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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: 2-96605403-C-G (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=2&pos=96605403&ref=C&alt=G&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "2",
      "pos": 96605403,
      "ref": "C",
      "alt": "G",
      "effect": "missense_variant",
      "transcript": "NM_001349256.2",
      "consequences": [
        {
          "aa_ref": "R",
          "aa_alt": "P",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 15,
          "exon_rank_end": null,
          "exon_count": 21,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "KANSL3",
          "gene_hgnc_id": 25473,
          "hgvs_c": "c.1850G>C",
          "hgvs_p": "p.Arg617Pro",
          "transcript": "NM_001115016.3",
          "protein_id": "NP_001108488.1",
          "transcript_support_level": null,
          "aa_start": 617,
          "aa_end": null,
          "aa_length": 878,
          "cds_start": 1850,
          "cds_end": null,
          "cds_length": 2637,
          "cdna_start": 1930,
          "cdna_end": null,
          "cdna_length": 5156,
          "mane_select": "ENST00000431828.6",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001115016.3"
        },
        {
          "aa_ref": "R",
          "aa_alt": "P",
          "canonical": true,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 15,
          "exon_rank_end": null,
          "exon_count": 21,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "KANSL3",
          "gene_hgnc_id": 25473,
          "hgvs_c": "c.1850G>C",
          "hgvs_p": "p.Arg617Pro",
          "transcript": "ENST00000431828.6",
          "protein_id": "ENSP00000396749.1",
          "transcript_support_level": 1,
          "aa_start": 617,
          "aa_end": null,
          "aa_length": 878,
          "cds_start": 1850,
          "cds_end": null,
          "cds_length": 2637,
          "cdna_start": 1930,
          "cdna_end": null,
          "cdna_length": 5156,
          "mane_select": "NM_001115016.3",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000431828.6"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 15,
          "exon_rank_end": null,
          "exon_count": 21,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "KANSL3",
          "gene_hgnc_id": 25473,
          "hgvs_c": "n.*1692G>C",
          "hgvs_p": null,
          "transcript": "ENST00000354204.10",
          "protein_id": "ENSP00000346144.7",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": null,
          "cds_start": null,
          "cds_end": null,
          "cds_length": null,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 5253,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "nonsense_mediated_decay",
          "feature": "ENST00000354204.10"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 16,
          "exon_rank_end": null,
          "exon_count": 21,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "KANSL3",
          "gene_hgnc_id": 25473,
          "hgvs_c": "n.1928G>C",
          "hgvs_p": null,
          "transcript": "ENST00000420155.5",
          "protein_id": "ENSP00000414426.1",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": null,
          "cds_start": null,
          "cds_end": null,
          "cds_length": null,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 5028,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "nonsense_mediated_decay",
          "feature": "ENST00000420155.5"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 15,
          "exon_rank_end": null,
          "exon_count": 20,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "KANSL3",
          "gene_hgnc_id": 25473,
          "hgvs_c": "n.1934G>C",
          "hgvs_p": null,
          "transcript": "ENST00000487070.5",
          "protein_id": null,
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": null,
          "cds_start": null,
          "cds_end": null,
          "cds_length": null,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 4937,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "pseudogene",
          "feature": "ENST00000487070.5"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "3_prime_UTR_variant"
          ],
          "exon_rank": 15,
          "exon_rank_end": null,
          "exon_count": 21,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "KANSL3",
          "gene_hgnc_id": 25473,
          "hgvs_c": "n.*1692G>C",
          "hgvs_p": null,
          "transcript": "ENST00000354204.10",
          "protein_id": "ENSP00000346144.7",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": null,
          "cds_start": null,
          "cds_end": null,
          "cds_length": null,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 5253,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "nonsense_mediated_decay",
          "feature": "ENST00000354204.10"
        },
        {
          "aa_ref": "R",
          "aa_alt": "P",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 16,
          "exon_rank_end": null,
          "exon_count": 22,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "KANSL3",
          "gene_hgnc_id": 25473,
          "hgvs_c": "c.1928G>C",
          "hgvs_p": "p.Arg643Pro",
          "transcript": "NM_001349256.2",
          "protein_id": "NP_001336185.1",
          "transcript_support_level": null,
          "aa_start": 643,
          "aa_end": null,
          "aa_length": 907,
          "cds_start": 1928,
          "cds_end": null,
          "cds_length": 2724,
          "cdna_start": 2008,
          "cdna_end": null,
          "cdna_length": 3625,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001349256.2"
        },
        {
          "aa_ref": "R",
          "aa_alt": "P",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 16,
          "exon_rank_end": null,
          "exon_count": 22,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "KANSL3",
          "gene_hgnc_id": 25473,
          "hgvs_c": "c.1928G>C",
          "hgvs_p": "p.Arg643Pro",
          "transcript": "NM_001349257.2",
          "protein_id": "NP_001336186.1",
          "transcript_support_level": null,
          "aa_start": 643,
          "aa_end": null,
          "aa_length": 904,
          "cds_start": 1928,
          "cds_end": null,
          "cds_length": 2715,
          "cdna_start": 2008,
          "cdna_end": null,
          "cdna_length": 5234,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001349257.2"
        },
        {
          "aa_ref": "R",
          "aa_alt": "P",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 16,
          "exon_rank_end": null,
          "exon_count": 22,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "KANSL3",
          "gene_hgnc_id": 25473,
          "hgvs_c": "c.1928G>C",
          "hgvs_p": "p.Arg643Pro",
          "transcript": "ENST00000666923.1",
          "protein_id": "ENSP00000499674.1",
          "transcript_support_level": null,
          "aa_start": 643,
          "aa_end": null,
          "aa_length": 904,
          "cds_start": 1928,
          "cds_end": null,
          "cds_length": 2715,
          "cdna_start": 2012,
          "cdna_end": null,
          "cdna_length": 5226,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000666923.1"
        },
        {
          "aa_ref": "R",
          "aa_alt": "P",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 16,
          "exon_rank_end": null,
          "exon_count": 22,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "KANSL3",
          "gene_hgnc_id": 25473,
          "hgvs_c": "c.1928G>C",
          "hgvs_p": "p.Arg643Pro",
          "transcript": "ENST00000883013.1",
          "protein_id": "ENSP00000553072.1",
          "transcript_support_level": null,
          "aa_start": 643,
          "aa_end": null,
          "aa_length": 904,
          "cds_start": 1928,
          "cds_end": null,
          "cds_length": 2715,
          "cdna_start": 2089,
          "cdna_end": null,
          "cdna_length": 5315,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000883013.1"
        },
        {
          "aa_ref": "R",
          "aa_alt": "P",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 16,
          "exon_rank_end": null,
          "exon_count": 22,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "KANSL3",
          "gene_hgnc_id": 25473,
          "hgvs_c": "c.1928G>C",
          "hgvs_p": "p.Arg643Pro",
          "transcript": "ENST00000948575.1",
          "protein_id": "ENSP00000618634.1",
          "transcript_support_level": null,
          "aa_start": 643,
          "aa_end": null,
          "aa_length": 904,
          "cds_start": 1928,
          "cds_end": null,
          "cds_length": 2715,
          "cdna_start": 2111,
          "cdna_end": null,
          "cdna_length": 5335,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000948575.1"
        },
        {
          "aa_ref": "R",
          "aa_alt": "P",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 16,
          "exon_rank_end": null,
          "exon_count": 22,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "KANSL3",
          "gene_hgnc_id": 25473,
          "hgvs_c": "c.1928G>C",
          "hgvs_p": "p.Arg643Pro",
          "transcript": "NM_001349258.2",
          "protein_id": "NP_001336187.1",
          "transcript_support_level": null,
          "aa_start": 643,
          "aa_end": null,
          "aa_length": 902,
          "cds_start": 1928,
          "cds_end": null,
          "cds_length": 2709,
          "cdna_start": 2008,
          "cdna_end": null,
          "cdna_length": 5228,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001349258.2"
        },
        {
          "aa_ref": "R",
          "aa_alt": "P",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 16,
          "exon_rank_end": null,
          "exon_count": 22,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "KANSL3",
          "gene_hgnc_id": 25473,
          "hgvs_c": "c.1928G>C",
          "hgvs_p": "p.Arg643Pro",
          "transcript": "ENST00000883015.1",
          "protein_id": "ENSP00000553074.1",
          "transcript_support_level": null,
          "aa_start": 643,
          "aa_end": null,
          "aa_length": 902,
          "cds_start": 1928,
          "cds_end": null,
          "cds_length": 2709,
          "cdna_start": 2053,
          "cdna_end": null,
          "cdna_length": 5275,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000883015.1"
        },
        {
          "aa_ref": "R",
          "aa_alt": "P",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 16,
          "exon_rank_end": null,
          "exon_count": 22,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "KANSL3",
          "gene_hgnc_id": 25473,
          "hgvs_c": "c.1928G>C",
          "hgvs_p": "p.Arg643Pro",
          "transcript": "ENST00000948573.1",
          "protein_id": "ENSP00000618632.1",
          "transcript_support_level": null,
          "aa_start": 643,
          "aa_end": null,
          "aa_length": 902,
          "cds_start": 1928,
          "cds_end": null,
          "cds_length": 2709,
          "cdna_start": 2005,
          "cdna_end": null,
          "cdna_length": 5195,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000948573.1"
        },
        {
          "aa_ref": "R",
          "aa_alt": "P",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 15,
          "exon_rank_end": null,
          "exon_count": 21,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "KANSL3",
          "gene_hgnc_id": 25473,
          "hgvs_c": "c.1850G>C",
          "hgvs_p": "p.Arg617Pro",
          "transcript": "ENST00000883014.1",
          "protein_id": "ENSP00000553073.1",
          "transcript_support_level": null,
          "aa_start": 617,
          "aa_end": null,
          "aa_length": 878,
          "cds_start": 1850,
          "cds_end": null,
          "cds_length": 2637,
          "cdna_start": 1980,
          "cdna_end": null,
          "cdna_length": 5207,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000883014.1"
        },
        {
          "aa_ref": "R",
          "aa_alt": "P",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 15,
          "exon_rank_end": null,
          "exon_count": 21,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "KANSL3",
          "gene_hgnc_id": 25473,
          "hgvs_c": "c.1850G>C",
          "hgvs_p": "p.Arg617Pro",
          "transcript": "ENST00000948574.1",
          "protein_id": "ENSP00000618633.1",
          "transcript_support_level": null,
          "aa_start": 617,
          "aa_end": null,
          "aa_length": 878,
          "cds_start": 1850,
          "cds_end": null,
          "cds_length": 2637,
          "cdna_start": 2084,
          "cdna_end": null,
          "cdna_length": 5280,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000948574.1"
        },
        {
          "aa_ref": "R",
          "aa_alt": "P",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 15,
          "exon_rank_end": null,
          "exon_count": 21,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "KANSL3",
          "gene_hgnc_id": 25473,
          "hgvs_c": "c.1850G>C",
          "hgvs_p": "p.Arg617Pro",
          "transcript": "ENST00000948576.1",
          "protein_id": "ENSP00000618635.1",
          "transcript_support_level": null,
          "aa_start": 617,
          "aa_end": null,
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          "cds_start": 1850,
          "cds_end": null,
          "cds_length": 2637,
          "cdna_start": 2007,
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          "cdna_length": 5223,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000948576.1"
        },
        {
          "aa_ref": "R",
          "aa_alt": "P",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 14,
          "exon_rank_end": null,
          "exon_count": 20,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "KANSL3",
          "gene_hgnc_id": 25473,
          "hgvs_c": "c.1850G>C",
          "hgvs_p": "p.Arg617Pro",
          "transcript": "ENST00000948577.1",
          "protein_id": "ENSP00000618636.1",
          "transcript_support_level": null,
          "aa_start": 617,
          "aa_end": null,
          "aa_length": 878,
          "cds_start": 1850,
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          "cds_length": 2637,
          "cdna_start": 2084,
          "cdna_end": null,
          "cdna_length": 3813,
          "mane_select": null,
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          "biotype": "protein_coding",
          "feature": "ENST00000948577.1"
        },
        {
          "aa_ref": "R",
          "aa_alt": "P",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 15,
          "exon_rank_end": null,
          "exon_count": 21,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "KANSL3",
          "gene_hgnc_id": 25473,
          "hgvs_c": "c.1850G>C",
          "hgvs_p": "p.Arg617Pro",
          "transcript": "ENST00000883008.1",
          "protein_id": "ENSP00000553067.1",
          "transcript_support_level": null,
          "aa_start": 617,
          "aa_end": null,
          "aa_length": 876,
          "cds_start": 1850,
          "cds_end": null,
          "cds_length": 2631,
          "cdna_start": 1992,
          "cdna_end": null,
          "cdna_length": 5212,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000883008.1"
        },
        {
          "aa_ref": "R",
          "aa_alt": "P",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 15,
          "exon_rank_end": null,
          "exon_count": 21,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "KANSL3",
          "gene_hgnc_id": 25473,
          "hgvs_c": "c.1835G>C",
          "hgvs_p": "p.Arg612Pro",
          "transcript": "ENST00000883011.1",
          "protein_id": "ENSP00000553070.1",
          "transcript_support_level": null,
          "aa_start": 612,
          "aa_end": null,
          "aa_length": 873,
          "cds_start": 1835,
          "cds_end": null,
          "cds_length": 2622,
          "cdna_start": 1935,
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      ],
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      "computational_score_selected": 0.34785398840904236,
      "computational_prediction_selected": "Benign",
      "computational_source_selected": "MetaRNN",
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      "splice_prediction_selected": "Benign",
      "splice_source_selected": "max_spliceai",
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      "revel_prediction": "Benign",
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      "alphamissense_prediction": "Uncertain_significance",
      "bayesdelnoaf_score": 0.07,
      "bayesdelnoaf_prediction": "Uncertain_significance",
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      "phylop100way_prediction": "Uncertain_significance",
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      "acmg_classification": "Uncertain_significance",
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      "acmg_by_gene": [
        {
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          "verdict": "Uncertain_significance",
          "transcript": "NM_001349256.2",
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          "hgvs_p": "p.Arg643Pro"
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      ],
      "clinvar_disease": "",
      "clinvar_classification": "",
      "clinvar_review_status": "",
      "clinvar_submissions_summary": "",
      "phenotype_combined": null,
      "pathogenicity_classification_combined": null,
      "custom_annotations": null
    }
  ],
  "message": null
}
For research and educational, non-commercial use only. Not for clinical or diagnostic use. GeneBe does not provide medical advice. Data use for AI modeling is prohibited: if used, the cost is $0.001 per byte of downloaded uncompressed data.