical_mass": 85514.0
                }
            ]
        },
        {
            "start_pos": "145",
            "site_seq": "SCINESAIDSR",
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            "glycoprotein": [
                {
                    "uniprot_canonical_ac": "P08473-1",
                    "start_pos": 145,
                    "end_pos": 145,
                    "residue": "Asn",
                    "evidence": [
                        {
                            "database": "PubMed",
                            "id": "37074911",
                            "url": "https://glygen.org/publication/PubMed/37074911"
                        },
                        {
                            "database": "PDC",
                            "id": "PDC000471",
                            "url": "https://proteomic.datacommons.cancer.gov/pdc/study/PDC000471"
                        }
                    ],
                    "protein_name": "Neprilysin",
                    "gene_name": "MME",
                    "tax_id": 9606,
                    "tax_name": "Homo sapiens",
                    "tax_common_name": "Human",
                    "length": 750,
                    "chemical_mass": 85514.0
                }
            ]
        },
        {
            "start_pos": "285",
            "site_seq": "EIAnATAKPEDRNDPMLLYNK",
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            "residue": "Asn",
            "glycoprotein": [
                {
                    "uniprot_canonical_ac": "P08473-1",
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                    "end_pos": 285,
                    "residue": "Asn",
                    "evidence": [
                        {
                            "database": "PubMed",
                            "id": "37074911",
                            "url": "https://glygen.org/publication/PubMed/37074911"
                        },
                        {
                            "database": "PDC",
                            "id": "PDC000471",
                            "url": "https://proteomic.datacommons.cancer.gov/pdc/study/PDC000471"
                        }
                    ],
                    "protein_name": "Neprilysin",
                    "gene_name": "MME",
                    "tax_id": 9606,
                    "tax_name": "Homo sapiens",
                    "tax_common_name": "Human",
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                    "chemical_mass": 85514.0
                }
            ]
        },
        {
            "start_pos": "285",
            "site_seq": "EIAnATAKPEDR",
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            "residue": "Asn",
            "glycoprotein": [
                {
                    "uniprot_canonical_ac": "P08473-1",
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                    "end_pos": 285,
                    "residue": "Asn",
                    "evidence": [
                        {
                            "database": "PubMed",
                            "id": "37074911",
                            "url": "https://glygen.org/publication/PubMed/37074911"
                        },
                        {
                            "database": "PDC",
                            "id": "PDC000471",
                            "url": "https://proteomic.datacommons.cancer.gov/pdc/study/PDC000471"
                        }
                    ],
                    "protein_name": "Neprilysin",
                    "gene_name": "MME",
                    "tax_id": 9606,
                    "tax_name": "Homo sapiens",
                    "tax_common_name": "Human",
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                    "chemical_mass": 85514.0
                }
            ]
        },
        {
            "start_pos": "285",
            "site_seq": "EIANATAKPEDR",
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            "residue": "Asn",
            "glycoprotein": [
                {
                    "uniprot_canonical_ac": "P08473-1",
                    "start_pos": 285,
                    "end_pos": 285,
                    "residue": "Asn",
                    "evidence": [
                        {
                            "database": "PubMed",
                            "id": "37074911",
                            "url": "https://glygen.org/publication/PubMed/37074911"
                        },
                        {
                            "database": "PDC",
                            "id": "PDC000471",
                            "url": "https://proteomic.datacommons.cancer.gov/pdc/study/PDC000471"
                        }
                    ],
                    "protein_name": "Neprilysin",
                    "gene_name": "MME",
                    "tax_id": 9606,
                    "tax_name": "Homo sapiens",
                    "tax_common_name": "Human",
                    "length": 750,
                    "chemical_mass": 85514.0
                }
            ]
        },
        {
            "start_pos": "285",
            "site_seq": "N",
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            "residue": "Asn",
            "glycoprotein": [
                {
                    "uniprot_canonical_ac": "P08473-1",
                    "start_pos": 285,
                    "end_pos": 285,
                    "residue": "Asn",
                    "evidence": [
                        {
                            "database": "PubMed",
                            "id": "37074911",
                            "url": "https://glygen.org/publication/PubMed/37074911"
                        },
                        {
                            "database": "PDC",
                            "id": "PDC000471",
                            "url": "https://proteomic.datacommons.cancer.gov/pdc/study/PDC000471"
                        }
                    ],
                    "protein_name": "Neprilysin",
                    "gene_name": "MME",
                    "tax_id": 9606,
                    "tax_name": "Homo sapiens",
                    "tax_common_name": "Human",
                    "length": 750,
                    "chemical_mass": 85514.0
                }
            ]
        },
        {
            "start_pos": "145",
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            "site_lbl": "N145",
            "residue": "",
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                {
                    "weight": 100,
                    "sequence_org": "N",
                    "sequence_mut": "H",
                    "comment": "Somatic mutation passed 1 out of 6 filters: n-glyco-sequon-loss (NES->HES).",
                    "chr_id": "3",
                    "chr_pos": "155116553",
                    "evidence": [
                        {
                            "id": "P08473",
                            "database": "BioMuta",
                            "url": "https://hivelab.biochemistry.gwu.edu/biomuta/proteinview/P08473"
                        }
                    ],
                    "disease": [
                        {
                            "disease_id": "DOID:10534",
                            "name": "stomach cancer",
                            "description": "A gastrointestinal system cancer that is located_in the stomach.",
                            "url": "http://disease-ontology.org/term/DOID:10534",
                            "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"
                                }
                            ]
                        }
                    ]
                }
            ],
            "glycoprotein": [
                {
                    "uniprot_canonical_ac": "P08473-1",
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                    "end_pos": 145,
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                    "evidence": [
                        {
                            "database": "PubMed",
                            "id": "37074911",
                            "url": "https://glygen.org/publication/PubMed/37074911"
                        },
                        {
                            "database": "PDC",
                            "id": "PDC000471",
                            "url": "https://proteomic.datacommons.cancer.gov/pdc/study/PDC000471"
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                    ],
                    "protein_name": "Neprilysin",
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                    "tax_name": "Homo sapiens",
                    "tax_common_name": "Human",
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                    "chemical_mass": 85514.0
                }
            ]
        },
        {
            "start_pos": "285",
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            "site_lbl": "N285",
            "residue": "",
            "snv": [
                {
                    "weight": 100,
                    "sequence_org": "N",
                    "sequence_mut": "D",
                    "comment": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-loss (NAT->DAT).",
                    "chr_id": "3",
                    "chr_pos": "155138234",
                    "evidence": [
                        {
                            "id": "rs1339178202",
                            "database": "dbSNP",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1339178202"
                        },
                        {
                            "id": "rs1339178202",
                            "database": "gnomAD",
                            "url": "http://gnomad.broadinstitute.org/awesome?query=rs1339178202"
                        }
                    ]
                },
                {
                    "weight": 100,
                    "sequence_org": "N",
                    "sequence_mut": "I",
                    "comment": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-loss (NAT->IAT).",
                    "chr_id": "3",
                    "chr_pos": "155138235",
                    "evidence": [
                        {
                            "id": "rs200961860",
                            "database": "dbSNP",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs200961860"
                        },
                        {
                            "id": "rs200961860",
                            "database": "1000Genomes",
                            "url": "https://www.ensembl.org/homo_sapiens/Variation/Explore?v=rs200961860"
                        },
                        {
                            "id": "rs200961860",
                            "database": "ExAC",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs200961860"
                        },
                        {
                            "id": "rs200961860",
                            "database": "TOPMed",
                            "url": "https://www.ncbi.nlm.nih.gov/snp/rs200961860#frequency_tab"
                        },
                        {
                            "id": "rs200961860",
                            "database": "gnomAD",
                            "url": "http://gnomad.broadinstitute.org/awesome?query=rs200961860"
                        }
                    ]
                },
                {
                    "weight": 100,
                    "sequence_org": "N",
                    "sequence_mut": "K",
                    "comment": "Somatic mutation passed 1 out of 6 filters: n-glyco-sequon-loss (NAT->KAT).",
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                    "chr_pos": "155138236",
                    "evidence": [
                        {
                            "id": "P08473",
                            "database": "BioMuta",
                            "url": "https://hivelab.biochemistry.gwu.edu/biomuta/proteinview/P08473"
                        },
                        {
                            "id": "rs1434664230",
                            "database": "dbSNP",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1434664230"
                        },
                        {
                            "id": "rs1434664230",
                            "database": "gnomAD",
                            "url": "http://gnomad.broadinstitute.org/awesome?query=rs1434664230"
                        },
                        {
                            "id": "rs1434664230",
                            "database": "COSMIC",
                            "url": "https://www.ensembl.org/homo_sapiens/Variation/Explore?v=rs1434664230"
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                    ],
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                            "url": "http://disease-ontology.org/term/DOID:1324",
                            "evidence": [
                                {
                                    "id": "1324",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:1324"
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                            ]
                        }
                    ]
                },
                {
                    "weight": 100,
                    "sequence_org": "N",
                    "sequence_mut": "S",
                    "comment": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-loss (NAT->SAT).",
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                    "chr_pos": "155138235",
                    "evidence": [
                        {
                            "id": "rs200961860",
                            "database": "dbSNP",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs200961860"
                        },
                        {
                            "id": "rs200961860",
                            "database": "1000Genomes",
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                        },
                        {
                            "id": "rs200961860",
                            "database": "ExAC",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs200961860"
                        },
                        {
                            "id": "rs200961860",
                            "database": "TOPMed",
                            "url": "https://www.ncbi.nlm.nih.gov/snp/rs200961860#frequency_tab"
                        },
                        {
                            "id": "rs200961860",
                            "database": "gnomAD",
                            "url": "http://gnomad.broadinstitute.org/awesome?query=rs200961860"
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                    ],
                    "disease": [
                        {
                            "disease_id": "DOID:0110160",
                            "name": "Charcot-Marie-Tooth disease axonal type 2T",
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                            "url": "http://disease-ontology.org/term/DOID:0110160",
                            "evidence": [
                                {
                                    "id": "0110160",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0110160"
                                },
                                {
                                    "id": "0110160",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0110160"
                                }
                            ]
                        },
                        {
                            "disease_id": "DOID:0110160",
                            "name": "Charcot-Marie-Tooth disease axonal type 2T",
                            "description": "A Charcot-Marie-Tooth disease type 2 that has_material_basis_in homozygous or compound heterozygous mutation in the MME gene on chromosome 3q25.",
                            "url": "http://disease-ontology.org/term/DOID:0110160",
                            "evidence": [
                                {
                                    "id": "0110160",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0110160"
                                },
                                {
                                    "id": "0110160",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0110160"
                                }
                            ]
                        },
                        {
                            "disease_id": "DOID:0110160",
                            "name": "Charcot-Marie-Tooth disease axonal type 2T",
                            "description": "A Charcot-Marie-Tooth disease type 2 that has_material_basis_in homozygous or compound heterozygous mutation in the MME gene on chromosome 3q25.",
                            "url": "http://disease-ontology.org/term/DOID:0110160",
                            "evidence": [
                                {
                                    "id": "0110160",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0110160"
                                },
                                {
                                    "id": "0110160",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0110160"
                                }
                            ]
                        },
                        {
                            "disease_id": "DOID:0110160",
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                            "evidence": [
                                {
                                    "id": "0110160",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0110160"
                                },
                                {
                                    "id": "0110160",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0110160"
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                            ]
                        },
                        {
                            "disease_id": "DOID:0110160",
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                            "evidence": [
                                {
                                    "id": "0110160",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0110160"
                                },
                                {
                                    "id": "0110160",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0110160"
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                            ]
                        },
                        {
                            "disease_id": "DOID:0111745",
                            "name": "cerebellar ataxia type 43",
                            "description": "An autosomal dominant cerebellar ataxia characterized by adult-onset, slowly progressive, gait and limb ataxia, often associated with peripheral neuropathy typically affecting the motor system that has_material_basis_in heterozygous mutation in MME on chromosome 3q25.2.",
                            "url": "http://disease-ontology.org/term/DOID:0111745",
                            "evidence": [
                                {
                                    "id": "0111745",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0111745"
                                },
                                {
                                    "id": "0111745",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0111745"
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                            ]
                        },
                        {
                            "disease_id": "DOID:0111745",
                            "name": "cerebellar ataxia type 43",
                            "description": "An autosomal dominant cerebellar ataxia characterized by adult-onset, slowly progressive, gait and limb ataxia, often associated with peripheral neuropathy typically affecting the motor system that has_material_basis_in heterozygous mutation in MME on chromosome 3q25.2.",
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                            "evidence": [
                                {
                                    "id": "0111745",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0111745"
                                },
                                {
                                    "id": "0111745",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0111745"
                                }
                            ]
                        },
                        {
                            "disease_id": "DOID:0111745",
                            "name": "cerebellar ataxia type 43",
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                            "evidence": [
                                {
                                    "id": "0111745",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0111745"
                                },
                                {
                                    "id": "0111745",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0111745"
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                            ]
                        },
                        {
                            "disease_id": "DOID:0111745",
                            "name": "cerebellar ataxia type 43",
                            "description": "An autosomal dominant cerebellar ataxia characterized by adult-onset, slowly progressive, gait and limb ataxia, often associated with peripheral neuropathy typically affecting the motor system that has_material_basis_in heterozygous mutation in MME on chromosome 3q25.2.",
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                            "evidence": [
                                {
                                    "id": "0111745",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0111745"
                                },
                                {
                                    "id": "0111745",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0111745"
                                }
                            ]
                        },
                        {
                            "disease_id": "DOID:0111745",
                            "name": "cerebellar ataxia type 43",
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                            "evidence": [
                                {
                                    "id": "0111745",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0111745"
                                },
                                {
                                    "id": "0111745",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0111745"
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                            ]
                        }
                    ]
                }
            ],
            "glycoprotein": [
                {
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                        {
                            "database": "PubMed",
                            "id": "37074911",
                            "url": "https://glygen.org/publication/PubMed/37074911"
                        },
                        {
                            "database": "PDC",
                            "id": "PDC000471",
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                    ],
                    "protein_name": "Neprilysin",
                    "gene_name": "MME",
                    "tax_id": 9606,
                    "tax_name": "Homo sapiens",
                    "tax_common_name": "Human",
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                    "chemical_mass": 85514.0
                }
            ]
        },
        {
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            "glycoprotein": [
                {
                    "uniprot_canonical_ac": "P08473-1",
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                        {
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                            "id": "37074911",
                            "url": "https://glygen.org/publication/PubMed/37074911"
                        },
                        {
                            "database": "PDC",
                            "id": "PDC000471",
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                    ],
                    "protein_name": "Neprilysin",
                    "gene_name": "MME",
                    "tax_id": 9606,
                    "tax_name": "Homo sapiens",
                    "tax_common_name": "Human",
                    "length": 750,
                    "chemical_mass": 85514.0
                }
            ]
        },
        {
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            "glycoprotein": [
                {
                    "uniprot_canonical_ac": "P08473-1",
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                    "end_pos": 145,
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                    "evidence": [
                        {
                            "database": "PubMed",
                            "id": "37074911",
                            "url": "https://glygen.org/publication/PubMed/37074911"
                        },
                        {
                            "database": "PDC",
                            "id": "PDC000471",
                            "url": "https://proteomic.datacommons.cancer.gov/pdc/study/PDC000471"
                        }
                    ],
                    "protein_name": "Neprilysin",
                    "gene_name": "MME",
                    "tax_id": 9606,
                    "tax_name": "Homo sapiens",
                    "tax_common_name": "Human",
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                    "chemical_mass": 85514.0
                }
            ]
        },
        {
            "start_pos": "145",
            "site_seq": "SCINESAIDSR",
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            "glycoprotein": [
                {
                    "uniprot_canonical_ac": "P08473-1",
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                    "end_pos": 145,
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                        {
                            "database": "PubMed",
                            "id": "37074911",
                            "url": "https://glygen.org/publication/PubMed/37074911"
                        },
                        {
                            "database": "PDC",
                            "id": "PDC000471",
                            "url": "https://proteomic.datacommons.cancer.gov/pdc/study/PDC000471"
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                    ],
                    "protein_name": "Neprilysin",
                    "gene_name": "MME",
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                    "tax_name": "Homo sapiens",
                    "tax_common_name": "Human",
                    "length": 750,
                    "chemical_mass": 85514.0
                }
            ]
        },
        {
            "start_pos": "285",
            "site_seq": "EIAnATAKPEDRNDPMLLYNK",
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            "residue": "Asn",
            "glycoprotein": [
                {
                    "uniprot_canonical_ac": "P08473-1",
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                    "end_pos": 285,
                    "residue": "Asn",
                    "evidence": [
                        {
                            "database": "PubMed",
                            "id": "37074911",
                            "url": "https://glygen.org/publication/PubMed/37074911"
                        },
                        {
                            "database": "PDC",
                            "id": "PDC000471",
                            "url": "https://proteomic.datacommons.cancer.gov/pdc/study/PDC000471"
                        }
                    ],
                    "protein_name": "Neprilysin",
                    "gene_name": "MME",
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                    "tax_name": "Homo sapiens",
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                    "chemical_mass": 85514.0
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            ]
        },
        {
            "start_pos": "285",
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            "glycoprotein": [
                {
                    "uniprot_canonical_ac": "P08473-1",
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                        {
                            "database": "PubMed",
                            "id": "37074911",
                            "url": "https://glygen.org/publication/PubMed/37074911"
                        },
                        {
                            "database": "PDC",
                            "id": "PDC000471",
                            "url": "https://proteomic.datacommons.cancer.gov/pdc/study/PDC000471"
                        }
                    ],
                    "protein_name": "Neprilysin",
                    "gene_name": "MME",
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                    "tax_name": "Homo sapiens",
                    "tax_common_name": "Human",
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                    "chemical_mass": 85514.0
                }
            ]
        },
        {
            "start_pos": "285",
            "site_seq": "EIANATAKPEDR",
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            "glycoprotein": [
                {
                    "uniprot_canonical_ac": "P08473-1",
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                    "end_pos": 285,
                    "residue": "Asn",
                    "evidence": [
                        {
                            "database": "PubMed",
                            "id": "37074911",
                            "url": "https://glygen.org/publication/PubMed/37074911"
                        },
                        {
                            "database": "PDC",
                            "id": "PDC000471",
                            "url": "https://proteomic.datacommons.cancer.gov/pdc/study/PDC000471"
                        }
                    ],
                    "protein_name": "Neprilysin",
                    "gene_name": "MME",
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                    "tax_name": "Homo sapiens",
                    "tax_common_name": "Human",
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                    "chemical_mass": 85514.0
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            ]
        },
        {
            "start_pos": "285",
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            "glycoprotein": [
                {
                    "uniprot_canonical_ac": "P08473-1",
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                    "evidence": [
                        {
                            "database": "PubMed",
                            "id": "37074911",
                            "url": "https://glygen.org/publication/PubMed/37074911"
                        },
                        {
                            "database": "PDC",
                            "id": "PDC000471",
                            "url": "https://proteomic.datacommons.cancer.gov/pdc/study/PDC000471"
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                    ],
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                    "gene_name": "MME",
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                    "tax_common_name": "Human",
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                    "chemical_mass": 85514.0
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            ]
        },
        {
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            "residue": "",
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                    "sequence_org": "N",
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                    "comment": "Somatic mutation passed 1 out of 6 filters: n-glyco-sequon-loss (NES->HES).",
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                    "chr_pos": "155116553",
                    "evidence": [
                        {
                            "id": "P08473",
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                    ],
                    "disease": [
                        {
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                            "name": "stomach cancer",
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                            "url": "http://disease-ontology.org/term/DOID:10534",
                            "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"
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                            ]
                        }
                    ]
                }
            ],
            "glycoprotein": [
                {
                    "uniprot_canonical_ac": "P08473-1",
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                    "evidence": [
                        {
                            "database": "PubMed",
                            "id": "37074911",
                            "url": "https://glygen.org/publication/PubMed/37074911"
                        },
                        {
                            "database": "PDC",
                            "id": "PDC000471",
                            "url": "https://proteomic.datacommons.cancer.gov/pdc/study/PDC000471"
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                    ],
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                    "chemical_mass": 85514.0
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            ]
        },
        {
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                {
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                    "comment": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-loss (NAT->DAT).",
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                    "chr_pos": "155138234",
                    "evidence": [
                        {
                            "id": "rs1339178202",
                            "database": "dbSNP",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1339178202"
                        },
                        {
                            "id": "rs1339178202",
                            "database": "gnomAD",
                            "url": "http://gnomad.broadinstitute.org/awesome?query=rs1339178202"
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                    ]
                },
                {
                    "weight": 100,
                    "sequence_org": "N",
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                    "comment": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-loss (NAT->IAT).",
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                    "chr_pos": "155138235",
                    "evidence": [
                        {
                            "id": "rs200961860",
                            "database": "dbSNP",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs200961860"
                        },
                        {
                            "id": "rs200961860",
                            "database": "1000Genomes",
                            "url": "https://www.ensembl.org/homo_sapiens/Variation/Explore?v=rs200961860"
                        },
                        {
                            "id": "rs200961860",
                            "database": "ExAC",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs200961860"
                        },
                        {
                            "id": "rs200961860",
                            "database": "TOPMed",
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                        },
                        {
                            "id": "rs200961860",
                            "database": "gnomAD",
                            "url": "http://gnomad.broadinstitute.org/awesome?query=rs200961860"
                        }
                    ]
                },
                {
                    "weight": 100,
                    "sequence_org": "N",
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                    "comment": "Somatic mutation passed 1 out of 6 filters: n-glyco-sequon-loss (NAT->KAT).",
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                    "chr_pos": "155138236",
                    "evidence": [
                        {
                            "id": "P08473",
                            "database": "BioMuta",
                            "url": "https://hivelab.biochemistry.gwu.edu/biomuta/proteinview/P08473"
                        },
                        {
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                            "database": "dbSNP",
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                        },
                        {
                            "id": "rs1434664230",
                            "database": "gnomAD",
                            "url": "http://gnomad.broadinstitute.org/awesome?query=rs1434664230"
                        },
                        {
                            "id": "rs1434664230",
                            "database": "COSMIC",
                            "url": "https://www.ensembl.org/homo_sapiens/Variation/Explore?v=rs1434664230"
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                    ],
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                                {
                                    "id": "1324",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:1324"
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                            ]
                        }
                    ]
                },
                {
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                    "sequence_org": "N",
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                    "comment": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-loss (NAT->SAT).",
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                    "chr_pos": "155138235",
                    "evidence": [
                        {
                            "id": "rs200961860",
                            "database": "dbSNP",
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                        },
                        {
                            "id": "rs200961860",
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                        },
                        {
                            "id": "rs200961860",
                            "database": "ExAC",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs200961860"
                        },
                        {
                            "id": "rs200961860",
                            "database": "TOPMed",
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                        },
                        {
                            "id": "rs200961860",
                            "database": "gnomAD",
                            "url": "http://gnomad.broadinstitute.org/awesome?query=rs200961860"
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                    ],
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                        {
                            "disease_id": "DOID:0110160",
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                            "url": "http://disease-ontology.org/term/DOID:0110160",
                            "evidence": [
                                {
                                    "id": "0110160",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0110160"
                                },
                                {
                                    "id": "0110160",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0110160"
                                }
                            ]
                        },
                        {
                            "disease_id": "DOID:0110160",
                            "name": "Charcot-Marie-Tooth disease axonal type 2T",
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                            "url": "http://disease-ontology.org/term/DOID:0110160",
                            "evidence": [
                                {
                                    "id": "0110160",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0110160"
                                },
                                {
                                    "id": "0110160",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0110160"
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                            ]
                        },
                        {
                            "disease_id": "DOID:0110160",
                            "name": "Charcot-Marie-Tooth disease axonal type 2T",
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                            "evidence": [
                                {
                                    "id": "0110160",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0110160"
                                },
                                {
                                    "id": "0110160",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0110160"
                                }
                            ]
                        },
                        {
                            "disease_id": "DOID:0110160",
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                            "evidence": [
                                {
                                    "id": "0110160",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0110160"
                                },
                                {
                                    "id": "0110160",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0110160"
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                            ]
                        },
                        {
                            "disease_id": "DOID:0110160",
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                                {
                                    "id": "0110160",
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                                },
                                {
                                    "id": "0110160",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0110160"
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                            ]
                        },
                        {
                            "disease_id": "DOID:0111745",
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                            "evidence": [
                                {
                                    "id": "0111745",
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                                    "url": "https://www.alliancegenome.org/disease/DOID:0111745"
                                },
                                {
                                    "id": "0111745",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0111745"
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                            ]
                        },
                        {
                            "disease_id": "DOID:0111745",
                            "name": "cerebellar ataxia type 43",
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                            "evidence": [
                                {
                                    "id": "0111745",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0111745"
                                },
                                {
                                    "id": "0111745",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0111745"
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                            ]
                        },
                        {
                            "disease_id": "DOID:0111745",
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                                {
                                    "id": "0111745",
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                                    "url": "https://www.alliancegenome.org/disease/DOID:0111745"
                                },
                                {
                                    "id": "0111745",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0111745"
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                            ]
                        },
                        {
                            "disease_id": "DOID:0111745",
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                            "evidence": [
                                {
                                    "id": "0111745",
                                    "database": "AGR",
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                                },
                                {
                                    "id": "0111745",
                                    "database": "AGR",
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                            ]
                        },
                        {
                            "disease_id": "DOID:0111745",
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                                {
                                    "id": "0111745",
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                                    "url": "https://www.alliancegenome.org/disease/DOID:0111745"
                                },
                                {
                                    "id": "0111745",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0111745"
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                }
            ],
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                        {
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                    ],
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            ]
        },
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                    "gene_name": "LAMB2",
                    "tax_id": 9606,
                    "tax_name": "Homo sapiens",
                    "tax_common_name": "Human",
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                    "chemical_mass": 195981.0
                }
            ]
        },
        {
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                {
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                        },
                        {
                            "database": "PDC",
                            "id": "PDC000471",
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                    ],
                    "protein_name": "Laminin subunit beta-2",
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            ]
        },
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                        {
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                    ],
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            ]
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                        {
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                    ],
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            ]
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                        {
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                    ],
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            ]
        },
        {
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                        {
                            "id": "rs1459957730",
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                        },
                        {
                            "id": "rs1459957730",
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                        }
                    ]
                },
                {
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                        {
                            "id": "rs1459957730",
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                        },
                        {
                            "id": "rs1459957730",
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                    ]
                },
                {
                    "weight": 100,
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                    "comment": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-loss (NTS->ITS).",
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                    "chr_pos": "49123313",
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                        {
                            "id": "rs771215576",
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                        },
                        {
                            "id": "rs771215576",
                            "database": "ExAC",
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                        {
                            "id": "rs771215576",
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                        },
                        {
                            "id": "rs771215576",
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                    ]
                },
                {
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                    "comment": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-loss (NTS->STS).",
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                        {
                            "id": "rs771215576",
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                        },
                        {
                            "id": "rs771215576",
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                        },
                        {
                            "id": "rs771215576",
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                        },
                        {
                            "id": "rs771215576",
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                    ],
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                            "url": "http://disease-ontology.org/term/DOID:0080380",
                            "evidence": [
                                {
                                    "id": "0080380",
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                                    "url": "https://www.alliancegenome.org/disease/DOID:0080380"
                                },
                                {
                                    "id": "0080380",
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                            ]
                        },
                        {
                            "disease_id": "DOID:0080380",
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                                {
                                    "id": "0080380",
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                                    "url": "https://www.alliancegenome.org/disease/DOID:0080380"
                                },
                                {
                                    "id": "0080380",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0080380"
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                            ]
                        },
                        {
                            "disease_id": "DOID:0080380",
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                                {
                                    "id": "0080380",
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                                    "url": "https://www.alliancegenome.org/disease/DOID:0080380"
                                },
                                {
                                    "id": "0080380",
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                                    "url": "https://www.alliancegenome.org/disease/DOID:0080380"
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                            ]
                        },
                        {
                            "disease_id": "DOID:0080380",
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                                {
                                    "id": "0080380",
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                                },
                                {
                                    "id": "0080380",
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                                    "url": "https://www.alliancegenome.org/disease/DOID:0080380"
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                            ]
                        },
                        {
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                                {
                                    "id": "0060852",
                                    "database": "AGR",
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                            ]
                        },
                        {
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                                    "id": "0060852",
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                            ]
                        },
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                                {
                                    "id": "0060852",
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                            ]
                        },
                        {
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        },
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                        {
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        },
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                    ],
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            ]
        },
        {
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                        {
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                    ]
                },
                {
                    "weight": 100,
                    "sequence_org": "N",
                    "sequence_mut": "K",
                    "comment": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-loss (NGS->KGS).",
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                    "chr_pos": "186617302",
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                        {
                            "id": "rs770113523",
                            "database": "dbSNP",
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                        {
                            "id": "rs770113523",
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                    ]
                },
                {
                    "weight": 100,
                    "sequence_org": "N",
                    "sequence_mut": "S",
                    "comment": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-loss (NGS->SGS).",
                    "chr_id": "3",
                    "chr_pos": "186617301",
                    "evidence": [
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                            "id": "rs556158119",
                            "database": "dbSNP",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs556158119"
                        },
                        {
                            "id": "rs556158119",
                            "database": "1000Genomes",
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                        },
                        {
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                            "id": "rs2124243120",
                            "database": "dbSNP",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs2124243120"
                        }
                    ]
                }
            ],
            "glycoprotein": [
                {
                    "uniprot_canonical_ac": "P21810-1",
                    "start_pos": 311,
                    "end_pos": 311,
                    "residue": "Asn",
                    "evidence": [
                        {
                            "database": "PubMed",
                            "id": "37074911",
                            "url": "https://glygen.org/publication/PubMed/37074911"
                        },
                        {
                            "database": "PDC",
                            "id": "PDC000471",
                            "url": "https://proteomic.datacommons.cancer.gov/pdc/study/PDC000471"
                        }
                    ],
                    "protein_name": "Biglycan",
                    "gene_name": "BGN",
                    "tax_id": 9606,
                    "tax_name": "Homo sapiens",
                    "tax_common_name": "Human",
                    "length": 368,
                    "chemical_mass": 41654.0
                }
            ]
        }
    ],
    "record_id": "G02528FI"
}
