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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: 12-109124475-G-C (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=12&pos=109124475&ref=G&alt=C&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "12",
      "pos": 109124475,
      "ref": "G",
      "alt": "C",
      "effect": "intron_variant",
      "transcript": "ENST00000338432.12",
      "consequences": [
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 53,
          "intron_rank": 1,
          "intron_rank_end": null,
          "gene_symbol": "ACACB",
          "gene_hgnc_id": 85,
          "hgvs_c": "c.-10+7771G>C",
          "hgvs_p": null,
          "transcript": "NM_001093.4",
          "protein_id": "NP_001084.3",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 2458,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 7377,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 9368,
          "mane_select": "ENST00000338432.12",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": true,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 53,
          "intron_rank": 1,
          "intron_rank_end": null,
          "gene_symbol": "ACACB",
          "gene_hgnc_id": 85,
          "hgvs_c": "c.-10+7771G>C",
          "hgvs_p": null,
          "transcript": "ENST00000338432.12",
          "protein_id": "ENSP00000341044.7",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 2458,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 7377,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 9368,
          "mane_select": "NM_001093.4",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 2,
          "exon_rank_end": null,
          "exon_count": 3,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "LOC105369974",
          "gene_hgnc_id": null,
          "hgvs_c": "n.3322C>G",
          "hgvs_p": null,
          "transcript": "XR_945332.3",
          "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": 3782,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 54,
          "intron_rank": 2,
          "intron_rank_end": null,
          "gene_symbol": "ACACB",
          "gene_hgnc_id": 85,
          "hgvs_c": "c.-10+11060G>C",
          "hgvs_p": null,
          "transcript": "NM_001412734.1",
          "protein_id": "NP_001399663.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 2458,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 7377,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 9855,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 53,
          "intron_rank": 2,
          "intron_rank_end": null,
          "gene_symbol": "ACACB",
          "gene_hgnc_id": 85,
          "hgvs_c": "c.26+11060G>C",
          "hgvs_p": null,
          "transcript": "NM_001412737.1",
          "protein_id": "NP_001399666.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 2249,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 6750,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 9027,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 6,
          "intron_rank": 5,
          "intron_rank_end": null,
          "gene_symbol": "UNG",
          "gene_hgnc_id": 12572,
          "hgvs_c": "c.775-1470G>C",
          "hgvs_p": null,
          "transcript": "ENST00000699563.1",
          "protein_id": "ENSP00000514437.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 269,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 810,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 1710,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "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": "ENSG00000256139",
          "gene_hgnc_id": null,
          "hgvs_c": "n.577-786G>C",
          "hgvs_p": null,
          "transcript": "ENST00000541704.2",
          "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": 910,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 52,
          "intron_rank": 1,
          "intron_rank_end": null,
          "gene_symbol": "ACACB",
          "gene_hgnc_id": 85,
          "hgvs_c": "c.-10+11060G>C",
          "hgvs_p": null,
          "transcript": "XM_011538263.4",
          "protein_id": "XP_011536565.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 2395,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 7188,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 10900,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 52,
          "intron_rank": 1,
          "intron_rank_end": null,
          "gene_symbol": "ACACB",
          "gene_hgnc_id": 85,
          "hgvs_c": "c.26+11060G>C",
          "hgvs_p": null,
          "transcript": "XM_011538264.4",
          "protein_id": "XP_011536566.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 2249,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 6750,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 10427,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 53,
          "intron_rank": 2,
          "intron_rank_end": null,
          "gene_symbol": "ACACB",
          "gene_hgnc_id": 85,
          "hgvs_c": "c.26+11060G>C",
          "hgvs_p": null,
          "transcript": "XM_047428764.1",
          "protein_id": "XP_047284720.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 2249,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 6750,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 9222,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 49,
          "intron_rank": 1,
          "intron_rank_end": null,
          "gene_symbol": "ACACB",
          "gene_hgnc_id": 85,
          "hgvs_c": "c.-10+11060G>C",
          "hgvs_p": null,
          "transcript": "XM_047428766.1",
          "protein_id": "XP_047284722.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 2204,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 6615,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 8559,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 49,
          "intron_rank": 1,
          "intron_rank_end": null,
          "gene_symbol": "ACACB",
          "gene_hgnc_id": 85,
          "hgvs_c": "c.-10+11060G>C",
          "hgvs_p": null,
          "transcript": "XM_047428767.1",
          "protein_id": "XP_047284723.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 2192,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 6579,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 8522,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 48,
          "intron_rank": 1,
          "intron_rank_end": null,
          "gene_symbol": "ACACB",
          "gene_hgnc_id": 85,
          "hgvs_c": "c.-10+11060G>C",
          "hgvs_p": null,
          "transcript": "XM_047428768.1",
          "protein_id": "XP_047284724.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 2172,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 6519,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 8535,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 28,
          "intron_rank": 1,
          "intron_rank_end": null,
          "gene_symbol": "ACACB",
          "gene_hgnc_id": 85,
          "hgvs_c": "c.-10+11060G>C",
          "hgvs_p": null,
          "transcript": "XM_011538265.3",
          "protein_id": "XP_011536567.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1304,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 3915,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 5868,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "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": 41,
          "intron_rank": 1,
          "intron_rank_end": null,
          "gene_symbol": "ACACB",
          "gene_hgnc_id": 85,
          "hgvs_c": "n.1839+11060G>C",
          "hgvs_p": null,
          "transcript": "XR_007063072.1",
          "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": 7645,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "downstream_gene_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 3,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ENSG00000256139",
          "gene_hgnc_id": null,
          "hgvs_c": "n.*185G>C",
          "hgvs_p": null,
          "transcript": "ENST00000755021.1",
          "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": 902,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        }
      ],
      "gene_symbol": "ACACB",
      "gene_hgnc_id": 85,
      "dbsnp": "rs2430682",
      "frequency_reference_population": null,
      "hom_count_reference_population": 0,
      "allele_count_reference_population": 0,
      "gnomad_exomes_af": null,
      "gnomad_genomes_af": null,
      "gnomad_exomes_ac": null,
      "gnomad_genomes_ac": null,
      "gnomad_exomes_homalt": null,
      "gnomad_genomes_homalt": null,
      "gnomad_mito_homoplasmic": null,
      "gnomad_mito_heteroplasmic": null,
      "computational_score_selected": -0.9900000095367432,
      "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": -0.99,
      "bayesdelnoaf_prediction": "Benign",
      "phylop100way_score": -0.943,
      "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": -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": "ENST00000338432.12",
          "gene_symbol": "ACACB",
          "hgnc_id": 85,
          "effects": [
            "intron_variant"
          ],
          "inheritance_mode": "Unknown",
          "hgvs_c": "c.-10+7771G>C",
          "hgvs_p": null
        },
        {
          "score": -2,
          "benign_score": 4,
          "pathogenic_score": 2,
          "criteria": [
            "PM2",
            "BP4_Strong"
          ],
          "verdict": "Likely_benign",
          "transcript": "XR_945332.3",
          "gene_symbol": "LOC105369974",
          "hgnc_id": null,
          "effects": [
            "non_coding_transcript_exon_variant"
          ],
          "inheritance_mode": "",
          "hgvs_c": "n.3322C>G",
          "hgvs_p": null
        },
        {
          "score": -2,
          "benign_score": 4,
          "pathogenic_score": 2,
          "criteria": [
            "PM2",
            "BP4_Strong"
          ],
          "verdict": "Likely_benign",
          "transcript": "ENST00000699563.1",
          "gene_symbol": "UNG",
          "hgnc_id": 12572,
          "effects": [
            "intron_variant"
          ],
          "inheritance_mode": "AR",
          "hgvs_c": "c.775-1470G>C",
          "hgvs_p": null
        },
        {
          "score": -2,
          "benign_score": 4,
          "pathogenic_score": 2,
          "criteria": [
            "PM2",
            "BP4_Strong"
          ],
          "verdict": "Likely_benign",
          "transcript": "ENST00000541704.2",
          "gene_symbol": "ENSG00000256139",
          "hgnc_id": null,
          "effects": [
            "intron_variant"
          ],
          "inheritance_mode": "",
          "hgvs_c": "n.577-786G>C",
          "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
}