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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: 22-41663764-G-A (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=22&pos=41663764&ref=G&alt=A&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "22",
      "pos": 41663764,
      "ref": "G",
      "alt": "A",
      "effect": "synonymous_variant",
      "transcript": "NM_001469.5",
      "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": 13,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "XRCC6",
          "gene_hgnc_id": 4055,
          "hgvs_c": "c.1779G>A",
          "hgvs_p": "p.Gly593Gly",
          "transcript": "NM_001469.5",
          "protein_id": "NP_001460.1",
          "transcript_support_level": null,
          "aa_start": 593,
          "aa_end": null,
          "aa_length": 609,
          "cds_start": 1779,
          "cds_end": null,
          "cds_length": 1830,
          "cdna_start": 1845,
          "cdna_end": null,
          "cdna_length": 2122,
          "mane_select": "ENST00000360079.8",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001469.5"
        },
        {
          "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": 13,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "XRCC6",
          "gene_hgnc_id": 4055,
          "hgvs_c": "c.1779G>A",
          "hgvs_p": "p.Gly593Gly",
          "transcript": "ENST00000360079.8",
          "protein_id": "ENSP00000353192.3",
          "transcript_support_level": 1,
          "aa_start": 593,
          "aa_end": null,
          "aa_length": 609,
          "cds_start": 1779,
          "cds_end": null,
          "cds_length": 1830,
          "cdna_start": 1845,
          "cdna_end": null,
          "cdna_length": 2122,
          "mane_select": "NM_001469.5",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000360079.8"
        },
        {
          "aa_ref": "G",
          "aa_alt": "G",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 12,
          "exon_rank_end": null,
          "exon_count": 12,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "XRCC6",
          "gene_hgnc_id": 4055,
          "hgvs_c": "c.1779G>A",
          "hgvs_p": "p.Gly593Gly",
          "transcript": "ENST00000359308.8",
          "protein_id": "ENSP00000352257.4",
          "transcript_support_level": 1,
          "aa_start": 593,
          "aa_end": null,
          "aa_length": 609,
          "cds_start": 1779,
          "cds_end": null,
          "cds_length": 1830,
          "cdna_start": 2434,
          "cdna_end": null,
          "cdna_length": 2709,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000359308.8"
        },
        {
          "aa_ref": "G",
          "aa_alt": "G",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 14,
          "exon_rank_end": null,
          "exon_count": 14,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "XRCC6",
          "gene_hgnc_id": 4055,
          "hgvs_c": "c.1854G>A",
          "hgvs_p": "p.Gly618Gly",
          "transcript": "ENST00000938034.1",
          "protein_id": "ENSP00000608093.1",
          "transcript_support_level": null,
          "aa_start": 618,
          "aa_end": null,
          "aa_length": 634,
          "cds_start": 1854,
          "cds_end": null,
          "cds_length": 1905,
          "cdna_start": 1924,
          "cdna_end": null,
          "cdna_length": 2199,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000938034.1"
        },
        {
          "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": "XRCC6",
          "gene_hgnc_id": 4055,
          "hgvs_c": "c.1815G>A",
          "hgvs_p": "p.Gly605Gly",
          "transcript": "ENST00000892848.1",
          "protein_id": "ENSP00000562907.1",
          "transcript_support_level": null,
          "aa_start": 605,
          "aa_end": null,
          "aa_length": 621,
          "cds_start": 1815,
          "cds_end": null,
          "cds_length": 1866,
          "cdna_start": 1870,
          "cdna_end": null,
          "cdna_length": 2145,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000892848.1"
        },
        {
          "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": "XRCC6",
          "gene_hgnc_id": 4055,
          "hgvs_c": "c.1812G>A",
          "hgvs_p": "p.Gly604Gly",
          "transcript": "ENST00000970533.1",
          "protein_id": "ENSP00000640592.1",
          "transcript_support_level": null,
          "aa_start": 604,
          "aa_end": null,
          "aa_length": 620,
          "cds_start": 1812,
          "cds_end": null,
          "cds_length": 1863,
          "cdna_start": 1880,
          "cdna_end": null,
          "cdna_length": 2156,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000970533.1"
        },
        {
          "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": "XRCC6",
          "gene_hgnc_id": 4055,
          "hgvs_c": "c.1779G>A",
          "hgvs_p": "p.Gly593Gly",
          "transcript": "NM_001288976.2",
          "protein_id": "NP_001275905.1",
          "transcript_support_level": null,
          "aa_start": 593,
          "aa_end": null,
          "aa_length": 609,
          "cds_start": 1779,
          "cds_end": null,
          "cds_length": 1830,
          "cdna_start": 1910,
          "cdna_end": null,
          "cdna_length": 2187,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001288976.2"
        },
        {
          "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": "XRCC6",
          "gene_hgnc_id": 4055,
          "hgvs_c": "c.1779G>A",
          "hgvs_p": "p.Gly593Gly",
          "transcript": "ENST00000405878.5",
          "protein_id": "ENSP00000384257.1",
          "transcript_support_level": 5,
          "aa_start": 593,
          "aa_end": null,
          "aa_length": 609,
          "cds_start": 1779,
          "cds_end": null,
          "cds_length": 1830,
          "cdna_start": 1925,
          "cdna_end": null,
          "cdna_length": 2200,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000405878.5"
        },
        {
          "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": "XRCC6",
          "gene_hgnc_id": 4055,
          "hgvs_c": "c.1779G>A",
          "hgvs_p": "p.Gly593Gly",
          "transcript": "ENST00000892843.1",
          "protein_id": "ENSP00000562902.1",
          "transcript_support_level": null,
          "aa_start": 593,
          "aa_end": null,
          "aa_length": 609,
          "cds_start": 1779,
          "cds_end": null,
          "cds_length": 1830,
          "cdna_start": 1840,
          "cdna_end": null,
          "cdna_length": 2115,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000892843.1"
        },
        {
          "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": "XRCC6",
          "gene_hgnc_id": 4055,
          "hgvs_c": "c.1779G>A",
          "hgvs_p": "p.Gly593Gly",
          "transcript": "ENST00000892849.1",
          "protein_id": "ENSP00000562908.1",
          "transcript_support_level": null,
          "aa_start": 593,
          "aa_end": null,
          "aa_length": 609,
          "cds_start": 1779,
          "cds_end": null,
          "cds_length": 1830,
          "cdna_start": 1866,
          "cdna_end": null,
          "cdna_length": 2143,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000892849.1"
        },
        {
          "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": "XRCC6",
          "gene_hgnc_id": 4055,
          "hgvs_c": "c.1779G>A",
          "hgvs_p": "p.Gly593Gly",
          "transcript": "ENST00000892850.1",
          "protein_id": "ENSP00000562909.1",
          "transcript_support_level": null,
          "aa_start": 593,
          "aa_end": null,
          "aa_length": 609,
          "cds_start": 1779,
          "cds_end": null,
          "cds_length": 1830,
          "cdna_start": 1901,
          "cdna_end": null,
          "cdna_length": 2176,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000892850.1"
        },
        {
          "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": "XRCC6",
          "gene_hgnc_id": 4055,
          "hgvs_c": "c.1779G>A",
          "hgvs_p": "p.Gly593Gly",
          "transcript": "ENST00000892852.1",
          "protein_id": "ENSP00000562911.1",
          "transcript_support_level": null,
          "aa_start": 593,
          "aa_end": null,
          "aa_length": 609,
          "cds_start": 1779,
          "cds_end": null,
          "cds_length": 1830,
          "cdna_start": 1850,
          "cdna_end": null,
          "cdna_length": 2123,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000892852.1"
        },
        {
          "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": "XRCC6",
          "gene_hgnc_id": 4055,
          "hgvs_c": "c.1779G>A",
          "hgvs_p": "p.Gly593Gly",
          "transcript": "ENST00000892853.1",
          "protein_id": "ENSP00000562912.1",
          "transcript_support_level": null,
          "aa_start": 593,
          "aa_end": null,
          "aa_length": 609,
          "cds_start": 1779,
          "cds_end": null,
          "cds_length": 1830,
          "cdna_start": 2022,
          "cdna_end": null,
          "cdna_length": 2297,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000892853.1"
        },
        {
          "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": "XRCC6",
          "gene_hgnc_id": 4055,
          "hgvs_c": "c.1779G>A",
          "hgvs_p": "p.Gly593Gly",
          "transcript": "ENST00000938028.1",
          "protein_id": "ENSP00000608087.1",
          "transcript_support_level": null,
          "aa_start": 593,
          "aa_end": null,
          "aa_length": 609,
          "cds_start": 1779,
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          "cdna_start": 2041,
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          "mane_select": null,
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          "biotype": "protein_coding",
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        },
        {
          "aa_ref": "G",
          "aa_alt": "G",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 13,
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          "intron_rank": null,
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          "gene_symbol": "XRCC6",
          "gene_hgnc_id": 4055,
          "hgvs_c": "c.1779G>A",
          "hgvs_p": "p.Gly593Gly",
          "transcript": "ENST00000938030.1",
          "protein_id": "ENSP00000608089.1",
          "transcript_support_level": null,
          "aa_start": 593,
          "aa_end": null,
          "aa_length": 609,
          "cds_start": 1779,
          "cds_end": null,
          "cds_length": 1830,
          "cdna_start": 1868,
          "cdna_end": null,
          "cdna_length": 2191,
          "mane_select": null,
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          "biotype": "protein_coding",
          "feature": "ENST00000938030.1"
        },
        {
          "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": "XRCC6",
          "gene_hgnc_id": 4055,
          "hgvs_c": "c.1779G>A",
          "hgvs_p": "p.Gly593Gly",
          "transcript": "ENST00000938031.1",
          "protein_id": "ENSP00000608090.1",
          "transcript_support_level": null,
          "aa_start": 593,
          "aa_end": null,
          "aa_length": 609,
          "cds_start": 1779,
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          "cdna_start": 1862,
          "cdna_end": null,
          "cdna_length": 2139,
          "mane_select": null,
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          "biotype": "protein_coding",
          "feature": "ENST00000938031.1"
        },
        {
          "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": "XRCC6",
          "gene_hgnc_id": 4055,
          "hgvs_c": "c.1779G>A",
          "hgvs_p": "p.Gly593Gly",
          "transcript": "ENST00000938039.1",
          "protein_id": "ENSP00000608098.1",
          "transcript_support_level": null,
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          "cds_start": 1779,
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          "cdna_start": 2039,
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          "mane_select": null,
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          "biotype": "protein_coding",
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        },
        {
          "aa_ref": "G",
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          "protein_coding": true,
          "strand": true,
          "consequences": [
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          ],
          "exon_rank": 13,
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          "exon_count": 13,
          "intron_rank": null,
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          "gene_symbol": "XRCC6",
          "gene_hgnc_id": 4055,
          "hgvs_c": "c.1776G>A",
          "hgvs_p": "p.Gly592Gly",
          "transcript": "ENST00000892844.1",
          "protein_id": "ENSP00000562903.1",
          "transcript_support_level": null,
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          "cdna_start": 1842,
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          "mane_select": null,
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          "biotype": "protein_coding",
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        },
        {
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          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
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          ],
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          "exon_count": 13,
          "intron_rank": null,
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          "gene_symbol": "XRCC6",
          "gene_hgnc_id": 4055,
          "hgvs_c": "c.1776G>A",
          "hgvs_p": "p.Gly592Gly",
          "transcript": "ENST00000938029.1",
          "protein_id": "ENSP00000608088.1",
          "transcript_support_level": null,
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          "cds_start": 1776,
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          "cdna_start": 1912,
          "cdna_end": null,
          "cdna_length": 2196,
          "mane_select": null,
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          "biotype": "protein_coding",
          "feature": "ENST00000938029.1"
        },
        {
          "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": "XRCC6",
          "gene_hgnc_id": 4055,
          "hgvs_c": "c.1776G>A",
          "hgvs_p": "p.Gly592Gly",
          "transcript": "ENST00000938040.1",
          "protein_id": "ENSP00000608099.1",
          "transcript_support_level": null,
          "aa_start": 592,
          "aa_end": null,
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          "cds_start": 1776,
          "cds_end": null,
          "cds_length": 1827,
          "cdna_start": 1859,
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          "aa_end": null,
          "aa_length": 559,
          "cds_start": 1629,
          "cds_end": null,
          "cds_length": 1680,
          "cdna_start": 1797,
          "cdna_end": null,
          "cdna_length": 2074,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "XM_047441304.1"
        }
      ],
      "gene_symbol": "XRCC6",
      "gene_hgnc_id": 4055,
      "dbsnp": "rs132788",
      "frequency_reference_population": 0.0000117743,
      "hom_count_reference_population": 0,
      "allele_count_reference_population": 19,
      "gnomad_exomes_af": 0.0000102636,
      "gnomad_genomes_af": 0.0000262805,
      "gnomad_exomes_ac": 15,
      "gnomad_genomes_ac": 4,
      "gnomad_exomes_homalt": 0,
      "gnomad_genomes_homalt": 0,
      "gnomad_mito_homoplasmic": null,
      "gnomad_mito_heteroplasmic": null,
      "computational_score_selected": -0.7099999785423279,
      "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": -0.71,
      "bayesdelnoaf_prediction": "Benign",
      "phylop100way_score": -1.059,
      "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": -9,
      "acmg_classification": "Benign",
      "acmg_criteria": "BP4_Strong,BP7,BS2",
      "acmg_by_gene": [
        {
          "score": -9,
          "benign_score": 9,
          "pathogenic_score": 0,
          "criteria": [
            "BP4_Strong",
            "BP7",
            "BS2"
          ],
          "verdict": "Benign",
          "transcript": "NM_001469.5",
          "gene_symbol": "XRCC6",
          "hgnc_id": 4055,
          "effects": [
            "synonymous_variant"
          ],
          "inheritance_mode": "AD",
          "hgvs_c": "c.1779G>A",
          "hgvs_p": "p.Gly593Gly"
        }
      ],
      "clinvar_disease": "",
      "clinvar_classification": "",
      "clinvar_review_status": "",
      "clinvar_submissions_summary": "",
      "phenotype_combined": null,
      "pathogenicity_classification_combined": null,
      "custom_annotations": null
    }
  ],
  "message": null
}
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