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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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                    "tax_id": 9606,
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                    "tax_common_name": "Human",
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            ]
        },
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                        {
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                    ],
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                        {
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                        {
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                            "id": "G00912UN",
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                        {
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                        {
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            ]
        },
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                        {
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                            "id": "G00912UN",
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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": "G00912UN",
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                        },
                        {
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                        {
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            ]
        },
        {
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            "glycoprotein": [
                {
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                        {
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                        },
                        {
                            "database": "GPTwiki",
                            "id": "G00912UN",
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                        },
                        {
                            "database": "PubMed",
                            "id": "37074911",
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                        },
                        {
                            "database": "PDC",
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                    ],
                    "protein_name": "Complement factor I",
                    "gene_name": "CFI",
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                    "chemical_mass": 65750.0
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            ]
        },
        {
            "start_pos": "464",
            "site_seq": "SIPACVPWSPYLFQPnDTCIVSGWGR",
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                {
                    "uniprot_canonical_ac": "P05156-1",
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                        {
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                        },
                        {
                            "database": "GPTwiki",
                            "id": "G00912UN",
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                        },
                        {
                            "database": "PubMed",
                            "id": "37074911",
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                        {
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                    ],
                    "protein_name": "Complement factor I",
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            ]
        },
        {
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                        {
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                        },
                        {
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                            "id": "G00912UN",
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                        {
                            "database": "PubMed",
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                        {
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                    ],
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            ]
        },
        {
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                {
                    "uniprot_canonical_ac": "P05156-1",
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                        {
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                    ],
                    "protein_name": "Complement factor I",
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            ]
        },
        {
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                {
                    "uniprot_canonical_ac": "P05156-1",
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                        {
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                    ],
                    "protein_name": "Complement factor I",
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            ]
        },
        {
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                {
                    "uniprot_canonical_ac": "P05156-1",
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                        {
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                    ],
                    "protein_name": "Complement factor I",
                    "gene_name": "CFI",
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            ]
        },
        {
            "start_pos": "536",
            "site_seq": "N",
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            "glycoprotein": [
                {
                    "uniprot_canonical_ac": "P05156-1",
                    "start_pos": 536,
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                        {
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                    ],
                    "protein_name": "Complement factor I",
                    "gene_name": "CFI",
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                    "chemical_mass": 65750.0
                }
            ]
        },
        {
            "start_pos": "70",
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                {
                    "uniprot_canonical_ac": "P05156-1",
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                            "id": "G00912UN",
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                        {
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                    ],
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                    "chemical_mass": 65750.0
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            ]
        },
        {
            "start_pos": "70",
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                {
                    "uniprot_canonical_ac": "P05156-1",
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                        {
                            "database": "GPTwiki",
                            "id": "G00912UN",
                            "url": "https://edwardslab.bmcb.georgetown.edu/gptwiki/G00912UN"
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                        {
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                            "id": "37074911",
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                        },
                        {
                            "database": "PDC",
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                    ],
                    "protein_name": "Complement factor I",
                    "gene_name": "CFI",
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                    "tax_common_name": "Human",
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            ]
        },
        {
            "start_pos": "70",
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                {
                    "uniprot_canonical_ac": "P05156-1",
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                        {
                            "database": "GPTwiki",
                            "id": "G00912UN",
                            "url": "https://edwardslab.bmcb.georgetown.edu/gptwiki/G00912UN"
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                        {
                            "database": "PubMed",
                            "id": "37074911",
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                        },
                        {
                            "database": "PDC",
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                    ],
                    "protein_name": "Complement factor I",
                    "gene_name": "CFI",
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                    "tax_common_name": "Human",
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                    "chemical_mass": 65750.0
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            ]
        },
        {
            "start_pos": "177",
            "site_seq": "",
            "site_lbl": "N177",
            "residue": "",
            "snv": [
                {
                    "weight": 100,
                    "sequence_org": "N",
                    "sequence_mut": "H",
                    "comment": "Somatic mutation passed 1 out of 6 filters: n-glyco-sequon-loss (NST->HST).",
                    "chr_id": "4",
                    "chr_pos": "109761646",
                    "evidence": [
                        {
                            "id": "P05156",
                            "database": "BioMuta",
                            "url": "https://hivelab.biochemistry.gwu.edu/biomuta/proteinview/P05156"
                        }
                    ],
                    "disease": [
                        {
                            "disease_id": "DOID:9256",
                            "name": "colorectal cancer",
                            "description": "A large intestine cancer that is located_in the colon and/or located_in the rectum.",
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                            "evidence": [
                                {
                                    "id": "9256",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:9256"
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                            ]
                        }
                    ]
                },
                {
                    "weight": 100,
                    "sequence_org": "N",
                    "sequence_mut": "I",
                    "comment": "Somatic mutation passed 1 out of 6 filters: n-glyco-sequon-loss (NST->IST).",
                    "chr_id": "4",
                    "chr_pos": "109761645",
                    "evidence": [
                        {
                            "id": "P05156",
                            "database": "BioMuta",
                            "url": "https://hivelab.biochemistry.gwu.edu/biomuta/proteinview/P05156"
                        },
                        {
                            "id": "rs753060374",
                            "database": "dbSNP",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs753060374"
                        },
                        {
                            "id": "rs753060374",
                            "database": "ExAC",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs753060374"
                        },
                        {
                            "id": "rs753060374",
                            "database": "TOPMed",
                            "url": "https://www.ncbi.nlm.nih.gov/snp/rs753060374#frequency_tab"
                        },
                        {
                            "id": "rs753060374",
                            "database": "gnomAD",
                            "url": "http://gnomad.broadinstitute.org/awesome?query=rs753060374"
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                    ],
                    "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"
                                }
                            ]
                        },
                        {
                            "disease_id": "DOID:0110025",
                            "name": "age related macular degeneration 13",
                            "description": "An age related macular degeneration conferred by heterozygous mutation in the CFI gene on chromosome 4q25.",
                            "url": "http://disease-ontology.org/term/DOID:0110025",
                            "evidence": [
                                {
                                    "id": "615439",
                                    "database": "MIM",
                                    "url": "https://www.omim.org/entry/615439"
                                },
                                {
                                    "id": "0110025",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0110025"
                                }
                            ]
                        },
                        {
                            "disease_id": "DOID:0110025",
                            "name": "age related macular degeneration 13",
                            "description": "An age related macular degeneration conferred by heterozygous mutation in the CFI gene on chromosome 4q25.",
                            "url": "http://disease-ontology.org/term/DOID:0110025",
                            "evidence": [
                                {
                                    "id": "615439",
                                    "database": "MIM",
                                    "url": "https://www.omim.org/entry/615439"
                                },
                                {
                                    "id": "0110025",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0110025"
                                }
                            ]
                        },
                        {
                            "disease_id": "DOID:0110025",
                            "name": "age related macular degeneration 13",
                            "description": "An age related macular degeneration conferred by heterozygous mutation in the CFI gene on chromosome 4q25.",
                            "url": "http://disease-ontology.org/term/DOID:0110025",
                            "evidence": [
                                {
                                    "id": "615439",
                                    "database": "MIM",
                                    "url": "https://www.omim.org/entry/615439"
                                },
                                {
                                    "id": "0110025",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0110025"
                                }
                            ]
                        },
                        {
                            "disease_id": "DOID:0110025",
                            "name": "age related macular degeneration 13",
                            "description": "An age related macular degeneration conferred by heterozygous mutation in the CFI gene on chromosome 4q25.",
                            "url": "http://disease-ontology.org/term/DOID:0110025",
                            "evidence": [
                                {
                                    "id": "615439",
                                    "database": "MIM",
                                    "url": "https://www.omim.org/entry/615439"
                                },
                                {
                                    "id": "0110025",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0110025"
                                }
                            ]
                        },
                        {
                            "disease_id": "DOID:0050419",
                            "name": "complement factor I deficiency",
                            "description": "A complement deficiency that is characterized by recurrent pyogenic bacterial infections that is the result of complement component 3 deficiency.",
                            "url": "http://disease-ontology.org/term/DOID:0050419",
                            "evidence": [
                                {
                                    "id": "610984",
                                    "database": "MIM",
                                    "url": "https://www.omim.org/entry/610984"
                                },
                                {
                                    "id": "0050419",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0050419"
                                }
                            ]
                        },
                        {
                            "disease_id": "DOID:0050419",
                            "name": "complement factor I deficiency",
                            "description": "A complement deficiency that is characterized by recurrent pyogenic bacterial infections that is the result of complement component 3 deficiency.",
                            "url": "http://disease-ontology.org/term/DOID:0050419",
                            "evidence": [
                                {
                                    "id": "610984",
                                    "database": "MIM",
                                    "url": "https://www.omim.org/entry/610984"
                                },
                                {
                                    "id": "0050419",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0050419"
                                }
                            ]
                        },
                        {
                            "disease_id": "DOID:0050419",
                            "name": "complement factor I deficiency",
                            "description": "A complement deficiency that is characterized by recurrent pyogenic bacterial infections that is the result of complement component 3 deficiency.",
                            "url": "http://disease-ontology.org/term/DOID:0050419",
                            "evidence": [
                                {
                                    "id": "610984",
                                    "database": "MIM",
                                    "url": "https://www.omim.org/entry/610984"
                                },
                                {
                                    "id": "0050419",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0050419"
                                }
                            ]
                        },
                        {
                            "disease_id": "DOID:0050419",
                            "name": "complement factor I deficiency",
                            "description": "A complement deficiency that is characterized by recurrent pyogenic bacterial infections that is the result of complement component 3 deficiency.",
                            "url": "http://disease-ontology.org/term/DOID:0050419",
                            "evidence": [
                                {
                                    "id": "610984",
                                    "database": "MIM",
                                    "url": "https://www.omim.org/entry/610984"
                                },
                                {
                                    "id": "0050419",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0050419"
                                }
                            ]
                        },
                        {
                            "disease_id": "DOID:0110025",
                            "name": "age related macular degeneration 13",
                            "description": "An age related macular degeneration conferred by heterozygous mutation in the CFI gene on chromosome 4q25.",
                            "url": "http://disease-ontology.org/term/DOID:0110025",
                            "evidence": [
                                {
                                    "id": "615439",
                                    "database": "MIM",
                                    "url": "https://www.omim.org/entry/615439"
                                },
                                {
                                    "id": "0110025",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0110025"
                                }
                            ]
                        },
                        {
                            "disease_id": "DOID:0110025",
                            "name": "age related macular degeneration 13",
                            "description": "An age related macular degeneration conferred by heterozygous mutation in the CFI gene on chromosome 4q25.",
                            "url": "http://disease-ontology.org/term/DOID:0110025",
                            "evidence": [
                                {
                                    "id": "615439",
                                    "database": "MIM",
                                    "url": "https://www.omim.org/entry/615439"
                                },
                                {
                                    "id": "0110025",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0110025"
                                }
                            ]
                        },
                        {
                            "disease_id": "DOID:0110025",
                            "name": "age related macular degeneration 13",
                            "description": "An age related macular degeneration conferred by heterozygous mutation in the CFI gene on chromosome 4q25.",
                            "url": "http://disease-ontology.org/term/DOID:0110025",
                            "evidence": [
                                {
                                    "id": "615439",
                                    "database": "MIM",
                                    "url": "https://www.omim.org/entry/615439"
                                },
                                {
                                    "id": "0110025",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0110025"
                                }
                            ]
                        },
                        {
                            "disease_id": "DOID:0110025",
                            "name": "age related macular degeneration 13",
                            "description": "An age related macular degeneration conferred by heterozygous mutation in the CFI gene on chromosome 4q25.",
                            "url": "http://disease-ontology.org/term/DOID:0110025",
                            "evidence": [
                                {
                                    "id": "615439",
                                    "database": "MIM",
                                    "url": "https://www.omim.org/entry/615439"
                                },
                                {
                                    "id": "0110025",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0110025"
                                }
                            ]
                        },
                        {
                            "disease_id": "DOID:0050419",
                            "name": "complement factor I deficiency",
                            "description": "A complement deficiency that is characterized by recurrent pyogenic bacterial infections that is the result of complement component 3 deficiency.",
                            "url": "http://disease-ontology.org/term/DOID:0050419",
                            "evidence": [
                                {
                                    "id": "610984",
                                    "database": "MIM",
                                    "url": "https://www.omim.org/entry/610984"
                                },
                                {
                                    "id": "0050419",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0050419"
                                }
                            ]
                        },
                        {
                            "disease_id": "DOID:0050419",
                            "name": "complement factor I deficiency",
                            "description": "A complement deficiency that is characterized by recurrent pyogenic bacterial infections that is the result of complement component 3 deficiency.",
                            "url": "http://disease-ontology.org/term/DOID:0050419",
                            "evidence": [
                                {
                                    "id": "610984",
                                    "database": "MIM",
                                    "url": "https://www.omim.org/entry/610984"
                                },
                                {
                                    "id": "0050419",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0050419"
                                }
                            ]
                        },
                        {
                            "disease_id": "DOID:0050419",
                            "name": "complement factor I deficiency",
                            "description": "A complement deficiency that is characterized by recurrent pyogenic bacterial infections that is the result of complement component 3 deficiency.",
                            "url": "http://disease-ontology.org/term/DOID:0050419",
                            "evidence": [
                                {
                                    "id": "610984",
                                    "database": "MIM",
                                    "url": "https://www.omim.org/entry/610984"
                                },
                                {
                                    "id": "0050419",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0050419"
                                }
                            ]
                        },
                        {
                            "disease_id": "DOID:0050419",
                            "name": "complement factor I deficiency",
                            "description": "A complement deficiency that is characterized by recurrent pyogenic bacterial infections that is the result of complement component 3 deficiency.",
                            "url": "http://disease-ontology.org/term/DOID:0050419",
                            "evidence": [
                                {
                                    "id": "610984",
                                    "database": "MIM",
                                    "url": "https://www.omim.org/entry/610984"
                                },
                                {
                                    "id": "0050419",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0050419"
                                }
                            ]
                        }
                    ]
                }
            ],
            "glycoprotein": [
                {
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                    "end_pos": 177,
                    "residue": "asn",
                    "evidence": [
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                            "database": "PubMed",
                            "id": "29671580",
                            "url": "https://glygen.org/publication/PubMed/29671580"
                        },
                        {
                            "database": "UniCarbKB",
                            "id": "GLY_000040",
                            "url": "http://data.glygen.org/GLY_000040"
                        },
                        {
                            "database": "GPTwiki",
                            "id": "G00912UN",
                            "url": "https://edwardslab.bmcb.georgetown.edu/gptwiki/G00912UN"
                        },
                        {
                            "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": "Complement factor I",
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                    "tax_name": "Homo sapiens",
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                    "chemical_mass": 65750.0
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            ]
        },
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            "site_lbl": "N464",
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                {
                    "weight": 100,
                    "sequence_org": "N",
                    "sequence_mut": "K",
                    "comment": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-loss (NDT->KDT).",
                    "chr_id": "4",
                    "chr_pos": "109746259",
                    "evidence": [
                        {
                            "id": "rs759927335",
                            "database": "dbSNP",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs759927335"
                        },
                        {
                            "id": "rs759927335",
                            "database": "ExAC",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs759927335"
                        },
                        {
                            "id": "rs759927335",
                            "database": "TOPMed",
                            "url": "https://www.ncbi.nlm.nih.gov/snp/rs759927335#frequency_tab"
                        },
                        {
                            "id": "rs759927335",
                            "database": "gnomAD",
                            "url": "http://gnomad.broadinstitute.org/awesome?query=rs759927335"
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                    ]
                }
            ],
            "glycoprotein": [
                {
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                    "end_pos": 464,
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                    "evidence": [
                        {
                            "database": "PubMed",
                            "id": "29671580",
                            "url": "https://glygen.org/publication/PubMed/29671580"
                        },
                        {
                            "database": "UniCarbKB",
                            "id": "GLY_000040",
                            "url": "http://data.glygen.org/GLY_000040"
                        },
                        {
                            "database": "GPTwiki",
                            "id": "G00912UN",
                            "url": "https://edwardslab.bmcb.georgetown.edu/gptwiki/G00912UN"
                        },
                        {
                            "database": "PubMed",
                            "id": "37074911",
                            "url": "https://glygen.org/publication/PubMed/37074911"
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                        {
                            "database": "PDC",
                            "id": "PDC000471",
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                    ],
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                    "gene_name": "CFI",
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                    "tax_common_name": "Human",
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            ]
        },
        {
            "start_pos": "494",
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            "snv": [
                {
                    "weight": 100,
                    "sequence_org": "N",
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                    "comment": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-loss (NCS->TCS).",
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                    "chr_pos": "109742544",
                    "evidence": [
                        {
                            "id": "rs1723931486",
                            "database": "dbSNP",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1723931486"
                        },
                        {
                            "id": "rs1723931486",
                            "database": "gnomAD",
                            "url": "http://gnomad.broadinstitute.org/awesome?query=rs1723931486"
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                    ]
                }
            ],
            "glycoprotein": [
                {
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                        {
                            "database": "PubMed",
                            "id": "37074911",
                            "url": "https://glygen.org/publication/PubMed/37074911"
                        },
                        {
                            "database": "PDC",
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                            "url": "https://proteomic.datacommons.cancer.gov/pdc/study/PDC000471"
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                    ],
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            ]
        },
        {
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            "snv": [
                {
                    "weight": 100,
                    "sequence_org": "N",
                    "sequence_mut": "D",
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                    "chr_pos": "109741039",
                    "evidence": [
                        {
                            "id": "rs1314998523",
                            "database": "dbSNP",
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                        },
                        {
                            "id": "rs1314998523",
                            "database": "TOPMed",
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                        },
                        {
                            "id": "rs1314998523",
                            "database": "gnomAD",
                            "url": "http://gnomad.broadinstitute.org/awesome?query=rs1314998523"
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                    ]
                },
                {
                    "weight": 100,
                    "sequence_org": "N",
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                    "comment": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-loss (NVT->KVT).",
                    "chr_id": "4",
                    "chr_pos": "109741037",
                    "evidence": [
                        {
                            "id": "rs1336453366",
                            "database": "dbSNP",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1336453366"
                        },
                        {
                            "id": "rs1336453366",
                            "database": "TOPMed",
                            "url": "https://www.ncbi.nlm.nih.gov/snp/rs1336453366#frequency_tab"
                        },
                        {
                            "id": "rs1336453366",
                            "database": "gnomAD",
                            "url": "http://gnomad.broadinstitute.org/awesome?query=rs1336453366"
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                    ]
                },
                {
                    "weight": 100,
                    "sequence_org": "N",
                    "sequence_mut": "S",
                    "comment": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-loss (NVT->SVT).",
                    "chr_id": "4",
                    "chr_pos": "109741038",
                    "evidence": [
                        {
                            "id": "rs1357609555",
                            "database": "dbSNP",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1357609555"
                        },
                        {
                            "id": "rs1357609555",
                            "database": "TOPMed",
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                        },
                        {
                            "id": "rs1357609555",
                            "database": "gnomAD",
                            "url": "http://gnomad.broadinstitute.org/awesome?query=rs1357609555"
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                    ]
                }
            ],
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                {
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                        {
                            "database": "GPTwiki",
                            "id": "G00912UN",
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                    ],
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                    "gene_name": "CFI",
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            ]
        },
        {
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                {
                    "weight": 100,
                    "sequence_org": "N",
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                    "comment": "Somatic mutation passed 1 out of 6 filters: n-glyco-sequon-loss (NGT->IGT).",
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                    "chr_pos": "109766673",
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                        {
                            "id": "P05156",
                            "database": "BioMuta",
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                    ],
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                            "description": "An integumentary system cancer located_in the skin that is the uncontrolled growth of abnormal skin cells.",
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                            "evidence": [
                                {
                                    "id": "4159",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:4159"
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                            ]
                        }
                    ]
                },
                {
                    "weight": 100,
                    "sequence_org": "N",
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                    "comment": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-loss (NGT->TGT).",
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                        {
                            "id": "rs749553820",
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                        {
                            "id": "rs749553820",
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                        {
                            "id": "rs749553820",
                            "database": "TOPMed",
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                        },
                        {
                            "id": "rs749553820",
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                    ]
                }
            ],
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                    ],
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                    "tax_common_name": "Human",
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                    "chemical_mass": 65750.0
                }
            ]
        },
        {
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            "site_seq": "N",
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                {
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                        {
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                            "id": "GLY_000040",
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                        {
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                            "id": "G00912UN",
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                        {
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                        {
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                    ],
                    "protein_name": "Complement factor I",
                    "gene_name": "CFI",
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                    "tax_name": "Homo sapiens",
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                    "chemical_mass": 65750.0
                }
            ]
        },
        {
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                {
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                        {
                            "database": "UniCarbKB",
                            "id": "GLY_000040",
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                        {
                            "database": "GPTwiki",
                            "id": "G00912UN",
                            "url": "https://edwardslab.bmcb.georgetown.edu/gptwiki/G00912UN"
                        },
                        {
                            "database": "PubMed",
                            "id": "37074911",
                            "url": "https://glygen.org/publication/PubMed/37074911"
                        },
                        {
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                            "id": "PDC000471",
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                    ],
                    "protein_name": "Complement factor I",
                    "gene_name": "CFI",
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                    "tax_name": "Homo sapiens",
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                    "chemical_mass": 65750.0
                }
            ]
        },
        {
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            "site_seq": "LSDLSINSTECLHVHCR",
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                {
                    "uniprot_canonical_ac": "P05156-1",
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                        {
                            "database": "UniCarbKB",
                            "id": "GLY_000040",
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                        },
                        {
                            "database": "GPTwiki",
                            "id": "G00912UN",
                            "url": "https://edwardslab.bmcb.georgetown.edu/gptwiki/G00912UN"
                        },
                        {
                            "database": "PubMed",
                            "id": "37074911",
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                        },
                        {
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                            "id": "PDC000471",
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                    ],
                    "protein_name": "Complement factor I",
                    "gene_name": "CFI",
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                    "tax_name": "Homo sapiens",
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                    "chemical_mass": 65750.0
                }
            ]
        },
        {
            "start_pos": "464",
            "site_seq": "N",
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            "glycoprotein": [
                {
                    "uniprot_canonical_ac": "P05156-1",
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                    "end_pos": 464,
                    "residue": "asn",
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                        {
                            "database": "PubMed",
                            "id": "29671580",
                            "url": "https://glygen.org/publication/PubMed/29671580"
                        },
                        {
                            "database": "UniCarbKB",
                            "id": "GLY_000040",
                            "url": "http://data.glygen.org/GLY_000040"
                        },
                        {
                            "database": "GPTwiki",
                            "id": "G00912UN",
                            "url": "https://edwardslab.bmcb.georgetown.edu/gptwiki/G00912UN"
                        },
                        {
                            "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": "Complement factor I",
                    "gene_name": "CFI",
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                    "tax_name": "Homo sapiens",
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                    "length": 583,
                    "chemical_mass": 65750.0
                }
            ]
        },
        {
            "start_pos": "464",
            "site_seq": "SIPACVPWSPYLFQPnDTCIVSGWGR",
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                {
                    "uniprot_canonical_ac": "P05156-1",
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                    "end_pos": 464,
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                    "evidence": [
                        {
                            "database": "PubMed",
                            "id": "29671580",
                            "url": "https://glygen.org/publication/PubMed/29671580"
                        },
                        {
                            "database": "UniCarbKB",
                            "id": "GLY_000040",
                            "url": "http://data.glygen.org/GLY_000040"
                        },
                        {
                            "database": "GPTwiki",
                            "id": "G00912UN",
                            "url": "https://edwardslab.bmcb.georgetown.edu/gptwiki/G00912UN"
                        },
                        {
                            "database": "PubMed",
                            "id": "37074911",
                            "url": "https://glygen.org/publication/PubMed/37074911"
                        },
                        {
                            "database": "PDC",
                            "id": "PDC000471",
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                        }
                    ],
                    "protein_name": "Complement factor I",
                    "gene_name": "CFI",
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                    "tax_name": "Homo sapiens",
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            ]
        },
        {
            "start_pos": "464",
            "site_seq": "SIPACVPWSPYLFQPNDTCIVSGWGR",
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                {
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                        {
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                            "id": "GLY_000040",
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                        },
                        {
                            "database": "GPTwiki",
                            "id": "G00912UN",
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                        },
                        {
                            "database": "PubMed",
                            "id": "37074911",
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                        },
                        {
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                    ],
                    "protein_name": "Complement factor I",
                    "gene_name": "CFI",
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                    "tax_name": "Homo sapiens",
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                    "chemical_mass": 65750.0
                }
            ]
        },
        {
            "start_pos": "494",
            "site_seq": "LISnCSK",
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            "residue": "Asn",
            "glycoprotein": [
                {
                    "uniprot_canonical_ac": "P05156-1",
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                    "end_pos": 494,
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                    "evidence": [
                        {
                            "database": "PubMed",
                            "id": "37074911",
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                        },
                        {
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                    ],
                    "protein_name": "Complement factor I",
                    "gene_name": "CFI",
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                    "tax_name": "Homo sapiens",
                    "tax_common_name": "Human",
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                    "chemical_mass": 65750.0
                }
            ]
        },
        {
            "start_pos": "494",
            "site_seq": "N",
            "site_lbl": "Asn494",
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            "glycoprotein": [
                {
                    "uniprot_canonical_ac": "P05156-1",
                    "start_pos": 494,
                    "end_pos": 494,
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                    "evidence": [
                        {
                            "database": "PubMed",
                            "id": "37074911",
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                        {
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                    ],
                    "protein_name": "Complement factor I",
                    "gene_name": "CFI",
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                    "tax_common_name": "Human",
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                    "chemical_mass": 65750.0
                }
            ]
        },
        {
            "start_pos": "494",
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            "glycoprotein": [
                {
                    "uniprot_canonical_ac": "P05156-1",
                    "start_pos": 494,
                    "end_pos": 494,
                    "residue": "Asn",
                    "evidence": [
                        {
                            "database": "PubMed",
                            "id": "37074911",
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                        },
                        {
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                            "id": "PDC000471",
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                    ],
                    "protein_name": "Complement factor I",
                    "gene_name": "CFI",
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                    "tax_common_name": "Human",
                    "length": 583,
                    "chemical_mass": 65750.0
                }
            ]
        },
        {
            "start_pos": "536",
            "site_seq": "N",
            "site_lbl": "Asn536",
            "residue": "Asn",
            "glycoprotein": [
                {
                    "uniprot_canonical_ac": "P05156-1",
                    "start_pos": 536,
                    "end_pos": 536,
                    "residue": "Asn",
                    "evidence": [
                        {
                            "database": "GPTwiki",
                            "id": "G00912UN",
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                    ],
                    "protein_name": "Complement factor I",
                    "gene_name": "CFI",
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                    "tax_name": "Homo sapiens",
                    "tax_common_name": "Human",
                    "length": 583,
                    "chemical_mass": 65750.0
                }
            ]
        },
        {
            "start_pos": "70",
            "site_seq": "N",
            "site_lbl": "Asn70",
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            "glycoprotein": [
                {
                    "uniprot_canonical_ac": "P05156-1",
                    "start_pos": 70,
                    "end_pos": 70,
                    "residue": "Asn",
                    "evidence": [
                        {
                            "database": "GPTwiki",
                            "id": "G00912UN",
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                        },
                        {
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                        {
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                    ],
                    "protein_name": "Complement factor I",
                    "gene_name": "CFI",
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                    "tax_common_name": "Human",
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                    "chemical_mass": 65750.0
                }
            ]
        },
        {
            "start_pos": "70",
            "site_seq": "nGTAVCATNR",
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            "residue": "Asn",
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                {
                    "uniprot_canonical_ac": "P05156-1",
                    "start_pos": 70,
                    "end_pos": 70,
                    "residue": "Asn",
                    "evidence": [
                        {
                            "database": "GPTwiki",
                            "id": "G00912UN",
                            "url": "https://edwardslab.bmcb.georgetown.edu/gptwiki/G00912UN"
                        },
                        {
                            "database": "PubMed",
                            "id": "37074911",
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                        },
                        {
                            "database": "PDC",
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                    ],
                    "protein_name": "Complement factor I",
                    "gene_name": "CFI",
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                    "tax_name": "Homo sapiens",
                    "tax_common_name": "Human",
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                    "chemical_mass": 65750.0
                }
            ]
        },
        {
            "start_pos": "70",
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                {
                    "uniprot_canonical_ac": "P05156-1",
                    "start_pos": 70,
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                    "residue": "Asn",
                    "evidence": [
                        {
                            "database": "GPTwiki",
                            "id": "G00912UN",
                            "url": "https://edwardslab.bmcb.georgetown.edu/gptwiki/G00912UN"
                        },
                        {
                            "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": "Complement factor I",
                    "gene_name": "CFI",
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                    "tax_name": "Homo sapiens",
                    "tax_common_name": "Human",
                    "length": 583,
                    "chemical_mass": 65750.0
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            ]
        },
        {
            "start_pos": "177",
            "site_seq": "",
            "site_lbl": "N177",
            "residue": "",
            "snv": [
                {
                    "weight": 100,
                    "sequence_org": "N",
                    "sequence_mut": "H",
                    "comment": "Somatic mutation passed 1 out of 6 filters: n-glyco-sequon-loss (NST->HST).",
                    "chr_id": "4",
                    "chr_pos": "109761646",
                    "evidence": [
                        {
                            "id": "P05156",
                            "database": "BioMuta",
                            "url": "https://hivelab.biochemistry.gwu.edu/biomuta/proteinview/P05156"
                        }
                    ],
                    "disease": [
                        {
                            "disease_id": "DOID:9256",
                            "name": "colorectal cancer",
                            "description": "A large intestine cancer that is located_in the colon and/or located_in the rectum.",
                            "url": "http://disease-ontology.org/term/DOID:9256",
                            "evidence": [
                                {
                                    "id": "9256",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:9256"
                                }
                            ]
                        }
                    ]
                },
                {
                    "weight": 100,
                    "sequence_org": "N",
                    "sequence_mut": "I",
                    "comment": "Somatic mutation passed 1 out of 6 filters: n-glyco-sequon-loss (NST->IST).",
                    "chr_id": "4",
                    "chr_pos": "109761645",
                    "evidence": [
                        {
                            "id": "P05156",
                            "database": "BioMuta",
                            "url": "https://hivelab.biochemistry.gwu.edu/biomuta/proteinview/P05156"
                        },
                        {
                            "id": "rs753060374",
                            "database": "dbSNP",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs753060374"
                        },
                        {
                            "id": "rs753060374",
                            "database": "ExAC",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs753060374"
                        },
                        {
                            "id": "rs753060374",
                            "database": "TOPMed",
                            "url": "https://www.ncbi.nlm.nih.gov/snp/rs753060374#frequency_tab"
                        },
                        {
                            "id": "rs753060374",
                            "database": "gnomAD",
                            "url": "http://gnomad.broadinstitute.org/awesome?query=rs753060374"
                        }
                    ],
                    "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"
                                }
                            ]
                        },
                        {
                            "disease_id": "DOID:0110025",
                            "name": "age related macular degeneration 13",
                            "description": "An age related macular degeneration conferred by heterozygous mutation in the CFI gene on chromosome 4q25.",
                            "url": "http://disease-ontology.org/term/DOID:0110025",
                            "evidence": [
                                {
                                    "id": "615439",
                                    "database": "MIM",
                                    "url": "https://www.omim.org/entry/615439"
                                },
                                {
                                    "id": "0110025",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0110025"
                                }
                            ]
                        },
                        {
                            "disease_id": "DOID:0110025",
                            "name": "age related macular degeneration 13",
                            "description": "An age related macular degeneration conferred by heterozygous mutation in the CFI gene on chromosome 4q25.",
                            "url": "http://disease-ontology.org/term/DOID:0110025",
                            "evidence": [
                                {
                                    "id": "615439",
                                    "database": "MIM",
                                    "url": "https://www.omim.org/entry/615439"
                                },
                                {
                                    "id": "0110025",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0110025"
                                }
                            ]
                        },
                        {
                            "disease_id": "DOID:0110025",
                            "name": "age related macular degeneration 13",
                            "description": "An age related macular degeneration conferred by heterozygous mutation in the CFI gene on chromosome 4q25.",
                            "url": "http://disease-ontology.org/term/DOID:0110025",
                            "evidence": [
                                {
                                    "id": "615439",
                                    "database": "MIM",
                                    "url": "https://www.omim.org/entry/615439"
                                },
                                {
                                    "id": "0110025",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0110025"
                                }
                            ]
                        },
                        {
                            "disease_id": "DOID:0110025",
                            "name": "age related macular degeneration 13",
                            "description": "An age related macular degeneration conferred by heterozygous mutation in the CFI gene on chromosome 4q25.",
                            "url": "http://disease-ontology.org/term/DOID:0110025",
                            "evidence": [
                                {
                                    "id": "615439",
                                    "database": "MIM",
                                    "url": "https://www.omim.org/entry/615439"
                                },
                                {
                                    "id": "0110025",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0110025"
                                }
                            ]
                        },
                        {
                            "disease_id": "DOID:0050419",
                            "name": "complement factor I deficiency",
                            "description": "A complement deficiency that is characterized by recurrent pyogenic bacterial infections that is the result of complement component 3 deficiency.",
                            "url": "http://disease-ontology.org/term/DOID:0050419",
                            "evidence": [
                                {
                                    "id": "610984",
                                    "database": "MIM",
                                    "url": "https://www.omim.org/entry/610984"
                                },
                                {
                                    "id": "0050419",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0050419"
                                }
                            ]
                        },
                        {
                            "disease_id": "DOID:0050419",
                            "name": "complement factor I deficiency",
                            "description": "A complement deficiency that is characterized by recurrent pyogenic bacterial infections that is the result of complement component 3 deficiency.",
                            "url": "http://disease-ontology.org/term/DOID:0050419",
                            "evidence": [
                                {
                                    "id": "610984",
                                    "database": "MIM",
                                    "url": "https://www.omim.org/entry/610984"
                                },
                                {
                                    "id": "0050419",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0050419"
                                }
                            ]
                        },
                        {
                            "disease_id": "DOID:0050419",
                            "name": "complement factor I deficiency",
                            "description": "A complement deficiency that is characterized by recurrent pyogenic bacterial infections that is the result of complement component 3 deficiency.",
                            "url": "http://disease-ontology.org/term/DOID:0050419",
                            "evidence": [
                                {
                                    "id": "610984",
                                    "database": "MIM",
                                    "url": "https://www.omim.org/entry/610984"
                                },
                                {
                                    "id": "0050419",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0050419"
                                }
                            ]
                        },
                        {
                            "disease_id": "DOID:0050419",
                            "name": "complement factor I deficiency",
                            "description": "A complement deficiency that is characterized by recurrent pyogenic bacterial infections that is the result of complement component 3 deficiency.",
                            "url": "http://disease-ontology.org/term/DOID:0050419",
                            "evidence": [
                                {
                                    "id": "610984",
                                    "database": "MIM",
                                    "url": "https://www.omim.org/entry/610984"
                                },
                                {
                                    "id": "0050419",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0050419"
                                }
                            ]
                        },
                        {
                            "disease_id": "DOID:0110025",
                            "name": "age related macular degeneration 13",
                            "description": "An age related macular degeneration conferred by heterozygous mutation in the CFI gene on chromosome 4q25.",
                            "url": "http://disease-ontology.org/term/DOID:0110025",
                            "evidence": [
                                {
                                    "id": "615439",
                                    "database": "MIM",
                                    "url": "https://www.omim.org/entry/615439"
                                },
                                {
                                    "id": "0110025",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0110025"
                                }
                            ]
                        },
                        {
                            "disease_id": "DOID:0110025",
                            "name": "age related macular degeneration 13",
                            "description": "An age related macular degeneration conferred by heterozygous mutation in the CFI gene on chromosome 4q25.",
                            "url": "http://disease-ontology.org/term/DOID:0110025",
                            "evidence": [
                                {
                                    "id": "615439",
                                    "database": "MIM",
                                    "url": "https://www.omim.org/entry/615439"
                                },
                                {
                                    "id": "0110025",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0110025"
                                }
                            ]
                        },
                        {
                            "disease_id": "DOID:0110025",
                            "name": "age related macular degeneration 13",
                            "description": "An age related macular degeneration conferred by heterozygous mutation in the CFI gene on chromosome 4q25.",
                            "url": "http://disease-ontology.org/term/DOID:0110025",
                            "evidence": [
                                {
                                    "id": "615439",
                                    "database": "MIM",
                                    "url": "https://www.omim.org/entry/615439"
                                },
                                {
                                    "id": "0110025",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0110025"
                                }
                            ]
                        },
                        {
                            "disease_id": "DOID:0110025",
                            "name": "age related macular degeneration 13",
                            "description": "An age related macular degeneration conferred by heterozygous mutation in the CFI gene on chromosome 4q25.",
                            "url": "http://disease-ontology.org/term/DOID:0110025",
                            "evidence": [
                                {
                                    "id": "615439",
                                    "database": "MIM",
                                    "url": "https://www.omim.org/entry/615439"
                                },
                                {
                                    "id": "0110025",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0110025"
                                }
                            ]
                        },
                        {
                            "disease_id": "DOID:0050419",
                            "name": "complement factor I deficiency",
                            "description": "A complement deficiency that is characterized by recurrent pyogenic bacterial infections that is the result of complement component 3 deficiency.",
                            "url": "http://disease-ontology.org/term/DOID:0050419",
                            "evidence": [
                                {
                                    "id": "610984",
                                    "database": "MIM",
                                    "url": "https://www.omim.org/entry/610984"
                                },
                                {
                                    "id": "0050419",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0050419"
                                }
                            ]
                        },
                        {
                            "disease_id": "DOID:0050419",
                            "name": "complement factor I deficiency",
                            "description": "A complement deficiency that is characterized by recurrent pyogenic bacterial infections that is the result of complement component 3 deficiency.",
                            "url": "http://disease-ontology.org/term/DOID:0050419",
                            "evidence": [
                                {
                                    "id": "610984",
                                    "database": "MIM",
                                    "url": "https://www.omim.org/entry/610984"
                                },
                                {
                                    "id": "0050419",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0050419"
                                }
                            ]
                        },
                        {
                            "disease_id": "DOID:0050419",
                            "name": "complement factor I deficiency",
                            "description": "A complement deficiency that is characterized by recurrent pyogenic bacterial infections that is the result of complement component 3 deficiency.",
                            "url": "http://disease-ontology.org/term/DOID:0050419",
                            "evidence": [
                                {
                                    "id": "610984",
                                    "database": "MIM",
                                    "url": "https://www.omim.org/entry/610984"
                                },
                                {
                                    "id": "0050419",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0050419"
                                }
                            ]
                        },
                        {
                            "disease_id": "DOID:0050419",
                            "name": "complement factor I deficiency",
                            "description": "A complement deficiency that is characterized by recurrent pyogenic bacterial infections that is the result of complement component 3 deficiency.",
                            "url": "http://disease-ontology.org/term/DOID:0050419",
                            "evidence": [
                                {
                                    "id": "610984",
                                    "database": "MIM",
                                    "url": "https://www.omim.org/entry/610984"
                                },
                                {
                                    "id": "0050419",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0050419"
                                }
                            ]
                        }
                    ]
                }
            ],
            "glycoprotein": [
                {
                    "uniprot_canonical_ac": "P05156-1",
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                    "end_pos": 177,
                    "residue": "asn",
                    "evidence": [
                        {
                            "database": "PubMed",
                            "id": "29671580",
                            "url": "https://glygen.org/publication/PubMed/29671580"
                        },
                        {
                            "database": "UniCarbKB",
                            "id": "GLY_000040",
                            "url": "http://data.glygen.org/GLY_000040"
                        },
                        {
                            "database": "GPTwiki",
                            "id": "G00912UN",
                            "url": "https://edwardslab.bmcb.georgetown.edu/gptwiki/G00912UN"
                        },
                        {
                            "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": "Complement factor I",
                    "gene_name": "CFI",
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                    "tax_name": "Homo sapiens",
                    "tax_common_name": "Human",
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                    "chemical_mass": 65750.0
                }
            ]
        },
        {
            "start_pos": "464",
            "site_seq": "",
            "site_lbl": "N464",
            "residue": "",
            "snv": [
                {
                    "weight": 100,
                    "sequence_org": "N",
                    "sequence_mut": "K",
                    "comment": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-loss (NDT->KDT).",
                    "chr_id": "4",
                    "chr_pos": "109746259",
                    "evidence": [
                        {
                            "id": "rs759927335",
                            "database": "dbSNP",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs759927335"
                        },
                        {
                            "id": "rs759927335",
                            "database": "ExAC",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs759927335"
                        },
                        {
                            "id": "rs759927335",
                            "database": "TOPMed",
                            "url": "https://www.ncbi.nlm.nih.gov/snp/rs759927335#frequency_tab"
                        },
                        {
                            "id": "rs759927335",
                            "database": "gnomAD",
                            "url": "http://gnomad.broadinstitute.org/awesome?query=rs759927335"
                        }
                    ]
                }
            ],
            "glycoprotein": [
                {
                    "uniprot_canonical_ac": "P05156-1",
                    "start_pos": 464,
                    "end_pos": 464,
                    "residue": "asn",
                    "evidence": [
                        {
                            "database": "PubMed",
                            "id": "29671580",
                            "url": "https://glygen.org/publication/PubMed/29671580"
                        },
                        {
                            "database": "UniCarbKB",
                            "id": "GLY_000040",
                            "url": "http://data.glygen.org/GLY_000040"
                        },
                        {
                            "database": "GPTwiki",
                            "id": "G00912UN",
                            "url": "https://edwardslab.bmcb.georgetown.edu/gptwiki/G00912UN"
                        },
                        {
                            "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": "Complement factor I",
                    "gene_name": "CFI",
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                    "tax_common_name": "Human",
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                    "chemical_mass": 65750.0
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            ]
        },
        {
            "start_pos": "494",
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            "site_lbl": "N494",
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            "snv": [
                {
                    "weight": 100,
                    "sequence_org": "N",
                    "sequence_mut": "T",
                    "comment": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-loss (NCS->TCS).",
                    "chr_id": "4",
                    "chr_pos": "109742544",
                    "evidence": [
                        {
                            "id": "rs1723931486",
                            "database": "dbSNP",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1723931486"
                        },
                        {
                            "id": "rs1723931486",
                            "database": "gnomAD",
                            "url": "http://gnomad.broadinstitute.org/awesome?query=rs1723931486"
                        }
                    ]
                }
            ],
            "glycoprotein": [
                {
                    "uniprot_canonical_ac": "P05156-1",
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                    "evidence": [
                        {
                            "database": "PubMed",
                            "id": "37074911",
                            "url": "https://glygen.org/publication/PubMed/37074911"
                        },
                        {
                            "database": "PDC",
                            "id": "PDC000471",
                            "url": "https://proteomic.datacommons.cancer.gov/pdc/study/PDC000471"
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                    ],
                    "protein_name": "Complement factor I",
                    "gene_name": "CFI",
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                    "tax_common_name": "Human",
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                    "chemical_mass": 65750.0
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            ]
        },
        {
            "start_pos": "536",
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            "site_lbl": "N536",
            "residue": "",
            "snv": [
                {
                    "weight": 100,
                    "sequence_org": "N",
                    "sequence_mut": "D",
                    "comment": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-loss (NVT->DVT).",
                    "chr_id": "4",
                    "chr_pos": "109741039",
                    "evidence": [
                        {
                            "id": "rs1314998523",
                            "database": "dbSNP",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1314998523"
                        },
                        {
                            "id": "rs1314998523",
                            "database": "TOPMed",
                            "url": "https://www.ncbi.nlm.nih.gov/snp/rs1314998523#frequency_tab"
                        },
                        {
                            "id": "rs1314998523",
                            "database": "gnomAD",
                            "url": "http://gnomad.broadinstitute.org/awesome?query=rs1314998523"
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                    ]
                },
                {
                    "weight": 100,
                    "sequence_org": "N",
                    "sequence_mut": "K",
                    "comment": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-loss (NVT->KVT).",
                    "chr_id": "4",
                    "chr_pos": "109741037",
                    "evidence": [
                        {
                            "id": "rs1336453366",
                            "database": "dbSNP",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1336453366"
                        },
                        {
                            "id": "rs1336453366",
                            "database": "TOPMed",
                            "url": "https://www.ncbi.nlm.nih.gov/snp/rs1336453366#frequency_tab"
                        },
                        {
                            "id": "rs1336453366",
                            "database": "gnomAD",
                            "url": "http://gnomad.broadinstitute.org/awesome?query=rs1336453366"
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                    ]
                },
                {
                    "weight": 100,
                    "sequence_org": "N",
                    "sequence_mut": "S",
                    "comment": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-loss (NVT->SVT).",
                    "chr_id": "4",
                    "chr_pos": "109741038",
                    "evidence": [
                        {
                            "id": "rs1357609555",
                            "database": "dbSNP",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1357609555"
                        },
                        {
                            "id": "rs1357609555",
                            "database": "TOPMed",
                            "url": "https://www.ncbi.nlm.nih.gov/snp/rs1357609555#frequency_tab"
                        },
                        {
                            "id": "rs1357609555",
                            "database": "gnomAD",
                            "url": "http://gnomad.broadinstitute.org/awesome?query=rs1357609555"
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                    ]
                }
            ],
            "glycoprotein": [
                {
                    "uniprot_canonical_ac": "P05156-1",
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                    "end_pos": 536,
                    "residue": "Asn",
                    "evidence": [
                        {
                            "database": "GPTwiki",
                            "id": "G00912UN",
                            "url": "https://edwardslab.bmcb.georgetown.edu/gptwiki/G00912UN"
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                    ],
                    "protein_name": "Complement factor I",
                    "gene_name": "CFI",
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                    "tax_common_name": "Human",
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                    "chemical_mass": 65750.0
                }
            ]
        },
        {
            "start_pos": "70",
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            "site_lbl": "N70",
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            "snv": [
                {
                    "weight": 100,
                    "sequence_org": "N",
                    "sequence_mut": "I",
                    "comment": "Somatic mutation passed 1 out of 6 filters: n-glyco-sequon-loss (NGT->IGT).",
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                    "chr_pos": "109766673",
                    "evidence": [
                        {
                            "id": "P05156",
                            "database": "BioMuta",
                            "url": "https://hivelab.biochemistry.gwu.edu/biomuta/proteinview/P05156"
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                    ],
                    "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.",
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                            "evidence": [
                                {
                                    "id": "4159",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:4159"
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                            ]
                        }
                    ]
                },
                {
                    "weight": 100,
                    "sequence_org": "N",
                    "sequence_mut": "T",
                    "comment": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-loss (NGT->TGT).",
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                    "chr_pos": "109766673",
                    "evidence": [
                        {
                            "id": "rs749553820",
                            "database": "dbSNP",
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                        },
                        {
                            "id": "rs749553820",
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                        },
                        {
                            "id": "rs749553820",
                            "database": "TOPMed",
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                        },
                        {
                            "id": "rs749553820",
                            "database": "gnomAD",
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                    ]
                }
            ],
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                            "database": "GPTwiki",
                            "id": "G00912UN",
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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": "G00912UN",
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                        {
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                        {
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                    "chemical_mass": 71957.0
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            ]
        },
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                        {
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                        {
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                        {
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                        {
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                        {
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                        {
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        {
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                        {
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                        {
                            "database": "PubMed",
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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": "rs2108623235",
                            "database": "ENSEMBL",
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                    ]
                },
                {
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                        {
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                            "database": "dbSNP",
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                        {
                            "id": "rs2108623237",
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                    ]
                },
                {
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                        {
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                            "id": "rs2108623235",
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                        {
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                        {
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                        {
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                        {
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                        {
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                        {
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                        {
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                {
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                        {
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                    ]
                },
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                    ]
                },
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                        {
                            "id": "rs1157292917",
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                    ]
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                        {
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        },
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        {
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                        {
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                        {
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                        {
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                        {
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                        {
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                        {
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                        {
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                {
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                },
                {
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                        {
                            "id": "rs1157292917",
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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": "G00912UN",
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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": "rs755851961",
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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": "UniCarbKB",
                            "id": "GLY_000040",
                            "url": "http://data.glygen.org/GLY_000040"
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                        {
                            "database": "PubMed",
                            "id": "37074911",
                            "url": "https://glygen.org/publication/PubMed/37074911"
                        },
                        {
                            "database": "PDC",
                            "id": "PDC000471",
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                    ],
                    "protein_name": "Apolipoprotein B-100",
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                    "chemical_mass": 515545.0
                }
            ]
        },
        {
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                            "id": "29671580",
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                        },
                        {
                            "database": "UniCarbKB",
                            "id": "GLY_000040",
                            "url": "http://data.glygen.org/GLY_000040"
                        },
                        {
                            "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": "Apolipoprotein B-100",
                    "gene_name": "APOB",
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                    "tax_name": "Homo sapiens",
                    "tax_common_name": "Human",
                    "length": 4563,
                    "chemical_mass": 515545.0
                }
            ]
        },
        {
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            "site_seq": "N",
            "site_lbl": "Asn3895",
            "residue": "Asn",
            "glycoprotein": [
                {
                    "uniprot_canonical_ac": "P04114-1",
                    "start_pos": 3895,
                    "end_pos": 3895,
                    "residue": "asn",
                    "evidence": [
                        {
                            "database": "PubMed",
                            "id": "29671580",
                            "url": "https://glygen.org/publication/PubMed/29671580"
                        },
                        {
                            "database": "UniCarbKB",
                            "id": "GLY_000040",
                            "url": "http://data.glygen.org/GLY_000040"
                        },
                        {
                            "database": "GPTwiki",
                            "id": "G00912UN",
                            "url": "https://edwardslab.bmcb.georgetown.edu/gptwiki/G00912UN"
                        },
                        {
                            "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": "Apolipoprotein B-100",
                    "gene_name": "APOB",
                    "tax_id": 9606,
                    "tax_name": "Homo sapiens",
                    "tax_common_name": "Human",
                    "length": 4563,
                    "chemical_mass": 515545.0
                }
            ]
        },
        {
            "start_pos": "3895",
            "site_seq": "FEVDSPVYnATWSASLK",
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            "residue": "Asn",
            "glycoprotein": [
                {
                    "uniprot_canonical_ac": "P04114-1",
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                    "end_pos": 3895,
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                            "database": "PubMed",
                            "id": "29671580",
                            "url": "https://glygen.org/publication/PubMed/29671580"
                        },
                        {
                            "database": "UniCarbKB",
                            "id": "GLY_000040",
                            "url": "http://data.glygen.org/GLY_000040"
                        },
                        {
                            "database": "GPTwiki",
                            "id": "G00912UN",
                            "url": "https://edwardslab.bmcb.georgetown.edu/gptwiki/G00912UN"
                        },
                        {
                            "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": "Apolipoprotein B-100",
                    "gene_name": "APOB",
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                    "tax_name": "Homo sapiens",
                    "tax_common_name": "Human",
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                    "chemical_mass": 515545.0
                }
            ]
        },
        {
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            "site_seq": "DFHSEYIVSASnFTSQLSSQVEQFLHR",
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            "glycoprotein": [
                {
                    "uniprot_canonical_ac": "P04114-1",
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                    "residue": "Asn",
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                        {
                            "database": "PubMed",
                            "id": "37074911",
                            "url": "https://glygen.org/publication/PubMed/37074911"
                        },
                        {
                            "database": "PDC",
                            "id": "PDC000471",
                            "url": "https://proteomic.datacommons.cancer.gov/pdc/study/PDC000471"
                        }
                    ],
                    "protein_name": "Apolipoprotein B-100",
                    "gene_name": "APOB",
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                    "tax_name": "Homo sapiens",
                    "tax_common_name": "Human",
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                    "chemical_mass": 515545.0
                }
            ]
        },
        {
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                {
                    "uniprot_canonical_ac": "P04114-1",
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                    "residue": "Asn",
                    "evidence": [
                        {
                            "database": "PubMed",
                            "id": "37074911",
                            "url": "https://glygen.org/publication/PubMed/37074911"
                        },
                        {
                            "database": "PDC",
                            "id": "PDC000471",
                            "url": "https://proteomic.datacommons.cancer.gov/pdc/study/PDC000471"
                        }
                    ],
                    "protein_name": "Apolipoprotein B-100",
                    "gene_name": "APOB",
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                    "tax_name": "Homo sapiens",
                    "tax_common_name": "Human",
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                    "chemical_mass": 515545.0
                }
            ]
        },
        {
            "start_pos": "983",
            "site_seq": "N",
            "site_lbl": "Asn983",
            "residue": "Asn",
            "glycoprotein": [
                {
                    "uniprot_canonical_ac": "P04114-1",
                    "start_pos": 983,
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                    "residue": "asn",
                    "evidence": [
                        {
                            "database": "PubMed",
                            "id": "29671580",
                            "url": "https://glygen.org/publication/PubMed/29671580"
                        },
                        {
                            "database": "UniCarbKB",
                            "id": "GLY_000040",
                            "url": "http://data.glygen.org/GLY_000040"
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                    ],
                    "protein_name": "Apolipoprotein B-100",
                    "gene_name": "APOB",
                    "tax_id": 9606,
                    "tax_name": "Homo sapiens",
                    "tax_common_name": "Human",
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                    "chemical_mass": 515545.0
                }
            ]
        },
        {
            "start_pos": "2239",
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            "site_lbl": "N2239",
            "residue": "",
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                {
                    "weight": 100,
                    "sequence_org": "N",
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                    "comment": "Somatic mutation passed 1 out of 6 filters: n-glyco-sequon-loss (NKS->KKS).",
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                    "chr_pos": "21010151",
                    "evidence": [
                        {
                            "id": "P04114",
                            "database": "BioMuta",
                            "url": "https://hivelab.biochemistry.gwu.edu/biomuta/proteinview/P04114"
                        }
                    ],
                    "disease": [
                        {
                            "disease_id": "DOID:9256",
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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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                            ]
                        }
                    ]
                }
            ],
            "glycoprotein": [
                {
                    "uniprot_canonical_ac": "P04114-1",
                    "start_pos": 2239,
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                    "residue": "Asn",
                    "evidence": [
                        {
                            "database": "GPTwiki",
                            "id": "G00912UN",
                            "url": "https://edwardslab.bmcb.georgetown.edu/gptwiki/G00912UN"
                        },
                        {
                            "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": "Apolipoprotein B-100",
                    "gene_name": "APOB",
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                    "tax_common_name": "Human",
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                    "chemical_mass": 515545.0
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            ]
        },
        {
            "start_pos": "2982",
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            "residue": "",
            "snv": [
                {
                    "weight": 100,
                    "sequence_org": "N",
                    "sequence_mut": "H",
                    "comment": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-loss (NFS->HFS).",
                    "chr_id": "2",
                    "chr_pos": "21007924",
                    "evidence": [
                        {
                            "id": "rs1460637587",
                            "database": "dbSNP",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1460637587"
                        },
                        {
                            "id": "rs1460637587",
                            "database": "gnomAD",
                            "url": "http://gnomad.broadinstitute.org/awesome?query=rs1460637587"
                        }
                    ],
                    "disease": [
                        {
                            "disease_id": "DOID:0111062",
                            "name": "familial hypobetalipoproteinemia 1",
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                                {
                                    "id": "615558",
                                    "database": "MIM",
                                    "url": "https://www.omim.org/entry/615558"
                                },
                                {
                                    "id": "0111062",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0111062"
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                            ]
                        },
                        {
                            "disease_id": "DOID:0111062",
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                            "description": "A hypobetalipoproteinemia that has_material_basis_in mutation in the APOB gene on chromosome 2p24.",
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                            "evidence": [
                                {
                                    "id": "615558",
                                    "database": "MIM",
                                    "url": "https://www.omim.org/entry/615558"
                                },
                                {
                                    "id": "0111062",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0111062"
                                }
                            ]
                        }
                    ]
                },
                {
                    "weight": 100,
                    "sequence_org": "N",
                    "sequence_mut": "K",
                    "comment": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-loss (NFS->KFS).",
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                    "chr_pos": "21007922",
                    "evidence": [
                        {
                            "id": "rs775661185",
                            "database": "dbSNP",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs775661185"
                        },
                        {
                            "id": "rs775661185",
                            "database": "ExAC",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs775661185"
                        },
                        {
                            "id": "rs775661185",
                            "database": "gnomAD",
                            "url": "http://gnomad.broadinstitute.org/awesome?query=rs775661185"
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                    ]
                }
            ],
            "glycoprotein": [
                {
                    "uniprot_canonical_ac": "P04114-1",
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                        {
                            "database": "PubMed",
                            "id": "29671580",
                            "url": "https://glygen.org/publication/PubMed/29671580"
                        },
                        {
                            "database": "UniCarbKB",
                            "id": "GLY_000040",
                            "url": "http://data.glygen.org/GLY_000040"
                        },
                        {
                            "database": "GPTwiki",
                            "id": "G00912UN",
                            "url": "https://edwardslab.bmcb.georgetown.edu/gptwiki/G00912UN"
                        },
                        {
                            "database": "PubMed",
                            "id": "37074911",
                            "url": "https://glygen.org/publication/PubMed/37074911"
                        },
                        {
                            "database": "PDC",
                            "id": "PDC000471",
                            "url": "https://proteomic.datacommons.cancer.gov/pdc/study/PDC000471"
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                    ],
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                    "tax_common_name": "Human",
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                    "chemical_mass": 515545.0
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            ]
        },
        {
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            "site_lbl": "N3224",
            "residue": "",
            "snv": [
                {
                    "weight": 100,
                    "sequence_org": "N",
                    "sequence_mut": "S",
                    "comment": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-loss (NET->SET).",
                    "chr_id": "2",
                    "chr_pos": "21007197",
                    "evidence": [
                        {
                            "id": "rs1663168031",
                            "database": "dbSNP",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1663168031"
                        },
                        {
                            "id": "rs1663168031",
                            "database": "ENSEMBL",
                            "url": "https://www.ensembl.org/id/rs1663168031"
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                    ]
                }
            ],
            "glycoprotein": [
                {
                    "uniprot_canonical_ac": "P04114-1",
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                    "end_pos": 3224,
                    "residue": "Asn",
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                        {
                            "database": "PubMed",
                            "id": "37074911",
                            "url": "https://glygen.org/publication/PubMed/37074911"
                        },
                        {
                            "database": "PDC",
                            "id": "PDC000471",
                            "url": "https://proteomic.datacommons.cancer.gov/pdc/study/PDC000471"
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                    ],
                    "protein_name": "Apolipoprotein B-100",
                    "gene_name": "APOB",
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                    "tax_common_name": "Human",
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                    "chemical_mass": 515545.0
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            ]
        },
        {
            "start_pos": "3411",
            "site_seq": "",
            "site_lbl": "N3411",
            "residue": "",
            "snv": [
                {
                    "weight": 100,
                    "sequence_org": "N",
                    "sequence_mut": "K",
                    "comment": "Somatic mutation passed 1 out of 6 filters: n-glyco-sequon-loss (NST->KST).",
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                    "chr_pos": "21006635",
                    "evidence": [
                        {
                            "id": "P04114",
                            "database": "BioMuta",
                            "url": "https://hivelab.biochemistry.gwu.edu/biomuta/proteinview/P04114"
                        },
                        {
                            "id": "rs771372599",
                            "database": "dbSNP",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs771372599"
                        },
                        {
                            "id": "rs771372599",
                            "database": "ExAC",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs771372599"
                        },
                        {
                            "id": "rs771372599",
                            "database": "TOPMed",
                            "url": "https://www.ncbi.nlm.nih.gov/snp/rs771372599#frequency_tab"
                        },
                        {
                            "id": "rs771372599",
                            "database": "gnomAD",
                            "url": "http://gnomad.broadinstitute.org/awesome?query=rs771372599"
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                    ],
                    "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"
                                }
                            ]
                        },
                        {
                            "disease_id": "DOID:2394",
                            "name": "ovarian cancer",
                            "description": "A female reproductive organ cancer that is located_in the ovary.",
                            "url": "http://disease-ontology.org/term/DOID:2394",
                            "evidence": [
                                {
                                    "id": "2394",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:2394"
                                }
                            ]
                        }
                    ]
                },
                {
                    "weight": 100,
                    "sequence_org": "N",
                    "sequence_mut": "S",
                    "comment": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-loss (NST->SST).",
                    "chr_id": "2",
                    "chr_pos": "21006636",
                    "evidence": [
                        {
                            "id": "rs773958267",
                            "database": "dbSNP",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs773958267"
                        },
                        {
                            "id": "rs773958267",
                            "database": "ExAC",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs773958267"
                        },
                        {
                            "id": "rs773958267",
                            "database": "gnomAD",
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                        {
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                    ]
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                                    "id": "4159",
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                {
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                        {
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                        {
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                        {
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            ]
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                        {
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                        {
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                        {
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                        {
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                        {
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                    ],
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                                    "url": "https://www.alliancegenome.org/disease/DOID:9256"
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                        {
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                    ],
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                                {
                                    "id": "0111062",
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                        {
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                                {
                                    "id": "0111062",
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                    ]
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                        {
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                        {
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                        {
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                            "id": "rs1663168031",
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                        {
                            "id": "rs1663168031",
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                    "weight": 100,
                    "sequence_org": "N",
                    "sequence_mut": "K",
                    "comment": "Somatic mutation passed 1 out of 6 filters: n-glyco-sequon-loss (NST->KST).",
                    "chr_id": "2",
                    "chr_pos": "21006635",
                    "evidence": [
                        {
                            "id": "P04114",
                            "database": "BioMuta",
                            "url": "https://hivelab.biochemistry.gwu.edu/biomuta/proteinview/P04114"
                        },
                        {
                            "id": "rs771372599",
                            "database": "dbSNP",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs771372599"
                        },
                        {
                            "id": "rs771372599",
                            "database": "ExAC",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs771372599"
                        },
                        {
                            "id": "rs771372599",
                            "database": "TOPMed",
                            "url": "https://www.ncbi.nlm.nih.gov/snp/rs771372599#frequency_tab"
                        },
                        {
                            "id": "rs771372599",
                            "database": "gnomAD",
                            "url": "http://gnomad.broadinstitute.org/awesome?query=rs771372599"
                        }
                    ],
                    "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"
                                }
                            ]
                        },
                        {
                            "disease_id": "DOID:2394",
                            "name": "ovarian cancer",
                            "description": "A female reproductive organ cancer that is located_in the ovary.",
                            "url": "http://disease-ontology.org/term/DOID:2394",
                            "evidence": [
                                {
                                    "id": "2394",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:2394"
                                }
                            ]
                        }
                    ]
                },
                {
                    "weight": 100,
                    "sequence_org": "N",
                    "sequence_mut": "S",
                    "comment": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-loss (NST->SST).",
                    "chr_id": "2",
                    "chr_pos": "21006636",
                    "evidence": [
                        {
                            "id": "rs773958267",
                            "database": "dbSNP",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs773958267"
                        },
                        {
                            "id": "rs773958267",
                            "database": "ExAC",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs773958267"
                        },
                        {
                            "id": "rs773958267",
                            "database": "gnomAD",
                            "url": "http://gnomad.broadinstitute.org/awesome?query=rs773958267"
                        }
                    ]
                }
            ],
            "glycoprotein": [
                {
                    "uniprot_canonical_ac": "P04114-1",
                    "start_pos": 3411,
                    "end_pos": 3411,
                    "residue": "asn",
                    "evidence": [
                        {
                            "database": "PubMed",
                            "id": "29671580",
                            "url": "https://glygen.org/publication/PubMed/29671580"
                        },
                        {
                            "database": "UniCarbKB",
                            "id": "GLY_000040",
                            "url": "http://data.glygen.org/GLY_000040"
                        }
                    ],
                    "protein_name": "Apolipoprotein B-100",
                    "gene_name": "APOB",
                    "tax_id": 9606,
                    "tax_name": "Homo sapiens",
                    "tax_common_name": "Human",
                    "length": 4563,
                    "chemical_mass": 515545.0
                }
            ]
        },
        {
            "start_pos": "3465",
            "site_seq": "",
            "site_lbl": "N3465",
            "residue": "",
            "snv": [
                {
                    "weight": 100,
                    "sequence_org": "N",
                    "sequence_mut": "D",
                    "comment": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-loss (NSS->DSS).",
                    "chr_id": "2",
                    "chr_pos": "21006475",
                    "evidence": [
                        {
                            "id": "rs751227728",
                            "database": "dbSNP",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs751227728"
                        },
                        {
                            "id": "rs751227728",
                            "database": "ExAC",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs751227728"
                        },
                        {
                            "id": "rs751227728",
                            "database": "gnomAD",
                            "url": "http://gnomad.broadinstitute.org/awesome?query=rs751227728"
                        }
                    ]
                },
                {
                    "weight": 100,
                    "sequence_org": "N",
                    "sequence_mut": "S",
                    "comment": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-loss (NSS->SSS).",
                    "chr_id": "2",
                    "chr_pos": "21006474",
                    "evidence": [
                        {
                            "id": "rs1663141372",
                            "database": "dbSNP",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1663141372"
                        },
                        {
                            "id": "rs1663141372",
                            "database": "ENSEMBL",
                            "url": "https://www.ensembl.org/id/rs1663141372"
                        }
                    ]
                }
            ],
            "glycoprotein": [
                {
                    "uniprot_canonical_ac": "P04114-1",
                    "start_pos": 3465,
                    "end_pos": 3465,
                    "residue": "asn",
                    "evidence": [
                        {
                            "database": "PubMed",
                            "id": "29671580",
                            "url": "https://glygen.org/publication/PubMed/29671580"
                        },
                        {
                            "database": "UniCarbKB",
                            "id": "GLY_000040",
                            "url": "http://data.glygen.org/GLY_000040"
                        },
                        {
                            "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": "Apolipoprotein B-100",
                    "gene_name": "APOB",
                    "tax_id": 9606,
                    "tax_name": "Homo sapiens",
                    "tax_common_name": "Human",
                    "length": 4563,
                    "chemical_mass": 515545.0
                }
            ]
        },
        {
            "start_pos": "3895",
            "site_seq": "",
            "site_lbl": "N3895",
            "residue": "",
            "snv": [
                {
                    "weight": 100,
                    "sequence_org": "N",
                    "sequence_mut": "H",
                    "comment": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-loss (NAT->HAT).",
                    "chr_id": "2",
                    "chr_pos": "21005185",
                    "evidence": [
                        {
                            "id": "rs2103350346",
                            "database": "dbSNP",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs2103350346"
                        },
                        {
                            "id": "rs2103350346",
                            "database": "ENSEMBL",
                            "url": "https://www.ensembl.org/id/rs2103350346"
                        }
                    ]
                },
                {
                    "weight": 100,
                    "sequence_org": "N",
                    "sequence_mut": "S",
                    "comment": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-loss (NAT->SAT).",
                    "chr_id": "2",
                    "chr_pos": "21005184",
                    "evidence": [
                        {
                            "id": "rs1434488061",
                            "database": "dbSNP",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1434488061"
                        },
                        {
                            "id": "rs1434488061",
                            "database": "TOPMed",
                            "url": "https://www.ncbi.nlm.nih.gov/snp/rs1434488061#frequency_tab"
                        },
                        {
                            "id": "rs1434488061",
                            "database": "gnomAD",
                            "url": "http://gnomad.broadinstitute.org/awesome?query=rs1434488061"
                        }
                    ]
                }
            ],
            "glycoprotein": [
                {
                    "uniprot_canonical_ac": "P04114-1",
                    "start_pos": 3895,
                    "end_pos": 3895,
                    "residue": "asn",
                    "evidence": [
                        {
                            "database": "PubMed",
                            "id": "29671580",
                            "url": "https://glygen.org/publication/PubMed/29671580"
                        },
                        {
                            "database": "UniCarbKB",
                            "id": "GLY_000040",
                            "url": "http://data.glygen.org/GLY_000040"
                        },
                        {
                            "database": "GPTwiki",
                            "id": "G00912UN",
                            "url": "https://edwardslab.bmcb.georgetown.edu/gptwiki/G00912UN"
                        },
                        {
                            "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": "Apolipoprotein B-100",
                    "gene_name": "APOB",
                    "tax_id": 9606,
                    "tax_name": "Homo sapiens",
                    "tax_common_name": "Human",
                    "length": 4563,
                    "chemical_mass": 515545.0
                }
            ]
        },
        {
            "start_pos": "4431",
            "site_seq": "",
            "site_lbl": "N4431",
            "residue": "",
            "snv": [
                {
                    "weight": 100,
                    "sequence_org": "N",
                    "sequence_mut": "D",
                    "comment": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-loss (NFT->DFT).",
                    "chr_id": "2",
                    "chr_pos": "21002131",
                    "evidence": [
                        {
                            "id": "rs761556176",
                            "database": "dbSNP",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs761556176"
                        },
                        {
                            "id": "rs761556176",
                            "database": "ENSEMBL",
                            "url": "https://www.ensembl.org/id/rs761556176"
                        }
                    ]
                },
                {
                    "weight": 100,
                    "sequence_org": "N",
                    "sequence_mut": "K",
                    "comment": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-loss (NFT->KFT).",
                    "chr_id": "2",
                    "chr_pos": "21002129",
                    "evidence": [
                        {
                            "id": "rs2465348156",
                            "database": "dbSNP",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs2465348156"
                        }
                    ]
                },
                {
                    "weight": 100,
                    "sequence_org": "N",
                    "sequence_mut": "S",
                    "comment": "Somatic mutation passed 1 out of 6 filters: n-glyco-sequon-loss (NFT->SFT).",
                    "chr_id": "2",
                    "chr_pos": "21002130",
                    "evidence": [
                        {
                            "id": "P04114",
                            "database": "BioMuta",
                            "url": "https://hivelab.biochemistry.gwu.edu/biomuta/proteinview/P04114"
                        }
                    ],
                    "disease": [
                        {
                            "disease_id": "DOID:4159",
                            "name": "skin cancer",
                            "description": "An integumentary system cancer located_in the skin that is the uncontrolled growth of abnormal skin cells.",
                            "url": "http://disease-ontology.org/term/DOID:4159",
                            "evidence": [
                                {
                                    "id": "4159",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:4159"
                                }
                            ]
                        }
                    ]
                },
                {
                    "weight": 100,
                    "sequence_org": "N",
                    "sequence_mut": "Y",
                    "comment": "Somatic mutation passed 1 out of 6 filters: n-glyco-sequon-loss (NFT->YFT).",
                    "chr_id": "2",
                    "chr_pos": "21002131",
                    "evidence": [
                        {
                            "id": "P04114",
                            "database": "BioMuta",
                            "url": "https://hivelab.biochemistry.gwu.edu/biomuta/proteinview/P04114"
                        }
                    ],
                    "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"
                                }
                            ]
                        }
                    ]
                }
            ],
            "glycoprotein": [
                {
                    "uniprot_canonical_ac": "P04114-1",
                    "start_pos": 4431,
                    "end_pos": 4431,
                    "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": "Apolipoprotein B-100",
                    "gene_name": "APOB",
                    "tax_id": 9606,
                    "tax_name": "Homo sapiens",
                    "tax_common_name": "Human",
                    "length": 4563,
                    "chemical_mass": 515545.0
                }
            ]
        },
        {
            "start_pos": "983",
            "site_seq": "",
            "site_lbl": "N983",
            "residue": "",
            "snv": [
                {
                    "weight": 100,
                    "sequence_org": "N",
                    "sequence_mut": "S",
                    "comment": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-loss (NAS->SAS).",
                    "chr_id": "2",
                    "chr_pos": "21019774",
                    "evidence": [
                        {
                            "id": "rs1407756735",
                            "database": "dbSNP",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1407756735"
                        },
                        {
                            "id": "rs1407756735",
                            "database": "gnomAD",
                            "url": "http://gnomad.broadinstitute.org/awesome?query=rs1407756735"
                        }
                    ]
                },
                {
                    "weight": 100,
                    "sequence_org": "N",
                    "sequence_mut": "Y",
                    "comment": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-loss (NAS->YAS).",
                    "chr_id": "2",
                    "chr_pos": "21019775",
                    "evidence": [
                        {
                            "id": "rs767190489",
                            "database": "dbSNP",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs767190489"
                        },
                        {
                            "id": "rs767190489",
                            "database": "ExAC",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs767190489"
                        },
                        {
                            "id": "rs767190489",
                            "database": "gnomAD",
                            "url": "http://gnomad.broadinstitute.org/awesome?query=rs767190489"
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                    ]
                }
            ],
            "glycoprotein": [
                {
                    "uniprot_canonical_ac": "P04114-1",
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                    "evidence": [
                        {
                            "database": "PubMed",
                            "id": "29671580",
                            "url": "https://glygen.org/publication/PubMed/29671580"
                        },
                        {
                            "database": "UniCarbKB",
                            "id": "GLY_000040",
                            "url": "http://data.glygen.org/GLY_000040"
                        }
                    ],
                    "protein_name": "Apolipoprotein B-100",
                    "gene_name": "APOB",
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                    "tax_common_name": "Human",
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                    "chemical_mass": 515545.0
                }
            ]
        },
        {
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            "site_seq": "N",
            "site_lbl": "Asn493",
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            "glycoprotein": [
                {
                    "uniprot_canonical_ac": "Q8N3X6-1",
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                            "database": "PubMed",
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                        {
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                            "id": "GLY_000040",
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                    ],
                    "protein_name": "Ligand-dependent nuclear receptor corepressor-like protein",
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            ]
        },
        {
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                {
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                            "id": "29671580",
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                        {
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                    ],
                    "protein_name": "Ligand-dependent nuclear receptor corepressor-like protein",
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            ]
        },
        {
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                            "database": "PubMed",
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                        },
                        {
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                    ],
                    "protein_name": "Ligand-dependent nuclear receptor corepressor-like protein",
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                    "chemical_mass": 66964.0
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            ]
        },
        {
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                {
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                        {
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            ]
        },
        {
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                        },
                        {
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                        },
                        {
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                        },
                        {
                            "database": "PDC",
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                    ],
                    "protein_name": "C4b-binding protein beta chain",
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                    "chemical_mass": 28357.0
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            ]
        },
        {
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                {
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                            "url": "https://glygen.org/publication/PubMed/29671580"
                        },
                        {
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                            "url": "http://data.glygen.org/GLY_000040"
                        },
                        {
                            "database": "PubMed",
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                        },
                        {
                            "database": "PDC",
                            "id": "PDC000471",
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                                {
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                {
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                        {
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                            "database": "BioMuta",
                            "url": "https://hivelab.biochemistry.gwu.edu/biomuta/proteinview/P01011"
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                        {
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                            "database": "dbSNP",
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                        {
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                            "database": "ExAC",
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                        {
                            "id": "rs145819878",
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                        },
                        {
                            "id": "rs145819878",
                            "database": "gnomAD",
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                        },
                        {
                            "id": "rs145819878",
                            "database": "COSMIC",
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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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                        {
                            "database": "GPTwiki",
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                        {
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                        {
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        },
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                        {
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                    ]
                },
                {
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                        {
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                    ]
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            ],
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                        {
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                    ]
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            ],
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                        {
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                        {
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                        {
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            ]
        },
        {
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                        {
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                        {
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                        {
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                    ]
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                        {
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                        },
                        {
                            "database": "GPTwiki",
                            "id": "G00912UN",
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                        {
                            "database": "PubMed",
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                        },
                        {
                            "database": "PDC",
                            "id": "PDC000471",
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                    ],
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                    "tax_name": "Homo sapiens",
                    "tax_common_name": "Human",
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                    "chemical_mass": 47651.0
                }
            ]
        },
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                        {
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                        },
                        {
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                            "id": "G00912UN",
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                        {
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                        {
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                    ],
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                }
            ]
        },
        {
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                {
                    "uniprot_canonical_ac": "P01011-1",
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                        {
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                        },
                        {
                            "database": "GPTwiki",
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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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                        },
                        {
                            "database": "GPTwiki",
                            "id": "G00912UN",
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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": "rs1885922817",
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                        {
                            "id": "rs1885922817",
                            "database": "ENSEMBL",
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                    ]
                }
            ],
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                {
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                        {
                            "database": "GPTwiki",
                            "id": "G00912UN",
                            "url": "https://edwardslab.bmcb.georgetown.edu/gptwiki/G00912UN"
                        },
                        {
                            "database": "PubMed",
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                        },
                        {
                            "database": "PDC",
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                    ],
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            ]
        },
        {
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                {
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                    "evidence": [
                        {
                            "id": "P01011",
                            "database": "BioMuta",
                            "url": "https://hivelab.biochemistry.gwu.edu/biomuta/proteinview/P01011"
                        },
                        {
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                        {
                            "id": "rs145819878",
                            "database": "ExAC",
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                        },
                        {
                            "id": "rs145819878",
                            "database": "TOPMed",
                            "url": "https://www.ncbi.nlm.nih.gov/snp/rs145819878#frequency_tab"
                        },
                        {
                            "id": "rs145819878",
                            "database": "gnomAD",
                            "url": "http://gnomad.broadinstitute.org/awesome?query=rs145819878"
                        },
                        {
                            "id": "rs145819878",
                            "database": "COSMIC",
                            "url": "https://www.ensembl.org/homo_sapiens/Variation/Explore?v=rs145819878"
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                    ],
                    "disease": [
                        {
                            "disease_id": "DOID:263",
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                            "url": "http://disease-ontology.org/term/DOID:263",
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                                {
                                    "id": "263",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:263"
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                            ]
                        }
                    ]
                }
            ],
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                        {
                            "database": "PubMed",
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                            "url": "https://glygen.org/publication/PubMed/29671580"
                        },
                        {
                            "database": "UniCarbKB",
                            "id": "GLY_000040",
                            "url": "http://data.glygen.org/GLY_000040"
                        },
                        {
                            "database": "GPTwiki",
                            "id": "G00912UN",
                            "url": "https://edwardslab.bmcb.georgetown.edu/gptwiki/G00912UN"
                        },
                        {
                            "database": "PubMed",
                            "id": "37074911",
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                        },
                        {
                            "database": "PDC",
                            "id": "PDC000471",
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                    ],
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            ]
        },
        {
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                {
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                    "evidence": [
                        {
                            "id": "P01011",
                            "database": "BioMuta",
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                    ],
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                                {
                                    "id": "4159",
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                            ]
                        }
                    ]
                },
                {
                    "weight": 100,
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                    "evidence": [
                        {
                            "id": "rs950804088",
                            "database": "dbSNP",
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                        {
                            "id": "rs950804088",
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                    ]
                }
            ],
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                        {
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                            "id": "G00912UN",
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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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                        {
                            "id": "rs534010283",
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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": "rs542942614",
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                        {
                            "id": "rs542942614",
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                        {
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                        {
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                        {
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                    ]
                },
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                    ]
                },
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                        {
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            ]
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                        {
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            ]
        },
        {
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                        {
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                        {
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                        {
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                        {
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                        {
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                        {
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                        {
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                            "id": "GLY_000040",
                            "url": "http://data.glygen.org/GLY_000040"
                        },
                        {
                            "database": "GPTwiki",
                            "id": "G00912UN",
                            "url": "https://edwardslab.bmcb.georgetown.edu/gptwiki/G00912UN"
                        },
                        {
                            "database": "PubMed",
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                        },
                        {
                            "database": "PDC",
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                    ],
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                    "gene_name": "SERPING1",
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                    "tax_common_name": "Human",
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                    "chemical_mass": 55154.0
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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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                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs776553402"
                        },
                        {
                            "id": "rs776553402",
                            "database": "ExAC",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs776553402"
                        },
                        {
                            "id": "rs776553402",
                            "database": "gnomAD",
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                            "id": "G00912UN",
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                        {
                            "database": "PubMed",
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                    ],
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                        {
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                                    "id": "363",
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                        {
                            "id": "rs1945329565",
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            ]
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                        {
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                        {
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                        {
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                        {
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                    "tax_common_name": "Human",
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                    "chemical_mass": 62217.0
                }
            ]
        },
        {
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                        {
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                            "id": "GLY_000040",
                            "url": "http://data.glygen.org/GLY_000040"
                        },
                        {
                            "database": "GPTwiki",
                            "id": "G00912UN",
                            "url": "https://edwardslab.bmcb.georgetown.edu/gptwiki/G00912UN"
                        },
                        {
                            "database": "PubMed",
                            "id": "37074911",
                            "url": "https://glygen.org/publication/PubMed/37074911"
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                        {
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                            "id": "PDC000471",
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                    ],
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            ]
        },
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                        {
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                        },
                        {
                            "database": "GPTwiki",
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                        {
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                        {
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                    ],
                    "protein_name": "N-acetylmuramoyl-L-alanine amidase",
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            ]
        },
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                {
                    "uniprot_canonical_ac": "Q96PD5-1",
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                        {
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                            "id": "G00912UN",
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                        },
                        {
                            "database": "PubMed",
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                            "url": "https://glygen.org/publication/PubMed/37074911"
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                        {
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                    ],
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                    "chemical_mass": 62217.0
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            ]
        },
        {
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                        {
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                            "id": "G00912UN",
                            "url": "https://edwardslab.bmcb.georgetown.edu/gptwiki/G00912UN"
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                        {
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                            "id": "37074911",
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                        },
                        {
                            "database": "PDC",
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                    ],
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                    "chemical_mass": 62217.0
                }
            ]
        },
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                {
                    "uniprot_canonical_ac": "Q96PD5-1",
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                        {
                            "database": "GPTwiki",
                            "id": "G00912UN",
                            "url": "https://edwardslab.bmcb.georgetown.edu/gptwiki/G00912UN"
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                        {
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                        {
                            "database": "PDC",
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                    ],
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                    "chemical_mass": 62217.0
                }
            ]
        },
        {
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                    "uniprot_canonical_ac": "Q96PD5-1",
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                        {
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                        {
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                    ],
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                    "chemical_mass": 62217.0
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            ]
        },
        {
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                        {
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                        {
                            "id": "rs758375344",
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                    ]
                },
                {
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                        {
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                        {
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                        {
                            "id": "rs752659784",
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                    ]
                }
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                        {
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                    ]
                },
                {
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                    ],
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                            "url": "http://disease-ontology.org/term/DOID:263",
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                                {
                                    "id": "263",
                                    "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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                                    "id": "1324",
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                    ]
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                                {
                                    "id": "9256",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:9256"
                                }
                            ]
                        }
                    ]
                },
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                    "weight": 100,
                    "sequence_org": "N",
                    "sequence_mut": "T",
                    "comment": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-loss (NYS->TYS).",
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                    "chr_pos": "58352360",
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                        {
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                            "database": "dbSNP",
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                        {
                            "id": "rs2051968507",
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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": "rs773884016",
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                        {
                            "id": "rs773884016",
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                    "protein_name": "Alpha-1B-glycoprotein",
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                        {
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                        {
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                        {
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                    ]
                },
                {
                    "weight": 100,
                    "sequence_org": "N",
                    "sequence_mut": "S",
                    "comment": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-loss (NMT->SMT).",
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                        {
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                        {
                            "id": "rs759037089",
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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": "PDC000471",
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                    ],
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            ]
        },
        {
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            ]
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                        {
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            ]
        },
        {
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            ]
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        {
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            ]
        },
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                    ]
                },
                {
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                        {
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                        {
                            "id": "rs1252153468",
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                    ]
                }
            ],
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                    ],
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        },
        {
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                        {
                            "id": "rs1945295028",
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                    ]
                },
                {
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                            "id": "rs371953822",
                            "database": "dbSNP",
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                        {
                            "id": "rs371953822",
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                        },
                        {
                            "id": "rs371953822",
                            "database": "ExAC",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs371953822"
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                        {
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                                    "url": "https://www.alliancegenome.org/disease/DOID:0060574"
                                }
                            ]
                        },
                        {
                            "disease_id": "DOID:0060574",
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                            "description": "A von Willebrand's disease characterized by qualitative but not quantitative abnormalities of the VWF protein that has_material_basis_in mutation in the VWF gene which maps to chromosome 12p13.",
                            "url": "http://disease-ontology.org/term/DOID:0060574",
                            "evidence": [
                                {
                                    "id": "0060574",
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                                }
                            ]
                        },
                        {
                            "disease_id": "DOID:0060574",
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                            "url": "http://disease-ontology.org/term/DOID:0060574",
                            "evidence": [
                                {
                                    "id": "0060574",
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                                    "url": "https://www.alliancegenome.org/disease/DOID:0060574"
                                }
                            ]
                        },
                        {
                            "disease_id": "DOID:0111054",
                            "name": "von Willebrand's disease 3",
                            "description": "A von Willebrand's disease characterized by autosomal recessive inheritance of a severe quantitative defect or virtual absence of VWF in plasma, prolonged bleeding time, and more severe bleeding tendencies compared to the other types of von Willebrand disease that has_material_basis_in homozygous or compound heterozygous mutation in the VWF gene which maps to chromosome 12p13.",
                            "url": "http://disease-ontology.org/term/DOID:0111054",
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                                },
                                {
                                    "id": "0111054",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0111054"
                                }
                            ]
                        },
                        {
                            "disease_id": "DOID:0111054",
                            "name": "von Willebrand's disease 3",
                            "description": "A von Willebrand's disease characterized by autosomal recessive inheritance of a severe quantitative defect or virtual absence of VWF in plasma, prolonged bleeding time, and more severe bleeding tendencies compared to the other types of von Willebrand disease that has_material_basis_in homozygous or compound heterozygous mutation in the VWF gene which maps to chromosome 12p13.",
                            "url": "http://disease-ontology.org/term/DOID:0111054",
                            "evidence": [
                                {
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                                {
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                        },
                        {
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                                {
                                    "id": "0111054",
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                        },
                        {
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                                {
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        {
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        {
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                                {
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                                {
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                            ]
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                                {
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            ]
        },
        {
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                        {
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                        {
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            ]
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                        {
                            "id": "rs767674762",
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                        {
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                        {
                            "id": "rs767674762",
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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": "rs1212144452",
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                        {
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                        {
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                        {
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            ]
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                        {
                            "id": "rs1372954090",
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                        {
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                        {
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                        {
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                        {
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                    ],
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                                {
                                    "id": "9256",
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                                    "url": "https://www.alliancegenome.org/disease/DOID:9256"
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                        {
                            "id": "rs758383871",
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                        {
                            "id": "rs758383871",
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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": "rs750365345",
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                        {
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                        {
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                        {
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                        {
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                                {
                                    "id": "1324",
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                    ]
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                {
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                        {
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                        {
                            "database": "PDC",
                            "id": "PDC000471",
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                    ],
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            ]
        },
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                        {
                            "database": "PDC",
                            "id": "PDC000471",
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                    ],
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            ]
        },
        {
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                        {
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                        {
                            "id": "rs778454792",
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                    ]
                },
                {
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                        {
                            "id": "Q08380",
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                            "url": "https://hivelab.biochemistry.gwu.edu/biomuta/proteinview/Q08380"
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                        {
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                        },
                        {
                            "id": "rs1461262648",
                            "database": "gnomAD",
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                        },
                        {
                            "id": "rs1461262648",
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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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                        {
                            "id": "rs923974095",
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                            "database": "PubMed",
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                        {
                            "database": "UniCarbKB",
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                        {
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                            "url": "https://glygen.org/publication/PubMed/37074911"
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                        {
                            "database": "PDC",
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                            "url": "https://proteomic.datacommons.cancer.gov/pdc/study/PDC000471"
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                    ],
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            ]
        },
        {
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                {
                    "weight": 100,
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                    "evidence": [
                        {
                            "id": "rs773114062",
                            "database": "dbSNP",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs773114062"
                        },
                        {
                            "id": "rs773114062",
                            "database": "ExAC",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs773114062"
                        },
                        {
                            "id": "rs773114062",
                            "database": "gnomAD",
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                    ]
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                            "database": "dbSNP",
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                        {
                            "id": "rs907549693",
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                {
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                        {
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                    ]
                },
                {
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                        {
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                        {
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                        {
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                                {
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                            ]
                        }
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                },
                {
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                        {
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                        {
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                        {
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                        {
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                        {
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                        {
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                                {
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                                {
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                                {
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                                {
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                                {
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                                {
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                        {
                            "database": "UniCarbKB",
                            "id": "GLY_000040",
                            "url": "http://data.glygen.org/GLY_000040"
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                    ],
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            ]
        },
        {
            "start_pos": "202",
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                {
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            ]
        },
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                        {
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            ]
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                        {
                            "id": "rs1168132530",
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                    ]
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                        {
                            "id": "rs1168132530",
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                    ]
                },
                {
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                    "chr_pos": "40945235",
                    "evidence": [
                        {
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                        },
                        {
                            "id": "rs199587630",
                            "database": "ExAC",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs199587630"
                        },
                        {
                            "id": "rs199587630",
                            "database": "TOPMed",
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                        },
                        {
                            "id": "rs199587630",
                            "database": "gnomAD",
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                    ],
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                                {
                                    "id": "610102",
                                    "database": "MIM",
                                    "url": "https://www.omim.org/entry/610102"
                                },
                                {
                                    "id": "0060300",
                                    "database": "AGR",
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                            ]
                        },
                        {
                            "disease_id": "DOID:0060300",
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                                {
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                                {
                                    "id": "0060300",
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                            ]
                        },
                        {
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                                {
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                            ]
                        },
                        {
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                                {
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                            ]
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                        {
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                                {
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                            ]
                        },
                        {
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                                {
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                                {
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                        {
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                                {
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                        },
                        {
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                                {
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                        {
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                        {
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            ]
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            ]
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        {
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                        {
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                        },
                        {
                            "id": "rs11052883",
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                        },
                        {
                            "id": "rs11052883",
                            "database": "ExAC",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs11052883"
                        },
                        {
                            "id": "rs11052883",
                            "database": "TOPMed",
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                        },
                        {
                            "id": "rs11052883",
                            "database": "gnomAD",
                            "url": "http://gnomad.broadinstitute.org/awesome?query=rs11052883"
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                    ]
                },
                {
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                            "database": "BioMuta",
                            "url": "https://hivelab.biochemistry.gwu.edu/biomuta/proteinview/Q07108"
                        },
                        {
                            "id": "rs771435497",
                            "database": "dbSNP",
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                        },
                        {
                            "id": "rs771435497",
                            "database": "1000Genomes",
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                        },
                        {
                            "id": "rs771435497",
                            "database": "ExAC",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs771435497"
                        },
                        {
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                        {
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                    ],
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                                {
                                    "id": "1324",
                                    "database": "AGR",
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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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                        {
                            "id": "rs746003601",
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                        {
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                        {
                            "id": "rs746003601",
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                    "chemical_mass": 38178.0
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            ]
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            ]
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                        {
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            ]
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                    "chemical_mass": 38178.0
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            ]
        },
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                        {
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                    ],
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                    "chemical_mass": 38178.0
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            ]
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                        {
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                }
            ]
        },
        {
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                {
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            ]
        },
        {
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                        {
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                        {
                            "id": "rs771381352",
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                        {
                            "id": "rs771381352",
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                    ]
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                        {
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                        {
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                        {
                            "id": "rs751236906",
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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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                    "tax_common_name": "Human",
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                    "chemical_mass": 35399.0
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            ]
        },
        {
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                {
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                        {
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            ]
        },
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                    "chemical_mass": 35399.0
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            ]
        },
        {
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                        {
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                        {
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                            "database": "TOPMed",
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                        {
                            "id": "rs750714330",
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                    ]
                }
            ],
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                        {
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            ]
        },
        {
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                        {
                            "id": "rs760294047",
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                        {
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                        {
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                        {
                            "id": "rs760294047",
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                    ]
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                {
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            ]
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            ]
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            ]
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            ]
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            ]
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            ]
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            ]
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                        {
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            ]
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                        {
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                        {
                            "id": "rs369893643",
                            "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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            ]
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                        {
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                    ]
                },
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                        {
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                        {
                            "id": "rs770788791",
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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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                    "tax_common_name": "Human",
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            ]
        },
        {
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                            "id": "37074911",
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                        },
                        {
                            "database": "PDC",
                            "id": "PDC000471",
                            "url": "https://proteomic.datacommons.cancer.gov/pdc/study/PDC000471"
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                    ],
                    "protein_name": "Laminin subunit alpha-2",
                    "gene_name": "LAMA2",
                    "tax_id": 9606,
                    "tax_name": "Homo sapiens",
                    "tax_common_name": "Human",
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                    "chemical_mass": 343905.0
                }
            ]
        },
        {
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                {
                    "uniprot_canonical_ac": "P24043-1",
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                    "evidence": [
                        {
                            "database": "PubMed",
                            "id": "37074911",
                            "url": "https://glygen.org/publication/PubMed/37074911"
                        },
                        {
                            "database": "PDC",
                            "id": "PDC000471",
                            "url": "https://proteomic.datacommons.cancer.gov/pdc/study/PDC000471"
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                    ],
                    "protein_name": "Laminin subunit alpha-2",
                    "gene_name": "LAMA2",
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                    "tax_name": "Homo sapiens",
                    "tax_common_name": "Human",
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                    "chemical_mass": 343905.0
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            ]
        },
        {
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                    "uniprot_canonical_ac": "P24043-1",
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                        {
                            "database": "PubMed",
                            "id": "37074911",
                            "url": "https://glygen.org/publication/PubMed/37074911"
                        },
                        {
                            "database": "PDC",
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                    ],
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                    "chemical_mass": 343905.0
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            ]
        },
        {
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                    "uniprot_canonical_ac": "P24043-1",
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                        {
                            "database": "PubMed",
                            "id": "37074911",
                            "url": "https://glygen.org/publication/PubMed/37074911"
                        },
                        {
                            "database": "PDC",
                            "id": "PDC000471",
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                    ],
                    "protein_name": "Laminin subunit alpha-2",
                    "gene_name": "LAMA2",
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                    "tax_common_name": "Human",
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                    "chemical_mass": 343905.0
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            ]
        },
        {
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                {
                    "uniprot_canonical_ac": "P24043-1",
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                        {
                            "database": "PubMed",
                            "id": "37074911",
                            "url": "https://glygen.org/publication/PubMed/37074911"
                        },
                        {
                            "database": "PDC",
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                    ],
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            ]
        },
        {
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                        {
                            "database": "PubMed",
                            "id": "37074911",
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                        },
                        {
                            "database": "PDC",
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                    ],
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            ]
        },
        {
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                        {
                            "database": "PubMed",
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                        {
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                    ],
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            ]
        },
        {
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                {
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                            "id": "37074911",
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                        },
                        {
                            "database": "PDC",
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                    ],
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            ]
        },
        {
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                {
                    "weight": 100,
                    "sequence_org": "N",
                    "sequence_mut": "K",
                    "comment": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-loss (NMT->KMT).",
                    "chr_id": "6",
                    "chr_pos": "129393240",
                    "evidence": [
                        {
                            "id": "rs1005888452",
                            "database": "dbSNP",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1005888452"
                        },
                        {
                            "id": "rs1005888452",
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                            "url": "https://www.ncbi.nlm.nih.gov/snp/rs1005888452#frequency_tab"
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                    ]
                },
                {
                    "weight": 100,
                    "sequence_org": "N",
                    "sequence_mut": "S",
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                    "chr_pos": "129393239",
                    "evidence": [
                        {
                            "id": "P24043",
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                            "url": "https://hivelab.biochemistry.gwu.edu/biomuta/proteinview/P24043"
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                    ],
                    "disease": [
                        {
                            "disease_id": "DOID:363",
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                            "description": "A female reproductive organ cancer that is located_in the uterus.",
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                                {
                                    "id": "363",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:363"
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                            ]
                        }
                    ]
                },
                {
                    "weight": 100,
                    "sequence_org": "N",
                    "sequence_mut": "null",
                    "comment": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-loss (NMT->nullMT).",
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                    "chr_pos": "129393239",
                    "evidence": [
                        {
                            "id": "rs1211886873",
                            "database": "dbSNP",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1211886873"
                        }
                    ]
                }
            ],
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                {
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                        {
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                            "id": "37074911",
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                        {
                            "database": "PDC",
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                    ],
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            ]
        },
        {
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                {
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                    "sequence_org": "N",
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                    "chr_pos": "129505255",
                    "evidence": [
                        {
                            "id": "P24043",
                            "database": "BioMuta",
                            "url": "https://hivelab.biochemistry.gwu.edu/biomuta/proteinview/P24043"
                        }
                    ],
                    "disease": [
                        {
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                                {
                                    "id": "1324",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:1324"
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                            ]
                        }
                    ]
                },
                {
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                    "sequence_org": "N",
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                    "comment": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-loss (NRT->nullRT).",
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                    "chr_pos": "129505255",
                    "evidence": [
                        {
                            "id": "rs2533549889",
                            "database": "dbSNP",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs2533549889"
                        }
                    ],
                    "disease": [
                        {
                            "disease_id": "DOID:0110636",
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                            "url": "http://disease-ontology.org/term/DOID:0110636",
                            "evidence": [
                                {
                                    "id": "607855",
                                    "database": "MIM",
                                    "url": "https://www.omim.org/entry/607855"
                                },
                                {
                                    "id": "0110636",
                                    "database": "AGR",
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                            ]
                        },
                        {
                            "disease_id": "DOID:0061132",
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                            "url": "http://disease-ontology.org/term/DOID:0061132",
                            "evidence": [
                                {
                                    "id": "618138",
                                    "database": "MIM",
                                    "url": "https://www.omim.org/entry/618138"
                                },
                                {
                                    "id": "0061132",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0061132"
                                }
                            ]
                        }
                    ]
                }
            ],
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                            "database": "PubMed",
                            "id": "37074911",
                            "url": "https://glygen.org/publication/PubMed/37074911"
                        },
                        {
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                    ],
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            ]
        },
        {
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                            "database": "PubMed",
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                            "url": "https://glygen.org/publication/PubMed/37074911"
                        },
                        {
                            "database": "PDC",
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                            "url": "https://proteomic.datacommons.cancer.gov/pdc/study/PDC000471"
                        }
                    ],
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                    "gene_name": "LAMA2",
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                    "tax_name": "Homo sapiens",
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                }
            ]
        },
        {
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                {
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                            "database": "PubMed",
                            "id": "37074911",
                            "url": "https://glygen.org/publication/PubMed/37074911"
                        },
                        {
                            "database": "PDC",
                            "id": "PDC000471",
                            "url": "https://proteomic.datacommons.cancer.gov/pdc/study/PDC000471"
                        }
                    ],
                    "protein_name": "Laminin subunit alpha-2",
                    "gene_name": "LAMA2",
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                    "tax_common_name": "Human",
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                    "chemical_mass": 343905.0
                }
            ]
        },
        {
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            "residue": "Asn",
            "glycoprotein": [
                {
                    "uniprot_canonical_ac": "P24043-1",
                    "start_pos": 2126,
                    "end_pos": 2126,
                    "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-2",
                    "gene_name": "LAMA2",
                    "tax_id": 9606,
                    "tax_name": "Homo sapiens",
                    "tax_common_name": "Human",
                    "length": 3122,
                    "chemical_mass": 343905.0
                }
            ]
        },
        {
            "start_pos": "2126",
            "site_seq": "N",
            "site_lbl": "Asn2126",
            "residue": "Asn",
            "glycoprotein": [
                {
                    "uniprot_canonical_ac": "P24043-1",
                    "start_pos": 2126,
                    "end_pos": 2126,
                    "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-2",
                    "gene_name": "LAMA2",
                    "tax_id": 9606,
                    "tax_name": "Homo sapiens",
                    "tax_common_name": "Human",
                    "length": 3122,
                    "chemical_mass": 343905.0
                }
            ]
        },
        {
            "start_pos": "2240",
            "site_seq": "nGTISVR",
            "site_lbl": "Asn2240",
            "residue": "Asn",
            "glycoprotein": [
                {
                    "uniprot_canonical_ac": "P24043-1",
                    "start_pos": 2240,
                    "end_pos": 2240,
                    "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-2",
                    "gene_name": "LAMA2",
                    "tax_id": 9606,
                    "tax_name": "Homo sapiens",
                    "tax_common_name": "Human",
                    "length": 3122,
                    "chemical_mass": 343905.0
                }
            ]
        },
        {
            "start_pos": "2240",
            "site_seq": "N",
            "site_lbl": "Asn2240",
            "residue": "Asn",
            "glycoprotein": [
                {
                    "uniprot_canonical_ac": "P24043-1",
                    "start_pos": 2240,
                    "end_pos": 2240,
                    "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-2",
                    "gene_name": "LAMA2",
                    "tax_id": 9606,
                    "tax_name": "Homo sapiens",
                    "tax_common_name": "Human",
                    "length": 3122,
                    "chemical_mass": 343905.0
                }
            ]
        },
        {
            "start_pos": "2868",
            "site_seq": "QEGILYVDGASnR",
            "site_lbl": "Asn2868",
            "residue": "Asn",
            "glycoprotein": [
                {
                    "uniprot_canonical_ac": "P24043-1",
                    "start_pos": 2868,
                    "end_pos": 2868,
                    "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-2",
                    "gene_name": "LAMA2",
                    "tax_id": 9606,
                    "tax_name": "Homo sapiens",
                    "tax_common_name": "Human",
                    "length": 3122,
                    "chemical_mass": 343905.0
                }
            ]
        },
        {
            "start_pos": "2868",
            "site_seq": "QEGILYVDGASNRTISPK",
            "site_lbl": "Asn2868",
            "residue": "Asn",
            "glycoprotein": [
                {
                    "uniprot_canonical_ac": "P24043-1",
                    "start_pos": 2868,
                    "end_pos": 2868,
                    "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-2",
                    "gene_name": "LAMA2",
                    "tax_id": 9606,
                    "tax_name": "Homo sapiens",
                    "tax_common_name": "Human",
                    "length": 3122,
                    "chemical_mass": 343905.0
                }
            ]
        },
        {
            "start_pos": "2868",
            "site_seq": "N",
            "site_lbl": "Asn2868",
            "residue": "Asn",
            "glycoprotein": [
                {
                    "uniprot_canonical_ac": "P24043-1",
                    "start_pos": 2868,
                    "end_pos": 2868,
                    "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-2",
                    "gene_name": "LAMA2",
                    "tax_id": 9606,
                    "tax_name": "Homo sapiens",
                    "tax_common_name": "Human",
                    "length": 3122,
                    "chemical_mass": 343905.0
                }
            ]
        },
        {
            "start_pos": "1810",
            "site_seq": "",
            "site_lbl": "N1810",
            "residue": "",
            "snv": [
                {
                    "weight": 100,
                    "sequence_org": "N",
                    "sequence_mut": "K",
                    "comment": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-loss (NMT->KMT).",
                    "chr_id": "6",
                    "chr_pos": "129393240",
                    "evidence": [
                        {
                            "id": "rs1005888452",
                            "database": "dbSNP",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1005888452"
                        },
                        {
                            "id": "rs1005888452",
                            "database": "TOPMed",
                            "url": "https://www.ncbi.nlm.nih.gov/snp/rs1005888452#frequency_tab"
                        }
                    ]
                },
                {
                    "weight": 100,
                    "sequence_org": "N",
                    "sequence_mut": "S",
                    "comment": "Somatic mutation passed 1 out of 6 filters: n-glyco-sequon-loss (NMT->SMT).",
                    "chr_id": "6",
                    "chr_pos": "129393239",
                    "evidence": [
                        {
                            "id": "P24043",
                            "database": "BioMuta",
                            "url": "https://hivelab.biochemistry.gwu.edu/biomuta/proteinview/P24043"
                        }
                    ],
                    "disease": [
                        {
                            "disease_id": "DOID:363",
                            "name": "uterine cancer",
                            "description": "A female reproductive organ cancer that is located_in the uterus.",
                            "url": "http://disease-ontology.org/term/DOID:363",
                            "evidence": [
                                {
                                    "id": "363",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:363"
                                }
                            ]
                        }
                    ]
                },
                {
                    "weight": 100,
                    "sequence_org": "N",
                    "sequence_mut": "null",
                    "comment": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-loss (NMT->nullMT).",
                    "chr_id": "6",
                    "chr_pos": "129393239",
                    "evidence": [
                        {
                            "id": "rs1211886873",
                            "database": "dbSNP",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1211886873"
                        }
                    ]
                }
            ],
            "glycoprotein": [
                {
                    "uniprot_canonical_ac": "P24043-1",
                    "start_pos": 1810,
                    "end_pos": 1810,
                    "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-2",
                    "gene_name": "LAMA2",
                    "tax_id": 9606,
                    "tax_name": "Homo sapiens",
                    "tax_common_name": "Human",
                    "length": 3122,
                    "chemical_mass": 343905.0
                }
            ]
        },
        {
            "start_pos": "2868",
            "site_seq": "",
            "site_lbl": "N2868",
            "residue": "",
            "snv": [
                {
                    "weight": 100,
                    "sequence_org": "N",
                    "sequence_mut": "T",
                    "comment": "Somatic mutation passed 1 out of 6 filters: n-glyco-sequon-loss (NRT->TRT).",
                    "chr_id": "6",
                    "chr_pos": "129505255",
                    "evidence": [
                        {
                            "id": "P24043",
                            "database": "BioMuta",
                            "url": "https://hivelab.biochemistry.gwu.edu/biomuta/proteinview/P24043"
                        }
                    ],
                    "disease": [
                        {
                            "disease_id": "DOID:1324",
                            "name": "lung cancer",
                            "description": "A respiratory system cancer that is located_in the lung.",
                            "url": "http://disease-ontology.org/term/DOID:1324",
                            "evidence": [
                                {
                                    "id": "1324",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:1324"
                                }
                            ]
                        }
                    ]
                },
                {
                    "weight": 100,
                    "sequence_org": "N",
                    "sequence_mut": "null",
                    "comment": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-loss (NRT->nullRT).",
                    "chr_id": "6",
                    "chr_pos": "129505255",
                    "evidence": [
                        {
                            "id": "rs2533549889",
                            "database": "dbSNP",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs2533549889"
                        }
                    ],
                    "disease": [
                        {
                            "disease_id": "DOID:0110636",
                            "name": "congenital merosin-deficient muscular dystrophy 1A",
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                            "url": "http://disease-ontology.org/term/DOID:0110636",
                            "evidence": [
                                {
                                    "id": "607855",
                                    "database": "MIM",
                                    "url": "https://www.omim.org/entry/607855"
                                },
                                {
                                    "id": "0110636",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0110636"
                                }
                            ]
                        },
                        {
                            "disease_id": "DOID:0061132",
                            "name": "autosomal recessive limb-girdle muscular dystrophy type 23",
                            "description": "An autosomal recessive limb-girdle muscular dystrophy characterized by slowly progressive proximal muscle weakness primarily affecting the lower limbs and resulting in gait difficulties that has_material_basis_in y homozygous or compound heterozygous mutation in the LAMA2 gene on chromosome 6q22.",
                            "url": "http://disease-ontology.org/term/DOID:0061132",
                            "evidence": [
                                {
                                    "id": "618138",
                                    "database": "MIM",
                                    "url": "https://www.omim.org/entry/618138"
                                },
                                {
                                    "id": "0061132",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0061132"
                                }
                            ]
                        }
                    ]
                }
            ],
            "glycoprotein": [
                {
                    "uniprot_canonical_ac": "P24043-1",
                    "start_pos": 2868,
                    "end_pos": 2868,
                    "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-2",
                    "gene_name": "LAMA2",
                    "tax_id": 9606,
                    "tax_name": "Homo sapiens",
                    "tax_common_name": "Human",
                    "length": 3122,
                    "chemical_mass": 343905.0
                }
            ]
        },
        {
            "start_pos": "112",
            "site_seq": "DTGELnVTSILDREETPFFLLTGYALDAR",
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            "glycoprotein": [
                {
                    "uniprot_canonical_ac": "Q14126-1",
                    "start_pos": 112,
                    "end_pos": 112,
                    "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": "Desmoglein-2",
                    "gene_name": "DSG2",
                    "tax_id": 9606,
                    "tax_name": "Homo sapiens",
                    "tax_common_name": "Human",
                    "length": 1118,
                    "chemical_mass": 122294.0
                }
            ]
        },
        {
            "start_pos": "112",
            "site_seq": "N",
            "site_lbl": "Asn112",
            "residue": "Asn",
            "glycoprotein": [
                {
                    "uniprot_canonical_ac": "Q14126-1",
                    "start_pos": 112,
                    "end_pos": 112,
                    "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": "Desmoglein-2",
                    "gene_name": "DSG2",
                    "tax_id": 9606,
                    "tax_name": "Homo sapiens",
                    "tax_common_name": "Human",
                    "length": 1118,
                    "chemical_mass": 122294.0
                }
            ]
        },
        {
            "start_pos": "112",
            "site_seq": "DTGELNVTSILDR",
            "site_lbl": "Asn112",
            "residue": "Asn",
            "glycoprotein": [
                {
                    "uniprot_canonical_ac": "Q14126-1",
                    "start_pos": 112,
                    "end_pos": 112,
                    "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": "Desmoglein-2",
                    "gene_name": "DSG2",
                    "tax_id": 9606,
                    "tax_name": "Homo sapiens",
                    "tax_common_name": "Human",
                    "length": 1118,
                    "chemical_mass": 122294.0
                }
            ]
        },
        {
            "start_pos": "182",
            "site_seq": "InATDADEPNTLNSK",
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            "residue": "Asn",
            "glycoprotein": [
                {
                    "uniprot_canonical_ac": "Q14126-1",
                    "start_pos": 182,
                    "end_pos": 182,
                    "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": "Desmoglein-2",
                    "gene_name": "DSG2",
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                    "tax_name": "Homo sapiens",
                    "tax_common_name": "Human",
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            ]
        },
        {
            "start_pos": "182",
            "site_seq": "INATDADEPNTLNSK",
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            "glycoprotein": [
                {
                    "uniprot_canonical_ac": "Q14126-1",
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                        {
                            "database": "PubMed",
                            "id": "37074911",
                            "url": "https://glygen.org/publication/PubMed/37074911"
                        },
                        {
                            "database": "PDC",
                            "id": "PDC000471",
                            "url": "https://proteomic.datacommons.cancer.gov/pdc/study/PDC000471"
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                    ],
                    "protein_name": "Desmoglein-2",
                    "gene_name": "DSG2",
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                    "tax_common_name": "Human",
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                    "chemical_mass": 122294.0
                }
            ]
        },
        {
            "start_pos": "182",
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            "glycoprotein": [
                {
                    "uniprot_canonical_ac": "Q14126-1",
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                    "residue": "Asn",
                    "evidence": [
                        {
                            "database": "PubMed",
                            "id": "37074911",
                            "url": "https://glygen.org/publication/PubMed/37074911"
                        },
                        {
                            "database": "PDC",
                            "id": "PDC000471",
                            "url": "https://proteomic.datacommons.cancer.gov/pdc/study/PDC000471"
                        }
                    ],
                    "protein_name": "Desmoglein-2",
                    "gene_name": "DSG2",
                    "tax_id": 9606,
                    "tax_name": "Homo sapiens",
                    "tax_common_name": "Human",
                    "length": 1118,
                    "chemical_mass": 122294.0
                }
            ]
        },
        {
            "start_pos": "462",
            "site_seq": "YVQnGTYTVK",
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            "residue": "Asn",
            "glycoprotein": [
                {
                    "uniprot_canonical_ac": "Q14126-1",
                    "start_pos": 462,
                    "end_pos": 462,
                    "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": "Desmoglein-2",
                    "gene_name": "DSG2",
                    "tax_id": 9606,
                    "tax_name": "Homo sapiens",
                    "tax_common_name": "Human",
                    "length": 1118,
                    "chemical_mass": 122294.0
                }
            ]
        },
        {
            "start_pos": "462",
            "site_seq": "LPDFESRYVQnGTYTVK",
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            "residue": "Asn",
            "glycoprotein": [
                {
                    "uniprot_canonical_ac": "Q14126-1",
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                    "end_pos": 462,
                    "residue": "Asn",
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                        {
                            "database": "PubMed",
                            "id": "37074911",
                            "url": "https://glygen.org/publication/PubMed/37074911"
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                        {
                            "database": "PDC",
                            "id": "PDC000471",
                            "url": "https://proteomic.datacommons.cancer.gov/pdc/study/PDC000471"
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                    ],
                    "protein_name": "Desmoglein-2",
                    "gene_name": "DSG2",
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                    "tax_common_name": "Human",
                    "length": 1118,
                    "chemical_mass": 122294.0
                }
            ]
        },
        {
            "start_pos": "462",
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            "glycoprotein": [
                {
                    "uniprot_canonical_ac": "Q14126-1",
                    "start_pos": 462,
                    "end_pos": 462,
                    "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": "Desmoglein-2",
                    "gene_name": "DSG2",
                    "tax_id": 9606,
                    "tax_name": "Homo sapiens",
                    "tax_common_name": "Human",
                    "length": 1118,
                    "chemical_mass": 122294.0
                }
            ]
        },
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                }
            ],
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                {
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                    ],
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                    "tax_id": 9606,
                    "tax_name": "Homo sapiens",
                    "tax_common_name": "Human",
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            ]
        },
        {
            "start_pos": "182",
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            "site_lbl": "N182",
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                    "weight": 100,
                    "sequence_org": "N",
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                            "id": "rs368512832",
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                        {
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                                {
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                                {
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                            "id": "rs368512832",
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                        {
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                        {
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                        {
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                    "tax_common_name": "Human",
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            ]
        },
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                    "protein_name": "Laminin subunit beta-2",
                    "gene_name": "LAMB2",
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                    "chemical_mass": 195981.0
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            ]
        },
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                {
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                        {
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                        {
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            ]
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                        {
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                    ],
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            ]
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                        {
                            "id": "rs1459957730",
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                        {
                            "id": "rs1459957730",
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                    ]
                },
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                        {
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                        },
                        {
                            "id": "rs1459957730",
                            "database": "gnomAD",
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                    ]
                },
                {
                    "weight": 100,
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                    "comment": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-loss (NTS->ITS).",
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                            "id": "rs771215576",
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                        {
                            "id": "rs771215576",
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                        {
                            "id": "rs771215576",
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                        },
                        {
                            "id": "rs771215576",
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                    ]
                },
                {
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                    "comment": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-loss (NTS->STS).",
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                        {
                            "id": "rs771215576",
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                        {
                            "id": "rs771215576",
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                        },
                        {
                            "id": "rs771215576",
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                        },
                        {
                            "id": "rs771215576",
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                            "disease_id": "DOID:0080380",
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                            "url": "http://disease-ontology.org/term/DOID:0080380",
                            "evidence": [
                                {
                                    "id": "0080380",
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                                    "url": "https://www.alliancegenome.org/disease/DOID:0080380"
                                },
                                {
                                    "id": "0080380",
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                            ]
                        },
                        {
                            "disease_id": "DOID:0080380",
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                                {
                                    "id": "0080380",
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                                    "url": "https://www.alliancegenome.org/disease/DOID:0080380"
                                },
                                {
                                    "id": "0080380",
                                    "database": "AGR",
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                            ]
                        },
                        {
                            "disease_id": "DOID:0080380",
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                                {
                                    "id": "0080380",
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                                    "url": "https://www.alliancegenome.org/disease/DOID:0080380"
                                },
                                {
                                    "id": "0080380",
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                                    "url": "https://www.alliancegenome.org/disease/DOID:0080380"
                                }
                            ]
                        },
                        {
                            "disease_id": "DOID:0080380",
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                                {
                                    "id": "0080380",
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                                    "url": "https://www.alliancegenome.org/disease/DOID:0080380"
                                },
                                {
                                    "id": "0080380",
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                                    "url": "https://www.alliancegenome.org/disease/DOID:0080380"
                                }
                            ]
                        },
                        {
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                                {
                                    "id": "0060852",
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                            ]
                        },
                        {
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                                    "id": "0060852",
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                            ]
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            ]
        },
        {
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                        {
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                            "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"
                                }
                            ]
                        }
                    ]
                }
            ],
            "glycoprotein": [
                {
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                            "url": "https://glygen.org/publication/PubMed/37074911"
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                        {
                            "database": "PDC",
                            "id": "PDC000471",
                            "url": "https://proteomic.datacommons.cancer.gov/pdc/study/PDC000471"
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                    ],
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                    "gene_name": "LAMA5",
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                    "tax_name": "Homo sapiens",
                    "tax_common_name": "Human",
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            ]
        },
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                {
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                    "sequence_org": "N",
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                    "comment": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-loss (NAT->HAT).",
                    "chr_id": "20",
                    "chr_pos": "62317751",
                    "evidence": [
                        {
                            "id": "rs748430953",
                            "database": "dbSNP",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs748430953"
                        },
                        {
                            "id": "rs748430953",
                            "database": "ExAC",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs748430953"
                        },
                        {
                            "id": "rs748430953",
                            "database": "gnomAD",
                            "url": "http://gnomad.broadinstitute.org/awesome?query=rs748430953"
                        }
                    ]
                },
                {
                    "weight": 100,
                    "sequence_org": "N",
                    "sequence_mut": "S",
                    "comment": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-loss (NAT->SAT).",
                    "chr_id": "20",
                    "chr_pos": "62317750",
                    "evidence": [
                        {
                            "id": "rs979598123",
                            "database": "dbSNP",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs979598123"
                        },
                        {
                            "id": "rs979598123",
                            "database": "TOPMed",
                            "url": "https://www.ncbi.nlm.nih.gov/snp/rs979598123#frequency_tab"
                        },
                        {
                            "id": "rs979598123",
                            "database": "gnomAD",
                            "url": "http://gnomad.broadinstitute.org/awesome?query=rs979598123"
                        }
                    ]
                }
            ],
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                {
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                        {
                            "database": "PubMed",
                            "id": "37074911",
                            "url": "https://glygen.org/publication/PubMed/37074911"
                        },
                        {
                            "database": "PDC",
                            "id": "PDC000471",
                            "url": "https://proteomic.datacommons.cancer.gov/pdc/study/PDC000471"
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                    ],
                    "protein_name": "Laminin subunit alpha-5",
                    "gene_name": "LAMA5",
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                    "tax_common_name": "Human",
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            ]
        },
        {
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            "snv": [
                {
                    "weight": 100,
                    "sequence_org": "N",
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                    "chr_pos": "62317354",
                    "evidence": [
                        {
                            "id": "O15230",
                            "database": "BioMuta",
                            "url": "https://hivelab.biochemistry.gwu.edu/biomuta/proteinview/O15230"
                        },
                        {
                            "id": "rs766523334",
                            "database": "dbSNP",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs766523334"
                        },
                        {
                            "id": "rs766523334",
                            "database": "ExAC",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs766523334"
                        },
                        {
                            "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"
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                            ]
                        }
                    ]
                }
            ],
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                {
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                        {
                            "database": "PubMed",
                            "id": "37074911",
                            "url": "https://glygen.org/publication/PubMed/37074911"
                        },
                        {
                            "database": "PDC",
                            "id": "PDC000471",
                            "url": "https://proteomic.datacommons.cancer.gov/pdc/study/PDC000471"
                        }
                    ],
                    "protein_name": "Laminin subunit alpha-5",
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                    "tax_name": "Homo sapiens",
                    "tax_common_name": "Human",
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            ]
        },
        {
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            "site_lbl": "N3107",
            "residue": "",
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                {
                    "weight": 100,
                    "sequence_org": "N",
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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"
                                }
                            ]
                        }
                    ]
                },
                {
                    "weight": 100,
                    "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",
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                        },
                        {
                            "id": "rs759232226",
                            "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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                        {
                            "id": "O15230",
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                    ],
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                                {
                                    "id": "1793",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:1793"
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                            ]
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            ],
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                        {
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            ]
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                            "id": "rs1981055552",
                            "database": "dbSNP",
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                        {
                            "id": "rs1981055552",
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                    ]
                },
                {
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                        {
                            "id": "rs2146208511",
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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": "rs2126518883",
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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": "rs1340244712",
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                        {
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                {
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                        {
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                                {
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                                {
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                                {
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                {
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                            "url": "https://glygen.org/publication/PubMed/37074911"
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                        {
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                            "id": "PDC000471",
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                    ],
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                    "tax_name": "Homo sapiens",
                    "tax_common_name": "Human",
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                    "chemical_mass": 116612.0
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            ]
        },
        {
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                {
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                        {
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                    ],
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            ]
        },
        {
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                {
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                        {
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                    ],
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                    "tax_common_name": "Human",
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            ]
        },
        {
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                {
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                    "chr_pos": "50071353",
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                        {
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                        {
                            "id": "rs1380877482",
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                            "url": "http://gnomad.broadinstitute.org/awesome?query=rs1380877482"
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                    ]
                }
            ],
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                {
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                        {
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                            "id": "37074911",
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                        },
                        {
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                    ],
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            ]
        },
        {
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                {
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                        {
                            "id": "rs530445034",
                            "database": "1000Genomes",
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                        },
                        {
                            "id": "rs530445034",
                            "database": "ExAC",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs530445034"
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                        {
                            "id": "rs530445034",
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                        },
                        {
                            "id": "rs530445034",
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                    ]
                },
                {
                    "weight": 100,
                    "sequence_org": "N",
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                    "chr_pos": "50080332",
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                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1567703793"
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                        {
                            "id": "rs1567703793",
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                            "url": "https://www.ensembl.org/id/rs1567703793"
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                    ]
                }
            ],
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            ]
        },
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                            "id": "rs1447627958",
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                        {
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                        {
                            "id": "rs1447627958",
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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": "10581",
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                        {
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                                {
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                        {
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                                    "id": "10581",
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                                {
                                    "id": "10581",
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                            "evidence": [
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                                    "id": "0111330",
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                        },
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                            "disease_id": "DOID:0111330",
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                            "evidence": [
                                {
                                    "id": "0111330",
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                                    "url": "https://www.alliancegenome.org/disease/DOID:0111330"
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                            ]
                        },
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                            "evidence": [
                                {
                                    "id": "0111330",
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                                    "url": "https://www.alliancegenome.org/disease/DOID:0111330"
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                        },
                        {
                            "disease_id": "DOID:0110961",
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                                {
                                    "id": "0110961",
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                                },
                                {
                                    "id": "0110961",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0110961"
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                        },
                        {
                            "disease_id": "DOID:0110961",
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                                {
                                    "id": "0110961",
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                                    "url": "https://www.alliancegenome.org/disease/DOID:0110961"
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                                {
                                    "id": "0110961",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0110961"
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                            ]
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                        {
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                                {
                                    "id": "0110961",
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                                {
                                    "id": "0110961",
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                                {
                                    "id": "10581",
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                        {
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                        {
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                                {
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                        {
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                                    "id": "10581",
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                {
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                    ],
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            ]
        },
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                        {
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                        {
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                        {
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                    ]
                },
                {
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                        {
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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": "10581",
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                        },
                        {
                            "disease_id": "DOID:10581",
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                        {
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                                    "url": "https://www.alliancegenome.org/disease/DOID:10581"
                                }
                            ]
                        },
                        {
                            "disease_id": "DOID:10581",
                            "name": "metachromatic leukodystrophy",
                            "description": "A sphingolipidosis characterized by the accumulation of sulfatides in cells, especially the myelin producing cells of the nervous system.",
                            "url": "http://disease-ontology.org/term/DOID:10581",
                            "evidence": [
                                {
                                    "id": "10581",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:10581"
                                }
                            ]
                        },
                        {
                            "disease_id": "DOID:10581",
                            "name": "metachromatic leukodystrophy",
                            "description": "A sphingolipidosis characterized by the accumulation of sulfatides in cells, especially the myelin producing cells of the nervous system.",
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                            "evidence": [
                                {
                                    "id": "10581",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:10581"
                                }
                            ]
                        },
                        {
                            "disease_id": "DOID:10581",
                            "name": "metachromatic leukodystrophy",
                            "description": "A sphingolipidosis characterized by the accumulation of sulfatides in cells, especially the myelin producing cells of the nervous system.",
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                            "evidence": [
                                {
                                    "id": "10581",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:10581"
                                }
                            ]
                        },
                        {
                            "disease_id": "DOID:10581",
                            "name": "metachromatic leukodystrophy",
                            "description": "A sphingolipidosis characterized by the accumulation of sulfatides in cells, especially the myelin producing cells of the nervous system.",
                            "url": "http://disease-ontology.org/term/DOID:10581",
                            "evidence": [
                                {
                                    "id": "10581",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:10581"
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                            ]
                        }
                    ]
                },
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                    "sequence_mut": "K",
                    "comment": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-loss (NST->KST).",
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                        {
                            "id": "rs770171865",
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                        },
                        {
                            "id": "rs770171865",
                            "database": "ExAC",
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                        },
                        {
                            "id": "rs770171865",
                            "database": "gnomAD",
                            "url": "http://gnomad.broadinstitute.org/awesome?query=rs770171865"
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                    ],
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                            "disease_id": "DOID:0111330",
                            "name": "combined saposin deficiency",
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                            "url": "http://disease-ontology.org/term/DOID:0111330",
                            "evidence": [
                                {
                                    "id": "0111330",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0111330"
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                            ]
                        },
                        {
                            "disease_id": "DOID:0111330",
                            "name": "combined saposin deficiency",
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                            "url": "http://disease-ontology.org/term/DOID:0111330",
                            "evidence": [
                                {
                                    "id": "0111330",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0111330"
                                }
                            ]
                        },
                        {
                            "disease_id": "DOID:0111330",
                            "name": "combined saposin deficiency",
                            "description": "A sphingolipidosis characterized by absence of expression of both isoforms of PSAP (SAP1 and SAP2) resulting in hepatosplenomegaly and severe neurological disease that has_material_basis_in homozygous or compound heterozygous mutation in PSAP on 10q22.1.",
                            "url": "http://disease-ontology.org/term/DOID:0111330",
                            "evidence": [
                                {
                                    "id": "0111330",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0111330"
                                }
                            ]
                        },
                        {
                            "disease_id": "DOID:0110961",
                            "name": "atypical Gaucher's disease due to saposin c deficiency",
                            "description": "A Gaucher's disease that has_material_basis_in compound heterozygous mutation in the PSAP gene on chromosome 10q22.1.",
                            "url": "http://disease-ontology.org/term/DOID:0110961",
                            "evidence": [
                                {
                                    "id": "0110961",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0110961"
                                },
                                {
                                    "id": "0110961",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0110961"
                                }
                            ]
                        },
                        {
                            "disease_id": "DOID:0110961",
                            "name": "atypical Gaucher's disease due to saposin c deficiency",
                            "description": "A Gaucher's disease that has_material_basis_in compound heterozygous mutation in the PSAP gene on chromosome 10q22.1.",
                            "url": "http://disease-ontology.org/term/DOID:0110961",
                            "evidence": [
                                {
                                    "id": "0110961",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0110961"
                                },
                                {
                                    "id": "0110961",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0110961"
                                }
                            ]
                        },
                        {
                            "disease_id": "DOID:0110961",
                            "name": "atypical Gaucher's disease due to saposin c deficiency",
                            "description": "A Gaucher's disease that has_material_basis_in compound heterozygous mutation in the PSAP gene on chromosome 10q22.1.",
                            "url": "http://disease-ontology.org/term/DOID:0110961",
                            "evidence": [
                                {
                                    "id": "0110961",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0110961"
                                },
                                {
                                    "id": "0110961",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0110961"
                                }
                            ]
                        },
                        {
                            "disease_id": "DOID:10581",
                            "name": "metachromatic leukodystrophy",
                            "description": "A sphingolipidosis characterized by the accumulation of sulfatides in cells, especially the myelin producing cells of the nervous system.",
                            "url": "http://disease-ontology.org/term/DOID:10581",
                            "evidence": [
                                {
                                    "id": "10581",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:10581"
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                            ]
                        },
                        {
                            "disease_id": "DOID:10581",
                            "name": "metachromatic leukodystrophy",
                            "description": "A sphingolipidosis characterized by the accumulation of sulfatides in cells, especially the myelin producing cells of the nervous system.",
                            "url": "http://disease-ontology.org/term/DOID:10581",
                            "evidence": [
                                {
                                    "id": "10581",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:10581"
                                }
                            ]
                        },
                        {
                            "disease_id": "DOID:10581",
                            "name": "metachromatic leukodystrophy",
                            "description": "A sphingolipidosis characterized by the accumulation of sulfatides in cells, especially the myelin producing cells of the nervous system.",
                            "url": "http://disease-ontology.org/term/DOID:10581",
                            "evidence": [
                                {
                                    "id": "10581",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:10581"
                                }
                            ]
                        },
                        {
                            "disease_id": "DOID:10581",
                            "name": "metachromatic leukodystrophy",
                            "description": "A sphingolipidosis characterized by the accumulation of sulfatides in cells, especially the myelin producing cells of the nervous system.",
                            "url": "http://disease-ontology.org/term/DOID:10581",
                            "evidence": [
                                {
                                    "id": "10581",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:10581"
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                            ]
                        },
                        {
                            "disease_id": "DOID:10581",
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                            "url": "http://disease-ontology.org/term/DOID:10581",
                            "evidence": [
                                {
                                    "id": "10581",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:10581"
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                            ]
                        },
                        {
                            "disease_id": "DOID:10581",
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                                {
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                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:10581"
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                            ]
                        },
                        {
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                                {
                                    "id": "10581",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:10581"
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                            ]
                        },
                        {
                            "disease_id": "DOID:10581",
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                            "evidence": [
                                {
                                    "id": "10581",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:10581"
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                            ]
                        },
                        {
                            "disease_id": "DOID:10581",
                            "name": "metachromatic leukodystrophy",
                            "description": "A sphingolipidosis characterized by the accumulation of sulfatides in cells, especially the myelin producing cells of the nervous system.",
                            "url": "http://disease-ontology.org/term/DOID:10581",
                            "evidence": [
                                {
                                    "id": "10581",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:10581"
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                            ]
                        }
                    ]
                }
            ],
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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": "rs546727182",
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                    ]
                },
                {
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                                    "id": "10581",
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                    ],
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                        {
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                        {
                            "id": "rs1842525967",
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                    ]
                },
                {
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                    "chr_pos": "71831856",
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                        {
                            "id": "rs570654892",
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                        {
                            "id": "rs570654892",
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                        {
                            "id": "rs570654892",
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                        {
                            "id": "rs570654892",
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                        {
                            "id": "rs570654892",
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                                {
                                    "id": "10581",
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                            ]
                        },
                        {
                            "disease_id": "DOID:10581",
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                            ]
                        },
                        {
                            "disease_id": "DOID:10581",
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                        {
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                        {
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                        },
                        {
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                        },
                        {
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                            ]
                        },
                        {
                            "disease_id": "DOID:10581",
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                                {
                                    "id": "10581",
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                                    "url": "https://www.alliancegenome.org/disease/DOID:10581"
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                            ]
                        },
                        {
                            "disease_id": "DOID:10581",
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                                {
                                    "id": "10581",
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                                    "url": "https://www.alliancegenome.org/disease/DOID:10581"
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                            ]
                        },
                        {
                            "disease_id": "DOID:10581",
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                                {
                                    "id": "10581",
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                    "gene_name": "LRP2",
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            ]
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        {
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                        {
                            "id": "rs747142179",
                            "database": "ExAC",
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                        },
                        {
                            "id": "rs747142179",
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                },
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                        {
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                        },
                        {
                            "id": "rs747142179",
                            "database": "ExAC",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs747142179"
                        },
                        {
                            "id": "rs747142179",
                            "database": "gnomAD",
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                        {
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                        {
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                        {
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                        },
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                                {
                                    "id": "222448",
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                                    "url": "https://www.omim.org/entry/222448"
                                },
                                {
                                    "id": "0090144",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0090144"
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                            ]
                        },
                        {
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                            "evidence": [
                                {
                                    "id": "222448",
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                                },
                                {
                                    "id": "0090144",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0090144"
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                            ]
                        },
                        {
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                                {
                                    "id": "222448",
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                                    "url": "https://www.omim.org/entry/222448"
                                },
                                {
                                    "id": "0090144",
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                                    "url": "https://www.alliancegenome.org/disease/DOID:0090144"
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                        {
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                        {
                            "id": "rs764422443",
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                        {
                            "id": "rs764422443",
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                                {
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                            ]
                        },
                        {
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                                {
                                    "id": "10534",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:10534"
                                },
                                {
                                    "id": "10534",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:10534"
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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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                    "evidence": [
                        {
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            ]
        },
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                        {
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                    ],
                    "protein_name": "Low-density lipoprotein receptor-related protein 2",
                    "gene_name": "LRP2",
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            ]
        },
        {
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                            "id": "37074911",
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                        },
                        {
                            "database": "PDC",
                            "id": "PDC000471",
                            "url": "https://proteomic.datacommons.cancer.gov/pdc/study/PDC000471"
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                    ],
                    "protein_name": "Low-density lipoprotein receptor-related protein 2",
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            ]
        },
        {
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                {
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                        {
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                        },
                        {
                            "database": "PDC",
                            "id": "PDC000471",
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                    ],
                    "protein_name": "Low-density lipoprotein receptor-related protein 2",
                    "gene_name": "LRP2",
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            ]
        },
        {
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                        {
                            "database": "PDC",
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                    ],
                    "protein_name": "Low-density lipoprotein receptor-related protein 2",
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            ]
        },
        {
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                        {
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                    ],
                    "protein_name": "Low-density lipoprotein receptor-related protein 2",
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            ]
        },
        {
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                        {
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                    ],
                    "protein_name": "Low-density lipoprotein receptor-related protein 2",
                    "gene_name": "LRP2",
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                    "tax_name": "Homo sapiens",
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            ]
        },
        {
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            "site_seq": "AWSDGSHLLPVInTTLGWPNGLAIDWAASR",
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                {
                    "uniprot_canonical_ac": "P98164-1",
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                        {
                            "database": "PubMed",
                            "id": "37074911",
                            "url": "https://glygen.org/publication/PubMed/37074911"
                        },
                        {
                            "database": "PDC",
                            "id": "PDC000471",
                            "url": "https://proteomic.datacommons.cancer.gov/pdc/study/PDC000471"
                        }
                    ],
                    "protein_name": "Low-density lipoprotein receptor-related protein 2",
                    "gene_name": "LRP2",
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            ]
        },
        {
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                {
                    "uniprot_canonical_ac": "P98164-1",
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                        {
                            "database": "PubMed",
                            "id": "37074911",
                            "url": "https://glygen.org/publication/PubMed/37074911"
                        },
                        {
                            "database": "PDC",
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                    ],
                    "protein_name": "Low-density lipoprotein receptor-related protein 2",
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            ]
        },
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                {
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                        {
                            "id": "rs1689734706",
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                    ]
                },
                {
                    "weight": 100,
                    "sequence_org": "N",
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                    "comment": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-loss (NDS->IDS).",
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                    "evidence": [
                        {
                            "id": "rs747142179",
                            "database": "dbSNP",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs747142179"
                        },
                        {
                            "id": "rs747142179",
                            "database": "ExAC",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs747142179"
                        },
                        {
                            "id": "rs747142179",
                            "database": "gnomAD",
                            "url": "http://gnomad.broadinstitute.org/awesome?query=rs747142179"
                        }
                    ]
                },
                {
                    "weight": 100,
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                    "comment": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-loss (NDS->SDS).",
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                    "chr_pos": "169239673",
                    "evidence": [
                        {
                            "id": "rs747142179",
                            "database": "dbSNP",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs747142179"
                        },
                        {
                            "id": "rs747142179",
                            "database": "ExAC",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs747142179"
                        },
                        {
                            "id": "rs747142179",
                            "database": "gnomAD",
                            "url": "http://gnomad.broadinstitute.org/awesome?query=rs747142179"
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                    ]
                }
            ],
            "glycoprotein": [
                {
                    "uniprot_canonical_ac": "P98164-1",
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                        {
                            "database": "PubMed",
                            "id": "37074911",
                            "url": "https://glygen.org/publication/PubMed/37074911"
                        },
                        {
                            "database": "PDC",
                            "id": "PDC000471",
                            "url": "https://proteomic.datacommons.cancer.gov/pdc/study/PDC000471"
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                    ],
                    "protein_name": "Low-density lipoprotein receptor-related protein 2",
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            ]
        },
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                {
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                        {
                            "id": "P98164",
                            "database": "BioMuta",
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                        },
                        {
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                        },
                        {
                            "id": "rs957137487",
                            "database": "TOPMed",
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                        },
                        {
                            "id": "rs957137487",
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                    ],
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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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                                {
                                    "id": "9256",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:9256"
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                            ]
                        },
                        {
                            "disease_id": "DOID:0090144",
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                            "url": "http://disease-ontology.org/term/DOID:0090144",
                            "evidence": [
                                {
                                    "id": "222448",
                                    "database": "MIM",
                                    "url": "https://www.omim.org/entry/222448"
                                },
                                {
                                    "id": "0090144",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0090144"
                                }
                            ]
                        },
                        {
                            "disease_id": "DOID:0090144",
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                            "url": "http://disease-ontology.org/term/DOID:0090144",
                            "evidence": [
                                {
                                    "id": "222448",
                                    "database": "MIM",
                                    "url": "https://www.omim.org/entry/222448"
                                },
                                {
                                    "id": "0090144",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0090144"
                                }
                            ]
                        },
                        {
                            "disease_id": "DOID:0090144",
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                            "url": "http://disease-ontology.org/term/DOID:0090144",
                            "evidence": [
                                {
                                    "id": "222448",
                                    "database": "MIM",
                                    "url": "https://www.omim.org/entry/222448"
                                },
                                {
                                    "id": "0090144",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0090144"
                                }
                            ]
                        }
                    ]
                }
            ],
            "glycoprotein": [
                {
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                        {
                            "database": "PubMed",
                            "id": "37074911",
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                        },
                        {
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                            "url": "https://proteomic.datacommons.cancer.gov/pdc/study/PDC000471"
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                    ],
                    "protein_name": "Low-density lipoprotein receptor-related protein 2",
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                    "tax_common_name": "Human",
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            ]
        },
        {
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                {
                    "weight": 100,
                    "sequence_org": "N",
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                    "chr_pos": "169206084",
                    "evidence": [
                        {
                            "id": "rs1688374769",
                            "database": "dbSNP",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1688374769"
                        },
                        {
                            "id": "rs1688374769",
                            "database": "ENSEMBL",
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                    ]
                },
                {
                    "weight": 100,
                    "sequence_org": "N",
                    "sequence_mut": "K",
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                    "chr_id": "2",
                    "chr_pos": "169206082",
                    "evidence": [
                        {
                            "id": "rs764422443",
                            "database": "dbSNP",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs764422443"
                        },
                        {
                            "id": "rs764422443",
                            "database": "ExAC",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs764422443"
                        },
                        {
                            "id": "rs764422443",
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                        },
                        {
                            "id": "rs764422443",
                            "database": "gnomAD",
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                    ]
                },
                {
                    "weight": 100,
                    "sequence_org": "N",
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                    "chr_pos": "169206083",
                    "evidence": [
                        {
                            "id": "P98164",
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                    ],
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                            "name": "esophageal cancer",
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                            "evidence": [
                                {
                                    "id": "5041",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:5041"
                                }
                            ]
                        },
                        {
                            "disease_id": "DOID:10534",
                            "name": "stomach cancer",
                            "description": "A gastrointestinal system cancer that is located_in the stomach.",
                            "url": "http://disease-ontology.org/term/DOID:10534",
                            "evidence": [
                                {
                                    "id": "10534",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:10534"
                                },
                                {
                                    "id": "10534",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:10534"
                                }
                            ]
                        }
                    ]
                }
            ],
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                {
                    "uniprot_canonical_ac": "P98164-1",
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                        {
                            "database": "PubMed",
                            "id": "37074911",
                            "url": "https://glygen.org/publication/PubMed/37074911"
                        },
                        {
                            "database": "PDC",
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                    ],
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                    "tax_name": "Homo sapiens",
                    "tax_common_name": "Human",
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                    "chemical_mass": 521958.0
                }
            ]
        },
        {
            "start_pos": "3315",
            "site_seq": "",
            "site_lbl": "N3315",
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            "snv": [
                {
                    "weight": 100,
                    "sequence_org": "N",
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                    "comment": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-loss (NNT->DNT).",
                    "chr_id": "2",
                    "chr_pos": "169182222",
                    "evidence": [
                        {
                            "id": "rs2545747867",
                            "database": "dbSNP",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs2545747867"
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                    ]
                },
                {
                    "weight": 100,
                    "sequence_org": "N",
                    "sequence_mut": "K",
                    "comment": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-loss (NNT->KNT).",
                    "chr_id": "2",
                    "chr_pos": "169182220",
                    "evidence": [
                        {
                            "id": "rs201808907",
                            "database": "dbSNP",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs201808907"
                        },
                        {
                            "id": "rs201808907",
                            "database": "ExAC",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs201808907"
                        },
                        {
                            "id": "rs201808907",
                            "database": "TOPMed",
                            "url": "https://www.ncbi.nlm.nih.gov/snp/rs201808907#frequency_tab"
                        },
                        {
                            "id": "rs201808907",
                            "database": "gnomAD",
                            "url": "http://gnomad.broadinstitute.org/awesome?query=rs201808907"
                        }
                    ],
                    "disease": [
                        {
                            "disease_id": "DOID:0090144",
                            "name": "Donnai-Barrow syndrome",
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                            "url": "http://disease-ontology.org/term/DOID:0090144",
                            "evidence": [
                                {
                                    "id": "222448",
                                    "database": "MIM",
                                    "url": "https://www.omim.org/entry/222448"
                                },
                                {
                                    "id": "0090144",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0090144"
                                }
                            ]
                        },
                        {
                            "disease_id": "DOID:0090144",
                            "name": "Donnai-Barrow syndrome",
                            "description": "A syndrome that is characterized by facial and ocular abnormalities, sensorineural hearing loss, agenesis of the corpus callosum, variable intellectual disability, and proteinuria that has_material_basis_in homozygous or compound heterozygous mutation in the LDL receptor related protein 2 gene (LRP2) on chromosome 2q31.",
                            "url": "http://disease-ontology.org/term/DOID:0090144",
                            "evidence": [
                                {
                                    "id": "222448",
                                    "database": "MIM",
                                    "url": "https://www.omim.org/entry/222448"
                                },
                                {
                                    "id": "0090144",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0090144"
                                }
                            ]
                        },
                        {
                            "disease_id": "DOID:0090144",
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                            "url": "http://disease-ontology.org/term/DOID:0090144",
                            "evidence": [
                                {
                                    "id": "222448",
                                    "database": "MIM",
                                    "url": "https://www.omim.org/entry/222448"
                                },
                                {
                                    "id": "0090144",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0090144"
                                }
                            ]
                        },
                        {
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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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                                {
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                    "comment": "Affects glycosylation status. Affects glycosylation status; when associated with Q-448.",
                    "evidence": [
                        {
                            "database": "UniProtKB",
                            "id": "Q9NUN5",
                            "url": "https://www.uniprot.org/uniprotkb/Q9NUN5"
                        },
                        {
                            "database": "PubMed",
                            "id": "19136951",
                            "url": "https://glygen.org/publication/PubMed/19136951"
                        }
                    ]
                }
            ],
            "glycoprotein": [
                {
                    "uniprot_canonical_ac": "Q9NUN5-1",
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                    "end_pos": 457,
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                    "evidence": [
                        {
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                            "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": "Lysosomal cobalamin transport escort protein LMBD1",
                    "gene_name": "LMBRD1",
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                    "tax_name": "Homo sapiens",
                    "tax_common_name": "Human",
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                    "chemical_mass": 61389.0
                }
            ]
        },
        {
            "start_pos": "189",
            "site_seq": "NEPQnATGAPGR",
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                {
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                        {
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                    ],
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                    "tax_common_name": "Human",
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                    "chemical_mass": 23483.0
                }
            ]
        },
        {
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                {
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                            "url": "https://glygen.org/publication/PubMed/37074911"
                        },
                        {
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                    ],
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                    "gene_name": "RAB5C",
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                    "tax_common_name": "Human",
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                    "chemical_mass": 23483.0
                }
            ]
        },
        {
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                {
                    "uniprot_canonical_ac": "P51148-1",
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                    "end_pos": 189,
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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": "Ras-related protein Rab-5C",
                    "gene_name": "RAB5C",
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                    "tax_name": "Homo sapiens",
                    "tax_common_name": "Human",
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                    "chemical_mass": 23483.0
                }
            ]
        },
        {
            "start_pos": "189",
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                {
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                    "comment": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-loss (NAT->DAT).",
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                    "chr_pos": "42125869",
                    "evidence": [
                        {
                            "id": "rs782299857",
                            "database": "dbSNP",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs782299857"
                        },
                        {
                            "id": "rs782299857",
                            "database": "ExAC",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs782299857"
                        },
                        {
                            "id": "rs782299857",
                            "database": "gnomAD",
                            "url": "http://gnomad.broadinstitute.org/awesome?query=rs782299857"
                        }
                    ]
                },
                {
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                    "comment": "Somatic mutation passed 1 out of 6 filters: n-glyco-sequon-loss (NAT->IAT).",
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                        {
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                            "url": "https://hivelab.biochemistry.gwu.edu/biomuta/proteinview/P51148"
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                    ],
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                        {
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                            "name": "uterine cancer",
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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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                            "id": "37074911",
                            "url": "https://glygen.org/publication/PubMed/37074911"
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                        {
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                    ],
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                    "tax_common_name": "Human",
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                    "chemical_mass": 23483.0
                }
            ]
        },
        {
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                {
                    "uniprot_canonical_ac": "P51148-1",
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                        {
                            "database": "PubMed",
                            "id": "37074911",
                            "url": "https://glygen.org/publication/PubMed/37074911"
                        },
                        {
                            "database": "PDC",
                            "id": "PDC000471",
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                    ],
                    "protein_name": "Ras-related protein Rab-5C",
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                    "tax_common_name": "Human",
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                }
            ]
        },
        {
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                {
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                    "chr_pos": "42125869",
                    "evidence": [
                        {
                            "id": "rs782299857",
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                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs782299857"
                        },
                        {
                            "id": "rs782299857",
                            "database": "ExAC",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs782299857"
                        },
                        {
                            "id": "rs782299857",
                            "database": "gnomAD",
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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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                        {
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                        {
                            "id": "rs780532486",
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                },
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                            "id": "rs2103747069",
                            "database": "dbSNP",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs2103747069"
                        },
                        {
                            "id": "rs2103747069",
                            "database": "ENSEMBL",
                            "url": "https://www.ensembl.org/id/rs2103747069"
                        }
                    ]
                }
            ],
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                {
                    "uniprot_canonical_ac": "P16422-1",
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                    "end_pos": 74,
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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": "Epithelial cell adhesion molecule",
                    "gene_name": "EPCAM",
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                    "tax_name": "Homo sapiens",
                    "tax_common_name": "Human",
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                    "chemical_mass": 34932.0
                }
            ]
        },
        {
            "start_pos": "198",
            "site_seq": "FITSILYENNVITIDLVQnSSQK",
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            "residue": "Asn",
            "glycoprotein": [
                {
                    "uniprot_canonical_ac": "P16422-1",
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                    "end_pos": 198,
                    "residue": "Asn",
                    "evidence": [
                        {
                            "database": "PubMed",
                            "id": "37074911",
                            "url": "https://glygen.org/publication/PubMed/37074911"
                        },
                        {
                            "database": "PDC",
                            "id": "PDC000471",
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                        }
                    ],
                    "protein_name": "Epithelial cell adhesion molecule",
                    "gene_name": "EPCAM",
                    "tax_id": 9606,
                    "tax_name": "Homo sapiens",
                    "tax_common_name": "Human",
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                    "chemical_mass": 34932.0
                }
            ]
        },
        {
            "start_pos": "198",
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            "glycoprotein": [
                {
                    "uniprot_canonical_ac": "P16422-1",
                    "start_pos": 198,
                    "end_pos": 198,
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                    "evidence": [
                        {
                            "database": "PubMed",
                            "id": "37074911",
                            "url": "https://glygen.org/publication/PubMed/37074911"
                        },
                        {
                            "database": "PDC",
                            "id": "PDC000471",
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                        }
                    ],
                    "protein_name": "Epithelial cell adhesion molecule",
                    "gene_name": "EPCAM",
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                    "tax_name": "Homo sapiens",
                    "tax_common_name": "Human",
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                    "chemical_mass": 34932.0
                }
            ]
        },
        {
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                {
                    "uniprot_canonical_ac": "P16422-1",
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                    "evidence": [
                        {
                            "database": "PubMed",
                            "id": "37074911",
                            "url": "https://glygen.org/publication/PubMed/37074911"
                        },
                        {
                            "database": "PDC",
                            "id": "PDC000471",
                            "url": "https://proteomic.datacommons.cancer.gov/pdc/study/PDC000471"
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                    ],
                    "protein_name": "Epithelial cell adhesion molecule",
                    "gene_name": "EPCAM",
                    "tax_id": 9606,
                    "tax_name": "Homo sapiens",
                    "tax_common_name": "Human",
                    "length": 314,
                    "chemical_mass": 34932.0
                }
            ]
        },
        {
            "start_pos": "74",
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            "residue": "Asn",
            "glycoprotein": [
                {
                    "uniprot_canonical_ac": "P16422-1",
                    "start_pos": 74,
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                    "residue": "Asn",
                    "evidence": [
                        {
                            "database": "PubMed",
                            "id": "37074911",
                            "url": "https://glygen.org/publication/PubMed/37074911"
                        },
                        {
                            "database": "PDC",
                            "id": "PDC000471",
                            "url": "https://proteomic.datacommons.cancer.gov/pdc/study/PDC000471"
                        }
                    ],
                    "protein_name": "Epithelial cell adhesion molecule",
                    "gene_name": "EPCAM",
                    "tax_id": 9606,
                    "tax_name": "Homo sapiens",
                    "tax_common_name": "Human",
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                    "chemical_mass": 34932.0
                }
            ]
        },
        {
            "start_pos": "74",
            "site_seq": "AEMnGSKLGR",
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            "glycoprotein": [
                {
                    "uniprot_canonical_ac": "P16422-1",
                    "start_pos": 74,
                    "end_pos": 74,
                    "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": "Epithelial cell adhesion molecule",
                    "gene_name": "EPCAM",
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                    "tax_common_name": "Human",
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                    "chemical_mass": 34932.0
                }
            ]
        },
        {
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            "snv": [
                {
                    "weight": 100,
                    "sequence_org": "N",
                    "sequence_mut": "H",
                    "comment": "Somatic mutation passed 1 out of 6 filters: n-glyco-sequon-loss (NSS->HSS).",
                    "chr_id": "2",
                    "chr_pos": "47378989",
                    "evidence": [
                        {
                            "id": "P16422",
                            "database": "BioMuta",
                            "url": "https://hivelab.biochemistry.gwu.edu/biomuta/proteinview/P16422"
                        }
                    ],
                    "disease": [
                        {
                            "disease_id": "DOID:363",
                            "name": "uterine cancer",
                            "description": "A female reproductive organ cancer that is located_in the uterus.",
                            "url": "http://disease-ontology.org/term/DOID:363",
                            "evidence": [
                                {
                                    "id": "363",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:363"
                                }
                            ]
                        }
                    ]
                },
                {
                    "weight": 100,
                    "sequence_org": "N",
                    "sequence_mut": "Y",
                    "comment": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-loss (NSS->YSS).",
                    "chr_id": "2",
                    "chr_pos": "47378989",
                    "evidence": [
                        {
                            "id": "rs1671503097",
                            "database": "dbSNP",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1671503097"
                        },
                        {
                            "id": "rs1671503097",
                            "database": "ENSEMBL",
                            "url": "https://www.ensembl.org/id/rs1671503097"
                        }
                    ]
                }
            ],
            "glycoprotein": [
                {
                    "uniprot_canonical_ac": "P16422-1",
                    "start_pos": 198,
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                    "evidence": [
                        {
                            "database": "PubMed",
                            "id": "37074911",
                            "url": "https://glygen.org/publication/PubMed/37074911"
                        },
                        {
                            "database": "PDC",
                            "id": "PDC000471",
                            "url": "https://proteomic.datacommons.cancer.gov/pdc/study/PDC000471"
                        }
                    ],
                    "protein_name": "Epithelial cell adhesion molecule",
                    "gene_name": "EPCAM",
                    "tax_id": 9606,
                    "tax_name": "Homo sapiens",
                    "tax_common_name": "Human",
                    "length": 314,
                    "chemical_mass": 34932.0
                }
            ]
        },
        {
            "start_pos": "74",
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            "site_lbl": "N74",
            "residue": "",
            "snv": [
                {
                    "weight": 100,
                    "sequence_org": "N",
                    "sequence_mut": "K",
                    "comment": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-loss (NGS->KGS).",
                    "chr_id": "2",
                    "chr_pos": "47373845",
                    "evidence": [
                        {
                            "id": "rs2103747074",
                            "database": "dbSNP",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs2103747074"
                        },
                        {
                            "id": "rs2103747074",
                            "database": "ENSEMBL",
                            "url": "https://www.ensembl.org/id/rs2103747074"
                        }
                    ]
                },
                {
                    "weight": 100,
                    "sequence_org": "N",
                    "sequence_mut": "S",
                    "comment": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-loss (NGS->SGS).",
                    "chr_id": "2",
                    "chr_pos": "47373844",
                    "evidence": [
                        {
                            "id": "rs780532486",
                            "database": "dbSNP",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs780532486"
                        },
                        {
                            "id": "rs780532486",
                            "database": "ExAC",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs780532486"
                        },
                        {
                            "id": "rs780532486",
                            "database": "gnomAD",
                            "url": "http://gnomad.broadinstitute.org/awesome?query=rs780532486"
                        }
                    ]
                },
                {
                    "weight": 100,
                    "sequence_org": "N",
                    "sequence_mut": "Y",
                    "comment": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-loss (NGS->YGS).",
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                    "chr_pos": "47373843",
                    "evidence": [
                        {
                            "id": "rs2103747069",
                            "database": "dbSNP",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs2103747069"
                        },
                        {
                            "id": "rs2103747069",
                            "database": "ENSEMBL",
                            "url": "https://www.ensembl.org/id/rs2103747069"
                        }
                    ]
                }
            ],
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                {
                    "uniprot_canonical_ac": "P16422-1",
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                        {
                            "database": "PubMed",
                            "id": "37074911",
                            "url": "https://glygen.org/publication/PubMed/37074911"
                        },
                        {
                            "database": "PDC",
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                    ],
                    "protein_name": "Epithelial cell adhesion molecule",
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                }
            ]
        },
        {
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                {
                    "weight": 100,
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                        {
                            "database": "UniProtKB",
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                        },
                        {
                            "database": "PubMed",
                            "id": "18508581",
                            "url": "https://glygen.org/publication/PubMed/18508581"
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                    ]
                }
            ],
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                {
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                        {
                            "database": "PubMed",
                            "id": "37074911",
                            "url": "https://glygen.org/publication/PubMed/37074911"
                        },
                        {
                            "database": "PDC",
                            "id": "PDC000471",
                            "url": "https://proteomic.datacommons.cancer.gov/pdc/study/PDC000471"
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                    ],
                    "protein_name": "Epithelial cell adhesion molecule",
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                }
            ]
        },
        {
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                {
                    "weight": 100,
                    "sequence_org": "N",
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                        {
                            "database": "UniProtKB",
                            "id": "P16422",
                            "url": "https://www.uniprot.org/uniprotkb/P16422"
                        },
                        {
                            "database": "PubMed",
                            "id": "18508581",
                            "url": "https://glygen.org/publication/PubMed/18508581"
                        }
                    ]
                }
            ],
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                {
                    "uniprot_canonical_ac": "P16422-1",
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                        {
                            "database": "PubMed",
                            "id": "37074911",
                            "url": "https://glygen.org/publication/PubMed/37074911"
                        },
                        {
                            "database": "PDC",
                            "id": "PDC000471",
                            "url": "https://proteomic.datacommons.cancer.gov/pdc/study/PDC000471"
                        }
                    ],
                    "protein_name": "Epithelial cell adhesion molecule",
                    "gene_name": "EPCAM",
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                    "tax_common_name": "Human",
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                }
            ]
        },
        {
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                {
                    "uniprot_canonical_ac": "P34059-1",
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                        {
                            "database": "PubMed",
                            "id": "37074911",
                            "url": "https://glygen.org/publication/PubMed/37074911"
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                        {
                            "database": "PDC",
                            "id": "PDC000471",
                            "url": "https://proteomic.datacommons.cancer.gov/pdc/study/PDC000471"
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                    ],
                    "protein_name": "N-acetylgalactosamine-6-sulfatase",
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            ]
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                        {
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                    ],
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            ]
        },
        {
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                            "id": "37074911",
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                        {
                            "database": "PDC",
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                    ],
                    "protein_name": "N-acetylgalactosamine-6-sulfatase",
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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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                    "end_pos": 145,
                    "residue": "Asn",
                    "evidence": [
                        {
                            "database": "PubMed",
                            "id": "37074911",
                            "url": "https://glygen.org/publication/PubMed/37074911"
                        },
                        {
                            "database": "PDC",
                            "id": "PDC000471",
                            "url": "https://proteomic.datacommons.cancer.gov/pdc/study/PDC000471"
                        }
                    ],
                    "protein_name": "Neprilysin",
                    "gene_name": "MME",
                    "tax_id": 9606,
                    "tax_name": "Homo sapiens",
                    "tax_common_name": "Human",
                    "length": 750,
                    "chemical_mass": 85514.0
                }
            ]
        },
        {
            "start_pos": "145",
            "site_seq": "SCINESAIDSR",
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            "glycoprotein": [
                {
                    "uniprot_canonical_ac": "P08473-1",
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                    "end_pos": 145,
                    "residue": "Asn",
                    "evidence": [
                        {
                            "database": "PubMed",
                            "id": "37074911",
                            "url": "https://glygen.org/publication/PubMed/37074911"
                        },
                        {
                            "database": "PDC",
                            "id": "PDC000471",
                            "url": "https://proteomic.datacommons.cancer.gov/pdc/study/PDC000471"
                        }
                    ],
                    "protein_name": "Neprilysin",
                    "gene_name": "MME",
                    "tax_id": 9606,
                    "tax_name": "Homo sapiens",
                    "tax_common_name": "Human",
                    "length": 750,
                    "chemical_mass": 85514.0
                }
            ]
        },
        {
            "start_pos": "285",
            "site_seq": "EIAnATAKPEDRNDPMLLYNK",
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            "residue": "Asn",
            "glycoprotein": [
                {
                    "uniprot_canonical_ac": "P08473-1",
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                    "end_pos": 285,
                    "residue": "Asn",
                    "evidence": [
                        {
                            "database": "PubMed",
                            "id": "37074911",
                            "url": "https://glygen.org/publication/PubMed/37074911"
                        },
                        {
                            "database": "PDC",
                            "id": "PDC000471",
                            "url": "https://proteomic.datacommons.cancer.gov/pdc/study/PDC000471"
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                    ],
                    "protein_name": "Neprilysin",
                    "gene_name": "MME",
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                    "tax_name": "Homo sapiens",
                    "tax_common_name": "Human",
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                    "chemical_mass": 85514.0
                }
            ]
        },
        {
            "start_pos": "285",
            "site_seq": "EIAnATAKPEDR",
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            "glycoprotein": [
                {
                    "uniprot_canonical_ac": "P08473-1",
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                    "residue": "Asn",
                    "evidence": [
                        {
                            "database": "PubMed",
                            "id": "37074911",
                            "url": "https://glygen.org/publication/PubMed/37074911"
                        },
                        {
                            "database": "PDC",
                            "id": "PDC000471",
                            "url": "https://proteomic.datacommons.cancer.gov/pdc/study/PDC000471"
                        }
                    ],
                    "protein_name": "Neprilysin",
                    "gene_name": "MME",
                    "tax_id": 9606,
                    "tax_name": "Homo sapiens",
                    "tax_common_name": "Human",
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                    "chemical_mass": 85514.0
                }
            ]
        },
        {
            "start_pos": "285",
            "site_seq": "EIANATAKPEDR",
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            "glycoprotein": [
                {
                    "uniprot_canonical_ac": "P08473-1",
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                    "end_pos": 285,
                    "residue": "Asn",
                    "evidence": [
                        {
                            "database": "PubMed",
                            "id": "37074911",
                            "url": "https://glygen.org/publication/PubMed/37074911"
                        },
                        {
                            "database": "PDC",
                            "id": "PDC000471",
                            "url": "https://proteomic.datacommons.cancer.gov/pdc/study/PDC000471"
                        }
                    ],
                    "protein_name": "Neprilysin",
                    "gene_name": "MME",
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                    "tax_name": "Homo sapiens",
                    "tax_common_name": "Human",
                    "length": 750,
                    "chemical_mass": 85514.0
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            ]
        },
        {
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            "glycoprotein": [
                {
                    "uniprot_canonical_ac": "P08473-1",
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                    "evidence": [
                        {
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                            "id": "37074911",
                            "url": "https://glygen.org/publication/PubMed/37074911"
                        },
                        {
                            "database": "PDC",
                            "id": "PDC000471",
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                    ],
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                    "gene_name": "MME",
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                    "tax_common_name": "Human",
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                    "chemical_mass": 85514.0
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            ]
        },
        {
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            "residue": "",
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                    "sequence_org": "N",
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                    "comment": "Somatic mutation passed 1 out of 6 filters: n-glyco-sequon-loss (NES->HES).",
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                    "chr_pos": "155116553",
                    "evidence": [
                        {
                            "id": "P08473",
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                            "url": "https://hivelab.biochemistry.gwu.edu/biomuta/proteinview/P08473"
                        }
                    ],
                    "disease": [
                        {
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                            "name": "stomach cancer",
                            "description": "A gastrointestinal system cancer that is located_in the stomach.",
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                            "evidence": [
                                {
                                    "id": "10534",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:10534"
                                },
                                {
                                    "id": "10534",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:10534"
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                            ]
                        }
                    ]
                }
            ],
            "glycoprotein": [
                {
                    "uniprot_canonical_ac": "P08473-1",
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                    "evidence": [
                        {
                            "database": "PubMed",
                            "id": "37074911",
                            "url": "https://glygen.org/publication/PubMed/37074911"
                        },
                        {
                            "database": "PDC",
                            "id": "PDC000471",
                            "url": "https://proteomic.datacommons.cancer.gov/pdc/study/PDC000471"
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                    ],
                    "protein_name": "Neprilysin",
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                    "tax_common_name": "Human",
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                    "chemical_mass": 85514.0
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            ]
        },
        {
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            "residue": "",
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                {
                    "weight": 100,
                    "sequence_org": "N",
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                    "comment": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-loss (NAT->DAT).",
                    "chr_id": "3",
                    "chr_pos": "155138234",
                    "evidence": [
                        {
                            "id": "rs1339178202",
                            "database": "dbSNP",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1339178202"
                        },
                        {
                            "id": "rs1339178202",
                            "database": "gnomAD",
                            "url": "http://gnomad.broadinstitute.org/awesome?query=rs1339178202"
                        }
                    ]
                },
                {
                    "weight": 100,
                    "sequence_org": "N",
                    "sequence_mut": "I",
                    "comment": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-loss (NAT->IAT).",
                    "chr_id": "3",
                    "chr_pos": "155138235",
                    "evidence": [
                        {
                            "id": "rs200961860",
                            "database": "dbSNP",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs200961860"
                        },
                        {
                            "id": "rs200961860",
                            "database": "1000Genomes",
                            "url": "https://www.ensembl.org/homo_sapiens/Variation/Explore?v=rs200961860"
                        },
                        {
                            "id": "rs200961860",
                            "database": "ExAC",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs200961860"
                        },
                        {
                            "id": "rs200961860",
                            "database": "TOPMed",
                            "url": "https://www.ncbi.nlm.nih.gov/snp/rs200961860#frequency_tab"
                        },
                        {
                            "id": "rs200961860",
                            "database": "gnomAD",
                            "url": "http://gnomad.broadinstitute.org/awesome?query=rs200961860"
                        }
                    ]
                },
                {
                    "weight": 100,
                    "sequence_org": "N",
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                    "comment": "Somatic mutation passed 1 out of 6 filters: n-glyco-sequon-loss (NAT->KAT).",
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                    "chr_pos": "155138236",
                    "evidence": [
                        {
                            "id": "P08473",
                            "database": "BioMuta",
                            "url": "https://hivelab.biochemistry.gwu.edu/biomuta/proteinview/P08473"
                        },
                        {
                            "id": "rs1434664230",
                            "database": "dbSNP",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1434664230"
                        },
                        {
                            "id": "rs1434664230",
                            "database": "gnomAD",
                            "url": "http://gnomad.broadinstitute.org/awesome?query=rs1434664230"
                        },
                        {
                            "id": "rs1434664230",
                            "database": "COSMIC",
                            "url": "https://www.ensembl.org/homo_sapiens/Variation/Explore?v=rs1434664230"
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                    ],
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                                {
                                    "id": "1324",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:1324"
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                            ]
                        }
                    ]
                },
                {
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                    "sequence_org": "N",
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                    "comment": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-loss (NAT->SAT).",
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                    "chr_pos": "155138235",
                    "evidence": [
                        {
                            "id": "rs200961860",
                            "database": "dbSNP",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs200961860"
                        },
                        {
                            "id": "rs200961860",
                            "database": "1000Genomes",
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                        },
                        {
                            "id": "rs200961860",
                            "database": "ExAC",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs200961860"
                        },
                        {
                            "id": "rs200961860",
                            "database": "TOPMed",
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                        },
                        {
                            "id": "rs200961860",
                            "database": "gnomAD",
                            "url": "http://gnomad.broadinstitute.org/awesome?query=rs200961860"
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                    ],
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                        {
                            "disease_id": "DOID:0110160",
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                            "url": "http://disease-ontology.org/term/DOID:0110160",
                            "evidence": [
                                {
                                    "id": "0110160",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0110160"
                                },
                                {
                                    "id": "0110160",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0110160"
                                }
                            ]
                        },
                        {
                            "disease_id": "DOID:0110160",
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                            "url": "http://disease-ontology.org/term/DOID:0110160",
                            "evidence": [
                                {
                                    "id": "0110160",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0110160"
                                },
                                {
                                    "id": "0110160",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0110160"
                                }
                            ]
                        },
                        {
                            "disease_id": "DOID:0110160",
                            "name": "Charcot-Marie-Tooth disease axonal type 2T",
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                            "evidence": [
                                {
                                    "id": "0110160",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0110160"
                                },
                                {
                                    "id": "0110160",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0110160"
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                            ]
                        },
                        {
                            "disease_id": "DOID:0110160",
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                                {
                                    "id": "0110160",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0110160"
                                },
                                {
                                    "id": "0110160",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0110160"
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                            ]
                        },
                        {
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                                {
                                    "id": "0110160",
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                                },
                                {
                                    "id": "0110160",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0110160"
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                            ]
                        },
                        {
                            "disease_id": "DOID:0111745",
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                            "evidence": [
                                {
                                    "id": "0111745",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0111745"
                                },
                                {
                                    "id": "0111745",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0111745"
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                            ]
                        },
                        {
                            "disease_id": "DOID:0111745",
                            "name": "cerebellar ataxia type 43",
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                            "evidence": [
                                {
                                    "id": "0111745",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0111745"
                                },
                                {
                                    "id": "0111745",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0111745"
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                            ]
                        },
                        {
                            "disease_id": "DOID:0111745",
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                                {
                                    "id": "0111745",
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                                    "url": "https://www.alliancegenome.org/disease/DOID:0111745"
                                },
                                {
                                    "id": "0111745",
                                    "database": "AGR",
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                            ]
                        },
                        {
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                                {
                                    "id": "0111745",
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                                },
                                {
                                    "id": "0111745",
                                    "database": "AGR",
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                            ]
                        },
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                                {
                                    "id": "0111745",
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                                },
                                {
                                    "id": "0111745",
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                    ],
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        },
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                    ],
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            ]
        },
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                    ],
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            ]
        },
        {
            "start_pos": "145",
            "site_seq": "SCINESAIDSR",
            "site_lbl": "Asn145",
            "residue": "Asn",
            "glycoprotein": [
                {
                    "uniprot_canonical_ac": "P08473-1",
                    "start_pos": 145,
                    "end_pos": 145,
                    "residue": "Asn",
                    "evidence": [
                        {
                            "database": "PubMed",
                            "id": "37074911",
                            "url": "https://glygen.org/publication/PubMed/37074911"
                        },
                        {
                            "database": "PDC",
                            "id": "PDC000471",
                            "url": "https://proteomic.datacommons.cancer.gov/pdc/study/PDC000471"
                        }
                    ],
                    "protein_name": "Neprilysin",
                    "gene_name": "MME",
                    "tax_id": 9606,
                    "tax_name": "Homo sapiens",
                    "tax_common_name": "Human",
                    "length": 750,
                    "chemical_mass": 85514.0
                }
            ]
        },
        {
            "start_pos": "285",
            "site_seq": "EIAnATAKPEDRNDPMLLYNK",
            "site_lbl": "Asn285",
            "residue": "Asn",
            "glycoprotein": [
                {
                    "uniprot_canonical_ac": "P08473-1",
                    "start_pos": 285,
                    "end_pos": 285,
                    "residue": "Asn",
                    "evidence": [
                        {
                            "database": "PubMed",
                            "id": "37074911",
                            "url": "https://glygen.org/publication/PubMed/37074911"
                        },
                        {
                            "database": "PDC",
                            "id": "PDC000471",
                            "url": "https://proteomic.datacommons.cancer.gov/pdc/study/PDC000471"
                        }
                    ],
                    "protein_name": "Neprilysin",
                    "gene_name": "MME",
                    "tax_id": 9606,
                    "tax_name": "Homo sapiens",
                    "tax_common_name": "Human",
                    "length": 750,
                    "chemical_mass": 85514.0
                }
            ]
        },
        {
            "start_pos": "285",
            "site_seq": "EIAnATAKPEDR",
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            "glycoprotein": [
                {
                    "uniprot_canonical_ac": "P08473-1",
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                    "end_pos": 285,
                    "residue": "Asn",
                    "evidence": [
                        {
                            "database": "PubMed",
                            "id": "37074911",
                            "url": "https://glygen.org/publication/PubMed/37074911"
                        },
                        {
                            "database": "PDC",
                            "id": "PDC000471",
                            "url": "https://proteomic.datacommons.cancer.gov/pdc/study/PDC000471"
                        }
                    ],
                    "protein_name": "Neprilysin",
                    "gene_name": "MME",
                    "tax_id": 9606,
                    "tax_name": "Homo sapiens",
                    "tax_common_name": "Human",
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                    "chemical_mass": 85514.0
                }
            ]
        },
        {
            "start_pos": "285",
            "site_seq": "EIANATAKPEDR",
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            "glycoprotein": [
                {
                    "uniprot_canonical_ac": "P08473-1",
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                    "end_pos": 285,
                    "residue": "Asn",
                    "evidence": [
                        {
                            "database": "PubMed",
                            "id": "37074911",
                            "url": "https://glygen.org/publication/PubMed/37074911"
                        },
                        {
                            "database": "PDC",
                            "id": "PDC000471",
                            "url": "https://proteomic.datacommons.cancer.gov/pdc/study/PDC000471"
                        }
                    ],
                    "protein_name": "Neprilysin",
                    "gene_name": "MME",
                    "tax_id": 9606,
                    "tax_name": "Homo sapiens",
                    "tax_common_name": "Human",
                    "length": 750,
                    "chemical_mass": 85514.0
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            ]
        },
        {
            "start_pos": "285",
            "site_seq": "N",
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            "glycoprotein": [
                {
                    "uniprot_canonical_ac": "P08473-1",
                    "start_pos": 285,
                    "end_pos": 285,
                    "residue": "Asn",
                    "evidence": [
                        {
                            "database": "PubMed",
                            "id": "37074911",
                            "url": "https://glygen.org/publication/PubMed/37074911"
                        },
                        {
                            "database": "PDC",
                            "id": "PDC000471",
                            "url": "https://proteomic.datacommons.cancer.gov/pdc/study/PDC000471"
                        }
                    ],
                    "protein_name": "Neprilysin",
                    "gene_name": "MME",
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                    "tax_name": "Homo sapiens",
                    "tax_common_name": "Human",
                    "length": 750,
                    "chemical_mass": 85514.0
                }
            ]
        },
        {
            "start_pos": "145",
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            "site_lbl": "N145",
            "residue": "",
            "snv": [
                {
                    "weight": 100,
                    "sequence_org": "N",
                    "sequence_mut": "H",
                    "comment": "Somatic mutation passed 1 out of 6 filters: n-glyco-sequon-loss (NES->HES).",
                    "chr_id": "3",
                    "chr_pos": "155116553",
                    "evidence": [
                        {
                            "id": "P08473",
                            "database": "BioMuta",
                            "url": "https://hivelab.biochemistry.gwu.edu/biomuta/proteinview/P08473"
                        }
                    ],
                    "disease": [
                        {
                            "disease_id": "DOID:10534",
                            "name": "stomach cancer",
                            "description": "A gastrointestinal system cancer that is located_in the stomach.",
                            "url": "http://disease-ontology.org/term/DOID:10534",
                            "evidence": [
                                {
                                    "id": "10534",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:10534"
                                },
                                {
                                    "id": "10534",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:10534"
                                }
                            ]
                        }
                    ]
                }
            ],
            "glycoprotein": [
                {
                    "uniprot_canonical_ac": "P08473-1",
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                    "end_pos": 145,
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                    "evidence": [
                        {
                            "database": "PubMed",
                            "id": "37074911",
                            "url": "https://glygen.org/publication/PubMed/37074911"
                        },
                        {
                            "database": "PDC",
                            "id": "PDC000471",
                            "url": "https://proteomic.datacommons.cancer.gov/pdc/study/PDC000471"
                        }
                    ],
                    "protein_name": "Neprilysin",
                    "gene_name": "MME",
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                    "tax_name": "Homo sapiens",
                    "tax_common_name": "Human",
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                    "chemical_mass": 85514.0
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            ]
        },
        {
            "start_pos": "285",
            "site_seq": "",
            "site_lbl": "N285",
            "residue": "",
            "snv": [
                {
                    "weight": 100,
                    "sequence_org": "N",
                    "sequence_mut": "D",
                    "comment": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-loss (NAT->DAT).",
                    "chr_id": "3",
                    "chr_pos": "155138234",
                    "evidence": [
                        {
                            "id": "rs1339178202",
                            "database": "dbSNP",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1339178202"
                        },
                        {
                            "id": "rs1339178202",
                            "database": "gnomAD",
                            "url": "http://gnomad.broadinstitute.org/awesome?query=rs1339178202"
                        }
                    ]
                },
                {
                    "weight": 100,
                    "sequence_org": "N",
                    "sequence_mut": "I",
                    "comment": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-loss (NAT->IAT).",
                    "chr_id": "3",
                    "chr_pos": "155138235",
                    "evidence": [
                        {
                            "id": "rs200961860",
                            "database": "dbSNP",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs200961860"
                        },
                        {
                            "id": "rs200961860",
                            "database": "1000Genomes",
                            "url": "https://www.ensembl.org/homo_sapiens/Variation/Explore?v=rs200961860"
                        },
                        {
                            "id": "rs200961860",
                            "database": "ExAC",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs200961860"
                        },
                        {
                            "id": "rs200961860",
                            "database": "TOPMed",
                            "url": "https://www.ncbi.nlm.nih.gov/snp/rs200961860#frequency_tab"
                        },
                        {
                            "id": "rs200961860",
                            "database": "gnomAD",
                            "url": "http://gnomad.broadinstitute.org/awesome?query=rs200961860"
                        }
                    ]
                },
                {
                    "weight": 100,
                    "sequence_org": "N",
                    "sequence_mut": "K",
                    "comment": "Somatic mutation passed 1 out of 6 filters: n-glyco-sequon-loss (NAT->KAT).",
                    "chr_id": "3",
                    "chr_pos": "155138236",
                    "evidence": [
                        {
                            "id": "P08473",
                            "database": "BioMuta",
                            "url": "https://hivelab.biochemistry.gwu.edu/biomuta/proteinview/P08473"
                        },
                        {
                            "id": "rs1434664230",
                            "database": "dbSNP",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1434664230"
                        },
                        {
                            "id": "rs1434664230",
                            "database": "gnomAD",
                            "url": "http://gnomad.broadinstitute.org/awesome?query=rs1434664230"
                        },
                        {
                            "id": "rs1434664230",
                            "database": "COSMIC",
                            "url": "https://www.ensembl.org/homo_sapiens/Variation/Explore?v=rs1434664230"
                        }
                    ],
                    "disease": [
                        {
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                            "name": "lung cancer",
                            "description": "A respiratory system cancer that is located_in the lung.",
                            "url": "http://disease-ontology.org/term/DOID:1324",
                            "evidence": [
                                {
                                    "id": "1324",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:1324"
                                }
                            ]
                        }
                    ]
                },
                {
                    "weight": 100,
                    "sequence_org": "N",
                    "sequence_mut": "S",
                    "comment": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-loss (NAT->SAT).",
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                    "chr_pos": "155138235",
                    "evidence": [
                        {
                            "id": "rs200961860",
                            "database": "dbSNP",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs200961860"
                        },
                        {
                            "id": "rs200961860",
                            "database": "1000Genomes",
                            "url": "https://www.ensembl.org/homo_sapiens/Variation/Explore?v=rs200961860"
                        },
                        {
                            "id": "rs200961860",
                            "database": "ExAC",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs200961860"
                        },
                        {
                            "id": "rs200961860",
                            "database": "TOPMed",
                            "url": "https://www.ncbi.nlm.nih.gov/snp/rs200961860#frequency_tab"
                        },
                        {
                            "id": "rs200961860",
                            "database": "gnomAD",
                            "url": "http://gnomad.broadinstitute.org/awesome?query=rs200961860"
                        }
                    ],
                    "disease": [
                        {
                            "disease_id": "DOID:0110160",
                            "name": "Charcot-Marie-Tooth disease axonal type 2T",
                            "description": "A Charcot-Marie-Tooth disease type 2 that has_material_basis_in homozygous or compound heterozygous mutation in the MME gene on chromosome 3q25.",
                            "url": "http://disease-ontology.org/term/DOID:0110160",
                            "evidence": [
                                {
                                    "id": "0110160",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0110160"
                                },
                                {
                                    "id": "0110160",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0110160"
                                }
                            ]
                        },
                        {
                            "disease_id": "DOID:0110160",
                            "name": "Charcot-Marie-Tooth disease axonal type 2T",
                            "description": "A Charcot-Marie-Tooth disease type 2 that has_material_basis_in homozygous or compound heterozygous mutation in the MME gene on chromosome 3q25.",
                            "url": "http://disease-ontology.org/term/DOID:0110160",
                            "evidence": [
                                {
                                    "id": "0110160",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0110160"
                                },
                                {
                                    "id": "0110160",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0110160"
                                }
                            ]
                        },
                        {
                            "disease_id": "DOID:0110160",
                            "name": "Charcot-Marie-Tooth disease axonal type 2T",
                            "description": "A Charcot-Marie-Tooth disease type 2 that has_material_basis_in homozygous or compound heterozygous mutation in the MME gene on chromosome 3q25.",
                            "url": "http://disease-ontology.org/term/DOID:0110160",
                            "evidence": [
                                {
                                    "id": "0110160",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0110160"
                                },
                                {
                                    "id": "0110160",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0110160"
                                }
                            ]
                        },
                        {
                            "disease_id": "DOID:0110160",
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                            "evidence": [
                                {
                                    "id": "0110160",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0110160"
                                },
                                {
                                    "id": "0110160",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0110160"
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                            ]
                        },
                        {
                            "disease_id": "DOID:0110160",
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                            "evidence": [
                                {
                                    "id": "0110160",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0110160"
                                },
                                {
                                    "id": "0110160",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0110160"
                                }
                            ]
                        },
                        {
                            "disease_id": "DOID:0111745",
                            "name": "cerebellar ataxia type 43",
                            "description": "An autosomal dominant cerebellar ataxia characterized by adult-onset, slowly progressive, gait and limb ataxia, often associated with peripheral neuropathy typically affecting the motor system that has_material_basis_in heterozygous mutation in MME on chromosome 3q25.2.",
                            "url": "http://disease-ontology.org/term/DOID:0111745",
                            "evidence": [
                                {
                                    "id": "0111745",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0111745"
                                },
                                {
                                    "id": "0111745",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0111745"
                                }
                            ]
                        },
                        {
                            "disease_id": "DOID:0111745",
                            "name": "cerebellar ataxia type 43",
                            "description": "An autosomal dominant cerebellar ataxia characterized by adult-onset, slowly progressive, gait and limb ataxia, often associated with peripheral neuropathy typically affecting the motor system that has_material_basis_in heterozygous mutation in MME on chromosome 3q25.2.",
                            "url": "http://disease-ontology.org/term/DOID:0111745",
                            "evidence": [
                                {
                                    "id": "0111745",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0111745"
                                },
                                {
                                    "id": "0111745",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0111745"
                                }
                            ]
                        },
                        {
                            "disease_id": "DOID:0111745",
                            "name": "cerebellar ataxia type 43",
                            "description": "An autosomal dominant cerebellar ataxia characterized by adult-onset, slowly progressive, gait and limb ataxia, often associated with peripheral neuropathy typically affecting the motor system that has_material_basis_in heterozygous mutation in MME on chromosome 3q25.2.",
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                            "evidence": [
                                {
                                    "id": "0111745",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0111745"
                                },
                                {
                                    "id": "0111745",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0111745"
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                            ]
                        },
                        {
                            "disease_id": "DOID:0111745",
                            "name": "cerebellar ataxia type 43",
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                            "evidence": [
                                {
                                    "id": "0111745",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0111745"
                                },
                                {
                                    "id": "0111745",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0111745"
                                }
                            ]
                        },
                        {
                            "disease_id": "DOID:0111745",
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                                {
                                    "id": "0111745",
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                                    "url": "https://www.alliancegenome.org/disease/DOID:0111745"
                                },
                                {
                                    "id": "0111745",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0111745"
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            ],
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                    ],
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            ]
        },
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                    ],
                    "protein_name": "Epididymis-specific alpha-mannosidase",
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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": "rs753921101",
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                    "tax_common_name": "Human",
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            ]
        },
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                {
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            ]
        },
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                        {
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            ]
        },
        {
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                    ],
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            ]
        },
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                        {
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                        },
                        {
                            "id": "rs771212555",
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                    ]
                },
                {
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                },
                {
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                        {
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                        {
                            "id": "rs771212555",
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                    ],
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                                {
                                    "id": "1324",
                                    "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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                        {
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                        {
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            ]
        },
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        },
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                },
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                        {
                            "id": "rs371154344",
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                        {
                            "id": "rs371154344",
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                        {
                            "id": "rs371154344",
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                            "id": "rs1799575422",
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                    ]
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                        {
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                        {
                            "id": "rs372554004",
                            "database": "TOPMed",
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                        {
                            "id": "rs372554004",
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                            "database": "BioMuta",
                            "url": "https://hivelab.biochemistry.gwu.edu/biomuta/proteinview/P16444"
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                            "description": "An integumentary system cancer located_in the skin that is the uncontrolled growth of abnormal skin cells.",
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                            "evidence": [
                                {
                                    "id": "4159",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:4159"
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                        },
                        {
                            "disease_id": "DOID:1324",
                            "name": "lung cancer",
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                        {
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        {
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                        {
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                    ],
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                        {
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                                    "id": "4159",
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                                {
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                                {
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                            ]
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                                {
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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:0080678",
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                                {
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                        },
                        {
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                                {
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                        },
                        {
                            "disease_id": "DOID:0080678",
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                                {
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                                {
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                                    "url": "https://www.alliancegenome.org/disease/DOID:10534"
                                },
                                {
                                    "id": "10534",
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                            ]
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                                {
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                                },
                                {
                                    "id": "252940",
                                    "database": "MIM",
                                    "url": "https://www.omim.org/entry/252940"
                                },
                                {
                                    "id": "2799",
                                    "database": "GlyCosmos",
                                    "url": "https://glycosmos.org/glycogenes/show/2799#disease"
                                },
                                {
                                    "id": "0111402",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0111402"
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                            ]
                        },
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                                {
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                                    "url": "https://www.omim.org/entry/252940"
                                },
                                {
                                    "id": "2799",
                                    "database": "GlyCosmos",
                                    "url": "https://glycosmos.org/glycogenes/show/2799#disease"
                                },
                                {
                                    "id": "0111402",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0111402"
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                            ]
                        },
                        {
                            "disease_id": "DOID:0111402",
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                                {
                                    "id": "0009658",
                                    "database": "MONDO",
                                    "url": "https://monarchinitiative.org/disease/MONDO:0009658"
                                },
                                {
                                    "id": "252940",
                                    "database": "MIM",
                                    "url": "https://www.omim.org/entry/252940"
                                },
                                {
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                                    "url": "https://glycosmos.org/glycogenes/show/2799#disease"
                                },
                                {
                                    "id": "0111402",
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            ]
        },
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                        {
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                        {
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                            "id": "rs1199190795",
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                            "id": "rs1199190795",
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                            "name": "Ullrich congenital muscular dystrophy 2",
                            "description": "An Ullrich congenital muscular dystrophy characterized by joint hypermobility, proximal contractures, and muscle weakness precluding ambulation that has_material_basis_in homozygous mutation in the COL12A1 gene on chromosome 6q.",
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                        {
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                                {
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                                    "url": "https://www.alliancegenome.org/disease/DOID:13359"
                                }
                            ]
                        },
                        {
                            "disease_id": "DOID:13359",
                            "name": "Ehlers-Danlos syndrome",
                            "description": "A collagen disease that is characterized by extremely flexible joints, elastic skin, and excessive bruising caused by a heritable defect in collagen synthesis, which leads to marked healing difficulties. EDS has five cardinal signs, which may be present to some degree in all of the subtypes. These five cardinal signs are skin fragility, blood vessel fragility, skin hyperelasticity, joint hypermobility, and characteristic subcutaneous nodules.",
                            "url": "http://disease-ontology.org/term/DOID:13359",
                            "evidence": [
                                {
                                    "id": "13359",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:13359"
                                }
                            ]
                        },
                        {
                            "disease_id": "DOID:14720",
                            "name": "Ehlers-Danlos syndrome classic type 1",
                            "description": "An Ehlers-Danlos syndrome that is characterized by loose-jointedness and fragile, bruisable skin that heals with peculiar 'cigarette-paper' scars and that has_material_basis_in heterozygous mutation in the collagen alpha-1(V) gene (COL5A1) on chromosome 9q34.",
                            "url": "http://disease-ontology.org/term/DOID:14720",
                            "evidence": [
                                {
                                    "id": "14720",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:14720"
                                },
                                {
                                    "id": "14720",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:14720"
                                }
                            ]
                        },
                        {
                            "disease_id": "DOID:14720",
                            "name": "Ehlers-Danlos syndrome classic type 1",
                            "description": "An Ehlers-Danlos syndrome that is characterized by loose-jointedness and fragile, bruisable skin that heals with peculiar 'cigarette-paper' scars and that has_material_basis_in heterozygous mutation in the collagen alpha-1(V) gene (COL5A1) on chromosome 9q34.",
                            "url": "http://disease-ontology.org/term/DOID:14720",
                            "evidence": [
                                {
                                    "id": "14720",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:14720"
                                },
                                {
                                    "id": "14720",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:14720"
                                }
                            ]
                        },
                        {
                            "disease_id": "DOID:14720",
                            "name": "Ehlers-Danlos syndrome classic type 1",
                            "description": "An Ehlers-Danlos syndrome that is characterized by loose-jointedness and fragile, bruisable skin that heals with peculiar 'cigarette-paper' scars and that has_material_basis_in heterozygous mutation in the collagen alpha-1(V) gene (COL5A1) on chromosome 9q34.",
                            "url": "http://disease-ontology.org/term/DOID:14720",
                            "evidence": [
                                {
                                    "id": "14720",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:14720"
                                },
                                {
                                    "id": "14720",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:14720"
                                }
                            ]
                        }
                    ]
                }
            ],
            "glycoprotein": [
                {
                    "uniprot_canonical_ac": "P20908-1",
                    "start_pos": 176,
                    "end_pos": 176,
                    "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": "Collagen alpha-1(V) chain",
                    "gene_name": "COL5A1",
                    "tax_id": 9606,
                    "tax_name": "Homo sapiens",
                    "tax_common_name": "Human",
                    "length": 1838,
                    "chemical_mass": 183560.0
                }
            ]
        },
        {
            "start_pos": "153",
            "site_seq": "QIATGVSDTICEPCPVGFFSnVSSAFEK",
            "site_lbl": "Asn153",
            "residue": "Asn",
            "glycoprotein": [
                {
                    "uniprot_canonical_ac": "P25942-1",
                    "start_pos": 153,
                    "end_pos": 153,
                    "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": "Tumor necrosis factor receptor superfamily member 5",
                    "gene_name": "CD40",
                    "tax_id": 9606,
                    "tax_name": "Homo sapiens",
                    "tax_common_name": "Human",
                    "length": 277,
                    "chemical_mass": 30619.0
                }
            ]
        },
        {
            "start_pos": "153",
            "site_seq": "N",
            "site_lbl": "Asn153",
            "residue": "Asn",
            "glycoprotein": [
                {
                    "uniprot_canonical_ac": "P25942-1",
                    "start_pos": 153,
                    "end_pos": 153,
                    "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": "Tumor necrosis factor receptor superfamily member 5",
                    "gene_name": "CD40",
                    "tax_id": 9606,
                    "tax_name": "Homo sapiens",
                    "tax_common_name": "Human",
                    "length": 277,
                    "chemical_mass": 30619.0
                }
            ]
        },
        {
            "start_pos": "153",
            "site_seq": "QIATGVSDTICEPCPVGFFSnVSSAFEK",
            "site_lbl": "Asn153",
            "residue": "Asn",
            "glycoprotein": [
                {
                    "uniprot_canonical_ac": "P25942-1",
                    "start_pos": 153,
                    "end_pos": 153,
                    "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": "Tumor necrosis factor receptor superfamily member 5",
                    "gene_name": "CD40",
                    "tax_id": 9606,
                    "tax_name": "Homo sapiens",
                    "tax_common_name": "Human",
                    "length": 277,
                    "chemical_mass": 30619.0
                }
            ]
        },
        {
            "start_pos": "153",
            "site_seq": "N",
            "site_lbl": "Asn153",
            "residue": "Asn",
            "glycoprotein": [
                {
                    "uniprot_canonical_ac": "P25942-1",
                    "start_pos": 153,
                    "end_pos": 153,
                    "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": "Tumor necrosis factor receptor superfamily member 5",
                    "gene_name": "CD40",
                    "tax_id": 9606,
                    "tax_name": "Homo sapiens",
                    "tax_common_name": "Human",
                    "length": 277,
                    "chemical_mass": 30619.0
                }
            ]
        },
        {
            "start_pos": "153",
            "site_seq": "QIATGVSDTICEPCPVGFFSnVSSAFEK",
            "site_lbl": "Asn153",
            "residue": "Asn",
            "glycoprotein": [
                {
                    "uniprot_canonical_ac": "P25942-1",
                    "start_pos": 153,
                    "end_pos": 153,
                    "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": "Tumor necrosis factor receptor superfamily member 5",
                    "gene_name": "CD40",
                    "tax_id": 9606,
                    "tax_name": "Homo sapiens",
                    "tax_common_name": "Human",
                    "length": 277,
                    "chemical_mass": 30619.0
                }
            ]
        },
        {
            "start_pos": "153",
            "site_seq": "N",
            "site_lbl": "Asn153",
            "residue": "Asn",
            "glycoprotein": [
                {
                    "uniprot_canonical_ac": "P25942-1",
                    "start_pos": 153,
                    "end_pos": 153,
                    "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": "Tumor necrosis factor receptor superfamily member 5",
                    "gene_name": "CD40",
                    "tax_id": 9606,
                    "tax_name": "Homo sapiens",
                    "tax_common_name": "Human",
                    "length": 277,
                    "chemical_mass": 30619.0
                }
            ]
        },
        {
            "start_pos": "153",
            "site_seq": "",
            "site_lbl": "N153",
            "residue": "",
            "snv": [
                {
                    "weight": 100,
                    "sequence_org": "N",
                    "sequence_mut": "D",
                    "comment": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-loss (NVS->DVS).",
                    "chr_id": "20",
                    "chr_pos": "46123179",
                    "evidence": [
                        {
                            "id": "rs2085353847",
                            "database": "dbSNP",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs2085353847"
                        },
                        {
                            "id": "rs2085353847",
                            "database": "TOPMed",
                            "url": "https://www.ncbi.nlm.nih.gov/snp/rs2085353847#frequency_tab"
                        }
                    ]
                },
                {
                    "weight": 100,
                    "sequence_org": "N",
                    "sequence_mut": "I",
                    "comment": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-loss (NVS->IVS).",
                    "chr_id": "20",
                    "chr_pos": "46123180",
                    "evidence": [
                        {
                            "id": "rs745551504",
                            "database": "dbSNP",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs745551504"
                        },
                        {
                            "id": "rs745551504",
                            "database": "ExAC",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs745551504"
                        },
                        {
                            "id": "rs745551504",
                            "database": "gnomAD",
                            "url": "http://gnomad.broadinstitute.org/awesome?query=rs745551504"
                        }
                    ]
                },
                {
                    "weight": 100,
                    "sequence_org": "N",
                    "sequence_mut": "S",
                    "comment": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-loss (NVS->SVS).",
                    "chr_id": "20",
                    "chr_pos": "46123180",
                    "evidence": [
                        {
                            "id": "rs745551504",
                            "database": "dbSNP",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs745551504"
                        },
                        {
                            "id": "rs745551504",
                            "database": "ExAC",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs745551504"
                        },
                        {
                            "id": "rs745551504",
                            "database": "gnomAD",
                            "url": "http://gnomad.broadinstitute.org/awesome?query=rs745551504"
                        }
                    ]
                }
            ],
            "glycoprotein": [
                {
                    "uniprot_canonical_ac": "P25942-1",
                    "start_pos": 153,
                    "end_pos": 153,
                    "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": "Tumor necrosis factor receptor superfamily member 5",
                    "gene_name": "CD40",
                    "tax_id": 9606,
                    "tax_name": "Homo sapiens",
                    "tax_common_name": "Human",
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                    "chemical_mass": 30619.0
                }
            ]
        },
        {
            "start_pos": "153",
            "site_seq": "QIATGVSDTICEPCPVGFFSnVSSAFEK",
            "site_lbl": "Asn153",
            "residue": "Asn",
            "glycoprotein": [
                {
                    "uniprot_canonical_ac": "P25942-1",
                    "start_pos": 153,
                    "end_pos": 153,
                    "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": "Tumor necrosis factor receptor superfamily member 5",
                    "gene_name": "CD40",
                    "tax_id": 9606,
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                }
            ]
        },
        {
            "start_pos": "153",
            "site_seq": "N",
            "site_lbl": "Asn153",
            "residue": "Asn",
            "glycoprotein": [
                {
                    "uniprot_canonical_ac": "P25942-1",
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                    "end_pos": 153,
                    "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": "Tumor necrosis factor receptor superfamily member 5",
                    "gene_name": "CD40",
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                    "tax_common_name": "Human",
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                    "chemical_mass": 30619.0
                }
            ]
        },
        {
            "start_pos": "153",
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            "site_lbl": "N153",
            "residue": "",
            "snv": [
                {
                    "weight": 100,
                    "sequence_org": "N",
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                    "comment": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-loss (NVS->DVS).",
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                        {
                            "id": "rs2085353847",
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                        {
                            "id": "rs2085353847",
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                    ]
                },
                {
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                    "sequence_org": "N",
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                    "evidence": [
                        {
                            "id": "rs745551504",
                            "database": "dbSNP",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs745551504"
                        },
                        {
                            "id": "rs745551504",
                            "database": "ExAC",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs745551504"
                        },
                        {
                            "id": "rs745551504",
                            "database": "gnomAD",
                            "url": "http://gnomad.broadinstitute.org/awesome?query=rs745551504"
                        }
                    ]
                },
                {
                    "weight": 100,
                    "sequence_org": "N",
                    "sequence_mut": "S",
                    "comment": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-loss (NVS->SVS).",
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                        {
                            "id": "rs745551504",
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                        },
                        {
                            "id": "rs745551504",
                            "database": "ExAC",
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                        },
                        {
                            "id": "rs745551504",
                            "database": "gnomAD",
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                        }
                    ]
                }
            ],
            "glycoprotein": [
                {
                    "uniprot_canonical_ac": "P25942-1",
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                    "end_pos": 153,
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                        {
                            "database": "PubMed",
                            "id": "37074911",
                            "url": "https://glygen.org/publication/PubMed/37074911"
                        },
                        {
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                    ],
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            ]
        },
        {
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            "residue": "Asn",
            "glycoprotein": [
                {
                    "uniprot_canonical_ac": "Q9Y5Y6-1",
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                    "end_pos": 109,
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                        {
                            "database": "PubMed",
                            "id": "37074911",
                            "url": "https://glygen.org/publication/PubMed/37074911"
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                        {
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                            "id": "PDC000471",
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                    ],
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            ]
        },
        {
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                {
                    "uniprot_canonical_ac": "Q9Y5Y6-1",
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                            "database": "PubMed",
                            "id": "37074911",
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                        {
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                    ],
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            ]
        },
        {
            "start_pos": "772",
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                {
                    "uniprot_canonical_ac": "Q9Y5Y6-1",
                    "start_pos": 772,
                    "end_pos": 772,
                    "residue": "Asn",
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                        {
                            "database": "PubMed",
                            "id": "37074911",
                            "url": "https://glygen.org/publication/PubMed/37074911"
                        },
                        {
                            "database": "PDC",
                            "id": "PDC000471",
                            "url": "https://proteomic.datacommons.cancer.gov/pdc/study/PDC000471"
                        }
                    ],
                    "protein_name": "Suppressor of tumorigenicity 14 protein",
                    "gene_name": "ST14",
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                    "tax_common_name": "Human",
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                    "chemical_mass": 94770.0
                }
            ]
        },
        {
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                {
                    "uniprot_canonical_ac": "Q9Y5Y6-1",
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                    "end_pos": 772,
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                        {
                            "database": "PubMed",
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                            "url": "https://glygen.org/publication/PubMed/37074911"
                        },
                        {
                            "database": "PDC",
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                        }
                    ],
                    "protein_name": "Suppressor of tumorigenicity 14 protein",
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                        {
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        {
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                        {
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                {
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                        {
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                        {
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                        {
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                        {
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                        {
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                        {
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                        {
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                                {
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                    ]
                },
                {
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                        {
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                },
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            ]
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                                {
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                        {
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                        {
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                        {
                            "id": "rs899133377",
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                            "url": "http://gnomad.broadinstitute.org/awesome?query=rs899133377"
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                    ],
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                                    "id": "162800",
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                                    "url": "https://www.omim.org/entry/162800"
                                },
                                {
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                            ]
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                        {
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                                {
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                                {
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                                {
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                                {
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                                {
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                    ]
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                                {
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                            ]
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                                {
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        },
        {
            "start_pos": "172",
            "site_seq": "N",
            "site_lbl": "Asn172",
            "residue": "Asn",
            "glycoprotein": [
                {
                    "uniprot_canonical_ac": "Q9UNN8-1",
                    "start_pos": 172,
                    "end_pos": 172,
                    "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": "Endothelial protein C receptor",
                    "gene_name": "PROCR",
                    "tax_id": 9606,
                    "tax_name": "Homo sapiens",
                    "tax_common_name": "Human",
                    "length": 238,
                    "chemical_mass": 26671.0
                }
            ]
        },
        {
            "start_pos": "172",
            "site_seq": "",
            "site_lbl": "N172",
            "residue": "",
            "snv": [
                {
                    "weight": 100,
                    "sequence_org": "N",
                    "sequence_mut": "Y",
                    "comment": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-loss (NRT->YRT).",
                    "chr_id": "20",
                    "chr_pos": "35176359",
                    "evidence": [
                        {
                            "id": "rs2146145956",
                            "database": "dbSNP",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs2146145956"
                        },
                        {
                            "id": "rs2146145956",
                            "database": "ENSEMBL",
                            "url": "https://www.ensembl.org/id/rs2146145956"
                        }
                    ]
                }
            ],
            "glycoprotein": [
                {
                    "uniprot_canonical_ac": "Q9UNN8-1",
                    "start_pos": 172,
                    "end_pos": 172,
                    "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": "Endothelial protein C receptor",
                    "gene_name": "PROCR",
                    "tax_id": 9606,
                    "tax_name": "Homo sapiens",
                    "tax_common_name": "Human",
                    "length": 238,
                    "chemical_mass": 26671.0
                }
            ]
        }
    ],
    "record_id": "G00912UN"
}
