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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: 16-2081593-A-AGGGAACACCAGCTGGCT (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=16&pos=2081593&ref=A&alt=AGGGAACACCAGCTGGCT&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "16",
      "pos": 2081593,
      "ref": "A",
      "alt": "AGGGAACACCAGCTGGCT",
      "effect": "frameshift_variant,stop_gained",
      "transcript": "ENST00000219476.9",
      "consequences": [
        {
          "aa_ref": "M",
          "aa_alt": "GTPAG*?",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "frameshift_variant",
            "stop_gained"
          ],
          "exon_rank": 31,
          "exon_rank_end": null,
          "exon_count": 42,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TSC2",
          "gene_hgnc_id": 12363,
          "hgvs_c": "c.3611_3627dupGGAACACCAGCTGGCTG",
          "hgvs_p": "p.Met1210fs",
          "transcript": "NM_000548.5",
          "protein_id": "NP_000539.2",
          "transcript_support_level": null,
          "aa_start": 1210,
          "aa_end": null,
          "aa_length": 1807,
          "cds_start": 3628,
          "cds_end": null,
          "cds_length": 5424,
          "cdna_start": 3738,
          "cdna_end": null,
          "cdna_length": 6415,
          "mane_select": "ENST00000219476.9",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "M",
          "aa_alt": "GTPAG*?",
          "canonical": true,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "frameshift_variant",
            "stop_gained"
          ],
          "exon_rank": 31,
          "exon_rank_end": null,
          "exon_count": 42,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TSC2",
          "gene_hgnc_id": 12363,
          "hgvs_c": "c.3611_3627dupGGAACACCAGCTGGCTG",
          "hgvs_p": "p.Met1210fs",
          "transcript": "ENST00000219476.9",
          "protein_id": "ENSP00000219476.3",
          "transcript_support_level": 5,
          "aa_start": 1210,
          "aa_end": null,
          "aa_length": 1807,
          "cds_start": 3628,
          "cds_end": null,
          "cds_length": 5424,
          "cdna_start": 3738,
          "cdna_end": null,
          "cdna_length": 6415,
          "mane_select": "NM_000548.5",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "M",
          "aa_alt": "GTPAG*?",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "frameshift_variant",
            "stop_gained"
          ],
          "exon_rank": 31,
          "exon_rank_end": null,
          "exon_count": 41,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TSC2",
          "gene_hgnc_id": 12363,
          "hgvs_c": "c.3611_3627dupGGAACACCAGCTGGCTG",
          "hgvs_p": "p.Met1210fs",
          "transcript": "ENST00000350773.9",
          "protein_id": "ENSP00000344383.4",
          "transcript_support_level": 1,
          "aa_start": 1210,
          "aa_end": null,
          "aa_length": 1784,
          "cds_start": 3628,
          "cds_end": null,
          "cds_length": 5355,
          "cdna_start": 3703,
          "cdna_end": null,
          "cdna_length": 5538,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "M",
          "aa_alt": "GTPAG*?",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "frameshift_variant",
            "stop_gained"
          ],
          "exon_rank": 30,
          "exon_rank_end": null,
          "exon_count": 40,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TSC2",
          "gene_hgnc_id": 12363,
          "hgvs_c": "c.3479_3495dupGGAACACCAGCTGGCTG",
          "hgvs_p": "p.Met1166fs",
          "transcript": "ENST00000401874.7",
          "protein_id": "ENSP00000384468.2",
          "transcript_support_level": 1,
          "aa_start": 1166,
          "aa_end": null,
          "aa_length": 1740,
          "cds_start": 3496,
          "cds_end": null,
          "cds_length": 5223,
          "cdna_start": 3602,
          "cdna_end": null,
          "cdna_length": 5437,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 27,
          "exon_rank_end": null,
          "exon_count": 38,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TSC2",
          "gene_hgnc_id": 12363,
          "hgvs_c": "n.*2778_*2794dupGGAACACCAGCTGGCTG",
          "hgvs_p": null,
          "transcript": "ENST00000439117.6",
          "protein_id": "ENSP00000406980.2",
          "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": 5073,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "3_prime_UTR_variant"
          ],
          "exon_rank": 27,
          "exon_rank_end": null,
          "exon_count": 38,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TSC2",
          "gene_hgnc_id": 12363,
          "hgvs_c": "n.*2778_*2794dupGGAACACCAGCTGGCTG",
          "hgvs_p": null,
          "transcript": "ENST00000439117.6",
          "protein_id": "ENSP00000406980.2",
          "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": 5073,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "M",
          "aa_alt": "GTPAG*?",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "frameshift_variant",
            "stop_gained"
          ],
          "exon_rank": 31,
          "exon_rank_end": null,
          "exon_count": 42,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TSC2",
          "gene_hgnc_id": 12363,
          "hgvs_c": "c.3611_3627dupGGAACACCAGCTGGCTG",
          "hgvs_p": "p.Met1210fs",
          "transcript": "ENST00000645186.2",
          "protein_id": "ENSP00000495110.2",
          "transcript_support_level": null,
          "aa_start": 1210,
          "aa_end": null,
          "aa_length": 1837,
          "cds_start": 3628,
          "cds_end": null,
          "cds_length": 5514,
          "cdna_start": 3738,
          "cdna_end": null,
          "cdna_length": 6505,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "M",
          "aa_alt": "GTPAG*?",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "frameshift_variant",
            "stop_gained"
          ],
          "exon_rank": 31,
          "exon_rank_end": null,
          "exon_count": 42,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TSC2",
          "gene_hgnc_id": 12363,
          "hgvs_c": "c.3608_3624dupGGAACACCAGCTGGCTG",
          "hgvs_p": "p.Met1209fs",
          "transcript": "NM_001406663.1",
          "protein_id": "NP_001393592.1",
          "transcript_support_level": null,
          "aa_start": 1209,
          "aa_end": null,
          "aa_length": 1806,
          "cds_start": 3625,
          "cds_end": null,
          "cds_length": 5421,
          "cdna_start": 3735,
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          "cdna_length": 6412,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "M",
          "aa_alt": "GTPAG*?",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "frameshift_variant",
            "stop_gained"
          ],
          "exon_rank": 31,
          "exon_rank_end": null,
          "exon_count": 42,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TSC2",
          "gene_hgnc_id": 12363,
          "hgvs_c": "c.3608_3624dupGGAACACCAGCTGGCTG",
          "hgvs_p": "p.Met1209fs",
          "transcript": "ENST00000642365.2",
          "protein_id": "ENSP00000495459.2",
          "transcript_support_level": null,
          "aa_start": 1209,
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          "cds_start": 3625,
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          "cdna_start": 3696,
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          "cdna_length": 5574,
          "mane_select": null,
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          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "M",
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          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "frameshift_variant",
            "stop_gained"
          ],
          "exon_rank": 31,
          "exon_rank_end": null,
          "exon_count": 42,
          "intron_rank": null,
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          "gene_symbol": "TSC2",
          "gene_hgnc_id": 12363,
          "hgvs_c": "c.3611_3627dupGGAACACCAGCTGGCTG",
          "hgvs_p": "p.Met1210fs",
          "transcript": "ENST00000646388.1",
          "protein_id": "ENSP00000495921.1",
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        },
        {
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          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "frameshift_variant",
            "stop_gained"
          ],
          "exon_rank": 31,
          "exon_rank_end": null,
          "exon_count": 41,
          "intron_rank": null,
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          "gene_symbol": "TSC2",
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          "hgvs_c": "c.3611_3627dupGGAACACCAGCTGGCTG",
          "hgvs_p": "p.Met1210fs",
          "transcript": "NM_001114382.3",
          "protein_id": "NP_001107854.1",
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        {
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          "strand": true,
          "consequences": [
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          ],
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          "intron_rank": null,
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          "gene_symbol": "TSC2",
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          "hgvs_c": "c.3608_3624dupGGAACACCAGCTGGCTG",
          "hgvs_p": "p.Met1209fs",
          "transcript": "NM_001406664.1",
          "protein_id": "NP_001393593.1",
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        {
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          ],
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          "intron_rank": null,
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          "gene_symbol": "TSC2",
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          "hgvs_c": "c.3611_3627dupGGAACACCAGCTGGCTG",
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        {
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          ],
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        {
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          "gene_symbol": "TSC2",
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          "transcript": "ENST00000644399.1",
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        {
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        {
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        {
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        {
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          ],
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          "gene_symbol": "TSC2",
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          "hgvs_c": "c.3482_3498dupGGAACACCAGCTGGCTG",
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          "transcript": "NM_021055.3",
          "protein_id": "NP_066399.2",
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        {
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          ],
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        {
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        }
      ],
      "gene_symbol": "TSC2",
      "gene_hgnc_id": 12363,
      "dbsnp": "rs137854088",
      "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": null,
      "splice_prediction_selected": null,
      "splice_source_selected": null,
      "revel_score": null,
      "revel_prediction": null,
      "alphamissense_score": null,
      "alphamissense_prediction": null,
      "bayesdelnoaf_score": null,
      "bayesdelnoaf_prediction": null,
      "phylop100way_score": 9.92,
      "phylop100way_prediction": "Pathogenic",
      "spliceai_max_score": null,
      "spliceai_max_prediction": null,
      "dbscsnv_ada_score": null,
      "dbscsnv_ada_prediction": null,
      "apogee2_score": null,
      "apogee2_prediction": null,
      "mitotip_score": null,
      "mitotip_prediction": null,
      "acmg_score": 8,
      "acmg_classification": "Likely_pathogenic",
      "acmg_criteria": "PVS1",
      "acmg_by_gene": [
        {
          "score": 8,
          "benign_score": 0,
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          "criteria": [
            "PVS1"
          ],
          "verdict": "Likely_pathogenic",
          "transcript": "ENST00000219476.9",
          "gene_symbol": "TSC2",
          "hgnc_id": 12363,
          "effects": [
            "frameshift_variant",
            "stop_gained"
          ],
          "inheritance_mode": "AD",
          "hgvs_c": "c.3611_3627dupGGAACACCAGCTGGCTG",
          "hgvs_p": "p.Met1210fs"
        }
      ],
      "clinvar_disease": "Tuberous sclerosis syndrome",
      "clinvar_classification": "not provided",
      "clinvar_review_status": "no classification provided",
      "clinvar_submissions_summary": "O:1",
      "phenotype_combined": "Tuberous sclerosis syndrome",
      "pathogenicity_classification_combined": "not provided",
      "custom_annotations": null
    }
  ],
  "message": null
}