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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: 11-61304043-G-T (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=11&pos=61304043&ref=G&alt=T&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "11",
      "pos": 61304043,
      "ref": "G",
      "alt": "T",
      "effect": "splice_region_variant,intron_variant",
      "transcript": "NM_001923.5",
      "consequences": [
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 27,
          "intron_rank": 21,
          "intron_rank_end": null,
          "gene_symbol": "DDB1",
          "gene_hgnc_id": 2717,
          "hgvs_c": "c.2662-8C>A",
          "hgvs_p": null,
          "transcript": "NM_001923.5",
          "protein_id": "NP_001914.3",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1140,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 3423,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 4245,
          "mane_select": "ENST00000301764.12",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": true,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 27,
          "intron_rank": 21,
          "intron_rank_end": null,
          "gene_symbol": "DDB1",
          "gene_hgnc_id": 2717,
          "hgvs_c": "c.2662-8C>A",
          "hgvs_p": null,
          "transcript": "ENST00000301764.12",
          "protein_id": "ENSP00000301764.7",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1140,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 3423,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 4245,
          "mane_select": "NM_001923.5",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": true,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 29,
          "intron_rank": 23,
          "intron_rank_end": null,
          "gene_symbol": "DDB1",
          "gene_hgnc_id": 2717,
          "hgvs_c": "n.2662-8C>A",
          "hgvs_p": null,
          "transcript": "ENST00000540166.5",
          "protein_id": "ENSP00000440269.1",
          "transcript_support_level": 2,
          "aa_start": null,
          "aa_end": null,
          "aa_length": null,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": null,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 3906,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 28,
          "intron_rank": 22,
          "intron_rank_end": null,
          "gene_symbol": "DDB1",
          "gene_hgnc_id": 2717,
          "hgvs_c": "c.2662-8C>A",
          "hgvs_p": null,
          "transcript": "ENST00000680367.1",
          "protein_id": "ENSP00000506223.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1140,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 3423,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 4426,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 28,
          "intron_rank": 22,
          "intron_rank_end": null,
          "gene_symbol": "DDB1",
          "gene_hgnc_id": 2717,
          "hgvs_c": "c.2662-8C>A",
          "hgvs_p": null,
          "transcript": "ENST00000681803.1",
          "protein_id": "ENSP00000506685.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1140,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 3423,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 4348,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 27,
          "intron_rank": 21,
          "intron_rank_end": null,
          "gene_symbol": "DDB1",
          "gene_hgnc_id": 2717,
          "hgvs_c": "c.2563-8C>A",
          "hgvs_p": null,
          "transcript": "ENST00000681935.1",
          "protein_id": "ENSP00000505717.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1107,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 3324,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 4138,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 27,
          "intron_rank": 21,
          "intron_rank_end": null,
          "gene_symbol": "DDB1",
          "gene_hgnc_id": 2717,
          "hgvs_c": "c.2494-8C>A",
          "hgvs_p": null,
          "transcript": "ENST00000679588.1",
          "protein_id": "ENSP00000506134.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1084,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 3255,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 4184,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 25,
          "intron_rank": 19,
          "intron_rank_end": null,
          "gene_symbol": "DDB1",
          "gene_hgnc_id": 2717,
          "hgvs_c": "c.2449-8C>A",
          "hgvs_p": null,
          "transcript": "ENST00000679712.1",
          "protein_id": "ENSP00000504878.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1069,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 3210,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 4033,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 26,
          "intron_rank": 20,
          "intron_rank_end": null,
          "gene_symbol": "DDB1",
          "gene_hgnc_id": 2717,
          "hgvs_c": "c.2440-8C>A",
          "hgvs_p": null,
          "transcript": "ENST00000680075.1",
          "protein_id": "ENSP00000504954.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1066,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 3201,
          "cdna_start": null,
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          "cdna_length": 3981,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
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          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 25,
          "intron_rank": 19,
          "intron_rank_end": null,
          "gene_symbol": "DDB1",
          "gene_hgnc_id": 2717,
          "hgvs_c": "c.2425-8C>A",
          "hgvs_p": null,
          "transcript": "ENST00000680602.1",
          "protein_id": "ENSP00000505437.1",
          "transcript_support_level": null,
          "aa_start": null,
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          "cds_start": -4,
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          "cdna_start": null,
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          "mane_select": null,
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        {
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          "intron_rank": 19,
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          "gene_symbol": "DDB1",
          "gene_hgnc_id": 2717,
          "hgvs_c": "c.2323-8C>A",
          "hgvs_p": null,
          "transcript": "ENST00000680717.1",
          "protein_id": "ENSP00000506457.1",
          "transcript_support_level": null,
          "aa_start": null,
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          "aa_length": 1027,
          "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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        {
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          "canonical": false,
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          "strand": false,
          "consequences": [
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          ],
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          "intron_rank": 18,
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        {
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          "intron_rank": 3,
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          "gene_symbol": "DDB1",
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          "transcript": "ENST00000539332.2",
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        {
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          "consequences": [
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            "intron_variant"
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          "exon_count": 25,
          "intron_rank": 21,
          "intron_rank_end": null,
          "gene_symbol": "DDB1",
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          "hgvs_c": "n.2804-8C>A",
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        {
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        {
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          "canonical": false,
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          "consequences": [
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            "intron_variant"
          ],
          "exon_rank": null,
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          "exon_count": 28,
          "intron_rank": 22,
          "intron_rank_end": null,
          "gene_symbol": "DDB1",
          "gene_hgnc_id": 2717,
          "hgvs_c": "n.*2125-8C>A",
          "hgvs_p": null,
          "transcript": "ENST00000680357.1",
          "protein_id": "ENSP00000506385.1",
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        {
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          "consequences": [
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          "exon_count": 14,
          "intron_rank": 8,
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          "gene_symbol": "DDB1",
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          "hgvs_c": "n.1676-8C>A",
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          "transcript": "ENST00000680452.1",
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          "gene_symbol": "DDB1",
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        {
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          "gene_symbol": "DDB1",
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        },
        {
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          "consequences": [
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          "exon_count": 27,
          "intron_rank": 21,
          "intron_rank_end": null,
          "gene_symbol": "DDB1",
          "gene_hgnc_id": 2717,
          "hgvs_c": "n.*2526-8C>A",
          "hgvs_p": null,
          "transcript": "ENST00000681188.1",
          "protein_id": "ENSP00000506472.1",
          "transcript_support_level": null,
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          "cds_start": -4,
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          "cdna_length": 4329,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
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        {
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          "canonical": false,
          "protein_coding": false,
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          "consequences": [
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            "intron_variant"
          ],
          "exon_rank": null,
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          "exon_count": 22,
          "intron_rank": 21,
          "intron_rank_end": null,
          "gene_symbol": "DDB1",
          "gene_hgnc_id": 2717,
          "hgvs_c": "n.2804-8C>A",
          "hgvs_p": null,
          "transcript": "ENST00000681368.1",
          "protein_id": null,
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": null,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": null,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 3088,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        }
      ],
      "gene_symbol": "DDB1",
      "gene_hgnc_id": 2717,
      "dbsnp": "rs1156756276",
      "frequency_reference_population": 0.0000027372587,
      "hom_count_reference_population": 0,
      "allele_count_reference_population": 4,
      "gnomad_exomes_af": 0.00000273726,
      "gnomad_genomes_af": null,
      "gnomad_exomes_ac": 4,
      "gnomad_genomes_ac": null,
      "gnomad_exomes_homalt": 0,
      "gnomad_genomes_homalt": null,
      "gnomad_mito_homoplasmic": null,
      "gnomad_mito_heteroplasmic": null,
      "computational_score_selected": -0.7400000095367432,
      "computational_prediction_selected": "Benign",
      "computational_source_selected": "BayesDel_noAF",
      "splice_score_selected": 0.09399999678134918,
      "splice_prediction_selected": "Benign",
      "splice_source_selected": "dbscSNV1_RF",
      "revel_score": null,
      "revel_prediction": null,
      "alphamissense_score": null,
      "alphamissense_prediction": null,
      "bayesdelnoaf_score": -0.74,
      "bayesdelnoaf_prediction": "Benign",
      "phylop100way_score": 0.584,
      "phylop100way_prediction": "Benign",
      "spliceai_max_score": 0,
      "spliceai_max_prediction": "Benign",
      "dbscsnv_ada_score": 0.0070435530751636,
      "dbscsnv_ada_prediction": "Benign",
      "apogee2_score": null,
      "apogee2_prediction": null,
      "mitotip_score": null,
      "mitotip_prediction": null,
      "acmg_score": -2,
      "acmg_classification": "Likely_benign",
      "acmg_criteria": "PM2,BP4_Strong",
      "acmg_by_gene": [
        {
          "score": -2,
          "benign_score": 4,
          "pathogenic_score": 2,
          "criteria": [
            "PM2",
            "BP4_Strong"
          ],
          "verdict": "Likely_benign",
          "transcript": "NM_001923.5",
          "gene_symbol": "DDB1",
          "hgnc_id": 2717,
          "effects": [
            "splice_region_variant",
            "intron_variant"
          ],
          "inheritance_mode": "AD",
          "hgvs_c": "c.2662-8C>A",
          "hgvs_p": null
        }
      ],
      "clinvar_disease": "not specified",
      "clinvar_classification": "Uncertain significance",
      "clinvar_review_status": "criteria provided, single submitter",
      "clinvar_submissions_summary": "US:1",
      "phenotype_combined": "not specified",
      "pathogenicity_classification_combined": "Uncertain significance",
      "custom_annotations": null
    }
  ],
  "message": null
}