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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: 15-87932935-A-T (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=15&pos=87932935&ref=A&alt=T&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "15",
      "pos": 87932935,
      "ref": "A",
      "alt": "T",
      "effect": "intron_variant",
      "transcript": "NM_001012338.3",
      "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": 20,
          "intron_rank": 16,
          "intron_rank_end": null,
          "gene_symbol": "NTRK3",
          "gene_hgnc_id": 8033,
          "hgvs_c": "c.1889+77T>A",
          "hgvs_p": null,
          "transcript": "NM_001012338.3",
          "protein_id": "NP_001012338.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 839,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 2520,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": "ENST00000629765.3",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001012338.3"
        },
        {
          "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": 20,
          "intron_rank": 16,
          "intron_rank_end": null,
          "gene_symbol": "NTRK3",
          "gene_hgnc_id": 8033,
          "hgvs_c": "c.1889+77T>A",
          "hgvs_p": null,
          "transcript": "ENST00000629765.3",
          "protein_id": "ENSP00000485864.1",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 839,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 2520,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": "NM_001012338.3",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000629765.3"
        },
        {
          "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": 16,
          "intron_rank": 13,
          "intron_rank_end": null,
          "gene_symbol": "NTRK3",
          "gene_hgnc_id": 8033,
          "hgvs_c": "c.1865+77T>A",
          "hgvs_p": null,
          "transcript": "ENST00000557856.5",
          "protein_id": "ENSP00000453959.1",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 817,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 2454,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000557856.5"
        },
        {
          "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": 14,
          "intron_rank": 13,
          "intron_rank_end": null,
          "gene_symbol": "NTRK3",
          "gene_hgnc_id": 8033,
          "hgvs_c": "c.1865+77T>A",
          "hgvs_p": null,
          "transcript": "ENST00000558676.5",
          "protein_id": "ENSP00000453511.1",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 705,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 2118,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000558676.5"
        },
        {
          "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": 2,
          "intron_rank_end": null,
          "gene_symbol": "NTRK3",
          "gene_hgnc_id": 8033,
          "hgvs_c": "n.286+77T>A",
          "hgvs_p": null,
          "transcript": "ENST00000559680.1",
          "protein_id": null,
          "transcript_support_level": 1,
          "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": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "pseudogene",
          "feature": "ENST00000559680.1"
        },
        {
          "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": 18,
          "intron_rank": 15,
          "intron_rank_end": null,
          "gene_symbol": "NTRK3",
          "gene_hgnc_id": 8033,
          "hgvs_c": "c.2024+77T>A",
          "hgvs_p": null,
          "transcript": "ENST00000889753.1",
          "protein_id": "ENSP00000559812.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 870,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 2613,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000889753.1"
        },
        {
          "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": 19,
          "intron_rank": 14,
          "intron_rank_end": null,
          "gene_symbol": "NTRK3",
          "gene_hgnc_id": 8033,
          "hgvs_c": "c.1889+77T>A",
          "hgvs_p": null,
          "transcript": "ENST00000626019.2",
          "protein_id": "ENSP00000486784.1",
          "transcript_support_level": 5,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 864,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 2595,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000626019.2"
        },
        {
          "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": 17,
          "intron_rank": 13,
          "intron_rank_end": null,
          "gene_symbol": "NTRK3",
          "gene_hgnc_id": 8033,
          "hgvs_c": "c.1865+77T>A",
          "hgvs_p": null,
          "transcript": "ENST00000889752.1",
          "protein_id": "ENSP00000559811.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 842,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 2529,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000889752.1"
        },
        {
          "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": 18,
          "intron_rank": 14,
          "intron_rank_end": null,
          "gene_symbol": "NTRK3",
          "gene_hgnc_id": 8033,
          "hgvs_c": "c.1889+77T>A",
          "hgvs_p": null,
          "transcript": "NM_001375810.1",
          "protein_id": "NP_001362739.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 839,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 2520,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001375810.1"
        },
        {
          "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": 20,
          "intron_rank": 16,
          "intron_rank_end": null,
          "gene_symbol": "NTRK3",
          "gene_hgnc_id": 8033,
          "hgvs_c": "c.1889+77T>A",
          "hgvs_p": null,
          "transcript": "ENST00000695462.1",
          "protein_id": "ENSP00000511942.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 839,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 2520,
          "cdna_start": null,
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          "mane_select": null,
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          "biotype": "protein_coding",
          "feature": "ENST00000695462.1"
        },
        {
          "aa_ref": null,
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          "canonical": false,
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          "strand": false,
          "consequences": [
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          ],
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          "intron_rank": 14,
          "intron_rank_end": null,
          "gene_symbol": "NTRK3",
          "gene_hgnc_id": 8033,
          "hgvs_c": "c.1889+77T>A",
          "hgvs_p": null,
          "transcript": "ENST00000889747.1",
          "protein_id": "ENSP00000559806.1",
          "transcript_support_level": null,
          "aa_start": null,
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          "aa_length": 839,
          "cds_start": null,
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          "cds_length": 2520,
          "cdna_start": null,
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          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000889747.1"
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        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
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          ],
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          "exon_count": 19,
          "intron_rank": 15,
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          "gene_symbol": "NTRK3",
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          "cds_start": null,
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        {
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          "gene_symbol": "NTRK3",
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          "hgvs_c": "c.1865+77T>A",
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        {
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          "intron_rank": 14,
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          "gene_symbol": "NTRK3",
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          "transcript": "ENST00000889749.1",
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        {
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        {
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          "intron_rank_end": null,
          "gene_symbol": "NTRK3",
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          "transcript": "NM_002530.4",
          "protein_id": "NP_002521.2",
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          "gene_symbol": "NTRK3",
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          "hgvs_c": "c.1889+77T>A",
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          "transcript": "ENST00000394480.6",
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          ],
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          "exon_count": 17,
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          "gene_symbol": "NTRK3",
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          "hgvs_c": "c.1889+77T>A",
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          "transcript": "ENST00000889750.1",
          "protein_id": "ENSP00000559809.1",
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          "cdna_start": null,
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        {
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      "gnomad_genomes_ac": null,
      "gnomad_exomes_homalt": null,
      "gnomad_genomes_homalt": null,
      "gnomad_mito_homoplasmic": null,
      "gnomad_mito_heteroplasmic": null,
      "computational_score_selected": -0.9200000166893005,
      "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": -0.92,
      "bayesdelnoaf_prediction": "Benign",
      "phylop100way_score": -0.545,
      "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": "NM_001012338.3",
          "gene_symbol": "NTRK3",
          "hgnc_id": 8033,
          "effects": [
            "intron_variant"
          ],
          "inheritance_mode": "AD",
          "hgvs_c": "c.1889+77T>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
}