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            ]
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                        {
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                        {
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                    "protein_name": "Vascular endothelial growth factor receptor 1",
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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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                        {
                            "database": "PubMed",
                            "id": "37074911",
                            "url": "https://glygen.org/publication/PubMed/37074911"
                        },
                        {
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                            "id": "PDC000471",
                            "url": "https://proteomic.datacommons.cancer.gov/pdc/study/PDC000471"
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                    ],
                    "protein_name": "Vascular endothelial growth factor receptor 1",
                    "gene_name": "FLT1",
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            ]
        },
        {
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                        {
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                            "id": "PDC000471",
                            "url": "https://proteomic.datacommons.cancer.gov/pdc/study/PDC000471"
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                    ],
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                    "gene_name": "FLT1",
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                    "tax_common_name": "Human",
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            ]
        },
        {
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                        {
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                            "url": "https://hivelab.biochemistry.gwu.edu/biomuta/proteinview/P17948"
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                    ],
                    "disease": [
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                                    "database": "AGR",
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                            ]
                        }
                    ]
                },
                {
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                        {
                            "id": "P17948",
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                            "url": "https://hivelab.biochemistry.gwu.edu/biomuta/proteinview/P17948"
                        },
                        {
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                        },
                        {
                            "id": "rs1387615627",
                            "database": "TOPMed",
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                        },
                        {
                            "id": "rs1387615627",
                            "database": "gnomAD",
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                        },
                        {
                            "id": "rs1387615627",
                            "database": "COSMIC",
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                    ],
                    "disease": [
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                                {
                                    "id": "1324",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:1324"
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                            ]
                        }
                    ]
                },
                {
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                    "evidence": [
                        {
                            "id": "rs1290255117",
                            "database": "dbSNP",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1290255117"
                        },
                        {
                            "id": "rs1290255117",
                            "database": "ENSEMBL",
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                    ]
                }
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            ]
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                        {
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                    ],
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                                {
                                    "id": "9256",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:9256"
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                            ]
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                    ]
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                    ],
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            ]
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                        {
                            "id": "rs772751830",
                            "database": "ExAC",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs772751830"
                        },
                        {
                            "id": "rs772751830",
                            "database": "gnomAD",
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                    ]
                },
                {
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                    "sequence_org": "N",
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                    "evidence": [
                        {
                            "id": "rs772751830",
                            "database": "dbSNP",
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                        },
                        {
                            "id": "rs772751830",
                            "database": "ExAC",
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                        },
                        {
                            "id": "rs772751830",
                            "database": "gnomAD",
                            "url": "http://gnomad.broadinstitute.org/awesome?query=rs772751830"
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                    ]
                },
                {
                    "weight": 100,
                    "sequence_org": "N",
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                    "chr_pos": "28433880",
                    "evidence": [
                        {
                            "id": "rs767050810",
                            "database": "dbSNP",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs767050810"
                        },
                        {
                            "id": "rs767050810",
                            "database": "ExAC",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs767050810"
                        },
                        {
                            "id": "rs767050810",
                            "database": "TOPMed",
                            "url": "https://www.ncbi.nlm.nih.gov/snp/rs767050810#frequency_tab"
                        },
                        {
                            "id": "rs767050810",
                            "database": "gnomAD",
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                        },
                        {
                            "id": "rs767050810",
                            "database": "COSMIC",
                            "url": "https://www.ensembl.org/homo_sapiens/Variation/Explore?v=rs767050810"
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                    ]
                },
                {
                    "weight": 100,
                    "sequence_org": "N",
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                        {
                            "id": "rs772751830",
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                        {
                            "id": "rs772751830",
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                        },
                        {
                            "id": "rs772751830",
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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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                {
                    "uniprot_canonical_ac": "P17948-1",
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                    "end_pos": 164,
                    "residue": "Asn",
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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": "Vascular endothelial growth factor receptor 1",
                    "gene_name": "FLT1",
                    "tax_id": 9606,
                    "tax_name": "Homo sapiens",
                    "tax_common_name": "Human",
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                    "chemical_mass": 150769.0
                }
            ]
        },
        {
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            "site_seq": "N",
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            "residue": "Asn",
            "glycoprotein": [
                {
                    "uniprot_canonical_ac": "P17948-1",
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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": "Vascular endothelial growth factor receptor 1",
                    "gene_name": "FLT1",
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                    "tax_name": "Homo sapiens",
                    "tax_common_name": "Human",
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                    "chemical_mass": 150769.0
                }
            ]
        },
        {
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            "site_seq": "GFIISnATYK",
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            "glycoprotein": [
                {
                    "uniprot_canonical_ac": "P17948-1",
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                    "end_pos": 196,
                    "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": "Vascular endothelial growth factor receptor 1",
                    "gene_name": "FLT1",
                    "tax_id": 9606,
                    "tax_name": "Homo sapiens",
                    "tax_common_name": "Human",
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                    "chemical_mass": 150769.0
                }
            ]
        },
        {
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            "residue": "Asn",
            "glycoprotein": [
                {
                    "uniprot_canonical_ac": "P17948-1",
                    "start_pos": 196,
                    "end_pos": 196,
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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": "Vascular endothelial growth factor receptor 1",
                    "gene_name": "FLT1",
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                    "tax_name": "Homo sapiens",
                    "tax_common_name": "Human",
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                    "chemical_mass": 150769.0
                }
            ]
        },
        {
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            "glycoprotein": [
                {
                    "uniprot_canonical_ac": "P17948-1",
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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": "Vascular endothelial growth factor receptor 1",
                    "gene_name": "FLT1",
                    "tax_id": 9606,
                    "tax_name": "Homo sapiens",
                    "tax_common_name": "Human",
                    "length": 1338,
                    "chemical_mass": 150769.0
                }
            ]
        },
        {
            "start_pos": "251",
            "site_seq": "GHTLVLnCTATTPLNTR",
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            "residue": "Asn",
            "glycoprotein": [
                {
                    "uniprot_canonical_ac": "P17948-1",
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                    "end_pos": 251,
                    "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": "Vascular endothelial growth factor receptor 1",
                    "gene_name": "FLT1",
                    "tax_id": 9606,
                    "tax_name": "Homo sapiens",
                    "tax_common_name": "Human",
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                    "chemical_mass": 150769.0
                }
            ]
        },
        {
            "start_pos": "251",
            "site_seq": "N",
            "site_lbl": "Asn251",
            "residue": "Asn",
            "glycoprotein": [
                {
                    "uniprot_canonical_ac": "P17948-1",
                    "start_pos": 251,
                    "end_pos": 251,
                    "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": "Vascular endothelial growth factor receptor 1",
                    "gene_name": "FLT1",
                    "tax_id": 9606,
                    "tax_name": "Homo sapiens",
                    "tax_common_name": "Human",
                    "length": 1338,
                    "chemical_mass": 150769.0
                }
            ]
        },
        {
            "start_pos": "251",
            "site_seq": "GHTLVLNCTATTPLNTR",
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            "glycoprotein": [
                {
                    "uniprot_canonical_ac": "P17948-1",
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                    "end_pos": 251,
                    "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": "Vascular endothelial growth factor receptor 1",
                    "gene_name": "FLT1",
                    "tax_id": 9606,
                    "tax_name": "Homo sapiens",
                    "tax_common_name": "Human",
                    "length": 1338,
                    "chemical_mass": 150769.0
                }
            ]
        },
        {
            "start_pos": "164",
            "site_seq": "",
            "site_lbl": "N164",
            "residue": "",
            "snv": [
                {
                    "weight": 100,
                    "sequence_org": "N",
                    "sequence_mut": "I",
                    "comment": "Somatic mutation passed 1 out of 6 filters: n-glyco-sequon-loss (NIT->IIT).",
                    "chr_id": "13",
                    "chr_pos": "28438243",
                    "evidence": [
                        {
                            "id": "P17948",
                            "database": "BioMuta",
                            "url": "https://hivelab.biochemistry.gwu.edu/biomuta/proteinview/P17948"
                        }
                    ],
                    "disease": [
                        {
                            "disease_id": "DOID:363",
                            "name": "uterine cancer",
                            "description": "A female reproductive organ cancer that is located_in the uterus.",
                            "url": "http://disease-ontology.org/term/DOID:363",
                            "evidence": [
                                {
                                    "id": "363",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:363"
                                }
                            ]
                        }
                    ]
                },
                {
                    "weight": 100,
                    "sequence_org": "N",
                    "sequence_mut": "K",
                    "comment": "Somatic mutation passed 1 out of 6 filters: n-glyco-sequon-loss (NIT->KIT).",
                    "chr_id": "13",
                    "chr_pos": "28438242",
                    "evidence": [
                        {
                            "id": "P17948",
                            "database": "BioMuta",
                            "url": "https://hivelab.biochemistry.gwu.edu/biomuta/proteinview/P17948"
                        },
                        {
                            "id": "rs1387615627",
                            "database": "dbSNP",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1387615627"
                        },
                        {
                            "id": "rs1387615627",
                            "database": "TOPMed",
                            "url": "https://www.ncbi.nlm.nih.gov/snp/rs1387615627#frequency_tab"
                        },
                        {
                            "id": "rs1387615627",
                            "database": "gnomAD",
                            "url": "http://gnomad.broadinstitute.org/awesome?query=rs1387615627"
                        },
                        {
                            "id": "rs1387615627",
                            "database": "COSMIC",
                            "url": "https://www.ensembl.org/homo_sapiens/Variation/Explore?v=rs1387615627"
                        }
                    ],
                    "disease": [
                        {
                            "disease_id": "DOID:1324",
                            "name": "lung cancer",
                            "description": "A respiratory system cancer that is located_in the lung.",
                            "url": "http://disease-ontology.org/term/DOID:1324",
                            "evidence": [
                                {
                                    "id": "1324",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:1324"
                                }
                            ]
                        }
                    ]
                },
                {
                    "weight": 100,
                    "sequence_org": "N",
                    "sequence_mut": "S",
                    "comment": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-loss (NIT->SIT).",
                    "chr_id": "13",
                    "chr_pos": "28438243",
                    "evidence": [
                        {
                            "id": "rs1290255117",
                            "database": "dbSNP",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1290255117"
                        },
                        {
                            "id": "rs1290255117",
                            "database": "ENSEMBL",
                            "url": "https://www.ensembl.org/id/rs1290255117"
                        }
                    ]
                }
            ],
            "glycoprotein": [
                {
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                        {
                            "database": "PubMed",
                            "id": "37074911",
                            "url": "https://glygen.org/publication/PubMed/37074911"
                        },
                        {
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                    ],
                    "protein_name": "Vascular endothelial growth factor receptor 1",
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                    "tax_common_name": "Human",
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                    "chemical_mass": 150769.0
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            ]
        },
        {
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            "residue": "",
            "snv": [
                {
                    "weight": 100,
                    "sequence_org": "N",
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                    "chr_pos": "28434148",
                    "evidence": [
                        {
                            "id": "P17948",
                            "database": "BioMuta",
                            "url": "https://hivelab.biochemistry.gwu.edu/biomuta/proteinview/P17948"
                        }
                    ],
                    "disease": [
                        {
                            "disease_id": "DOID:9256",
                            "name": "colorectal cancer",
                            "description": "A large intestine cancer that is located_in the colon and/or located_in the rectum.",
                            "url": "http://disease-ontology.org/term/DOID:9256",
                            "evidence": [
                                {
                                    "id": "9256",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:9256"
                                }
                            ]
                        }
                    ]
                }
            ],
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                {
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                        {
                            "database": "PubMed",
                            "id": "37074911",
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                        },
                        {
                            "database": "PDC",
                            "id": "PDC000471",
                            "url": "https://proteomic.datacommons.cancer.gov/pdc/study/PDC000471"
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                    ],
                    "protein_name": "Vascular endothelial growth factor receptor 1",
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                    "tax_common_name": "Human",
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                    "chemical_mass": 150769.0
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            ]
        },
        {
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            "residue": "",
            "snv": [
                {
                    "weight": 100,
                    "sequence_org": "N",
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                    "chr_pos": "28433881",
                    "evidence": [
                        {
                            "id": "rs772751830",
                            "database": "dbSNP",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs772751830"
                        },
                        {
                            "id": "rs772751830",
                            "database": "ExAC",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs772751830"
                        },
                        {
                            "id": "rs772751830",
                            "database": "gnomAD",
                            "url": "http://gnomad.broadinstitute.org/awesome?query=rs772751830"
                        }
                    ]
                },
                {
                    "weight": 100,
                    "sequence_org": "N",
                    "sequence_mut": "H",
                    "comment": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-loss (NCT->HCT).",
                    "chr_id": "13",
                    "chr_pos": "28433881",
                    "evidence": [
                        {
                            "id": "rs772751830",
                            "database": "dbSNP",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs772751830"
                        },
                        {
                            "id": "rs772751830",
                            "database": "ExAC",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs772751830"
                        },
                        {
                            "id": "rs772751830",
                            "database": "gnomAD",
                            "url": "http://gnomad.broadinstitute.org/awesome?query=rs772751830"
                        }
                    ]
                },
                {
                    "weight": 100,
                    "sequence_org": "N",
                    "sequence_mut": "S",
                    "comment": "Somatic mutation passed 1 out of 1 filters: n-glyco-sequon-loss (NCT->SCT).",
                    "chr_id": "13",
                    "chr_pos": "28433880",
                    "evidence": [
                        {
                            "id": "rs767050810",
                            "database": "dbSNP",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs767050810"
                        },
                        {
                            "id": "rs767050810",
                            "database": "ExAC",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs767050810"
                        },
                        {
                            "id": "rs767050810",
                            "database": "TOPMed",
                            "url": "https://www.ncbi.nlm.nih.gov/snp/rs767050810#frequency_tab"
                        },
                        {
                            "id": "rs767050810",
                            "database": "gnomAD",
                            "url": "http://gnomad.broadinstitute.org/awesome?query=rs767050810"
                        },
                        {
                            "id": "rs767050810",
                            "database": "COSMIC",
                            "url": "https://www.ensembl.org/homo_sapiens/Variation/Explore?v=rs767050810"
                        }
                    ]
                },
                {
                    "weight": 100,
                    "sequence_org": "N",
                    "sequence_mut": "Y",
                    "comment": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-loss (NCT->YCT).",
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                    "chr_pos": "28433881",
                    "evidence": [
                        {
                            "id": "rs772751830",
                            "database": "dbSNP",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs772751830"
                        },
                        {
                            "id": "rs772751830",
                            "database": "ExAC",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs772751830"
                        },
                        {
                            "id": "rs772751830",
                            "database": "gnomAD",
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                    ]
                }
            ],
            "glycoprotein": [
                {
                    "uniprot_canonical_ac": "P17948-1",
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                    "evidence": [
                        {
                            "database": "PubMed",
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                            "url": "https://glygen.org/publication/PubMed/37074911"
                        },
                        {
                            "database": "PDC",
                            "id": "PDC000471",
                            "url": "https://proteomic.datacommons.cancer.gov/pdc/study/PDC000471"
                        }
                    ],
                    "protein_name": "Vascular endothelial growth factor receptor 1",
                    "gene_name": "FLT1",
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                    "tax_common_name": "Human",
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            ]
        },
        {
            "start_pos": "599",
            "site_seq": "EVnDTLLVNELK",
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            "residue": "Asn",
            "glycoprotein": [
                {
                    "uniprot_canonical_ac": "Q15063-1",
                    "start_pos": 599,
                    "end_pos": 599,
                    "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": "Periostin",
                    "gene_name": "POSTN",
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                    "tax_name": "Homo sapiens",
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                    "chemical_mass": 93314.0
                }
            ]
        },
        {
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            "site_seq": "N",
            "site_lbl": "Asn599",
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            "glycoprotein": [
                {
                    "uniprot_canonical_ac": "Q15063-1",
                    "start_pos": 599,
                    "end_pos": 599,
                    "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": "Periostin",
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                    "tax_common_name": "Human",
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                    "chemical_mass": 93314.0
                }
            ]
        },
        {
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            "site_lbl": "Asn599",
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            "glycoprotein": [
                {
                    "uniprot_canonical_ac": "Q15063-1",
                    "start_pos": 599,
                    "end_pos": 599,
                    "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": "Periostin",
                    "gene_name": "POSTN",
                    "tax_id": 9606,
                    "tax_name": "Homo sapiens",
                    "tax_common_name": "Human",
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                }
            ]
        },
        {
            "start_pos": "599",
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            "glycoprotein": [
                {
                    "uniprot_canonical_ac": "Q15063-1",
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                    "end_pos": 599,
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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": "Periostin",
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            ]
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                            ]
                        },
                        {
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                            "name": "metachromatic leukodystrophy",
                            "description": "A sphingolipidosis characterized by the accumulation of sulfatides in cells, especially the myelin producing cells of the nervous system.",
                            "url": "http://disease-ontology.org/term/DOID:10581",
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                                {
                                    "id": "10581",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:10581"
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                            ]
                        },
                        {
                            "disease_id": "DOID:10581",
                            "name": "metachromatic leukodystrophy",
                            "description": "A sphingolipidosis characterized by the accumulation of sulfatides in cells, especially the myelin producing cells of the nervous system.",
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                            "evidence": [
                                {
                                    "id": "10581",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:10581"
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                            ]
                        },
                        {
                            "disease_id": "DOID:10581",
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                            "description": "A sphingolipidosis characterized by the accumulation of sulfatides in cells, especially the myelin producing cells of the nervous system.",
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                                {
                                    "id": "10581",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:10581"
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                            ]
                        },
                        {
                            "disease_id": "DOID:10581",
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                                {
                                    "id": "10581",
                                    "database": "AGR",
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                        {
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                                {
                                    "id": "10581",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:10581"
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                            ]
                        },
                        {
                            "disease_id": "DOID:10581",
                            "name": "metachromatic leukodystrophy",
                            "description": "A sphingolipidosis characterized by the accumulation of sulfatides in cells, especially the myelin producing cells of the nervous system.",
                            "url": "http://disease-ontology.org/term/DOID:10581",
                            "evidence": [
                                {
                                    "id": "10581",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:10581"
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                            ]
                        },
                        {
                            "disease_id": "DOID:10581",
                            "name": "metachromatic leukodystrophy",
                            "description": "A sphingolipidosis characterized by the accumulation of sulfatides in cells, especially the myelin producing cells of the nervous system.",
                            "url": "http://disease-ontology.org/term/DOID:10581",
                            "evidence": [
                                {
                                    "id": "10581",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:10581"
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                            ]
                        },
                        {
                            "disease_id": "DOID:10581",
                            "name": "metachromatic leukodystrophy",
                            "description": "A sphingolipidosis characterized by the accumulation of sulfatides in cells, especially the myelin producing cells of the nervous system.",
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                            "evidence": [
                                {
                                    "id": "10581",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:10581"
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                            ]
                        },
                        {
                            "disease_id": "DOID:10581",
                            "name": "metachromatic leukodystrophy",
                            "description": "A sphingolipidosis characterized by the accumulation of sulfatides in cells, especially the myelin producing cells of the nervous system.",
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                            "evidence": [
                                {
                                    "id": "10581",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:10581"
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                            ]
                        },
                        {
                            "disease_id": "DOID:10581",
                            "name": "metachromatic leukodystrophy",
                            "description": "A sphingolipidosis characterized by the accumulation of sulfatides in cells, especially the myelin producing cells of the nervous system.",
                            "url": "http://disease-ontology.org/term/DOID:10581",
                            "evidence": [
                                {
                                    "id": "10581",
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                        {
                            "id": "rs770171865",
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                        {
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                        {
                            "id": "rs770171865",
                            "database": "gnomAD",
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                    ],
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                            "url": "http://disease-ontology.org/term/DOID:0111330",
                            "evidence": [
                                {
                                    "id": "0111330",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0111330"
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                            ]
                        },
                        {
                            "disease_id": "DOID:0111330",
                            "name": "combined saposin deficiency",
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                            "url": "http://disease-ontology.org/term/DOID:0111330",
                            "evidence": [
                                {
                                    "id": "0111330",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0111330"
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                            ]
                        },
                        {
                            "disease_id": "DOID:0111330",
                            "name": "combined saposin deficiency",
                            "description": "A sphingolipidosis characterized by absence of expression of both isoforms of PSAP (SAP1 and SAP2) resulting in hepatosplenomegaly and severe neurological disease that has_material_basis_in homozygous or compound heterozygous mutation in PSAP on 10q22.1.",
                            "url": "http://disease-ontology.org/term/DOID:0111330",
                            "evidence": [
                                {
                                    "id": "0111330",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0111330"
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                            ]
                        },
                        {
                            "disease_id": "DOID:0110961",
                            "name": "atypical Gaucher's disease due to saposin c deficiency",
                            "description": "A Gaucher's disease that has_material_basis_in compound heterozygous mutation in the PSAP gene on chromosome 10q22.1.",
                            "url": "http://disease-ontology.org/term/DOID:0110961",
                            "evidence": [
                                {
                                    "id": "0110961",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0110961"
                                },
                                {
                                    "id": "0110961",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0110961"
                                }
                            ]
                        },
                        {
                            "disease_id": "DOID:0110961",
                            "name": "atypical Gaucher's disease due to saposin c deficiency",
                            "description": "A Gaucher's disease that has_material_basis_in compound heterozygous mutation in the PSAP gene on chromosome 10q22.1.",
                            "url": "http://disease-ontology.org/term/DOID:0110961",
                            "evidence": [
                                {
                                    "id": "0110961",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0110961"
                                },
                                {
                                    "id": "0110961",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0110961"
                                }
                            ]
                        },
                        {
                            "disease_id": "DOID:0110961",
                            "name": "atypical Gaucher's disease due to saposin c deficiency",
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                            "url": "http://disease-ontology.org/term/DOID:0110961",
                            "evidence": [
                                {
                                    "id": "0110961",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0110961"
                                },
                                {
                                    "id": "0110961",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0110961"
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                            ]
                        },
                        {
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                            "description": "A sphingolipidosis characterized by the accumulation of sulfatides in cells, especially the myelin producing cells of the nervous system.",
                            "url": "http://disease-ontology.org/term/DOID:10581",
                            "evidence": [
                                {
                                    "id": "10581",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:10581"
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                            ]
                        },
                        {
                            "disease_id": "DOID:10581",
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                            "evidence": [
                                {
                                    "id": "10581",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:10581"
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                            ]
                        },
                        {
                            "disease_id": "DOID:10581",
                            "name": "metachromatic leukodystrophy",
                            "description": "A sphingolipidosis characterized by the accumulation of sulfatides in cells, especially the myelin producing cells of the nervous system.",
                            "url": "http://disease-ontology.org/term/DOID:10581",
                            "evidence": [
                                {
                                    "id": "10581",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:10581"
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                            ]
                        },
                        {
                            "disease_id": "DOID:10581",
                            "name": "metachromatic leukodystrophy",
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                            "url": "http://disease-ontology.org/term/DOID:10581",
                            "evidence": [
                                {
                                    "id": "10581",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:10581"
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                            ]
                        },
                        {
                            "disease_id": "DOID:10581",
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                                {
                                    "id": "10581",
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                            ]
                        },
                        {
                            "disease_id": "DOID:10581",
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                                {
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                            ]
                        },
                        {
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                                {
                                    "id": "10581",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:10581"
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                            ]
                        },
                        {
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                            "evidence": [
                                {
                                    "id": "10581",
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                                    "url": "https://www.alliancegenome.org/disease/DOID:10581"
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                            ]
                        },
                        {
                            "disease_id": "DOID:10581",
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                            "description": "A sphingolipidosis characterized by the accumulation of sulfatides in cells, especially the myelin producing cells of the nervous system.",
                            "url": "http://disease-ontology.org/term/DOID:10581",
                            "evidence": [
                                {
                                    "id": "10581",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:10581"
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                            ]
                        }
                    ]
                }
            ],
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                {
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                        {
                            "database": "PDC",
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                    ],
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                    "chemical_mass": 58113.0
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            ]
        },
        {
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                    "chr_pos": "71820249",
                    "evidence": [
                        {
                            "id": "rs546727182",
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                        {
                            "id": "rs546727182",
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                        },
                        {
                            "id": "rs546727182",
                            "database": "ExAC",
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                        },
                        {
                            "id": "rs546727182",
                            "database": "TOPMed",
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                        },
                        {
                            "id": "rs546727182",
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                    ]
                },
                {
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                    "sequence_org": "N",
                    "sequence_mut": "null",
                    "comment": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-loss (NKT->nullKT).",
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                    "chr_pos": "71820248TGT",
                    "evidence": [
                        {
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                            "database": "dbSNP",
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                                    "id": "10581",
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                    ],
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                        {
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                        {
                            "id": "rs1842525967",
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                    ]
                },
                {
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                    "comment": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-loss (NAT->SAT).",
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                    "evidence": [
                        {
                            "id": "rs570654892",
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                        {
                            "id": "rs570654892",
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                        {
                            "id": "rs570654892",
                            "database": "ExAC",
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                        {
                            "id": "rs570654892",
                            "database": "TOPMed",
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                        {
                            "id": "rs570654892",
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                            "description": "A sphingolipidosis characterized by the accumulation of sulfatides in cells, especially the myelin producing cells of the nervous system.",
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                            "evidence": [
                                {
                                    "id": "10581",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:10581"
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                            ]
                        },
                        {
                            "disease_id": "DOID:10581",
                            "name": "metachromatic leukodystrophy",
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                                {
                                    "id": "10581",
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                            ]
                        },
                        {
                            "disease_id": "DOID:10581",
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                            ]
                        },
                        {
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                        },
                        {
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                    "chemical_mass": 521958.0
                }
            ]
        },
        {
            "start_pos": "3315",
            "site_seq": "MLAQHCVDANNTFCFDNPR",
            "site_lbl": "Asn3315",
            "residue": "Asn",
            "glycoprotein": [
                {
                    "uniprot_canonical_ac": "P98164-1",
                    "start_pos": 3315,
                    "end_pos": 3315,
                    "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": "Low-density lipoprotein receptor-related protein 2",
                    "gene_name": "LRP2",
                    "tax_id": 9606,
                    "tax_name": "Homo sapiens",
                    "tax_common_name": "Human",
                    "length": 4655,
                    "chemical_mass": 521958.0
                }
            ]
        },
        {
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            "site_seq": "N",
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            "glycoprotein": [
                {
                    "uniprot_canonical_ac": "P98164-1",
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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": "Low-density lipoprotein receptor-related protein 2",
                    "gene_name": "LRP2",
                    "tax_id": 9606,
                    "tax_name": "Homo sapiens",
                    "tax_common_name": "Human",
                    "length": 4655,
                    "chemical_mass": 521958.0
                }
            ]
        },
        {
            "start_pos": "866",
            "site_seq": "AWSDGSHLLPVInTTLGWPNGLAIDWAASR",
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            "glycoprotein": [
                {
                    "uniprot_canonical_ac": "P98164-1",
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                    "end_pos": 866,
                    "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": "Low-density lipoprotein receptor-related protein 2",
                    "gene_name": "LRP2",
                    "tax_id": 9606,
                    "tax_name": "Homo sapiens",
                    "tax_common_name": "Human",
                    "length": 4655,
                    "chemical_mass": 521958.0
                }
            ]
        },
        {
            "start_pos": "866",
            "site_seq": "N",
            "site_lbl": "Asn866",
            "residue": "Asn",
            "glycoprotein": [
                {
                    "uniprot_canonical_ac": "P98164-1",
                    "start_pos": 866,
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                    "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": "Low-density lipoprotein receptor-related protein 2",
                    "gene_name": "LRP2",
                    "tax_id": 9606,
                    "tax_name": "Homo sapiens",
                    "tax_common_name": "Human",
                    "length": 4655,
                    "chemical_mass": 521958.0
                }
            ]
        },
        {
            "start_pos": "1144",
            "site_seq": "",
            "site_lbl": "N1144",
            "residue": "",
            "snv": [
                {
                    "weight": 100,
                    "sequence_org": "N",
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                    "comment": "Somatic mutation passed 1 out of 6 filters: n-glyco-sequon-loss (NST->SST); n-glyco-sequon-gain (NCN->NCS).",
                    "chr_id": "2",
                    "chr_pos": "169243522",
                    "evidence": [
                        {
                            "id": "P98164",
                            "database": "BioMuta",
                            "url": "https://hivelab.biochemistry.gwu.edu/biomuta/proteinview/P98164"
                        }
                    ],
                    "disease": [
                        {
                            "disease_id": "DOID:4159",
                            "name": "skin cancer",
                            "description": "An integumentary system cancer located_in the skin that is the uncontrolled growth of abnormal skin cells.",
                            "url": "http://disease-ontology.org/term/DOID:4159",
                            "evidence": [
                                {
                                    "id": "4159",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:4159"
                                }
                            ]
                        }
                    ]
                },
                {
                    "weight": 100,
                    "sequence_org": "N",
                    "sequence_mut": "D",
                    "comment": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-loss (NST->DST).",
                    "chr_id": "2",
                    "chr_pos": "169244693",
                    "evidence": [
                        {
                            "id": "rs1689938007",
                            "database": "dbSNP",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1689938007"
                        },
                        {
                            "id": "rs1689938007",
                            "database": "ENSEMBL",
                            "url": "https://www.ensembl.org/id/rs1689938007"
                        }
                    ]
                }
            ],
            "glycoprotein": [
                {
                    "uniprot_canonical_ac": "P98164-1",
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                    "end_pos": 1144,
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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": "Low-density lipoprotein receptor-related protein 2",
                    "gene_name": "LRP2",
                    "tax_id": 9606,
                    "tax_name": "Homo sapiens",
                    "tax_common_name": "Human",
                    "length": 4655,
                    "chemical_mass": 521958.0
                }
            ]
        },
        {
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            "site_seq": "",
            "site_lbl": "N2499",
            "residue": "",
            "snv": [
                {
                    "weight": 100,
                    "sequence_org": "N",
                    "sequence_mut": "D",
                    "comment": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-loss (NRT->DRT).",
                    "chr_id": "2",
                    "chr_pos": "169206084",
                    "evidence": [
                        {
                            "id": "rs1688374769",
                            "database": "dbSNP",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1688374769"
                        },
                        {
                            "id": "rs1688374769",
                            "database": "ENSEMBL",
                            "url": "https://www.ensembl.org/id/rs1688374769"
                        }
                    ]
                },
                {
                    "weight": 100,
                    "sequence_org": "N",
                    "sequence_mut": "K",
                    "comment": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-loss (NRT->KRT).",
                    "chr_id": "2",
                    "chr_pos": "169206082",
                    "evidence": [
                        {
                            "id": "rs764422443",
                            "database": "dbSNP",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs764422443"
                        },
                        {
                            "id": "rs764422443",
                            "database": "ExAC",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs764422443"
                        },
                        {
                            "id": "rs764422443",
                            "database": "TOPMed",
                            "url": "https://www.ncbi.nlm.nih.gov/snp/rs764422443#frequency_tab"
                        },
                        {
                            "id": "rs764422443",
                            "database": "gnomAD",
                            "url": "http://gnomad.broadinstitute.org/awesome?query=rs764422443"
                        }
                    ]
                },
                {
                    "weight": 100,
                    "sequence_org": "N",
                    "sequence_mut": "T",
                    "comment": "Somatic mutation passed 1 out of 6 filters: n-glyco-sequon-loss (NRT->TRT).",
                    "chr_id": "2",
                    "chr_pos": "169206083",
                    "evidence": [
                        {
                            "id": "P98164",
                            "database": "BioMuta",
                            "url": "https://hivelab.biochemistry.gwu.edu/biomuta/proteinview/P98164"
                        }
                    ],
                    "disease": [
                        {
                            "disease_id": "DOID:5041",
                            "name": "esophageal cancer",
                            "description": "A gastrointestinal system cancer that is located_in the esophagus.",
                            "url": "http://disease-ontology.org/term/DOID:5041",
                            "evidence": [
                                {
                                    "id": "5041",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:5041"
                                }
                            ]
                        },
                        {
                            "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": [
                {
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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": "Low-density lipoprotein receptor-related protein 2",
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                    "tax_common_name": "Human",
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                    "chemical_mass": 521958.0
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            ]
        },
        {
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            "residue": "",
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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 (NNT->HNT).",
                    "chr_id": "2",
                    "chr_pos": "169201655",
                    "evidence": [
                        {
                            "id": "rs768363457",
                            "database": "dbSNP",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs768363457"
                        },
                        {
                            "id": "rs768363457",
                            "database": "ExAC",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs768363457"
                        },
                        {
                            "id": "rs768363457",
                            "database": "gnomAD",
                            "url": "http://gnomad.broadinstitute.org/awesome?query=rs768363457"
                        }
                    ]
                },
                {
                    "weight": 100,
                    "sequence_org": "N",
                    "sequence_mut": "S",
                    "comment": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-loss (NNT->SNT).",
                    "chr_id": "2",
                    "chr_pos": "169201654",
                    "evidence": [
                        {
                            "id": "rs191087468",
                            "database": "dbSNP",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs191087468"
                        },
                        {
                            "id": "rs191087468",
                            "database": "1000Genomes",
                            "url": "https://www.ensembl.org/homo_sapiens/Variation/Explore?v=rs191087468"
                        },
                        {
                            "id": "rs191087468",
                            "database": "TOPMed",
                            "url": "https://www.ncbi.nlm.nih.gov/snp/rs191087468#frequency_tab"
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                    ]
                }
            ],
            "glycoprotein": [
                {
                    "uniprot_canonical_ac": "P98164-1",
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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"
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                    ],
                    "protein_name": "Low-density lipoprotein receptor-related protein 2",
                    "gene_name": "LRP2",
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            ]
        },
        {
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            "snv": [
                {
                    "weight": 100,
                    "sequence_org": "N",
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                    "chr_pos": "169182222",
                    "evidence": [
                        {
                            "id": "rs2545747867",
                            "database": "dbSNP",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs2545747867"
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                    ]
                },
                {
                    "weight": 100,
                    "sequence_org": "N",
                    "sequence_mut": "K",
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                    "chr_pos": "169182220",
                    "evidence": [
                        {
                            "id": "rs201808907",
                            "database": "dbSNP",
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                        },
                        {
                            "id": "rs201808907",
                            "database": "ExAC",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs201808907"
                        },
                        {
                            "id": "rs201808907",
                            "database": "TOPMed",
                            "url": "https://www.ncbi.nlm.nih.gov/snp/rs201808907#frequency_tab"
                        },
                        {
                            "id": "rs201808907",
                            "database": "gnomAD",
                            "url": "http://gnomad.broadinstitute.org/awesome?query=rs201808907"
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                    ],
                    "disease": [
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                            "url": "http://disease-ontology.org/term/DOID:0090144",
                            "evidence": [
                                {
                                    "id": "222448",
                                    "database": "MIM",
                                    "url": "https://www.omim.org/entry/222448"
                                },
                                {
                                    "id": "0090144",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0090144"
                                }
                            ]
                        },
                        {
                            "disease_id": "DOID:0090144",
                            "name": "Donnai-Barrow syndrome",
                            "description": "A syndrome that is characterized by facial and ocular abnormalities, sensorineural hearing loss, agenesis of the corpus callosum, variable intellectual disability, and proteinuria that has_material_basis_in homozygous or compound heterozygous mutation in the LDL receptor related protein 2 gene (LRP2) on chromosome 2q31.",
                            "url": "http://disease-ontology.org/term/DOID:0090144",
                            "evidence": [
                                {
                                    "id": "222448",
                                    "database": "MIM",
                                    "url": "https://www.omim.org/entry/222448"
                                },
                                {
                                    "id": "0090144",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0090144"
                                }
                            ]
                        },
                        {
                            "disease_id": "DOID:0090144",
                            "name": "Donnai-Barrow syndrome",
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                            "url": "http://disease-ontology.org/term/DOID:0090144",
                            "evidence": [
                                {
                                    "id": "222448",
                                    "database": "MIM",
                                    "url": "https://www.omim.org/entry/222448"
                                },
                                {
                                    "id": "0090144",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0090144"
                                }
                            ]
                        },
                        {
                            "disease_id": "DOID:0090144",
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                            "evidence": [
                                {
                                    "id": "222448",
                                    "database": "MIM",
                                    "url": "https://www.omim.org/entry/222448"
                                },
                                {
                                    "id": "0090144",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0090144"
                                }
                            ]
                        }
                    ]
                },
                {
                    "weight": 100,
                    "sequence_org": "N",
                    "sequence_mut": "S",
                    "comment": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-loss (NNT->SNT).",
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                    "chr_pos": "169182221",
                    "evidence": [
                        {
                            "id": "rs772442505",
                            "database": "dbSNP",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs772442505"
                        },
                        {
                            "id": "rs772442505",
                            "database": "ExAC",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs772442505"
                        },
                        {
                            "id": "rs772442505",
                            "database": "TOPMed",
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                        },
                        {
                            "id": "rs772442505",
                            "database": "gnomAD",
                            "url": "http://gnomad.broadinstitute.org/awesome?query=rs772442505"
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                    ]
                }
            ],
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                        {
                            "database": "PubMed",
                            "id": "37074911",
                            "url": "https://glygen.org/publication/PubMed/37074911"
                        },
                        {
                            "database": "PDC",
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                            "url": "https://proteomic.datacommons.cancer.gov/pdc/study/PDC000471"
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                    ],
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                    "chemical_mass": 521958.0
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            ]
        },
        {
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                        {
                            "database": "PubMed",
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                            "url": "https://glygen.org/publication/PubMed/37074911"
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                        {
                            "database": "PDC",
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                    ],
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                    "chemical_mass": 521958.0
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            ]
        },
        {
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                            "database": "PubMed",
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                        },
                        {
                            "database": "PDC",
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                            "url": "https://proteomic.datacommons.cancer.gov/pdc/study/PDC000471"
                        }
                    ],
                    "protein_name": "Low-density lipoprotein receptor-related protein 2",
                    "gene_name": "LRP2",
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                    "tax_name": "Homo sapiens",
                    "tax_common_name": "Human",
                    "length": 4655,
                    "chemical_mass": 521958.0
                }
            ]
        },
        {
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            ]
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                        {
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            ]
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                        {
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                            "id": "PDC000471",
                            "url": "https://proteomic.datacommons.cancer.gov/pdc/study/PDC000471"
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                    "tax_name": "Homo sapiens",
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                }
            ]
        },
        {
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                {
                    "uniprot_canonical_ac": "P98164-1",
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                        {
                            "database": "PubMed",
                            "id": "37074911",
                            "url": "https://glygen.org/publication/PubMed/37074911"
                        },
                        {
                            "database": "PDC",
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                    ],
                    "protein_name": "Low-density lipoprotein receptor-related protein 2",
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                    "tax_name": "Homo sapiens",
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                }
            ]
        },
        {
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                {
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                        {
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                        },
                        {
                            "database": "PDC",
                            "id": "PDC000471",
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                    ],
                    "protein_name": "Low-density lipoprotein receptor-related protein 2",
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                    "chemical_mass": 521958.0
                }
            ]
        },
        {
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                {
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                        {
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                        {
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                    ],
                    "protein_name": "Low-density lipoprotein receptor-related protein 2",
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                    "tax_name": "Homo sapiens",
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            ]
        },
        {
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                {
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                        {
                            "database": "PubMed",
                            "id": "37074911",
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                        {
                            "database": "PDC",
                            "id": "PDC000471",
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                    ],
                    "protein_name": "Low-density lipoprotein receptor-related protein 2",
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            ]
        },
        {
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                {
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                        {
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                            "id": "37074911",
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                        {
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                    ],
                    "protein_name": "Low-density lipoprotein receptor-related protein 2",
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            ]
        },
        {
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                {
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                        {
                            "database": "PubMed",
                            "id": "37074911",
                            "url": "https://glygen.org/publication/PubMed/37074911"
                        },
                        {
                            "database": "PDC",
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                    ],
                    "protein_name": "Low-density lipoprotein receptor-related protein 2",
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                    "chemical_mass": 521958.0
                }
            ]
        },
        {
            "start_pos": "866",
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                {
                    "uniprot_canonical_ac": "P98164-1",
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                        {
                            "database": "PubMed",
                            "id": "37074911",
                            "url": "https://glygen.org/publication/PubMed/37074911"
                        },
                        {
                            "database": "PDC",
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                    ],
                    "protein_name": "Low-density lipoprotein receptor-related protein 2",
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            ]
        },
        {
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                {
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                        {
                            "database": "PubMed",
                            "id": "37074911",
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                        },
                        {
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                    ],
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            ]
        },
        {
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                {
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                        {
                            "id": "P98164",
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                    ],
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                                {
                                    "id": "4159",
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                                    "url": "https://www.alliancegenome.org/disease/DOID:4159"
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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 (NST->DST).",
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                    "chr_pos": "169244693",
                    "evidence": [
                        {
                            "id": "rs1689938007",
                            "database": "dbSNP",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1689938007"
                        },
                        {
                            "id": "rs1689938007",
                            "database": "ENSEMBL",
                            "url": "https://www.ensembl.org/id/rs1689938007"
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                    ]
                }
            ],
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                {
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                        {
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                            "url": "https://glygen.org/publication/PubMed/37074911"
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                        {
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                    ],
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            ]
        },
        {
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                {
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                        {
                            "id": "rs1688374769",
                            "database": "dbSNP",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1688374769"
                        },
                        {
                            "id": "rs1688374769",
                            "database": "ENSEMBL",
                            "url": "https://www.ensembl.org/id/rs1688374769"
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                    ]
                },
                {
                    "weight": 100,
                    "sequence_org": "N",
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                    "evidence": [
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                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs764422443"
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                        {
                            "id": "rs764422443",
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                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs764422443"
                        },
                        {
                            "id": "rs764422443",
                            "database": "TOPMed",
                            "url": "https://www.ncbi.nlm.nih.gov/snp/rs764422443#frequency_tab"
                        },
                        {
                            "id": "rs764422443",
                            "database": "gnomAD",
                            "url": "http://gnomad.broadinstitute.org/awesome?query=rs764422443"
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                    ]
                },
                {
                    "weight": 100,
                    "sequence_org": "N",
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                    "comment": "Somatic mutation passed 1 out of 6 filters: n-glyco-sequon-loss (NRT->TRT).",
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                    "chr_pos": "169206083",
                    "evidence": [
                        {
                            "id": "P98164",
                            "database": "BioMuta",
                            "url": "https://hivelab.biochemistry.gwu.edu/biomuta/proteinview/P98164"
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                    ],
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                                {
                                    "id": "5041",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:5041"
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                            ]
                        },
                        {
                            "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"
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                            ]
                        }
                    ]
                }
            ],
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                            "database": "PubMed",
                            "id": "37074911",
                            "url": "https://glygen.org/publication/PubMed/37074911"
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                            "id": "PDC000471",
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                            "evidence": [
                                {
                                    "id": "0112297",
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                                    "url": "https://www.alliancegenome.org/disease/DOID:0112297"
                                },
                                {
                                    "id": "0112297",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0112297"
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                            ]
                        },
                        {
                            "disease_id": "DOID:0112297",
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                            "evidence": [
                                {
                                    "id": "0112297",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0112297"
                                },
                                {
                                    "id": "0112297",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0112297"
                                }
                            ]
                        },
                        {
                            "disease_id": "DOID:0112297",
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                            "evidence": [
                                {
                                    "id": "0112297",
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                                    "url": "https://www.alliancegenome.org/disease/DOID:0112297"
                                },
                                {
                                    "id": "0112297",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0112297"
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                            ]
                        },
                        {
                            "disease_id": "DOID:0112297",
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                            "evidence": [
                                {
                                    "id": "0112297",
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                                    "url": "https://www.alliancegenome.org/disease/DOID:0112297"
                                },
                                {
                                    "id": "0112297",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0112297"
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                            ]
                        },
                        {
                            "disease_id": "DOID:0112297",
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                                {
                                    "id": "0112297",
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                                    "url": "https://www.alliancegenome.org/disease/DOID:0112297"
                                },
                                {
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                                    "url": "https://www.alliancegenome.org/disease/DOID:0112297"
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                            ]
                        }
                    ]
                },
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                        {
                            "id": "rs768650910",
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                        {
                            "id": "rs768650910",
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                        {
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                        {
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            ]
        },
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                        {
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                        },
                        {
                            "id": "rs749189506",
                            "database": "ExAC",
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                        },
                        {
                            "id": "rs749189506",
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                    ]
                },
                {
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                        {
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                        {
                            "id": "rs138144264",
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                        {
                            "id": "rs138144264",
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                    ]
                },
                {
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                    "sequence_org": "N",
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                            "id": "rs576328100",
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                        {
                            "id": "rs576328100",
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                        {
                            "id": "rs576328100",
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                        {
                            "id": "rs576328100",
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            ]
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                        {
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            ]
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                                {
                                    "id": "363",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:363"
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                        {
                            "id": "rs1294027053",
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            ]
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                {
                    "weight": 100,
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                            ]
                        },
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                            "disease_id": "DOID:0060573",
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                        {
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                        },
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                        {
                            "id": "rs1450907470",
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            ]
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                    ]
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}
