← Back to variant description

GeneBe API Showcase

This page demonstrates how to use the GeneBe API to query variant information. The API provides programmatic access to genomic annotations and variant data.

API presented here should be used for checking single variants. If you want to check many variants at once, please use other API endpoints that you will find in the documentation.

Documentation & Advanced Usage

Complete API documentation:docs.genebe.net/docs/api/overview/

Interactive endpoint tester:api.genebe.net/cloud/gb-api-doc/swagger-ui/

Python client for pandas:pypi.org/project/genebe/

Java CLI for VCF files:github.com/pstawinski/genebe-cli

All tools documented at:docs.genebe.net

API Request Examples for Variant: 1-150950536-C-A (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=1&pos=150950536&ref=C&alt=A&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "1",
      "pos": 150950536,
      "ref": "C",
      "alt": "A",
      "effect": "synonymous_variant",
      "transcript": "NM_001366418.1",
      "consequences": [
        {
          "aa_ref": "G",
          "aa_alt": "G",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 13,
          "exon_rank_end": null,
          "exon_count": 22,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SETDB1",
          "gene_hgnc_id": 10761,
          "hgvs_c": "c.1662C>A",
          "hgvs_p": "p.Gly554Gly",
          "transcript": "NM_001366418.1",
          "protein_id": "NP_001353347.1",
          "transcript_support_level": null,
          "aa_start": 554,
          "aa_end": null,
          "aa_length": 1292,
          "cds_start": 1662,
          "cds_end": null,
          "cds_length": 3879,
          "cdna_start": 1828,
          "cdna_end": null,
          "cdna_length": 4418,
          "mane_select": "ENST00000692827.1",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "G",
          "aa_alt": "G",
          "canonical": true,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 13,
          "exon_rank_end": null,
          "exon_count": 22,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SETDB1",
          "gene_hgnc_id": 10761,
          "hgvs_c": "c.1662C>A",
          "hgvs_p": "p.Gly554Gly",
          "transcript": "ENST00000692827.1",
          "protein_id": "ENSP00000509425.1",
          "transcript_support_level": null,
          "aa_start": 554,
          "aa_end": null,
          "aa_length": 1292,
          "cds_start": 1662,
          "cds_end": null,
          "cds_length": 3879,
          "cdna_start": 1828,
          "cdna_end": null,
          "cdna_length": 4418,
          "mane_select": "NM_001366418.1",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "G",
          "aa_alt": "G",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 13,
          "exon_rank_end": null,
          "exon_count": 22,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SETDB1",
          "gene_hgnc_id": 10761,
          "hgvs_c": "c.1659C>A",
          "hgvs_p": "p.Gly553Gly",
          "transcript": "ENST00000271640.9",
          "protein_id": "ENSP00000271640.5",
          "transcript_support_level": 1,
          "aa_start": 553,
          "aa_end": null,
          "aa_length": 1291,
          "cds_start": 1659,
          "cds_end": null,
          "cds_length": 3876,
          "cdna_start": 1849,
          "cdna_end": null,
          "cdna_length": 4437,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "G",
          "aa_alt": "G",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 13,
          "exon_rank_end": null,
          "exon_count": 22,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SETDB1",
          "gene_hgnc_id": 10761,
          "hgvs_c": "c.1659C>A",
          "hgvs_p": "p.Gly553Gly",
          "transcript": "ENST00000368969.8",
          "protein_id": "ENSP00000357965.4",
          "transcript_support_level": 1,
          "aa_start": 553,
          "aa_end": null,
          "aa_length": 1290,
          "cds_start": 1659,
          "cds_end": null,
          "cds_length": 3873,
          "cdna_start": 1776,
          "cdna_end": null,
          "cdna_length": 4370,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "G",
          "aa_alt": "G",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 13,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SETDB1",
          "gene_hgnc_id": 10761,
          "hgvs_c": "c.1662C>A",
          "hgvs_p": "p.Gly554Gly",
          "transcript": "ENST00000534805.5",
          "protein_id": "ENSP00000436148.1",
          "transcript_support_level": 1,
          "aa_start": 554,
          "aa_end": null,
          "aa_length": 635,
          "cds_start": 1662,
          "cds_end": null,
          "cds_length": 1909,
          "cdna_start": 1796,
          "cdna_end": null,
          "cdna_length": 2043,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "G",
          "aa_alt": "G",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 13,
          "exon_rank_end": null,
          "exon_count": 22,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SETDB1",
          "gene_hgnc_id": 10761,
          "hgvs_c": "c.1662C>A",
          "hgvs_p": "p.Gly554Gly",
          "transcript": "NM_001366417.1",
          "protein_id": "NP_001353346.1",
          "transcript_support_level": null,
          "aa_start": 554,
          "aa_end": null,
          "aa_length": 1292,
          "cds_start": 1662,
          "cds_end": null,
          "cds_length": 3879,
          "cdna_start": 1759,
          "cdna_end": null,
          "cdna_length": 4349,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "G",
          "aa_alt": "G",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 13,
          "exon_rank_end": null,
          "exon_count": 22,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SETDB1",
          "gene_hgnc_id": 10761,
          "hgvs_c": "c.1662C>A",
          "hgvs_p": "p.Gly554Gly",
          "transcript": "NM_001393958.1",
          "protein_id": "NP_001380887.1",
          "transcript_support_level": null,
          "aa_start": 554,
          "aa_end": null,
          "aa_length": 1292,
          "cds_start": 1662,
          "cds_end": null,
          "cds_length": 3879,
          "cdna_start": 1855,
          "cdna_end": null,
          "cdna_length": 4445,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "G",
          "aa_alt": "G",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 13,
          "exon_rank_end": null,
          "exon_count": 22,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SETDB1",
          "gene_hgnc_id": 10761,
          "hgvs_c": "c.1662C>A",
          "hgvs_p": "p.Gly554Gly",
          "transcript": "NM_001393959.1",
          "protein_id": "NP_001380888.1",
          "transcript_support_level": null,
          "aa_start": 554,
          "aa_end": null,
          "aa_length": 1292,
          "cds_start": 1662,
          "cds_end": null,
          "cds_length": 3879,
          "cdna_start": 1774,
          "cdna_end": null,
          "cdna_length": 4364,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "G",
          "aa_alt": "G",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 13,
          "exon_rank_end": null,
          "exon_count": 22,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SETDB1",
          "gene_hgnc_id": 10761,
          "hgvs_c": "c.1662C>A",
          "hgvs_p": "p.Gly554Gly",
          "transcript": "ENST00000692314.1",
          "protein_id": "ENSP00000508664.1",
          "transcript_support_level": null,
          "aa_start": 554,
          "aa_end": null,
          "aa_length": 1292,
          "cds_start": 1662,
          "cds_end": null,
          "cds_length": 3879,
          "cdna_start": 1717,
          "cdna_end": null,
          "cdna_length": 4295,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "G",
          "aa_alt": "G",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 13,
          "exon_rank_end": null,
          "exon_count": 22,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SETDB1",
          "gene_hgnc_id": 10761,
          "hgvs_c": "c.1659C>A",
          "hgvs_p": "p.Gly553Gly",
          "transcript": "NM_001145415.2",
          "protein_id": "NP_001138887.1",
          "transcript_support_level": null,
          "aa_start": 553,
          "aa_end": null,
          "aa_length": 1291,
          "cds_start": 1659,
          "cds_end": null,
          "cds_length": 3876,
          "cdna_start": 1825,
          "cdna_end": null,
          "cdna_length": 4415,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "G",
          "aa_alt": "G",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 13,
          "exon_rank_end": null,
          "exon_count": 22,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SETDB1",
          "gene_hgnc_id": 10761,
          "hgvs_c": "c.1659C>A",
          "hgvs_p": "p.Gly553Gly",
          "transcript": "NM_001393960.1",
          "protein_id": "NP_001380889.1",
          "transcript_support_level": null,
          "aa_start": 553,
          "aa_end": null,
          "aa_length": 1291,
          "cds_start": 1659,
          "cds_end": null,
          "cds_length": 3876,
          "cdna_start": 1756,
          "cdna_end": null,
          "cdna_length": 4346,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "G",
          "aa_alt": "G",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 13,
          "exon_rank_end": null,
          "exon_count": 22,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SETDB1",
          "gene_hgnc_id": 10761,
          "hgvs_c": "c.1662C>A",
          "hgvs_p": "p.Gly554Gly",
          "transcript": "NM_001393961.1",
          "protein_id": "NP_001380890.1",
          "transcript_support_level": null,
          "aa_start": 554,
          "aa_end": null,
          "aa_length": 1291,
          "cds_start": 1662,
          "cds_end": null,
          "cds_length": 3876,
          "cdna_start": 1759,
          "cdna_end": null,
          "cdna_length": 4346,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "G",
          "aa_alt": "G",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 13,
          "exon_rank_end": null,
          "exon_count": 22,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SETDB1",
          "gene_hgnc_id": 10761,
          "hgvs_c": "c.1659C>A",
          "hgvs_p": "p.Gly553Gly",
          "transcript": "NM_012432.4",
          "protein_id": "NP_036564.3",
          "transcript_support_level": null,
          "aa_start": 553,
          "aa_end": null,
          "aa_length": 1290,
          "cds_start": 1659,
          "cds_end": null,
          "cds_length": 3873,
          "cdna_start": 1825,
          "cdna_end": null,
          "cdna_length": 4412,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "G",
          "aa_alt": "G",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 13,
          "exon_rank_end": null,
          "exon_count": 20,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SETDB1",
          "gene_hgnc_id": 10761,
          "hgvs_c": "c.1659C>A",
          "hgvs_p": "p.Gly553Gly",
          "transcript": "ENST00000498193.5",
          "protein_id": "ENSP00000432348.1",
          "transcript_support_level": 2,
          "aa_start": 553,
          "aa_end": null,
          "aa_length": 1258,
          "cds_start": 1659,
          "cds_end": null,
          "cds_length": 3779,
          "cdna_start": 1734,
          "cdna_end": null,
          "cdna_length": 3854,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "G",
          "aa_alt": "G",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 13,
          "exon_rank_end": null,
          "exon_count": 22,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SETDB1",
          "gene_hgnc_id": 10761,
          "hgvs_c": "c.1662C>A",
          "hgvs_p": "p.Gly554Gly",
          "transcript": "XM_047435567.1",
          "protein_id": "XP_047291523.1",
          "transcript_support_level": null,
          "aa_start": 554,
          "aa_end": null,
          "aa_length": 1292,
          "cds_start": 1662,
          "cds_end": null,
          "cds_length": 3879,
          "cdna_start": 1842,
          "cdna_end": null,
          "cdna_length": 4432,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "G",
          "aa_alt": "G",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 13,
          "exon_rank_end": null,
          "exon_count": 22,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SETDB1",
          "gene_hgnc_id": 10761,
          "hgvs_c": "c.1659C>A",
          "hgvs_p": "p.Gly553Gly",
          "transcript": "XM_047435573.1",
          "protein_id": "XP_047291529.1",
          "transcript_support_level": null,
          "aa_start": 553,
          "aa_end": null,
          "aa_length": 1291,
          "cds_start": 1659,
          "cds_end": null,
          "cds_length": 3876,
          "cdna_start": 1771,
          "cdna_end": null,
          "cdna_length": 4361,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "G",
          "aa_alt": "G",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 13,
          "exon_rank_end": null,
          "exon_count": 22,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SETDB1",
          "gene_hgnc_id": 10761,
          "hgvs_c": "c.1659C>A",
          "hgvs_p": "p.Gly553Gly",
          "transcript": "XM_047435579.1",
          "protein_id": "XP_047291535.1",
          "transcript_support_level": null,
          "aa_start": 553,
          "aa_end": null,
          "aa_length": 1291,
          "cds_start": 1659,
          "cds_end": null,
          "cds_length": 3876,
          "cdna_start": 1839,
          "cdna_end": null,
          "cdna_length": 4429,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "G",
          "aa_alt": "G",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 13,
          "exon_rank_end": null,
          "exon_count": 22,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SETDB1",
          "gene_hgnc_id": 10761,
          "hgvs_c": "c.1659C>A",
          "hgvs_p": "p.Gly553Gly",
          "transcript": "XM_047435582.1",
          "protein_id": "XP_047291538.1",
          "transcript_support_level": null,
          "aa_start": 553,
          "aa_end": null,
          "aa_length": 1291,
          "cds_start": 1659,
          "cds_end": null,
          "cds_length": 3876,
          "cdna_start": 1852,
          "cdna_end": null,
          "cdna_length": 4442,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "G",
          "aa_alt": "G",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 13,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SETDB1",
          "gene_hgnc_id": 10761,
          "hgvs_c": "c.1659C>A",
          "hgvs_p": "p.Gly553Gly",
          "transcript": "XM_047435587.1",
          "protein_id": "XP_047291543.1",
          "transcript_support_level": null,
          "aa_start": 553,
          "aa_end": null,
          "aa_length": 738,
          "cds_start": 1659,
          "cds_end": null,
          "cds_length": 2217,
          "cdna_start": 1825,
          "cdna_end": null,
          "cdna_length": 2383,
          "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": 13,
          "exon_rank_end": null,
          "exon_count": 16,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SETDB1",
          "gene_hgnc_id": 10761,
          "hgvs_c": "n.1861C>A",
          "hgvs_p": null,
          "transcript": "ENST00000690229.1",
          "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": 2984,
          "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": 21,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SETDB1",
          "gene_hgnc_id": 10761,
          "hgvs_c": "n.1557C>A",
          "hgvs_p": null,
          "transcript": "NR_172060.1",
          "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": 4147,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "5_prime_UTR_variant"
          ],
          "exon_rank": 3,
          "exon_rank_end": null,
          "exon_count": 12,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SETDB1",
          "gene_hgnc_id": 10761,
          "hgvs_c": "c.-1C>A",
          "hgvs_p": null,
          "transcript": "XM_047435586.1",
          "protein_id": "XP_047291542.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 738,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 2217,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 2882,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 4,
          "intron_rank": 3,
          "intron_rank_end": null,
          "gene_symbol": "SETDB1",
          "gene_hgnc_id": 10761,
          "hgvs_c": "n.464-10027C>A",
          "hgvs_p": null,
          "transcript": "ENST00000459773.1",
          "protein_id": null,
          "transcript_support_level": 3,
          "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": 791,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        }
      ],
      "gene_symbol": "SETDB1",
      "gene_hgnc_id": 10761,
      "dbsnp": "rs752794321",
      "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": -0.36000001430511475,
      "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": -0.36,
      "bayesdelnoaf_prediction": "Benign",
      "phylop100way_score": -0.022,
      "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": -3,
      "acmg_classification": "Likely_benign",
      "acmg_criteria": "PM2,BP4_Moderate,BP6_Moderate,BP7",
      "acmg_by_gene": [
        {
          "score": -3,
          "benign_score": 5,
          "pathogenic_score": 2,
          "criteria": [
            "PM2",
            "BP4_Moderate",
            "BP6_Moderate",
            "BP7"
          ],
          "verdict": "Likely_benign",
          "transcript": "NM_001366418.1",
          "gene_symbol": "SETDB1",
          "hgnc_id": 10761,
          "effects": [
            "synonymous_variant"
          ],
          "inheritance_mode": "AD",
          "hgvs_c": "c.1662C>A",
          "hgvs_p": "p.Gly554Gly"
        }
      ],
      "clinvar_disease": "not provided",
      "clinvar_classification": "Likely benign",
      "clinvar_review_status": "criteria provided, single submitter",
      "clinvar_submissions_summary": "LB:1",
      "phenotype_combined": "not provided",
      "pathogenicity_classification_combined": "Likely benign",
      "custom_annotations": null
    }
  ],
  "message": null
}