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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: 5-91150218-G-A (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=5&pos=91150218&ref=G&alt=A&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "5",
      "pos": 91150218,
      "ref": "G",
      "alt": "A",
      "effect": "synonymous_variant",
      "transcript": "ENST00000405460.9",
      "consequences": [
        {
          "aa_ref": "E",
          "aa_alt": "E",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 88,
          "exon_rank_end": null,
          "exon_count": 90,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ADGRV1",
          "gene_hgnc_id": 17416,
          "hgvs_c": "c.18621G>A",
          "hgvs_p": "p.Glu6207Glu",
          "transcript": "NM_032119.4",
          "protein_id": "NP_115495.3",
          "transcript_support_level": null,
          "aa_start": 6207,
          "aa_end": null,
          "aa_length": 6306,
          "cds_start": 18621,
          "cds_end": null,
          "cds_length": 18921,
          "cdna_start": 18720,
          "cdna_end": null,
          "cdna_length": 19557,
          "mane_select": "ENST00000405460.9",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "E",
          "aa_alt": "E",
          "canonical": true,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 88,
          "exon_rank_end": null,
          "exon_count": 90,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ADGRV1",
          "gene_hgnc_id": 17416,
          "hgvs_c": "c.18621G>A",
          "hgvs_p": "p.Glu6207Glu",
          "transcript": "ENST00000405460.9",
          "protein_id": "ENSP00000384582.2",
          "transcript_support_level": 1,
          "aa_start": 6207,
          "aa_end": null,
          "aa_length": 6306,
          "cds_start": 18621,
          "cds_end": null,
          "cds_length": 18921,
          "cdna_start": 18720,
          "cdna_end": null,
          "cdna_length": 19557,
          "mane_select": "NM_032119.4",
          "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": 24,
          "exon_rank_end": null,
          "exon_count": 26,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ADGRV1",
          "gene_hgnc_id": 17416,
          "hgvs_c": "n.5888G>A",
          "hgvs_p": null,
          "transcript": "ENST00000638510.1",
          "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": 6503,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "E",
          "aa_alt": "E",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 36,
          "exon_rank_end": null,
          "exon_count": 38,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ADGRV1",
          "gene_hgnc_id": 17416,
          "hgvs_c": "c.7575G>A",
          "hgvs_p": "p.Glu2525Glu",
          "transcript": "ENST00000425867.3",
          "protein_id": "ENSP00000392618.3",
          "transcript_support_level": 5,
          "aa_start": 2525,
          "aa_end": null,
          "aa_length": 2624,
          "cds_start": 7575,
          "cds_end": null,
          "cds_length": 7875,
          "cdna_start": 7575,
          "cdna_end": null,
          "cdna_length": 8141,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "E",
          "aa_alt": "E",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 6,
          "exon_rank_end": null,
          "exon_count": 8,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ADGRV1",
          "gene_hgnc_id": 17416,
          "hgvs_c": "c.705G>A",
          "hgvs_p": "p.Glu235Glu",
          "transcript": "ENST00000640815.1",
          "protein_id": "ENSP00000491767.1",
          "transcript_support_level": 2,
          "aa_start": 235,
          "aa_end": null,
          "aa_length": 334,
          "cds_start": 705,
          "cds_end": null,
          "cds_length": 1005,
          "cdna_start": 906,
          "cdna_end": null,
          "cdna_length": 1522,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "E",
          "aa_alt": "E",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 88,
          "exon_rank_end": null,
          "exon_count": 90,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ADGRV1",
          "gene_hgnc_id": 17416,
          "hgvs_c": "c.18642G>A",
          "hgvs_p": "p.Glu6214Glu",
          "transcript": "XM_017009963.3",
          "protein_id": "XP_016865452.1",
          "transcript_support_level": null,
          "aa_start": 6214,
          "aa_end": null,
          "aa_length": 6313,
          "cds_start": 18642,
          "cds_end": null,
          "cds_length": 18942,
          "cdna_start": 18741,
          "cdna_end": null,
          "cdna_length": 19578,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "E",
          "aa_alt": "E",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 88,
          "exon_rank_end": null,
          "exon_count": 90,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ADGRV1",
          "gene_hgnc_id": 17416,
          "hgvs_c": "c.18639G>A",
          "hgvs_p": "p.Glu6213Glu",
          "transcript": "XM_017009964.3",
          "protein_id": "XP_016865453.1",
          "transcript_support_level": null,
          "aa_start": 6213,
          "aa_end": null,
          "aa_length": 6312,
          "cds_start": 18639,
          "cds_end": null,
          "cds_length": 18939,
          "cdna_start": 18738,
          "cdna_end": null,
          "cdna_length": 19575,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "E",
          "aa_alt": "E",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 88,
          "exon_rank_end": null,
          "exon_count": 90,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ADGRV1",
          "gene_hgnc_id": 17416,
          "hgvs_c": "c.18639G>A",
          "hgvs_p": "p.Glu6213Glu",
          "transcript": "XM_017009965.2",
          "protein_id": "XP_016865454.1",
          "transcript_support_level": null,
          "aa_start": 6213,
          "aa_end": null,
          "aa_length": 6312,
          "cds_start": 18639,
          "cds_end": null,
          "cds_length": 18939,
          "cdna_start": 18757,
          "cdna_end": null,
          "cdna_length": 19594,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "E",
          "aa_alt": "E",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 88,
          "exon_rank_end": null,
          "exon_count": 90,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ADGRV1",
          "gene_hgnc_id": 17416,
          "hgvs_c": "c.18618G>A",
          "hgvs_p": "p.Glu6206Glu",
          "transcript": "XM_047417824.1",
          "protein_id": "XP_047273780.1",
          "transcript_support_level": null,
          "aa_start": 6206,
          "aa_end": null,
          "aa_length": 6305,
          "cds_start": 18618,
          "cds_end": null,
          "cds_length": 18918,
          "cdna_start": 18717,
          "cdna_end": null,
          "cdna_length": 19554,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "E",
          "aa_alt": "E",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 87,
          "exon_rank_end": null,
          "exon_count": 89,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ADGRV1",
          "gene_hgnc_id": 17416,
          "hgvs_c": "c.18561G>A",
          "hgvs_p": "p.Glu6187Glu",
          "transcript": "XM_017009966.3",
          "protein_id": "XP_016865455.1",
          "transcript_support_level": null,
          "aa_start": 6187,
          "aa_end": null,
          "aa_length": 6286,
          "cds_start": 18561,
          "cds_end": null,
          "cds_length": 18861,
          "cdna_start": 18660,
          "cdna_end": null,
          "cdna_length": 19497,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "E",
          "aa_alt": "E",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 87,
          "exon_rank_end": null,
          "exon_count": 89,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ADGRV1",
          "gene_hgnc_id": 17416,
          "hgvs_c": "c.18546G>A",
          "hgvs_p": "p.Glu6182Glu",
          "transcript": "XM_017009967.2",
          "protein_id": "XP_016865456.1",
          "transcript_support_level": null,
          "aa_start": 6182,
          "aa_end": null,
          "aa_length": 6281,
          "cds_start": 18546,
          "cds_end": null,
          "cds_length": 18846,
          "cdna_start": 18645,
          "cdna_end": null,
          "cdna_length": 19482,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "E",
          "aa_alt": "E",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 87,
          "exon_rank_end": null,
          "exon_count": 89,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ADGRV1",
          "gene_hgnc_id": 17416,
          "hgvs_c": "c.18462G>A",
          "hgvs_p": "p.Glu6154Glu",
          "transcript": "XM_017009968.3",
          "protein_id": "XP_016865457.1",
          "transcript_support_level": null,
          "aa_start": 6154,
          "aa_end": null,
          "aa_length": 6253,
          "cds_start": 18462,
          "cds_end": null,
          "cds_length": 18762,
          "cdna_start": 18561,
          "cdna_end": null,
          "cdna_length": 19398,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "E",
          "aa_alt": "E",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 58,
          "exon_rank_end": null,
          "exon_count": 60,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ADGRV1",
          "gene_hgnc_id": 17416,
          "hgvs_c": "c.11760G>A",
          "hgvs_p": "p.Glu3920Glu",
          "transcript": "XM_017009972.2",
          "protein_id": "XP_016865461.1",
          "transcript_support_level": null,
          "aa_start": 3920,
          "aa_end": null,
          "aa_length": 4019,
          "cds_start": 11760,
          "cds_end": null,
          "cds_length": 12060,
          "cdna_start": 11847,
          "cdna_end": null,
          "cdna_length": 12684,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "E",
          "aa_alt": "E",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 58,
          "exon_rank_end": null,
          "exon_count": 60,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ADGRV1",
          "gene_hgnc_id": 17416,
          "hgvs_c": "c.11739G>A",
          "hgvs_p": "p.Glu3913Glu",
          "transcript": "XM_017009973.2",
          "protein_id": "XP_016865462.1",
          "transcript_support_level": null,
          "aa_start": 3913,
          "aa_end": null,
          "aa_length": 4012,
          "cds_start": 11739,
          "cds_end": null,
          "cds_length": 12039,
          "cdna_start": 11833,
          "cdna_end": null,
          "cdna_length": 12670,
          "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": 12,
          "exon_rank_end": null,
          "exon_count": 14,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ADGRV1",
          "gene_hgnc_id": 17416,
          "hgvs_c": "n.*1592G>A",
          "hgvs_p": null,
          "transcript": "ENST00000638990.1",
          "protein_id": "ENSP00000492781.1",
          "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": 2433,
          "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": 4,
          "exon_rank_end": null,
          "exon_count": 6,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ADGRV1",
          "gene_hgnc_id": 17416,
          "hgvs_c": "n.541G>A",
          "hgvs_p": null,
          "transcript": "ENST00000639212.1",
          "protein_id": null,
          "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": 1167,
          "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": 3,
          "exon_rank_end": null,
          "exon_count": 5,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ADGRV1",
          "gene_hgnc_id": 17416,
          "hgvs_c": "n.489G>A",
          "hgvs_p": null,
          "transcript": "ENST00000639530.1",
          "protein_id": null,
          "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": 1101,
          "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": 23,
          "exon_rank_end": null,
          "exon_count": 25,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ADGRV1",
          "gene_hgnc_id": 17416,
          "hgvs_c": "n.*2253G>A",
          "hgvs_p": null,
          "transcript": "ENST00000640407.1",
          "protein_id": "ENSP00000491425.1",
          "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": 5673,
          "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": 88,
          "exon_rank_end": null,
          "exon_count": 90,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ADGRV1",
          "gene_hgnc_id": 17416,
          "hgvs_c": "n.18637G>A",
          "hgvs_p": null,
          "transcript": "NR_003149.2",
          "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": 19474,
          "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": 12,
          "exon_rank_end": null,
          "exon_count": 14,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ADGRV1",
          "gene_hgnc_id": 17416,
          "hgvs_c": "n.*1592G>A",
          "hgvs_p": null,
          "transcript": "ENST00000638990.1",
          "protein_id": "ENSP00000492781.1",
          "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": 2433,
          "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": 23,
          "exon_rank_end": null,
          "exon_count": 25,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ADGRV1",
          "gene_hgnc_id": 17416,
          "hgvs_c": "n.*2253G>A",
          "hgvs_p": null,
          "transcript": "ENST00000640407.1",
          "protein_id": "ENSP00000491425.1",
          "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,
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          "cdna_length": 5673,
          "mane_select": null,
          "mane_plus": null,
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          "feature": null
        },
        {
          "aa_ref": null,
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          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 6,
          "intron_rank": 5,
          "intron_rank_end": null,
          "gene_symbol": "ADGRV1",
          "gene_hgnc_id": 17416,
          "hgvs_c": "c.517-13564G>A",
          "hgvs_p": null,
          "transcript": "ENST00000639821.1",
          "protein_id": "ENSP00000492216.1",
          "transcript_support_level": 3,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 192,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 579,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 893,
          "mane_select": null,
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          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
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          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 4,
          "intron_rank": 2,
          "intron_rank_end": null,
          "gene_symbol": "ADGRV1",
          "gene_hgnc_id": 17416,
          "hgvs_c": "n.301-3003G>A",
          "hgvs_p": null,
          "transcript": "ENST00000640256.1",
          "protein_id": null,
          "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": 904,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
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          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 3,
          "intron_rank": 2,
          "intron_rank_end": null,
          "gene_symbol": "LUCAT1",
          "gene_hgnc_id": 48498,
          "hgvs_c": "n.155+52393C>T",
          "hgvs_p": null,
          "transcript": "ENST00000650017.1",
          "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": 2176,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
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          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 88,
          "intron_rank": 87,
          "intron_rank_end": null,
          "gene_symbol": "ADGRV1",
          "gene_hgnc_id": 17416,
          "hgvs_c": "c.18454-13564G>A",
          "hgvs_p": null,
          "transcript": "XM_017009969.3",
          "protein_id": "XP_016865458.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 6171,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 18516,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 19208,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        }
      ],
      "gene_symbol": "ADGRV1",
      "gene_hgnc_id": 17416,
      "dbsnp": "rs543269561",
      "frequency_reference_population": 0.000021223503,
      "hom_count_reference_population": 0,
      "allele_count_reference_population": 33,
      "gnomad_exomes_af": 0.0000171082,
      "gnomad_genomes_af": 0.0000591942,
      "gnomad_exomes_ac": 24,
      "gnomad_genomes_ac": 9,
      "gnomad_exomes_homalt": 0,
      "gnomad_genomes_homalt": 0,
      "gnomad_mito_homoplasmic": null,
      "gnomad_mito_heteroplasmic": null,
      "computational_score_selected": -0.4699999988079071,
      "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": -0.47,
      "bayesdelnoaf_prediction": "Benign",
      "phylop100way_score": -0.055,
      "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": -13,
      "acmg_classification": "Benign",
      "acmg_criteria": "BP4_Strong,BP6_Very_Strong,BP7",
      "acmg_by_gene": [
        {
          "score": -13,
          "benign_score": 13,
          "pathogenic_score": 0,
          "criteria": [
            "BP4_Strong",
            "BP6_Very_Strong",
            "BP7"
          ],
          "verdict": "Benign",
          "transcript": "ENST00000405460.9",
          "gene_symbol": "ADGRV1",
          "hgnc_id": 17416,
          "effects": [
            "synonymous_variant"
          ],
          "inheritance_mode": "AR,AD",
          "hgvs_c": "c.18621G>A",
          "hgvs_p": "p.Glu6207Glu"
        },
        {
          "score": -12,
          "benign_score": 12,
          "pathogenic_score": 0,
          "criteria": [
            "BP4_Strong",
            "BP6_Very_Strong"
          ],
          "verdict": "Benign",
          "transcript": "ENST00000650017.1",
          "gene_symbol": "LUCAT1",
          "hgnc_id": 48498,
          "effects": [
            "intron_variant"
          ],
          "inheritance_mode": "",
          "hgvs_c": "n.155+52393C>T",
          "hgvs_p": null
        }
      ],
      "clinvar_disease": "ADGRV1-related disorder,not provided,not specified",
      "clinvar_classification": "Likely benign",
      "clinvar_review_status": "criteria provided, multiple submitters, no conflicts",
      "clinvar_submissions_summary": "LB:2",
      "phenotype_combined": "not specified|not provided|ADGRV1-related disorder",
      "pathogenicity_classification_combined": "Likely benign",
      "custom_annotations": null
    }
  ],
  "message": null
}