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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: 14-95094004-C-A (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=14&pos=95094004&ref=C&alt=A&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "14",
      "pos": 95094004,
      "ref": "C",
      "alt": "A",
      "effect": "missense_variant",
      "transcript": "ENST00000343455.8",
      "consequences": [
        {
          "aa_ref": "V",
          "aa_alt": "L",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 24,
          "exon_rank_end": null,
          "exon_count": 27,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "DICER1",
          "gene_hgnc_id": 17098,
          "hgvs_c": "c.5248G>T",
          "hgvs_p": "p.Val1750Leu",
          "transcript": "NM_177438.3",
          "protein_id": "NP_803187.1",
          "transcript_support_level": null,
          "aa_start": 1750,
          "aa_end": null,
          "aa_length": 1922,
          "cds_start": 5248,
          "cds_end": null,
          "cds_length": 5769,
          "cdna_start": 5593,
          "cdna_end": null,
          "cdna_length": 10384,
          "mane_select": "ENST00000343455.8",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "V",
          "aa_alt": "L",
          "canonical": true,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 24,
          "exon_rank_end": null,
          "exon_count": 27,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "DICER1",
          "gene_hgnc_id": 17098,
          "hgvs_c": "c.5248G>T",
          "hgvs_p": "p.Val1750Leu",
          "transcript": "ENST00000343455.8",
          "protein_id": "ENSP00000343745.3",
          "transcript_support_level": 1,
          "aa_start": 1750,
          "aa_end": null,
          "aa_length": 1922,
          "cds_start": 5248,
          "cds_end": null,
          "cds_length": 5769,
          "cdna_start": 5593,
          "cdna_end": null,
          "cdna_length": 10384,
          "mane_select": "NM_177438.3",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "V",
          "aa_alt": "L",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 26,
          "exon_rank_end": null,
          "exon_count": 29,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "DICER1",
          "gene_hgnc_id": 17098,
          "hgvs_c": "c.5248G>T",
          "hgvs_p": "p.Val1750Leu",
          "transcript": "ENST00000393063.6",
          "protein_id": "ENSP00000376783.1",
          "transcript_support_level": 1,
          "aa_start": 1750,
          "aa_end": null,
          "aa_length": 1922,
          "cds_start": 5248,
          "cds_end": null,
          "cds_length": 5769,
          "cdna_start": 5651,
          "cdna_end": null,
          "cdna_length": 7423,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "V",
          "aa_alt": "L",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 24,
          "exon_rank_end": null,
          "exon_count": 27,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "DICER1",
          "gene_hgnc_id": 17098,
          "hgvs_c": "c.5248G>T",
          "hgvs_p": "p.Val1750Leu",
          "transcript": "ENST00000527414.5",
          "protein_id": "ENSP00000435681.1",
          "transcript_support_level": 1,
          "aa_start": 1750,
          "aa_end": null,
          "aa_length": 1922,
          "cds_start": 5248,
          "cds_end": null,
          "cds_length": 5769,
          "cdna_start": 5481,
          "cdna_end": null,
          "cdna_length": 6179,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "V",
          "aa_alt": "L",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 27,
          "exon_rank_end": null,
          "exon_count": 30,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "DICER1",
          "gene_hgnc_id": 17098,
          "hgvs_c": "c.5248G>T",
          "hgvs_p": "p.Val1750Leu",
          "transcript": "ENST00000529720.2",
          "protein_id": "ENSP00000433926.2",
          "transcript_support_level": 1,
          "aa_start": 1750,
          "aa_end": null,
          "aa_length": 1922,
          "cds_start": 5248,
          "cds_end": null,
          "cds_length": 5769,
          "cdna_start": 5583,
          "cdna_end": null,
          "cdna_length": 10374,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "V",
          "aa_alt": "L",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 26,
          "exon_rank_end": null,
          "exon_count": 29,
          "intron_rank": null,
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          "gene_symbol": "DICER1",
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          "hgvs_c": "c.5248G>T",
          "hgvs_p": "p.Val1750Leu",
          "transcript": "ENST00000531162.7",
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          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "V",
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          "protein_coding": true,
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          "consequences": [
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          ],
          "exon_rank": 23,
          "exon_rank_end": null,
          "exon_count": 25,
          "intron_rank": null,
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          "gene_symbol": "DICER1",
          "gene_hgnc_id": 17098,
          "hgvs_c": "c.5248G>T",
          "hgvs_p": "p.Val1750Leu",
          "transcript": "ENST00000541352.5",
          "protein_id": "ENSP00000444719.1",
          "transcript_support_level": 1,
          "aa_start": 1750,
          "aa_end": null,
          "aa_length": 1829,
          "cds_start": 5248,
          "cds_end": null,
          "cds_length": 5490,
          "cdna_start": 5257,
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          "cdna_length": 5621,
          "mane_select": null,
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          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "V",
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          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 24,
          "exon_rank_end": null,
          "exon_count": 27,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "DICER1",
          "gene_hgnc_id": 17098,
          "hgvs_c": "c.5248G>T",
          "hgvs_p": "p.Val1750Leu",
          "transcript": "NM_001271282.3",
          "protein_id": "NP_001258211.1",
          "transcript_support_level": null,
          "aa_start": 1750,
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          "aa_length": 1922,
          "cds_start": 5248,
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          "cdna_start": 5472,
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          "mane_select": null,
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        {
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        {
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        {
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      ],
      "gene_symbol": "DICER1",
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      "dbsnp": "rs1184678913",
      "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": 0.8347547054290771,
      "computational_prediction_selected": "Pathogenic",
      "computational_source_selected": "MetaRNN",
      "splice_score_selected": 0.029999999329447746,
      "splice_prediction_selected": "Benign",
      "splice_source_selected": "max_spliceai",
      "revel_score": 0.588,
      "revel_prediction": "Uncertain_significance",
      "alphamissense_score": 0.9156,
      "alphamissense_prediction": null,
      "bayesdelnoaf_score": 0.28,
      "bayesdelnoaf_prediction": "Pathogenic",
      "phylop100way_score": 7.505,
      "phylop100way_prediction": "Uncertain_significance",
      "spliceai_max_score": 0.03,
      "spliceai_max_prediction": "Benign",
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      "apogee2_prediction": null,
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      "acmg_score": 5,
      "acmg_classification": "Uncertain_significance",
      "acmg_criteria": "PM1,PM2,PP3",
      "acmg_by_gene": [
        {
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          "benign_score": 0,
          "pathogenic_score": 5,
          "criteria": [
            "PM1",
            "PM2",
            "PP3"
          ],
          "verdict": "Uncertain_significance",
          "transcript": "ENST00000343455.8",
          "gene_symbol": "DICER1",
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          "effects": [
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          "inheritance_mode": "AD,Unknown",
          "hgvs_c": "c.5248G>T",
          "hgvs_p": "p.Val1750Leu"
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      ],
      "clinvar_disease": "",
      "clinvar_classification": "",
      "clinvar_review_status": "",
      "clinvar_submissions_summary": "",
      "phenotype_combined": null,
      "pathogenicity_classification_combined": null,
      "custom_annotations": null
    }
  ],
  "message": null
}