← 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: 11-108250928-G-A (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=11&pos=108250928&ref=G&alt=A&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "11",
      "pos": 108250928,
      "ref": "G",
      "alt": "A",
      "effect": "stop_gained",
      "transcript": "NM_000051.4",
      "consequences": [
        {
          "aa_ref": "W",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 10,
          "exon_rank_end": null,
          "exon_count": 63,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATM",
          "gene_hgnc_id": 795,
          "hgvs_c": "c.1463G>A",
          "hgvs_p": "p.Trp488*",
          "transcript": "NM_000051.4",
          "protein_id": "NP_000042.3",
          "transcript_support_level": null,
          "aa_start": 488,
          "aa_end": null,
          "aa_length": 3056,
          "cds_start": 1463,
          "cds_end": null,
          "cds_length": 9171,
          "cdna_start": 1613,
          "cdna_end": null,
          "cdna_length": 12915,
          "mane_select": "ENST00000675843.1",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "W",
          "aa_alt": "*",
          "canonical": true,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 10,
          "exon_rank_end": null,
          "exon_count": 63,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATM",
          "gene_hgnc_id": 795,
          "hgvs_c": "c.1463G>A",
          "hgvs_p": "p.Trp488*",
          "transcript": "ENST00000675843.1",
          "protein_id": "ENSP00000501606.1",
          "transcript_support_level": null,
          "aa_start": 488,
          "aa_end": null,
          "aa_length": 3056,
          "cds_start": 1463,
          "cds_end": null,
          "cds_length": 9171,
          "cdna_start": 1613,
          "cdna_end": null,
          "cdna_length": 12915,
          "mane_select": "NM_000051.4",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "W",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 11,
          "exon_rank_end": null,
          "exon_count": 64,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATM",
          "gene_hgnc_id": 795,
          "hgvs_c": "c.1463G>A",
          "hgvs_p": "p.Trp488*",
          "transcript": "ENST00000452508.7",
          "protein_id": "ENSP00000388058.2",
          "transcript_support_level": 1,
          "aa_start": 488,
          "aa_end": null,
          "aa_length": 3056,
          "cds_start": 1463,
          "cds_end": null,
          "cds_length": 9171,
          "cdna_start": 1945,
          "cdna_end": null,
          "cdna_length": 13247,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "W",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 10,
          "exon_rank_end": null,
          "exon_count": 30,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATM",
          "gene_hgnc_id": 795,
          "hgvs_c": "c.1463G>A",
          "hgvs_p": "p.Trp488*",
          "transcript": "ENST00000531525.3",
          "protein_id": "ENSP00000434327.3",
          "transcript_support_level": 1,
          "aa_start": 488,
          "aa_end": null,
          "aa_length": 1486,
          "cds_start": 1463,
          "cds_end": null,
          "cds_length": 4461,
          "cdna_start": 1613,
          "cdna_end": null,
          "cdna_length": 5656,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 10,
          "exon_rank_end": null,
          "exon_count": 61,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATM",
          "gene_hgnc_id": 795,
          "hgvs_c": "n.1463G>A",
          "hgvs_p": null,
          "transcript": "ENST00000527805.6",
          "protein_id": "ENSP00000435747.2",
          "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": 9287,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "W",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 11,
          "exon_rank_end": null,
          "exon_count": 64,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATM",
          "gene_hgnc_id": 795,
          "hgvs_c": "c.1463G>A",
          "hgvs_p": "p.Trp488*",
          "transcript": "NM_001351834.2",
          "protein_id": "NP_001338763.1",
          "transcript_support_level": null,
          "aa_start": 488,
          "aa_end": null,
          "aa_length": 3056,
          "cds_start": 1463,
          "cds_end": null,
          "cds_length": 9171,
          "cdna_start": 1701,
          "cdna_end": null,
          "cdna_length": 13003,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "W",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 10,
          "exon_rank_end": null,
          "exon_count": 63,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATM",
          "gene_hgnc_id": 795,
          "hgvs_c": "c.1463G>A",
          "hgvs_p": "p.Trp488*",
          "transcript": "ENST00000278616.10",
          "protein_id": "ENSP00000278616.4",
          "transcript_support_level": 5,
          "aa_start": 488,
          "aa_end": null,
          "aa_length": 3056,
          "cds_start": 1463,
          "cds_end": null,
          "cds_length": 9171,
          "cdna_start": 1769,
          "cdna_end": null,
          "cdna_length": 11233,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "W",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 11,
          "exon_rank_end": null,
          "exon_count": 64,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATM",
          "gene_hgnc_id": 795,
          "hgvs_c": "c.1463G>A",
          "hgvs_p": "p.Trp488*",
          "transcript": "ENST00000601453.3",
          "protein_id": "ENSP00000469471.2",
          "transcript_support_level": 3,
          "aa_start": 488,
          "aa_end": null,
          "aa_length": 3056,
          "cds_start": 1463,
          "cds_end": null,
          "cds_length": 9171,
          "cdna_start": 2914,
          "cdna_end": null,
          "cdna_length": 14216,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "W",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 11,
          "exon_rank_end": null,
          "exon_count": 64,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATM",
          "gene_hgnc_id": 795,
          "hgvs_c": "c.1463G>A",
          "hgvs_p": "p.Trp488*",
          "transcript": "ENST00000713844.1",
          "protein_id": "ENSP00000519149.1",
          "transcript_support_level": null,
          "aa_start": 488,
          "aa_end": null,
          "aa_length": 3056,
          "cds_start": 1463,
          "cds_end": null,
          "cds_length": 9171,
          "cdna_start": 1627,
          "cdna_end": null,
          "cdna_length": 9550,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "W",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 10,
          "exon_rank_end": null,
          "exon_count": 63,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATM",
          "gene_hgnc_id": 795,
          "hgvs_c": "c.1463G>A",
          "hgvs_p": "p.Trp488*",
          "transcript": "XM_005271562.6",
          "protein_id": "XP_005271619.2",
          "transcript_support_level": null,
          "aa_start": 488,
          "aa_end": null,
          "aa_length": 3056,
          "cds_start": 1463,
          "cds_end": null,
          "cds_length": 9171,
          "cdna_start": 1855,
          "cdna_end": null,
          "cdna_length": 13157,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "W",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 10,
          "exon_rank_end": null,
          "exon_count": 63,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATM",
          "gene_hgnc_id": 795,
          "hgvs_c": "c.1463G>A",
          "hgvs_p": "p.Trp488*",
          "transcript": "XM_006718843.5",
          "protein_id": "XP_006718906.1",
          "transcript_support_level": null,
          "aa_start": 488,
          "aa_end": null,
          "aa_length": 3056,
          "cds_start": 1463,
          "cds_end": null,
          "cds_length": 9171,
          "cdna_start": 2563,
          "cdna_end": null,
          "cdna_length": 13865,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "W",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 11,
          "exon_rank_end": null,
          "exon_count": 64,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATM",
          "gene_hgnc_id": 795,
          "hgvs_c": "c.1463G>A",
          "hgvs_p": "p.Trp488*",
          "transcript": "XM_011542840.4",
          "protein_id": "XP_011541142.1",
          "transcript_support_level": null,
          "aa_start": 488,
          "aa_end": null,
          "aa_length": 3056,
          "cds_start": 1463,
          "cds_end": null,
          "cds_length": 9171,
          "cdna_start": 2651,
          "cdna_end": null,
          "cdna_length": 13953,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "W",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 10,
          "exon_rank_end": null,
          "exon_count": 63,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATM",
          "gene_hgnc_id": 795,
          "hgvs_c": "c.1463G>A",
          "hgvs_p": "p.Trp488*",
          "transcript": "XM_017017790.3",
          "protein_id": "XP_016873279.1",
          "transcript_support_level": null,
          "aa_start": 488,
          "aa_end": null,
          "aa_length": 3056,
          "cds_start": 1463,
          "cds_end": null,
          "cds_length": 9171,
          "cdna_start": 2431,
          "cdna_end": null,
          "cdna_length": 13733,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "W",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 11,
          "exon_rank_end": null,
          "exon_count": 64,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATM",
          "gene_hgnc_id": 795,
          "hgvs_c": "c.1463G>A",
          "hgvs_p": "p.Trp488*",
          "transcript": "XM_047426975.1",
          "protein_id": "XP_047282931.1",
          "transcript_support_level": null,
          "aa_start": 488,
          "aa_end": null,
          "aa_length": 3056,
          "cds_start": 1463,
          "cds_end": null,
          "cds_length": 9171,
          "cdna_start": 2404,
          "cdna_end": null,
          "cdna_length": 13706,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "W",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 11,
          "exon_rank_end": null,
          "exon_count": 64,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATM",
          "gene_hgnc_id": 795,
          "hgvs_c": "c.1463G>A",
          "hgvs_p": "p.Trp488*",
          "transcript": "XM_047426976.1",
          "protein_id": "XP_047282932.1",
          "transcript_support_level": null,
          "aa_start": 488,
          "aa_end": null,
          "aa_length": 3056,
          "cds_start": 1463,
          "cds_end": null,
          "cds_length": 9171,
          "cdna_start": 1943,
          "cdna_end": null,
          "cdna_length": 13245,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "W",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 9,
          "exon_rank_end": null,
          "exon_count": 62,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATM",
          "gene_hgnc_id": 795,
          "hgvs_c": "c.1298G>A",
          "hgvs_p": "p.Trp433*",
          "transcript": "XM_011542842.4",
          "protein_id": "XP_011541144.1",
          "transcript_support_level": null,
          "aa_start": 433,
          "aa_end": null,
          "aa_length": 3001,
          "cds_start": 1298,
          "cds_end": null,
          "cds_length": 9006,
          "cdna_start": 1448,
          "cdna_end": null,
          "cdna_length": 12750,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "W",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 10,
          "exon_rank_end": null,
          "exon_count": 63,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATM",
          "gene_hgnc_id": 795,
          "hgvs_c": "c.1298G>A",
          "hgvs_p": "p.Trp433*",
          "transcript": "XM_047426977.1",
          "protein_id": "XP_047282933.1",
          "transcript_support_level": null,
          "aa_start": 433,
          "aa_end": null,
          "aa_length": 3001,
          "cds_start": 1298,
          "cds_end": null,
          "cds_length": 9006,
          "cdna_start": 2486,
          "cdna_end": null,
          "cdna_length": 13788,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "W",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 10,
          "exon_rank_end": null,
          "exon_count": 63,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATM",
          "gene_hgnc_id": 795,
          "hgvs_c": "c.1298G>A",
          "hgvs_p": "p.Trp433*",
          "transcript": "XM_047426978.1",
          "protein_id": "XP_047282934.1",
          "transcript_support_level": null,
          "aa_start": 433,
          "aa_end": null,
          "aa_length": 3001,
          "cds_start": 1298,
          "cds_end": null,
          "cds_length": 9006,
          "cdna_start": 1536,
          "cdna_end": null,
          "cdna_length": 12838,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "W",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 9,
          "exon_rank_end": null,
          "exon_count": 62,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATM",
          "gene_hgnc_id": 795,
          "hgvs_c": "c.1298G>A",
          "hgvs_p": "p.Trp433*",
          "transcript": "XM_047426979.1",
          "protein_id": "XP_047282935.1",
          "transcript_support_level": null,
          "aa_start": 433,
          "aa_end": null,
          "aa_length": 3001,
          "cds_start": 1298,
          "cds_end": null,
          "cds_length": 9006,
          "cdna_start": 2398,
          "cdna_end": null,
          "cdna_length": 13700,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "W",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 10,
          "exon_rank_end": null,
          "exon_count": 60,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATM",
          "gene_hgnc_id": 795,
          "hgvs_c": "c.1463G>A",
          "hgvs_p": "p.Trp488*",
          "transcript": "XM_011542843.3",
          "protein_id": "XP_011541145.1",
          "transcript_support_level": null,
          "aa_start": 488,
          "aa_end": null,
          "aa_length": 2912,
          "cds_start": 1463,
          "cds_end": null,
          "cds_length": 8739,
          "cdna_start": 1613,
          "cdna_end": null,
          "cdna_length": 8923,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "W",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 6,
          "exon_rank_end": null,
          "exon_count": 59,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATM",
          "gene_hgnc_id": 795,
          "hgvs_c": "c.419G>A",
          "hgvs_p": "p.Trp140*",
          "transcript": "XM_011542844.4",
          "protein_id": "XP_011541146.1",
          "transcript_support_level": null,
          "aa_start": 140,
          "aa_end": null,
          "aa_length": 2708,
          "cds_start": 419,
          "cds_end": null,
          "cds_length": 8127,
          "cdna_start": 1034,
          "cdna_end": null,
          "cdna_length": 12336,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "W",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 10,
          "exon_rank_end": null,
          "exon_count": 32,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATM",
          "gene_hgnc_id": 795,
          "hgvs_c": "c.1463G>A",
          "hgvs_p": "p.Trp488*",
          "transcript": "XM_047426981.1",
          "protein_id": "XP_047282937.1",
          "transcript_support_level": null,
          "aa_start": 488,
          "aa_end": null,
          "aa_length": 1600,
          "cds_start": 1463,
          "cds_end": null,
          "cds_length": 4803,
          "cdna_start": 1613,
          "cdna_end": null,
          "cdna_length": 5015,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 10,
          "exon_rank_end": null,
          "exon_count": 62,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATM",
          "gene_hgnc_id": 795,
          "hgvs_c": "n.1463G>A",
          "hgvs_p": null,
          "transcript": "ENST00000529588.6",
          "protein_id": "ENSP00000435524.2",
          "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": 12827,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 9,
          "exon_rank_end": null,
          "exon_count": 62,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATM",
          "gene_hgnc_id": 795,
          "hgvs_c": "n.1298G>A",
          "hgvs_p": null,
          "transcript": "ENST00000675595.1",
          "protein_id": "ENSP00000502563.1",
          "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": 9309,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 10,
          "exon_rank_end": null,
          "exon_count": 19,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATM",
          "gene_hgnc_id": 795,
          "hgvs_c": "n.1597G>A",
          "hgvs_p": null,
          "transcript": "ENST00000682516.1",
          "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": 3011,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 10,
          "exon_rank_end": null,
          "exon_count": 10,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATM",
          "gene_hgnc_id": 795,
          "hgvs_c": "n.1597G>A",
          "hgvs_p": null,
          "transcript": "ENST00000682956.1",
          "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": 2353,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 10,
          "exon_rank_end": null,
          "exon_count": 63,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATM",
          "gene_hgnc_id": 795,
          "hgvs_c": "n.1463G>A",
          "hgvs_p": null,
          "transcript": "ENST00000683174.2",
          "protein_id": "ENSP00000519136.1",
          "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": 13130,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 5,
          "exon_rank_end": null,
          "exon_count": 12,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATM",
          "gene_hgnc_id": 795,
          "hgvs_c": "n.958G>A",
          "hgvs_p": null,
          "transcript": "ENST00000683605.1",
          "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": 2884,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 10,
          "exon_rank_end": null,
          "exon_count": 19,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATM",
          "gene_hgnc_id": 795,
          "hgvs_c": "n.*398G>A",
          "hgvs_p": null,
          "transcript": "ENST00000684037.1",
          "protein_id": "ENSP00000508245.1",
          "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": 3020,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 10,
          "exon_rank_end": null,
          "exon_count": 14,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATM",
          "gene_hgnc_id": 795,
          "hgvs_c": "n.1597G>A",
          "hgvs_p": null,
          "transcript": "ENST00000684061.1",
          "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": 2529,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 9,
          "exon_rank_end": null,
          "exon_count": 9,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATM",
          "gene_hgnc_id": 795,
          "hgvs_c": "n.1432G>A",
          "hgvs_p": null,
          "transcript": "ENST00000684179.1",
          "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": 2243,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 10,
          "exon_rank_end": null,
          "exon_count": 63,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATM",
          "gene_hgnc_id": 795,
          "hgvs_c": "n.*934G>A",
          "hgvs_p": null,
          "transcript": "ENST00000713593.1",
          "protein_id": "ENSP00000518889.1",
          "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": 12893,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 10,
          "exon_rank_end": null,
          "exon_count": 63,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATM",
          "gene_hgnc_id": 795,
          "hgvs_c": "n.1463G>A",
          "hgvs_p": null,
          "transcript": "ENST00000713840.1",
          "protein_id": "ENSP00000519145.1",
          "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": 9933,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 10,
          "exon_rank_end": null,
          "exon_count": 64,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATM",
          "gene_hgnc_id": 795,
          "hgvs_c": "n.1463G>A",
          "hgvs_p": null,
          "transcript": "ENST00000713841.1",
          "protein_id": "ENSP00000519146.1",
          "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": 11890,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 10,
          "exon_rank_end": null,
          "exon_count": 63,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATM",
          "gene_hgnc_id": 795,
          "hgvs_c": "n.1463G>A",
          "hgvs_p": null,
          "transcript": "ENST00000713842.1",
          "protein_id": "ENSP00000519147.1",
          "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": 11758,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 10,
          "exon_rank_end": null,
          "exon_count": 64,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATM",
          "gene_hgnc_id": 795,
          "hgvs_c": "n.1463G>A",
          "hgvs_p": null,
          "transcript": "ENST00000713843.1",
          "protein_id": "ENSP00000519148.1",
          "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": 13126,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "3_prime_UTR_variant"
          ],
          "exon_rank": 10,
          "exon_rank_end": null,
          "exon_count": 19,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATM",
          "gene_hgnc_id": 795,
          "hgvs_c": "n.*398G>A",
          "hgvs_p": null,
          "transcript": "ENST00000684037.1",
          "protein_id": "ENSP00000508245.1",
          "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": 3020,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "3_prime_UTR_variant"
          ],
          "exon_rank": 10,
          "exon_rank_end": null,
          "exon_count": 63,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATM",
          "gene_hgnc_id": 795,
          "hgvs_c": "n.*934G>A",
          "hgvs_p": null,
          "transcript": "ENST00000713593.1",
          "protein_id": "ENSP00000518889.1",
          "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": 12893,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        }
      ],
      "gene_symbol": "ATM",
      "gene_hgnc_id": 795,
      "dbsnp": "rs879254093",
      "frequency_reference_population": 0.000006574276,
      "hom_count_reference_population": 0,
      "allele_count_reference_population": 1,
      "gnomad_exomes_af": null,
      "gnomad_genomes_af": 0.00000657428,
      "gnomad_exomes_ac": null,
      "gnomad_genomes_ac": 1,
      "gnomad_exomes_homalt": null,
      "gnomad_genomes_homalt": 0,
      "gnomad_mito_homoplasmic": null,
      "gnomad_mito_heteroplasmic": null,
      "computational_score_selected": 0.6600000262260437,
      "computational_prediction_selected": "Pathogenic",
      "computational_source_selected": "BayesDel_noAF",
      "splice_score_selected": 0.05999999865889549,
      "splice_prediction_selected": "Benign",
      "splice_source_selected": "max_spliceai",
      "revel_score": null,
      "revel_prediction": null,
      "alphamissense_score": null,
      "alphamissense_prediction": null,
      "bayesdelnoaf_score": 0.66,
      "bayesdelnoaf_prediction": "Pathogenic",
      "phylop100way_score": 9.442,
      "phylop100way_prediction": "Pathogenic",
      "spliceai_max_score": 0.06,
      "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": 18,
      "acmg_classification": "Pathogenic",
      "acmg_criteria": "PVS1,PM2,PP5_Very_Strong",
      "acmg_by_gene": [
        {
          "score": 18,
          "benign_score": 0,
          "pathogenic_score": 18,
          "criteria": [
            "PVS1",
            "PM2",
            "PP5_Very_Strong"
          ],
          "verdict": "Pathogenic",
          "transcript": "NM_000051.4",
          "gene_symbol": "ATM",
          "hgnc_id": 795,
          "effects": [
            "stop_gained"
          ],
          "inheritance_mode": "AD,AR",
          "hgvs_c": "c.1463G>A",
          "hgvs_p": "p.Trp488*"
        }
      ],
      "clinvar_disease": "Ataxia-telangiectasia syndrome,Familial cancer of breast,Hereditary cancer-predisposing syndrome,not provided",
      "clinvar_classification": "Pathogenic",
      "clinvar_review_status": "criteria provided, multiple submitters, no conflicts",
      "clinvar_submissions_summary": "P:6",
      "phenotype_combined": "Ataxia-telangiectasia syndrome|not provided|Hereditary cancer-predisposing syndrome|Familial cancer of breast",
      "pathogenicity_classification_combined": "Pathogenic",
      "custom_annotations": null
    }
  ],
  "message": null
}