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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: 2-213007940-T-C (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=2&pos=213007940&ref=T&alt=C&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "2",
      "pos": 213007940,
      "ref": "T",
      "alt": "C",
      "effect": "missense_variant",
      "transcript": "NM_016260.3",
      "consequences": [
        {
          "aa_ref": "H",
          "aa_alt": "R",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 9,
          "exon_rank_end": null,
          "exon_count": 9,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "IKZF2",
          "gene_hgnc_id": 13177,
          "hgvs_c": "c.1001A>G",
          "hgvs_p": "p.His334Arg",
          "transcript": "NM_001387220.1",
          "protein_id": "NP_001374149.1",
          "transcript_support_level": null,
          "aa_start": 334,
          "aa_end": null,
          "aa_length": 526,
          "cds_start": 1001,
          "cds_end": null,
          "cds_length": 1581,
          "cdna_start": 1320,
          "cdna_end": null,
          "cdna_length": 9562,
          "mane_select": "ENST00000434687.6",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001387220.1"
        },
        {
          "aa_ref": "H",
          "aa_alt": "R",
          "canonical": true,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 9,
          "exon_rank_end": null,
          "exon_count": 9,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "IKZF2",
          "gene_hgnc_id": 13177,
          "hgvs_c": "c.1001A>G",
          "hgvs_p": "p.His334Arg",
          "transcript": "ENST00000434687.6",
          "protein_id": "ENSP00000412869.1",
          "transcript_support_level": 5,
          "aa_start": 334,
          "aa_end": null,
          "aa_length": 526,
          "cds_start": 1001,
          "cds_end": null,
          "cds_length": 1581,
          "cdna_start": 1320,
          "cdna_end": null,
          "cdna_length": 9562,
          "mane_select": "NM_001387220.1",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000434687.6"
        },
        {
          "aa_ref": "H",
          "aa_alt": "R",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 8,
          "exon_rank_end": null,
          "exon_count": 8,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "IKZF2",
          "gene_hgnc_id": 13177,
          "hgvs_c": "c.1019A>G",
          "hgvs_p": "p.His340Arg",
          "transcript": "ENST00000342002.6",
          "protein_id": "ENSP00000342876.2",
          "transcript_support_level": 1,
          "aa_start": 340,
          "aa_end": null,
          "aa_length": 532,
          "cds_start": 1019,
          "cds_end": null,
          "cds_length": 1599,
          "cdna_start": 1170,
          "cdna_end": null,
          "cdna_length": 3747,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000342002.6"
        },
        {
          "aa_ref": "H",
          "aa_alt": "R",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 9,
          "exon_rank_end": null,
          "exon_count": 9,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "IKZF2",
          "gene_hgnc_id": 13177,
          "hgvs_c": "c.923A>G",
          "hgvs_p": "p.His308Arg",
          "transcript": "ENST00000374319.8",
          "protein_id": "ENSP00000363439.4",
          "transcript_support_level": 1,
          "aa_start": 308,
          "aa_end": null,
          "aa_length": 500,
          "cds_start": 923,
          "cds_end": null,
          "cds_length": 1503,
          "cdna_start": 1233,
          "cdna_end": null,
          "cdna_length": 2001,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000374319.8"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 7,
          "exon_rank_end": null,
          "exon_count": 7,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "IKZF2",
          "gene_hgnc_id": 13177,
          "hgvs_c": "n.*659A>G",
          "hgvs_p": null,
          "transcript": "ENST00000374326.7",
          "protein_id": "ENSP00000363446.3",
          "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": 1401,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "nonsense_mediated_decay",
          "feature": "ENST00000374326.7"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 9,
          "exon_rank_end": null,
          "exon_count": 9,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "IKZF2",
          "gene_hgnc_id": 13177,
          "hgvs_c": "n.*995A>G",
          "hgvs_p": null,
          "transcript": "ENST00000412444.5",
          "protein_id": "ENSP00000413680.1",
          "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": 1737,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "nonsense_mediated_decay",
          "feature": "ENST00000412444.5"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 9,
          "exon_rank_end": null,
          "exon_count": 9,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "IKZF2",
          "gene_hgnc_id": 13177,
          "hgvs_c": "n.*480A>G",
          "hgvs_p": null,
          "transcript": "ENST00000431520.5",
          "protein_id": "ENSP00000396253.1",
          "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": 1780,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "nonsense_mediated_decay",
          "feature": "ENST00000431520.5"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 8,
          "exon_rank_end": null,
          "exon_count": 8,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "IKZF2",
          "gene_hgnc_id": 13177,
          "hgvs_c": "n.*733A>G",
          "hgvs_p": null,
          "transcript": "ENST00000439848.5",
          "protein_id": "ENSP00000389548.1",
          "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": 1763,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "nonsense_mediated_decay",
          "feature": "ENST00000439848.5"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 8,
          "exon_rank_end": null,
          "exon_count": 8,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "IKZF2",
          "gene_hgnc_id": 13177,
          "hgvs_c": "n.*848A>G",
          "hgvs_p": null,
          "transcript": "ENST00000453575.5",
          "protein_id": "ENSP00000411444.1",
          "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": 1594,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "nonsense_mediated_decay",
          "feature": "ENST00000453575.5"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 2,
          "exon_rank_end": null,
          "exon_count": 2,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "IKZF2",
          "gene_hgnc_id": 13177,
          "hgvs_c": "n.1633A>G",
          "hgvs_p": null,
          "transcript": "ENST00000484040.1",
          "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": 3534,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "retained_intron",
          "feature": "ENST00000484040.1"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "3_prime_UTR_variant"
          ],
          "exon_rank": 7,
          "exon_rank_end": null,
          "exon_count": 7,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "IKZF2",
          "gene_hgnc_id": 13177,
          "hgvs_c": "n.*659A>G",
          "hgvs_p": null,
          "transcript": "ENST00000374326.7",
          "protein_id": "ENSP00000363446.3",
          "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": 1401,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "nonsense_mediated_decay",
          "feature": "ENST00000374326.7"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "3_prime_UTR_variant"
          ],
          "exon_rank": 9,
          "exon_rank_end": null,
          "exon_count": 9,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "IKZF2",
          "gene_hgnc_id": 13177,
          "hgvs_c": "n.*995A>G",
          "hgvs_p": null,
          "transcript": "ENST00000412444.5",
          "protein_id": "ENSP00000413680.1",
          "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": 1737,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "nonsense_mediated_decay",
          "feature": "ENST00000412444.5"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "3_prime_UTR_variant"
          ],
          "exon_rank": 9,
          "exon_rank_end": null,
          "exon_count": 9,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "IKZF2",
          "gene_hgnc_id": 13177,
          "hgvs_c": "n.*480A>G",
          "hgvs_p": null,
          "transcript": "ENST00000431520.5",
          "protein_id": "ENSP00000396253.1",
          "transcript_support_level": 1,
          "aa_start": null,
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          "aa_length": null,
          "cds_start": null,
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          "cds_length": null,
          "cdna_start": null,
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          "cdna_length": 1780,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "nonsense_mediated_decay",
          "feature": "ENST00000431520.5"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "3_prime_UTR_variant"
          ],
          "exon_rank": 8,
          "exon_rank_end": null,
          "exon_count": 8,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "IKZF2",
          "gene_hgnc_id": 13177,
          "hgvs_c": "n.*733A>G",
          "hgvs_p": null,
          "transcript": "ENST00000439848.5",
          "protein_id": "ENSP00000389548.1",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": null,
          "cds_start": null,
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          "mane_select": null,
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        },
        {
          "aa_ref": null,
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          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
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          ],
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          "exon_count": 8,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "IKZF2",
          "gene_hgnc_id": 13177,
          "hgvs_c": "n.*848A>G",
          "hgvs_p": null,
          "transcript": "ENST00000453575.5",
          "protein_id": "ENSP00000411444.1",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": null,
          "cds_start": null,
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          "cds_length": null,
          "cdna_start": null,
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          "cdna_length": 1594,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "nonsense_mediated_decay",
          "feature": "ENST00000453575.5"
        },
        {
          "aa_ref": "H",
          "aa_alt": "R",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 8,
          "exon_rank_end": null,
          "exon_count": 8,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "IKZF2",
          "gene_hgnc_id": 13177,
          "hgvs_c": "c.1004A>G",
          "hgvs_p": "p.His335Arg",
          "transcript": "ENST00000852783.1",
          "protein_id": "ENSP00000522842.1",
          "transcript_support_level": null,
          "aa_start": 335,
          "aa_end": null,
          "aa_length": 527,
          "cds_start": 1004,
          "cds_end": null,
          "cds_length": 1584,
          "cdna_start": 1210,
          "cdna_end": null,
          "cdna_length": 5796,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000852783.1"
        },
        {
          "aa_ref": "H",
          "aa_alt": "R",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 8,
          "exon_rank_end": null,
          "exon_count": 8,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "IKZF2",
          "gene_hgnc_id": 13177,
          "hgvs_c": "c.1001A>G",
          "hgvs_p": "p.His334Arg",
          "transcript": "NM_001371274.1",
          "protein_id": "NP_001358203.1",
          "transcript_support_level": null,
          "aa_start": 334,
          "aa_end": null,
          "aa_length": 526,
          "cds_start": 1001,
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          "cdna_start": 1347,
          "cdna_end": null,
          "cdna_length": 9589,
          "mane_select": null,
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          "biotype": "protein_coding",
          "feature": "NM_001371274.1"
        },
        {
          "aa_ref": "H",
          "aa_alt": "R",
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          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 8,
          "exon_rank_end": null,
          "exon_count": 8,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "IKZF2",
          "gene_hgnc_id": 13177,
          "hgvs_c": "c.1001A>G",
          "hgvs_p": "p.His334Arg",
          "transcript": "NM_016260.3",
          "protein_id": "NP_057344.2",
          "transcript_support_level": null,
          "aa_start": 334,
          "aa_end": null,
          "aa_length": 526,
          "cds_start": 1001,
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          "cds_length": 1581,
          "cdna_start": 1273,
          "cdna_end": null,
          "cdna_length": 9515,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_016260.3"
        },
        {
          "aa_ref": "H",
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          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 8,
          "exon_rank_end": null,
          "exon_count": 8,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "IKZF2",
          "gene_hgnc_id": 13177,
          "hgvs_c": "c.1001A>G",
          "hgvs_p": "p.His334Arg",
          "transcript": "ENST00000852782.1",
          "protein_id": "ENSP00000522841.1",
          "transcript_support_level": null,
          "aa_start": 334,
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          "cds_start": 1001,
          "cds_end": null,
          "cds_length": 1581,
          "cdna_start": 1218,
          "cdna_end": null,
          "cdna_length": 5804,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000852782.1"
        },
        {
          "aa_ref": "H",
          "aa_alt": "R",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 9,
          "exon_rank_end": null,
          "exon_count": 9,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "IKZF2",
          "gene_hgnc_id": 13177,
          "hgvs_c": "c.1001A>G",
          "hgvs_p": "p.His334Arg",
          "transcript": "ENST00000852786.1",
          "protein_id": "ENSP00000522845.1",
          "transcript_support_level": null,
          "aa_start": 334,
          "aa_end": null,
          "aa_length": 526,
          "cds_start": 1001,
          "cds_end": null,
          "cds_length": 1581,
          "cdna_start": 1271,
          "cdna_end": null,
          "cdna_length": 3206,
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      "gnomad_mito_heteroplasmic": null,
      "computational_score_selected": 0.07864701747894287,
      "computational_prediction_selected": "Benign",
      "computational_source_selected": "MetaRNN",
      "splice_score_selected": 0,
      "splice_prediction_selected": "Benign",
      "splice_source_selected": "max_spliceai",
      "revel_score": 0.097,
      "revel_prediction": "Benign",
      "alphamissense_score": 0.1703,
      "alphamissense_prediction": null,
      "bayesdelnoaf_score": -0.57,
      "bayesdelnoaf_prediction": "Benign",
      "phylop100way_score": 4.47,
      "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": -2,
      "acmg_classification": "Likely_benign",
      "acmg_criteria": "BP4_Moderate",
      "acmg_by_gene": [
        {
          "score": -2,
          "benign_score": 2,
          "pathogenic_score": 0,
          "criteria": [
            "BP4_Moderate"
          ],
          "verdict": "Likely_benign",
          "transcript": "NM_016260.3",
          "gene_symbol": "IKZF2",
          "hgnc_id": 13177,
          "effects": [
            "missense_variant"
          ],
          "inheritance_mode": "AD,AR,SD",
          "hgvs_c": "c.1001A>G",
          "hgvs_p": "p.His334Arg"
        },
        {
          "score": 0,
          "benign_score": 2,
          "pathogenic_score": 2,
          "criteria": [
            "PM2",
            "BP4_Moderate"
          ],
          "verdict": "Uncertain_significance",
          "transcript": "ENST00000415387.1",
          "gene_symbol": "ENSG00000273118",
          "hgnc_id": null,
          "effects": [
            "intron_variant"
          ],
          "inheritance_mode": "",
          "hgvs_c": "n.81+13525A>G",
          "hgvs_p": null
        }
      ],
      "clinvar_disease": "not provided",
      "clinvar_classification": "Uncertain significance",
      "clinvar_review_status": "criteria provided, single submitter",
      "clinvar_submissions_summary": "US:1",
      "phenotype_combined": "not provided",
      "pathogenicity_classification_combined": "Uncertain significance",
      "custom_annotations": null
    }
  ],
  "message": null
}
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