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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: 2-174571869-A-C (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=2&pos=174571869&ref=A&alt=C&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "2",
      "pos": 174571869,
      "ref": "A",
      "alt": "C",
      "effect": "synonymous_variant",
      "transcript": "ENST00000679041.1",
      "consequences": [
        {
          "aa_ref": "P",
          "aa_alt": "P",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 5,
          "exon_rank_end": null,
          "exon_count": 8,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "WIPF1",
          "gene_hgnc_id": 12736,
          "hgvs_c": "c.936T>G",
          "hgvs_p": "p.Pro312Pro",
          "transcript": "NM_001375834.1",
          "protein_id": "NP_001362763.1",
          "transcript_support_level": null,
          "aa_start": 312,
          "aa_end": null,
          "aa_length": 503,
          "cds_start": 936,
          "cds_end": null,
          "cds_length": 1512,
          "cdna_start": 1178,
          "cdna_end": null,
          "cdna_length": 4727,
          "mane_select": "ENST00000679041.1",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "P",
          "aa_alt": "P",
          "canonical": true,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 5,
          "exon_rank_end": null,
          "exon_count": 8,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "WIPF1",
          "gene_hgnc_id": 12736,
          "hgvs_c": "c.936T>G",
          "hgvs_p": "p.Pro312Pro",
          "transcript": "ENST00000679041.1",
          "protein_id": "ENSP00000503603.1",
          "transcript_support_level": null,
          "aa_start": 312,
          "aa_end": null,
          "aa_length": 503,
          "cds_start": 936,
          "cds_end": null,
          "cds_length": 1512,
          "cdna_start": 1178,
          "cdna_end": null,
          "cdna_length": 4727,
          "mane_select": "NM_001375834.1",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "P",
          "aa_alt": "P",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 5,
          "exon_rank_end": null,
          "exon_count": 9,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "WIPF1",
          "gene_hgnc_id": 12736,
          "hgvs_c": "c.936T>G",
          "hgvs_p": "p.Pro312Pro",
          "transcript": "ENST00000272746.9",
          "protein_id": "ENSP00000272746.5",
          "transcript_support_level": 1,
          "aa_start": 312,
          "aa_end": null,
          "aa_length": 510,
          "cds_start": 936,
          "cds_end": null,
          "cds_length": 1533,
          "cdna_start": 1100,
          "cdna_end": null,
          "cdna_length": 3028,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "P",
          "aa_alt": "P",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 5,
          "exon_rank_end": null,
          "exon_count": 8,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "WIPF1",
          "gene_hgnc_id": 12736,
          "hgvs_c": "c.936T>G",
          "hgvs_p": "p.Pro312Pro",
          "transcript": "ENST00000359761.7",
          "protein_id": "ENSP00000352802.3",
          "transcript_support_level": 1,
          "aa_start": 312,
          "aa_end": null,
          "aa_length": 503,
          "cds_start": 936,
          "cds_end": null,
          "cds_length": 1512,
          "cdna_start": 1084,
          "cdna_end": null,
          "cdna_length": 2003,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "P",
          "aa_alt": "P",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 5,
          "exon_rank_end": null,
          "exon_count": 8,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "WIPF1",
          "gene_hgnc_id": 12736,
          "hgvs_c": "c.936T>G",
          "hgvs_p": "p.Pro312Pro",
          "transcript": "ENST00000392547.6",
          "protein_id": "ENSP00000376330.2",
          "transcript_support_level": 1,
          "aa_start": 312,
          "aa_end": null,
          "aa_length": 503,
          "cds_start": 936,
          "cds_end": null,
          "cds_length": 1512,
          "cdna_start": 1036,
          "cdna_end": null,
          "cdna_length": 4587,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "P",
          "aa_alt": "P",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 5,
          "exon_rank_end": null,
          "exon_count": 7,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "WIPF1",
          "gene_hgnc_id": 12736,
          "hgvs_c": "c.936T>G",
          "hgvs_p": "p.Pro312Pro",
          "transcript": "ENST00000409891.5",
          "protein_id": "ENSP00000386431.1",
          "transcript_support_level": 1,
          "aa_start": 312,
          "aa_end": null,
          "aa_length": 493,
          "cds_start": 936,
          "cds_end": null,
          "cds_length": 1482,
          "cdna_start": 1139,
          "cdna_end": null,
          "cdna_length": 2568,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "P",
          "aa_alt": "P",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 5,
          "exon_rank_end": null,
          "exon_count": 5,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "WIPF1",
          "gene_hgnc_id": 12736,
          "hgvs_c": "c.936T>G",
          "hgvs_p": "p.Pro312Pro",
          "transcript": "ENST00000409415.7",
          "protein_id": "ENSP00000387150.3",
          "transcript_support_level": 1,
          "aa_start": 312,
          "aa_end": null,
          "aa_length": 403,
          "cds_start": 936,
          "cds_end": null,
          "cds_length": 1212,
          "cdna_start": 1072,
          "cdna_end": null,
          "cdna_length": 1772,
          "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": 4,
          "intron_rank": 2,
          "intron_rank_end": null,
          "gene_symbol": "ENSG00000236449",
          "gene_hgnc_id": null,
          "hgvs_c": "n.217+24392A>C",
          "hgvs_p": null,
          "transcript": "ENST00000442996.1",
          "protein_id": null,
          "transcript_support_level": 1,
          "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": 2400,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "P",
          "aa_alt": "P",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 5,
          "exon_rank_end": null,
          "exon_count": 9,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "WIPF1",
          "gene_hgnc_id": 12736,
          "hgvs_c": "c.936T>G",
          "hgvs_p": "p.Pro312Pro",
          "transcript": "NM_001375835.1",
          "protein_id": "NP_001362764.1",
          "transcript_support_level": null,
          "aa_start": 312,
          "aa_end": null,
          "aa_length": 510,
          "cds_start": 936,
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          "cdna_start": 1114,
          "cdna_end": null,
          "cdna_length": 4238,
          "mane_select": null,
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        },
        {
          "aa_ref": "P",
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          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 5,
          "exon_rank_end": null,
          "exon_count": 8,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "WIPF1",
          "gene_hgnc_id": 12736,
          "hgvs_c": "c.936T>G",
          "hgvs_p": "p.Pro312Pro",
          "transcript": "NM_001077269.1",
          "protein_id": "NP_001070737.1",
          "transcript_support_level": null,
          "aa_start": 312,
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          "cds_start": 936,
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          "cdna_start": 1100,
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          "mane_select": null,
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        },
        {
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          "strand": false,
          "consequences": [
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          "exon_rank": 6,
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          "intron_rank": null,
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          "hgvs_c": "c.936T>G",
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          "transcript": "NM_001375832.1",
          "protein_id": "NP_001362761.1",
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          "cds_start": 936,
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          "cdna_start": 1265,
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          "mane_select": null,
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        {
          "aa_ref": "P",
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          "protein_coding": true,
          "strand": false,
          "consequences": [
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          "exon_rank": 6,
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        {
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      "frequency_reference_population": 6.842529e-7,
      "hom_count_reference_population": 0,
      "allele_count_reference_population": 1,
      "gnomad_exomes_af": 6.84253e-7,
      "gnomad_genomes_af": null,
      "gnomad_exomes_ac": 1,
      "gnomad_genomes_ac": null,
      "gnomad_exomes_homalt": 0,
      "gnomad_genomes_homalt": null,
      "gnomad_mito_homoplasmic": null,
      "gnomad_mito_heteroplasmic": null,
      "computational_score_selected": -0.8299999833106995,
      "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": -0.83,
      "bayesdelnoaf_prediction": "Benign",
      "phylop100way_score": -1.829,
      "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": -5,
      "acmg_classification": "Likely_benign",
      "acmg_criteria": "PM2,BP4_Strong,BP6_Moderate,BP7",
      "acmg_by_gene": [
        {
          "score": -5,
          "benign_score": 7,
          "pathogenic_score": 2,
          "criteria": [
            "PM2",
            "BP4_Strong",
            "BP6_Moderate",
            "BP7"
          ],
          "verdict": "Likely_benign",
          "transcript": "ENST00000679041.1",
          "gene_symbol": "WIPF1",
          "hgnc_id": 12736,
          "effects": [
            "synonymous_variant"
          ],
          "inheritance_mode": "AR,AD",
          "hgvs_c": "c.936T>G",
          "hgvs_p": "p.Pro312Pro"
        },
        {
          "score": -4,
          "benign_score": 6,
          "pathogenic_score": 2,
          "criteria": [
            "PM2",
            "BP4_Strong",
            "BP6_Moderate"
          ],
          "verdict": "Likely_benign",
          "transcript": "ENST00000442996.1",
          "gene_symbol": "ENSG00000236449",
          "hgnc_id": null,
          "effects": [
            "intron_variant"
          ],
          "inheritance_mode": "",
          "hgvs_c": "n.217+24392A>C",
          "hgvs_p": null
        }
      ],
      "clinvar_disease": "Wiskott-Aldrich syndrome 2",
      "clinvar_classification": "Likely benign",
      "clinvar_review_status": "criteria provided, single submitter",
      "clinvar_submissions_summary": "LB:1",
      "phenotype_combined": "Wiskott-Aldrich syndrome 2",
      "pathogenicity_classification_combined": "Likely benign",
      "custom_annotations": null
    }
  ],
  "message": null
}