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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: 18-55234619-AC-A (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=18&pos=55234619&ref=AC&alt=A&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "18",
      "pos": 55234619,
      "ref": "AC",
      "alt": "A",
      "effect": "frameshift_variant",
      "transcript": "ENST00000354452.8",
      "consequences": [
        {
          "aa_ref": "V",
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 16,
          "exon_rank_end": null,
          "exon_count": 20,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TCF4",
          "gene_hgnc_id": 11634,
          "hgvs_c": "c.1414delG",
          "hgvs_p": "p.Val472fs",
          "transcript": "NM_001083962.2",
          "protein_id": "NP_001077431.1",
          "transcript_support_level": null,
          "aa_start": 472,
          "aa_end": null,
          "aa_length": 671,
          "cds_start": 1414,
          "cds_end": null,
          "cds_length": 2016,
          "cdna_start": 1589,
          "cdna_end": null,
          "cdna_length": 8041,
          "mane_select": "ENST00000354452.8",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "V",
          "aa_alt": null,
          "canonical": true,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 16,
          "exon_rank_end": null,
          "exon_count": 20,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TCF4",
          "gene_hgnc_id": 11634,
          "hgvs_c": "c.1414delG",
          "hgvs_p": "p.Val472fs",
          "transcript": "ENST00000354452.8",
          "protein_id": "ENSP00000346440.3",
          "transcript_support_level": 5,
          "aa_start": 472,
          "aa_end": null,
          "aa_length": 671,
          "cds_start": 1414,
          "cds_end": null,
          "cds_length": 2016,
          "cdna_start": 1589,
          "cdna_end": null,
          "cdna_length": 8041,
          "mane_select": "NM_001083962.2",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "V",
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 17,
          "exon_rank_end": null,
          "exon_count": 21,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TCF4",
          "gene_hgnc_id": 11634,
          "hgvs_c": "c.1720delG",
          "hgvs_p": "p.Val574fs",
          "transcript": "ENST00000398339.5",
          "protein_id": "ENSP00000381382.1",
          "transcript_support_level": 1,
          "aa_start": 574,
          "aa_end": null,
          "aa_length": 773,
          "cds_start": 1720,
          "cds_end": null,
          "cds_length": 2322,
          "cdna_start": 1850,
          "cdna_end": null,
          "cdna_length": 2551,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "V",
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 16,
          "exon_rank_end": null,
          "exon_count": 20,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TCF4",
          "gene_hgnc_id": 11634,
          "hgvs_c": "c.1414delG",
          "hgvs_p": "p.Val472fs",
          "transcript": "ENST00000356073.8",
          "protein_id": "ENSP00000348374.4",
          "transcript_support_level": 1,
          "aa_start": 472,
          "aa_end": null,
          "aa_length": 667,
          "cds_start": 1414,
          "cds_end": null,
          "cds_length": 2004,
          "cdna_start": 2026,
          "cdna_end": null,
          "cdna_length": 8317,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "V",
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 15,
          "exon_rank_end": null,
          "exon_count": 19,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TCF4",
          "gene_hgnc_id": 11634,
          "hgvs_c": "c.1405delG",
          "hgvs_p": "p.Val469fs",
          "transcript": "ENST00000566286.5",
          "protein_id": "ENSP00000455418.2",
          "transcript_support_level": 1,
          "aa_start": 469,
          "aa_end": null,
          "aa_length": 664,
          "cds_start": 1405,
          "cds_end": null,
          "cds_length": 1995,
          "cdna_start": 1405,
          "cdna_end": null,
          "cdna_length": 2119,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "V",
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 14,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TCF4",
          "gene_hgnc_id": 11634,
          "hgvs_c": "c.1288delG",
          "hgvs_p": "p.Val430fs",
          "transcript": "ENST00000543082.5",
          "protein_id": "ENSP00000439656.1",
          "transcript_support_level": 1,
          "aa_start": 430,
          "aa_end": null,
          "aa_length": 625,
          "cds_start": 1288,
          "cds_end": null,
          "cds_length": 1878,
          "cdna_start": 1463,
          "cdna_end": null,
          "cdna_length": 2399,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "V",
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 13,
          "exon_rank_end": null,
          "exon_count": 17,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TCF4",
          "gene_hgnc_id": 11634,
          "hgvs_c": "c.1234delG",
          "hgvs_p": "p.Val412fs",
          "transcript": "ENST00000567880.5",
          "protein_id": "ENSP00000454366.1",
          "transcript_support_level": 1,
          "aa_start": 412,
          "aa_end": null,
          "aa_length": 607,
          "cds_start": 1234,
          "cds_end": null,
          "cds_length": 1824,
          "cdna_start": 1234,
          "cdna_end": null,
          "cdna_length": 1948,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "V",
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 12,
          "exon_rank_end": null,
          "exon_count": 16,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TCF4",
          "gene_hgnc_id": 11634,
          "hgvs_c": "c.1201delG",
          "hgvs_p": "p.Val401fs",
          "transcript": "ENST00000564228.5",
          "protein_id": "ENSP00000455261.1",
          "transcript_support_level": 1,
          "aa_start": 401,
          "aa_end": null,
          "aa_length": 596,
          "cds_start": 1201,
          "cds_end": null,
          "cds_length": 1791,
          "cdna_start": 1201,
          "cdna_end": null,
          "cdna_length": 1915,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "V",
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 9,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TCF4",
          "gene_hgnc_id": 11634,
          "hgvs_c": "c.934delG",
          "hgvs_p": "p.Val312fs",
          "transcript": "ENST00000457482.7",
          "protein_id": "ENSP00000409447.2",
          "transcript_support_level": 1,
          "aa_start": 312,
          "aa_end": null,
          "aa_length": 511,
          "cds_start": 934,
          "cds_end": null,
          "cds_length": 1536,
          "cdna_start": 1418,
          "cdna_end": null,
          "cdna_length": 2372,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "V",
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 9,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TCF4",
          "gene_hgnc_id": 11634,
          "hgvs_c": "c.934delG",
          "hgvs_p": "p.Val312fs",
          "transcript": "ENST00000561831.7",
          "protein_id": "ENSP00000457765.1",
          "transcript_support_level": 1,
          "aa_start": 312,
          "aa_end": null,
          "aa_length": 507,
          "cds_start": 934,
          "cds_end": null,
          "cds_length": 1524,
          "cdna_start": 1076,
          "cdna_end": null,
          "cdna_length": 1823,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "V",
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          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 9,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TCF4",
          "gene_hgnc_id": 11634,
          "hgvs_c": "c.934delG",
          "hgvs_p": "p.Val312fs",
          "transcript": "ENST00000570287.6",
          "protein_id": "ENSP00000455763.1",
          "transcript_support_level": 1,
          "aa_start": 312,
          "aa_end": null,
          "aa_length": 507,
          "cds_start": 934,
          "cds_end": null,
          "cds_length": 1524,
          "cdna_start": 1182,
          "cdna_end": null,
          "cdna_length": 3163,
          "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": "TCF4",
          "gene_hgnc_id": 11634,
          "hgvs_c": "n.1505delG",
          "hgvs_p": null,
          "transcript": "ENST00000562680.5",
          "protein_id": null,
          "transcript_support_level": 1,
          "aa_start": null,
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          "aa_length": null,
          "cds_start": -4,
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          "cdna_start": null,
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          "cdna_length": 5733,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
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        },
        {
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          "canonical": false,
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          "strand": false,
          "consequences": [
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          ],
          "exon_rank": 17,
          "exon_rank_end": null,
          "exon_count": 21,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TCF4",
          "gene_hgnc_id": 11634,
          "hgvs_c": "c.1720delG",
          "hgvs_p": "p.Val574fs",
          "transcript": "NM_001243226.3",
          "protein_id": "NP_001230155.2",
          "transcript_support_level": null,
          "aa_start": 574,
          "aa_end": null,
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          "cds_start": 1720,
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          "cdna_start": 1780,
          "cdna_end": null,
          "cdna_length": 8232,
          "mane_select": null,
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          "biotype": null,
          "feature": null
        },
        {
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          "protein_coding": true,
          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 15,
          "exon_rank_end": null,
          "exon_count": 19,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TCF4",
          "gene_hgnc_id": 11634,
          "hgvs_c": "c.1441delG",
          "hgvs_p": "p.Val481fs",
          "transcript": "ENST00000638154.3",
          "protein_id": "ENSP00000490625.2",
          "transcript_support_level": 5,
          "aa_start": 481,
          "aa_end": null,
          "aa_length": 680,
          "cds_start": 1441,
          "cds_end": null,
          "cds_length": 2043,
          "cdna_start": 1644,
          "cdna_end": null,
          "cdna_length": 7946,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "V",
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 16,
          "exon_rank_end": null,
          "exon_count": 20,
          "intron_rank": null,
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          "gene_symbol": "TCF4",
          "gene_hgnc_id": 11634,
          "hgvs_c": "c.1432delG",
          "hgvs_p": "p.Val478fs",
          "transcript": "NM_001243228.2",
          "protein_id": "NP_001230157.1",
          "transcript_support_level": null,
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          "cdna_start": 1967,
          "cdna_end": null,
          "cdna_length": 8419,
          "mane_select": null,
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          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "V",
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          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 16,
          "exon_rank_end": null,
          "exon_count": 20,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TCF4",
          "gene_hgnc_id": 11634,
          "hgvs_c": "c.1432delG",
          "hgvs_p": "p.Val478fs",
          "transcript": "ENST00000564403.6",
          "protein_id": "ENSP00000457263.1",
          "transcript_support_level": 5,
          "aa_start": 478,
          "aa_end": null,
          "aa_length": 677,
          "cds_start": 1432,
          "cds_end": null,
          "cds_length": 2034,
          "cdna_start": 1995,
          "cdna_end": null,
          "cdna_length": 2696,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "V",
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
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          ],
          "exon_rank": 16,
          "exon_rank_end": null,
          "exon_count": 20,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TCF4",
          "gene_hgnc_id": 11634,
          "hgvs_c": "c.1414delG",
          "hgvs_p": "p.Val472fs",
          "transcript": "NM_001369567.1",
          "protein_id": "NP_001356496.1",
          "transcript_support_level": null,
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          "cds_start": 1414,
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          "cdna_start": 1949,
          "cdna_end": null,
          "cdna_length": 8401,
          "mane_select": null,
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          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "V",
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          "canonical": false,
          "protein_coding": true,
          "strand": false,
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            "frameshift_variant"
          ],
          "exon_rank": 16,
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          "exon_count": 20,
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          "intron_rank_end": null,
          "gene_symbol": "TCF4",
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          "hgvs_c": "c.1414delG",
          "hgvs_p": "p.Val472fs",
          "transcript": "NM_001369568.1",
          "protein_id": "NP_001356497.1",
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          "cdna_end": null,
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          "biotype": null,
          "feature": null
        },
        {
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          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 16,
          "exon_rank_end": null,
          "exon_count": 20,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TCF4",
          "gene_hgnc_id": 11634,
          "hgvs_c": "c.1414delG",
          "hgvs_p": "p.Val472fs",
          "transcript": "ENST00000629387.2",
          "protein_id": "ENSP00000486670.1",
          "transcript_support_level": 5,
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          "cds_start": 1414,
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          "cds_length": 2016,
          "cdna_start": 1945,
          "cdna_end": null,
          "cdna_length": 3789,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "V",
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 16,
          "exon_rank_end": null,
          "exon_count": 20,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TCF4",
          "gene_hgnc_id": 11634,
          "hgvs_c": "c.1411delG",
          "hgvs_p": "p.Val471fs",
          "transcript": "NM_001330604.3",
          "protein_id": "NP_001317533.1",
          "transcript_support_level": null,
          "aa_start": 471,
          "aa_end": null,
          "aa_length": 670,
          "cds_start": 1411,
          "cds_end": null,
          "cds_length": 2013,
          "cdna_start": 1586,
          "cdna_end": null,
          "cdna_length": 8038,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "V",
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 16,
          "exon_rank_end": null,
          "exon_count": 20,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TCF4",
          "gene_hgnc_id": 11634,
          "hgvs_c": "c.1411delG",
          "hgvs_p": "p.Val471fs",
          "transcript": "NM_001369569.1",
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        },
        {
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          "protein_coding": false,
          "strand": false,
          "consequences": [
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          "exon_rank": 10,
          "exon_rank_end": null,
          "exon_count": 14,
          "intron_rank": null,
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          "hgvs_c": "n.*714delG",
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        },
        {
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          "protein_coding": false,
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          "consequences": [
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          "exon_rank": 13,
          "exon_rank_end": null,
          "exon_count": 17,
          "intron_rank": null,
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          "gene_symbol": "TCF4",
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          "hgvs_c": "n.*1025delG",
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          "transcript": "ENST00000674764.1",
          "protein_id": "ENSP00000502213.1",
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          "cdna_length": 2057,
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          "feature": null
        },
        {
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          "protein_coding": false,
          "strand": false,
          "consequences": [
            "3_prime_UTR_variant"
          ],
          "exon_rank": 16,
          "exon_rank_end": null,
          "exon_count": 20,
          "intron_rank": null,
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          "gene_symbol": "TCF4",
          "gene_hgnc_id": 11634,
          "hgvs_c": "n.*1122delG",
          "hgvs_p": null,
          "transcript": "ENST00000636751.2",
          "protein_id": "ENSP00000489783.1",
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          "aa_start": null,
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          "cdna_start": null,
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        },
        {
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          "protein_coding": false,
          "strand": false,
          "consequences": [
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          ],
          "exon_rank": 17,
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          "exon_count": 21,
          "intron_rank": null,
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          "gene_symbol": "TCF4",
          "gene_hgnc_id": 11634,
          "hgvs_c": "n.*1304delG",
          "hgvs_p": null,
          "transcript": "ENST00000637115.2",
          "protein_id": "ENSP00000490234.1",
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          "cdna_length": 7883,
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          "feature": null
        },
        {
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          "protein_coding": false,
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          "consequences": [
            "3_prime_UTR_variant"
          ],
          "exon_rank": 10,
          "exon_rank_end": null,
          "exon_count": 14,
          "intron_rank": null,
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          "gene_symbol": "TCF4",
          "gene_hgnc_id": 11634,
          "hgvs_c": "n.*714delG",
          "hgvs_p": null,
          "transcript": "ENST00000637923.2",
          "protein_id": "ENSP00000490329.1",
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          "feature": null
        },
        {
          "aa_ref": null,
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          "protein_coding": false,
          "strand": false,
          "consequences": [
            "3_prime_UTR_variant"
          ],
          "exon_rank": 13,
          "exon_rank_end": null,
          "exon_count": 17,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TCF4",
          "gene_hgnc_id": 11634,
          "hgvs_c": "n.*1025delG",
          "hgvs_p": null,
          "transcript": "ENST00000674764.1",
          "protein_id": "ENSP00000502213.1",
          "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": 2057,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        }
      ],
      "gene_symbol": "TCF4",
      "gene_hgnc_id": 11634,
      "dbsnp": "rs727504174",
      "frequency_reference_population": null,
      "hom_count_reference_population": 0,
      "allele_count_reference_population": 0,
      "gnomad_exomes_af": null,
      "gnomad_genomes_af": null,
      "gnomad_exomes_ac": null,
      "gnomad_genomes_ac": null,
      "gnomad_exomes_homalt": null,
      "gnomad_genomes_homalt": null,
      "gnomad_mito_homoplasmic": null,
      "gnomad_mito_heteroplasmic": null,
      "computational_score_selected": null,
      "computational_prediction_selected": null,
      "computational_source_selected": null,
      "splice_score_selected": 0,
      "splice_prediction_selected": "Benign",
      "splice_source_selected": "max_spliceai",
      "revel_score": null,
      "revel_prediction": null,
      "alphamissense_score": null,
      "alphamissense_prediction": null,
      "bayesdelnoaf_score": null,
      "bayesdelnoaf_prediction": null,
      "phylop100way_score": 6.472,
      "phylop100way_prediction": "Uncertain_significance",
      "spliceai_max_score": 0,
      "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": 12,
      "acmg_classification": "Pathogenic",
      "acmg_criteria": "PVS1,PM2,PP5_Moderate",
      "acmg_by_gene": [
        {
          "score": 12,
          "benign_score": 0,
          "pathogenic_score": 12,
          "criteria": [
            "PVS1",
            "PM2",
            "PP5_Moderate"
          ],
          "verdict": "Pathogenic",
          "transcript": "ENST00000354452.8",
          "gene_symbol": "TCF4",
          "hgnc_id": 11634,
          "effects": [
            "frameshift_variant"
          ],
          "inheritance_mode": "AD",
          "hgvs_c": "c.1414delG",
          "hgvs_p": "p.Val472fs"
        }
      ],
      "clinvar_disease": "not provided",
      "clinvar_classification": "Pathogenic",
      "clinvar_review_status": "criteria provided, single submitter",
      "clinvar_submissions_summary": "P:1",
      "phenotype_combined": "not provided",
      "pathogenicity_classification_combined": "Pathogenic",
      "custom_annotations": null
    }
  ],
  "message": null
}