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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: 17-44114525-G-T (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=17&pos=44114525&ref=G&alt=T&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "17",
      "pos": 44114525,
      "ref": "G",
      "alt": "T",
      "effect": "intron_variant",
      "transcript": "ENST00000682912.1",
      "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": 27,
          "intron_rank": 2,
          "intron_rank_end": null,
          "gene_symbol": "HDAC5",
          "gene_hgnc_id": 14068,
          "hgvs_c": "c.22+2969C>A",
          "hgvs_p": null,
          "transcript": "NM_005474.5",
          "protein_id": "NP_005465.2",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1122,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 3369,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 5319,
          "mane_select": "ENST00000682912.1",
          "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": 27,
          "intron_rank": 2,
          "intron_rank_end": null,
          "gene_symbol": "HDAC5",
          "gene_hgnc_id": 14068,
          "hgvs_c": "c.22+2969C>A",
          "hgvs_p": null,
          "transcript": "ENST00000682912.1",
          "protein_id": "ENSP00000507606.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1122,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 3369,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 5319,
          "mane_select": "NM_005474.5",
          "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": 27,
          "intron_rank": 2,
          "intron_rank_end": null,
          "gene_symbol": "HDAC5",
          "gene_hgnc_id": 14068,
          "hgvs_c": "c.22+2969C>A",
          "hgvs_p": null,
          "transcript": "ENST00000586802.5",
          "protein_id": "ENSP00000468004.1",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1122,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 3369,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 3662,
          "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": 25,
          "intron_rank": 2,
          "intron_rank_end": null,
          "gene_symbol": "HDAC5",
          "gene_hgnc_id": 14068,
          "hgvs_c": "c.22+2969C>A",
          "hgvs_p": null,
          "transcript": "ENST00000336057.9",
          "protein_id": "ENSP00000337290.4",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1037,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 3114,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 5040,
          "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": 27,
          "intron_rank": 2,
          "intron_rank_end": null,
          "gene_symbol": "HDAC5",
          "gene_hgnc_id": 14068,
          "hgvs_c": "c.22+2969C>A",
          "hgvs_p": null,
          "transcript": "NM_001015053.2",
          "protein_id": "NP_001015053.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1123,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 3372,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 5322,
          "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": 27,
          "intron_rank": 2,
          "intron_rank_end": null,
          "gene_symbol": "HDAC5",
          "gene_hgnc_id": 14068,
          "hgvs_c": "c.22+2969C>A",
          "hgvs_p": null,
          "transcript": "ENST00000225983.10",
          "protein_id": "ENSP00000225983.5",
          "transcript_support_level": 5,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1123,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 3372,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 5326,
          "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": 27,
          "intron_rank": 2,
          "intron_rank_end": null,
          "gene_symbol": "HDAC5",
          "gene_hgnc_id": 14068,
          "hgvs_c": "c.22+2969C>A",
          "hgvs_p": null,
          "transcript": "NM_001382393.1",
          "protein_id": "NP_001369322.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1122,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 3369,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 5569,
          "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": 27,
          "intron_rank": 2,
          "intron_rank_end": null,
          "gene_symbol": "HDAC5",
          "gene_hgnc_id": 14068,
          "hgvs_c": "c.22+2969C>A",
          "hgvs_p": null,
          "transcript": "ENST00000715273.1",
          "protein_id": "ENSP00000520442.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1122,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 3369,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 5321,
          "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": 3,
          "intron_rank": 1,
          "intron_rank_end": null,
          "gene_symbol": "HDAC5",
          "gene_hgnc_id": 14068,
          "hgvs_c": "c.-8-3722C>A",
          "hgvs_p": null,
          "transcript": "ENST00000588703.5",
          "protein_id": "ENSP00000465229.1",
          "transcript_support_level": 3,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 78,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 238,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 445,
          "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": 3,
          "intron_rank": 1,
          "intron_rank_end": null,
          "gene_symbol": "HDAC5",
          "gene_hgnc_id": 14068,
          "hgvs_c": "c.-8-3722C>A",
          "hgvs_p": null,
          "transcript": "ENST00000587135.1",
          "protein_id": "ENSP00000465393.1",
          "transcript_support_level": 2,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 39,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 121,
          "cdna_start": null,
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          "cdna_length": 504,
          "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": [
            "intron_variant"
          ],
          "exon_rank": null,
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          "exon_count": 27,
          "intron_rank": 2,
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          "gene_symbol": "HDAC5",
          "gene_hgnc_id": 14068,
          "hgvs_c": "c.22+2969C>A",
          "hgvs_p": null,
          "transcript": "XM_047435047.1",
          "protein_id": "XP_047291003.1",
          "transcript_support_level": null,
          "aa_start": null,
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          "aa_length": 1123,
          "cds_start": -4,
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          "cdna_start": null,
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          "cdna_length": 5572,
          "mane_select": null,
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          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
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          "exon_count": 27,
          "intron_rank": 2,
          "intron_rank_end": null,
          "gene_symbol": "HDAC5",
          "gene_hgnc_id": 14068,
          "hgvs_c": "c.22+2969C>A",
          "hgvs_p": null,
          "transcript": "XM_047435048.1",
          "protein_id": "XP_047291004.1",
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          "cds_start": -4,
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        },
        {
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          "consequences": [
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          "intron_rank": 2,
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          "gene_symbol": "HDAC5",
          "gene_hgnc_id": 14068,
          "hgvs_c": "c.22+2969C>A",
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          "transcript": "XM_047435049.1",
          "protein_id": "XP_047291005.1",
          "transcript_support_level": null,
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        {
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            "intron_variant"
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          "intron_rank": 2,
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          "gene_symbol": "HDAC5",
          "gene_hgnc_id": 14068,
          "hgvs_c": "c.22+2969C>A",
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          "transcript": "XM_047435050.1",
          "protein_id": "XP_047291006.1",
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        },
        {
          "aa_ref": null,
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            "intron_variant"
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          "gene_symbol": "HDAC5",
          "gene_hgnc_id": 14068,
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          "transcript": "XM_047435051.1",
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        {
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          "intron_rank": 2,
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          "gene_symbol": "HDAC5",
          "gene_hgnc_id": 14068,
          "hgvs_c": "c.22+2969C>A",
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          "transcript": "XM_011524149.3",
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        {
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          "exon_count": 27,
          "intron_rank": 2,
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          "gene_symbol": "HDAC5",
          "gene_hgnc_id": 14068,
          "hgvs_c": "c.22+2969C>A",
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          "transcript": "XM_047435052.1",
          "protein_id": "XP_047291008.1",
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          "cdna_length": 5292,
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        },
        {
          "aa_ref": null,
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          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
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          "exon_count": 27,
          "intron_rank": 2,
          "intron_rank_end": null,
          "gene_symbol": "HDAC5",
          "gene_hgnc_id": 14068,
          "hgvs_c": "c.22+2969C>A",
          "hgvs_p": null,
          "transcript": "XM_047435054.1",
          "protein_id": "XP_047291010.1",
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        },
        {
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          "strand": false,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
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          "exon_count": 15,
          "intron_rank": 2,
          "intron_rank_end": null,
          "gene_symbol": "HDAC5",
          "gene_hgnc_id": 14068,
          "hgvs_c": "c.22+2969C>A",
          "hgvs_p": null,
          "transcript": "XM_047435057.1",
          "protein_id": "XP_047291013.1",
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          "cdna_length": 2496,
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        }
      ],
      "gene_symbol": "HDAC5",
      "gene_hgnc_id": 14068,
      "dbsnp": "rs228768",
      "frequency_reference_population": 0.5010258,
      "hom_count_reference_population": 23870,
      "allele_count_reference_population": 76193,
      "gnomad_exomes_af": null,
      "gnomad_genomes_af": 0.501026,
      "gnomad_exomes_ac": null,
      "gnomad_genomes_ac": 76193,
      "gnomad_exomes_homalt": null,
      "gnomad_genomes_homalt": 23870,
      "gnomad_mito_homoplasmic": null,
      "gnomad_mito_heteroplasmic": null,
      "computational_score_selected": -0.4000000059604645,
      "computational_prediction_selected": "Benign",
      "computational_source_selected": "BayesDel_noAF",
      "splice_score_selected": 0,
      "splice_prediction_selected": "Benign",
      "splice_source_selected": "max_spliceai",
      "revel_score": null,
      "revel_prediction": null,
      "alphamissense_score": null,
      "alphamissense_prediction": null,
      "bayesdelnoaf_score": -0.4,
      "bayesdelnoaf_prediction": "Benign",
      "phylop100way_score": 1.638,
      "phylop100way_prediction": "Benign",
      "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": -10,
      "acmg_classification": "Benign",
      "acmg_criteria": "BP4_Moderate,BA1",
      "acmg_by_gene": [
        {
          "score": -10,
          "benign_score": 10,
          "pathogenic_score": 0,
          "criteria": [
            "BP4_Moderate",
            "BA1"
          ],
          "verdict": "Benign",
          "transcript": "ENST00000682912.1",
          "gene_symbol": "HDAC5",
          "hgnc_id": 14068,
          "effects": [
            "intron_variant"
          ],
          "inheritance_mode": "Unknown",
          "hgvs_c": "c.22+2969C>A",
          "hgvs_p": null
        }
      ],
      "clinvar_disease": "",
      "clinvar_classification": "",
      "clinvar_review_status": "",
      "clinvar_submissions_summary": "",
      "phenotype_combined": null,
      "pathogenicity_classification_combined": null,
      "custom_annotations": null
    }
  ],
  "message": null
}