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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: 9-131523066-G-C (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=9&pos=131523066&ref=G&alt=C&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "9",
      "pos": 131523066,
      "ref": "G",
      "alt": "C",
      "effect": "missense_variant",
      "transcript": "ENST00000402686.8",
      "consequences": [
        {
          "aa_ref": "R",
          "aa_alt": "P",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 20,
          "exon_rank_end": null,
          "exon_count": 20,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "POMT1",
          "gene_hgnc_id": 9202,
          "hgvs_c": "c.2138G>C",
          "hgvs_p": "p.Arg713Pro",
          "transcript": "NM_001077365.2",
          "protein_id": "NP_001070833.1",
          "transcript_support_level": null,
          "aa_start": 713,
          "aa_end": null,
          "aa_length": 725,
          "cds_start": 2138,
          "cds_end": null,
          "cds_length": 2178,
          "cdna_start": 2324,
          "cdna_end": null,
          "cdna_length": 3057,
          "mane_select": "ENST00000402686.8",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "P",
          "canonical": true,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 20,
          "exon_rank_end": null,
          "exon_count": 20,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "POMT1",
          "gene_hgnc_id": 9202,
          "hgvs_c": "c.2138G>C",
          "hgvs_p": "p.Arg713Pro",
          "transcript": "ENST00000402686.8",
          "protein_id": "ENSP00000385797.4",
          "transcript_support_level": 1,
          "aa_start": 713,
          "aa_end": null,
          "aa_length": 725,
          "cds_start": 2138,
          "cds_end": null,
          "cds_length": 2178,
          "cdna_start": 2324,
          "cdna_end": null,
          "cdna_length": 3057,
          "mane_select": "NM_001077365.2",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "P",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 20,
          "exon_rank_end": null,
          "exon_count": 20,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "POMT1",
          "gene_hgnc_id": 9202,
          "hgvs_c": "c.2204G>C",
          "hgvs_p": "p.Arg735Pro",
          "transcript": "ENST00000372228.9",
          "protein_id": "ENSP00000361302.3",
          "transcript_support_level": 1,
          "aa_start": 735,
          "aa_end": null,
          "aa_length": 747,
          "cds_start": 2204,
          "cds_end": null,
          "cds_length": 2244,
          "cdna_start": 2519,
          "cdna_end": null,
          "cdna_length": 3252,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "P",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 19,
          "exon_rank_end": null,
          "exon_count": 19,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "POMT1",
          "gene_hgnc_id": 9202,
          "hgvs_c": "c.2195G>C",
          "hgvs_p": "p.Arg732Pro",
          "transcript": "ENST00000423007.6",
          "protein_id": "ENSP00000404119.2",
          "transcript_support_level": 1,
          "aa_start": 732,
          "aa_end": null,
          "aa_length": 744,
          "cds_start": 2195,
          "cds_end": null,
          "cds_length": 2235,
          "cdna_start": 2195,
          "cdna_end": null,
          "cdna_length": 2235,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "P",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 20,
          "exon_rank_end": null,
          "exon_count": 20,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "POMT1",
          "gene_hgnc_id": 9202,
          "hgvs_c": "c.2204G>C",
          "hgvs_p": "p.Arg735Pro",
          "transcript": "NM_001353193.2",
          "protein_id": "NP_001340122.2",
          "transcript_support_level": null,
          "aa_start": 735,
          "aa_end": null,
          "aa_length": 747,
          "cds_start": 2204,
          "cds_end": null,
          "cds_length": 2244,
          "cdna_start": 2630,
          "cdna_end": null,
          "cdna_length": 3363,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "P",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 20,
          "exon_rank_end": null,
          "exon_count": 20,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "POMT1",
          "gene_hgnc_id": 9202,
          "hgvs_c": "c.2204G>C",
          "hgvs_p": "p.Arg735Pro",
          "transcript": "NM_007171.4",
          "protein_id": "NP_009102.4",
          "transcript_support_level": null,
          "aa_start": 735,
          "aa_end": null,
          "aa_length": 747,
          "cds_start": 2204,
          "cds_end": null,
          "cds_length": 2244,
          "cdna_start": 2390,
          "cdna_end": null,
          "cdna_length": 3123,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "P",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 20,
          "exon_rank_end": null,
          "exon_count": 20,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "POMT1",
          "gene_hgnc_id": 9202,
          "hgvs_c": "c.2138G>C",
          "hgvs_p": "p.Arg713Pro",
          "transcript": "NM_001136113.2",
          "protein_id": "NP_001129585.1",
          "transcript_support_level": null,
          "aa_start": 713,
          "aa_end": null,
          "aa_length": 725,
          "cds_start": 2138,
          "cds_end": null,
          "cds_length": 2178,
          "cdna_start": 2564,
          "cdna_end": null,
          "cdna_length": 3297,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "P",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 20,
          "exon_rank_end": null,
          "exon_count": 20,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "POMT1",
          "gene_hgnc_id": 9202,
          "hgvs_c": "c.2138G>C",
          "hgvs_p": "p.Arg713Pro",
          "transcript": "ENST00000676640.1",
          "protein_id": "ENSP00000503281.1",
          "transcript_support_level": null,
          "aa_start": 713,
          "aa_end": null,
          "aa_length": 725,
          "cds_start": 2138,
          "cds_end": null,
          "cds_length": 2178,
          "cdna_start": 2576,
          "cdna_end": null,
          "cdna_length": 3309,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "P",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 19,
          "exon_rank_end": null,
          "exon_count": 19,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "POMT1",
          "gene_hgnc_id": 9202,
          "hgvs_c": "c.2126G>C",
          "hgvs_p": "p.Arg709Pro",
          "transcript": "NM_001374689.1",
          "protein_id": "NP_001361618.1",
          "transcript_support_level": null,
          "aa_start": 709,
          "aa_end": null,
          "aa_length": 721,
          "cds_start": 2126,
          "cds_end": null,
          "cds_length": 2166,
          "cdna_start": 2322,
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          "mane_select": null,
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        },
        {
          "aa_ref": "R",
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          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 19,
          "exon_rank_end": null,
          "exon_count": 19,
          "intron_rank": null,
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          "gene_symbol": "POMT1",
          "gene_hgnc_id": 9202,
          "hgvs_c": "c.2048G>C",
          "hgvs_p": "p.Arg683Pro",
          "transcript": "NM_001353196.2",
          "protein_id": "NP_001340125.1",
          "transcript_support_level": null,
          "aa_start": 683,
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          "aa_length": 695,
          "cds_start": 2048,
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          "cdna_start": 2234,
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          "mane_select": null,
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        {
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          "gene_symbol": "POMT1",
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          "hgvs_c": "c.2048G>C",
          "hgvs_p": "p.Arg683Pro",
          "transcript": "ENST00000678303.1",
          "protein_id": "ENSP00000503696.1",
          "transcript_support_level": null,
          "aa_start": 683,
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          "cds_start": 2048,
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          "cdna_start": 2204,
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        {
          "aa_ref": "R",
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          "strand": true,
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          "exon_count": 19,
          "intron_rank": null,
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          "hgvs_c": "c.2042G>C",
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          "transcript": "NM_001353197.2",
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        {
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          ],
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          "hgvs_c": "c.2042G>C",
          "hgvs_p": "p.Arg681Pro",
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        {
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          "intron_rank": null,
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          "gene_symbol": "POMT1",
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          "hgvs_c": "c.1976G>C",
          "hgvs_p": "p.Arg659Pro",
          "transcript": "NM_001077366.2",
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        {
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        {
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          "gene_symbol": "POMT1",
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          "hgvs_c": "c.1976G>C",
          "hgvs_p": "p.Arg659Pro",
          "transcript": "ENST00000341012.13",
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        {
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          "gene_symbol": "POMT1",
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          "hgvs_p": "p.Arg640Pro",
          "transcript": "NM_001374690.1",
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        {
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        {
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        {
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          "gene_symbol": "POMT1",
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          "hgvs_c": "c.1787G>C",
          "hgvs_p": "p.Arg596Pro",
          "transcript": "NM_001353195.2",
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        },
        {
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      "phylop100way_prediction": "Uncertain_significance",
      "spliceai_max_score": 0,
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      "acmg_score": 4,
      "acmg_classification": "Uncertain_significance",
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      "acmg_by_gene": [
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          "verdict": "Uncertain_significance",
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      "clinvar_disease": "",
      "clinvar_classification": "",
      "clinvar_review_status": "",
      "clinvar_submissions_summary": "",
      "phenotype_combined": null,
      "pathogenicity_classification_combined": null,
      "custom_annotations": null
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  "message": null
}