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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: 9-132897255-C-T (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=9&pos=132897255&ref=C&alt=T&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "9",
      "pos": 132897255,
      "ref": "C",
      "alt": "T",
      "effect": "synonymous_variant",
      "transcript": "ENST00000298552.9",
      "consequences": [
        {
          "aa_ref": "R",
          "aa_alt": "R",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 22,
          "exon_rank_end": null,
          "exon_count": 23,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TSC1",
          "gene_hgnc_id": 12362,
          "hgvs_c": "c.2904G>A",
          "hgvs_p": "p.Arg968Arg",
          "transcript": "NM_000368.5",
          "protein_id": "NP_000359.1",
          "transcript_support_level": null,
          "aa_start": 968,
          "aa_end": null,
          "aa_length": 1164,
          "cds_start": 2904,
          "cds_end": null,
          "cds_length": 3495,
          "cdna_start": 3121,
          "cdna_end": null,
          "cdna_length": 8598,
          "mane_select": "ENST00000298552.9",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "R",
          "canonical": true,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 22,
          "exon_rank_end": null,
          "exon_count": 23,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TSC1",
          "gene_hgnc_id": 12362,
          "hgvs_c": "c.2904G>A",
          "hgvs_p": "p.Arg968Arg",
          "transcript": "ENST00000298552.9",
          "protein_id": "ENSP00000298552.3",
          "transcript_support_level": 1,
          "aa_start": 968,
          "aa_end": null,
          "aa_length": 1164,
          "cds_start": 2904,
          "cds_end": null,
          "cds_length": 3495,
          "cdna_start": 3121,
          "cdna_end": null,
          "cdna_length": 8598,
          "mane_select": "NM_000368.5",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "R",
          "canonical": true,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 23,
          "exon_rank_end": null,
          "exon_count": 24,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TSC1",
          "gene_hgnc_id": 12362,
          "hgvs_c": "c.2904G>A",
          "hgvs_p": "p.Arg968Arg",
          "transcript": "ENST00000490179.4",
          "protein_id": "ENSP00000495533.2",
          "transcript_support_level": 3,
          "aa_start": 968,
          "aa_end": null,
          "aa_length": 1164,
          "cds_start": 2904,
          "cds_end": null,
          "cds_length": 3495,
          "cdna_start": 3213,
          "cdna_end": null,
          "cdna_length": 8690,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "R",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 22,
          "exon_rank_end": null,
          "exon_count": 23,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TSC1",
          "gene_hgnc_id": 12362,
          "hgvs_c": "c.2904G>A",
          "hgvs_p": "p.Arg968Arg",
          "transcript": "NM_001406592.1",
          "protein_id": "NP_001393521.1",
          "transcript_support_level": null,
          "aa_start": 968,
          "aa_end": null,
          "aa_length": 1164,
          "cds_start": 2904,
          "cds_end": null,
          "cds_length": 3495,
          "cdna_start": 3092,
          "cdna_end": null,
          "cdna_length": 8569,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "R",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 22,
          "exon_rank_end": null,
          "exon_count": 23,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TSC1",
          "gene_hgnc_id": 12362,
          "hgvs_c": "c.2904G>A",
          "hgvs_p": "p.Arg968Arg",
          "transcript": "NM_001406593.1",
          "protein_id": "NP_001393522.1",
          "transcript_support_level": null,
          "aa_start": 968,
          "aa_end": null,
          "aa_length": 1164,
          "cds_start": 2904,
          "cds_end": null,
          "cds_length": 3495,
          "cdna_start": 3117,
          "cdna_end": null,
          "cdna_length": 8594,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "R",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 23,
          "exon_rank_end": null,
          "exon_count": 24,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TSC1",
          "gene_hgnc_id": 12362,
          "hgvs_c": "c.2904G>A",
          "hgvs_p": "p.Arg968Arg",
          "transcript": "NM_001406594.1",
          "protein_id": "NP_001393523.1",
          "transcript_support_level": null,
          "aa_start": 968,
          "aa_end": null,
          "aa_length": 1164,
          "cds_start": 2904,
          "cds_end": null,
          "cds_length": 3495,
          "cdna_start": 3340,
          "cdna_end": null,
          "cdna_length": 8817,
          "mane_select": null,
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          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "R",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 23,
          "exon_rank_end": null,
          "exon_count": 24,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TSC1",
          "gene_hgnc_id": 12362,
          "hgvs_c": "c.2904G>A",
          "hgvs_p": "p.Arg968Arg",
          "transcript": "NM_001406595.1",
          "protein_id": "NP_001393524.1",
          "transcript_support_level": null,
          "aa_start": 968,
          "aa_end": null,
          "aa_length": 1164,
          "cds_start": 2904,
          "cds_end": null,
          "cds_length": 3495,
          "cdna_start": 3311,
          "cdna_end": null,
          "cdna_length": 8788,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "R",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 21,
          "exon_rank_end": null,
          "exon_count": 22,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TSC1",
          "gene_hgnc_id": 12362,
          "hgvs_c": "c.2904G>A",
          "hgvs_p": "p.Arg968Arg",
          "transcript": "NM_001406596.1",
          "protein_id": "NP_001393525.1",
          "transcript_support_level": null,
          "aa_start": 968,
          "aa_end": null,
          "aa_length": 1164,
          "cds_start": 2904,
          "cds_end": null,
          "cds_length": 3495,
          "cdna_start": 3058,
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          "cdna_length": 8535,
          "mane_select": null,
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        },
        {
          "aa_ref": "R",
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          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 22,
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          "exon_count": 23,
          "intron_rank": null,
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          "gene_symbol": "TSC1",
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          "hgvs_c": "c.2904G>A",
          "hgvs_p": "p.Arg968Arg",
          "transcript": "ENST00000643875.1",
          "protein_id": "ENSP00000495158.1",
          "transcript_support_level": null,
          "aa_start": 968,
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          "cds_start": 2904,
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          "cds_length": 3495,
          "cdna_start": 3118,
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        {
          "aa_ref": "R",
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          "consequences": [
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          ],
          "exon_rank": 22,
          "exon_rank_end": null,
          "exon_count": 23,
          "intron_rank": null,
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          "gene_symbol": "TSC1",
          "gene_hgnc_id": 12362,
          "hgvs_c": "c.2904G>A",
          "hgvs_p": "p.Arg968Arg",
          "transcript": "ENST00000646440.2",
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          "hgvs_c": "c.2904G>A",
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      ],
      "gene_symbol": "TSC1",
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      "dbsnp": "rs1554813280",
      "frequency_reference_population": 0.0000027361764,
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      "gnomad_exomes_af": 0.00000273618,
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      "gnomad_genomes_ac": null,
      "gnomad_exomes_homalt": 0,
      "gnomad_genomes_homalt": null,
      "gnomad_mito_homoplasmic": null,
      "gnomad_mito_heteroplasmic": null,
      "computational_score_selected": -0.5699999928474426,
      "computational_prediction_selected": "Benign",
      "computational_source_selected": "BayesDel_noAF",
      "splice_score_selected": 0,
      "splice_prediction_selected": "Benign",
      "splice_source_selected": "max_spliceai",
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      "alphamissense_score": null,
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      "bayesdelnoaf_score": -0.57,
      "bayesdelnoaf_prediction": "Benign",
      "phylop100way_score": -0.303,
      "phylop100way_prediction": "Benign",
      "spliceai_max_score": 0,
      "spliceai_max_prediction": "Benign",
      "dbscsnv_ada_score": null,
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      "acmg_score": -11,
      "acmg_classification": "Benign",
      "acmg_criteria": "PM2,BP4_Strong,BP6_Very_Strong,BP7",
      "acmg_by_gene": [
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          "verdict": "Benign",
          "transcript": "ENST00000298552.9",
          "gene_symbol": "TSC1",
          "hgnc_id": 12362,
          "effects": [
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          "hgvs_p": "p.Arg968Arg"
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      "clinvar_disease": "Hereditary cancer-predisposing syndrome,Tuberous sclerosis 1,Tuberous sclerosis syndrome",
      "clinvar_classification": "Benign/Likely benign",
      "clinvar_review_status": "criteria provided, multiple submitters, no conflicts",
      "clinvar_submissions_summary": "LB:4 B:1",
      "phenotype_combined": "Hereditary cancer-predisposing syndrome|Tuberous sclerosis 1|Tuberous sclerosis syndrome",
      "pathogenicity_classification_combined": "Benign/Likely benign",
      "custom_annotations": null
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  ],
  "message": null
}