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                        {
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                        {
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                    ],
                    "protein_name": "Inactive dipeptidyl peptidase 10",
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            ]
        },
        {
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                        {
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                    ],
                    "protein_name": "ADAM DEC1",
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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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                        }
                    ],
                    "protein_name": "Neural cell adhesion molecule L1-like protein",
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            ]
        },
        {
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                {
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                        },
                        {
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                    ],
                    "protein_name": "Ligand-dependent nuclear receptor corepressor-like protein",
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                    "tax_name": "Homo sapiens",
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                    "chemical_mass": 66964.0
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            ]
        },
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                        {
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                        {
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                        },
                        {
                            "id": "rs1251925440",
                            "database": "gnomAD",
                            "url": "http://gnomad.broadinstitute.org/awesome?query=rs1251925440"
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                    ]
                }
            ],
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                {
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                        {
                            "database": "PubMed",
                            "id": "29671580",
                            "url": "https://glygen.org/publication/PubMed/29671580"
                        },
                        {
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                            "id": "GLY_000040",
                            "url": "http://data.glygen.org/GLY_000040"
                        }
                    ],
                    "protein_name": "Sulfhydryl oxidase 1",
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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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                    "evidence": [
                        {
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                            "url": "https://hivelab.biochemistry.gwu.edu/biomuta/proteinview/Q70UQ0"
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                    ],
                    "disease": [
                        {
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                            "evidence": [
                                {
                                    "id": "9256",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:9256"
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                            ]
                        }
                    ]
                }
            ],
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                {
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                            "url": "https://glygen.org/publication/PubMed/29671580"
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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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                            ]
                        },
                        {
                            "disease_id": "DOID:0110178",
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                                {
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                                {
                                    "id": "0110178",
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                            ]
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                        {
                            "disease_id": "DOID:0110178",
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                                },
                                {
                                    "id": "0110178",
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                            ]
                        },
                        {
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                            "evidence": [
                                {
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                                },
                                {
                                    "id": "252920",
                                    "database": "MIM",
                                    "url": "https://www.omim.org/entry/252920"
                                },
                                {
                                    "id": "4669",
                                    "database": "GlyCosmos",
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                                },
                                {
                                    "id": "0111394",
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                            ]
                        },
                        {
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                                },
                                {
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                                    "database": "MIM",
                                    "url": "https://www.omim.org/entry/252920"
                                },
                                {
                                    "id": "4669",
                                    "database": "GlyCosmos",
                                    "url": "https://glycosmos.org/glycogenes/show/4669#disease"
                                },
                                {
                                    "id": "0111394",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0111394"
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                            ]
                        },
                        {
                            "disease_id": "DOID:0111394",
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                                {
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                                },
                                {
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                            ]
                        },
                        {
                            "disease_id": "DOID:0111394",
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                                    "url": "https://monarchinitiative.org/disease/MONDO:0009656"
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                                {
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                                    "database": "MIM",
                                    "url": "https://www.omim.org/entry/252920"
                                },
                                {
                                    "id": "4669",
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                                    "url": "https://glycosmos.org/glycogenes/show/4669#disease"
                                },
                                {
                                    "id": "0111394",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0111394"
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                        {
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                    ],
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            ]
        },
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                        {
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                            "disease_id": "DOID:0110178",
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                            "evidence": [
                                {
                                    "id": "616491",
                                    "database": "MIM",
                                    "url": "https://www.omim.org/entry/616491"
                                },
                                {
                                    "id": "0110178",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0110178"
                                }
                            ]
                        },
                        {
                            "disease_id": "DOID:0110178",
                            "name": "Charcot-Marie-Tooth disease axonal type 2V",
                            "description": "A Charcot-Marie-Tooth disease type 2 that has_material_basis_in heterozygous mutation in the NAGLU gene on chromosome 17q21.",
                            "url": "http://disease-ontology.org/term/DOID:0110178",
                            "evidence": [
                                {
                                    "id": "616491",
                                    "database": "MIM",
                                    "url": "https://www.omim.org/entry/616491"
                                },
                                {
                                    "id": "0110178",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0110178"
                                }
                            ]
                        },
                        {
                            "disease_id": "DOID:0110178",
                            "name": "Charcot-Marie-Tooth disease axonal type 2V",
                            "description": "A Charcot-Marie-Tooth disease type 2 that has_material_basis_in heterozygous mutation in the NAGLU gene on chromosome 17q21.",
                            "url": "http://disease-ontology.org/term/DOID:0110178",
                            "evidence": [
                                {
                                    "id": "616491",
                                    "database": "MIM",
                                    "url": "https://www.omim.org/entry/616491"
                                },
                                {
                                    "id": "0110178",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0110178"
                                }
                            ]
                        },
                        {
                            "disease_id": "DOID:0111394",
                            "name": "mucopolysaccharidosis type IIIB",
                            "description": "A mucopolysaccharidosis III characterized by neurodegeneration, behavioral problems, mild skeletal changes, and shortened life span that has_material_basis_in homozygous or compound heterozygous mutation in NAGLU on chromosome 17q21.2.",
                            "url": "http://disease-ontology.org/term/DOID:0111394",
                            "evidence": [
                                {
                                    "id": "0009656",
                                    "database": "MONDO",
                                    "url": "https://monarchinitiative.org/disease/MONDO:0009656"
                                },
                                {
                                    "id": "252920",
                                    "database": "MIM",
                                    "url": "https://www.omim.org/entry/252920"
                                },
                                {
                                    "id": "4669",
                                    "database": "GlyCosmos",
                                    "url": "https://glycosmos.org/glycogenes/show/4669#disease"
                                },
                                {
                                    "id": "0111394",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0111394"
                                }
                            ]
                        },
                        {
                            "disease_id": "DOID:0111394",
                            "name": "mucopolysaccharidosis type IIIB",
                            "description": "A mucopolysaccharidosis III characterized by neurodegeneration, behavioral problems, mild skeletal changes, and shortened life span that has_material_basis_in homozygous or compound heterozygous mutation in NAGLU on chromosome 17q21.2.",
                            "url": "http://disease-ontology.org/term/DOID:0111394",
                            "evidence": [
                                {
                                    "id": "0009656",
                                    "database": "MONDO",
                                    "url": "https://monarchinitiative.org/disease/MONDO:0009656"
                                },
                                {
                                    "id": "252920",
                                    "database": "MIM",
                                    "url": "https://www.omim.org/entry/252920"
                                },
                                {
                                    "id": "4669",
                                    "database": "GlyCosmos",
                                    "url": "https://glycosmos.org/glycogenes/show/4669#disease"
                                },
                                {
                                    "id": "0111394",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0111394"
                                }
                            ]
                        },
                        {
                            "disease_id": "DOID:0111394",
                            "name": "mucopolysaccharidosis type IIIB",
                            "description": "A mucopolysaccharidosis III characterized by neurodegeneration, behavioral problems, mild skeletal changes, and shortened life span that has_material_basis_in homozygous or compound heterozygous mutation in NAGLU on chromosome 17q21.2.",
                            "url": "http://disease-ontology.org/term/DOID:0111394",
                            "evidence": [
                                {
                                    "id": "0009656",
                                    "database": "MONDO",
                                    "url": "https://monarchinitiative.org/disease/MONDO:0009656"
                                },
                                {
                                    "id": "252920",
                                    "database": "MIM",
                                    "url": "https://www.omim.org/entry/252920"
                                },
                                {
                                    "id": "4669",
                                    "database": "GlyCosmos",
                                    "url": "https://glycosmos.org/glycogenes/show/4669#disease"
                                },
                                {
                                    "id": "0111394",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0111394"
                                }
                            ]
                        }
                    ]
                },
                {
                    "sequence_org": "N",
                    "sequence_mut": "S",
                    "comment": "Germline mutation passed 0 out of 0 filters:",
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                    "chr_pos": "42543310",
                    "evidence": [
                        {
                            "id": "rs764815033",
                            "database": "dbSNP",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs764815033"
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                        {
                            "id": "rs764815033",
                            "database": "ExAC",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs764815033"
                        },
                        {
                            "id": "rs764815033",
                            "database": "TOPMed",
                            "url": "https://www.ncbi.nlm.nih.gov/snp/rs764815033#frequency_tab"
                        },
                        {
                            "id": "rs764815033",
                            "database": "gnomAD",
                            "url": "http://gnomad.broadinstitute.org/awesome?query=rs764815033"
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                    ],
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                        {
                            "disease_id": "DOID:0110178",
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                            "url": "http://disease-ontology.org/term/DOID:0110178",
                            "evidence": [
                                {
                                    "id": "616491",
                                    "database": "MIM",
                                    "url": "https://www.omim.org/entry/616491"
                                },
                                {
                                    "id": "0110178",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0110178"
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                            ]
                        },
                        {
                            "disease_id": "DOID:0110178",
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                            "description": "A Charcot-Marie-Tooth disease type 2 that has_material_basis_in heterozygous mutation in the NAGLU gene on chromosome 17q21.",
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                            "evidence": [
                                {
                                    "id": "616491",
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                                    "url": "https://www.omim.org/entry/616491"
                                },
                                {
                                    "id": "0110178",
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                            ]
                        },
                        {
                            "disease_id": "DOID:0110178",
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                            "url": "http://disease-ontology.org/term/DOID:0110178",
                            "evidence": [
                                {
                                    "id": "616491",
                                    "database": "MIM",
                                    "url": "https://www.omim.org/entry/616491"
                                },
                                {
                                    "id": "0110178",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0110178"
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                            ]
                        },
                        {
                            "disease_id": "DOID:0110178",
                            "name": "Charcot-Marie-Tooth disease axonal type 2V",
                            "description": "A Charcot-Marie-Tooth disease type 2 that has_material_basis_in heterozygous mutation in the NAGLU gene on chromosome 17q21.",
                            "url": "http://disease-ontology.org/term/DOID:0110178",
                            "evidence": [
                                {
                                    "id": "616491",
                                    "database": "MIM",
                                    "url": "https://www.omim.org/entry/616491"
                                },
                                {
                                    "id": "0110178",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0110178"
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                            ]
                        },
                        {
                            "disease_id": "DOID:0111394",
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                            "evidence": [
                                {
                                    "id": "0009656",
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                                    "url": "https://monarchinitiative.org/disease/MONDO:0009656"
                                },
                                {
                                    "id": "252920",
                                    "database": "MIM",
                                    "url": "https://www.omim.org/entry/252920"
                                },
                                {
                                    "id": "4669",
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                                {
                                    "id": "0111394",
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                                    "url": "https://www.alliancegenome.org/disease/DOID:0111394"
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                            ]
                        },
                        {
                            "disease_id": "DOID:0111394",
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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": "0009656",
                                    "database": "MONDO",
                                    "url": "https://monarchinitiative.org/disease/MONDO:0009656"
                                },
                                {
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                                },
                                {
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                                {
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                            ]
                        },
                        {
                            "disease_id": "DOID:0111394",
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                                    "id": "0009656",
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                                {
                                    "id": "252920",
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                                },
                                {
                                    "id": "4669",
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                                    "url": "https://glycosmos.org/glycogenes/show/4669#disease"
                                },
                                {
                                    "id": "0111394",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0111394"
                                }
                            ]
                        }
                    ]
                },
                {
                    "sequence_org": "N",
                    "sequence_mut": "T",
                    "comment": "Germline mutation passed 0 out of 0 filters:",
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                        {
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                        {
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                        },
                        {
                            "id": "rs764815033",
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                                {
                                    "id": "616491",
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                                    "url": "https://www.omim.org/entry/616491"
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                                {
                                    "id": "0110178",
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                        },
                        {
                            "disease_id": "DOID:0110178",
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                            "evidence": [
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                                    "id": "616491",
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                                {
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                        },
                        {
                            "disease_id": "DOID:0110178",
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                                    "id": "616491",
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                                },
                                {
                                    "id": "0110178",
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                            ]
                        },
                        {
                            "disease_id": "DOID:0110178",
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                                    "id": "616491",
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                                },
                                {
                                    "id": "0110178",
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                            ]
                        },
                        {
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                                    "id": "0009656",
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                                    "url": "https://monarchinitiative.org/disease/MONDO:0009656"
                                },
                                {
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                                    "url": "https://www.omim.org/entry/252920"
                                },
                                {
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                                {
                                    "id": "0111394",
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                            ]
                        },
                        {
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                                {
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                                },
                                {
                                    "id": "4669",
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                                {
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                                    "database": "AGR",
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                            ]
                        },
                        {
                            "disease_id": "DOID:0111394",
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                                {
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                                },
                                {
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                        },
                        {
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                                    "url": "https://monarchinitiative.org/disease/MONDO:0009656"
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                                    "url": "https://www.omim.org/entry/252920"
                                },
                                {
                                    "id": "4669",
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                                {
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                                    "url": "https://www.alliancegenome.org/disease/DOID:0111394"
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                        }
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                    "end_pos": 435,
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                            "url": "https://glygen.org/publication/PubMed/29671580"
                        },
                        {
                            "database": "UniCarbKB",
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                    ],
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                    "tax_name": "Homo sapiens",
                    "tax_common_name": "Human",
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                    "length": 743,
                    "chemical_mass": 82266.0
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            ]
        },
        {
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                    "sequence_org": "N",
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                    "comment": "Germline mutation passed 0 out of 0 filters:",
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                        {
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                        {
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                    ],
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                        {
                            "disease_id": "DOID:0110178",
                            "name": "Charcot-Marie-Tooth disease axonal type 2V",
                            "description": "A Charcot-Marie-Tooth disease type 2 that has_material_basis_in heterozygous mutation in the NAGLU gene on chromosome 17q21.",
                            "url": "http://disease-ontology.org/term/DOID:0110178",
                            "evidence": [
                                {
                                    "id": "616491",
                                    "database": "MIM",
                                    "url": "https://www.omim.org/entry/616491"
                                },
                                {
                                    "id": "0110178",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0110178"
                                }
                            ]
                        },
                        {
                            "disease_id": "DOID:0110178",
                            "name": "Charcot-Marie-Tooth disease axonal type 2V",
                            "description": "A Charcot-Marie-Tooth disease type 2 that has_material_basis_in heterozygous mutation in the NAGLU gene on chromosome 17q21.",
                            "url": "http://disease-ontology.org/term/DOID:0110178",
                            "evidence": [
                                {
                                    "id": "616491",
                                    "database": "MIM",
                                    "url": "https://www.omim.org/entry/616491"
                                },
                                {
                                    "id": "0110178",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0110178"
                                }
                            ]
                        },
                        {
                            "disease_id": "DOID:0110178",
                            "name": "Charcot-Marie-Tooth disease axonal type 2V",
                            "description": "A Charcot-Marie-Tooth disease type 2 that has_material_basis_in heterozygous mutation in the NAGLU gene on chromosome 17q21.",
                            "url": "http://disease-ontology.org/term/DOID:0110178",
                            "evidence": [
                                {
                                    "id": "616491",
                                    "database": "MIM",
                                    "url": "https://www.omim.org/entry/616491"
                                },
                                {
                                    "id": "0110178",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0110178"
                                }
                            ]
                        },
                        {
                            "disease_id": "DOID:0111394",
                            "name": "mucopolysaccharidosis type IIIB",
                            "description": "A mucopolysaccharidosis III characterized by neurodegeneration, behavioral problems, mild skeletal changes, and shortened life span that has_material_basis_in homozygous or compound heterozygous mutation in NAGLU on chromosome 17q21.2.",
                            "url": "http://disease-ontology.org/term/DOID:0111394",
                            "evidence": [
                                {
                                    "id": "0009656",
                                    "database": "MONDO",
                                    "url": "https://monarchinitiative.org/disease/MONDO:0009656"
                                },
                                {
                                    "id": "252920",
                                    "database": "MIM",
                                    "url": "https://www.omim.org/entry/252920"
                                },
                                {
                                    "id": "4669",
                                    "database": "GlyCosmos",
                                    "url": "https://glycosmos.org/glycogenes/show/4669#disease"
                                },
                                {
                                    "id": "0111394",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0111394"
                                }
                            ]
                        },
                        {
                            "disease_id": "DOID:0111394",
                            "name": "mucopolysaccharidosis type IIIB",
                            "description": "A mucopolysaccharidosis III characterized by neurodegeneration, behavioral problems, mild skeletal changes, and shortened life span that has_material_basis_in homozygous or compound heterozygous mutation in NAGLU on chromosome 17q21.2.",
                            "url": "http://disease-ontology.org/term/DOID:0111394",
                            "evidence": [
                                {
                                    "id": "0009656",
                                    "database": "MONDO",
                                    "url": "https://monarchinitiative.org/disease/MONDO:0009656"
                                },
                                {
                                    "id": "252920",
                                    "database": "MIM",
                                    "url": "https://www.omim.org/entry/252920"
                                },
                                {
                                    "id": "4669",
                                    "database": "GlyCosmos",
                                    "url": "https://glycosmos.org/glycogenes/show/4669#disease"
                                },
                                {
                                    "id": "0111394",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0111394"
                                }
                            ]
                        },
                        {
                            "disease_id": "DOID:0111394",
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                            "url": "http://disease-ontology.org/term/DOID:0111394",
                            "evidence": [
                                {
                                    "id": "0009656",
                                    "database": "MONDO",
                                    "url": "https://monarchinitiative.org/disease/MONDO:0009656"
                                },
                                {
                                    "id": "252920",
                                    "database": "MIM",
                                    "url": "https://www.omim.org/entry/252920"
                                },
                                {
                                    "id": "4669",
                                    "database": "GlyCosmos",
                                    "url": "https://glycosmos.org/glycogenes/show/4669#disease"
                                },
                                {
                                    "id": "0111394",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0111394"
                                }
                            ]
                        }
                    ]
                },
                {
                    "sequence_org": "N",
                    "sequence_mut": "S",
                    "comment": "Germline mutation passed 0 out of 0 filters:",
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                        {
                            "id": "rs757325483",
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                        {
                            "id": "rs757325483",
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                        },
                        {
                            "id": "rs757325483",
                            "database": "TOPMed",
                            "url": "https://www.ncbi.nlm.nih.gov/snp/rs757325483#frequency_tab"
                        },
                        {
                            "id": "rs757325483",
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                    ],
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                        {
                            "disease_id": "DOID:0110178",
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                            "url": "http://disease-ontology.org/term/DOID:0110178",
                            "evidence": [
                                {
                                    "id": "616491",
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                                    "url": "https://www.omim.org/entry/616491"
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                                {
                                    "id": "0110178",
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                        },
                        {
                            "disease_id": "DOID:0110178",
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                            "description": "A Charcot-Marie-Tooth disease type 2 that has_material_basis_in heterozygous mutation in the NAGLU gene on chromosome 17q21.",
                            "url": "http://disease-ontology.org/term/DOID:0110178",
                            "evidence": [
                                {
                                    "id": "616491",
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                                    "url": "https://www.omim.org/entry/616491"
                                },
                                {
                                    "id": "0110178",
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                        },
                        {
                            "disease_id": "DOID:0110178",
                            "name": "Charcot-Marie-Tooth disease axonal type 2V",
                            "description": "A Charcot-Marie-Tooth disease type 2 that has_material_basis_in heterozygous mutation in the NAGLU gene on chromosome 17q21.",
                            "url": "http://disease-ontology.org/term/DOID:0110178",
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                                {
                                    "id": "616491",
                                    "database": "MIM",
                                    "url": "https://www.omim.org/entry/616491"
                                },
                                {
                                    "id": "0110178",
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                                    "url": "https://www.alliancegenome.org/disease/DOID:0110178"
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                        },
                        {
                            "disease_id": "DOID:0110178",
                            "name": "Charcot-Marie-Tooth disease axonal type 2V",
                            "description": "A Charcot-Marie-Tooth disease type 2 that has_material_basis_in heterozygous mutation in the NAGLU gene on chromosome 17q21.",
                            "url": "http://disease-ontology.org/term/DOID:0110178",
                            "evidence": [
                                {
                                    "id": "616491",
                                    "database": "MIM",
                                    "url": "https://www.omim.org/entry/616491"
                                },
                                {
                                    "id": "0110178",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0110178"
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                            ]
                        },
                        {
                            "disease_id": "DOID:0111394",
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                            "description": "A mucopolysaccharidosis III characterized by neurodegeneration, behavioral problems, mild skeletal changes, and shortened life span that has_material_basis_in homozygous or compound heterozygous mutation in NAGLU on chromosome 17q21.2.",
                            "url": "http://disease-ontology.org/term/DOID:0111394",
                            "evidence": [
                                {
                                    "id": "0009656",
                                    "database": "MONDO",
                                    "url": "https://monarchinitiative.org/disease/MONDO:0009656"
                                },
                                {
                                    "id": "252920",
                                    "database": "MIM",
                                    "url": "https://www.omim.org/entry/252920"
                                },
                                {
                                    "id": "4669",
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                                    "url": "https://glycosmos.org/glycogenes/show/4669#disease"
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                                {
                                    "id": "0111394",
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                                    "url": "https://www.alliancegenome.org/disease/DOID:0111394"
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                            ]
                        },
                        {
                            "disease_id": "DOID:0111394",
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                            "description": "A mucopolysaccharidosis III characterized by neurodegeneration, behavioral problems, mild skeletal changes, and shortened life span that has_material_basis_in homozygous or compound heterozygous mutation in NAGLU on chromosome 17q21.2.",
                            "url": "http://disease-ontology.org/term/DOID:0111394",
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                                {
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                                    "database": "MONDO",
                                    "url": "https://monarchinitiative.org/disease/MONDO:0009656"
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                                {
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                                },
                                {
                                    "id": "4669",
                                    "database": "GlyCosmos",
                                    "url": "https://glycosmos.org/glycogenes/show/4669#disease"
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                                {
                                    "id": "0111394",
                                    "database": "AGR",
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                            ]
                        },
                        {
                            "disease_id": "DOID:0111394",
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                                {
                                    "id": "0009656",
                                    "database": "MONDO",
                                    "url": "https://monarchinitiative.org/disease/MONDO:0009656"
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                                {
                                    "id": "252920",
                                    "database": "MIM",
                                    "url": "https://www.omim.org/entry/252920"
                                },
                                {
                                    "id": "4669",
                                    "database": "GlyCosmos",
                                    "url": "https://glycosmos.org/glycogenes/show/4669#disease"
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                                {
                                    "id": "0111394",
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                                    "url": "https://www.alliancegenome.org/disease/DOID:0111394"
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                        },
                        {
                            "disease_id": "DOID:0111394",
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                            "url": "http://disease-ontology.org/term/DOID:0111394",
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                                {
                                    "id": "0009656",
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                                {
                                    "id": "252920",
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                                    "url": "https://www.omim.org/entry/252920"
                                },
                                {
                                    "id": "4669",
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                                    "url": "https://glycosmos.org/glycogenes/show/4669#disease"
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                                {
                                    "id": "0111394",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0111394"
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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": "rs758810828",
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                    ]
                },
                {
                    "sequence_org": "N",
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                            "id": "rs1208202746",
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                        {
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                        {
                            "id": "rs1208202746",
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                        {
                            "database": "PubMed",
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                        {
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                    ],
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                        {
                            "id": "rs149732546",
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                        {
                            "id": "rs149732546",
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                        {
                            "id": "rs149732546",
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            ],
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                    ],
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            ]
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                {
                    "sequence_org": "N",
                    "sequence_mut": "K",
                    "comment": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-loss (NMS->KMS).",
                    "chr_id": "20",
                    "chr_pos": "24970322",
                    "evidence": [
                        {
                            "id": "rs2122491348",
                            "database": "dbSNP",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs2122491348"
                        },
                        {
                            "id": "rs2122491348",
                            "database": "ENSEMBL",
                            "url": "https://www.ensembl.org/id/rs2122491348"
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                    ]
                }
            ],
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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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                            "id": "PDC000471",
                            "url": "https://proteomic.datacommons.cancer.gov/pdc/study/PDC000471"
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                    ],
                    "protein_name": "Adipocyte plasma membrane-associated protein",
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                    "tax_name": "Homo sapiens",
                    "tax_common_name": "Human",
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                    "length": 416,
                    "chemical_mass": 46480.0
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            ]
        },
        {
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                {
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                    "comment": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-loss (NFT->SFT).",
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                    "chr_pos": "94294529",
                    "evidence": [
                        {
                            "id": "rs1465641590",
                            "database": "dbSNP",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1465641590"
                        },
                        {
                            "id": "rs1465641590",
                            "database": "TOPMed",
                            "url": "https://www.ncbi.nlm.nih.gov/snp/rs1465641590#frequency_tab"
                        }
                    ]
                },
                {
                    "sequence_org": "N",
                    "sequence_mut": "T",
                    "comment": "Somatic mutation passed 1 out of 6 filters: n-glyco-sequon-loss (NFT->TFT).",
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                    "chr_pos": "94294529",
                    "evidence": [
                        {
                            "id": "O60486",
                            "database": "BioMuta",
                            "url": "https://hivelab.biochemistry.gwu.edu/biomuta/proteinview/O60486"
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                    ],
                    "disease": [
                        {
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                            "description": "A female reproductive organ cancer that is located_in the uterus.",
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                            "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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                        {
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                            "id": "23345538",
                            "url": "https://glygen.org/publication/PubMed/23345538"
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                        {
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                            "url": "http://data.glygen.org/GLY_000040"
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                    ],
                    "protein_name": "Plexin-C1",
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                    "tax_name": "Homo sapiens",
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                    "length": 1568,
                    "chemical_mass": 175742.0
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            ]
        },
        {
            "start_pos": "105",
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            "snv": [
                {
                    "sequence_org": "N",
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                    "comment": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-loss (NIS->DIS).",
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                    "chr_pos": "17127864",
                    "evidence": [
                        {
                            "id": "rs2492161163",
                            "database": "dbSNP",
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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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                        {
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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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                {
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                    "evidence": [
                        {
                            "id": "rs1842615728",
                            "database": "dbSNP",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1842615728"
                        },
                        {
                            "id": "rs1842615728",
                            "database": "TOPMed",
                            "url": "https://www.ncbi.nlm.nih.gov/snp/rs1842615728#frequency_tab"
                        }
                    ]
                },
                {
                    "sequence_org": "N",
                    "sequence_mut": "S",
                    "comment": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-loss (NAT->SAT).",
                    "chr_id": "10",
                    "chr_pos": "16940175",
                    "evidence": [
                        {
                            "id": "rs765059540",
                            "database": "dbSNP",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs765059540"
                        },
                        {
                            "id": "rs765059540",
                            "database": "ExAC",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs765059540"
                        },
                        {
                            "id": "rs765059540",
                            "database": "gnomAD",
                            "url": "http://gnomad.broadinstitute.org/awesome?query=rs765059540"
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                    ]
                }
            ],
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                        {
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            ]
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                        {
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                            "database": "dbSNP",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs555761842"
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                        {
                            "id": "rs555761842",
                            "database": "1000Genomes",
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                        },
                        {
                            "id": "rs555761842",
                            "database": "ExAC",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs555761842"
                        },
                        {
                            "id": "rs555761842",
                            "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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                {
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                            "database": "dbSNP",
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                        {
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                            "database": "ENSEMBL",
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                    ]
                },
                {
                    "sequence_org": "N",
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                    "evidence": [
                        {
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                            "database": "dbSNP",
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                        {
                            "id": "rs756429821",
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                        {
                            "id": "rs756429821",
                            "database": "gnomAD",
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                        {
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                    ],
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        {
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                {
                    "sequence_org": "N",
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                        {
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                            "database": "dbSNP",
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                        {
                            "id": "rs149758972",
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                        {
                            "id": "rs149758972",
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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": "rs1443611996",
                            "database": "TOPMed",
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                        {
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                    ],
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                            ]
                        }
                    ]
                },
                {
                    "sequence_org": "N",
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                        {
                            "id": "Q6EMK4",
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                    ],
                    "disease": [
                        {
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                            "description": "A large intestine cancer that is located_in the colon and/or located_in the rectum.",
                            "url": "http://disease-ontology.org/term/DOID:9256",
                            "evidence": [
                                {
                                    "id": "9256",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:9256"
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                            ]
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                    ]
                }
            ],
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                {
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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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                    "tax_name": "Homo sapiens",
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            ]
        },
        {
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                    "chr_pos": "4382460",
                    "evidence": [
                        {
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                            "database": "dbSNP",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs758383871"
                        },
                        {
                            "id": "rs758383871",
                            "database": "ExAC",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs758383871"
                        },
                        {
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                            "database": "gnomAD",
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                    ]
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            ],
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                {
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                            "url": "https://glygen.org/publication/PubMed/37074911"
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                        {
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                    ],
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                    "tax_name": "Homo sapiens",
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            ]
        },
        {
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                    "chr_pos": "112659398",
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                            "database": "dbSNP",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1335835565"
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                        {
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                        },
                        {
                            "id": "rs1335835565",
                            "database": "gnomAD",
                            "url": "http://gnomad.broadinstitute.org/awesome?query=rs1335835565"
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                    ]
                },
                {
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                    "chr_pos": "112659399",
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                        {
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                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1414886098"
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                        {
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                            "url": "https://www.ncbi.nlm.nih.gov/snp/rs1414886098#frequency_tab"
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            ],
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                    ],
                    "protein_name": "Sodium-dependent phosphate transporter 1",
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            ]
        },
        {
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                        {
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                            "database": "TOPMed",
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                        {
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                            "url": "http://gnomad.broadinstitute.org/awesome?query=rs1256351609"
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                    ]
                },
                {
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                    "evidence": []
                },
                {
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                            "url": "https://hivelab.biochemistry.gwu.edu/biomuta/proteinview/O43157"
                        },
                        {
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                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1256351609"
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                        {
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                        {
                            "id": "rs1256351609",
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                            "url": "http://gnomad.broadinstitute.org/awesome?query=rs1256351609"
                        },
                        {
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                            "url": "https://www.ensembl.org/homo_sapiens/Variation/Explore?v=rs1256351609"
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                    ],
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                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:263"
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                    ],
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                        {
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            ],
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                    ],
                    "protein_name": "Protein phosphatase 1 regulatory subunit 21",
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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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                    "comment": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-loss (NGT->KGT).",
                    "chr_id": "11",
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                        {
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                            "database": "dbSNP",
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                        {
                            "id": "rs1699102",
                            "database": "1000Genomes",
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                        },
                        {
                            "id": "rs1699102",
                            "database": "ExAC",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1699102"
                        },
                        {
                            "id": "rs1699102",
                            "database": "TOPMed",
                            "url": "https://www.ncbi.nlm.nih.gov/snp/rs1699102#frequency_tab"
                        },
                        {
                            "id": "rs1699102",
                            "database": "gnomAD",
                            "url": "http://gnomad.broadinstitute.org/awesome?query=rs1699102"
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                }
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                {
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                            "database": "PubMed",
                            "id": "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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                        {
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                            "database": "dbSNP",
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                        },
                        {
                            "id": "rs769962217",
                            "database": "TOPMed",
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                        },
                        {
                            "id": "rs769962217",
                            "database": "gnomAD",
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                }
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                        {
                            "database": "PubMed",
                            "id": "37074911",
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                        },
                        {
                            "database": "PDC",
                            "id": "PDC000471",
                            "url": "https://proteomic.datacommons.cancer.gov/pdc/study/PDC000471"
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                    ],
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                    "chemical_mass": 248426.0
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            ]
        },
        {
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                {
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                    "evidence": [
                        {
                            "id": "Q92673",
                            "database": "BioMuta",
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                    ],
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                                {
                                    "id": "4159",
                                    "database": "AGR",
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                            ]
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                        {
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                            "id": "37074911",
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                        {
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                            "id": "PDC000471",
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                    ],
                    "protein_name": "Sortilin-related receptor",
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            ]
        },
        {
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                {
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                    "evidence": [
                        {
                            "id": "rs1863717703",
                            "database": "dbSNP",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1863717703"
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                        {
                            "id": "rs1863717703",
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            ],
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                            "url": "https://glygen.org/publication/PubMed/37074911"
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                        {
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                    ],
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                    "tax_name": "Homo sapiens",
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            ]
        },
        {
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                {
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                        {
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                        {
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                    ],
                    "protein_name": "Sortilin-related receptor",
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            ]
        },
        {
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                        {
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                        {
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                    ]
                },
                {
                    "sequence_org": "N",
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                        {
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                        {
                            "id": "rs1262906894",
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                        {
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                    ]
                },
                {
                    "sequence_org": "N",
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                    "evidence": [
                        {
                            "id": "rs1186245679",
                            "database": "dbSNP",
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                        {
                            "id": "rs1186245679",
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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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                                    "database": "AGR",
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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": "rs766523334",
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                        {
                            "id": "rs766523334",
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                        {
                            "id": "rs766523334",
                            "database": "TOPMed",
                            "url": "https://www.ncbi.nlm.nih.gov/snp/rs766523334#frequency_tab"
                        },
                        {
                            "id": "rs766523334",
                            "database": "gnomAD",
                            "url": "http://gnomad.broadinstitute.org/awesome?query=rs766523334"
                        }
                    ],
                    "disease": [
                        {
                            "disease_id": "DOID:2531",
                            "name": "hematologic cancer",
                            "description": "An organ system cancer located in the hematological system that is characterized by uncontrolled cellular proliferation in blood, bone marrow and lymph nodes.",
                            "url": "http://disease-ontology.org/term/DOID:2531",
                            "evidence": [
                                {
                                    "id": "2531",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:2531"
                                }
                            ]
                        }
                    ]
                }
            ],
            "uniprot_canonical_ac": "O15230-1",
            "glycoprotein": [
                {
                    "uniprot_canonical_ac": "O15230-1",
                    "start_pos": 2501,
                    "end_pos": 2501,
                    "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": "Laminin subunit alpha-5",
                    "gene_name": "LAMA5",
                    "tax_id": 9606,
                    "tax_name": "Homo sapiens",
                    "tax_common_name": "Human",
                    "weight": 100.3,
                    "length": 3695,
                    "chemical_mass": 399737.0
                }
            ]
        },
        {
            "start_pos": "2568",
            "end_pos": "961",
            "site_lbl": "Asn2568",
            "weight": 0.0,
            "uniprot_canonical_ac": "O15230-1",
            "glycoprotein": [
                {
                    "uniprot_canonical_ac": "O15230-1",
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                    "end_pos": 2568,
                    "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": "Laminin subunit alpha-5",
                    "gene_name": "LAMA5",
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                    "tax_name": "Homo sapiens",
                    "tax_common_name": "Human",
                    "weight": 100.3,
                    "length": 3695,
                    "chemical_mass": 399737.0
                }
            ]
        },
        {
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            "end_pos": "961",
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                {
                    "sequence_org": "N",
                    "sequence_mut": "H",
                    "comment": "Somatic mutation passed 1 out of 6 filters: n-glyco-sequon-loss (NTT->HTT).",
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                    "chr_pos": "62312441",
                    "evidence": [
                        {
                            "id": "O15230",
                            "database": "BioMuta",
                            "url": "https://hivelab.biochemistry.gwu.edu/biomuta/proteinview/O15230"
                        }
                    ],
                    "disease": [
                        {
                            "disease_id": "DOID:10283",
                            "name": "prostate cancer",
                            "description": "A male reproductive organ cancer that is located_in the prostate.",
                            "url": "http://disease-ontology.org/term/DOID:10283",
                            "evidence": [
                                {
                                    "id": "10283",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:10283"
                                }
                            ]
                        }
                    ]
                },
                {
                    "sequence_org": "N",
                    "sequence_mut": "K",
                    "comment": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-loss (NTT->KTT).",
                    "chr_id": "20",
                    "chr_pos": "62312439",
                    "evidence": [
                        {
                            "id": "rs759232226",
                            "database": "dbSNP",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs759232226"
                        },
                        {
                            "id": "rs759232226",
                            "database": "ExAC",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs759232226"
                        },
                        {
                            "id": "rs759232226",
                            "database": "TOPMed",
                            "url": "https://www.ncbi.nlm.nih.gov/snp/rs759232226#frequency_tab"
                        },
                        {
                            "id": "rs759232226",
                            "database": "gnomAD",
                            "url": "http://gnomad.broadinstitute.org/awesome?query=rs759232226"
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                    ]
                }
            ],
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                {
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                        {
                            "database": "PubMed",
                            "id": "37074911",
                            "url": "https://glygen.org/publication/PubMed/37074911"
                        },
                        {
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                            "url": "https://proteomic.datacommons.cancer.gov/pdc/study/PDC000471"
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                    ],
                    "protein_name": "Laminin subunit alpha-5",
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                    "tax_name": "Homo sapiens",
                    "tax_common_name": "Human",
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                    "length": 3695,
                    "chemical_mass": 399737.0
                }
            ]
        },
        {
            "start_pos": "900",
            "end_pos": "961",
            "site_lbl": "Asn900",
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            "snv": [
                {
                    "sequence_org": "N",
                    "sequence_mut": "D",
                    "comment": "Somatic mutation passed 1 out of 6 filters: n-glyco-sequon-loss (NFS->DFS).",
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                    "chr_pos": "62334227",
                    "evidence": [
                        {
                            "id": "O15230",
                            "database": "BioMuta",
                            "url": "https://hivelab.biochemistry.gwu.edu/biomuta/proteinview/O15230"
                        }
                    ],
                    "disease": [
                        {
                            "disease_id": "DOID:1793",
                            "name": "pancreatic cancer",
                            "description": "An endocrine gland cancer located_in the pancreas.",
                            "url": "http://disease-ontology.org/term/DOID:1793",
                            "evidence": [
                                {
                                    "id": "1793",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:1793"
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                            ]
                        }
                    ]
                }
            ],
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            "glycoprotein": [
                {
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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"
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                    ],
                    "protein_name": "Laminin subunit alpha-5",
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                    "tax_name": "Homo sapiens",
                    "tax_common_name": "Human",
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                    "length": 3695,
                    "chemical_mass": 399737.0
                }
            ]
        },
        {
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                {
                    "sequence_org": "N",
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                    "comment": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-loss (NLT->KLT).",
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                    "chr_pos": "62334016",
                    "evidence": [
                        {
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                            "database": "dbSNP",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1981055552"
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                        {
                            "id": "rs1981055552",
                            "database": "TOPMed",
                            "url": "https://www.ncbi.nlm.nih.gov/snp/rs1981055552#frequency_tab"
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                    ]
                },
                {
                    "sequence_org": "N",
                    "sequence_mut": "T",
                    "comment": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-loss (NLT->TLT).",
                    "chr_id": "20",
                    "chr_pos": "62334017",
                    "evidence": [
                        {
                            "id": "rs2146208511",
                            "database": "dbSNP",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs2146208511"
                        },
                        {
                            "id": "rs2146208511",
                            "database": "ENSEMBL",
                            "url": "https://www.ensembl.org/id/rs2146208511"
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                    ]
                }
            ],
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                {
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                        {
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                    ],
                    "protein_name": "Laminin subunit alpha-5",
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                    "chemical_mass": 399737.0
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            ]
        },
        {
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                {
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                    "sequence_mut": "K",
                    "comment": "Germline mutation passed 0 out of 0 filters:",
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                    "chr_pos": "12650193",
                    "evidence": [
                        {
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                            "database": "dbSNP",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs376110556"
                        },
                        {
                            "id": "rs376110556",
                            "database": "TOPMed",
                            "url": "https://www.ncbi.nlm.nih.gov/snp/rs376110556#frequency_tab"
                        },
                        {
                            "id": "rs376110556",
                            "database": "gnomAD",
                            "url": "http://gnomad.broadinstitute.org/awesome?query=rs376110556"
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                    ]
                }
            ],
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                {
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                        {
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                        },
                        {
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                            "url": "https://proteomic.datacommons.cancer.gov/pdc/study/PDC000471"
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                    ],
                    "protein_name": "Lysosomal alpha-mannosidase",
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                    "tax_name": "Homo sapiens",
                    "tax_common_name": "Human",
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                    "chemical_mass": 113744.0
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            ]
        },
        {
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            "snv": [
                {
                    "sequence_org": "N",
                    "sequence_mut": "null",
                    "comment": "Germline mutation passed 0 out of 0 filters:",
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                    "chr_pos": "12649404_12649410",
                    "evidence": [
                        {
                            "id": "rs2512488403",
                            "database": "dbSNP",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs2512488403"
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                    ],
                    "disease": [
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                            "evidence": [
                                {
                                    "id": "3413",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:3413"
                                },
                                {
                                    "id": "3413",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:3413"
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                            ]
                        }
                    ]
                }
            ],
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                {
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                        {
                            "database": "PubMed",
                            "id": "37074911",
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                        },
                        {
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                    ],
                    "protein_name": "Lysosomal alpha-mannosidase",
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            ]
        },
        {
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                    "chr_pos": "35466626",
                    "evidence": [
                        {
                            "id": "Q8IZA0",
                            "database": "BioMuta",
                            "url": "https://hivelab.biochemistry.gwu.edu/biomuta/proteinview/Q8IZA0"
                        }
                    ],
                    "disease": [
                        {
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                            "name": "uterine cancer",
                            "description": "A female reproductive organ cancer that is located_in the uterus.",
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                            "evidence": [
                                {
                                    "id": "363",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:363"
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                            ]
                        }
                    ]
                }
            ],
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            "glycoprotein": [
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                        {
                            "database": "PubMed",
                            "id": "37074911",
                            "url": "https://glygen.org/publication/PubMed/37074911"
                        },
                        {
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                            "url": "https://proteomic.datacommons.cancer.gov/pdc/study/PDC000471"
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                    ],
                    "protein_name": "Dyslexia-associated protein KIAA0319-like protein",
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                    "tax_name": "Homo sapiens",
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            ]
        },
        {
            "start_pos": "214",
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                        {
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                            "database": "dbSNP",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1383536185"
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                        {
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                            "database": "TOPMed",
                            "url": "https://www.ncbi.nlm.nih.gov/snp/rs1383536185#frequency_tab"
                        },
                        {
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                            "database": "gnomAD",
                            "url": "http://gnomad.broadinstitute.org/awesome?query=rs1383536185"
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                    ]
                }
            ],
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                {
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                        {
                            "database": "PubMed",
                            "id": "37074911",
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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": "Spondin-1",
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            ]
        },
        {
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                            "url": "https://glygen.org/publication/PubMed/37074911"
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                    ],
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                    "length": 388,
                    "chemical_mass": 42785.0
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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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                            "id": "PDC000471",
                            "url": "https://proteomic.datacommons.cancer.gov/pdc/study/PDC000471"
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                    ],
                    "protein_name": "CD276 antigen",
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                    "chemical_mass": 57235.0
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            ]
        },
        {
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                            "url": "https://glygen.org/publication/PubMed/37074911"
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                        {
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                    ],
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            ]
        },
        {
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                            "id": "rs145158897",
                            "database": "dbSNP",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs145158897"
                        },
                        {
                            "id": "rs145158897",
                            "database": "1000Genomes",
                            "url": "https://www.ensembl.org/homo_sapiens/Variation/Explore?v=rs145158897"
                        },
                        {
                            "id": "rs145158897",
                            "database": "ExAC",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs145158897"
                        },
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                    "length": 523,
                    "chemical_mass": 59151.0
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            ]
        },
        {
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                {
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                        {
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                            "url": "https://glygen.org/publication/PubMed/37074911"
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                        {
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                    ],
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            ]
        },
        {
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                        {
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                            "database": "dbSNP",
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                        {
                            "id": "rs771212555",
                            "database": "ExAC",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs771212555"
                        },
                        {
                            "id": "rs771212555",
                            "database": "gnomAD",
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                    ]
                },
                {
                    "sequence_org": "N",
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                    "comment": "Somatic mutation passed 1 out of 1 filters: n-glyco-sequon-loss (NKT->KKT).",
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                },
                {
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                        {
                            "id": "Q9H3G5",
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                        },
                        {
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                        },
                        {
                            "id": "rs771212555",
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                        },
                        {
                            "id": "rs771212555",
                            "database": "gnomAD",
                            "url": "http://gnomad.broadinstitute.org/awesome?query=rs771212555"
                        },
                        {
                            "id": "rs771212555",
                            "database": "COSMIC",
                            "url": "https://www.ensembl.org/homo_sapiens/Variation/Explore?v=rs771212555"
                        }
                    ],
                    "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"
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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": "213",
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                {
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                    "comment": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-loss (NTS->KTS).",
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                    "chr_pos": "41479216",
                    "evidence": [
                        {
                            "id": "rs1326192818",
                            "database": "dbSNP",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1326192818"
                        },
                        {
                            "id": "rs1326192818",
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                            "url": "https://www.ncbi.nlm.nih.gov/snp/rs1326192818#frequency_tab"
                        },
                        {
                            "id": "rs1326192818",
                            "database": "gnomAD",
                            "url": "http://gnomad.broadinstitute.org/awesome?query=rs1326192818"
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                }
            ],
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                        {
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                        {
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                    ],
                    "protein_name": "Transmembrane protease serine 2",
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            ]
        },
        {
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                        {
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                            "database": "dbSNP",
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                        {
                            "id": "rs1794392557",
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                    ]
                }
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                        {
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                    ],
                    "protein_name": "HEPACAM family member 2",
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            ]
        },
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                        },
                        {
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                        },
                        {
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                            "database": "gnomAD",
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                    ]
                },
                {
                    "sequence_org": "N",
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                    "comment": "Somatic mutation passed 1 out of 1 filters: n-glyco-sequon-loss (NDT->IDT).",
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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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                    ]
                },
                {
                    "sequence_org": "N",
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                        {
                            "id": "rs771733043",
                            "database": "dbSNP",
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                        {
                            "id": "rs771733043",
                            "database": "ExAC",
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                        {
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                            "database": "gnomAD",
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                        {
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                    ],
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                        {
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                    ]
                }
            ],
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                {
                    "uniprot_canonical_ac": "Q5KU26-1",
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                        {
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                        {
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                    ],
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            ]
        },
        {
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                {
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                    "chr_pos": "6615269",
                    "evidence": [
                        {
                            "id": "rs754243461",
                            "database": "dbSNP",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs754243461"
                        },
                        {
                            "id": "rs754243461",
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                        },
                        {
                            "id": "rs754243461",
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                            "url": "https://www.ncbi.nlm.nih.gov/snp/rs754243461#frequency_tab"
                        },
                        {
                            "id": "rs754243461",
                            "database": "gnomAD",
                            "url": "http://gnomad.broadinstitute.org/awesome?query=rs754243461"
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                    ]
                },
                {
                    "sequence_org": "N",
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                    "comment": "Somatic mutation passed 1 out of 1 filters: n-glyco-sequon-loss (NAS->SAS).",
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                    "chr_pos": "6615268",
                    "evidence": [
                        {
                            "id": "rs139343938",
                            "database": "dbSNP",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs139343938"
                        },
                        {
                            "id": "rs139343938",
                            "database": "ExAC",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs139343938"
                        },
                        {
                            "id": "rs139343938",
                            "database": "TOPMed",
                            "url": "https://www.ncbi.nlm.nih.gov/snp/rs139343938#frequency_tab"
                        },
                        {
                            "id": "rs139343938",
                            "database": "gnomAD",
                            "url": "http://gnomad.broadinstitute.org/awesome?query=rs139343938"
                        },
                        {
                            "id": "rs139343938",
                            "database": "COSMIC",
                            "url": "https://www.ensembl.org/homo_sapiens/Variation/Explore?v=rs139343938"
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                    ],
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                            "evidence": [
                                {
                                    "id": "204500",
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                                    "url": "https://www.omim.org/entry/204500"
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                                {
                                    "id": "0110726",
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                            ]
                        },
                        {
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                            "evidence": [
                                {
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                                },
                                {
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                        },
                        {
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                            "evidence": [
                                {
                                    "id": "204500",
                                    "database": "MIM",
                                    "url": "https://www.omim.org/entry/204500"
                                },
                                {
                                    "id": "0110726",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0110726"
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                            ]
                        },
                        {
                            "disease_id": "DOID:0110726",
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                            "url": "http://disease-ontology.org/term/DOID:0110726",
                            "evidence": [
                                {
                                    "id": "204500",
                                    "database": "MIM",
                                    "url": "https://www.omim.org/entry/204500"
                                },
                                {
                                    "id": "0110726",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0110726"
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                        },
                        {
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                            "url": "http://disease-ontology.org/term/DOID:0110726",
                            "evidence": [
                                {
                                    "id": "204500",
                                    "database": "MIM",
                                    "url": "https://www.omim.org/entry/204500"
                                },
                                {
                                    "id": "0110726",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0110726"
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                        }
                    ]
                }
            ],
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                {
                    "uniprot_canonical_ac": "O14773-1",
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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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                    ],
                    "protein_name": "Tripeptidyl-peptidase 1",
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                    "tax_name": "Homo sapiens",
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                    "length": 563,
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            ]
        },
        {
            "start_pos": "93",
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                {
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                    "chr_pos": "108074375",
                    "evidence": [
                        {
                            "id": "rs1204561499",
                            "database": "dbSNP",
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                        {
                            "id": "rs1204561499",
                            "database": "TOPMed",
                            "url": "https://www.ncbi.nlm.nih.gov/snp/rs1204561499#frequency_tab"
                        },
                        {
                            "id": "rs1204561499",
                            "database": "gnomAD",
                            "url": "http://gnomad.broadinstitute.org/awesome?query=rs1204561499"
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                    ]
                },
                {
                    "sequence_org": "N",
                    "sequence_mut": "S",
                    "comment": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-loss (NSS->SSS).",
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                    "chr_pos": "108074374",
                    "evidence": [
                        {
                            "id": "rs1354770509",
                            "database": "dbSNP",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1354770509"
                        },
                        {
                            "id": "rs1354770509",
                            "database": "TOPMed",
                            "url": "https://www.ncbi.nlm.nih.gov/snp/rs1354770509#frequency_tab"
                        },
                        {
                            "id": "rs1354770509",
                            "database": "gnomAD",
                            "url": "http://gnomad.broadinstitute.org/awesome?query=rs1354770509"
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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": "1076",
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                {
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                        {
                            "id": "rs776694891",
                            "database": "dbSNP",
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                        {
                            "id": "rs776694891",
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                        {
                            "id": "rs776694891",
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                        },
                        {
                            "id": "rs776694891",
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            ],
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                {
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                        {
                            "database": "PubMed",
                            "id": "37074911",
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                        },
                        {
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                    ],
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                    "length": 2923,
                    "chemical_mass": 317453.0
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            ]
        },
        {
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                {
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                    "comment": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-loss (NVS->DVS).",
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                        {
                            "id": "rs1247709684",
                            "database": "dbSNP",
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                        {
                            "id": "rs1247709684",
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                    ]
                },
                {
                    "sequence_org": "N",
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                    "comment": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-loss (NVS->SVS).",
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                        {
                            "id": "rs376984266",
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                        {
                            "id": "rs376984266",
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                        {
                            "id": "rs376984266",
                            "database": "TOPMed",
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                        {
                            "id": "rs376984266",
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                    ],
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                            "evidence": [
                                {
                                    "id": "616736",
                                    "database": "MIM",
                                    "url": "https://www.omim.org/entry/616736"
                                },
                                {
                                    "id": "0111432",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0111432"
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                            ]
                        },
                        {
                            "disease_id": "DOID:0111432",
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                                {
                                    "id": "616736",
                                    "database": "MIM",
                                    "url": "https://www.omim.org/entry/616736"
                                },
                                {
                                    "id": "0111432",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0111432"
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                            ]
                        },
                        {
                            "disease_id": "DOID:0111432",
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                            "evidence": [
                                {
                                    "id": "616736",
                                    "database": "MIM",
                                    "url": "https://www.omim.org/entry/616736"
                                },
                                {
                                    "id": "0111432",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0111432"
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                            ]
                        },
                        {
                            "disease_id": "DOID:0111432",
                            "name": "essential tremor 5",
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                            "evidence": [
                                {
                                    "id": "616736",
                                    "database": "MIM",
                                    "url": "https://www.omim.org/entry/616736"
                                },
                                {
                                    "id": "0111432",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0111432"
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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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                    ],
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            ]
        },
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                    "comment": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-loss (NNT->KNT).",
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                    "chr_pos": "69576190",
                    "evidence": [
                        {
                            "id": "rs1188766952",
                            "database": "dbSNP",
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                        {
                            "id": "rs1188766952",
                            "database": "gnomAD",
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                        {
                            "database": "PubMed",
                            "id": "37074911",
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                        {
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                    ],
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            ]
        },
        {
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                {
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                    "sequence_mut": "K",
                    "comment": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-loss (NIS->KIS).",
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                    "chr_pos": "105356251",
                    "evidence": [
                        {
                            "id": "rs780705243",
                            "database": "dbSNP",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs780705243"
                        },
                        {
                            "id": "rs780705243",
                            "database": "ExAC",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs780705243"
                        },
                        {
                            "id": "rs780705243",
                            "database": "gnomAD",
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                    ]
                },
                {
                    "sequence_org": "N",
                    "sequence_mut": "S",
                    "comment": "Somatic mutation passed 1 out of 6 filters: n-glyco-sequon-loss (NIS->SIS).",
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                    "chr_pos": "105356250",
                    "evidence": [
                        {
                            "id": "Q8WWI5",
                            "database": "BioMuta",
                            "url": "https://hivelab.biochemistry.gwu.edu/biomuta/proteinview/Q8WWI5"
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                    ],
                    "disease": [
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                            "description": "A large intestine cancer that is located_in the colon and/or located_in the rectum.",
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                            "evidence": [
                                {
                                    "id": "9256",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:9256"
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                            ]
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                    ]
                }
            ],
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            "glycoprotein": [
                {
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                        {
                            "database": "PubMed",
                            "id": "37074911",
                            "url": "https://glygen.org/publication/PubMed/37074911"
                        },
                        {
                            "database": "PDC",
                            "id": "PDC000471",
                            "url": "https://proteomic.datacommons.cancer.gov/pdc/study/PDC000471"
                        }
                    ],
                    "protein_name": "Choline transporter-like protein 1",
                    "gene_name": "SLC44A1",
                    "tax_id": 9606,
                    "tax_name": "Homo sapiens",
                    "tax_common_name": "Human",
                    "weight": 11.3,
                    "length": 657,
                    "chemical_mass": 73302.0
                }
            ]
        },
        {
            "start_pos": "70",
            "end_pos": "182",
            "site_lbl": "Asn70",
            "weight": 0.0,
            "uniprot_canonical_ac": "Q5VW38-1",
            "glycoprotein": [
                {
                    "uniprot_canonical_ac": "Q5VW38-1",
                    "start_pos": 70,
                    "end_pos": 70,
                    "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": "Protein GPR107",
                    "gene_name": "GPR107",
                    "tax_id": 9606,
                    "tax_name": "Homo sapiens",
                    "tax_common_name": "Human",
                    "weight": 9.5,
                    "length": 600,
                    "chemical_mass": 66990.0
                }
            ]
        },
        {
            "start_pos": "311",
            "end_pos": "202",
            "site_lbl": "Asn311",
            "weight": 0.0,
            "snv": [
                {
                    "sequence_org": "N",
                    "sequence_mut": "Y",
                    "comment": "Somatic mutation passed 1 out of 6 filters: n-glyco-sequon-loss (NVT->YVT).",
                    "chr_id": "6",
                    "chr_pos": "33780179",
                    "evidence": [
                        {
                            "id": "Q8NC56",
                            "database": "BioMuta",
                            "url": "https://hivelab.biochemistry.gwu.edu/biomuta/proteinview/Q8NC56"
                        }
                    ],
                    "disease": [
                        {
                            "disease_id": "DOID:3571",
                            "name": "liver cancer",
                            "description": "A hepatobiliary system cancer that is located_in the liver.",
                            "url": "http://disease-ontology.org/term/DOID:3571",
                            "evidence": [
                                {
                                    "id": "3571",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:3571"
                                }
                            ]
                        }
                    ]
                }
            ],
            "uniprot_canonical_ac": "Q8NC56-1",
            "glycoprotein": [
                {
                    "uniprot_canonical_ac": "Q8NC56-1",
                    "start_pos": 311,
                    "end_pos": 311,
                    "residue": "Asn",
                    "evidence": [
                        {
                            "database": "PubMed",
                            "id": "37074911",
                            "url": "https://glygen.org/publication/PubMed/37074911"
                        },
                        {
                            "database": "PDC",
                            "id": "PDC000471",
                            "url": "https://proteomic.datacommons.cancer.gov/pdc/study/PDC000471"
                        }
                    ],
                    "protein_name": "LEM domain-containing protein 2",
                    "gene_name": "LEMD2",
                    "tax_id": 9606,
                    "tax_name": "Homo sapiens",
                    "tax_common_name": "Human",
                    "weight": 14.1,
                    "length": 503,
                    "chemical_mass": 56975.0
                }
            ]
        },
        {
            "start_pos": "185",
            "end_pos": "97",
            "site_lbl": "Asn185",
            "weight": 0.0,
            "snv": [
                {
                    "sequence_org": "N",
                    "sequence_mut": "D",
                    "comment": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-loss (NAT->DAT).",
                    "chr_id": "18",
                    "chr_pos": "23561438",
                    "evidence": [
                        {
                            "id": "rs139485263",
                            "database": "dbSNP",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs139485263"
                        },
                        {
                            "id": "rs139485263",
                            "database": "ExAC",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs139485263"
                        },
                        {
                            "id": "rs139485263",
                            "database": "TOPMed",
                            "url": "https://www.ncbi.nlm.nih.gov/snp/rs139485263#frequency_tab"
                        },
                        {
                            "id": "rs139485263",
                            "database": "gnomAD",
                            "url": "http://gnomad.broadinstitute.org/awesome?query=rs139485263"
                        }
                    ],
                    "disease": [
                        {
                            "disease_id": "DOID:0070113",
                            "name": "Niemann-Pick disease type C1",
                            "description": "A Niemann-Pick disease that has_material_basis_in an autosomal recessive mutation of the NPC1 gene on chromosome 18q11.2.",
                            "url": "http://disease-ontology.org/term/DOID:0070113",
                            "evidence": [
                                {
                                    "id": "0070113",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0070113"
                                }
                            ]
                        },
                        {
                            "disease_id": "DOID:0070113",
                            "name": "Niemann-Pick disease type C1",
                            "description": "A Niemann-Pick disease that has_material_basis_in an autosomal recessive mutation of the NPC1 gene on chromosome 18q11.2.",
                            "url": "http://disease-ontology.org/term/DOID:0070113",
                            "evidence": [
                                {
                                    "id": "0070113",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0070113"
                                }
                            ]
                        },
                        {
                            "disease_id": "DOID:0070113",
                            "name": "Niemann-Pick disease type C1",
                            "description": "A Niemann-Pick disease that has_material_basis_in an autosomal recessive mutation of the NPC1 gene on chromosome 18q11.2.",
                            "url": "http://disease-ontology.org/term/DOID:0070113",
                            "evidence": [
                                {
                                    "id": "0070113",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0070113"
                                }
                            ]
                        },
                        {
                            "disease_id": "DOID:0070113",
                            "name": "Niemann-Pick disease type C1",
                            "description": "A Niemann-Pick disease that has_material_basis_in an autosomal recessive mutation of the NPC1 gene on chromosome 18q11.2.",
                            "url": "http://disease-ontology.org/term/DOID:0070113",
                            "evidence": [
                                {
                                    "id": "0070113",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0070113"
                                }
                            ]
                        }
                    ]
                }
            ],
            "mutagenesis": [
                {
                    "sequence_org": "N",
                    "sequence_mut": "Q",
                    "comment": "Reduces glycosylation; when associated with Q-70 and Q-122. No effect on cholesterol and 25-hydroxycholesterol binding. Strongly reduces cholesterol transfer to liposomes in a NPC2-dependent manner.",
                    "evidence": [
                        {
                            "database": "UniProtKB",
                            "id": "O15118",
                            "url": "https://www.uniprot.org/uniprotkb/O15118"
                        },
                        {
                            "database": "PubMed",
                            "id": "19563754",
                            "url": "https://glygen.org/publication/PubMed/19563754"
                        }
                    ]
                }
            ],
            "uniprot_canonical_ac": "O15118-1",
            "glycoprotein": [
                {
                    "uniprot_canonical_ac": "O15118-1",
                    "start_pos": 185,
                    "end_pos": 185,
                    "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": "NPC intracellular cholesterol transporter 1",
                    "gene_name": "NPC1",
                    "tax_id": 9606,
                    "tax_name": "Homo sapiens",
                    "tax_common_name": "Human",
                    "weight": 23.9,
                    "length": 1278,
                    "chemical_mass": 142167.0
                }
            ]
        },
        {
            "start_pos": "696",
            "end_pos": "84",
            "site_lbl": "Asn696",
            "weight": 0.0,
            "snv": [
                {
                    "sequence_org": "N",
                    "sequence_mut": "D",
                    "comment": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-loss (NCS->DCS).",
                    "chr_id": "3",
                    "chr_pos": "146070845",
                    "evidence": [
                        {
                            "id": "rs769059398",
                            "database": "dbSNP",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs769059398"
                        },
                        {
                            "id": "rs769059398",
                            "database": "ExAC",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs769059398"
                        },
                        {
                            "id": "rs769059398",
                            "database": "TOPMed",
                            "url": "https://www.ncbi.nlm.nih.gov/snp/rs769059398#frequency_tab"
                        },
                        {
                            "id": "rs769059398",
                            "database": "gnomAD",
                            "url": "http://gnomad.broadinstitute.org/awesome?query=rs769059398"
                        }
                    ]
                },
                {
                    "sequence_org": "N",
                    "sequence_mut": "S",
                    "comment": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-loss (NCS->SCS).",
                    "chr_id": "3",
                    "chr_pos": "146070844",
                    "evidence": [
                        {
                            "id": "rs1171673791",
                            "database": "dbSNP",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1171673791"
                        },
                        {
                            "id": "rs1171673791",
                            "database": "TOPMed",
                            "url": "https://www.ncbi.nlm.nih.gov/snp/rs1171673791#frequency_tab"
                        },
                        {
                            "id": "rs1171673791",
                            "database": "gnomAD",
                            "url": "http://gnomad.broadinstitute.org/awesome?query=rs1171673791"
                        }
                    ]
                }
            ],
            "uniprot_canonical_ac": "O00469-1",
            "glycoprotein": [
                {
                    "uniprot_canonical_ac": "O00469-1",
                    "start_pos": 696,
                    "end_pos": 696,
                    "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": "Procollagen-lysine,2-oxoglutarate 5-dioxygenase 2",
                    "gene_name": "PLOD2",
                    "tax_id": 9606,
                    "tax_name": "Homo sapiens",
                    "tax_common_name": "Human",
                    "weight": 24.3,
                    "length": 737,
                    "chemical_mass": 84686.0
                }
            ]
        },
        {
            "start_pos": "267",
            "end_pos": "656",
            "site_lbl": "Asn267",
            "weight": 0.0,
            "uniprot_canonical_ac": "O14672-1",
            "glycoprotein": [
                {
                    "uniprot_canonical_ac": "O14672-1",
                    "start_pos": 267,
                    "end_pos": 267,
                    "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": "Disintegrin and metalloproteinase domain-containing protein 10",
                    "gene_name": "ADAM10",
                    "tax_id": 9606,
                    "tax_name": "Homo sapiens",
                    "tax_common_name": "Human",
                    "weight": 60.9,
                    "length": 748,
                    "chemical_mass": 84142.0
                }
            ]
        },
        {
            "start_pos": "551",
            "end_pos": "656",
            "site_lbl": "Asn551",
            "weight": 0.0,
            "uniprot_canonical_ac": "O14672-1",
            "glycoprotein": [
                {
                    "uniprot_canonical_ac": "O14672-1",
                    "start_pos": 551,
                    "end_pos": 551,
                    "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": "Disintegrin and metalloproteinase domain-containing protein 10",
                    "gene_name": "ADAM10",
                    "tax_id": 9606,
                    "tax_name": "Homo sapiens",
                    "tax_common_name": "Human",
                    "weight": 60.9,
                    "length": 748,
                    "chemical_mass": 84142.0
                }
            ]
        },
        {
            "start_pos": "547",
            "end_pos": "74",
            "site_lbl": "Asn547",
            "weight": 0.0,
            "uniprot_canonical_ac": "O00187-1",
            "glycoprotein": [
                {
                    "uniprot_canonical_ac": "O00187-1",
                    "start_pos": 547,
                    "end_pos": 547,
                    "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": "Mannan-binding lectin serine protease 2",
                    "gene_name": "MASP2",
                    "tax_id": 9606,
                    "tax_name": "Homo sapiens",
                    "tax_common_name": "Human",
                    "weight": 2.8,
                    "length": 686,
                    "chemical_mass": 75702.0
                }
            ]
        },
        {
            "start_pos": "414",
            "end_pos": "754",
            "site_lbl": "Asn414",
            "weight": 0.0,
            "snv": [
                {
                    "sequence_org": "N",
                    "sequence_mut": "H",
                    "comment": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-loss (NLT->HLT).",
                    "chr_id": "4",
                    "chr_pos": "153704147",
                    "evidence": [
                        {
                            "id": "rs764391959",
                            "database": "dbSNP",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs764391959"
                        },
                        {
                            "id": "rs764391959",
                            "database": "ExAC",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs764391959"
                        },
                        {
                            "id": "rs764391959",
                            "database": "gnomAD",
                            "url": "http://gnomad.broadinstitute.org/awesome?query=rs764391959"
                        }
                    ]
                },
                {
                    "sequence_org": "N",
                    "sequence_mut": "Y",
                    "comment": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-loss (NLT->YLT).",
                    "chr_id": "4",
                    "chr_pos": "153704147",
                    "evidence": [
                        {
                            "id": "rs764391959",
                            "database": "dbSNP",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs764391959"
                        },
                        {
                            "id": "rs764391959",
                            "database": "ExAC",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs764391959"
                        },
                        {
                            "id": "rs764391959",
                            "database": "gnomAD",
                            "url": "http://gnomad.broadinstitute.org/awesome?query=rs764391959"
                        }
                    ]
                }
            ],
            "uniprot_canonical_ac": "O60603-1",
            "glycoprotein": [
                {
                    "uniprot_canonical_ac": "O60603-1",
                    "start_pos": 414,
                    "end_pos": 414,
                    "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": "Toll-like receptor 2",
                    "gene_name": "TLR2",
                    "tax_id": 9606,
                    "tax_name": "Homo sapiens",
                    "tax_common_name": "Human",
                    "weight": 26.6,
                    "length": 784,
                    "chemical_mass": 89838.0
                }
            ]
        },
        {
            "start_pos": "274",
            "end_pos": "264",
            "site_lbl": "Asn274",
            "weight": 0.0,
            "snv": [
                {
                    "sequence_org": "N",
                    "sequence_mut": "D",
                    "comment": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-loss (NST->DST).",
                    "chr_id": "4",
                    "chr_pos": "16018505",
                    "evidence": [
                        {
                            "id": "rs778490205",
                            "database": "dbSNP",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs778490205"
                        },
                        {
                            "id": "rs778490205",
                            "database": "ExAC",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs778490205"
                        },
                        {
                            "id": "rs778490205",
                            "database": "gnomAD",
                            "url": "http://gnomad.broadinstitute.org/awesome?query=rs778490205"
                        }
                    ]
                }
            ],
            "uniprot_canonical_ac": "O43490-1",
            "glycoprotein": [
                {
                    "uniprot_canonical_ac": "O43490-1",
                    "start_pos": 274,
                    "end_pos": 274,
                    "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": "Prominin-1",
                    "gene_name": "PROM1",
                    "tax_id": 9606,
                    "tax_name": "Homo sapiens",
                    "tax_common_name": "Human",
                    "weight": 13.2,
                    "length": 865,
                    "chemical_mass": 97202.0
                }
            ]
        },
        {
            "start_pos": "81",
            "end_pos": "845",
            "site_lbl": "Asn81",
            "weight": 0.0,
            "uniprot_canonical_ac": "Q9HBB8-1",
            "glycoprotein": [
                {
                    "uniprot_canonical_ac": "Q9HBB8-1",
                    "start_pos": 81,
                    "end_pos": 81,
                    "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": "Cadherin-related family member 5",
                    "gene_name": "CDHR5",
                    "tax_id": 9606,
                    "tax_name": "Homo sapiens",
                    "tax_common_name": "Human",
                    "weight": 16.1,
                    "length": 845,
                    "chemical_mass": 88223.0
                }
            ]
        },
        {
            "start_pos": "273",
            "end_pos": "263",
            "site_lbl": "Asn273",
            "weight": 0.0,
            "snv": [
                {
                    "sequence_org": "N",
                    "sequence_mut": "K",
                    "comment": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-loss (NSS->KSS).",
                    "chr_id": "19",
                    "chr_pos": "39025444",
                    "evidence": [
                        {
                            "id": "rs1385525052",
                            "database": "dbSNP",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1385525052"
                        },
                        {
                            "id": "rs1385525052",
                            "database": "gnomAD",
                            "url": "http://gnomad.broadinstitute.org/awesome?query=rs1385525052"
                        }
                    ]
                },
                {
                    "sequence_org": "N",
                    "sequence_mut": "S",
                    "comment": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-loss (NSS->SSS).",
                    "chr_id": "19",
                    "chr_pos": "39025445",
                    "evidence": [
                        {
                            "id": "rs112158067",
                            "database": "dbSNP",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs112158067"
                        },
                        {
                            "id": "rs112158067",
                            "database": "TOPMed",
                            "url": "https://www.ncbi.nlm.nih.gov/snp/rs112158067#frequency_tab"
                        },
                        {
                            "id": "rs112158067",
                            "database": "gnomAD",
                            "url": "http://gnomad.broadinstitute.org/awesome?query=rs112158067"
                        }
                    ]
                },
                {
                    "sequence_org": "N",
                    "sequence_mut": "T",
                    "comment": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-loss (NSS->TSS).",
                    "chr_id": "19",
                    "chr_pos": "39025445",
                    "evidence": [
                        {
                            "id": "rs112158067",
                            "database": "dbSNP",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs112158067"
                        },
                        {
                            "id": "rs112158067",
                            "database": "TOPMed",
                            "url": "https://www.ncbi.nlm.nih.gov/snp/rs112158067#frequency_tab"
                        },
                        {
                            "id": "rs112158067",
                            "database": "gnomAD",
                            "url": "http://gnomad.broadinstitute.org/awesome?query=rs112158067"
                        }
                    ]
                }
            ],
            "uniprot_canonical_ac": "Q8NI29-1",
            "glycoprotein": [
                {
                    "uniprot_canonical_ac": "Q8NI29-1",
                    "start_pos": 273,
                    "end_pos": 273,
                    "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": "F-box only protein 27",
                    "gene_name": "FBXO27",
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                    "tax_name": "Homo sapiens",
                    "tax_common_name": "Human",
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                    "length": 283,
                    "chemical_mass": 31623.0
                }
            ]
        },
        {
            "start_pos": "725",
            "end_pos": "814",
            "site_lbl": "Asn725",
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                {
                    "sequence_org": "N",
                    "sequence_mut": "K",
                    "comment": "Somatic mutation passed 1 out of 6 filters: n-glyco-sequon-loss (NVS->KVS).",
                    "chr_id": "2",
                    "chr_pos": "95287213",
                    "evidence": [
                        {
                            "id": "Q8N271",
                            "database": "BioMuta",
                            "url": "https://hivelab.biochemistry.gwu.edu/biomuta/proteinview/Q8N271"
                        },
                        {
                            "id": "rs1253314370",
                            "database": "dbSNP",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1253314370"
                        },
                        {
                            "id": "rs1253314370",
                            "database": "TOPMed",
                            "url": "https://www.ncbi.nlm.nih.gov/snp/rs1253314370#frequency_tab"
                        },
                        {
                            "id": "rs1253314370",
                            "database": "gnomAD",
                            "url": "http://gnomad.broadinstitute.org/awesome?query=rs1253314370"
                        }
                    ],
                    "disease": [
                        {
                            "disease_id": "DOID:1612",
                            "name": "breast cancer",
                            "description": "An organ system cancer that originates in the mammary gland.",
                            "url": "http://disease-ontology.org/term/DOID:1612",
                            "evidence": [
                                {
                                    "id": "1612",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:1612"
                                }
                            ]
                        }
                    ]
                }
            ],
            "uniprot_canonical_ac": "Q8N271-1",
            "glycoprotein": [
                {
                    "uniprot_canonical_ac": "Q8N271-1",
                    "start_pos": 725,
                    "end_pos": 725,
                    "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": "Prominin-2",
                    "gene_name": "PROM2",
                    "tax_id": 9606,
                    "tax_name": "Homo sapiens",
                    "tax_common_name": "Human",
                    "weight": 6.3,
                    "length": 834,
                    "chemical_mass": 91883.0
                }
            ]
        },
        {
            "start_pos": "382",
            "end_pos": "9",
            "site_lbl": "Asn382",
            "weight": 0.0,
            "snv": [
                {
                    "sequence_org": "N",
                    "sequence_mut": "D",
                    "comment": "Somatic mutation passed 0 out of 0 filters:",
                    "chr_id": "1",
                    "chr_pos": "183945557",
                    "evidence": [
                        {
                            "id": "rs759400909",
                            "database": "dbSNP",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs759400909"
                        },
                        {
                            "id": "rs759400909",
                            "database": "ExAC",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs759400909"
                        },
                        {
                            "id": "rs759400909",
                            "database": "COSMIC",
                            "url": "https://www.ensembl.org/homo_sapiens/Variation/Explore?v=rs759400909"
                        }
                    ]
                },
                {
                    "sequence_org": "N",
                    "sequence_mut": "S",
                    "comment": "Somatic mutation passed 1 out of 6 filters: n-glyco-sequon-loss (NTS->STS).",
                    "chr_id": "1",
                    "chr_pos": "183945556",
                    "evidence": [
                        {
                            "id": "Q8IYK4",
                            "database": "BioMuta",
                            "url": "https://hivelab.biochemistry.gwu.edu/biomuta/proteinview/Q8IYK4"
                        },
                        {
                            "id": "rs1227000124",
                            "database": "dbSNP",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1227000124"
                        },
                        {
                            "id": "rs1227000124",
                            "database": "TOPMed",
                            "url": "https://www.ncbi.nlm.nih.gov/snp/rs1227000124#frequency_tab"
                        },
                        {
                            "id": "rs1227000124",
                            "database": "gnomAD",
                            "url": "http://gnomad.broadinstitute.org/awesome?query=rs1227000124"
                        }
                    ],
                    "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"
                                }
                            ]
                        }
                    ]
                },
                {
                    "sequence_org": "N",
                    "sequence_mut": "T",
                    "comment": "Germline mutation passed 0 out of 0 filters:",
                    "chr_id": "1",
                    "chr_pos": "183945556",
                    "evidence": [
                        {
                            "id": "rs1227000124",
                            "database": "dbSNP",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1227000124"
                        },
                        {
                            "id": "rs1227000124",
                            "database": "TOPMed",
                            "url": "https://www.ncbi.nlm.nih.gov/snp/rs1227000124#frequency_tab"
                        },
                        {
                            "id": "rs1227000124",
                            "database": "gnomAD",
                            "url": "http://gnomad.broadinstitute.org/awesome?query=rs1227000124"
                        }
                    ]
                }
            ],
            "uniprot_canonical_ac": "Q8IYK4-1",
            "glycoprotein": [
                {
                    "uniprot_canonical_ac": "Q8IYK4-1",
                    "start_pos": 382,
                    "end_pos": 382,
                    "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": "Procollagen galactosyltransferase 2",
                    "gene_name": "COLGALT2",
                    "tax_id": 9606,
                    "tax_name": "Homo sapiens",
                    "tax_common_name": "Human",
                    "weight": 7.2,
                    "length": 626,
                    "chemical_mass": 72924.0
                }
            ]
        },
        {
            "start_pos": "236",
            "end_pos": "7",
            "site_lbl": "Asn236",
            "weight": 0.0,
            "snv": [
                {
                    "sequence_org": "N",
                    "sequence_mut": "S",
                    "comment": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-loss (NCS->SCS).",
                    "chr_id": "19",
                    "chr_pos": "40371701",
                    "evidence": [
                        {
                            "id": "rs375716725",
                            "database": "dbSNP",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs375716725"
                        },
                        {
                            "id": "rs375716725",
                            "database": "ExAC",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs375716725"
                        },
                        {
                            "id": "rs375716725",
                            "database": "TOPMed",
                            "url": "https://www.ncbi.nlm.nih.gov/snp/rs375716725#frequency_tab"
                        },
                        {
                            "id": "rs375716725",
                            "database": "gnomAD",
                            "url": "http://gnomad.broadinstitute.org/awesome?query=rs375716725"
                        }
                    ]
                }
            ],
            "mutagenesis": [
                {
                    "sequence_org": "N",
                    "sequence_mut": "S",
                    "comment": "Increases exonuclease activity toward CpG-free ssDNA substrates. Slightly decreases exonuclease activity toward a CpG-rich ATP6 ssDNA sequence. Loss of exonuclease activity toward a CpG-rich ND4L ssDNA sequence. Increases mitophagy rate. No effect on protein maturation or trafficking to lysosomes.",
                    "evidence": [
                        {
                            "database": "UniProtKB",
                            "id": "Q8IV08",
                            "url": "https://www.uniprot.org/uniprotkb/Q8IV08"
                        },
                        {
                            "database": "PubMed",
                            "id": "37225734",
                            "url": "https://glygen.org/publication/PubMed/37225734"
                        }
                    ]
                }
            ],
            "uniprot_canonical_ac": "Q8IV08-1",
            "glycoprotein": [
                {
                    "uniprot_canonical_ac": "Q8IV08-1",
                    "start_pos": 236,
                    "end_pos": 236,
                    "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": "5'-3' exonuclease PLD3",
                    "gene_name": "PLD3",
                    "tax_id": 9606,
                    "tax_name": "Homo sapiens",
                    "tax_common_name": "Human",
                    "weight": 21.2,
                    "length": 490,
                    "chemical_mass": 54705.0
                }
            ]
        },
        {
            "start_pos": "389",
            "end_pos": "76",
            "site_lbl": "Asn389",
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            "snv": [
                {
                    "sequence_org": "N",
                    "sequence_mut": "K",
                    "comment": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-loss (NGT->KGT).",
                    "chr_id": "16",
                    "chr_pos": "263754",
                    "evidence": [
                        {
                            "id": "rs563568001",
                            "database": "dbSNP",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs563568001"
                        },
                        {
                            "id": "rs563568001",
                            "database": "1000Genomes",
                            "url": "https://www.ensembl.org/homo_sapiens/Variation/Explore?v=rs563568001"
                        },
                        {
                            "id": "rs563568001",
                            "database": "ExAC",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs563568001"
                        },
                        {
                            "id": "rs563568001",
                            "database": "TOPMed",
                            "url": "https://www.ncbi.nlm.nih.gov/snp/rs563568001#frequency_tab"
                        },
                        {
                            "id": "rs563568001",
                            "database": "gnomAD",
                            "url": "http://gnomad.broadinstitute.org/awesome?query=rs563568001"
                        }
                    ]
                }
            ],
            "uniprot_canonical_ac": "Q9H0X4-1",
            "glycoprotein": [
                {
                    "uniprot_canonical_ac": "Q9H0X4-1",
                    "start_pos": 389,
                    "end_pos": 389,
                    "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": "Protein FAM234A",
                    "gene_name": "FAM234A",
                    "tax_id": 9606,
                    "tax_name": "Homo sapiens",
                    "tax_common_name": "Human",
                    "weight": 8.7,
                    "length": 552,
                    "chemical_mass": 59660.0
                }
            ]
        },
        {
            "start_pos": "508",
            "end_pos": "99",
            "site_lbl": "Asn508",
            "weight": 0.0,
            "snv": [
                {
                    "sequence_org": "N",
                    "sequence_mut": "K",
                    "comment": "Somatic mutation passed 1 out of 6 filters: n-glyco-sequon-loss (NGS->KGS).",
                    "chr_id": "10",
                    "chr_pos": "7576907",
                    "evidence": [
                        {
                            "id": "Q86UX2",
                            "database": "BioMuta",
                            "url": "https://hivelab.biochemistry.gwu.edu/biomuta/proteinview/Q86UX2"
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                    ],
                    "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"
                                }
                            ]
                        }
                    ]
                },
                {
                    "sequence_org": "N",
                    "sequence_mut": "S",
                    "comment": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-loss (NGS->SGS).",
                    "chr_id": "10",
                    "chr_pos": "7576908",
                    "evidence": [
                        {
                            "id": "rs765900247",
                            "database": "dbSNP",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs765900247"
                        },
                        {
                            "id": "rs765900247",
                            "database": "ExAC",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs765900247"
                        },
                        {
                            "id": "rs765900247",
                            "database": "gnomAD",
                            "url": "http://gnomad.broadinstitute.org/awesome?query=rs765900247"
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                    ]
                }
            ],
            "uniprot_canonical_ac": "Q86UX2-1",
            "glycoprotein": [
                {
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                    "start_pos": 508,
                    "end_pos": 508,
                    "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": "Inter-alpha-trypsin inhibitor heavy chain H5",
                    "gene_name": "ITIH5",
                    "tax_id": 9606,
                    "tax_name": "Homo sapiens",
                    "tax_common_name": "Human",
                    "weight": 14.6,
                    "length": 942,
                    "chemical_mass": 104576.0
                }
            ]
        },
        {
            "start_pos": "439",
            "end_pos": "904",
            "site_lbl": "Asn439",
            "weight": 0.0,
            "snv": [
                {
                    "sequence_org": "N",
                    "sequence_mut": "K",
                    "comment": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-loss (NHT->KHT).",
                    "chr_id": "10",
                    "chr_pos": "86943467",
                    "evidence": [
                        {
                            "id": "rs763050868",
                            "database": "dbSNP",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs763050868"
                        },
                        {
                            "id": "rs763050868",
                            "database": "ExAC",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs763050868"
                        },
                        {
                            "id": "rs763050868",
                            "database": "TOPMed",
                            "url": "https://www.ncbi.nlm.nih.gov/snp/rs763050868#frequency_tab"
                        },
                        {
                            "id": "rs763050868",
                            "database": "gnomAD",
                            "url": "http://gnomad.broadinstitute.org/awesome?query=rs763050868"
                        }
                    ]
                }
            ],
            "uniprot_canonical_ac": "Q9H8L6-1",
            "glycoprotein": [
                {
                    "uniprot_canonical_ac": "Q9H8L6-1",
                    "start_pos": 439,
                    "end_pos": 439,
                    "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": "Multimerin-2",
                    "gene_name": "MMRN2",
                    "tax_id": 9606,
                    "tax_name": "Homo sapiens",
                    "tax_common_name": "Human",
                    "weight": 30.6,
                    "length": 949,
                    "chemical_mass": 104409.0
                }
            ]
        },
        {
            "start_pos": "131",
            "end_pos": "60",
            "site_lbl": "Asn131",
            "weight": 0.0,
            "uniprot_canonical_ac": "O43852-1",
            "glycoprotein": [
                {
                    "uniprot_canonical_ac": "O43852-1",
                    "start_pos": 131,
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                    "residue": "Asn",
                    "evidence": [
                        {
                            "database": "PubMed",
                            "id": "37074911",
                            "url": "https://glygen.org/publication/PubMed/37074911"
                        },
                        {
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                            "id": "PDC000471",
                            "url": "https://proteomic.datacommons.cancer.gov/pdc/study/PDC000471"
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                    ],
                    "protein_name": "Calumenin",
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                    "tax_name": "Homo sapiens",
                    "tax_common_name": "Human",
                    "weight": 39.3,
                    "length": 315,
                    "chemical_mass": 37107.0
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            ]
        },
        {
            "start_pos": "517",
            "end_pos": "71",
            "site_lbl": "Asn517",
            "weight": 0.0,
            "snv": [
                {
                    "sequence_org": "N",
                    "sequence_mut": "K",
                    "comment": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-loss (NLS->KLS).",
                    "chr_id": "6",
                    "chr_pos": "132297913",
                    "evidence": [
                        {
                            "id": "rs761241376",
                            "database": "dbSNP",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs761241376"
                        },
                        {
                            "id": "rs761241376",
                            "database": "ExAC",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs761241376"
                        },
                        {
                            "id": "rs761241376",
                            "database": "TOPMed",
                            "url": "https://www.ncbi.nlm.nih.gov/snp/rs761241376#frequency_tab"
                        },
                        {
                            "id": "rs761241376",
                            "database": "gnomAD",
                            "url": "http://gnomad.broadinstitute.org/awesome?query=rs761241376"
                        }
                    ]
                }
            ],
            "uniprot_canonical_ac": "Q6UVY6-1",
            "glycoprotein": [
                {
                    "uniprot_canonical_ac": "Q6UVY6-1",
                    "start_pos": 517,
                    "end_pos": 517,
                    "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": "DBH-like monooxygenase protein 1",
                    "gene_name": "MOXD1",
                    "tax_id": 9606,
                    "tax_name": "Homo sapiens",
                    "tax_common_name": "Human",
                    "weight": 11.6,
                    "length": 613,
                    "chemical_mass": 69652.0
                }
            ]
        },
        {
            "start_pos": "273",
            "end_pos": "99",
            "site_lbl": "Asn273",
            "weight": 0.0,
            "snv": [
                {
                    "sequence_org": "N",
                    "sequence_mut": "K",
                    "comment": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-loss (NYT->KYT).",
                    "chr_id": "16",
                    "chr_pos": "68259237",
                    "evidence": [
                        {
                            "id": "rs371632429",
                            "database": "dbSNP",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs371632429"
                        },
                        {
                            "id": "rs371632429",
                            "database": "ExAC",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs371632429"
                        },
                        {
                            "id": "rs371632429",
                            "database": "TOPMed",
                            "url": "https://www.ncbi.nlm.nih.gov/snp/rs371632429#frequency_tab"
                        },
                        {
                            "id": "rs371632429",
                            "database": "gnomAD",
                            "url": "http://gnomad.broadinstitute.org/awesome?query=rs371632429"
                        }
                    ]
                }
            ],
            "mutagenesis": [
                {
                    "sequence_org": "N",
                    "sequence_mut": "A",
                    "comment": "Loss of glycosylation site. Mildly reduces production of the mature, active enzyme.",
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