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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: 2-214861027-G-A (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=2&pos=214861027&ref=G&alt=A&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "2",
      "pos": 214861027,
      "ref": "G",
      "alt": "A",
      "effect": "intron_variant",
      "transcript": "ENST00000607412.2",
      "consequences": [
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 4,
          "intron_rank": 2,
          "intron_rank_end": null,
          "gene_symbol": "SNHG31",
          "gene_hgnc_id": 54196,
          "hgvs_c": "n.350+26922G>A",
          "hgvs_p": null,
          "transcript": "ENST00000607412.2",
          "protein_id": null,
          "transcript_support_level": 2,
          "aa_start": null,
          "aa_end": null,
          "aa_length": null,
          "cds_start": null,
          "cds_end": null,
          "cds_length": null,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 1938,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "pseudogene",
          "feature": "ENST00000607412.2"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 4,
          "intron_rank": 2,
          "intron_rank_end": null,
          "gene_symbol": "SNHG31",
          "gene_hgnc_id": 54196,
          "hgvs_c": "n.369+26922G>A",
          "hgvs_p": null,
          "transcript": "ENST00000655899.1",
          "protein_id": null,
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": null,
          "cds_start": null,
          "cds_end": null,
          "cds_length": null,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 2104,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "pseudogene",
          "feature": "ENST00000655899.1"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 3,
          "intron_rank": 2,
          "intron_rank_end": null,
          "gene_symbol": "SNHG31",
          "gene_hgnc_id": 54196,
          "hgvs_c": "n.451+26922G>A",
          "hgvs_p": null,
          "transcript": "ENST00000664818.2",
          "protein_id": null,
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": null,
          "cds_start": null,
          "cds_end": null,
          "cds_length": null,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 2264,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "pseudogene",
          "feature": "ENST00000664818.2"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 4,
          "intron_rank": 3,
          "intron_rank_end": null,
          "gene_symbol": "SNHG31",
          "gene_hgnc_id": 54196,
          "hgvs_c": "n.610+18195G>A",
          "hgvs_p": null,
          "transcript": "ENST00000670391.2",
          "protein_id": null,
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": null,
          "cds_start": null,
          "cds_end": null,
          "cds_length": null,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 2376,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "pseudogene",
          "feature": "ENST00000670391.2"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 4,
          "intron_rank": 3,
          "intron_rank_end": null,
          "gene_symbol": "SNHG31",
          "gene_hgnc_id": 54196,
          "hgvs_c": "n.389+18195G>A",
          "hgvs_p": null,
          "transcript": "ENST00000797167.1",
          "protein_id": null,
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": null,
          "cds_start": null,
          "cds_end": null,
          "cds_length": null,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 642,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "pseudogene",
          "feature": "ENST00000797167.1"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 4,
          "intron_rank": 3,
          "intron_rank_end": null,
          "gene_symbol": "SNHG31",
          "gene_hgnc_id": 54196,
          "hgvs_c": "n.471+7236G>A",
          "hgvs_p": null,
          "transcript": "ENST00000797168.1",
          "protein_id": null,
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": null,
          "cds_start": null,
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          "cds_length": null,
          "cdna_start": null,
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          "cdna_length": 724,
          "mane_select": null,
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          "biotype": "pseudogene",
          "feature": "ENST00000797168.1"
        },
        {
          "aa_ref": null,
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          "protein_coding": false,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
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          "exon_count": 4,
          "intron_rank": 3,
          "intron_rank_end": null,
          "gene_symbol": "SNHG31",
          "gene_hgnc_id": 54196,
          "hgvs_c": "n.447+7236G>A",
          "hgvs_p": null,
          "transcript": "ENST00000797169.1",
          "protein_id": null,
          "transcript_support_level": null,
          "aa_start": null,
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          "cds_start": null,
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          "cds_length": null,
          "cdna_start": null,
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          "cdna_length": 700,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "pseudogene",
          "feature": "ENST00000797169.1"
        },
        {
          "aa_ref": null,
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          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
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          ],
          "exon_rank": null,
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          "exon_count": 4,
          "intron_rank": 2,
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          "gene_symbol": "SNHG31",
          "gene_hgnc_id": 54196,
          "hgvs_c": "n.341+26922G>A",
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          "transcript": "ENST00000797170.1",
          "protein_id": null,
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          "aa_start": null,
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          "cds_start": null,
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          "mane_select": null,
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          "feature": "ENST00000797170.1"
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        {
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          "canonical": false,
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          "strand": true,
          "consequences": [
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          ],
          "exon_rank": null,
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          "exon_count": 5,
          "intron_rank": 2,
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          "gene_symbol": "SNHG31",
          "gene_hgnc_id": 54196,
          "hgvs_c": "n.322+26922G>A",
          "hgvs_p": null,
          "transcript": "ENST00000797171.1",
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          "cds_start": null,
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          "cdna_start": null,
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          "biotype": "pseudogene",
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        },
        {
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          "protein_coding": false,
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          "consequences": [
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          "gene_symbol": "SNHG31",
          "gene_hgnc_id": 54196,
          "hgvs_c": "n.320+26922G>A",
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          "transcript": "ENST00000797173.1",
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          "hgvs_c": "n.512+26922G>A",
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        {
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          "gene_symbol": "SNHG31",
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          "strand": true,
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          "gene_symbol": "SNHG31",
          "gene_hgnc_id": 54196,
          "hgvs_c": "n.319+26922G>A",
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        {
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        {
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          "gene_symbol": "SNHG31",
          "gene_hgnc_id": 54196,
          "hgvs_c": "n.351+26922G>A",
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          "transcript": "ENST00000797179.1",
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          "feature": "ENST00000797179.1"
        },
        {
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          "exon_count": 4,
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          "gene_symbol": "SNHG31",
          "gene_hgnc_id": 54196,
          "hgvs_c": "n.321+26922G>A",
          "hgvs_p": null,
          "transcript": "NR_110292.1",
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          "cdna_length": 2240,
          "mane_select": null,
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          "biotype": "pseudogene",
          "feature": "NR_110292.1"
        }
      ],
      "gene_symbol": "SNHG31",
      "gene_hgnc_id": 54196,
      "dbsnp": "rs2592232",
      "frequency_reference_population": 0.73639727,
      "hom_count_reference_population": 41473,
      "allele_count_reference_population": 111872,
      "gnomad_exomes_af": null,
      "gnomad_genomes_af": 0.736397,
      "gnomad_exomes_ac": null,
      "gnomad_genomes_ac": 111872,
      "gnomad_exomes_homalt": null,
      "gnomad_genomes_homalt": 41473,
      "gnomad_mito_homoplasmic": null,
      "gnomad_mito_heteroplasmic": null,
      "computational_score_selected": -1.0499999523162842,
      "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": -1.05,
      "bayesdelnoaf_prediction": "Benign",
      "phylop100way_score": -0.837,
      "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": "ENST00000607412.2",
          "gene_symbol": "SNHG31",
          "hgnc_id": 54196,
          "effects": [
            "intron_variant"
          ],
          "inheritance_mode": "",
          "hgvs_c": "n.350+26922G>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
}
For research and educational, non-commercial use only. Not for clinical or diagnostic use. GeneBe does not provide medical advice. Data use for AI modeling is prohibited: if used, the cost is $0.001 per byte of downloaded uncompressed data.