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                        {
                            "database": "PDC",
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                    ],
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                    "gene_name": "LRP1",
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                    "tax_name": "Homo sapiens",
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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": "dbSNP",
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                        {
                            "id": "rs1565715511",
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                    ]
                },
                {
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                        {
                            "id": "rs2035343652",
                            "database": "TOPMed",
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                    ]
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                        {
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            ]
        },
        {
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                    ],
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                                {
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                            ]
                        }
                    ]
                },
                {
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                        }
                    ],
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                                {
                                    "id": "10283",
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                            ]
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                    ]
                }
            ],
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                        {
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                        },
                        {
                            "id": "rs1592653640",
                            "database": "gnomAD",
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                    ]
                },
                {
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                        {
                            "id": "rs758377934",
                            "database": "ExAC",
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                        {
                            "id": "rs758377934",
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                        {
                            "id": "rs758377934",
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                        {
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                    ]
                },
                {
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                        {
                            "id": "rs758377934",
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                        {
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                        {
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                        {
                            "id": "rs1800687134",
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                    ]
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                    "tax_name": "Homo sapiens",
                    "tax_common_name": "Human",
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                    "chemical_mass": 52495.0
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            ]
        },
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                {
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                        {
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                        {
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                        {
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                            "id": "PDC000471",
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                        {
                            "id": "rs1800687134",
                            "database": "ENSEMBL",
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                    ]
                }
            ],
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                        {
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                        {
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            ]
        },
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                        {
                            "id": "rs1313161587",
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            ]
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                                {
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                                {
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            ]
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            ]
        },
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                        {
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            ]
        },
        {
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                        {
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                            "id": "PDC000471",
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            ]
        },
        {
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                {
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                    "chr_pos": "89805181",
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                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs2141810244"
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                        {
                            "id": "rs2141810244",
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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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                    ],
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            ]
        },
        {
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                {
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                    "comment": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-loss (NVT->SVT); n-glyco-sequon-gain (NLN->NLS).",
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                    "chr_pos": "89799505",
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                            "database": "dbSNP",
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                        {
                            "id": "rs1567158374",
                            "database": "ENSEMBL",
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                    ]
                },
                {
                    "weight": 100,
                    "sequence_org": "N",
                    "sequence_mut": "H",
                    "comment": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-loss (NVT->HVT).",
                    "chr_id": "15",
                    "chr_pos": "89799506",
                    "evidence": [
                        {
                            "id": "rs1894541807",
                            "database": "dbSNP",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1894541807"
                        },
                        {
                            "id": "rs1894541807",
                            "database": "gnomAD",
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                    ]
                }
            ],
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                {
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                        {
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                        },
                        {
                            "database": "PDC",
                            "id": "PDC000471",
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                    ],
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            ]
        },
        {
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                {
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                    "chr_pos": "89805376",
                    "evidence": [
                        {
                            "id": "rs1338821581",
                            "database": "dbSNP",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1338821581"
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                        {
                            "id": "rs1338821581",
                            "database": "gnomAD",
                            "url": "http://gnomad.broadinstitute.org/awesome?query=rs1338821581"
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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 (NIT->SIT).",
                    "chr_id": "15",
                    "chr_pos": "89805377",
                    "evidence": [
                        {
                            "id": "rs1173509041",
                            "database": "dbSNP",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1173509041"
                        },
                        {
                            "id": "rs1173509041",
                            "database": "TOPMed",
                            "url": "https://www.ncbi.nlm.nih.gov/snp/rs1173509041#frequency_tab"
                        },
                        {
                            "id": "rs1173509041",
                            "database": "gnomAD",
                            "url": "http://gnomad.broadinstitute.org/awesome?query=rs1173509041"
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                    ]
                }
            ],
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                        {
                            "database": "PubMed",
                            "id": "37074911",
                            "url": "https://glygen.org/publication/PubMed/37074911"
                        },
                        {
                            "database": "PDC",
                            "id": "PDC000471",
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                    ],
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                {
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                    "chr_pos": "89792235",
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                        {
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                            "database": "dbSNP",
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                        {
                            "id": "rs1968642413",
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                    ]
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                        {
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                        {
                            "database": "UniProtKB",
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                        {
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                        {
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        {
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            ]
        },
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            ]
        },
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            ]
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                        {
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                        {
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                    ],
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                        {
                            "id": "rs781323112",
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                    ]
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            ]
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                        {
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                        {
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                        {
                            "id": "rs748430953",
                            "database": "gnomAD",
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                },
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                        {
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                        {
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                                {
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                        {
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                        {
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                        {
                            "id": "rs748430953",
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                },
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                }
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                {
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                        {
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                        {
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                        {
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                        {
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                        {
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            ]
        },
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        },
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                        {
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                },
                {
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                        {
                            "id": "rs747142179",
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                        {
                            "id": "rs747142179",
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                    ]
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                        {
                            "id": "rs747142179",
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                        {
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            ],
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                        {
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                        {
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                                },
                                {
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                        },
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                                {
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                        },
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                                },
                                {
                                    "id": "0090144",
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                        {
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                        {
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                                {
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                            ]
                        },
                        {
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                            "name": "stomach cancer",
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                                {
                                    "id": "10534",
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                                    "url": "https://www.alliancegenome.org/disease/DOID:10534"
                                },
                                {
                                    "id": "10534",
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                        {
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                        {
                            "id": "rs747432317",
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                },
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                        {
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                        {
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                                {
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                            ]
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                                {
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                        },
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                                {
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                                {
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                        {
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                        {
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            "start_pos": "3446",
            "site_seq": "QTLVnTTHRPFDIHVYHPYR",
            "site_lbl": "Asn3446",
            "residue": "Asn",
            "glycoprotein": [
                {
                    "uniprot_canonical_ac": "P98164-1",
                    "start_pos": 3446,
                    "end_pos": 3446,
                    "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": "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": "3446",
            "site_seq": "QTLVNTTHR",
            "site_lbl": "Asn3446",
            "residue": "Asn",
            "glycoprotein": [
                {
                    "uniprot_canonical_ac": "P98164-1",
                    "start_pos": 3446,
                    "end_pos": 3446,
                    "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": "3446",
            "site_seq": "N",
            "site_lbl": "Asn3446",
            "residue": "Asn",
            "glycoprotein": [
                {
                    "uniprot_canonical_ac": "P98164-1",
                    "start_pos": 3446,
                    "end_pos": 3446,
                    "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": "388",
            "site_seq": "AnDSFGEASIIFSNGR",
            "site_lbl": "Asn388",
            "residue": "Asn",
            "glycoprotein": [
                {
                    "uniprot_canonical_ac": "P98164-1",
                    "start_pos": 388,
                    "end_pos": 388,
                    "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": "388",
            "site_seq": "ANDSFGEASIIFSNGR",
            "site_lbl": "Asn388",
            "residue": "Asn",
            "glycoprotein": [
                {
                    "uniprot_canonical_ac": "P98164-1",
                    "start_pos": 388,
                    "end_pos": 388,
                    "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": "388",
            "site_seq": "N",
            "site_lbl": "Asn388",
            "residue": "Asn",
            "glycoprotein": [
                {
                    "uniprot_canonical_ac": "P98164-1",
                    "start_pos": 388,
                    "end_pos": 388,
                    "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",
                    "sequence_mut": "S",
                    "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",
                    "start_pos": 1144,
                    "end_pos": 1144,
                    "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": "1383",
            "site_seq": "",
            "site_lbl": "N1383",
            "residue": "",
            "snv": [
                {
                    "weight": 100,
                    "sequence_org": "N",
                    "sequence_mut": "D",
                    "comment": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-loss (NDS->DDS).",
                    "chr_id": "2",
                    "chr_pos": "169239674",
                    "evidence": [
                        {
                            "id": "rs1689734706",
                            "database": "dbSNP",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1689734706"
                        },
                        {
                            "id": "rs1689734706",
                            "database": "TOPMed",
                            "url": "https://www.ncbi.nlm.nih.gov/snp/rs1689734706#frequency_tab"
                        }
                    ]
                },
                {
                    "weight": 100,
                    "sequence_org": "N",
                    "sequence_mut": "I",
                    "comment": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-loss (NDS->IDS).",
                    "chr_id": "2",
                    "chr_pos": "169239673",
                    "evidence": [
                        {
                            "id": "rs747142179",
                            "database": "dbSNP",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs747142179"
                        },
                        {
                            "id": "rs747142179",
                            "database": "ExAC",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs747142179"
                        },
                        {
                            "id": "rs747142179",
                            "database": "gnomAD",
                            "url": "http://gnomad.broadinstitute.org/awesome?query=rs747142179"
                        }
                    ]
                },
                {
                    "weight": 100,
                    "sequence_org": "N",
                    "sequence_mut": "S",
                    "comment": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-loss (NDS->SDS).",
                    "chr_id": "2",
                    "chr_pos": "169239673",
                    "evidence": [
                        {
                            "id": "rs747142179",
                            "database": "dbSNP",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs747142179"
                        },
                        {
                            "id": "rs747142179",
                            "database": "ExAC",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs747142179"
                        },
                        {
                            "id": "rs747142179",
                            "database": "gnomAD",
                            "url": "http://gnomad.broadinstitute.org/awesome?query=rs747142179"
                        }
                    ]
                }
            ],
            "glycoprotein": [
                {
                    "uniprot_canonical_ac": "P98164-1",
                    "start_pos": 1383,
                    "end_pos": 1383,
                    "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": "2224",
            "site_seq": "",
            "site_lbl": "N2224",
            "residue": "",
            "snv": [
                {
                    "weight": 100,
                    "sequence_org": "N",
                    "sequence_mut": "S",
                    "comment": "Somatic mutation passed 1 out of 6 filters: n-glyco-sequon-loss (NRT->SRT).",
                    "chr_id": "2",
                    "chr_pos": "169207049",
                    "evidence": [
                        {
                            "id": "P98164",
                            "database": "BioMuta",
                            "url": "https://hivelab.biochemistry.gwu.edu/biomuta/proteinview/P98164"
                        },
                        {
                            "id": "rs957137487",
                            "database": "dbSNP",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs957137487"
                        },
                        {
                            "id": "rs957137487",
                            "database": "TOPMed",
                            "url": "https://www.ncbi.nlm.nih.gov/snp/rs957137487#frequency_tab"
                        },
                        {
                            "id": "rs957137487",
                            "database": "gnomAD",
                            "url": "http://gnomad.broadinstitute.org/awesome?query=rs957137487"
                        }
                    ],
                    "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"
                                }
                            ]
                        },
                        {
                            "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",
                            "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",
                            "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"
                                }
                            ]
                        }
                    ]
                }
            ],
            "glycoprotein": [
                {
                    "uniprot_canonical_ac": "P98164-1",
                    "start_pos": 2224,
                    "end_pos": 2224,
                    "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": "2499",
            "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": [
                {
                    "uniprot_canonical_ac": "P98164-1",
                    "start_pos": 2499,
                    "end_pos": 2499,
                    "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": "2781",
            "site_seq": "",
            "site_lbl": "N2781",
            "residue": "",
            "snv": [
                {
                    "weight": 100,
                    "sequence_org": "N",
                    "sequence_mut": "H",
                    "comment": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-loss (NAT->HAT).",
                    "chr_id": "2",
                    "chr_pos": "169201739",
                    "evidence": [
                        {
                            "id": "rs747432317",
                            "database": "dbSNP",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs747432317"
                        },
                        {
                            "id": "rs747432317",
                            "database": "ExAC",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs747432317"
                        },
                        {
                            "id": "rs747432317",
                            "database": "gnomAD",
                            "url": "http://gnomad.broadinstitute.org/awesome?query=rs747432317"
                        }
                    ]
                },
                {
                    "weight": 100,
                    "sequence_org": "N",
                    "sequence_mut": "S",
                    "comment": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-loss (NAT->SAT).",
                    "chr_id": "2",
                    "chr_pos": "169201738",
                    "evidence": [
                        {
                            "id": "rs1054438192",
                            "database": "dbSNP",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1054438192"
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            ]
        },
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                        {
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            ]
        },
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                        {
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                    ],
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                    ]
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                        {
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                    ],
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                        {
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                        {
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                        {
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                        {
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                        {
                            "id": "rs369440863",
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                    ],
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                        {
                            "id": "rs1267934922",
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                        {
                            "id": "rs1267934922",
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                    ],
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                        {
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            ]
        },
        {
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                        {
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            ]
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                        {
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            ]
        },
        {
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                        {
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            ]
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                        {
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            ]
        },
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                        {
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                },
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                },
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                        {
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                        {
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                        {
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                },
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                        {
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                    ],
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                                {
                                    "id": "13382",
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                                    "url": "https://www.alliancegenome.org/disease/DOID:13382"
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                            ]
                        },
                        {
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                            ]
                        },
                        {
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                                {
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                                    "url": "https://www.alliancegenome.org/disease/DOID:13382"
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                            ]
                        },
                        {
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                            ]
                        },
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                            ]
                        }
                    ]
                },
                {
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                    "comment": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-loss (NAS->TAS).",
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                        {
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                        {
                            "id": "rs569527072",
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                        {
                            "id": "rs569527072",
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                        },
                        {
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                        {
                            "database": "PDC",
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            ]
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                        {
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                },
                {
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                            "database": "TOPMed",
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                        {
                            "id": "rs1236634546",
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                        {
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                            "database": "dbSNP",
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                        {
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                                {
                                    "id": "3571",
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                    ]
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                        {
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                        {
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                        {
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                    ],
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                        {
                            "id": "rs142424994",
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                            "id": "rs142424994",
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                        {
                            "id": "rs142424994",
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        },
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                        {
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            ]
        },
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                {
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                        {
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            ]
        },
        {
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                {
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                        {
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            ]
        },
        {
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                        {
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                        {
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            ]
        },
        {
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            ]
        },
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                        {
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            ]
        },
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                        {
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            ]
        },
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                        {
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                    ]
                }
            ],
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                        {
                            "id": "rs763542055",
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                        {
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                        {
                            "id": "rs763542055",
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                    ]
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            ],
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                        {
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                            "id": "27958302",
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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": "Q8TCC7-1",
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                        {
                            "database": "PubMed",
                            "id": "37074911",
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                        {
                            "database": "PDC",
                            "id": "PDC000471",
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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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            "site_seq": "EHEGAIYPDNTTDFQR",
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                {
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                    "end_pos": 138,
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                        {
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                            "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": "Ceruloplasmin",
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                    "tax_id": 9606,
                    "tax_name": "Homo sapiens",
                    "tax_common_name": "Human",
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                    "chemical_mass": 122219.0
                }
            ]
        },
        {
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                {
                    "uniprot_canonical_ac": "P00450-1",
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                        {
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                            "id": "37074911",
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                        {
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                    ],
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                    "tax_name": "Homo sapiens",
                    "tax_common_name": "Human",
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                    "chemical_mass": 122219.0
                }
            ]
        },
        {
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                {
                    "uniprot_canonical_ac": "P00450-1",
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                    "evidence": [
                        {
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                            "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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                    ],
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                    "tax_common_name": "Human",
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                    "chemical_mass": 122219.0
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            ]
        },
        {
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                {
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                        {
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                    ],
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                    "chemical_mass": 122219.0
                }
            ]
        },
        {
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                    "chr_pos": "149210360",
                    "evidence": [
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                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs757785679"
                        },
                        {
                            "id": "rs757785679",
                            "database": "ExAC",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs757785679"
                        },
                        {
                            "id": "rs757785679",
                            "database": "TOPMed",
                            "url": "https://www.ncbi.nlm.nih.gov/snp/rs757785679#frequency_tab"
                        },
                        {
                            "id": "rs757785679",
                            "database": "gnomAD",
                            "url": "http://gnomad.broadinstitute.org/awesome?query=rs757785679"
                        }
                    ]
                }
            ],
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                {
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                        {
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                            "id": "37074911",
                            "url": "https://glygen.org/publication/PubMed/37074911"
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                        {
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                            "id": "PDC000471",
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                    ],
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            ]
        },
        {
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                {
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                            "url": "https://hivelab.biochemistry.gwu.edu/biomuta/proteinview/P00450"
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                        {
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                        {
                            "id": "rs1576737229",
                            "database": "ENSEMBL",
                            "url": "https://www.ensembl.org/id/rs1576737229"
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                    ],
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                            "description": "An endocrine gland cancer located in the thyroid gland located in the neck below the thyroid cartilage.",
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                            "evidence": [
                                {
                                    "id": "1781",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:1781"
                                }
                            ]
                        }
                    ]
                },
                {
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                    "comment": "Somatic mutation passed 1 out of 6 filters: n-glyco-sequon-loss (NVS->TVS).",
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                    ],
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                                {
                                    "id": "1612",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:1612"
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                            ]
                        }
                    ]
                }
            ],
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                    ],
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            ]
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            ]
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        {
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                    ],
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        {
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            ]
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            ]
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            ]
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        {
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            ]
        },
        {
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                    ],
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            ]
        },
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                    ],
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                        {
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                    "chemical_mass": 58113.0
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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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                    "protein_name": "Prosaposin",
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                    "tax_name": "Homo sapiens",
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                    "chemical_mass": 58113.0
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            ]
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        {
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                        {
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            ]
        },
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                            "id": "37074911",
                            "url": "https://glygen.org/publication/PubMed/37074911"
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                        {
                            "database": "PDC",
                            "id": "PDC000471",
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                    ],
                    "protein_name": "Prosaposin",
                    "gene_name": "PSAP",
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                    "tax_name": "Homo sapiens",
                    "tax_common_name": "Human",
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                    "chemical_mass": 58113.0
                }
            ]
        },
        {
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            "glycoprotein": [
                {
                    "uniprot_canonical_ac": "P07602-1",
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                    "evidence": [
                        {
                            "database": "PubMed",
                            "id": "37074911",
                            "url": "https://glygen.org/publication/PubMed/37074911"
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                        {
                            "database": "PDC",
                            "id": "PDC000471",
                            "url": "https://proteomic.datacommons.cancer.gov/pdc/study/PDC000471"
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                    ],
                    "protein_name": "Prosaposin",
                    "gene_name": "PSAP",
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                    "tax_name": "Homo sapiens",
                    "tax_common_name": "Human",
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                    "chemical_mass": 58113.0
                }
            ]
        },
        {
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                {
                    "uniprot_canonical_ac": "P07602-1",
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                    "evidence": [
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                            "database": "PubMed",
                            "id": "37074911",
                            "url": "https://glygen.org/publication/PubMed/37074911"
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                        {
                            "database": "PDC",
                            "id": "PDC000471",
                            "url": "https://proteomic.datacommons.cancer.gov/pdc/study/PDC000471"
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                    ],
                    "protein_name": "Prosaposin",
                    "gene_name": "PSAP",
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                    "chemical_mass": 58113.0
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            ]
        },
        {
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                        {
                            "database": "PDC",
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                    ],
                    "protein_name": "Prosaposin",
                    "gene_name": "PSAP",
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                    "tax_name": "Homo sapiens",
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            ]
        },
        {
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                        {
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                    ],
                    "protein_name": "Prosaposin",
                    "gene_name": "PSAP",
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                    "tax_common_name": "Human",
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            ]
        },
        {
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                {
                    "uniprot_canonical_ac": "P07602-1",
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                        {
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                    ],
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            ]
        },
        {
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                        {
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                    ],
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                                {
                                    "id": "4159",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:4159"
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                            ]
                        }
                    ]
                },
                {
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                    "sequence_org": "N",
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                    "evidence": [
                        {
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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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                        {
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                    ],
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            ]
        },
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                    "chr_pos": "71820249",
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                            "id": "rs546727182",
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                        {
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                        {
                            "id": "rs546727182",
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                        {
                            "id": "rs546727182",
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                        },
                        {
                            "id": "rs546727182",
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                    ]
                },
                {
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                    "sequence_org": "N",
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                        {
                            "id": "rs751974432",
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                    ],
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                    ],
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            ]
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                {
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                            "id": "rs1842525967",
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                        {
                            "id": "rs1842525967",
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                    ]
                },
                {
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                    "sequence_org": "N",
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                        {
                            "id": "rs570654892",
                            "database": "dbSNP",
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                        {
                            "id": "rs570654892",
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                        {
                            "id": "rs570654892",
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                        },
                        {
                            "id": "rs570654892",
                            "database": "TOPMed",
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                        },
                        {
                            "id": "rs570654892",
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                    ],
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                                {
                                    "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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                            "evidence": [
                                {
                                    "id": "10581",
                                    "database": "AGR",
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                            ]
                        },
                        {
                            "disease_id": "DOID:10581",
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                            ]
                        },
                        {
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                        },
                        {
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                            ]
                        },
                        {
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                        },
                        {
                            "disease_id": "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",
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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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                                {
                                    "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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                                {
                                    "id": "10581",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:10581"
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                    ],
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                    "tax_name": "Homo sapiens",
                    "tax_common_name": "Human",
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            ]
        },
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                        {
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                            "id": "PDC000471",
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                    ],
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                    "tax_name": "Homo sapiens",
                    "tax_common_name": "Human",
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                    "chemical_mass": 58113.0
                }
            ]
        },
        {
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                {
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                            "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": "Prosaposin",
                    "gene_name": "PSAP",
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                    "tax_name": "Homo sapiens",
                    "tax_common_name": "Human",
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                    "chemical_mass": 58113.0
                }
            ]
        },
        {
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                            "url": "https://glygen.org/publication/PubMed/37074911"
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                        {
                            "database": "PDC",
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                    "gene_name": "PSAP",
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                    "tax_common_name": "Human",
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                    "chemical_mass": 58113.0
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            ]
        },
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                            "id": "37074911",
                            "url": "https://glygen.org/publication/PubMed/37074911"
                        },
                        {
                            "database": "PDC",
                            "id": "PDC000471",
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                    ],
                    "protein_name": "Prosaposin",
                    "gene_name": "PSAP",
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                    "tax_name": "Homo sapiens",
                    "tax_common_name": "Human",
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                    "chemical_mass": 58113.0
                }
            ]
        },
        {
            "start_pos": "332",
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            "glycoprotein": [
                {
                    "uniprot_canonical_ac": "P07602-1",
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                    "end_pos": 332,
                    "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"
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                    ],
                    "protein_name": "Prosaposin",
                    "gene_name": "PSAP",
                    "tax_id": 9606,
                    "tax_name": "Homo sapiens",
                    "tax_common_name": "Human",
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                    "chemical_mass": 58113.0
                }
            ]
        },
        {
            "start_pos": "332",
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            "glycoprotein": [
                {
                    "uniprot_canonical_ac": "P07602-1",
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                    "end_pos": 332,
                    "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": "Prosaposin",
                    "gene_name": "PSAP",
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                    "tax_name": "Homo sapiens",
                    "tax_common_name": "Human",
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                    "chemical_mass": 58113.0
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            ]
        },
        {
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                {
                    "uniprot_canonical_ac": "P07602-1",
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                    "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"
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                    ],
                    "protein_name": "Prosaposin",
                    "gene_name": "PSAP",
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                    "tax_name": "Homo sapiens",
                    "tax_common_name": "Human",
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                    "chemical_mass": 58113.0
                }
            ]
        },
        {
            "start_pos": "80",
            "site_seq": "DnATEEEILVYLEK",
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            "glycoprotein": [
                {
                    "uniprot_canonical_ac": "P07602-1",
                    "start_pos": 80,
                    "end_pos": 80,
                    "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"
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                    ],
                    "protein_name": "Prosaposin",
                    "gene_name": "PSAP",
                    "tax_id": 9606,
                    "tax_name": "Homo sapiens",
                    "tax_common_name": "Human",
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                    "chemical_mass": 58113.0
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            ]
        },
        {
            "start_pos": "80",
            "site_seq": "DVVTAAGDMLKDNATEEEILVYLEK",
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                {
                    "uniprot_canonical_ac": "P07602-1",
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                        {
                            "database": "PubMed",
                            "id": "37074911",
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                        },
                        {
                            "database": "PDC",
                            "id": "PDC000471",
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                    ],
                    "protein_name": "Prosaposin",
                    "gene_name": "PSAP",
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                    "tax_name": "Homo sapiens",
                    "tax_common_name": "Human",
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                    "chemical_mass": 58113.0
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            ]
        },
        {
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                {
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                    "evidence": [
                        {
                            "id": "P07602",
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                    ],
                    "disease": [
                        {
                            "disease_id": "DOID:4159",
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                            "evidence": [
                                {
                                    "id": "4159",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:4159"
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                            ]
                        }
                    ]
                },
                {
                    "weight": 100,
                    "sequence_org": "N",
                    "sequence_mut": "T",
                    "comment": "Somatic mutation passed 1 out of 6 filters: n-glyco-sequon-loss (NMS->TMS).",
                    "chr_id": "10",
                    "chr_pos": "71831199",
                    "evidence": [
                        {
                            "id": "P07602",
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                        }
                    ],
                    "disease": [
                        {
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                            "evidence": [
                                {
                                    "id": "1324",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:1324"
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                            ]
                        }
                    ]
                }
            ],
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                {
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                        {
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                        },
                        {
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                    ],
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                    "tax_common_name": "Human",
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                    "chemical_mass": 58113.0
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            ]
        },
        {
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                {
                    "weight": 100,
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                    "comment": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-loss (NKT->KKT).",
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                    "chr_pos": "71820249",
                    "evidence": [
                        {
                            "id": "rs546727182",
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                        {
                            "id": "rs546727182",
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                        },
                        {
                            "id": "rs546727182",
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                        },
                        {
                            "id": "rs546727182",
                            "database": "TOPMed",
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                        },
                        {
                            "id": "rs546727182",
                            "database": "gnomAD",
                            "url": "http://gnomad.broadinstitute.org/awesome?query=rs546727182"
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                    ]
                },
                {
                    "weight": 100,
                    "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": [
                        {
                            "id": "rs751974432",
                            "database": "dbSNP",
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                    ],
                    "disease": [
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            ],
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                    ],
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            ]
        },
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                {
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                    "chr_pos": "71831857",
                    "evidence": [
                        {
                            "id": "rs1842525967",
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                        },
                        {
                            "id": "rs1842525967",
                            "database": "ENSEMBL",
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                    ]
                },
                {
                    "weight": 100,
                    "sequence_org": "N",
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                    "chr_pos": "71831856",
                    "evidence": [
                        {
                            "id": "rs570654892",
                            "database": "dbSNP",
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                        {
                            "id": "rs570654892",
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                        },
                        {
                            "id": "rs570654892",
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                        },
                        {
                            "id": "rs570654892",
                            "database": "TOPMed",
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                        },
                        {
                            "id": "rs570654892",
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                    ],
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                                {
                                    "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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                                {
                                    "id": "10581",
                                    "database": "AGR",
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                            ]
                        },
                        {
                            "disease_id": "DOID:10581",
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                            ]
                        },
                        {
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                        },
                        {
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                            ]
                        },
                        {
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                            ]
                        },
                        {
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        },
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                        {
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                        {
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                                    "id": "4159",
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                        {
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                        {
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        },
        {
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                    "chr_id": "3",
                    "chr_pos": "167807325",
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                    ],
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                        {
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                            "name": "familial encephalopathy with neuroserpin inclusion bodies",
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                            "url": "http://disease-ontology.org/term/DOID:0050831",
                            "evidence": [
                                {
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                                    "url": "https://www.alliancegenome.org/disease/DOID:0050831"
                                },
                                {
                                    "id": "0050831",
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                                    "url": "https://www.alliancegenome.org/disease/DOID:0050831"
                                }
                            ]
                        },
                        {
                            "disease_id": "DOID:0050831",
                            "name": "familial encephalopathy with neuroserpin inclusion bodies",
                            "description": "A neurodegenerative disease that is characterized by intraneuronal inclusions of mutant neuroserpin resulting in progressive encephalopathy, dementia and seizures and has_material_basis_in a mutation in the SERPINI1 gene inherited in an in autosomal dominant pattern.",
                            "url": "http://disease-ontology.org/term/DOID:0050831",
                            "evidence": [
                                {
                                    "id": "0050831",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0050831"
                                },
                                {
                                    "id": "0050831",
                                    "database": "AGR",
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                                }
                            ]
                        }
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                    "gene_name": "SERPINI1",
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                    "tax_name": "Homo sapiens",
                    "tax_common_name": "Human",
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        {
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                        {
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                        {
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                            "database": "gnomAD",
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                }
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                                    "id": "9256",
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                                    "url": "https://www.alliancegenome.org/disease/DOID:9256"
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                    ]
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        {
            "start_pos": "520",
            "site_seq": "KENSSEICSNNGECVCGQCVCRK",
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            "glycoprotein": [
                {
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                        {
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                            "id": "37074911",
                            "url": "https://glygen.org/publication/PubMed/37074911"
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                        {
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                            "id": "PDC000471",
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                    ],
                    "protein_name": "Integrin beta-1",
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            ]
        },
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                {
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                        {
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                    ],
                    "protein_name": "Integrin beta-1",
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                    "chemical_mass": 88415.0
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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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                    ],
                    "protein_name": "Integrin beta-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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                        },
                        {
                            "id": "rs2094945297",
                            "database": "gnomAD",
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                        {
                            "id": "rs2505884571",
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                    ]
                }
            ],
            "glycoprotein": [
                {
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                        {
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                            "id": "37074911",
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                        {
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                    ],
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            ]
        },
        {
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                {
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            ],
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                        {
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                        {
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            ]
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        {
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                                {
                                    "id": "9256",
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                                    "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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                        {
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                }
            ]
        },
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                    "uniprot_canonical_ac": "Q9BY67-1",
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                        {
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                    "chemical_mass": 48509.0
                }
            ]
        },
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                    "uniprot_canonical_ac": "Q9BY67-1",
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                        {
                            "database": "PDC",
                            "id": "PDC000471",
                            "url": "https://proteomic.datacommons.cancer.gov/pdc/study/PDC000471"
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                    ],
                    "protein_name": "Cell adhesion molecule 1",
                    "gene_name": "CADM1",
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                    "chemical_mass": 48509.0
                }
            ]
        },
        {
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                {
                    "uniprot_canonical_ac": "Q9BY67-1",
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                        {
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                            "id": "37074911",
                            "url": "https://glygen.org/publication/PubMed/37074911"
                        },
                        {
                            "database": "PDC",
                            "id": "PDC000471",
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                    ],
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                    "chemical_mass": 48509.0
                }
            ]
        },
        {
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                {
                    "uniprot_canonical_ac": "Q9BY67-1",
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                        {
                            "database": "PDC",
                            "id": "PDC000471",
                            "url": "https://proteomic.datacommons.cancer.gov/pdc/study/PDC000471"
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                    ],
                    "protein_name": "Cell adhesion molecule 1",
                    "gene_name": "CADM1",
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                    "tax_common_name": "Human",
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            ]
        },
        {
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                        {
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            ]
        },
        {
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                        {
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                        {
                            "database": "PDC",
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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": "Q9BY67-1",
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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": "Cell adhesion molecule 1",
                    "gene_name": "CADM1",
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                    "tax_common_name": "Human",
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            ]
        },
        {
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                {
                    "uniprot_canonical_ac": "Q9BY67-1",
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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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                    "gene_name": "CADM1",
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            ]
        },
        {
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                {
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                    "sequence_org": "N",
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                    "comment": "Somatic mutation passed 1 out of 6 filters: n-glyco-sequon-loss (NFS->HFS).",
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                    "chr_pos": "115238623",
                    "evidence": [
                        {
                            "id": "Q9BY67",
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                            "url": "https://hivelab.biochemistry.gwu.edu/biomuta/proteinview/Q9BY67"
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                    ],
                    "disease": [
                        {
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                                {
                                    "id": "10534",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:10534"
                                },
                                {
                                    "id": "10534",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:10534"
                                }
                            ]
                        },
                        {
                            "disease_id": "DOID:5041",
                            "name": "esophageal cancer",
                            "description": "A gastrointestinal system cancer that is located_in the esophagus.",
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                                {
                                    "id": "5041",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:5041"
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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 (NFS->KFS).",
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                    "evidence": [
                        {
                            "id": "rs1942095521",
                            "database": "dbSNP",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1942095521"
                        },
                        {
                            "id": "rs1942095521",
                            "database": "ENSEMBL",
                            "url": "https://www.ensembl.org/id/rs1942095521"
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                    ]
                },
                {
                    "weight": 100,
                    "sequence_org": "N",
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                        {
                            "id": "Q9BY67",
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                            "url": "https://hivelab.biochemistry.gwu.edu/biomuta/proteinview/Q9BY67"
                        }
                    ],
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                            "disease_id": "DOID:1319",
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                            "description": "A central nervous system cancer that is characterized by the growth of abnormal cells in the tissues of the brain.",
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                                {
                                    "id": "1319",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:1319"
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                            ]
                        }
                    ]
                }
            ],
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                {
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                        {
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                    ],
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            ]
        },
        {
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                {
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                        {
                            "id": "Q9BY67",
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                        }
                    ],
                    "disease": [
                        {
                            "disease_id": "DOID:363",
                            "name": "uterine cancer",
                            "description": "A female reproductive organ cancer that is located_in the uterus.",
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                                {
                                    "id": "363",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:363"
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                            ]
                        }
                    ]
                }
            ],
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                {
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                        {
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                        {
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                    ],
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            ]
        },
        {
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                {
                    "weight": 100,
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                    "comment": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-loss (NKS->DKS).",
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                    "chr_pos": "115240346",
                    "evidence": [
                        {
                            "id": "rs367800520",
                            "database": "dbSNP",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs367800520"
                        },
                        {
                            "id": "rs367800520",
                            "database": "ExAC",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs367800520"
                        },
                        {
                            "id": "rs367800520",
                            "database": "gnomAD",
                            "url": "http://gnomad.broadinstitute.org/awesome?query=rs367800520"
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                    ]
                },
                {
                    "weight": 100,
                    "sequence_org": "N",
                    "sequence_mut": "K",
                    "comment": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-loss (NKS->KKS).",
                    "chr_id": "11",
                    "chr_pos": "115240344",
                    "evidence": [
                        {
                            "id": "rs1335676735",
                            "database": "dbSNP",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1335676735"
                        },
                        {
                            "id": "rs1335676735",
                            "database": "gnomAD",
                            "url": "http://gnomad.broadinstitute.org/awesome?query=rs1335676735"
                        }
                    ]
                },
                {
                    "weight": 100,
                    "sequence_org": "N",
                    "sequence_mut": "S",
                    "comment": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-loss (NKS->SKS).",
                    "chr_id": "11",
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                    "evidence": [
                        {
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                        {
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                        {
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                }
            ]
        },
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                        {
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                            "id": "PDC000471",
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                    "gene_name": "CADM1",
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                }
            ]
        },
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                        {
                            "database": "PDC",
                            "id": "PDC000471",
                            "url": "https://proteomic.datacommons.cancer.gov/pdc/study/PDC000471"
                        }
                    ],
                    "protein_name": "Cell adhesion molecule 1",
                    "gene_name": "CADM1",
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                    "tax_name": "Homo sapiens",
                    "tax_common_name": "Human",
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                    "chemical_mass": 48509.0
                }
            ]
        },
        {
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                {
                    "uniprot_canonical_ac": "Q9BY67-1",
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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": "Cell adhesion molecule 1",
                    "gene_name": "CADM1",
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                    "tax_name": "Homo sapiens",
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                    "chemical_mass": 48509.0
                }
            ]
        },
        {
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                {
                    "uniprot_canonical_ac": "Q9BY67-1",
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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": "Cell adhesion molecule 1",
                    "gene_name": "CADM1",
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                    "tax_name": "Homo sapiens",
                    "tax_common_name": "Human",
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                    "chemical_mass": 48509.0
                }
            ]
        },
        {
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                {
                    "uniprot_canonical_ac": "Q9BY67-1",
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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"
                        }
                    ],
                    "protein_name": "Cell adhesion molecule 1",
                    "gene_name": "CADM1",
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                    "tax_name": "Homo sapiens",
                    "tax_common_name": "Human",
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                    "chemical_mass": 48509.0
                }
            ]
        },
        {
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            "site_seq": "VSLTNVSISDEGR",
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                {
                    "uniprot_canonical_ac": "Q9BY67-1",
                    "start_pos": 113,
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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": "Cell adhesion molecule 1",
                    "gene_name": "CADM1",
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                    "tax_name": "Homo sapiens",
                    "tax_common_name": "Human",
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                    "chemical_mass": 48509.0
                }
            ]
        },
        {
            "start_pos": "67",
            "site_seq": "DVTVIEGEVATISCQVnK",
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                {
                    "uniprot_canonical_ac": "Q9BY67-1",
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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": "Cell adhesion molecule 1",
                    "gene_name": "CADM1",
                    "tax_id": 9606,
                    "tax_name": "Homo sapiens",
                    "tax_common_name": "Human",
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                    "chemical_mass": 48509.0
                }
            ]
        },
        {
            "start_pos": "67",
            "site_seq": "DVTVIEGEVATISCQVNK",
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            "residue": "Asn",
            "glycoprotein": [
                {
                    "uniprot_canonical_ac": "Q9BY67-1",
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                    "evidence": [
                        {
                            "database": "PubMed",
                            "id": "37074911",
                            "url": "https://glygen.org/publication/PubMed/37074911"
                        },
                        {
                            "database": "PDC",
                            "id": "PDC000471",
                            "url": "https://proteomic.datacommons.cancer.gov/pdc/study/PDC000471"
                        }
                    ],
                    "protein_name": "Cell adhesion molecule 1",
                    "gene_name": "CADM1",
                    "tax_id": 9606,
                    "tax_name": "Homo sapiens",
                    "tax_common_name": "Human",
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                    "chemical_mass": 48509.0
                }
            ]
        },
        {
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                {
                    "uniprot_canonical_ac": "Q9BY67-1",
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                    "evidence": [
                        {
                            "database": "PubMed",
                            "id": "37074911",
                            "url": "https://glygen.org/publication/PubMed/37074911"
                        },
                        {
                            "database": "PDC",
                            "id": "PDC000471",
                            "url": "https://proteomic.datacommons.cancer.gov/pdc/study/PDC000471"
                        }
                    ],
                    "protein_name": "Cell adhesion molecule 1",
                    "gene_name": "CADM1",
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                    "tax_name": "Homo sapiens",
                    "tax_common_name": "Human",
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                    "chemical_mass": 48509.0
                }
            ]
        },
        {
            "start_pos": "101",
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            "residue": "",
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                {
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                    "sequence_org": "N",
                    "sequence_mut": "H",
                    "comment": "Somatic mutation passed 1 out of 6 filters: n-glyco-sequon-loss (NFS->HFS).",
                    "chr_id": "11",
                    "chr_pos": "115238623",
                    "evidence": [
                        {
                            "id": "Q9BY67",
                            "database": "BioMuta",
                            "url": "https://hivelab.biochemistry.gwu.edu/biomuta/proteinview/Q9BY67"
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                    ],
                    "disease": [
                        {
                            "disease_id": "DOID:10534",
                            "name": "stomach cancer",
                            "description": "A gastrointestinal system cancer that is located_in the stomach.",
                            "url": "http://disease-ontology.org/term/DOID:10534",
                            "evidence": [
                                {
                                    "id": "10534",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:10534"
                                },
                                {
                                    "id": "10534",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:10534"
                                }
                            ]
                        },
                        {
                            "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"
                                }
                            ]
                        }
                    ]
                },
                {
                    "weight": 100,
                    "sequence_org": "N",
                    "sequence_mut": "K",
                    "comment": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-loss (NFS->KFS).",
                    "chr_id": "11",
                    "chr_pos": "115238621",
                    "evidence": [
                        {
                            "id": "rs1942095521",
                            "database": "dbSNP",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1942095521"
                        },
                        {
                            "id": "rs1942095521",
                            "database": "ENSEMBL",
                            "url": "https://www.ensembl.org/id/rs1942095521"
                        }
                    ]
                },
                {
                    "weight": 100,
                    "sequence_org": "N",
                    "sequence_mut": "S",
                    "comment": "Somatic mutation passed 1 out of 6 filters: n-glyco-sequon-loss (NFS->SFS).",
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                    "chr_pos": "115238622",
                    "evidence": [
                        {
                            "id": "Q9BY67",
                            "database": "BioMuta",
                            "url": "https://hivelab.biochemistry.gwu.edu/biomuta/proteinview/Q9BY67"
                        }
                    ],
                    "disease": [
                        {
                            "disease_id": "DOID:1319",
                            "name": "brain cancer",
                            "description": "A central nervous system cancer that is characterized by the growth of abnormal cells in the tissues of the brain.",
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                            "evidence": [
                                {
                                    "id": "1319",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:1319"
                                }
                            ]
                        }
                    ]
                }
            ],
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                {
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                        {
                            "database": "PubMed",
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                        },
                        {
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                            "url": "https://proteomic.datacommons.cancer.gov/pdc/study/PDC000471"
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                    ],
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                }
            ]
        },
        {
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                {
                    "weight": 100,
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                    "evidence": [
                        {
                            "id": "Q9BY67",
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                            "url": "https://hivelab.biochemistry.gwu.edu/biomuta/proteinview/Q9BY67"
                        }
                    ],
                    "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"
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                            ]
                        }
                    ]
                }
            ],
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                {
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                        {
                            "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": "Cell adhesion molecule 1",
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                }
            ]
        },
        {
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                {
                    "weight": 100,
                    "sequence_org": "N",
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                    "chr_pos": "115240346",
                    "evidence": [
                        {
                            "id": "rs367800520",
                            "database": "dbSNP",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs367800520"
                        },
                        {
                            "id": "rs367800520",
                            "database": "ExAC",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs367800520"
                        },
                        {
                            "id": "rs367800520",
                            "database": "gnomAD",
                            "url": "http://gnomad.broadinstitute.org/awesome?query=rs367800520"
                        }
                    ]
                },
                {
                    "weight": 100,
                    "sequence_org": "N",
                    "sequence_mut": "K",
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                    "chr_id": "11",
                    "chr_pos": "115240344",
                    "evidence": [
                        {
                            "id": "rs1335676735",
                            "database": "dbSNP",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1335676735"
                        },
                        {
                            "id": "rs1335676735",
                            "database": "gnomAD",
                            "url": "http://gnomad.broadinstitute.org/awesome?query=rs1335676735"
                        }
                    ]
                },
                {
                    "weight": 100,
                    "sequence_org": "N",
                    "sequence_mut": "S",
                    "comment": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-loss (NKS->SKS).",
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                    "evidence": [
                        {
                            "id": "rs1179131916",
                            "database": "dbSNP",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1179131916"
                        },
                        {
                            "id": "rs1179131916",
                            "database": "TOPMed",
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                    ]
                }
            ],
            "glycoprotein": [
                {
                    "uniprot_canonical_ac": "Q9BY67-1",
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                        {
                            "database": "PubMed",
                            "id": "37074911",
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                        {
                            "database": "PDC",
                            "id": "PDC000471",
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                    ],
                    "protein_name": "Cell adhesion molecule 1",
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                }
            ]
        },
        {
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                {
                    "uniprot_canonical_ac": "Q8WWB7-1",
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                        {
                            "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"
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                    ],
                    "protein_name": "Glycosylated lysosomal membrane protein",
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                    "chemical_mass": 43864.0
                }
            ]
        },
        {
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                {
                    "uniprot_canonical_ac": "Q8WWB7-1",
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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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                    ],
                    "protein_name": "Glycosylated lysosomal membrane protein",
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                    "chemical_mass": 43864.0
                }
            ]
        },
        {
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                {
                    "uniprot_canonical_ac": "Q8WWB7-1",
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                        {
                            "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": "Glycosylated lysosomal membrane protein",
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                    "chemical_mass": 43864.0
                }
            ]
        },
        {
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                {
                    "uniprot_canonical_ac": "Q8WWB7-1",
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                    "evidence": [
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                        {
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                        {
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                        {
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                        {
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                        {
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                        {
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                        {
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                        {
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            ]
        },
        {
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                        {
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            ]
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                        {
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        },
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                        {
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                        {
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                        {
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                    ]
                },
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                        {
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                        {
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                        {
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                        {
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                },
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                        {
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                        {
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        },
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                                    "url": "https://www.omim.org/entry/614557"
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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": "PDC",
                            "id": "PDC000471",
                            "url": "https://proteomic.datacommons.cancer.gov/pdc/study/PDC000471"
                        }
                    ],
                    "protein_name": "Neprilysin",
                    "gene_name": "MME",
                    "tax_id": 9606,
                    "tax_name": "Homo sapiens",
                    "tax_common_name": "Human",
                    "length": 750,
                    "chemical_mass": 85514.0
                }
            ]
        },
        {
            "start_pos": "145",
            "site_seq": "SCINESAIDSR",
            "site_lbl": "Asn145",
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            "glycoprotein": [
                {
                    "uniprot_canonical_ac": "P08473-1",
                    "start_pos": 145,
                    "end_pos": 145,
                    "residue": "Asn",
                    "evidence": [
                        {
                            "database": "PubMed",
                            "id": "37074911",
                            "url": "https://glygen.org/publication/PubMed/37074911"
                        },
                        {
                            "database": "PDC",
                            "id": "PDC000471",
                            "url": "https://proteomic.datacommons.cancer.gov/pdc/study/PDC000471"
                        }
                    ],
                    "protein_name": "Neprilysin",
                    "gene_name": "MME",
                    "tax_id": 9606,
                    "tax_name": "Homo sapiens",
                    "tax_common_name": "Human",
                    "length": 750,
                    "chemical_mass": 85514.0
                }
            ]
        },
        {
            "start_pos": "285",
            "site_seq": "EIAnATAKPEDRNDPMLLYNK",
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            "residue": "Asn",
            "glycoprotein": [
                {
                    "uniprot_canonical_ac": "P08473-1",
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                    "end_pos": 285,
                    "residue": "Asn",
                    "evidence": [
                        {
                            "database": "PubMed",
                            "id": "37074911",
                            "url": "https://glygen.org/publication/PubMed/37074911"
                        },
                        {
                            "database": "PDC",
                            "id": "PDC000471",
                            "url": "https://proteomic.datacommons.cancer.gov/pdc/study/PDC000471"
                        }
                    ],
                    "protein_name": "Neprilysin",
                    "gene_name": "MME",
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                    "tax_name": "Homo sapiens",
                    "tax_common_name": "Human",
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                    "chemical_mass": 85514.0
                }
            ]
        },
        {
            "start_pos": "285",
            "site_seq": "EIAnATAKPEDR",
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            "glycoprotein": [
                {
                    "uniprot_canonical_ac": "P08473-1",
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                    "residue": "Asn",
                    "evidence": [
                        {
                            "database": "PubMed",
                            "id": "37074911",
                            "url": "https://glygen.org/publication/PubMed/37074911"
                        },
                        {
                            "database": "PDC",
                            "id": "PDC000471",
                            "url": "https://proteomic.datacommons.cancer.gov/pdc/study/PDC000471"
                        }
                    ],
                    "protein_name": "Neprilysin",
                    "gene_name": "MME",
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                    "tax_name": "Homo sapiens",
                    "tax_common_name": "Human",
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                    "chemical_mass": 85514.0
                }
            ]
        },
        {
            "start_pos": "285",
            "site_seq": "EIANATAKPEDR",
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            "glycoprotein": [
                {
                    "uniprot_canonical_ac": "P08473-1",
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                    "end_pos": 285,
                    "residue": "Asn",
                    "evidence": [
                        {
                            "database": "PubMed",
                            "id": "37074911",
                            "url": "https://glygen.org/publication/PubMed/37074911"
                        },
                        {
                            "database": "PDC",
                            "id": "PDC000471",
                            "url": "https://proteomic.datacommons.cancer.gov/pdc/study/PDC000471"
                        }
                    ],
                    "protein_name": "Neprilysin",
                    "gene_name": "MME",
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                    "tax_name": "Homo sapiens",
                    "tax_common_name": "Human",
                    "length": 750,
                    "chemical_mass": 85514.0
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            ]
        },
        {
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            "glycoprotein": [
                {
                    "uniprot_canonical_ac": "P08473-1",
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                    "evidence": [
                        {
                            "database": "PubMed",
                            "id": "37074911",
                            "url": "https://glygen.org/publication/PubMed/37074911"
                        },
                        {
                            "database": "PDC",
                            "id": "PDC000471",
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                    ],
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                    "gene_name": "MME",
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                    "tax_name": "Homo sapiens",
                    "tax_common_name": "Human",
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                    "chemical_mass": 85514.0
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            ]
        },
        {
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            "site_lbl": "N145",
            "residue": "",
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                    "sequence_org": "N",
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                    "comment": "Somatic mutation passed 1 out of 6 filters: n-glyco-sequon-loss (NES->HES).",
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                    "chr_pos": "155116553",
                    "evidence": [
                        {
                            "id": "P08473",
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                            "url": "https://hivelab.biochemistry.gwu.edu/biomuta/proteinview/P08473"
                        }
                    ],
                    "disease": [
                        {
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                            "name": "stomach cancer",
                            "description": "A gastrointestinal system cancer that is located_in the stomach.",
                            "url": "http://disease-ontology.org/term/DOID:10534",
                            "evidence": [
                                {
                                    "id": "10534",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:10534"
                                },
                                {
                                    "id": "10534",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:10534"
                                }
                            ]
                        }
                    ]
                }
            ],
            "glycoprotein": [
                {
                    "uniprot_canonical_ac": "P08473-1",
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                    "end_pos": 145,
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                    "evidence": [
                        {
                            "database": "PubMed",
                            "id": "37074911",
                            "url": "https://glygen.org/publication/PubMed/37074911"
                        },
                        {
                            "database": "PDC",
                            "id": "PDC000471",
                            "url": "https://proteomic.datacommons.cancer.gov/pdc/study/PDC000471"
                        }
                    ],
                    "protein_name": "Neprilysin",
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                    "tax_name": "Homo sapiens",
                    "tax_common_name": "Human",
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                    "chemical_mass": 85514.0
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            ]
        },
        {
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            "site_lbl": "N285",
            "residue": "",
            "snv": [
                {
                    "weight": 100,
                    "sequence_org": "N",
                    "sequence_mut": "D",
                    "comment": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-loss (NAT->DAT).",
                    "chr_id": "3",
                    "chr_pos": "155138234",
                    "evidence": [
                        {
                            "id": "rs1339178202",
                            "database": "dbSNP",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1339178202"
                        },
                        {
                            "id": "rs1339178202",
                            "database": "gnomAD",
                            "url": "http://gnomad.broadinstitute.org/awesome?query=rs1339178202"
                        }
                    ]
                },
                {
                    "weight": 100,
                    "sequence_org": "N",
                    "sequence_mut": "I",
                    "comment": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-loss (NAT->IAT).",
                    "chr_id": "3",
                    "chr_pos": "155138235",
                    "evidence": [
                        {
                            "id": "rs200961860",
                            "database": "dbSNP",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs200961860"
                        },
                        {
                            "id": "rs200961860",
                            "database": "1000Genomes",
                            "url": "https://www.ensembl.org/homo_sapiens/Variation/Explore?v=rs200961860"
                        },
                        {
                            "id": "rs200961860",
                            "database": "ExAC",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs200961860"
                        },
                        {
                            "id": "rs200961860",
                            "database": "TOPMed",
                            "url": "https://www.ncbi.nlm.nih.gov/snp/rs200961860#frequency_tab"
                        },
                        {
                            "id": "rs200961860",
                            "database": "gnomAD",
                            "url": "http://gnomad.broadinstitute.org/awesome?query=rs200961860"
                        }
                    ]
                },
                {
                    "weight": 100,
                    "sequence_org": "N",
                    "sequence_mut": "K",
                    "comment": "Somatic mutation passed 1 out of 6 filters: n-glyco-sequon-loss (NAT->KAT).",
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                    "chr_pos": "155138236",
                    "evidence": [
                        {
                            "id": "P08473",
                            "database": "BioMuta",
                            "url": "https://hivelab.biochemistry.gwu.edu/biomuta/proteinview/P08473"
                        },
                        {
                            "id": "rs1434664230",
                            "database": "dbSNP",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1434664230"
                        },
                        {
                            "id": "rs1434664230",
                            "database": "gnomAD",
                            "url": "http://gnomad.broadinstitute.org/awesome?query=rs1434664230"
                        },
                        {
                            "id": "rs1434664230",
                            "database": "COSMIC",
                            "url": "https://www.ensembl.org/homo_sapiens/Variation/Explore?v=rs1434664230"
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                    ],
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                            "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"
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                            ]
                        }
                    ]
                },
                {
                    "weight": 100,
                    "sequence_org": "N",
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                    "comment": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-loss (NAT->SAT).",
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                    "chr_pos": "155138235",
                    "evidence": [
                        {
                            "id": "rs200961860",
                            "database": "dbSNP",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs200961860"
                        },
                        {
                            "id": "rs200961860",
                            "database": "1000Genomes",
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                        },
                        {
                            "id": "rs200961860",
                            "database": "ExAC",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs200961860"
                        },
                        {
                            "id": "rs200961860",
                            "database": "TOPMed",
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                        },
                        {
                            "id": "rs200961860",
                            "database": "gnomAD",
                            "url": "http://gnomad.broadinstitute.org/awesome?query=rs200961860"
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                    ],
                    "disease": [
                        {
                            "disease_id": "DOID:0110160",
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                            "url": "http://disease-ontology.org/term/DOID:0110160",
                            "evidence": [
                                {
                                    "id": "0110160",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0110160"
                                },
                                {
                                    "id": "0110160",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0110160"
                                }
                            ]
                        },
                        {
                            "disease_id": "DOID:0110160",
                            "name": "Charcot-Marie-Tooth disease axonal type 2T",
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                            "url": "http://disease-ontology.org/term/DOID:0110160",
                            "evidence": [
                                {
                                    "id": "0110160",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0110160"
                                },
                                {
                                    "id": "0110160",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0110160"
                                }
                            ]
                        },
                        {
                            "disease_id": "DOID:0110160",
                            "name": "Charcot-Marie-Tooth disease axonal type 2T",
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                            "evidence": [
                                {
                                    "id": "0110160",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0110160"
                                },
                                {
                                    "id": "0110160",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0110160"
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                            ]
                        },
                        {
                            "disease_id": "DOID:0110160",
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                                {
                                    "id": "0110160",
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                                    "url": "https://www.alliancegenome.org/disease/DOID:0110160"
                                },
                                {
                                    "id": "0110160",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0110160"
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                            ]
                        },
                        {
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                                {
                                    "id": "0110160",
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                                },
                                {
                                    "id": "0110160",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0110160"
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                            ]
                        },
                        {
                            "disease_id": "DOID:0111745",
                            "name": "cerebellar ataxia type 43",
                            "description": "An autosomal dominant cerebellar ataxia characterized by adult-onset, slowly progressive, gait and limb ataxia, often associated with peripheral neuropathy typically affecting the motor system that has_material_basis_in heterozygous mutation in MME on chromosome 3q25.2.",
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                            "evidence": [
                                {
                                    "id": "0111745",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0111745"
                                },
                                {
                                    "id": "0111745",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0111745"
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                            ]
                        },
                        {
                            "disease_id": "DOID:0111745",
                            "name": "cerebellar ataxia type 43",
                            "description": "An autosomal dominant cerebellar ataxia characterized by adult-onset, slowly progressive, gait and limb ataxia, often associated with peripheral neuropathy typically affecting the motor system that has_material_basis_in heterozygous mutation in MME on chromosome 3q25.2.",
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                            "evidence": [
                                {
                                    "id": "0111745",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0111745"
                                },
                                {
                                    "id": "0111745",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0111745"
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                            ]
                        },
                        {
                            "disease_id": "DOID:0111745",
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                                {
                                    "id": "0111745",
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                                    "url": "https://www.alliancegenome.org/disease/DOID:0111745"
                                },
                                {
                                    "id": "0111745",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0111745"
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                            ]
                        },
                        {
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                                {
                                    "id": "0111745",
                                    "database": "AGR",
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                                },
                                {
                                    "id": "0111745",
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                            ]
                        },
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                                {
                                    "id": "0111745",
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                                },
                                {
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                    ],
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            ]
        },
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                    ],
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            ]
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                    "evidence": [
                        {
                            "database": "PubMed",
                            "id": "37074911",
                            "url": "https://glygen.org/publication/PubMed/37074911"
                        },
                        {
                            "database": "PDC",
                            "id": "PDC000471",
                            "url": "https://proteomic.datacommons.cancer.gov/pdc/study/PDC000471"
                        }
                    ],
                    "protein_name": "Neprilysin",
                    "gene_name": "MME",
                    "tax_id": 9606,
                    "tax_name": "Homo sapiens",
                    "tax_common_name": "Human",
                    "length": 750,
                    "chemical_mass": 85514.0
                }
            ]
        },
        {
            "start_pos": "285",
            "site_seq": "EIAnATAKPEDRNDPMLLYNK",
            "site_lbl": "Asn285",
            "residue": "Asn",
            "glycoprotein": [
                {
                    "uniprot_canonical_ac": "P08473-1",
                    "start_pos": 285,
                    "end_pos": 285,
                    "residue": "Asn",
                    "evidence": [
                        {
                            "database": "PubMed",
                            "id": "37074911",
                            "url": "https://glygen.org/publication/PubMed/37074911"
                        },
                        {
                            "database": "PDC",
                            "id": "PDC000471",
                            "url": "https://proteomic.datacommons.cancer.gov/pdc/study/PDC000471"
                        }
                    ],
                    "protein_name": "Neprilysin",
                    "gene_name": "MME",
                    "tax_id": 9606,
                    "tax_name": "Homo sapiens",
                    "tax_common_name": "Human",
                    "length": 750,
                    "chemical_mass": 85514.0
                }
            ]
        },
        {
            "start_pos": "285",
            "site_seq": "EIAnATAKPEDR",
            "site_lbl": "Asn285",
            "residue": "Asn",
            "glycoprotein": [
                {
                    "uniprot_canonical_ac": "P08473-1",
                    "start_pos": 285,
                    "end_pos": 285,
                    "residue": "Asn",
                    "evidence": [
                        {
                            "database": "PubMed",
                            "id": "37074911",
                            "url": "https://glygen.org/publication/PubMed/37074911"
                        },
                        {
                            "database": "PDC",
                            "id": "PDC000471",
                            "url": "https://proteomic.datacommons.cancer.gov/pdc/study/PDC000471"
                        }
                    ],
                    "protein_name": "Neprilysin",
                    "gene_name": "MME",
                    "tax_id": 9606,
                    "tax_name": "Homo sapiens",
                    "tax_common_name": "Human",
                    "length": 750,
                    "chemical_mass": 85514.0
                }
            ]
        },
        {
            "start_pos": "285",
            "site_seq": "EIANATAKPEDR",
            "site_lbl": "Asn285",
            "residue": "Asn",
            "glycoprotein": [
                {
                    "uniprot_canonical_ac": "P08473-1",
                    "start_pos": 285,
                    "end_pos": 285,
                    "residue": "Asn",
                    "evidence": [
                        {
                            "database": "PubMed",
                            "id": "37074911",
                            "url": "https://glygen.org/publication/PubMed/37074911"
                        },
                        {
                            "database": "PDC",
                            "id": "PDC000471",
                            "url": "https://proteomic.datacommons.cancer.gov/pdc/study/PDC000471"
                        }
                    ],
                    "protein_name": "Neprilysin",
                    "gene_name": "MME",
                    "tax_id": 9606,
                    "tax_name": "Homo sapiens",
                    "tax_common_name": "Human",
                    "length": 750,
                    "chemical_mass": 85514.0
                }
            ]
        },
        {
            "start_pos": "285",
            "site_seq": "N",
            "site_lbl": "Asn285",
            "residue": "Asn",
            "glycoprotein": [
                {
                    "uniprot_canonical_ac": "P08473-1",
                    "start_pos": 285,
                    "end_pos": 285,
                    "residue": "Asn",
                    "evidence": [
                        {
                            "database": "PubMed",
                            "id": "37074911",
                            "url": "https://glygen.org/publication/PubMed/37074911"
                        },
                        {
                            "database": "PDC",
                            "id": "PDC000471",
                            "url": "https://proteomic.datacommons.cancer.gov/pdc/study/PDC000471"
                        }
                    ],
                    "protein_name": "Neprilysin",
                    "gene_name": "MME",
                    "tax_id": 9606,
                    "tax_name": "Homo sapiens",
                    "tax_common_name": "Human",
                    "length": 750,
                    "chemical_mass": 85514.0
                }
            ]
        },
        {
            "start_pos": "145",
            "site_seq": "",
            "site_lbl": "N145",
            "residue": "",
            "snv": [
                {
                    "weight": 100,
                    "sequence_org": "N",
                    "sequence_mut": "H",
                    "comment": "Somatic mutation passed 1 out of 6 filters: n-glyco-sequon-loss (NES->HES).",
                    "chr_id": "3",
                    "chr_pos": "155116553",
                    "evidence": [
                        {
                            "id": "P08473",
                            "database": "BioMuta",
                            "url": "https://hivelab.biochemistry.gwu.edu/biomuta/proteinview/P08473"
                        }
                    ],
                    "disease": [
                        {
                            "disease_id": "DOID:10534",
                            "name": "stomach cancer",
                            "description": "A gastrointestinal system cancer that is located_in the stomach.",
                            "url": "http://disease-ontology.org/term/DOID:10534",
                            "evidence": [
                                {
                                    "id": "10534",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:10534"
                                },
                                {
                                    "id": "10534",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:10534"
                                }
                            ]
                        }
                    ]
                }
            ],
            "glycoprotein": [
                {
                    "uniprot_canonical_ac": "P08473-1",
                    "start_pos": 145,
                    "end_pos": 145,
                    "residue": "Asn",
                    "evidence": [
                        {
                            "database": "PubMed",
                            "id": "37074911",
                            "url": "https://glygen.org/publication/PubMed/37074911"
                        },
                        {
                            "database": "PDC",
                            "id": "PDC000471",
                            "url": "https://proteomic.datacommons.cancer.gov/pdc/study/PDC000471"
                        }
                    ],
                    "protein_name": "Neprilysin",
                    "gene_name": "MME",
                    "tax_id": 9606,
                    "tax_name": "Homo sapiens",
                    "tax_common_name": "Human",
                    "length": 750,
                    "chemical_mass": 85514.0
                }
            ]
        },
        {
            "start_pos": "285",
            "site_seq": "",
            "site_lbl": "N285",
            "residue": "",
            "snv": [
                {
                    "weight": 100,
                    "sequence_org": "N",
                    "sequence_mut": "D",
                    "comment": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-loss (NAT->DAT).",
                    "chr_id": "3",
                    "chr_pos": "155138234",
                    "evidence": [
                        {
                            "id": "rs1339178202",
                            "database": "dbSNP",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1339178202"
                        },
                        {
                            "id": "rs1339178202",
                            "database": "gnomAD",
                            "url": "http://gnomad.broadinstitute.org/awesome?query=rs1339178202"
                        }
                    ]
                },
                {
                    "weight": 100,
                    "sequence_org": "N",
                    "sequence_mut": "I",
                    "comment": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-loss (NAT->IAT).",
                    "chr_id": "3",
                    "chr_pos": "155138235",
                    "evidence": [
                        {
                            "id": "rs200961860",
                            "database": "dbSNP",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs200961860"
                        },
                        {
                            "id": "rs200961860",
                            "database": "1000Genomes",
                            "url": "https://www.ensembl.org/homo_sapiens/Variation/Explore?v=rs200961860"
                        },
                        {
                            "id": "rs200961860",
                            "database": "ExAC",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs200961860"
                        },
                        {
                            "id": "rs200961860",
                            "database": "TOPMed",
                            "url": "https://www.ncbi.nlm.nih.gov/snp/rs200961860#frequency_tab"
                        },
                        {
                            "id": "rs200961860",
                            "database": "gnomAD",
                            "url": "http://gnomad.broadinstitute.org/awesome?query=rs200961860"
                        }
                    ]
                },
                {
                    "weight": 100,
                    "sequence_org": "N",
                    "sequence_mut": "K",
                    "comment": "Somatic mutation passed 1 out of 6 filters: n-glyco-sequon-loss (NAT->KAT).",
                    "chr_id": "3",
                    "chr_pos": "155138236",
                    "evidence": [
                        {
                            "id": "P08473",
                            "database": "BioMuta",
                            "url": "https://hivelab.biochemistry.gwu.edu/biomuta/proteinview/P08473"
                        },
                        {
                            "id": "rs1434664230",
                            "database": "dbSNP",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1434664230"
                        },
                        {
                            "id": "rs1434664230",
                            "database": "gnomAD",
                            "url": "http://gnomad.broadinstitute.org/awesome?query=rs1434664230"
                        },
                        {
                            "id": "rs1434664230",
                            "database": "COSMIC",
                            "url": "https://www.ensembl.org/homo_sapiens/Variation/Explore?v=rs1434664230"
                        }
                    ],
                    "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 (NAT->SAT).",
                    "chr_id": "3",
                    "chr_pos": "155138235",
                    "evidence": [
                        {
                            "id": "rs200961860",
                            "database": "dbSNP",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs200961860"
                        },
                        {
                            "id": "rs200961860",
                            "database": "1000Genomes",
                            "url": "https://www.ensembl.org/homo_sapiens/Variation/Explore?v=rs200961860"
                        },
                        {
                            "id": "rs200961860",
                            "database": "ExAC",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs200961860"
                        },
                        {
                            "id": "rs200961860",
                            "database": "TOPMed",
                            "url": "https://www.ncbi.nlm.nih.gov/snp/rs200961860#frequency_tab"
                        },
                        {
                            "id": "rs200961860",
                            "database": "gnomAD",
                            "url": "http://gnomad.broadinstitute.org/awesome?query=rs200961860"
                        }
                    ],
                    "disease": [
                        {
                            "disease_id": "DOID:0110160",
                            "name": "Charcot-Marie-Tooth disease axonal type 2T",
                            "description": "A Charcot-Marie-Tooth disease type 2 that has_material_basis_in homozygous or compound heterozygous mutation in the MME gene on chromosome 3q25.",
                            "url": "http://disease-ontology.org/term/DOID:0110160",
                            "evidence": [
                                {
                                    "id": "0110160",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0110160"
                                },
                                {
                                    "id": "0110160",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0110160"
                                }
                            ]
                        },
                        {
                            "disease_id": "DOID:0110160",
                            "name": "Charcot-Marie-Tooth disease axonal type 2T",
                            "description": "A Charcot-Marie-Tooth disease type 2 that has_material_basis_in homozygous or compound heterozygous mutation in the MME gene on chromosome 3q25.",
                            "url": "http://disease-ontology.org/term/DOID:0110160",
                            "evidence": [
                                {
                                    "id": "0110160",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0110160"
                                },
                                {
                                    "id": "0110160",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0110160"
                                }
                            ]
                        },
                        {
                            "disease_id": "DOID:0110160",
                            "name": "Charcot-Marie-Tooth disease axonal type 2T",
                            "description": "A Charcot-Marie-Tooth disease type 2 that has_material_basis_in homozygous or compound heterozygous mutation in the MME gene on chromosome 3q25.",
                            "url": "http://disease-ontology.org/term/DOID:0110160",
                            "evidence": [
                                {
                                    "id": "0110160",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0110160"
                                },
                                {
                                    "id": "0110160",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0110160"
                                }
                            ]
                        },
                        {
                            "disease_id": "DOID:0110160",
                            "name": "Charcot-Marie-Tooth disease axonal type 2T",
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                            "evidence": [
                                {
                                    "id": "0110160",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0110160"
                                },
                                {
                                    "id": "0110160",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0110160"
                                }
                            ]
                        },
                        {
                            "disease_id": "DOID:0110160",
                            "name": "Charcot-Marie-Tooth disease axonal type 2T",
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                            "evidence": [
                                {
                                    "id": "0110160",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0110160"
                                },
                                {
                                    "id": "0110160",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0110160"
                                }
                            ]
                        },
                        {
                            "disease_id": "DOID:0111745",
                            "name": "cerebellar ataxia type 43",
                            "description": "An autosomal dominant cerebellar ataxia characterized by adult-onset, slowly progressive, gait and limb ataxia, often associated with peripheral neuropathy typically affecting the motor system that has_material_basis_in heterozygous mutation in MME on chromosome 3q25.2.",
                            "url": "http://disease-ontology.org/term/DOID:0111745",
                            "evidence": [
                                {
                                    "id": "0111745",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0111745"
                                },
                                {
                                    "id": "0111745",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0111745"
                                }
                            ]
                        },
                        {
                            "disease_id": "DOID:0111745",
                            "name": "cerebellar ataxia type 43",
                            "description": "An autosomal dominant cerebellar ataxia characterized by adult-onset, slowly progressive, gait and limb ataxia, often associated with peripheral neuropathy typically affecting the motor system that has_material_basis_in heterozygous mutation in MME on chromosome 3q25.2.",
                            "url": "http://disease-ontology.org/term/DOID:0111745",
                            "evidence": [
                                {
                                    "id": "0111745",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0111745"
                                },
                                {
                                    "id": "0111745",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0111745"
                                }
                            ]
                        },
                        {
                            "disease_id": "DOID:0111745",
                            "name": "cerebellar ataxia type 43",
                            "description": "An autosomal dominant cerebellar ataxia characterized by adult-onset, slowly progressive, gait and limb ataxia, often associated with peripheral neuropathy typically affecting the motor system that has_material_basis_in heterozygous mutation in MME on chromosome 3q25.2.",
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                            "evidence": [
                                {
                                    "id": "0111745",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0111745"
                                },
                                {
                                    "id": "0111745",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0111745"
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                            ]
                        },
                        {
                            "disease_id": "DOID:0111745",
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                            "evidence": [
                                {
                                    "id": "0111745",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0111745"
                                },
                                {
                                    "id": "0111745",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0111745"
                                }
                            ]
                        },
                        {
                            "disease_id": "DOID:0111745",
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                                {
                                    "id": "0111745",
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                                    "url": "https://www.alliancegenome.org/disease/DOID:0111745"
                                },
                                {
                                    "id": "0111745",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0111745"
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                            ]
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                }
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                            "database": "PubMed",
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                        },
                        {
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                    ],
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                    "chemical_mass": 85514.0
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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": "P50895-1",
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                            "database": "PubMed",
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                        },
                        {
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                    ],
                    "protein_name": "Basal cell adhesion molecule",
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                    "chemical_mass": 67405.0
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            ]
        },
        {
            "start_pos": "439",
            "site_seq": "TQnFTLLVQGSPELK",
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                                {
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                                {
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                    "chemical_mass": 71957.0
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            ]
        },
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                            "id": "rs768936464",
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                            "id": "rs768936464",
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                        {
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}
