← Back to variant description

GeneBe API Showcase

This page demonstrates how to use the GeneBe API to query variant information. The API provides programmatic access to genomic annotations and variant data.

API presented here should be used for checking single variants. If you want to check many variants at once, please use other API endpoints that you will find in the documentation.

Documentation & Advanced Usage

Complete API documentation:docs.genebe.net/docs/api/overview/

Interactive endpoint tester:api.genebe.net/cloud/gb-api-doc/swagger-ui/

Python client for pandas:pypi.org/project/genebe/

Java CLI for VCF files:github.com/pstawinski/genebe-cli

All tools documented at:docs.genebe.net

API Request Examples for Variant: 13-51937488-G-A (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=13&pos=51937488&ref=G&alt=A&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "13",
      "pos": 51937488,
      "ref": "G",
      "alt": "A",
      "effect": "synonymous_variant",
      "transcript": "ENST00000242839.10",
      "consequences": [
        {
          "aa_ref": "V",
          "aa_alt": "V",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 18,
          "exon_rank_end": null,
          "exon_count": 21,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATP7B",
          "gene_hgnc_id": 870,
          "hgvs_c": "c.3891C>T",
          "hgvs_p": "p.Val1297Val",
          "transcript": "NM_000053.4",
          "protein_id": "NP_000044.2",
          "transcript_support_level": null,
          "aa_start": 1297,
          "aa_end": null,
          "aa_length": 1465,
          "cds_start": 3891,
          "cds_end": null,
          "cds_length": 4398,
          "cdna_start": 4004,
          "cdna_end": null,
          "cdna_length": 6598,
          "mane_select": "ENST00000242839.10",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "V",
          "aa_alt": "V",
          "canonical": true,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 18,
          "exon_rank_end": null,
          "exon_count": 21,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATP7B",
          "gene_hgnc_id": 870,
          "hgvs_c": "c.3891C>T",
          "hgvs_p": "p.Val1297Val",
          "transcript": "ENST00000242839.10",
          "protein_id": "ENSP00000242839.5",
          "transcript_support_level": 1,
          "aa_start": 1297,
          "aa_end": null,
          "aa_length": 1465,
          "cds_start": 3891,
          "cds_end": null,
          "cds_length": 4398,
          "cdna_start": 4004,
          "cdna_end": null,
          "cdna_length": 6598,
          "mane_select": "NM_000053.4",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "V",
          "aa_alt": "V",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 18,
          "exon_rank_end": null,
          "exon_count": 21,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATP7B",
          "gene_hgnc_id": 870,
          "hgvs_c": "c.3747C>T",
          "hgvs_p": "p.Val1249Val",
          "transcript": "ENST00000634844.1",
          "protein_id": "ENSP00000489398.1",
          "transcript_support_level": 1,
          "aa_start": 1249,
          "aa_end": null,
          "aa_length": 1417,
          "cds_start": 3747,
          "cds_end": null,
          "cds_length": 4254,
          "cdna_start": 3821,
          "cdna_end": null,
          "cdna_length": 4398,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "V",
          "aa_alt": "V",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 17,
          "exon_rank_end": null,
          "exon_count": 20,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATP7B",
          "gene_hgnc_id": 870,
          "hgvs_c": "c.3696C>T",
          "hgvs_p": "p.Val1232Val",
          "transcript": "ENST00000418097.7",
          "protein_id": "ENSP00000393343.2",
          "transcript_support_level": 1,
          "aa_start": 1232,
          "aa_end": null,
          "aa_length": 1400,
          "cds_start": 3696,
          "cds_end": null,
          "cds_length": 4203,
          "cdna_start": 3770,
          "cdna_end": null,
          "cdna_length": 4340,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "V",
          "aa_alt": "V",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 16,
          "exon_rank_end": null,
          "exon_count": 19,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATP7B",
          "gene_hgnc_id": 870,
          "hgvs_c": "c.3639C>T",
          "hgvs_p": "p.Val1213Val",
          "transcript": "ENST00000448424.7",
          "protein_id": "ENSP00000416738.3",
          "transcript_support_level": 1,
          "aa_start": 1213,
          "aa_end": null,
          "aa_length": 1381,
          "cds_start": 3639,
          "cds_end": null,
          "cds_length": 4146,
          "cdna_start": 3892,
          "cdna_end": null,
          "cdna_length": 6451,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "V",
          "aa_alt": "V",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 19,
          "exon_rank_end": null,
          "exon_count": 22,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATP7B",
          "gene_hgnc_id": 870,
          "hgvs_c": "c.3558C>T",
          "hgvs_p": "p.Val1186Val",
          "transcript": "ENST00000400366.6",
          "protein_id": "ENSP00000383217.3",
          "transcript_support_level": 1,
          "aa_start": 1186,
          "aa_end": null,
          "aa_length": 1354,
          "cds_start": 3558,
          "cds_end": null,
          "cds_length": 4065,
          "cdna_start": 3558,
          "cdna_end": null,
          "cdna_length": 4065,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "V",
          "aa_alt": "V",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 10,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATP7B",
          "gene_hgnc_id": 870,
          "hgvs_c": "c.2601C>T",
          "hgvs_p": "p.Val867Val",
          "transcript": "ENST00000400370.8",
          "protein_id": "ENSP00000383221.3",
          "transcript_support_level": 1,
          "aa_start": 867,
          "aa_end": null,
          "aa_length": 1035,
          "cds_start": 2601,
          "cds_end": null,
          "cds_length": 3108,
          "cdna_start": 2675,
          "cdna_end": null,
          "cdna_length": 3252,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 18,
          "exon_rank_end": null,
          "exon_count": 21,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATP7B",
          "gene_hgnc_id": 870,
          "hgvs_c": "n.*992C>T",
          "hgvs_p": null,
          "transcript": "ENST00000634308.1",
          "protein_id": "ENSP00000489234.1",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": null,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": null,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 4321,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 14,
          "exon_rank_end": null,
          "exon_count": 17,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATP7B",
          "gene_hgnc_id": 870,
          "hgvs_c": "n.4635C>T",
          "hgvs_p": null,
          "transcript": "ENST00000634620.1",
          "protein_id": null,
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": null,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": null,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 5653,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 11,
          "exon_rank_end": null,
          "exon_count": 14,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATP7B",
          "gene_hgnc_id": 870,
          "hgvs_c": "n.3236C>T",
          "hgvs_p": null,
          "transcript": "ENST00000634810.1",
          "protein_id": null,
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": null,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": null,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 5825,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "3_prime_UTR_variant"
          ],
          "exon_rank": 18,
          "exon_rank_end": null,
          "exon_count": 21,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATP7B",
          "gene_hgnc_id": 870,
          "hgvs_c": "n.*992C>T",
          "hgvs_p": null,
          "transcript": "ENST00000634308.1",
          "protein_id": "ENSP00000489234.1",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": null,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": null,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 4321,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "V",
          "aa_alt": "V",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 19,
          "exon_rank_end": null,
          "exon_count": 22,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATP7B",
          "gene_hgnc_id": 870,
          "hgvs_c": "c.3891C>T",
          "hgvs_p": "p.Val1297Val",
          "transcript": "NM_001406511.1",
          "protein_id": "NP_001393440.1",
          "transcript_support_level": null,
          "aa_start": 1297,
          "aa_end": null,
          "aa_length": 1465,
          "cds_start": 3891,
          "cds_end": null,
          "cds_length": 4398,
          "cdna_start": 4058,
          "cdna_end": null,
          "cdna_length": 6652,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "V",
          "aa_alt": "V",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 19,
          "exon_rank_end": null,
          "exon_count": 22,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATP7B",
          "gene_hgnc_id": 870,
          "hgvs_c": "c.3891C>T",
          "hgvs_p": "p.Val1297Val",
          "transcript": "NM_001406512.1",
          "protein_id": "NP_001393441.1",
          "transcript_support_level": null,
          "aa_start": 1297,
          "aa_end": null,
          "aa_length": 1465,
          "cds_start": 3891,
          "cds_end": null,
          "cds_length": 4398,
          "cdna_start": 4297,
          "cdna_end": null,
          "cdna_length": 6891,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "V",
          "aa_alt": "V",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 19,
          "exon_rank_end": null,
          "exon_count": 22,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATP7B",
          "gene_hgnc_id": 870,
          "hgvs_c": "c.3885C>T",
          "hgvs_p": "p.Val1295Val",
          "transcript": "NM_001406513.1",
          "protein_id": "NP_001393442.1",
          "transcript_support_level": null,
          "aa_start": 1295,
          "aa_end": null,
          "aa_length": 1463,
          "cds_start": 3885,
          "cds_end": null,
          "cds_length": 4392,
          "cdna_start": 4052,
          "cdna_end": null,
          "cdna_length": 6646,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "V",
          "aa_alt": "V",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 18,
          "exon_rank_end": null,
          "exon_count": 21,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATP7B",
          "gene_hgnc_id": 870,
          "hgvs_c": "c.3858C>T",
          "hgvs_p": "p.Val1286Val",
          "transcript": "NM_001406514.1",
          "protein_id": "NP_001393443.1",
          "transcript_support_level": null,
          "aa_start": 1286,
          "aa_end": null,
          "aa_length": 1454,
          "cds_start": 3858,
          "cds_end": null,
          "cds_length": 4365,
          "cdna_start": 3971,
          "cdna_end": null,
          "cdna_length": 6565,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "V",
          "aa_alt": "V",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 18,
          "exon_rank_end": null,
          "exon_count": 21,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATP7B",
          "gene_hgnc_id": 870,
          "hgvs_c": "c.3837C>T",
          "hgvs_p": "p.Val1279Val",
          "transcript": "NM_001406515.1",
          "protein_id": "NP_001393444.1",
          "transcript_support_level": null,
          "aa_start": 1279,
          "aa_end": null,
          "aa_length": 1447,
          "cds_start": 3837,
          "cds_end": null,
          "cds_length": 4344,
          "cdna_start": 3950,
          "cdna_end": null,
          "cdna_length": 6544,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "V",
          "aa_alt": "V",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 19,
          "exon_rank_end": null,
          "exon_count": 22,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATP7B",
          "gene_hgnc_id": 870,
          "hgvs_c": "c.3837C>T",
          "hgvs_p": "p.Val1279Val",
          "transcript": "NM_001406516.1",
          "protein_id": "NP_001393445.1",
          "transcript_support_level": null,
          "aa_start": 1279,
          "aa_end": null,
          "aa_length": 1447,
          "cds_start": 3837,
          "cds_end": null,
          "cds_length": 4344,
          "cdna_start": 4243,
          "cdna_end": null,
          "cdna_length": 6837,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "V",
          "aa_alt": "V",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 18,
          "exon_rank_end": null,
          "exon_count": 21,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATP7B",
          "gene_hgnc_id": 870,
          "hgvs_c": "c.3795C>T",
          "hgvs_p": "p.Val1265Val",
          "transcript": "NM_001406517.1",
          "protein_id": "NP_001393446.1",
          "transcript_support_level": null,
          "aa_start": 1265,
          "aa_end": null,
          "aa_length": 1433,
          "cds_start": 3795,
          "cds_end": null,
          "cds_length": 4302,
          "cdna_start": 3908,
          "cdna_end": null,
          "cdna_length": 6502,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "V",
          "aa_alt": "V",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 19,
          "exon_rank_end": null,
          "exon_count": 22,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATP7B",
          "gene_hgnc_id": 870,
          "hgvs_c": "c.3795C>T",
          "hgvs_p": "p.Val1265Val",
          "transcript": "NM_001406518.1",
          "protein_id": "NP_001393447.1",
          "transcript_support_level": null,
          "aa_start": 1265,
          "aa_end": null,
          "aa_length": 1433,
          "cds_start": 3795,
          "cds_end": null,
          "cds_length": 4302,
          "cdna_start": 4095,
          "cdna_end": null,
          "cdna_length": 6689,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "V",
          "aa_alt": "V",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 17,
          "exon_rank_end": null,
          "exon_count": 20,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATP7B",
          "gene_hgnc_id": 870,
          "hgvs_c": "c.3756C>T",
          "hgvs_p": "p.Val1252Val",
          "transcript": "NM_001406519.1",
          "protein_id": "NP_001393448.1",
          "transcript_support_level": null,
          "aa_start": 1252,
          "aa_end": null,
          "aa_length": 1420,
          "cds_start": 3756,
          "cds_end": null,
          "cds_length": 4263,
          "cdna_start": 3869,
          "cdna_end": null,
          "cdna_length": 6463,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "V",
          "aa_alt": "V",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 18,
          "exon_rank_end": null,
          "exon_count": 21,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATP7B",
          "gene_hgnc_id": 870,
          "hgvs_c": "c.3747C>T",
          "hgvs_p": "p.Val1249Val",
          "transcript": "NM_001406520.1",
          "protein_id": "NP_001393449.1",
          "transcript_support_level": null,
          "aa_start": 1249,
          "aa_end": null,
          "aa_length": 1417,
          "cds_start": 3747,
          "cds_end": null,
          "cds_length": 4254,
          "cdna_start": 3860,
          "cdna_end": null,
          "cdna_length": 6454,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "V",
          "aa_alt": "V",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 19,
          "exon_rank_end": null,
          "exon_count": 22,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATP7B",
          "gene_hgnc_id": 870,
          "hgvs_c": "c.3747C>T",
          "hgvs_p": "p.Val1249Val",
          "transcript": "NM_001406521.1",
          "protein_id": "NP_001393450.1",
          "transcript_support_level": null,
          "aa_start": 1249,
          "aa_end": null,
          "aa_length": 1417,
          "cds_start": 3747,
          "cds_end": null,
          "cds_length": 4254,
          "cdna_start": 3914,
          "cdna_end": null,
          "cdna_length": 6508,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "V",
          "aa_alt": "V",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 19,
          "exon_rank_end": null,
          "exon_count": 22,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATP7B",
          "gene_hgnc_id": 870,
          "hgvs_c": "c.3747C>T",
          "hgvs_p": "p.Val1249Val",
          "transcript": "NM_001406522.1",
          "protein_id": "NP_001393451.1",
          "transcript_support_level": null,
          "aa_start": 1249,
          "aa_end": null,
          "aa_length": 1417,
          "cds_start": 3747,
          "cds_end": null,
          "cds_length": 4254,
          "cdna_start": 4153,
          "cdna_end": null,
          "cdna_length": 6747,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "V",
          "aa_alt": "V",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 18,
          "exon_rank_end": null,
          "exon_count": 21,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATP7B",
          "gene_hgnc_id": 870,
          "hgvs_c": "c.3714C>T",
          "hgvs_p": "p.Val1238Val",
          "transcript": "NM_001406524.1",
          "protein_id": "NP_001393453.1",
          "transcript_support_level": null,
          "aa_start": 1238,
          "aa_end": null,
          "aa_length": 1406,
          "cds_start": 3714,
          "cds_end": null,
          "cds_length": 4221,
          "cdna_start": 3827,
          "cdna_end": null,
          "cdna_length": 6421,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "V",
          "aa_alt": "V",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 17,
          "exon_rank_end": null,
          "exon_count": 20,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATP7B",
          "gene_hgnc_id": 870,
          "hgvs_c": "c.3708C>T",
          "hgvs_p": "p.Val1236Val",
          "transcript": "NM_001406523.1",
          "protein_id": "NP_001393452.1",
          "transcript_support_level": null,
          "aa_start": 1236,
          "aa_end": null,
          "aa_length": 1404,
          "cds_start": 3708,
          "cds_end": null,
          "cds_length": 4215,
          "cdna_start": 3821,
          "cdna_end": null,
          "cdna_length": 6415,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "V",
          "aa_alt": "V",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 17,
          "exon_rank_end": null,
          "exon_count": 20,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATP7B",
          "gene_hgnc_id": 870,
          "hgvs_c": "c.3696C>T",
          "hgvs_p": "p.Val1232Val",
          "transcript": "NM_001406525.1",
          "protein_id": "NP_001393454.1",
          "transcript_support_level": null,
          "aa_start": 1232,
          "aa_end": null,
          "aa_length": 1400,
          "cds_start": 3696,
          "cds_end": null,
          "cds_length": 4203,
          "cdna_start": 3809,
          "cdna_end": null,
          "cdna_length": 6403,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "V",
          "aa_alt": "V",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 17,
          "exon_rank_end": null,
          "exon_count": 20,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATP7B",
          "gene_hgnc_id": 870,
          "hgvs_c": "c.3657C>T",
          "hgvs_p": "p.Val1219Val",
          "transcript": "NM_001330578.2",
          "protein_id": "NP_001317507.1",
          "transcript_support_level": null,
          "aa_start": 1219,
          "aa_end": null,
          "aa_length": 1387,
          "cds_start": 3657,
          "cds_end": null,
          "cds_length": 4164,
          "cdna_start": 3770,
          "cdna_end": null,
          "cdna_length": 6364,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "V",
          "aa_alt": "V",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 18,
          "exon_rank_end": null,
          "exon_count": 21,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATP7B",
          "gene_hgnc_id": 870,
          "hgvs_c": "c.3657C>T",
          "hgvs_p": "p.Val1219Val",
          "transcript": "NM_001406527.1",
          "protein_id": "NP_001393456.1",
          "transcript_support_level": null,
          "aa_start": 1219,
          "aa_end": null,
          "aa_length": 1387,
          "cds_start": 3657,
          "cds_end": null,
          "cds_length": 4164,
          "cdna_start": 3824,
          "cdna_end": null,
          "cdna_length": 6418,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "V",
          "aa_alt": "V",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 18,
          "exon_rank_end": null,
          "exon_count": 21,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATP7B",
          "gene_hgnc_id": 870,
          "hgvs_c": "c.3657C>T",
          "hgvs_p": "p.Val1219Val",
          "transcript": "NM_001406528.1",
          "protein_id": "NP_001393457.1",
          "transcript_support_level": null,
          "aa_start": 1219,
          "aa_end": null,
          "aa_length": 1387,
          "cds_start": 3657,
          "cds_end": null,
          "cds_length": 4164,
          "cdna_start": 4008,
          "cdna_end": null,
          "cdna_length": 6602,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "V",
          "aa_alt": "V",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 17,
          "exon_rank_end": null,
          "exon_count": 20,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATP7B",
          "gene_hgnc_id": 870,
          "hgvs_c": "c.3657C>T",
          "hgvs_p": "p.Val1219Val",
          "transcript": "ENST00000673772.1",
          "protein_id": "ENSP00000501168.1",
          "transcript_support_level": null,
          "aa_start": 1219,
          "aa_end": null,
          "aa_length": 1387,
          "cds_start": 3657,
          "cds_end": null,
          "cds_length": 4164,
          "cdna_start": 3731,
          "cdna_end": null,
          "cdna_length": 4308,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "V",
          "aa_alt": "V",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 18,
          "exon_rank_end": null,
          "exon_count": 21,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATP7B",
          "gene_hgnc_id": 870,
          "hgvs_c": "c.3651C>T",
          "hgvs_p": "p.Val1217Val",
          "transcript": "NM_001406530.1",
          "protein_id": "NP_001393459.1",
          "transcript_support_level": null,
          "aa_start": 1217,
          "aa_end": null,
          "aa_length": 1385,
          "cds_start": 3651,
          "cds_end": null,
          "cds_length": 4158,
          "cdna_start": 3764,
          "cdna_end": null,
          "cdna_length": 6358,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "V",
          "aa_alt": "V",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 16,
          "exon_rank_end": null,
          "exon_count": 19,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATP7B",
          "gene_hgnc_id": 870,
          "hgvs_c": "c.3639C>T",
          "hgvs_p": "p.Val1213Val",
          "transcript": "NM_001330579.2",
          "protein_id": "NP_001317508.1",
          "transcript_support_level": null,
          "aa_start": 1213,
          "aa_end": null,
          "aa_length": 1381,
          "cds_start": 3639,
          "cds_end": null,
          "cds_length": 4146,
          "cdna_start": 3752,
          "cdna_end": null,
          "cdna_length": 6346,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "V",
          "aa_alt": "V",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 17,
          "exon_rank_end": null,
          "exon_count": 20,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATP7B",
          "gene_hgnc_id": 870,
          "hgvs_c": "c.3639C>T",
          "hgvs_p": "p.Val1213Val",
          "transcript": "NM_001406531.1",
          "protein_id": "NP_001393460.1",
          "transcript_support_level": null,
          "aa_start": 1213,
          "aa_end": null,
          "aa_length": 1381,
          "cds_start": 3639,
          "cds_end": null,
          "cds_length": 4146,
          "cdna_start": 3806,
          "cdna_end": null,
          "cdna_length": 6400,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "V",
          "aa_alt": "V",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 17,
          "exon_rank_end": null,
          "exon_count": 20,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATP7B",
          "gene_hgnc_id": 870,
          "hgvs_c": "c.3639C>T",
          "hgvs_p": "p.Val1213Val",
          "transcript": "NM_001406532.1",
          "protein_id": "NP_001393461.1",
          "transcript_support_level": null,
          "aa_start": 1213,
          "aa_end": null,
          "aa_length": 1381,
          "cds_start": 3639,
          "cds_end": null,
          "cds_length": 4146,
          "cdna_start": 4229,
          "cdna_end": null,
          "cdna_length": 6823,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "V",
          "aa_alt": "V",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 17,
          "exon_rank_end": null,
          "exon_count": 20,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATP7B",
          "gene_hgnc_id": 870,
          "hgvs_c": "c.3603C>T",
          "hgvs_p": "p.Val1201Val",
          "transcript": "NM_001406534.1",
          "protein_id": "NP_001393463.1",
          "transcript_support_level": null,
          "aa_start": 1201,
          "aa_end": null,
          "aa_length": 1369,
          "cds_start": 3603,
          "cds_end": null,
          "cds_length": 4110,
          "cdna_start": 3716,
          "cdna_end": null,
          "cdna_length": 6310,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "V",
          "aa_alt": "V",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 16,
          "exon_rank_end": null,
          "exon_count": 19,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATP7B",
          "gene_hgnc_id": 870,
          "hgvs_c": "c.3561C>T",
          "hgvs_p": "p.Val1187Val",
          "transcript": "NM_001406535.1",
          "protein_id": "NP_001393464.1",
          "transcript_support_level": null,
          "aa_start": 1187,
          "aa_end": null,
          "aa_length": 1355,
          "cds_start": 3561,
          "cds_end": null,
          "cds_length": 4068,
          "cdna_start": 3674,
          "cdna_end": null,
          "cdna_length": 6268,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "V",
          "aa_alt": "V",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 17,
          "exon_rank_end": null,
          "exon_count": 20,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATP7B",
          "gene_hgnc_id": 870,
          "hgvs_c": "c.3561C>T",
          "hgvs_p": "p.Val1187Val",
          "transcript": "NM_001406536.1",
          "protein_id": "NP_001393465.1",
          "transcript_support_level": null,
          "aa_start": 1187,
          "aa_end": null,
          "aa_length": 1355,
          "cds_start": 3561,
          "cds_end": null,
          "cds_length": 4068,
          "cdna_start": 3674,
          "cdna_end": null,
          "cdna_length": 6268,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "V",
          "aa_alt": "V",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 19,
          "exon_rank_end": null,
          "exon_count": 22,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATP7B",
          "gene_hgnc_id": 870,
          "hgvs_c": "c.3558C>T",
          "hgvs_p": "p.Val1186Val",
          "transcript": "NM_001243182.2",
          "protein_id": "NP_001230111.1",
          "transcript_support_level": null,
          "aa_start": 1186,
          "aa_end": null,
          "aa_length": 1354,
          "cds_start": 3558,
          "cds_end": null,
          "cds_length": 4065,
          "cdna_start": 3671,
          "cdna_end": null,
          "cdna_length": 6265,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "V",
          "aa_alt": "V",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 18,
          "exon_rank_end": null,
          "exon_count": 21,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATP7B",
          "gene_hgnc_id": 870,
          "hgvs_c": "c.3552C>T",
          "hgvs_p": "p.Val1184Val",
          "transcript": "NM_001406537.1",
          "protein_id": "NP_001393466.1",
          "transcript_support_level": null,
          "aa_start": 1184,
          "aa_end": null,
          "aa_length": 1352,
          "cds_start": 3552,
          "cds_end": null,
          "cds_length": 4059,
          "cdna_start": 3719,
          "cdna_end": null,
          "cdna_length": 6313,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "V",
          "aa_alt": "V",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 16,
          "exon_rank_end": null,
          "exon_count": 19,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATP7B",
          "gene_hgnc_id": 870,
          "hgvs_c": "c.3513C>T",
          "hgvs_p": "p.Val1171Val",
          "transcript": "NM_001406538.1",
          "protein_id": "NP_001393467.1",
          "transcript_support_level": null,
          "aa_start": 1171,
          "aa_end": null,
          "aa_length": 1339,
          "cds_start": 3513,
          "cds_end": null,
          "cds_length": 4020,
          "cdna_start": 3626,
          "cdna_end": null,
          "cdna_length": 6220,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "V",
          "aa_alt": "V",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 20,
          "exon_rank_end": null,
          "exon_count": 23,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATP7B",
          "gene_hgnc_id": 870,
          "hgvs_c": "c.3462C>T",
          "hgvs_p": "p.Val1154Val",
          "transcript": "NM_001406539.1",
          "protein_id": "NP_001393468.1",
          "transcript_support_level": null,
          "aa_start": 1154,
          "aa_end": null,
          "aa_length": 1322,
          "cds_start": 3462,
          "cds_end": null,
          "cds_length": 3969,
          "cdna_start": 3704,
          "cdna_end": null,
          "cdna_length": 6298,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "V",
          "aa_alt": "V",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 15,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATP7B",
          "gene_hgnc_id": 870,
          "hgvs_c": "c.3444C>T",
          "hgvs_p": "p.Val1148Val",
          "transcript": "NM_001406540.1",
          "protein_id": "NP_001393469.1",
          "transcript_support_level": null,
          "aa_start": 1148,
          "aa_end": null,
          "aa_length": 1316,
          "cds_start": 3444,
          "cds_end": null,
          "cds_length": 3951,
          "cdna_start": 3557,
          "cdna_end": null,
          "cdna_length": 6151,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "V",
          "aa_alt": "V",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 16,
          "exon_rank_end": null,
          "exon_count": 19,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATP7B",
          "gene_hgnc_id": 870,
          "hgvs_c": "c.3405C>T",
          "hgvs_p": "p.Val1135Val",
          "transcript": "NM_001406541.1",
          "protein_id": "NP_001393470.1",
          "transcript_support_level": null,
          "aa_start": 1135,
          "aa_end": null,
          "aa_length": 1303,
          "cds_start": 3405,
          "cds_end": null,
          "cds_length": 3912,
          "cdna_start": 3572,
          "cdna_end": null,
          "cdna_length": 6166,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "V",
          "aa_alt": "V",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 15,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATP7B",
          "gene_hgnc_id": 870,
          "hgvs_c": "c.3405C>T",
          "hgvs_p": "p.Val1135Val",
          "transcript": "NM_001406542.1",
          "protein_id": "NP_001393471.1",
          "transcript_support_level": null,
          "aa_start": 1135,
          "aa_end": null,
          "aa_length": 1303,
          "cds_start": 3405,
          "cds_end": null,
          "cds_length": 3912,
          "cdna_start": 3518,
          "cdna_end": null,
          "cdna_length": 6112,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "V",
          "aa_alt": "V",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 15,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATP7B",
          "gene_hgnc_id": 870,
          "hgvs_c": "c.3405C>T",
          "hgvs_p": "p.Val1135Val",
          "transcript": "ENST00000713660.1",
          "protein_id": "ENSP00000518962.1",
          "transcript_support_level": null,
          "aa_start": 1135,
          "aa_end": null,
          "aa_length": 1303,
          "cds_start": 3405,
          "cds_end": null,
          "cds_length": 3912,
          "cdna_start": 3459,
          "cdna_end": null,
          "cdna_length": 6048,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "V",
          "aa_alt": "V",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 17,
          "exon_rank_end": null,
          "exon_count": 20,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATP7B",
          "gene_hgnc_id": 870,
          "hgvs_c": "c.3399C>T",
          "hgvs_p": "p.Val1133Val",
          "transcript": "NM_001406543.1",
          "protein_id": "NP_001393472.1",
          "transcript_support_level": null,
          "aa_start": 1133,
          "aa_end": null,
          "aa_length": 1301,
          "cds_start": 3399,
          "cds_end": null,
          "cds_length": 3906,
          "cdna_start": 3695,
          "cdna_end": null,
          "cdna_length": 6289,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "V",
          "aa_alt": "V",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 15,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATP7B",
          "gene_hgnc_id": 870,
          "hgvs_c": "c.3309C>T",
          "hgvs_p": "p.Val1103Val",
          "transcript": "NM_001406544.1",
          "protein_id": "NP_001393473.1",
          "transcript_support_level": null,
          "aa_start": 1103,
          "aa_end": null,
          "aa_length": 1271,
          "cds_start": 3309,
          "cds_end": null,
          "cds_length": 3816,
          "cdna_start": 3422,
          "cdna_end": null,
          "cdna_length": 6016,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "V",
          "aa_alt": "V",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 14,
          "exon_rank_end": null,
          "exon_count": 17,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATP7B",
          "gene_hgnc_id": 870,
          "hgvs_c": "c.3270C>T",
          "hgvs_p": "p.Val1090Val",
          "transcript": "NM_001005918.3",
          "protein_id": "NP_001005918.1",
          "transcript_support_level": null,
          "aa_start": 1090,
          "aa_end": null,
          "aa_length": 1258,
          "cds_start": 3270,
          "cds_end": null,
          "cds_length": 3777,
          "cdna_start": 3383,
          "cdna_end": null,
          "cdna_length": 5977,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "V",
          "aa_alt": "V",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 14,
          "exon_rank_end": null,
          "exon_count": 17,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATP7B",
          "gene_hgnc_id": 870,
          "hgvs_c": "c.3270C>T",
          "hgvs_p": "p.Val1090Val",
          "transcript": "ENST00000674147.2",
          "protein_id": "ENSP00000500964.2",
          "transcript_support_level": null,
          "aa_start": 1090,
          "aa_end": null,
          "aa_length": 1258,
          "cds_start": 3270,
          "cds_end": null,
          "cds_length": 3777,
          "cdna_start": 3383,
          "cdna_end": null,
          "cdna_length": 5972,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "V",
          "aa_alt": "V",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 14,
          "exon_rank_end": null,
          "exon_count": 17,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATP7B",
          "gene_hgnc_id": 870,
          "hgvs_c": "c.3243C>T",
          "hgvs_p": "p.Val1081Val",
          "transcript": "NM_001406545.1",
          "protein_id": "NP_001393474.1",
          "transcript_support_level": null,
          "aa_start": 1081,
          "aa_end": null,
          "aa_length": 1249,
          "cds_start": 3243,
          "cds_end": null,
          "cds_length": 3750,
          "cdna_start": 3356,
          "cdna_end": null,
          "cdna_length": 5950,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "V",
          "aa_alt": "V",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 14,
          "exon_rank_end": null,
          "exon_count": 17,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATP7B",
          "gene_hgnc_id": 870,
          "hgvs_c": "c.3243C>T",
          "hgvs_p": "p.Val1081Val",
          "transcript": "ENST00000713659.1",
          "protein_id": "ENSP00000518961.1",
          "transcript_support_level": null,
          "aa_start": 1081,
          "aa_end": null,
          "aa_length": 1249,
          "cds_start": 3243,
          "cds_end": null,
          "cds_length": 3750,
          "cdna_start": 4021,
          "cdna_end": null,
          "cdna_length": 8132,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "V",
          "aa_alt": "V",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 14,
          "exon_rank_end": null,
          "exon_count": 17,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATP7B",
          "gene_hgnc_id": 870,
          "hgvs_c": "c.3210C>T",
          "hgvs_p": "p.Val1070Val",
          "transcript": "NM_001406546.1",
          "protein_id": "NP_001393475.1",
          "transcript_support_level": null,
          "aa_start": 1070,
          "aa_end": null,
          "aa_length": 1238,
          "cds_start": 3210,
          "cds_end": null,
          "cds_length": 3717,
          "cdna_start": 3323,
          "cdna_end": null,
          "cdna_length": 5917,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "V",
          "aa_alt": "V",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 13,
          "exon_rank_end": null,
          "exon_count": 16,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATP7B",
          "gene_hgnc_id": 870,
          "hgvs_c": "c.3048C>T",
          "hgvs_p": "p.Val1016Val",
          "transcript": "NM_001406547.1",
          "protein_id": "NP_001393476.1",
          "transcript_support_level": null,
          "aa_start": 1016,
          "aa_end": null,
          "aa_length": 1184,
          "cds_start": 3048,
          "cds_end": null,
          "cds_length": 3555,
          "cdna_start": 3161,
          "cdna_end": null,
          "cdna_length": 5755,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "V",
          "aa_alt": "V",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 10,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATP7B",
          "gene_hgnc_id": 870,
          "hgvs_c": "c.2601C>T",
          "hgvs_p": "p.Val867Val",
          "transcript": "NM_001406548.1",
          "protein_id": "NP_001393477.1",
          "transcript_support_level": null,
          "aa_start": 867,
          "aa_end": null,
          "aa_length": 1035,
          "cds_start": 2601,
          "cds_end": null,
          "cds_length": 3108,
          "cdna_start": 2714,
          "cdna_end": null,
          "cdna_length": 5308,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 16,
          "exon_rank_end": null,
          "exon_count": 19,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATP7B",
          "gene_hgnc_id": 870,
          "hgvs_c": "n.*1541C>T",
          "hgvs_p": null,
          "transcript": "ENST00000634296.2",
          "protein_id": "ENSP00000489512.2",
          "transcript_support_level": 5,
          "aa_start": null,
          "aa_end": null,
          "aa_length": null,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": null,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 4305,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 2,
          "exon_rank_end": null,
          "exon_count": 5,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATP7B",
          "gene_hgnc_id": 870,
          "hgvs_c": "n.1132C>T",
          "hgvs_p": null,
          "transcript": "ENST00000673696.1",
          "protein_id": null,
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": null,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": null,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 2800,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 19,
          "exon_rank_end": null,
          "exon_count": 22,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATP7B",
          "gene_hgnc_id": 870,
          "hgvs_c": "n.*2635C>T",
          "hgvs_p": null,
          "transcript": "ENST00000673864.2",
          "protein_id": "ENSP00000501045.2",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": null,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": null,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 7022,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 5,
          "exon_rank_end": null,
          "exon_count": 8,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATP7B",
          "gene_hgnc_id": 870,
          "hgvs_c": "n.4030C>T",
          "hgvs_p": null,
          "transcript": "ENST00000673867.1",
          "protein_id": null,
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": null,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": null,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 6613,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 2,
          "exon_rank_end": null,
          "exon_count": 5,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATP7B",
          "gene_hgnc_id": 870,
          "hgvs_c": "n.757C>T",
          "hgvs_p": null,
          "transcript": "ENST00000673923.1",
          "protein_id": null,
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": null,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": null,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 3336,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "3_prime_UTR_variant"
          ],
          "exon_rank": 16,
          "exon_rank_end": null,
          "exon_count": 19,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATP7B",
          "gene_hgnc_id": 870,
          "hgvs_c": "n.*1541C>T",
          "hgvs_p": null,
          "transcript": "ENST00000634296.2",
          "protein_id": "ENSP00000489512.2",
          "transcript_support_level": 5,
          "aa_start": null,
          "aa_end": null,
          "aa_length": null,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": null,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 4305,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "3_prime_UTR_variant"
          ],
          "exon_rank": 19,
          "exon_rank_end": null,
          "exon_count": 22,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATP7B",
          "gene_hgnc_id": 870,
          "hgvs_c": "n.*2635C>T",
          "hgvs_p": null,
          "transcript": "ENST00000673864.2",
          "protein_id": "ENSP00000501045.2",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": null,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": null,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 7022,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 20,
          "intron_rank": 17,
          "intron_rank_end": null,
          "gene_symbol": "ATP7B",
          "gene_hgnc_id": 870,
          "hgvs_c": "c.3700-95C>T",
          "hgvs_p": null,
          "transcript": "NM_001406526.1",
          "protein_id": "NP_001393455.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1397,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 4194,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 6394,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        }
      ],
      "gene_symbol": "ATP7B",
      "gene_hgnc_id": 870,
      "dbsnp": "rs114771537",
      "frequency_reference_population": 0.0019026507,
      "hom_count_reference_population": 52,
      "allele_count_reference_population": 3071,
      "gnomad_exomes_af": 0.00107681,
      "gnomad_genomes_af": 0.00982657,
      "gnomad_exomes_ac": 1574,
      "gnomad_genomes_ac": 1497,
      "gnomad_exomes_homalt": 22,
      "gnomad_genomes_homalt": 30,
      "gnomad_mito_homoplasmic": null,
      "gnomad_mito_heteroplasmic": null,
      "computational_score_selected": -0.8600000143051147,
      "computational_prediction_selected": "Benign",
      "computational_source_selected": "BayesDel_noAF",
      "splice_score_selected": 0.009999999776482582,
      "splice_prediction_selected": "Benign",
      "splice_source_selected": "max_spliceai",
      "revel_score": null,
      "revel_prediction": null,
      "alphamissense_score": null,
      "alphamissense_prediction": null,
      "bayesdelnoaf_score": -0.86,
      "bayesdelnoaf_prediction": "Benign",
      "phylop100way_score": -4.481,
      "phylop100way_prediction": "Benign",
      "spliceai_max_score": 0.01,
      "spliceai_max_prediction": "Benign",
      "dbscsnv_ada_score": null,
      "dbscsnv_ada_prediction": null,
      "apogee2_score": null,
      "apogee2_prediction": null,
      "mitotip_score": null,
      "mitotip_prediction": null,
      "acmg_score": -21,
      "acmg_classification": "Benign",
      "acmg_criteria": "BP4_Strong,BP6_Very_Strong,BP7,BS1,BS2",
      "acmg_by_gene": [
        {
          "score": -21,
          "benign_score": 21,
          "pathogenic_score": 0,
          "criteria": [
            "BP4_Strong",
            "BP6_Very_Strong",
            "BP7",
            "BS1",
            "BS2"
          ],
          "verdict": "Benign",
          "transcript": "ENST00000242839.10",
          "gene_symbol": "ATP7B",
          "hgnc_id": 870,
          "effects": [
            "synonymous_variant"
          ],
          "inheritance_mode": "AR",
          "hgvs_c": "c.3891C>T",
          "hgvs_p": "p.Val1297Val"
        }
      ],
      "clinvar_disease": "ATP7B-related disorder,Wilson disease,not provided,not specified",
      "clinvar_classification": "Benign/Likely benign",
      "clinvar_review_status": "criteria provided, multiple submitters, no conflicts",
      "clinvar_submissions_summary": "LB:2 B:7",
      "phenotype_combined": "not specified|Wilson disease|not provided|ATP7B-related disorder",
      "pathogenicity_classification_combined": "Benign/Likely benign",
      "custom_annotations": null
    }
  ],
  "message": null
}