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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: 15-100132006-C-A (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=15&pos=100132006&ref=C&alt=A&genome=hg38&allGenes=true"API Response
json
{
  "variants": [
    {
      "chr": "15",
      "pos": 100132006,
      "ref": "C",
      "alt": "A",
      "effect": "splice_donor_variant,intron_variant",
      "transcript": "ENST00000268070.9",
      "consequences": [
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_donor_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 22,
          "intron_rank": 12,
          "intron_rank_end": null,
          "gene_symbol": "ADAMTS17",
          "gene_hgnc_id": 17109,
          "hgvs_c": "c.1721+1G>T",
          "hgvs_p": null,
          "transcript": "NM_139057.4",
          "protein_id": "NP_620688.2",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1095,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 3288,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 6329,
          "mane_select": "ENST00000268070.9",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": true,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_donor_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 22,
          "intron_rank": 12,
          "intron_rank_end": null,
          "gene_symbol": "ADAMTS17",
          "gene_hgnc_id": 17109,
          "hgvs_c": "c.1721+1G>T",
          "hgvs_p": null,
          "transcript": "ENST00000268070.9",
          "protein_id": "ENSP00000268070.4",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1095,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 3288,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 6329,
          "mane_select": "NM_139057.4",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_donor_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 23,
          "intron_rank": 12,
          "intron_rank_end": null,
          "gene_symbol": "ADAMTS17",
          "gene_hgnc_id": 17109,
          "hgvs_c": "c.1721+1G>T",
          "hgvs_p": null,
          "transcript": "ENST00000568565.2",
          "protein_id": "ENSP00000456161.2",
          "transcript_support_level": 5,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1122,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 3369,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 3369,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "splice_donor_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 15,
          "intron_rank": 11,
          "intron_rank_end": null,
          "gene_symbol": "ADAMTS17",
          "gene_hgnc_id": 17109,
          "hgvs_c": "n.1402+1G>T",
          "hgvs_p": null,
          "transcript": "ENST00000378898.8",
          "protein_id": null,
          "transcript_support_level": 2,
          "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": 1964,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_donor_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 25,
          "intron_rank": 13,
          "intron_rank_end": null,
          "gene_symbol": "ADAMTS17",
          "gene_hgnc_id": 17109,
          "hgvs_c": "c.1853+1G>T",
          "hgvs_p": null,
          "transcript": "XM_017021973.3",
          "protein_id": "XP_016877462.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1189,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 3570,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 6611,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_donor_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 24,
          "intron_rank": 13,
          "intron_rank_end": null,
          "gene_symbol": "ADAMTS17",
          "gene_hgnc_id": 17109,
          "hgvs_c": "c.1853+1G>T",
          "hgvs_p": null,
          "transcript": "XM_017021974.2",
          "protein_id": "XP_016877463.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1181,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 3546,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 3658,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_donor_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 24,
          "intron_rank": 13,
          "intron_rank_end": null,
          "gene_symbol": "ADAMTS17",
          "gene_hgnc_id": 17109,
          "hgvs_c": "c.1853+1G>T",
          "hgvs_p": null,
          "transcript": "XM_017021975.2",
          "protein_id": "XP_016877464.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1166,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 3501,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 6542,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_donor_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 24,
          "intron_rank": 12,
          "intron_rank_end": null,
          "gene_symbol": "ADAMTS17",
          "gene_hgnc_id": 17109,
          "hgvs_c": "c.1721+1G>T",
          "hgvs_p": null,
          "transcript": "XM_011521312.3",
          "protein_id": "XP_011519614.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1145,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 3438,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 6479,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_donor_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 23,
          "intron_rank": 12,
          "intron_rank_end": null,
          "gene_symbol": "ADAMTS17",
          "gene_hgnc_id": 17109,
          "hgvs_c": "c.1721+1G>T",
          "hgvs_p": null,
          "transcript": "XM_005254872.4",
          "protein_id": "XP_005254929.1",
          "transcript_support_level": null,
          "aa_start": null,
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          "aa_length": 1122,
          "cds_start": -4,
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          "cds_length": 3369,
          "cdna_start": null,
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          "cdna_length": 6410,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
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          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_donor_variant",
            "intron_variant"
          ],
          "exon_rank": null,
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          "exon_count": 19,
          "intron_rank": 13,
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          "gene_symbol": "ADAMTS17",
          "gene_hgnc_id": 17109,
          "hgvs_c": "c.1853+1G>T",
          "hgvs_p": null,
          "transcript": "XM_017021977.2",
          "protein_id": "XP_016877466.1",
          "transcript_support_level": null,
          "aa_start": null,
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          "cds_start": -4,
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          "cdna_start": null,
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        {
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          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
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            "intron_variant"
          ],
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          "exon_count": 18,
          "intron_rank": 6,
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          "gene_symbol": "ADAMTS17",
          "gene_hgnc_id": 17109,
          "hgvs_c": "c.755+1G>T",
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          "transcript": "XM_017021978.2",
          "protein_id": "XP_016877467.1",
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          "cds_start": -4,
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          "mane_select": null,
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        {
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          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
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            "intron_variant"
          ],
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          "intron_rank": 5,
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          "gene_symbol": "ADAMTS17",
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          "hgvs_c": "c.533+1G>T",
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          "transcript": "XM_017021979.2",
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          "cds_start": -4,
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        {
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            "intron_variant"
          ],
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          "gene_symbol": "ADAMTS17",
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          "hgvs_c": "c.533+1G>T",
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        },
        {
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          "strand": false,
          "consequences": [
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            "intron_variant"
          ],
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          "exon_count": 16,
          "intron_rank": 13,
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          "gene_symbol": "ADAMTS17",
          "gene_hgnc_id": 17109,
          "hgvs_c": "c.1853+1G>T",
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          "transcript": "XM_017021981.2",
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          ],
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          "gene_symbol": "ADAMTS17",
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          "hgvs_c": "c.1853+1G>T",
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          "transcript": "XM_047432213.1",
          "protein_id": "XP_047288169.1",
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        {
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          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
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            "intron_variant"
          ],
          "exon_rank": null,
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          "exon_count": 15,
          "intron_rank": 3,
          "intron_rank_end": null,
          "gene_symbol": "ADAMTS17",
          "gene_hgnc_id": 17109,
          "hgvs_c": "c.242+1G>T",
          "hgvs_p": null,
          "transcript": "XM_017021982.2",
          "protein_id": "XP_016877471.1",
          "transcript_support_level": null,
          "aa_start": null,
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          "cds_start": -4,
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        {
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          ],
          "exon_rank": null,
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          "exon_count": 13,
          "intron_rank": 1,
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          "gene_symbol": "ADAMTS17",
          "gene_hgnc_id": 17109,
          "hgvs_c": "c.27-14993G>T",
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          "transcript": "XM_017021983.2",
          "protein_id": "XP_016877472.1",
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        {
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          "strand": false,
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            "intron_variant"
          ],
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          "intron_rank": 11,
          "intron_rank_end": null,
          "gene_symbol": "ADAMTS17",
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          "hgvs_c": "c.992+1G>T",
          "hgvs_p": null,
          "transcript": "XM_017021984.2",
          "protein_id": "XP_016877473.1",
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        },
        {
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          "consequences": [
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            "intron_variant"
          ],
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          "intron_rank": 13,
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          "gene_symbol": "ADAMTS17",
          "gene_hgnc_id": 17109,
          "hgvs_c": "n.1929+1G>T",
          "hgvs_p": null,
          "transcript": "XR_001751118.2",
          "protein_id": null,
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          "feature": null
        },
        {
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          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "splice_donor_variant",
            "intron_variant"
          ],
          "exon_rank": null,
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          "exon_count": 20,
          "intron_rank": 13,
          "intron_rank_end": null,
          "gene_symbol": "ADAMTS17",
          "gene_hgnc_id": 17109,
          "hgvs_c": "n.1929+1G>T",
          "hgvs_p": null,
          "transcript": "XR_001751119.2",
          "protein_id": null,
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          "cdna_start": null,
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        },
        {
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          "protein_coding": false,
          "strand": false,
          "consequences": [
            "splice_donor_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 20,
          "intron_rank": 13,
          "intron_rank_end": null,
          "gene_symbol": "ADAMTS17",
          "gene_hgnc_id": 17109,
          "hgvs_c": "n.1929+1G>T",
          "hgvs_p": null,
          "transcript": "XR_001751120.2",
          "protein_id": null,
          "transcript_support_level": null,
          "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": 2729,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        }
      ],
      "gene_symbol": "ADAMTS17",
      "gene_hgnc_id": 17109,
      "dbsnp": "rs749116256",
      "frequency_reference_population": 6.8409094e-7,
      "hom_count_reference_population": 0,
      "allele_count_reference_population": 1,
      "gnomad_exomes_af": 6.84091e-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": 0.36000001430511475,
      "computational_prediction_selected": "Pathogenic",
      "computational_source_selected": "BayesDel_noAF",
      "splice_score_selected": 0.9399999976158142,
      "splice_prediction_selected": "Pathogenic",
      "splice_source_selected": "dbscSNV1_RF",
      "revel_score": null,
      "revel_prediction": null,
      "alphamissense_score": null,
      "alphamissense_prediction": null,
      "bayesdelnoaf_score": 0.36,
      "bayesdelnoaf_prediction": "Pathogenic",
      "phylop100way_score": 7.195,
      "phylop100way_prediction": "Uncertain_significance",
      "spliceai_max_score": 0.94,
      "spliceai_max_prediction": "Pathogenic",
      "dbscsnv_ada_score": 0.999986675681007,
      "dbscsnv_ada_prediction": "Pathogenic",
      "apogee2_score": null,
      "apogee2_prediction": null,
      "mitotip_score": null,
      "mitotip_prediction": null,
      "acmg_score": 10,
      "acmg_classification": "Pathogenic",
      "acmg_criteria": "PVS1,PM2",
      "acmg_by_gene": [
        {
          "score": 10,
          "benign_score": 0,
          "pathogenic_score": 10,
          "criteria": [
            "PVS1",
            "PM2"
          ],
          "verdict": "Pathogenic",
          "transcript": "ENST00000268070.9",
          "gene_symbol": "ADAMTS17",
          "hgnc_id": 17109,
          "effects": [
            "splice_donor_variant",
            "intron_variant"
          ],
          "inheritance_mode": "AR",
          "hgvs_c": "c.1721+1G>T",
          "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
}