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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: 15-76572112-C-T (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=15&pos=76572112&ref=C&alt=T&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "15",
      "pos": 76572112,
      "ref": "C",
      "alt": "T",
      "effect": "intron_variant",
      "transcript": "NM_001353009.2",
      "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": 32,
          "intron_rank": 23,
          "intron_rank_end": null,
          "gene_symbol": "SCAPER",
          "gene_hgnc_id": 13081,
          "hgvs_c": "c.2838+2046G>A",
          "hgvs_p": null,
          "transcript": "NM_020843.4",
          "protein_id": "NP_065894.2",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1400,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 4203,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": "ENST00000563290.6",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_020843.4"
        },
        {
          "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": 32,
          "intron_rank": 23,
          "intron_rank_end": null,
          "gene_symbol": "SCAPER",
          "gene_hgnc_id": 13081,
          "hgvs_c": "c.2838+2046G>A",
          "hgvs_p": null,
          "transcript": "ENST00000563290.6",
          "protein_id": "ENSP00000454973.1",
          "transcript_support_level": 5,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1400,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 4203,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": "NM_020843.4",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000563290.6"
        },
        {
          "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": 31,
          "intron_rank": 22,
          "intron_rank_end": null,
          "gene_symbol": "SCAPER",
          "gene_hgnc_id": 13081,
          "hgvs_c": "c.2838+2046G>A",
          "hgvs_p": null,
          "transcript": "ENST00000324767.11",
          "protein_id": "ENSP00000326924.7",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1400,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 4203,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000324767.11"
        },
        {
          "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": 32,
          "intron_rank": 23,
          "intron_rank_end": null,
          "gene_symbol": "SCAPER",
          "gene_hgnc_id": 13081,
          "hgvs_c": "c.2100+2046G>A",
          "hgvs_p": null,
          "transcript": "ENST00000538941.6",
          "protein_id": "ENSP00000442190.2",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1154,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 3465,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000538941.6"
        },
        {
          "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": 33,
          "intron_rank": 24,
          "intron_rank_end": null,
          "gene_symbol": "SCAPER",
          "gene_hgnc_id": 13081,
          "hgvs_c": "c.2856+2046G>A",
          "hgvs_p": null,
          "transcript": "NM_001353009.2",
          "protein_id": "NP_001339938.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1406,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 4221,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001353009.2"
        },
        {
          "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": 32,
          "intron_rank": 23,
          "intron_rank_end": null,
          "gene_symbol": "SCAPER",
          "gene_hgnc_id": 13081,
          "hgvs_c": "c.2856+2046G>A",
          "hgvs_p": null,
          "transcript": "ENST00000867409.1",
          "protein_id": "ENSP00000537468.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1406,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 4221,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000867409.1"
        },
        {
          "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": 33,
          "intron_rank": 24,
          "intron_rank_end": null,
          "gene_symbol": "SCAPER",
          "gene_hgnc_id": 13081,
          "hgvs_c": "c.2856+2046G>A",
          "hgvs_p": null,
          "transcript": "ENST00000940731.1",
          "protein_id": "ENSP00000610790.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1406,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 4221,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000940731.1"
        },
        {
          "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": 32,
          "intron_rank": 23,
          "intron_rank_end": null,
          "gene_symbol": "SCAPER",
          "gene_hgnc_id": 13081,
          "hgvs_c": "c.2808+2046G>A",
          "hgvs_p": null,
          "transcript": "ENST00000867408.1",
          "protein_id": "ENSP00000537467.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1390,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 4173,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000867408.1"
        },
        {
          "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": 31,
          "intron_rank": 22,
          "intron_rank_end": null,
          "gene_symbol": "SCAPER",
          "gene_hgnc_id": 13081,
          "hgvs_c": "c.2772+2046G>A",
          "hgvs_p": null,
          "transcript": "ENST00000969238.1",
          "protein_id": "ENSP00000639297.1",
          "transcript_support_level": null,
          "aa_start": null,
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          "aa_length": 1378,
          "cds_start": null,
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          "cds_length": 4137,
          "cdna_start": null,
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          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000969238.1"
        },
        {
          "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": 31,
          "intron_rank": 23,
          "intron_rank_end": null,
          "gene_symbol": "SCAPER",
          "gene_hgnc_id": 13081,
          "hgvs_c": "c.2838+2046G>A",
          "hgvs_p": null,
          "transcript": "ENST00000969239.1",
          "protein_id": "ENSP00000639298.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1348,
          "cds_start": null,
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          "cdna_start": null,
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        {
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          "canonical": false,
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          "consequences": [
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          "intron_rank": 23,
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          "gene_symbol": "SCAPER",
          "gene_hgnc_id": 13081,
          "hgvs_c": "c.2658+2046G>A",
          "hgvs_p": null,
          "transcript": "ENST00000867407.1",
          "protein_id": "ENSP00000537466.1",
          "transcript_support_level": null,
          "aa_start": null,
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          "aa_length": 1340,
          "cds_start": null,
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          "cdna_start": null,
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          "mane_select": null,
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        {
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          "canonical": false,
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          "consequences": [
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          "gene_symbol": "SCAPER",
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          "cds_start": null,
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        {
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          "gene_symbol": "SCAPER",
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        {
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          "gene_symbol": "SCAPER",
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          "hgvs_c": "c.2436+2046G>A",
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          "transcript": "NM_001353010.2",
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        {
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          "intron_rank": 19,
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          "gene_symbol": "SCAPER",
          "gene_hgnc_id": 13081,
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          "transcript": "ENST00000940730.1",
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          "gene_symbol": "SCAPER",
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          "transcript": "NM_001145923.2",
          "protein_id": "NP_001139395.1",
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        {
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          ],
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          "intron_rank": 23,
          "intron_rank_end": null,
          "gene_symbol": "SCAPER",
          "gene_hgnc_id": 13081,
          "hgvs_c": "c.2913+2046G>A",
          "hgvs_p": null,
          "transcript": "XM_047432621.1",
          "protein_id": "XP_047288577.1",
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          "hgvs_c": "n.2996+2046G>A",
          "hgvs_p": null,
          "transcript": "NR_148227.2",
          "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": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "pseudogene",
          "feature": "NR_148227.2"
        },
        {
          "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": 27,
          "intron_rank": 23,
          "intron_rank_end": null,
          "gene_symbol": "SCAPER",
          "gene_hgnc_id": 13081,
          "hgvs_c": "n.3017+2046G>A",
          "hgvs_p": null,
          "transcript": "XR_007064448.1",
          "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": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "pseudogene",
          "feature": "XR_007064448.1"
        }
      ],
      "gene_symbol": "SCAPER",
      "gene_hgnc_id": 13081,
      "dbsnp": "rs62030374",
      "frequency_reference_population": 0.06696558,
      "hom_count_reference_population": 381,
      "allele_count_reference_population": 10186,
      "gnomad_exomes_af": null,
      "gnomad_genomes_af": 0.0669656,
      "gnomad_exomes_ac": null,
      "gnomad_genomes_ac": 10186,
      "gnomad_exomes_homalt": null,
      "gnomad_genomes_homalt": 381,
      "gnomad_mito_homoplasmic": null,
      "gnomad_mito_heteroplasmic": null,
      "computational_score_selected": -0.800000011920929,
      "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": -0.8,
      "bayesdelnoaf_prediction": "Benign",
      "phylop100way_score": 0.994,
      "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": -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": "NM_001353009.2",
          "gene_symbol": "SCAPER",
          "hgnc_id": 13081,
          "effects": [
            "intron_variant"
          ],
          "inheritance_mode": "AD,AR",
          "hgvs_c": "c.2856+2046G>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
}