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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: 10-75024983-GGGGT-G (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=10&pos=75024983&ref=GGGGT&alt=G&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "10",
      "pos": 75024983,
      "ref": "GGGGT",
      "alt": "G",
      "effect": "frameshift_variant",
      "transcript": "ENST00000287239.10",
      "consequences": [
        {
          "aa_ref": "RG",
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 17,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "KAT6B",
          "gene_hgnc_id": 17582,
          "hgvs_c": "c.3399_3402delGGGT",
          "hgvs_p": "p.Arg1133fs",
          "transcript": "NM_012330.4",
          "protein_id": "NP_036462.2",
          "transcript_support_level": null,
          "aa_start": 1133,
          "aa_end": null,
          "aa_length": 2073,
          "cds_start": 3399,
          "cds_end": null,
          "cds_length": 6222,
          "cdna_start": 3913,
          "cdna_end": null,
          "cdna_length": 8314,
          "mane_select": "ENST00000287239.10",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "RG",
          "aa_alt": null,
          "canonical": true,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 17,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "KAT6B",
          "gene_hgnc_id": 17582,
          "hgvs_c": "c.3399_3402delGGGT",
          "hgvs_p": "p.Arg1133fs",
          "transcript": "ENST00000287239.10",
          "protein_id": "ENSP00000287239.4",
          "transcript_support_level": 1,
          "aa_start": 1133,
          "aa_end": null,
          "aa_length": 2073,
          "cds_start": 3399,
          "cds_end": null,
          "cds_length": 6222,
          "cdna_start": 3913,
          "cdna_end": null,
          "cdna_length": 8314,
          "mane_select": "NM_012330.4",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "RG",
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 17,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "KAT6B",
          "gene_hgnc_id": 17582,
          "hgvs_c": "c.2850_2853delGGGT",
          "hgvs_p": "p.Arg950fs",
          "transcript": "ENST00000372711.2",
          "protein_id": "ENSP00000361796.1",
          "transcript_support_level": 1,
          "aa_start": 950,
          "aa_end": null,
          "aa_length": 1890,
          "cds_start": 2850,
          "cds_end": null,
          "cds_length": 5673,
          "cdna_start": 3235,
          "cdna_end": null,
          "cdna_length": 7297,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "RG",
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 17,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "KAT6B",
          "gene_hgnc_id": 17582,
          "hgvs_c": "c.3399_3402delGGGT",
          "hgvs_p": "p.Arg1133fs",
          "transcript": "NM_001370136.1",
          "protein_id": "NP_001357065.1",
          "transcript_support_level": null,
          "aa_start": 1133,
          "aa_end": null,
          "aa_length": 2073,
          "cds_start": 3399,
          "cds_end": null,
          "cds_length": 6222,
          "cdna_start": 3923,
          "cdna_end": null,
          "cdna_length": 8324,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "RG",
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 17,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "KAT6B",
          "gene_hgnc_id": 17582,
          "hgvs_c": "c.3399_3402delGGGT",
          "hgvs_p": "p.Arg1133fs",
          "transcript": "NM_001370137.1",
          "protein_id": "NP_001357066.1",
          "transcript_support_level": null,
          "aa_start": 1133,
          "aa_end": null,
          "aa_length": 2073,
          "cds_start": 3399,
          "cds_end": null,
          "cds_length": 6222,
          "cdna_start": 3944,
          "cdna_end": null,
          "cdna_length": 8345,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "RG",
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 17,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "KAT6B",
          "gene_hgnc_id": 17582,
          "hgvs_c": "c.3399_3402delGGGT",
          "hgvs_p": "p.Arg1133fs",
          "transcript": "ENST00000648725.1",
          "protein_id": "ENSP00000497841.1",
          "transcript_support_level": null,
          "aa_start": 1133,
          "aa_end": null,
          "aa_length": 2073,
          "cds_start": 3399,
          "cds_end": null,
          "cds_length": 6222,
          "cdna_start": 4148,
          "cdna_end": null,
          "cdna_length": 8209,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "RG",
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 17,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "KAT6B",
          "gene_hgnc_id": 17582,
          "hgvs_c": "c.3399_3402delGGGT",
          "hgvs_p": "p.Arg1133fs",
          "transcript": "ENST00000649463.1",
          "protein_id": "ENSP00000497166.1",
          "transcript_support_level": null,
          "aa_start": 1133,
          "aa_end": null,
          "aa_length": 2073,
          "cds_start": 3399,
          "cds_end": null,
          "cds_length": 6222,
          "cdna_start": 3910,
          "cdna_end": null,
          "cdna_length": 7908,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "RG",
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 17,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "KAT6B",
          "gene_hgnc_id": 17582,
          "hgvs_c": "c.2850_2853delGGGT",
          "hgvs_p": "p.Arg950fs",
          "transcript": "NM_001256468.2",
          "protein_id": "NP_001243397.1",
          "transcript_support_level": null,
          "aa_start": 950,
          "aa_end": null,
          "aa_length": 1890,
          "cds_start": 2850,
          "cds_end": null,
          "cds_length": 5673,
          "cdna_start": 3364,
          "cdna_end": null,
          "cdna_length": 7765,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "RG",
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          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 17,
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          "exon_count": 18,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "KAT6B",
          "gene_hgnc_id": 17582,
          "hgvs_c": "c.2850_2853delGGGT",
          "hgvs_p": "p.Arg950fs",
          "transcript": "NM_001370138.1",
          "protein_id": "NP_001357067.1",
          "transcript_support_level": null,
          "aa_start": 950,
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          "aa_length": 1890,
          "cds_start": 2850,
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          "cdna_start": 3374,
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          "mane_select": null,
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        },
        {
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          "strand": true,
          "consequences": [
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          ],
          "exon_rank": 17,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": null,
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          "gene_symbol": "KAT6B",
          "gene_hgnc_id": 17582,
          "hgvs_c": "c.2850_2853delGGGT",
          "hgvs_p": "p.Arg950fs",
          "transcript": "ENST00000372724.6",
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          "intron_rank": null,
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          "gene_symbol": "KAT6B",
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          "gene_symbol": "KAT6B",
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          "hgvs_c": "c.2361_2364delGGGT",
          "hgvs_p": "p.Arg787fs",
          "transcript": "NM_001370132.1",
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        },
        {
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        }
      ],
      "gene_symbol": "KAT6B",
      "gene_hgnc_id": 17582,
      "dbsnp": "rs1554844486",
      "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": null,
      "computational_prediction_selected": null,
      "computational_source_selected": null,
      "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": null,
      "bayesdelnoaf_prediction": null,
      "phylop100way_score": 9.602,
      "phylop100way_prediction": "Pathogenic",
      "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": "Pathogenic",
      "acmg_criteria": "PVS1,PM2,PP5_Moderate",
      "acmg_by_gene": [
        {
          "score": 12,
          "benign_score": 0,
          "pathogenic_score": 12,
          "criteria": [
            "PVS1",
            "PM2",
            "PP5_Moderate"
          ],
          "verdict": "Pathogenic",
          "transcript": "ENST00000287239.10",
          "gene_symbol": "KAT6B",
          "hgnc_id": 17582,
          "effects": [
            "frameshift_variant"
          ],
          "inheritance_mode": "AD",
          "hgvs_c": "c.3399_3402delGGGT",
          "hgvs_p": "p.Arg1133fs"
        },
        {
          "score": 4,
          "benign_score": 0,
          "pathogenic_score": 4,
          "criteria": [
            "PM2",
            "PP5_Moderate"
          ],
          "verdict": "Uncertain_significance",
          "transcript": "ENST00000413431.1",
          "gene_symbol": "ENSG00000234149",
          "hgnc_id": null,
          "effects": [
            "intron_variant"
          ],
          "inheritance_mode": "",
          "hgvs_c": "n.65+123_65+126delACCC",
          "hgvs_p": null
        }
      ],
      "clinvar_disease": "10 conditions",
      "clinvar_classification": "Likely pathogenic",
      "clinvar_review_status": "criteria provided, single submitter",
      "clinvar_submissions_summary": "LP:1",
      "phenotype_combined": "10 conditions",
      "pathogenicity_classification_combined": "Likely pathogenic",
      "custom_annotations": null
    }
  ],
  "message": null
}