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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: 2-151853537-G-C (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=2&pos=151853537&ref=G&alt=C&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "2",
      "pos": 151853537,
      "ref": "G",
      "alt": "C",
      "effect": "missense_variant",
      "transcript": "ENST00000539935.7",
      "consequences": [
        {
          "aa_ref": "Q",
          "aa_alt": "E",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 12,
          "exon_rank_end": null,
          "exon_count": 14,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CACNB4",
          "gene_hgnc_id": 1404,
          "hgvs_c": "c.1027C>G",
          "hgvs_p": "p.Gln343Glu",
          "transcript": "NM_000726.5",
          "protein_id": "NP_000717.2",
          "transcript_support_level": null,
          "aa_start": 343,
          "aa_end": null,
          "aa_length": 520,
          "cds_start": 1027,
          "cds_end": null,
          "cds_length": 1563,
          "cdna_start": 1060,
          "cdna_end": null,
          "cdna_length": 7944,
          "mane_select": "ENST00000539935.7",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Q",
          "aa_alt": "E",
          "canonical": true,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 12,
          "exon_rank_end": null,
          "exon_count": 14,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CACNB4",
          "gene_hgnc_id": 1404,
          "hgvs_c": "c.1027C>G",
          "hgvs_p": "p.Gln343Glu",
          "transcript": "ENST00000539935.7",
          "protein_id": "ENSP00000438949.1",
          "transcript_support_level": 1,
          "aa_start": 343,
          "aa_end": null,
          "aa_length": 520,
          "cds_start": 1027,
          "cds_end": null,
          "cds_length": 1563,
          "cdna_start": 1060,
          "cdna_end": null,
          "cdna_length": 7944,
          "mane_select": "NM_000726.5",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Q",
          "aa_alt": "E",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 11,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CACNB4",
          "gene_hgnc_id": 1404,
          "hgvs_c": "c.925C>G",
          "hgvs_p": "p.Gln309Glu",
          "transcript": "ENST00000534999.7",
          "protein_id": "ENSP00000443893.1",
          "transcript_support_level": 1,
          "aa_start": 309,
          "aa_end": null,
          "aa_length": 486,
          "cds_start": 925,
          "cds_end": null,
          "cds_length": 1461,
          "cdna_start": 1190,
          "cdna_end": null,
          "cdna_length": 8074,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Q",
          "aa_alt": "E",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 12,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CACNB4",
          "gene_hgnc_id": 1404,
          "hgvs_c": "c.1027C>G",
          "hgvs_p": "p.Gln343Glu",
          "transcript": "ENST00000201943.10",
          "protein_id": "ENSP00000201943.5",
          "transcript_support_level": 1,
          "aa_start": 343,
          "aa_end": null,
          "aa_length": 458,
          "cds_start": 1027,
          "cds_end": null,
          "cds_length": 1377,
          "cdna_start": 1039,
          "cdna_end": null,
          "cdna_length": 1389,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": true,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 9,
          "exon_rank_end": null,
          "exon_count": 12,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ENSG00000283228",
          "gene_hgnc_id": null,
          "hgvs_c": "n.*57C>G",
          "hgvs_p": null,
          "transcript": "ENST00000637559.1",
          "protein_id": "ENSP00000489697.1",
          "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": 1373,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": true,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "3_prime_UTR_variant"
          ],
          "exon_rank": 9,
          "exon_rank_end": null,
          "exon_count": 12,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ENSG00000283228",
          "gene_hgnc_id": null,
          "hgvs_c": "n.*57C>G",
          "hgvs_p": null,
          "transcript": "ENST00000637559.1",
          "protein_id": "ENSP00000489697.1",
          "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": 1373,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Q",
          "aa_alt": "E",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 12,
          "exon_rank_end": null,
          "exon_count": 14,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CACNB4",
          "gene_hgnc_id": 1404,
          "hgvs_c": "c.973C>G",
          "hgvs_p": "p.Gln325Glu",
          "transcript": "NM_001005746.4",
          "protein_id": "NP_001005746.1",
          "transcript_support_level": null,
          "aa_start": 325,
          "aa_end": null,
          "aa_length": 502,
          "cds_start": 973,
          "cds_end": null,
          "cds_length": 1509,
          "cdna_start": 1087,
          "cdna_end": null,
          "cdna_length": 7971,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Q",
          "aa_alt": "E",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 12,
          "exon_rank_end": null,
          "exon_count": 14,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CACNB4",
          "gene_hgnc_id": 1404,
          "hgvs_c": "c.973C>G",
          "hgvs_p": "p.Gln325Glu",
          "transcript": "ENST00000638005.1",
          "protein_id": "ENSP00000489677.1",
          "transcript_support_level": 2,
          "aa_start": 325,
          "aa_end": null,
          "aa_length": 502,
          "cds_start": 973,
          "cds_end": null,
          "cds_length": 1509,
          "cdna_start": 1168,
          "cdna_end": null,
          "cdna_length": 4615,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Q",
          "aa_alt": "E",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 13,
          "exon_rank_end": null,
          "exon_count": 15,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CACNB4",
          "gene_hgnc_id": 1404,
          "hgvs_c": "c.937C>G",
          "hgvs_p": "p.Gln313Glu",
          "transcript": "ENST00000637762.1",
          "protein_id": "ENSP00000489876.1",
          "transcript_support_level": 5,
          "aa_start": 313,
          "aa_end": null,
          "aa_length": 490,
          "cds_start": 937,
          "cds_end": null,
          "cds_length": 1473,
          "cdna_start": 1351,
          "cdna_end": null,
          "cdna_length": 3800,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Q",
          "aa_alt": "E",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 11,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CACNB4",
          "gene_hgnc_id": 1404,
          "hgvs_c": "c.925C>G",
          "hgvs_p": "p.Gln309Glu",
          "transcript": "NM_001005747.4",
          "protein_id": "NP_001005747.1",
          "transcript_support_level": null,
          "aa_start": 309,
          "aa_end": null,
          "aa_length": 486,
          "cds_start": 925,
          "cds_end": null,
          "cds_length": 1461,
          "cdna_start": 1190,
          "cdna_end": null,
          "cdna_length": 8074,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Q",
          "aa_alt": "E",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 11,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CACNB4",
          "gene_hgnc_id": 1404,
          "hgvs_c": "c.904C>G",
          "hgvs_p": "p.Gln302Glu",
          "transcript": "ENST00000427385.6",
          "protein_id": "ENSP00000410978.2",
          "transcript_support_level": 5,
          "aa_start": 302,
          "aa_end": null,
          "aa_length": 479,
          "cds_start": 904,
          "cds_end": null,
          "cds_length": 1440,
          "cdna_start": 926,
          "cdna_end": null,
          "cdna_length": 1776,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Q",
          "aa_alt": "E",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 12,
          "exon_rank_end": null,
          "exon_count": 14,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CACNB4",
          "gene_hgnc_id": 1404,
          "hgvs_c": "c.886C>G",
          "hgvs_p": "p.Gln296Glu",
          "transcript": "NM_001320722.3",
          "protein_id": "NP_001307651.1",
          "transcript_support_level": null,
          "aa_start": 296,
          "aa_end": null,
          "aa_length": 473,
          "cds_start": 886,
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          "cds_length": 1422,
          "cdna_start": 1350,
          "cdna_end": null,
          "cdna_length": 8234,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Q",
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          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 12,
          "exon_rank_end": null,
          "exon_count": 14,
          "intron_rank": null,
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          "gene_symbol": "CACNB4",
          "gene_hgnc_id": 1404,
          "hgvs_c": "c.886C>G",
          "hgvs_p": "p.Gln296Glu",
          "transcript": "NM_001330118.1",
          "protein_id": "NP_001317047.1",
          "transcript_support_level": null,
          "aa_start": 296,
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          "cds_start": 886,
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          "cdna_start": 1207,
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          "mane_select": null,
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          "biotype": null,
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        },
        {
          "aa_ref": "Q",
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          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 12,
          "exon_rank_end": null,
          "exon_count": 14,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CACNB4",
          "gene_hgnc_id": 1404,
          "hgvs_c": "c.886C>G",
          "hgvs_p": "p.Gln296Glu",
          "transcript": "ENST00000439467.6",
          "protein_id": "ENSP00000390161.2",
          "transcript_support_level": 5,
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          "aa_end": null,
          "aa_length": 473,
          "cds_start": 886,
          "cds_end": null,
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          "cdna_start": 1207,
          "cdna_end": null,
          "cdna_length": 2159,
          "mane_select": null,
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          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Q",
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          "strand": false,
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          ],
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          "gene_symbol": "CACNB4",
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          "hgvs_c": "c.886C>G",
          "hgvs_p": "p.Gln296Glu",
          "transcript": "ENST00000636598.1",
          "protein_id": "ENSP00000490247.1",
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        {
          "aa_ref": "Q",
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          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 12,
          "exon_rank_end": null,
          "exon_count": 14,
          "intron_rank": null,
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          "gene_symbol": "CACNB4",
          "gene_hgnc_id": 1404,
          "hgvs_c": "c.886C>G",
          "hgvs_p": "p.Gln296Glu",
          "transcript": "ENST00000637217.1",
          "protein_id": "ENSP00000490250.1",
          "transcript_support_level": 5,
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          "aa_length": 473,
          "cds_start": 886,
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          "cdna_start": 1399,
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          "mane_select": null,
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        },
        {
          "aa_ref": "Q",
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          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
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          ],
          "exon_rank": 11,
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          "exon_count": 13,
          "intron_rank": null,
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          "gene_symbol": "CACNB4",
          "gene_hgnc_id": 1404,
          "hgvs_c": "c.883C>G",
          "hgvs_p": "p.Gln295Glu",
          "transcript": "ENST00000360283.11",
          "protein_id": "ENSP00000353425.8",
          "transcript_support_level": 5,
          "aa_start": 295,
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          "cds_start": 883,
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          "cds_length": 1419,
          "cdna_start": 1221,
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          "cdna_length": 1885,
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        },
        {
          "aa_ref": "Q",
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          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
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          "intron_rank": null,
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          "gene_symbol": "CACNB4",
          "gene_hgnc_id": 1404,
          "hgvs_c": "c.850C>G",
          "hgvs_p": "p.Gln284Glu",
          "transcript": "ENST00000636442.1",
          "protein_id": "ENSP00000489779.1",
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        },
        {
          "aa_ref": "Q",
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          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 12,
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          "exon_count": 13,
          "intron_rank": null,
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          "gene_symbol": "CACNB4",
          "gene_hgnc_id": 1404,
          "hgvs_c": "c.1027C>G",
          "hgvs_p": "p.Gln343Glu",
          "transcript": "NM_001145798.2",
          "protein_id": "NP_001139270.1",
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          "cdna_start": 1183,
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          "cdna_length": 7881,
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          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Q",
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          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
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          "exon_count": 12,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CACNB4",
          "gene_hgnc_id": 1404,
          "hgvs_c": "c.823C>G",
          "hgvs_p": "p.Gln275Glu",
          "transcript": "ENST00000636350.1",
          "protein_id": "ENSP00000489621.1",
          "transcript_support_level": 5,
          "aa_start": 275,
          "aa_end": null,
          "aa_length": 452,
          "cds_start": 823,
          "cds_end": null,
          "cds_length": 1359,
          "cdna_start": 908,
          "cdna_end": null,
          "cdna_length": 7654,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Q",
          "aa_alt": "E",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 10,
          "exon_rank_end": null,
          "exon_count": 12,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CACNB4",
          "gene_hgnc_id": 1404,
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      ],
      "gene_symbol": "CACNB4",
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      "dbsnp": "rs1328517680",
      "frequency_reference_population": 0.000010161285,
      "hom_count_reference_population": 0,
      "allele_count_reference_population": 16,
      "gnomad_exomes_af": 0.00000843622,
      "gnomad_genomes_af": 0.0000262871,
      "gnomad_exomes_ac": 12,
      "gnomad_genomes_ac": 4,
      "gnomad_exomes_homalt": 0,
      "gnomad_genomes_homalt": 0,
      "gnomad_mito_homoplasmic": null,
      "gnomad_mito_heteroplasmic": null,
      "computational_score_selected": 0.7343443632125854,
      "computational_prediction_selected": "Uncertain_significance",
      "computational_source_selected": "MetaRNN",
      "splice_score_selected": 0.09000000357627869,
      "splice_prediction_selected": "Benign",
      "splice_source_selected": "max_spliceai",
      "revel_score": 0.489,
      "revel_prediction": "Uncertain_significance",
      "alphamissense_score": 0.6945,
      "alphamissense_prediction": null,
      "bayesdelnoaf_score": -0.1,
      "bayesdelnoaf_prediction": "Benign",
      "phylop100way_score": 10.003,
      "phylop100way_prediction": "Pathogenic",
      "spliceai_max_score": 0.09,
      "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": -4,
      "acmg_classification": "Likely_benign",
      "acmg_criteria": "BS2",
      "acmg_by_gene": [
        {
          "score": -4,
          "benign_score": 4,
          "pathogenic_score": 0,
          "criteria": [
            "BS2"
          ],
          "verdict": "Likely_benign",
          "transcript": "ENST00000539935.7",
          "gene_symbol": "CACNB4",
          "hgnc_id": 1404,
          "effects": [
            "missense_variant"
          ],
          "inheritance_mode": "AD",
          "hgvs_c": "c.1027C>G",
          "hgvs_p": "p.Gln343Glu"
        },
        {
          "score": 2,
          "benign_score": 0,
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          "criteria": [
            "PM2"
          ],
          "verdict": "Uncertain_significance",
          "transcript": "ENST00000637559.1",
          "gene_symbol": "ENSG00000283228",
          "hgnc_id": null,
          "effects": [
            "non_coding_transcript_exon_variant"
          ],
          "inheritance_mode": "",
          "hgvs_c": "n.*57C>G",
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        }
      ],
      "clinvar_disease": "Idiopathic generalized epilepsy,not specified",
      "clinvar_classification": "Uncertain significance",
      "clinvar_review_status": "criteria provided, multiple submitters, no conflicts",
      "clinvar_submissions_summary": "US:2",
      "phenotype_combined": "Idiopathic generalized epilepsy|not specified",
      "pathogenicity_classification_combined": "Uncertain significance",
      "custom_annotations": null
    }
  ],
  "message": null
}