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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: 10-52311959-G-A (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=10&pos=52311959&ref=G&alt=A&genome=hg38&allGenes=true"API Response
json
{
  "variants": [
    {
      "chr": "10",
      "pos": 52311959,
      "ref": "G",
      "alt": "A",
      "effect": "intron_variant",
      "transcript": "ENST00000420193.2",
      "consequences": [
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 9,
          "intron_rank": 2,
          "intron_rank_end": null,
          "gene_symbol": "PRKG1-AS1",
          "gene_hgnc_id": 45029,
          "hgvs_c": "n.583+1439C>T",
          "hgvs_p": null,
          "transcript": "ENST00000420193.2",
          "protein_id": null,
          "transcript_support_level": 3,
          "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": 2771,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 7,
          "intron_rank": 2,
          "intron_rank_end": null,
          "gene_symbol": "PRKG1-AS1",
          "gene_hgnc_id": 45029,
          "hgvs_c": "n.959+1439C>T",
          "hgvs_p": null,
          "transcript": "ENST00000452247.8",
          "protein_id": null,
          "transcript_support_level": 5,
          "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": 2462,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 8,
          "intron_rank": 2,
          "intron_rank_end": null,
          "gene_symbol": "PRKG1-AS1",
          "gene_hgnc_id": 45029,
          "hgvs_c": "n.962+1439C>T",
          "hgvs_p": null,
          "transcript": "ENST00000649494.1",
          "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": 2215,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 5,
          "intron_rank": 1,
          "intron_rank_end": null,
          "gene_symbol": "PRKG1-AS1",
          "gene_hgnc_id": 45029,
          "hgvs_c": "n.81+1439C>T",
          "hgvs_p": null,
          "transcript": "ENST00000658196.1",
          "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": 2977,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 8,
          "intron_rank": 1,
          "intron_rank_end": null,
          "gene_symbol": "PRKG1-AS1",
          "gene_hgnc_id": 45029,
          "hgvs_c": "n.105+1439C>T",
          "hgvs_p": null,
          "transcript": "ENST00000837171.1",
          "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": 859,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 7,
          "intron_rank": 1,
          "intron_rank_end": null,
          "gene_symbol": "PRKG1-AS1",
          "gene_hgnc_id": 45029,
          "hgvs_c": "n.59+1439C>T",
          "hgvs_p": null,
          "transcript": "ENST00000837172.1",
          "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": 687,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 3,
          "intron_rank": 1,
          "intron_rank_end": null,
          "gene_symbol": "PRKG1-AS1",
          "gene_hgnc_id": 45029,
          "hgvs_c": "n.88+1439C>T",
          "hgvs_p": null,
          "transcript": "ENST00000837173.1",
          "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": 324,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 5,
          "intron_rank": 1,
          "intron_rank_end": null,
          "gene_symbol": "PRKG1-AS1",
          "gene_hgnc_id": 45029,
          "hgvs_c": "n.209+1439C>T",
          "hgvs_p": null,
          "transcript": "ENST00000837174.1",
          "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": 639,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 5,
          "intron_rank": 2,
          "intron_rank_end": null,
          "gene_symbol": "PRKG1-AS1",
          "gene_hgnc_id": 45029,
          "hgvs_c": "n.291+1439C>T",
          "hgvs_p": null,
          "transcript": "ENST00000837175.1",
          "protein_id": null,
          "transcript_support_level": null,
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          "cdna_start": null,
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          "cdna_length": 1521,
          "mane_select": null,
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        },
        {
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          "protein_coding": false,
          "strand": false,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
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          "exon_count": 7,
          "intron_rank": 2,
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          "gene_symbol": "PRKG1-AS1",
          "gene_hgnc_id": 45029,
          "hgvs_c": "n.191+1439C>T",
          "hgvs_p": null,
          "transcript": "ENST00000837176.1",
          "protein_id": null,
          "transcript_support_level": null,
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          "cdna_length": 1675,
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        {
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          "consequences": [
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          "exon_rank": null,
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          "exon_count": 8,
          "intron_rank": 2,
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          "gene_symbol": "PRKG1-AS1",
          "gene_hgnc_id": 45029,
          "hgvs_c": "n.282+1439C>T",
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          "transcript": "ENST00000837177.1",
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        {
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          "consequences": [
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          "exon_count": 4,
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          "gene_symbol": "PRKG1-AS1",
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          "hgvs_c": "n.265+1171C>T",
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        {
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          "exon_count": 6,
          "intron_rank": 2,
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          "gene_symbol": "PRKG1-AS1",
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          "hgvs_c": "n.204+1439C>T",
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        {
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          "intron_rank": 2,
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          "gene_symbol": "PRKG1-AS1",
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          "hgvs_c": "n.251+1439C>T",
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          "transcript": "ENST00000837180.1",
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        },
        {
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          "intron_rank": 1,
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          "gene_symbol": "PRKG1-AS1",
          "gene_hgnc_id": 45029,
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        {
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          "intron_rank": 2,
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          "gene_symbol": "PRKG1-AS1",
          "gene_hgnc_id": 45029,
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          "transcript": "ENST00000837183.1",
          "protein_id": null,
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        },
        {
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          "strand": false,
          "consequences": [
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          ],
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          "exon_count": 5,
          "intron_rank": 2,
          "intron_rank_end": null,
          "gene_symbol": "PRKG1-AS1",
          "gene_hgnc_id": 45029,
          "hgvs_c": "n.191+1439C>T",
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          "transcript": "ENST00000837184.1",
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        },
        {
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          ],
          "exon_rank": null,
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          "intron_rank": 2,
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          "gene_symbol": "PRKG1-AS1",
          "gene_hgnc_id": 45029,
          "hgvs_c": "n.225+1439C>T",
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        },
        {
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          ],
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          "intron_rank": 2,
          "intron_rank_end": null,
          "gene_symbol": "PRKG1-AS1",
          "gene_hgnc_id": 45029,
          "hgvs_c": "n.583+1439C>T",
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          "transcript": "NR_038277.1",
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        }
      ],
      "gene_symbol": "PRKG1-AS1",
      "gene_hgnc_id": 45029,
      "dbsnp": "rs7069912",
      "frequency_reference_population": 0.09702346,
      "hom_count_reference_population": 1928,
      "allele_count_reference_population": 14766,
      "gnomad_exomes_af": null,
      "gnomad_genomes_af": 0.0970235,
      "gnomad_exomes_ac": null,
      "gnomad_genomes_ac": 14766,
      "gnomad_exomes_homalt": null,
      "gnomad_genomes_homalt": 1928,
      "gnomad_mito_homoplasmic": null,
      "gnomad_mito_heteroplasmic": null,
      "computational_score_selected": -0.9300000071525574,
      "computational_prediction_selected": "Benign",
      "computational_source_selected": "BayesDel_noAF",
      "splice_score_selected": null,
      "splice_prediction_selected": null,
      "splice_source_selected": null,
      "revel_score": null,
      "revel_prediction": null,
      "alphamissense_score": null,
      "alphamissense_prediction": null,
      "bayesdelnoaf_score": -0.93,
      "bayesdelnoaf_prediction": "Benign",
      "phylop100way_score": 0.119,
      "phylop100way_prediction": "Benign",
      "spliceai_max_score": null,
      "spliceai_max_prediction": null,
      "dbscsnv_ada_score": null,
      "dbscsnv_ada_prediction": null,
      "apogee2_score": null,
      "apogee2_prediction": null,
      "mitotip_score": null,
      "mitotip_prediction": null,
      "acmg_score": -12,
      "acmg_classification": "Benign",
      "acmg_criteria": "BP4_Strong,BA1",
      "acmg_by_gene": [
        {
          "score": -12,
          "benign_score": 12,
          "pathogenic_score": 0,
          "criteria": [
            "BP4_Strong",
            "BA1"
          ],
          "verdict": "Benign",
          "transcript": "ENST00000420193.2",
          "gene_symbol": "PRKG1-AS1",
          "hgnc_id": 45029,
          "effects": [
            "intron_variant"
          ],
          "inheritance_mode": "",
          "hgvs_c": "n.583+1439C>T",
          "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
}