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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: 10-18539557-C-A (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=10&pos=18539557&ref=C&alt=A&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "10",
      "pos": 18539557,
      "ref": "C",
      "alt": "A",
      "effect": "synonymous_variant",
      "transcript": "ENST00000324631.13",
      "consequences": [
        {
          "aa_ref": "R",
          "aa_alt": "R",
          "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": "CACNB2",
          "gene_hgnc_id": 1402,
          "hgvs_c": "c.1816C>A",
          "hgvs_p": "p.Arg606Arg",
          "transcript": "NM_201596.3",
          "protein_id": "NP_963890.2",
          "transcript_support_level": null,
          "aa_start": 606,
          "aa_end": null,
          "aa_length": 660,
          "cds_start": 1816,
          "cds_end": null,
          "cds_length": 1983,
          "cdna_start": 2129,
          "cdna_end": null,
          "cdna_length": 6129,
          "mane_select": "ENST00000324631.13",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "R",
          "canonical": true,
          "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": "CACNB2",
          "gene_hgnc_id": 1402,
          "hgvs_c": "c.1816C>A",
          "hgvs_p": "p.Arg606Arg",
          "transcript": "ENST00000324631.13",
          "protein_id": "ENSP00000320025.8",
          "transcript_support_level": 1,
          "aa_start": 606,
          "aa_end": null,
          "aa_length": 660,
          "cds_start": 1816,
          "cds_end": null,
          "cds_length": 1983,
          "cdna_start": 2129,
          "cdna_end": null,
          "cdna_length": 6129,
          "mane_select": "NM_201596.3",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "R",
          "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": "CACNB2",
          "gene_hgnc_id": 1402,
          "hgvs_c": "c.1654C>A",
          "hgvs_p": "p.Arg552Arg",
          "transcript": "NM_201590.3",
          "protein_id": "NP_963884.2",
          "transcript_support_level": null,
          "aa_start": 552,
          "aa_end": null,
          "aa_length": 606,
          "cds_start": 1654,
          "cds_end": null,
          "cds_length": 1821,
          "cdna_start": 1872,
          "cdna_end": null,
          "cdna_length": 5872,
          "mane_select": null,
          "mane_plus": "ENST00000377329.10",
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "R",
          "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": "CACNB2",
          "gene_hgnc_id": 1402,
          "hgvs_c": "c.1654C>A",
          "hgvs_p": "p.Arg552Arg",
          "transcript": "ENST00000377329.10",
          "protein_id": "ENSP00000366546.4",
          "transcript_support_level": 1,
          "aa_start": 552,
          "aa_end": null,
          "aa_length": 606,
          "cds_start": 1654,
          "cds_end": null,
          "cds_length": 1821,
          "cdna_start": 1872,
          "cdna_end": null,
          "cdna_length": 5872,
          "mane_select": null,
          "mane_plus": "NM_201590.3",
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "R",
          "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": "CACNB2",
          "gene_hgnc_id": 1402,
          "hgvs_c": "c.1744C>A",
          "hgvs_p": "p.Arg582Arg",
          "transcript": "ENST00000352115.10",
          "protein_id": "ENSP00000344474.6",
          "transcript_support_level": 1,
          "aa_start": 582,
          "aa_end": null,
          "aa_length": 636,
          "cds_start": 1744,
          "cds_end": null,
          "cds_length": 1911,
          "cdna_start": 1744,
          "cdna_end": null,
          "cdna_length": 1911,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "R",
          "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": "CACNB2",
          "gene_hgnc_id": 1402,
          "hgvs_c": "c.1732C>A",
          "hgvs_p": "p.Arg578Arg",
          "transcript": "ENST00000282343.13",
          "protein_id": "ENSP00000282343.8",
          "transcript_support_level": 1,
          "aa_start": 578,
          "aa_end": null,
          "aa_length": 632,
          "cds_start": 1732,
          "cds_end": null,
          "cds_length": 1899,
          "cdna_start": 1954,
          "cdna_end": null,
          "cdna_length": 3160,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "R",
          "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": "CACNB2",
          "gene_hgnc_id": 1402,
          "hgvs_c": "c.1672C>A",
          "hgvs_p": "p.Arg558Arg",
          "transcript": "ENST00000377315.6",
          "protein_id": "ENSP00000366532.4",
          "transcript_support_level": 1,
          "aa_start": 558,
          "aa_end": null,
          "aa_length": 612,
          "cds_start": 1672,
          "cds_end": null,
          "cds_length": 1839,
          "cdna_start": 2129,
          "cdna_end": null,
          "cdna_length": 6129,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "R",
          "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": "CACNB2",
          "gene_hgnc_id": 1402,
          "hgvs_c": "c.1651C>A",
          "hgvs_p": "p.Arg551Arg",
          "transcript": "ENST00000396576.6",
          "protein_id": "ENSP00000379821.2",
          "transcript_support_level": 1,
          "aa_start": 551,
          "aa_end": null,
          "aa_length": 605,
          "cds_start": 1651,
          "cds_end": null,
          "cds_length": 1818,
          "cdna_start": 2152,
          "cdna_end": null,
          "cdna_length": 4464,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "R",
          "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": "CACNB2",
          "gene_hgnc_id": 1402,
          "hgvs_c": "c.1537C>A",
          "hgvs_p": "p.Arg513Arg",
          "transcript": "ENST00000377319.9",
          "protein_id": "ENSP00000366536.3",
          "transcript_support_level": 1,
          "aa_start": 513,
          "aa_end": null,
          "aa_length": 567,
          "cds_start": 1537,
          "cds_end": null,
          "cds_length": 1704,
          "cdna_start": 2085,
          "cdna_end": null,
          "cdna_length": 6085,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "R",
          "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": "CACNB2",
          "gene_hgnc_id": 1402,
          "hgvs_c": "c.1441C>A",
          "hgvs_p": "p.Arg481Arg",
          "transcript": "ENST00000377331.8",
          "protein_id": "ENSP00000366548.4",
          "transcript_support_level": 1,
          "aa_start": 481,
          "aa_end": null,
          "aa_length": 528,
          "cds_start": 1441,
          "cds_end": null,
          "cds_length": 1589,
          "cdna_start": 1500,
          "cdna_end": null,
          "cdna_length": 1648,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "R",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 7,
          "exon_rank_end": null,
          "exon_count": 7,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CACNB2",
          "gene_hgnc_id": 1402,
          "hgvs_c": "c.1066C>A",
          "hgvs_p": "p.Arg356Arg",
          "transcript": "ENST00000377328.5",
          "protein_id": "ENSP00000366545.1",
          "transcript_support_level": 1,
          "aa_start": 356,
          "aa_end": null,
          "aa_length": 410,
          "cds_start": 1066,
          "cds_end": null,
          "cds_length": 1233,
          "cdna_start": 1066,
          "cdna_end": null,
          "cdna_length": 1233,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 5,
          "intron_rank": 3,
          "intron_rank_end": null,
          "gene_symbol": "ENSG00000240291",
          "gene_hgnc_id": 58168,
          "hgvs_c": "n.377-258G>T",
          "hgvs_p": null,
          "transcript": "ENST00000425669.1",
          "protein_id": null,
          "transcript_support_level": 1,
          "aa_start": null,
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          "aa_length": null,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": null,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 1028,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "R",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
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          ],
          "exon_rank": 14,
          "exon_rank_end": null,
          "exon_count": 14,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CACNB2",
          "gene_hgnc_id": 1402,
          "hgvs_c": "c.1744C>A",
          "hgvs_p": "p.Arg582Arg",
          "transcript": "NM_201597.3",
          "protein_id": "NP_963891.1",
          "transcript_support_level": null,
          "aa_start": 582,
          "aa_end": null,
          "aa_length": 636,
          "cds_start": 1744,
          "cds_end": null,
          "cds_length": 1911,
          "cdna_start": 2057,
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          "cdna_length": 6057,
          "mane_select": null,
          "mane_plus": null,
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          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "R",
          "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": "CACNB2",
          "gene_hgnc_id": 1402,
          "hgvs_c": "c.1732C>A",
          "hgvs_p": "p.Arg578Arg",
          "transcript": "NM_201571.4",
          "protein_id": "NP_963865.2",
          "transcript_support_level": null,
          "aa_start": 578,
          "aa_end": null,
          "aa_length": 632,
          "cds_start": 1732,
          "cds_end": null,
          "cds_length": 1899,
          "cdna_start": 2488,
          "cdna_end": null,
          "cdna_length": 6488,
          "mane_select": null,
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          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "R",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 14,
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          "exon_count": 14,
          "intron_rank": null,
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          "gene_symbol": "CACNB2",
          "gene_hgnc_id": 1402,
          "hgvs_c": "c.1702C>A",
          "hgvs_p": "p.Arg568Arg",
          "transcript": "NM_201593.3",
          "protein_id": "NP_963887.2",
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          "cds_start": 1702,
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          "cdna_start": 2015,
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          "mane_select": null,
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        },
        {
          "aa_ref": "R",
          "aa_alt": "R",
          "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": "CACNB2",
          "gene_hgnc_id": 1402,
          "hgvs_c": "c.1672C>A",
          "hgvs_p": "p.Arg558Arg",
          "transcript": "NM_201570.3",
          "protein_id": "NP_963864.1",
          "transcript_support_level": null,
          "aa_start": 558,
          "aa_end": null,
          "aa_length": 612,
          "cds_start": 1672,
          "cds_end": null,
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          "cdna_start": 2129,
          "cdna_end": null,
          "cdna_length": 6129,
          "mane_select": null,
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          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "R",
          "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": "CACNB2",
          "gene_hgnc_id": 1402,
          "hgvs_c": "c.1660C>A",
          "hgvs_p": "p.Arg554Arg",
          "transcript": "NM_201572.4",
          "protein_id": "NP_963866.2",
          "transcript_support_level": null,
          "aa_start": 554,
          "aa_end": null,
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          "cds_start": 1660,
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          "cds_length": 1827,
          "cdna_start": 2416,
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          "cdna_length": 6416,
          "mane_select": null,
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          "feature": null
        },
        {
          "aa_ref": "R",
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          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
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          ],
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          "exon_count": 14,
          "intron_rank": null,
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          "gene_symbol": "CACNB2",
          "gene_hgnc_id": 1402,
          "hgvs_c": "c.1660C>A",
          "hgvs_p": "p.Arg554Arg",
          "transcript": "ENST00000645287.2",
          "protein_id": "ENSP00000496203.1",
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        },
        {
          "aa_ref": "R",
          "aa_alt": "R",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 13,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
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          "gene_symbol": "CACNB2",
          "gene_hgnc_id": 1402,
          "hgvs_c": "c.1651C>A",
          "hgvs_p": "p.Arg551Arg",
          "transcript": "NM_000724.4",
          "protein_id": "NP_000715.2",
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          "cdna_start": 2199,
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          "cdna_length": 6199,
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          "feature": null
        },
        {
          "aa_ref": "R",
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          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
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          "exon_count": 13,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CACNB2",
          "gene_hgnc_id": 1402,
          "hgvs_c": "c.1636C>A",
          "hgvs_p": "p.Arg546Arg",
          "transcript": "ENST00000652391.1",
          "protein_id": "ENSP00000498938.1",
          "transcript_support_level": null,
          "aa_start": 546,
          "aa_end": null,
          "aa_length": 600,
          "cds_start": 1636,
          "cds_end": null,
          "cds_length": 1803,
          "cdna_start": 1783,
          "cdna_end": null,
          "cdna_length": 2501,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "R",
          "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": "CACNB2",
          "gene_hgnc_id": 1402,
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      "dbsnp": "rs61733968",
      "frequency_reference_population": 6.840619e-7,
      "hom_count_reference_population": 0,
      "allele_count_reference_population": 1,
      "gnomad_exomes_af": 6.84062e-7,
      "gnomad_genomes_af": null,
      "gnomad_exomes_ac": 1,
      "gnomad_genomes_ac": null,
      "gnomad_exomes_homalt": 0,
      "gnomad_genomes_homalt": null,
      "gnomad_mito_homoplasmic": null,
      "gnomad_mito_heteroplasmic": null,
      "computational_score_selected": -0.25,
      "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": -0.25,
      "bayesdelnoaf_prediction": "Benign",
      "phylop100way_score": 5.051,
      "phylop100way_prediction": "Uncertain_significance",
      "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": 0,
      "acmg_classification": "Uncertain_significance",
      "acmg_criteria": "PM2,BP4_Moderate",
      "acmg_by_gene": [
        {
          "score": 0,
          "benign_score": 2,
          "pathogenic_score": 2,
          "criteria": [
            "PM2",
            "BP4_Moderate"
          ],
          "verdict": "Uncertain_significance",
          "transcript": "ENST00000324631.13",
          "gene_symbol": "CACNB2",
          "hgnc_id": 1402,
          "effects": [
            "synonymous_variant"
          ],
          "inheritance_mode": "AD,Unknown",
          "hgvs_c": "c.1816C>A",
          "hgvs_p": "p.Arg606Arg"
        },
        {
          "score": 0,
          "benign_score": 2,
          "pathogenic_score": 2,
          "criteria": [
            "PM2",
            "BP4_Moderate"
          ],
          "verdict": "Uncertain_significance",
          "transcript": "ENST00000425669.1",
          "gene_symbol": "ENSG00000240291",
          "hgnc_id": 58168,
          "effects": [
            "intron_variant"
          ],
          "inheritance_mode": "",
          "hgvs_c": "n.377-258G>T",
          "hgvs_p": null
        }
      ],
      "clinvar_disease": "",
      "clinvar_classification": "",
      "clinvar_review_status": "",
      "clinvar_submissions_summary": "",
      "phenotype_combined": null,
      "pathogenicity_classification_combined": null,
      "custom_annotations": null
    }
  ],
  "message": null
}