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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: 17-5514787-G-A (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=17&pos=5514787&ref=G&alt=A&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "17",
      "pos": 5514787,
      "ref": "G",
      "alt": "A",
      "effect": "synonymous_variant",
      "transcript": "NM_033004.4",
      "consequences": [
        {
          "aa_ref": "G",
          "aa_alt": "G",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 17,
          "exon_rank_end": null,
          "exon_count": 17,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "NLRP1",
          "gene_hgnc_id": 14374,
          "hgvs_c": "c.4389C>T",
          "hgvs_p": "p.Gly1463Gly",
          "transcript": "NM_033004.4",
          "protein_id": "NP_127497.1",
          "transcript_support_level": null,
          "aa_start": 1463,
          "aa_end": null,
          "aa_length": 1473,
          "cds_start": 4389,
          "cds_end": null,
          "cds_length": 4422,
          "cdna_start": 4941,
          "cdna_end": null,
          "cdna_length": 5610,
          "mane_select": "ENST00000572272.6",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "G",
          "aa_alt": "G",
          "canonical": true,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 17,
          "exon_rank_end": null,
          "exon_count": 17,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "NLRP1",
          "gene_hgnc_id": 14374,
          "hgvs_c": "c.4389C>T",
          "hgvs_p": "p.Gly1463Gly",
          "transcript": "ENST00000572272.6",
          "protein_id": "ENSP00000460475.1",
          "transcript_support_level": 1,
          "aa_start": 1463,
          "aa_end": null,
          "aa_length": 1473,
          "cds_start": 4389,
          "cds_end": null,
          "cds_length": 4422,
          "cdna_start": 4941,
          "cdna_end": null,
          "cdna_length": 5610,
          "mane_select": "NM_033004.4",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "G",
          "aa_alt": "G",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 16,
          "exon_rank_end": null,
          "exon_count": 16,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "NLRP1",
          "gene_hgnc_id": 14374,
          "hgvs_c": "c.4299C>T",
          "hgvs_p": "p.Gly1433Gly",
          "transcript": "ENST00000354411.8",
          "protein_id": "ENSP00000346390.3",
          "transcript_support_level": 1,
          "aa_start": 1433,
          "aa_end": null,
          "aa_length": 1443,
          "cds_start": 4299,
          "cds_end": null,
          "cds_length": 4332,
          "cdna_start": 4299,
          "cdna_end": null,
          "cdna_length": 4780,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "G",
          "aa_alt": "G",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 17,
          "exon_rank_end": null,
          "exon_count": 17,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "NLRP1",
          "gene_hgnc_id": 14374,
          "hgvs_c": "c.4257C>T",
          "hgvs_p": "p.Gly1419Gly",
          "transcript": "ENST00000269280.9",
          "protein_id": "ENSP00000269280.4",
          "transcript_support_level": 1,
          "aa_start": 1419,
          "aa_end": null,
          "aa_length": 1429,
          "cds_start": 4257,
          "cds_end": null,
          "cds_length": 4290,
          "cdna_start": 4476,
          "cdna_end": null,
          "cdna_length": 5136,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "G",
          "aa_alt": "G",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 16,
          "exon_rank_end": null,
          "exon_count": 16,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "NLRP1",
          "gene_hgnc_id": 14374,
          "hgvs_c": "c.4257C>T",
          "hgvs_p": "p.Gly1419Gly",
          "transcript": "ENST00000571451.7",
          "protein_id": "ENSP00000459661.3",
          "transcript_support_level": 1,
          "aa_start": 1419,
          "aa_end": null,
          "aa_length": 1429,
          "cds_start": 4257,
          "cds_end": null,
          "cds_length": 4290,
          "cdna_start": 4779,
          "cdna_end": null,
          "cdna_length": 5450,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "G",
          "aa_alt": "G",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 15,
          "exon_rank_end": null,
          "exon_count": 15,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "NLRP1",
          "gene_hgnc_id": 14374,
          "hgvs_c": "c.4167C>T",
          "hgvs_p": "p.Gly1389Gly",
          "transcript": "ENST00000577119.5",
          "protein_id": "ENSP00000460216.1",
          "transcript_support_level": 1,
          "aa_start": 1389,
          "aa_end": null,
          "aa_length": 1399,
          "cds_start": 4167,
          "cds_end": null,
          "cds_length": 4200,
          "cdna_start": 4167,
          "cdna_end": null,
          "cdna_length": 4200,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 2,
          "intron_rank": 1,
          "intron_rank_end": null,
          "gene_symbol": "NLRP1",
          "gene_hgnc_id": 14374,
          "hgvs_c": "n.820+2959C>T",
          "hgvs_p": null,
          "transcript": "ENST00000574512.1",
          "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": 4506,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "G",
          "aa_alt": "G",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 17,
          "exon_rank_end": null,
          "exon_count": 17,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "NLRP1",
          "gene_hgnc_id": 14374,
          "hgvs_c": "c.4401C>T",
          "hgvs_p": "p.Gly1467Gly",
          "transcript": "ENST00000699633.1",
          "protein_id": "ENSP00000514491.1",
          "transcript_support_level": null,
          "aa_start": 1467,
          "aa_end": null,
          "aa_length": 1477,
          "cds_start": 4401,
          "cds_end": null,
          "cds_length": 4434,
          "cdna_start": 4946,
          "cdna_end": null,
          "cdna_length": 5606,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "G",
          "aa_alt": "G",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 18,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "NLRP1",
          "gene_hgnc_id": 14374,
          "hgvs_c": "c.4389C>T",
          "hgvs_p": "p.Gly1463Gly",
          "transcript": "ENST00000617618.5",
          "protein_id": "ENSP00000478516.1",
          "transcript_support_level": 5,
          "aa_start": 1463,
          "aa_end": null,
          "aa_length": 1473,
          "cds_start": 4389,
          "cds_end": null,
          "cds_length": 4422,
          "cdna_start": 4755,
          "cdna_end": null,
          "cdna_length": 5419,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "G",
          "aa_alt": "G",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 16,
          "exon_rank_end": null,
          "exon_count": 16,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "NLRP1",
          "gene_hgnc_id": 14374,
          "hgvs_c": "c.4299C>T",
          "hgvs_p": "p.Gly1433Gly",
          "transcript": "NM_033006.4",
          "protein_id": "NP_127499.1",
          "transcript_support_level": null,
          "aa_start": 1433,
          "aa_end": null,
          "aa_length": 1443,
          "cds_start": 4299,
          "cds_end": null,
          "cds_length": 4332,
          "cdna_start": 4851,
          "cdna_end": null,
          "cdna_length": 5520,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "G",
          "aa_alt": "G",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 16,
          "exon_rank_end": null,
          "exon_count": 16,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "NLRP1",
          "gene_hgnc_id": 14374,
          "hgvs_c": "c.4257C>T",
          "hgvs_p": "p.Gly1419Gly",
          "transcript": "NM_014922.5",
          "protein_id": "NP_055737.1",
          "transcript_support_level": null,
          "aa_start": 1419,
          "aa_end": null,
          "aa_length": 1429,
          "cds_start": 4257,
          "cds_end": null,
          "cds_length": 4290,
          "cdna_start": 4809,
          "cdna_end": null,
          "cdna_length": 5478,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "G",
          "aa_alt": "G",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 18,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "NLRP1",
          "gene_hgnc_id": 14374,
          "hgvs_c": "c.4257C>T",
          "hgvs_p": "p.Gly1419Gly",
          "transcript": "ENST00000576905.6",
          "protein_id": "ENSP00000458303.2",
          "transcript_support_level": 4,
          "aa_start": 1419,
          "aa_end": null,
          "aa_length": 1429,
          "cds_start": 4257,
          "cds_end": null,
          "cds_length": 4290,
          "cdna_start": 4705,
          "cdna_end": null,
          "cdna_length": 5337,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "G",
          "aa_alt": "G",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 15,
          "exon_rank_end": null,
          "exon_count": 15,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "NLRP1",
          "gene_hgnc_id": 14374,
          "hgvs_c": "c.4167C>T",
          "hgvs_p": "p.Gly1389Gly",
          "transcript": "NM_033007.4",
          "protein_id": "NP_127500.1",
          "transcript_support_level": null,
          "aa_start": 1389,
          "aa_end": null,
          "aa_length": 1399,
          "cds_start": 4167,
          "cds_end": null,
          "cds_length": 4200,
          "cdna_start": 4719,
          "cdna_end": null,
          "cdna_length": 5388,
          "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": 15,
          "exon_rank_end": null,
          "exon_count": 15,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "NLRP1",
          "gene_hgnc_id": 14374,
          "hgvs_c": "n.*1162C>T",
          "hgvs_p": null,
          "transcript": "ENST00000699586.1",
          "protein_id": "ENSP00000514458.1",
          "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": 5424,
          "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": 18,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "NLRP1",
          "gene_hgnc_id": 14374,
          "hgvs_c": "n.*2107C>T",
          "hgvs_p": null,
          "transcript": "ENST00000699615.1",
          "protein_id": "ENSP00000514479.1",
          "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": 5669,
          "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": 17,
          "exon_rank_end": null,
          "exon_count": 20,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "NLRP1",
          "gene_hgnc_id": 14374,
          "hgvs_c": "n.*1770C>T",
          "hgvs_p": null,
          "transcript": "ENST00000699629.1",
          "protein_id": "ENSP00000514488.1",
          "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": 7294,
          "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": 17,
          "exon_rank_end": null,
          "exon_count": 17,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "NLRP1",
          "gene_hgnc_id": 14374,
          "hgvs_c": "n.*1741C>T",
          "hgvs_p": null,
          "transcript": "ENST00000699632.1",
          "protein_id": "ENSP00000514490.1",
          "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": 5132,
          "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": 10,
          "exon_rank_end": null,
          "exon_count": 10,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "NLRP1",
          "gene_hgnc_id": 14374,
          "hgvs_c": "n.1551C>T",
          "hgvs_p": null,
          "transcript": "ENST00000699635.1",
          "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": 2068,
          "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": 15,
          "exon_rank_end": null,
          "exon_count": 15,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "NLRP1",
          "gene_hgnc_id": 14374,
          "hgvs_c": "n.7104C>T",
          "hgvs_p": null,
          "transcript": "ENST00000699636.1",
          "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": 7620,
          "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": 18,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "NLRP1",
          "gene_hgnc_id": 14374,
          "hgvs_c": "n.*3574C>T",
          "hgvs_p": null,
          "transcript": "ENST00000699642.1",
          "protein_id": "ENSP00000514495.1",
          "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": 5238,
          "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": 18,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "NLRP1",
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        },
        {
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          "exon_rank": null,
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          "exon_count": 11,
          "intron_rank": 8,
          "intron_rank_end": null,
          "gene_symbol": "NLRP1",
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          "hgvs_p": null,
          "transcript": "ENST00000699771.1",
          "protein_id": "ENSP00000514577.1",
          "transcript_support_level": null,
          "aa_start": null,
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          "cds_start": -4,
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          "cds_length": null,
          "cdna_start": null,
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        {
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          ],
          "exon_rank": null,
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          "exon_count": 7,
          "intron_rank": 5,
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          "gene_symbol": "NLRP1",
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          "hgvs_c": "n.*698+2959C>T",
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          "transcript": "ENST00000699772.1",
          "protein_id": "ENSP00000514578.1",
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          "cdna_length": 1620,
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        },
        {
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            "intron_variant"
          ],
          "exon_rank": null,
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          "exon_count": 8,
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          "gene_symbol": "NLRP1",
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          "hgvs_c": "n.805+686C>T",
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          "transcript": "ENST00000699773.1",
          "protein_id": "ENSP00000514579.1",
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          "aa_start": null,
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          "cdna_length": 1529,
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        },
        {
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          ],
          "exon_rank": null,
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          "exon_count": 3,
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          "gene_symbol": "NLRP1",
          "gene_hgnc_id": 14374,
          "hgvs_c": "n.142+2959C>T",
          "hgvs_p": null,
          "transcript": "ENST00000699802.1",
          "protein_id": "ENSP00000514605.1",
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          "cds_length": null,
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          "cdna_length": 408,
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        }
      ],
      "gene_symbol": "NLRP1",
      "gene_hgnc_id": 14374,
      "dbsnp": "rs74929853",
      "frequency_reference_population": 0.0137101235,
      "hom_count_reference_population": 1729,
      "allele_count_reference_population": 22126,
      "gnomad_exomes_af": 0.013998,
      "gnomad_genomes_af": 0.0109457,
      "gnomad_exomes_ac": 20460,
      "gnomad_genomes_ac": 1666,
      "gnomad_exomes_homalt": 1602,
      "gnomad_genomes_homalt": 127,
      "gnomad_mito_homoplasmic": null,
      "gnomad_mito_heteroplasmic": null,
      "computational_score_selected": -0.9100000262260437,
      "computational_prediction_selected": "Benign",
      "computational_source_selected": "BayesDel_noAF",
      "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": -0.91,
      "bayesdelnoaf_prediction": "Benign",
      "phylop100way_score": -1.002,
      "phylop100way_prediction": "Benign",
      "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": -21,
      "acmg_classification": "Benign",
      "acmg_criteria": "BP4_Strong,BP6_Very_Strong,BP7,BA1",
      "acmg_by_gene": [
        {
          "score": -21,
          "benign_score": 21,
          "pathogenic_score": 0,
          "criteria": [
            "BP4_Strong",
            "BP6_Very_Strong",
            "BP7",
            "BA1"
          ],
          "verdict": "Benign",
          "transcript": "NM_033004.4",
          "gene_symbol": "NLRP1",
          "hgnc_id": 14374,
          "effects": [
            "synonymous_variant"
          ],
          "inheritance_mode": "AD,AR,SD",
          "hgvs_c": "c.4389C>T",
          "hgvs_p": "p.Gly1463Gly"
        }
      ],
      "clinvar_disease": "not provided",
      "clinvar_classification": "Benign",
      "clinvar_review_status": "criteria provided, multiple submitters, no conflicts",
      "clinvar_submissions_summary": "B:2",
      "phenotype_combined": "not provided",
      "pathogenicity_classification_combined": "Benign",
      "custom_annotations": null
    }
  ],
  "message": null
}