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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: 17-40084693-C-A (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=17&pos=40084693&ref=C&alt=A&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "17",
      "pos": 40084693,
      "ref": "C",
      "alt": "A",
      "effect": "synonymous_variant",
      "transcript": "NM_199334.5",
      "consequences": [
        {
          "aa_ref": "R",
          "aa_alt": "R",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 6,
          "exon_rank_end": null,
          "exon_count": 9,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "THRA",
          "gene_hgnc_id": 11796,
          "hgvs_c": "c.454C>A",
          "hgvs_p": "p.Arg152Arg",
          "transcript": "NM_199334.5",
          "protein_id": "NP_955366.1",
          "transcript_support_level": null,
          "aa_start": 152,
          "aa_end": null,
          "aa_length": 410,
          "cds_start": 454,
          "cds_end": null,
          "cds_length": 1233,
          "cdna_start": 879,
          "cdna_end": null,
          "cdna_length": 5204,
          "mane_select": "ENST00000450525.7",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "R",
          "canonical": true,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 6,
          "exon_rank_end": null,
          "exon_count": 9,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "THRA",
          "gene_hgnc_id": 11796,
          "hgvs_c": "c.454C>A",
          "hgvs_p": "p.Arg152Arg",
          "transcript": "ENST00000450525.7",
          "protein_id": "ENSP00000395641.3",
          "transcript_support_level": 1,
          "aa_start": 152,
          "aa_end": null,
          "aa_length": 410,
          "cds_start": 454,
          "cds_end": null,
          "cds_length": 1233,
          "cdna_start": 879,
          "cdna_end": null,
          "cdna_length": 5204,
          "mane_select": "NM_199334.5",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "R",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 6,
          "exon_rank_end": null,
          "exon_count": 10,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "THRA",
          "gene_hgnc_id": 11796,
          "hgvs_c": "c.454C>A",
          "hgvs_p": "p.Arg152Arg",
          "transcript": "ENST00000264637.8",
          "protein_id": "ENSP00000264637.4",
          "transcript_support_level": 1,
          "aa_start": 152,
          "aa_end": null,
          "aa_length": 490,
          "cds_start": 454,
          "cds_end": null,
          "cds_length": 1473,
          "cdna_start": 1034,
          "cdna_end": null,
          "cdna_length": 2538,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "R",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 6,
          "exon_rank_end": null,
          "exon_count": 10,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "THRA",
          "gene_hgnc_id": 11796,
          "hgvs_c": "c.454C>A",
          "hgvs_p": "p.Arg152Arg",
          "transcript": "ENST00000584985.5",
          "protein_id": "ENSP00000463466.1",
          "transcript_support_level": 1,
          "aa_start": 152,
          "aa_end": null,
          "aa_length": 451,
          "cds_start": 454,
          "cds_end": null,
          "cds_length": 1356,
          "cdna_start": 1034,
          "cdna_end": null,
          "cdna_length": 2421,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "R",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 6,
          "exon_rank_end": null,
          "exon_count": 10,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "THRA",
          "gene_hgnc_id": 11796,
          "hgvs_c": "c.454C>A",
          "hgvs_p": "p.Arg152Arg",
          "transcript": "NM_001190919.2",
          "protein_id": "NP_001177848.1",
          "transcript_support_level": null,
          "aa_start": 152,
          "aa_end": null,
          "aa_length": 490,
          "cds_start": 454,
          "cds_end": null,
          "cds_length": 1473,
          "cdna_start": 1010,
          "cdna_end": null,
          "cdna_length": 2514,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "R",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 6,
          "exon_rank_end": null,
          "exon_count": 10,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "THRA",
          "gene_hgnc_id": 11796,
          "hgvs_c": "c.454C>A",
          "hgvs_p": "p.Arg152Arg",
          "transcript": "NM_003250.6",
          "protein_id": "NP_003241.2",
          "transcript_support_level": null,
          "aa_start": 152,
          "aa_end": null,
          "aa_length": 490,
          "cds_start": 454,
          "cds_end": null,
          "cds_length": 1473,
          "cdna_start": 879,
          "cdna_end": null,
          "cdna_length": 2383,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "R",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 6,
          "exon_rank_end": null,
          "exon_count": 10,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "THRA",
          "gene_hgnc_id": 11796,
          "hgvs_c": "c.454C>A",
          "hgvs_p": "p.Arg152Arg",
          "transcript": "ENST00000394121.8",
          "protein_id": "ENSP00000377679.4",
          "transcript_support_level": 2,
          "aa_start": 152,
          "aa_end": null,
          "aa_length": 490,
          "cds_start": 454,
          "cds_end": null,
          "cds_length": 1473,
          "cdna_start": 1010,
          "cdna_end": null,
          "cdna_length": 2260,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "R",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 6,
          "exon_rank_end": null,
          "exon_count": 10,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "THRA",
          "gene_hgnc_id": 11796,
          "hgvs_c": "c.454C>A",
          "hgvs_p": "p.Arg152Arg",
          "transcript": "NM_001190918.2",
          "protein_id": "NP_001177847.1",
          "transcript_support_level": null,
          "aa_start": 152,
          "aa_end": null,
          "aa_length": 451,
          "cds_start": 454,
          "cds_end": null,
          "cds_length": 1356,
          "cdna_start": 879,
          "cdna_end": null,
          "cdna_length": 2266,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "R",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 6,
          "exon_rank_end": null,
          "exon_count": 9,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "THRA",
          "gene_hgnc_id": 11796,
          "hgvs_c": "c.454C>A",
          "hgvs_p": "p.Arg152Arg",
          "transcript": "ENST00000546243.5",
          "protein_id": "ENSP00000443972.1",
          "transcript_support_level": 2,
          "aa_start": 152,
          "aa_end": null,
          "aa_length": 410,
          "cds_start": 454,
          "cds_end": null,
          "cds_length": 1233,
          "cdna_start": 856,
          "cdna_end": null,
          "cdna_length": 1909,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "R",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 6,
          "exon_rank_end": null,
          "exon_count": 9,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "THRA",
          "gene_hgnc_id": 11796,
          "hgvs_c": "c.454C>A",
          "hgvs_p": "p.Arg152Arg",
          "transcript": "XM_047436632.1",
          "protein_id": "XP_047292588.1",
          "transcript_support_level": null,
          "aa_start": 152,
          "aa_end": null,
          "aa_length": 410,
          "cds_start": 454,
          "cds_end": null,
          "cds_length": 1233,
          "cdna_start": 1831,
          "cdna_end": null,
          "cdna_length": 6156,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 1,
          "exon_rank_end": null,
          "exon_count": 2,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "THRA",
          "gene_hgnc_id": 11796,
          "hgvs_c": "n.260C>A",
          "hgvs_p": null,
          "transcript": "ENST00000577637.1",
          "protein_id": null,
          "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": 677,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        }
      ],
      "gene_symbol": "THRA",
      "gene_hgnc_id": 11796,
      "dbsnp": "rs746608683",
      "frequency_reference_population": 0.0000013681182,
      "hom_count_reference_population": 0,
      "allele_count_reference_population": 2,
      "gnomad_exomes_af": 0.00000136812,
      "gnomad_genomes_af": null,
      "gnomad_exomes_ac": 2,
      "gnomad_genomes_ac": null,
      "gnomad_exomes_homalt": 0,
      "gnomad_genomes_homalt": null,
      "gnomad_mito_homoplasmic": null,
      "gnomad_mito_heteroplasmic": null,
      "computational_score_selected": -0.2199999988079071,
      "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": -0.22,
      "bayesdelnoaf_prediction": "Benign",
      "phylop100way_score": 3.583,
      "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": 0,
      "acmg_classification": "Uncertain_significance",
      "acmg_criteria": "PM2,BP4_Moderate",
      "acmg_by_gene": [
        {
          "score": 0,
          "benign_score": 2,
          "pathogenic_score": 2,
          "criteria": [
            "PM2",
            "BP4_Moderate"
          ],
          "verdict": "Uncertain_significance",
          "transcript": "NM_199334.5",
          "gene_symbol": "THRA",
          "hgnc_id": 11796,
          "effects": [
            "synonymous_variant"
          ],
          "inheritance_mode": "AD",
          "hgvs_c": "c.454C>A",
          "hgvs_p": "p.Arg152Arg"
        }
      ],
      "clinvar_disease": "",
      "clinvar_classification": "",
      "clinvar_review_status": "",
      "clinvar_submissions_summary": "",
      "phenotype_combined": null,
      "pathogenicity_classification_combined": null,
      "custom_annotations": null
    }
  ],
  "message": null
}