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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: 2-166055402-G-A (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=2&pos=166055402&ref=G&alt=A&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "2",
      "pos": 166055402,
      "ref": "G",
      "alt": "A",
      "effect": "intron_variant",
      "transcript": "NM_001165963.4",
      "consequences": [
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 29,
          "intron_rank": 6,
          "intron_rank_end": null,
          "gene_symbol": "SCN1A",
          "gene_hgnc_id": 10585,
          "hgvs_c": "c.474-636C>T",
          "hgvs_p": null,
          "transcript": "NM_001165963.4",
          "protein_id": "NP_001159435.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 2009,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 6030,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 11940,
          "mane_select": "ENST00000674923.1",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": true,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 29,
          "intron_rank": 6,
          "intron_rank_end": null,
          "gene_symbol": "SCN1A",
          "gene_hgnc_id": 10585,
          "hgvs_c": "c.474-636C>T",
          "hgvs_p": null,
          "transcript": "ENST00000674923.1",
          "protein_id": "ENSP00000501589.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 2009,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 6030,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 11940,
          "mane_select": "NM_001165963.4",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": true,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 28,
          "intron_rank": 5,
          "intron_rank_end": null,
          "gene_symbol": "SCN1A",
          "gene_hgnc_id": 10585,
          "hgvs_c": "c.474-636C>T",
          "hgvs_p": null,
          "transcript": "ENST00000303395.9",
          "protein_id": "ENSP00000303540.4",
          "transcript_support_level": 5,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 2009,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 6030,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 11853,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": true,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 26,
          "intron_rank": 3,
          "intron_rank_end": null,
          "gene_symbol": "SCN1A",
          "gene_hgnc_id": 10585,
          "hgvs_c": "c.474-636C>T",
          "hgvs_p": null,
          "transcript": "ENST00000375405.7",
          "protein_id": "ENSP00000364554.3",
          "transcript_support_level": 5,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1998,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 5997,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 8097,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": true,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 28,
          "intron_rank": 5,
          "intron_rank_end": null,
          "gene_symbol": "SCN1A",
          "gene_hgnc_id": 10585,
          "hgvs_c": "c.474-636C>T",
          "hgvs_p": null,
          "transcript": "ENST00000409050.2",
          "protein_id": "ENSP00000386312.1",
          "transcript_support_level": 5,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1981,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 5946,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 7376,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 28,
          "intron_rank": 5,
          "intron_rank_end": null,
          "gene_symbol": "SCN1A",
          "gene_hgnc_id": 10585,
          "hgvs_c": "c.474-636C>T",
          "hgvs_p": null,
          "transcript": "NM_001202435.3",
          "protein_id": "NP_001189364.1",
          "transcript_support_level": null,
          "aa_start": null,
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          "aa_length": 2009,
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          "cdna_start": null,
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          "mane_select": null,
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          "biotype": null,
          "feature": null
        },
        {
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          "protein_coding": true,
          "strand": false,
          "consequences": [
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          ],
          "exon_rank": null,
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          "exon_count": 27,
          "intron_rank": 4,
          "intron_rank_end": null,
          "gene_symbol": "SCN1A",
          "gene_hgnc_id": 10585,
          "hgvs_c": "c.474-636C>T",
          "hgvs_p": null,
          "transcript": "NM_001353948.2",
          "protein_id": "NP_001340877.1",
          "transcript_support_level": null,
          "aa_start": null,
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          "aa_length": 2009,
          "cds_start": -4,
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          "cds_length": 6030,
          "cdna_start": null,
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          "cdna_length": 12933,
          "mane_select": null,
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          "biotype": null,
          "feature": null
        },
        {
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          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
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          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 27,
          "intron_rank": 4,
          "intron_rank_end": null,
          "gene_symbol": "SCN1A",
          "gene_hgnc_id": 10585,
          "hgvs_c": "c.474-636C>T",
          "hgvs_p": null,
          "transcript": "NM_001353949.2",
          "protein_id": "NP_001340878.1",
          "transcript_support_level": null,
          "aa_start": null,
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          "aa_length": 1998,
          "cds_start": -4,
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          "cdna_start": null,
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          "mane_select": null,
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          "feature": null
        },
        {
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          ],
          "exon_rank": null,
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          "gene_symbol": "SCN1A",
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          "transcript": "NM_001353950.2",
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          "gene_symbol": "SCN1A",
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      "computational_score_selected": -0.9300000071525574,
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      "computational_source_selected": "BayesDel_noAF",
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      "splice_source_selected": "max_spliceai",
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      "alphamissense_score": null,
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      "bayesdelnoaf_score": -0.93,
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      "phylop100way_score": -0.331,
      "phylop100way_prediction": "Benign",
      "spliceai_max_score": 0,
      "spliceai_max_prediction": "Benign",
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      "acmg_classification": "Benign",
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      "acmg_by_gene": [
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          "verdict": "Benign",
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          "verdict": "Benign",
          "transcript": "ENST00000651562.1",
          "gene_symbol": "SCN1A-AS1",
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          "effects": [
            "intron_variant"
          ],
          "inheritance_mode": "",
          "hgvs_c": "n.842-4727G>A",
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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
}