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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: 11-34651570-C-T (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=11&pos=34651570&ref=C&alt=T&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "11",
      "pos": 34651570,
      "ref": "C",
      "alt": "T",
      "effect": "synonymous_variant",
      "transcript": "NM_001206616.2",
      "consequences": [
        {
          "aa_ref": "D",
          "aa_alt": "D",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 5,
          "exon_rank_end": null,
          "exon_count": 9,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "EHF",
          "gene_hgnc_id": 3246,
          "hgvs_c": "c.435C>T",
          "hgvs_p": "p.Asp145Asp",
          "transcript": "NM_012153.6",
          "protein_id": "NP_036285.2",
          "transcript_support_level": null,
          "aa_start": 145,
          "aa_end": null,
          "aa_length": 300,
          "cds_start": 435,
          "cds_end": null,
          "cds_length": 903,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": "ENST00000257831.8",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_012153.6"
        },
        {
          "aa_ref": "D",
          "aa_alt": "D",
          "canonical": true,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 5,
          "exon_rank_end": null,
          "exon_count": 9,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "EHF",
          "gene_hgnc_id": 3246,
          "hgvs_c": "c.435C>T",
          "hgvs_p": "p.Asp145Asp",
          "transcript": "ENST00000257831.8",
          "protein_id": "ENSP00000257831.3",
          "transcript_support_level": 1,
          "aa_start": 145,
          "aa_end": null,
          "aa_length": 300,
          "cds_start": 435,
          "cds_end": null,
          "cds_length": 903,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": "NM_012153.6",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000257831.8"
        },
        {
          "aa_ref": "D",
          "aa_alt": "D",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 5,
          "exon_rank_end": null,
          "exon_count": 9,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "EHF",
          "gene_hgnc_id": 3246,
          "hgvs_c": "c.501C>T",
          "hgvs_p": "p.Asp167Asp",
          "transcript": "ENST00000531794.5",
          "protein_id": "ENSP00000435835.1",
          "transcript_support_level": 1,
          "aa_start": 167,
          "aa_end": null,
          "aa_length": 322,
          "cds_start": 501,
          "cds_end": null,
          "cds_length": 969,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000531794.5"
        },
        {
          "aa_ref": "D",
          "aa_alt": "D",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 5,
          "exon_rank_end": null,
          "exon_count": 9,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "EHF",
          "gene_hgnc_id": 3246,
          "hgvs_c": "c.435C>T",
          "hgvs_p": "p.Asp145Asp",
          "transcript": "ENST00000530286.5",
          "protein_id": "ENSP00000433508.1",
          "transcript_support_level": 1,
          "aa_start": 145,
          "aa_end": null,
          "aa_length": 300,
          "cds_start": 435,
          "cds_end": null,
          "cds_length": 903,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000530286.5"
        },
        {
          "aa_ref": "D",
          "aa_alt": "D",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 5,
          "exon_rank_end": null,
          "exon_count": 9,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "EHF",
          "gene_hgnc_id": 3246,
          "hgvs_c": "c.435C>T",
          "hgvs_p": "p.Asp145Asp",
          "transcript": "ENST00000533754.5",
          "protein_id": "ENSP00000435837.1",
          "transcript_support_level": 1,
          "aa_start": 145,
          "aa_end": null,
          "aa_length": 300,
          "cds_start": 435,
          "cds_end": null,
          "cds_length": 903,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000533754.5"
        },
        {
          "aa_ref": "D",
          "aa_alt": "D",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 5,
          "exon_rank_end": null,
          "exon_count": 8,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "EHF",
          "gene_hgnc_id": 3246,
          "hgvs_c": "c.435C>T",
          "hgvs_p": "p.Asp145Asp",
          "transcript": "ENST00000450654.6",
          "protein_id": "ENSP00000399733.2",
          "transcript_support_level": 1,
          "aa_start": 145,
          "aa_end": null,
          "aa_length": 277,
          "cds_start": 435,
          "cds_end": null,
          "cds_length": 834,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000450654.6"
        },
        {
          "aa_ref": "D",
          "aa_alt": "D",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 5,
          "exon_rank_end": null,
          "exon_count": 9,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "EHF",
          "gene_hgnc_id": 3246,
          "hgvs_c": "c.501C>T",
          "hgvs_p": "p.Asp167Asp",
          "transcript": "NM_001206616.2",
          "protein_id": "NP_001193545.1",
          "transcript_support_level": null,
          "aa_start": 167,
          "aa_end": null,
          "aa_length": 322,
          "cds_start": 501,
          "cds_end": null,
          "cds_length": 969,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001206616.2"
        },
        {
          "aa_ref": "D",
          "aa_alt": "D",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 5,
          "exon_rank_end": null,
          "exon_count": 9,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "EHF",
          "gene_hgnc_id": 3246,
          "hgvs_c": "c.501C>T",
          "hgvs_p": "p.Asp167Asp",
          "transcript": "NM_001378052.1",
          "protein_id": "NP_001364981.1",
          "transcript_support_level": null,
          "aa_start": 167,
          "aa_end": null,
          "aa_length": 321,
          "cds_start": 501,
          "cds_end": null,
          "cds_length": 966,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001378052.1"
        },
        {
          "aa_ref": "D",
          "aa_alt": "D",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 5,
          "exon_rank_end": null,
          "exon_count": 9,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "EHF",
          "gene_hgnc_id": 3246,
          "hgvs_c": "c.444C>T",
          "hgvs_p": "p.Asp148Asp",
          "transcript": "NM_001378053.1",
          "protein_id": "NP_001364982.1",
          "transcript_support_level": null,
          "aa_start": 148,
          "aa_end": null,
          "aa_length": 303,
          "cds_start": 444,
          "cds_end": null,
          "cds_length": 912,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001378053.1"
        },
        {
          "aa_ref": "D",
          "aa_alt": "D",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 6,
          "exon_rank_end": null,
          "exon_count": 10,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "EHF",
          "gene_hgnc_id": 3246,
          "hgvs_c": "c.435C>T",
          "hgvs_p": "p.Asp145Asp",
          "transcript": "NM_001378041.1",
          "protein_id": "NP_001364970.1",
          "transcript_support_level": null,
          "aa_start": 145,
          "aa_end": null,
          "aa_length": 300,
          "cds_start": 435,
          "cds_end": null,
          "cds_length": 903,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001378041.1"
        },
        {
          "aa_ref": "D",
          "aa_alt": "D",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 5,
          "exon_rank_end": null,
          "exon_count": 9,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "EHF",
          "gene_hgnc_id": 3246,
          "hgvs_c": "c.435C>T",
          "hgvs_p": "p.Asp145Asp",
          "transcript": "NM_001378042.1",
          "protein_id": "NP_001364971.1",
          "transcript_support_level": null,
          "aa_start": 145,
          "aa_end": null,
          "aa_length": 300,
          "cds_start": 435,
          "cds_end": null,
          "cds_length": 903,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001378042.1"
        },
        {
          "aa_ref": "D",
          "aa_alt": "D",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 6,
          "exon_rank_end": null,
          "exon_count": 10,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "EHF",
          "gene_hgnc_id": 3246,
          "hgvs_c": "c.435C>T",
          "hgvs_p": "p.Asp145Asp",
          "transcript": "NM_001378043.1",
          "protein_id": "NP_001364972.1",
          "transcript_support_level": null,
          "aa_start": 145,
          "aa_end": null,
          "aa_length": 300,
          "cds_start": 435,
          "cds_end": null,
          "cds_length": 903,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001378043.1"
        },
        {
          "aa_ref": "D",
          "aa_alt": "D",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 5,
          "exon_rank_end": null,
          "exon_count": 9,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "EHF",
          "gene_hgnc_id": 3246,
          "hgvs_c": "c.435C>T",
          "hgvs_p": "p.Asp145Asp",
          "transcript": "NM_001378044.1",
          "protein_id": "NP_001364973.1",
          "transcript_support_level": null,
          "aa_start": 145,
          "aa_end": null,
          "aa_length": 300,
          "cds_start": 435,
          "cds_end": null,
          "cds_length": 903,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001378044.1"
        },
        {
          "aa_ref": "D",
          "aa_alt": "D",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 5,
          "exon_rank_end": null,
          "exon_count": 9,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "EHF",
          "gene_hgnc_id": 3246,
          "hgvs_c": "c.435C>T",
          "hgvs_p": "p.Asp145Asp",
          "transcript": "NM_001378045.1",
          "protein_id": "NP_001364974.1",
          "transcript_support_level": null,
          "aa_start": 145,
          "aa_end": null,
          "aa_length": 300,
          "cds_start": 435,
          "cds_end": null,
          "cds_length": 903,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001378045.1"
        },
        {
          "aa_ref": "D",
          "aa_alt": "D",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 5,
          "exon_rank_end": null,
          "exon_count": 9,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "EHF",
          "gene_hgnc_id": 3246,
          "hgvs_c": "c.435C>T",
          "hgvs_p": "p.Asp145Asp",
          "transcript": "NM_001378046.1",
          "protein_id": "NP_001364975.1",
          "transcript_support_level": null,
          "aa_start": 145,
          "aa_end": null,
          "aa_length": 300,
          "cds_start": 435,
          "cds_end": null,
          "cds_length": 903,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001378046.1"
        },
        {
          "aa_ref": "D",
          "aa_alt": "D",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 5,
          "exon_rank_end": null,
          "exon_count": 9,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "EHF",
          "gene_hgnc_id": 3246,
          "hgvs_c": "c.435C>T",
          "hgvs_p": "p.Asp145Asp",
          "transcript": "NM_001378047.1",
          "protein_id": "NP_001364976.1",
          "transcript_support_level": null,
          "aa_start": 145,
          "aa_end": null,
          "aa_length": 300,
          "cds_start": 435,
          "cds_end": null,
          "cds_length": 903,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001378047.1"
        },
        {
          "aa_ref": "D",
          "aa_alt": "D",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 5,
          "exon_rank_end": null,
          "exon_count": 9,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "EHF",
          "gene_hgnc_id": 3246,
          "hgvs_c": "c.435C>T",
          "hgvs_p": "p.Asp145Asp",
          "transcript": "ENST00000907181.1",
          "protein_id": "ENSP00000577240.1",
          "transcript_support_level": null,
          "aa_start": 145,
          "aa_end": null,
          "aa_length": 300,
          "cds_start": 435,
          "cds_end": null,
          "cds_length": 903,
          "cdna_start": null,
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          "cdna_length": null,
          "mane_select": null,
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          "biotype": "protein_coding",
          "feature": "ENST00000907181.1"
        },
        {
          "aa_ref": "D",
          "aa_alt": "D",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 6,
          "exon_rank_end": null,
          "exon_count": 10,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "EHF",
          "gene_hgnc_id": 3246,
          "hgvs_c": "c.435C>T",
          "hgvs_p": "p.Asp145Asp",
          "transcript": "ENST00000907182.1",
          "protein_id": "ENSP00000577241.1",
          "transcript_support_level": null,
          "aa_start": 145,
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          "aa_length": 300,
          "cds_start": 435,
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          "cdna_start": null,
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          "mane_select": null,
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          "biotype": "protein_coding",
          "feature": "ENST00000907182.1"
        },
        {
          "aa_ref": "D",
          "aa_alt": "D",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 6,
          "exon_rank_end": null,
          "exon_count": 10,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "EHF",
          "gene_hgnc_id": 3246,
          "hgvs_c": "c.435C>T",
          "hgvs_p": "p.Asp145Asp",
          "transcript": "ENST00000907185.1",
          "protein_id": "ENSP00000577244.1",
          "transcript_support_level": null,
          "aa_start": 145,
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          "aa_length": 300,
          "cds_start": 435,
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          "cds_length": 903,
          "cdna_start": null,
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          "mane_select": null,
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          "biotype": "protein_coding",
          "feature": "ENST00000907185.1"
        },
        {
          "aa_ref": "D",
          "aa_alt": "D",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 5,
          "exon_rank_end": null,
          "exon_count": 9,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "EHF",
          "gene_hgnc_id": 3246,
          "hgvs_c": "c.435C>T",
          "hgvs_p": "p.Asp145Asp",
          "transcript": "ENST00000907188.1",
          "protein_id": "ENSP00000577247.1",
          "transcript_support_level": null,
          "aa_start": 145,
          "aa_end": null,
          "aa_length": 300,
          "cds_start": 435,
          "cds_end": null,
          "cds_length": 903,
          "cdna_start": null,
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          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000907188.1"
        },
        {
          "aa_ref": "D",
          "aa_alt": "D",
          "canonical": false,
          "protein_coding": true,
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        {
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          "protein_coding": false,
          "strand": true,
          "consequences": [
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          "exon_count": 8,
          "intron_rank": null,
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        },
        {
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          "exon_count": 6,
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          "gene_symbol": "ENSG00000309708",
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          "hgvs_c": "n.745-212G>A",
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          "transcript": "ENST00000843229.1",
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        {
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          "gene_symbol": "ENSG00000309708",
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          "hgvs_c": "n.618-212G>A",
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        {
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          "strand": false,
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          "exon_count": 4,
          "intron_rank": 3,
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          "gene_symbol": "ENSG00000309708",
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          "biotype": "pseudogene",
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        },
        {
          "aa_ref": null,
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          "protein_coding": false,
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          ],
          "exon_rank": null,
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          "exon_count": 5,
          "intron_rank": 4,
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          "gene_symbol": "ENSG00000309708",
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          "hgvs_c": "n.324-4824G>A",
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          "transcript": "ENST00000843232.1",
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          "mane_select": null,
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          "biotype": "pseudogene",
          "feature": "ENST00000843232.1"
        },
        {
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          "protein_coding": false,
          "strand": false,
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            "intron_variant"
          ],
          "exon_rank": null,
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          "exon_count": 4,
          "intron_rank": 3,
          "intron_rank_end": null,
          "gene_symbol": "ENSG00000309708",
          "gene_hgnc_id": null,
          "hgvs_c": "n.258-212G>A",
          "hgvs_p": null,
          "transcript": "ENST00000843233.1",
          "protein_id": null,
          "transcript_support_level": null,
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          "aa_length": null,
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          "cds_length": null,
          "cdna_start": null,
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          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "pseudogene",
          "feature": "ENST00000843233.1"
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      ],
      "gene_symbol": "EHF",
      "gene_hgnc_id": 3246,
      "dbsnp": "rs149874101",
      "frequency_reference_population": 0.000039036117,
      "hom_count_reference_population": 0,
      "allele_count_reference_population": 63,
      "gnomad_exomes_af": 0.0000376288,
      "gnomad_genomes_af": 0.0000525479,
      "gnomad_exomes_ac": 55,
      "gnomad_genomes_ac": 8,
      "gnomad_exomes_homalt": 0,
      "gnomad_genomes_homalt": 0,
      "gnomad_mito_homoplasmic": null,
      "gnomad_mito_heteroplasmic": null,
      "computational_score_selected": -0.4099999964237213,
      "computational_prediction_selected": "Benign",
      "computational_source_selected": "BayesDel_noAF",
      "splice_score_selected": 0.009999999776482582,
      "splice_prediction_selected": "Benign",
      "splice_source_selected": "max_spliceai",
      "revel_score": null,
      "revel_prediction": null,
      "alphamissense_score": null,
      "alphamissense_prediction": null,
      "bayesdelnoaf_score": -0.41,
      "bayesdelnoaf_prediction": "Benign",
      "phylop100way_score": 0.642,
      "phylop100way_prediction": "Benign",
      "spliceai_max_score": 0.01,
      "spliceai_max_prediction": "Benign",
      "dbscsnv_ada_score": null,
      "dbscsnv_ada_prediction": null,
      "apogee2_score": null,
      "apogee2_prediction": null,
      "mitotip_score": null,
      "mitotip_prediction": null,
      "acmg_score": -9,
      "acmg_classification": "Benign",
      "acmg_criteria": "BP4_Moderate,BP6_Moderate,BP7,BS2",
      "acmg_by_gene": [
        {
          "score": -9,
          "benign_score": 9,
          "pathogenic_score": 0,
          "criteria": [
            "BP4_Moderate",
            "BP6_Moderate",
            "BP7",
            "BS2"
          ],
          "verdict": "Benign",
          "transcript": "NM_001206616.2",
          "gene_symbol": "EHF",
          "hgnc_id": 3246,
          "effects": [
            "synonymous_variant"
          ],
          "inheritance_mode": "AD",
          "hgvs_c": "c.501C>T",
          "hgvs_p": "p.Asp167Asp"
        },
        {
          "score": -2,
          "benign_score": 4,
          "pathogenic_score": 2,
          "criteria": [
            "PM2",
            "BP4_Moderate",
            "BP6_Moderate"
          ],
          "verdict": "Likely_benign",
          "transcript": "ENST00000843245.1",
          "gene_symbol": "ENSG00000309708",
          "hgnc_id": null,
          "effects": [
            "non_coding_transcript_exon_variant"
          ],
          "inheritance_mode": "",
          "hgvs_c": "n.23G>A",
          "hgvs_p": null
        }
      ],
      "clinvar_disease": "not specified",
      "clinvar_classification": "Likely benign",
      "clinvar_review_status": "criteria provided, single submitter",
      "clinvar_submissions_summary": "LB:1",
      "phenotype_combined": "not specified",
      "pathogenicity_classification_combined": "Likely benign",
      "custom_annotations": null
    }
  ],
  "message": null
}