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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: 1-47251285-G-A (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=1&pos=47251285&ref=G&alt=A&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "1",
      "pos": 47251285,
      "ref": "G",
      "alt": "A",
      "effect": "stop_gained",
      "transcript": "ENST00000371877.8",
      "consequences": [
        {
          "aa_ref": "Q",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 17,
          "exon_rank_end": null,
          "exon_count": 17,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "STIL",
          "gene_hgnc_id": 10879,
          "hgvs_c": "c.3718C>T",
          "hgvs_p": "p.Gln1240*",
          "transcript": "NM_001048166.1",
          "protein_id": "NP_001041631.1",
          "transcript_support_level": null,
          "aa_start": 1240,
          "aa_end": null,
          "aa_length": 1288,
          "cds_start": 3718,
          "cds_end": null,
          "cds_length": 3867,
          "cdna_start": 3873,
          "cdna_end": null,
          "cdna_length": 5019,
          "mane_select": "ENST00000371877.8",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Q",
          "aa_alt": "*",
          "canonical": true,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 17,
          "exon_rank_end": null,
          "exon_count": 17,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "STIL",
          "gene_hgnc_id": 10879,
          "hgvs_c": "c.3718C>T",
          "hgvs_p": "p.Gln1240*",
          "transcript": "ENST00000371877.8",
          "protein_id": "ENSP00000360944.3",
          "transcript_support_level": 1,
          "aa_start": 1240,
          "aa_end": null,
          "aa_length": 1288,
          "cds_start": 3718,
          "cds_end": null,
          "cds_length": 3867,
          "cdna_start": 3873,
          "cdna_end": null,
          "cdna_length": 5019,
          "mane_select": "NM_001048166.1",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Q",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 18,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "STIL",
          "gene_hgnc_id": 10879,
          "hgvs_c": "c.3715C>T",
          "hgvs_p": "p.Gln1239*",
          "transcript": "ENST00000360380.7",
          "protein_id": "ENSP00000353544.3",
          "transcript_support_level": 1,
          "aa_start": 1239,
          "aa_end": null,
          "aa_length": 1287,
          "cds_start": 3715,
          "cds_end": null,
          "cds_length": 3864,
          "cdna_start": 4079,
          "cdna_end": null,
          "cdna_length": 5225,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Q",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 17,
          "exon_rank_end": null,
          "exon_count": 17,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "STIL",
          "gene_hgnc_id": 10879,
          "hgvs_c": "c.3664C>T",
          "hgvs_p": "p.Gln1222*",
          "transcript": "ENST00000396221.6",
          "protein_id": "ENSP00000379523.2",
          "transcript_support_level": 1,
          "aa_start": 1222,
          "aa_end": null,
          "aa_length": 1270,
          "cds_start": 3664,
          "cds_end": null,
          "cds_length": 3813,
          "cdna_start": 3895,
          "cdna_end": null,
          "cdna_length": 4558,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Q",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 19,
          "exon_rank_end": null,
          "exon_count": 19,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "STIL",
          "gene_hgnc_id": 10879,
          "hgvs_c": "c.3523C>T",
          "hgvs_p": "p.Gln1175*",
          "transcript": "ENST00000447475.7",
          "protein_id": "ENSP00000411664.3",
          "transcript_support_level": 1,
          "aa_start": 1175,
          "aa_end": null,
          "aa_length": 1223,
          "cds_start": 3523,
          "cds_end": null,
          "cds_length": 3672,
          "cdna_start": 3752,
          "cdna_end": null,
          "cdna_length": 3901,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Q",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 18,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "STIL",
          "gene_hgnc_id": 10879,
          "hgvs_c": "c.3715C>T",
          "hgvs_p": "p.Gln1239*",
          "transcript": "NM_001282936.1",
          "protein_id": "NP_001269865.1",
          "transcript_support_level": null,
          "aa_start": 1239,
          "aa_end": null,
          "aa_length": 1287,
          "cds_start": 3715,
          "cds_end": null,
          "cds_length": 3864,
          "cdna_start": 4079,
          "cdna_end": null,
          "cdna_length": 5225,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Q",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 17,
          "exon_rank_end": null,
          "exon_count": 17,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "STIL",
          "gene_hgnc_id": 10879,
          "hgvs_c": "c.3715C>T",
          "hgvs_p": "p.Gln1239*",
          "transcript": "NM_003035.2",
          "protein_id": "NP_003026.2",
          "transcript_support_level": null,
          "aa_start": 1239,
          "aa_end": null,
          "aa_length": 1287,
          "cds_start": 3715,
          "cds_end": null,
          "cds_length": 3864,
          "cdna_start": 3870,
          "cdna_end": null,
          "cdna_length": 5016,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Q",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 18,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "STIL",
          "gene_hgnc_id": 10879,
          "hgvs_c": "c.3664C>T",
          "hgvs_p": "p.Gln1222*",
          "transcript": "NM_001282937.1",
          "protein_id": "NP_001269866.1",
          "transcript_support_level": null,
          "aa_start": 1222,
          "aa_end": null,
          "aa_length": 1270,
          "cds_start": 3664,
          "cds_end": null,
          "cds_length": 3813,
          "cdna_start": 4028,
          "cdna_end": null,
          "cdna_length": 5174,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Q",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 19,
          "exon_rank_end": null,
          "exon_count": 19,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "STIL",
          "gene_hgnc_id": 10879,
          "hgvs_c": "c.3577C>T",
          "hgvs_p": "p.Gln1193*",
          "transcript": "NM_001282938.1",
          "protein_id": "NP_001269867.1",
          "transcript_support_level": null,
          "aa_start": 1193,
          "aa_end": null,
          "aa_length": 1241,
          "cds_start": 3577,
          "cds_end": null,
          "cds_length": 3726,
          "cdna_start": 3941,
          "cdna_end": null,
          "cdna_length": 5087,
          "mane_select": null,
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          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Q",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 19,
          "exon_rank_end": null,
          "exon_count": 19,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "STIL",
          "gene_hgnc_id": 10879,
          "hgvs_c": "c.3577C>T",
          "hgvs_p": "p.Gln1193*",
          "transcript": "NM_001377417.1",
          "protein_id": "NP_001364346.1",
          "transcript_support_level": null,
          "aa_start": 1193,
          "aa_end": null,
          "aa_length": 1241,
          "cds_start": 3577,
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          "cds_length": 3726,
          "cdna_start": 4243,
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          "cdna_length": 5389,
          "mane_select": null,
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        {
          "aa_ref": "Q",
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          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 19,
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          "intron_rank": null,
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          "gene_symbol": "STIL",
          "gene_hgnc_id": 10879,
          "hgvs_c": "c.3577C>T",
          "hgvs_p": "p.Gln1193*",
          "transcript": "ENST00000337817.10",
          "protein_id": "ENSP00000337367.6",
          "transcript_support_level": 5,
          "aa_start": 1193,
          "aa_end": null,
          "aa_length": 1241,
          "cds_start": 3577,
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          "cds_length": 3726,
          "cdna_start": 4239,
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          "cdna_length": 5351,
          "mane_select": null,
          "mane_plus": null,
          "biotype": 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": 18,
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          "exon_count": 18,
          "intron_rank": null,
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          "gene_symbol": "STIL",
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          "hgvs_c": "c.3577C>T",
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        {
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          "strand": false,
          "consequences": [
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          ],
          "exon_rank": 19,
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          "intron_rank": null,
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          "gene_symbol": "STIL",
          "gene_hgnc_id": 10879,
          "hgvs_c": "c.3523C>T",
          "hgvs_p": "p.Gln1175*",
          "transcript": "NM_001282939.1",
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        },
        {
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          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
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          ],
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          "exon_count": 18,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "STIL",
          "gene_hgnc_id": 10879,
          "hgvs_c": "c.3718C>T",
          "hgvs_p": "p.Gln1240*",
          "transcript": "XM_006710834.4",
          "protein_id": "XP_006710897.1",
          "transcript_support_level": null,
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        },
        {
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          "gene_symbol": "STIL",
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          "hgvs_c": "c.3718C>T",
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          "feature": null
        },
        {
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          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
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          ],
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          "exon_count": 18,
          "intron_rank": null,
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          "gene_symbol": "STIL",
          "gene_hgnc_id": 10879,
          "hgvs_c": "c.3718C>T",
          "hgvs_p": "p.Gln1240*",
          "transcript": "XM_011541992.3",
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        {
          "aa_ref": "Q",
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          "exon_rank": 18,
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          "exon_count": 18,
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          "gene_symbol": "STIL",
          "gene_hgnc_id": 10879,
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          "hgvs_p": "p.Gln1240*",
          "transcript": "XM_047428300.1",
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        {
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          "intron_rank": null,
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          "gene_symbol": "STIL",
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        {
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        },
        {
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          "exon_count": 18,
          "intron_rank": null,
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          "gene_symbol": "STIL",
          "gene_hgnc_id": 10879,
          "hgvs_c": "c.3718C>T",
          "hgvs_p": "p.Gln1240*",
          "transcript": "XM_047428312.1",
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          "mane_select": null,
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          "feature": null
        },
        {
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          "protein_coding": true,
          "strand": false,
          "consequences": [
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          ],
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          "exon_count": 18,
          "intron_rank": null,
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      "phenotype_combined": "Microcephaly 7, primary, autosomal recessive",
      "pathogenicity_classification_combined": "Pathogenic",
      "custom_annotations": null
    }
  ],
  "message": null
}