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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: 3-4818224-C-T (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=3&pos=4818224&ref=C&alt=T&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "3",
      "pos": 4818224,
      "ref": "C",
      "alt": "T",
      "effect": "synonymous_variant",
      "transcript": "ENST00000443694.5",
      "consequences": [
        {
          "aa_ref": "Y",
          "aa_alt": "Y",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 60,
          "exon_rank_end": null,
          "exon_count": 62,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ITPR1",
          "gene_hgnc_id": 6180,
          "hgvs_c": "c.8010C>T",
          "hgvs_p": "p.Tyr2670Tyr",
          "transcript": "NM_001378452.1",
          "protein_id": "NP_001365381.1",
          "transcript_support_level": null,
          "aa_start": 2670,
          "aa_end": null,
          "aa_length": 2758,
          "cds_start": 8010,
          "cds_end": null,
          "cds_length": 8277,
          "cdna_start": 8360,
          "cdna_end": null,
          "cdna_length": 9908,
          "mane_select": "ENST00000649015.2",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Y",
          "aa_alt": "Y",
          "canonical": true,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 60,
          "exon_rank_end": null,
          "exon_count": 62,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ITPR1",
          "gene_hgnc_id": 6180,
          "hgvs_c": "c.8010C>T",
          "hgvs_p": "p.Tyr2670Tyr",
          "transcript": "ENST00000649015.2",
          "protein_id": "ENSP00000497605.1",
          "transcript_support_level": null,
          "aa_start": 2670,
          "aa_end": null,
          "aa_length": 2758,
          "cds_start": 8010,
          "cds_end": null,
          "cds_length": 8277,
          "cdna_start": 8360,
          "cdna_end": null,
          "cdna_length": 9908,
          "mane_select": "NM_001378452.1",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Y",
          "aa_alt": "Y",
          "canonical": true,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 60,
          "exon_rank_end": null,
          "exon_count": 62,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ITPR1",
          "gene_hgnc_id": 6180,
          "hgvs_c": "c.7986C>T",
          "hgvs_p": "p.Tyr2662Tyr",
          "transcript": "ENST00000354582.12",
          "protein_id": "ENSP00000346595.8",
          "transcript_support_level": 5,
          "aa_start": 2662,
          "aa_end": null,
          "aa_length": 2750,
          "cds_start": 7986,
          "cds_end": null,
          "cds_length": 8253,
          "cdna_start": 8336,
          "cdna_end": null,
          "cdna_length": 9876,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Y",
          "aa_alt": "Y",
          "canonical": true,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 60,
          "exon_rank_end": null,
          "exon_count": 62,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ITPR1",
          "gene_hgnc_id": 6180,
          "hgvs_c": "c.7983C>T",
          "hgvs_p": "p.Tyr2661Tyr",
          "transcript": "ENST00000648266.1",
          "protein_id": "ENSP00000498014.1",
          "transcript_support_level": null,
          "aa_start": 2661,
          "aa_end": null,
          "aa_length": 2749,
          "cds_start": 7983,
          "cds_end": null,
          "cds_length": 8250,
          "cdna_start": 8227,
          "cdna_end": null,
          "cdna_length": 9767,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Y",
          "aa_alt": "Y",
          "canonical": true,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 59,
          "exon_rank_end": null,
          "exon_count": 61,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ITPR1",
          "gene_hgnc_id": 6180,
          "hgvs_c": "c.7968C>T",
          "hgvs_p": "p.Tyr2656Tyr",
          "transcript": "ENST00000650294.1",
          "protein_id": "ENSP00000498056.1",
          "transcript_support_level": null,
          "aa_start": 2656,
          "aa_end": null,
          "aa_length": 2744,
          "cds_start": 7968,
          "cds_end": null,
          "cds_length": 8235,
          "cdna_start": 8105,
          "cdna_end": null,
          "cdna_length": 9353,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Y",
          "aa_alt": "Y",
          "canonical": true,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 59,
          "exon_rank_end": null,
          "exon_count": 61,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ITPR1",
          "gene_hgnc_id": 6180,
          "hgvs_c": "c.7965C>T",
          "hgvs_p": "p.Tyr2655Tyr",
          "transcript": "ENST00000443694.5",
          "protein_id": "ENSP00000401671.2",
          "transcript_support_level": 1,
          "aa_start": 2655,
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          "aa_length": 2743,
          "cds_start": 7965,
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          "cds_length": 8232,
          "cdna_start": 8210,
          "cdna_end": null,
          "cdna_length": 9647,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Y",
          "aa_alt": "Y",
          "canonical": true,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 57,
          "exon_rank_end": null,
          "exon_count": 59,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ITPR1",
          "gene_hgnc_id": 6180,
          "hgvs_c": "c.7938C>T",
          "hgvs_p": "p.Tyr2646Tyr",
          "transcript": "ENST00000648309.1",
          "protein_id": "ENSP00000497026.1",
          "transcript_support_level": null,
          "aa_start": 2646,
          "aa_end": null,
          "aa_length": 2734,
          "cds_start": 7938,
          "cds_end": null,
          "cds_length": 8205,
          "cdna_start": 7943,
          "cdna_end": null,
          "cdna_length": 9311,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Y",
          "aa_alt": "Y",
          "canonical": true,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 57,
          "exon_rank_end": null,
          "exon_count": 59,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ITPR1",
          "gene_hgnc_id": 6180,
          "hgvs_c": "c.7866C>T",
          "hgvs_p": "p.Tyr2622Tyr",
          "transcript": "ENST00000357086.10",
          "protein_id": "ENSP00000349597.4",
          "transcript_support_level": 1,
          "aa_start": 2622,
          "aa_end": null,
          "aa_length": 2710,
          "cds_start": 7866,
          "cds_end": null,
          "cds_length": 8133,
          "cdna_start": 8219,
          "cdna_end": null,
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          "mane_select": null,
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          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Y",
          "aa_alt": "Y",
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          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 56,
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          "exon_count": 58,
          "intron_rank": null,
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          "gene_symbol": "ITPR1",
          "gene_hgnc_id": 6180,
          "hgvs_c": "c.7821C>T",
          "hgvs_p": "p.Tyr2607Tyr",
          "transcript": "ENST00000456211.8",
          "protein_id": "ENSP00000397885.2",
          "transcript_support_level": 1,
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        },
        {
          "aa_ref": "Y",
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          "consequences": [
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          ],
          "exon_rank": 40,
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          "intron_rank": null,
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          "gene_symbol": "ITPR1",
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          "hgvs_c": "c.5772C>T",
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          "gene_symbol": "ITPR1",
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        {
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          "hgvs_c": "n.725-3793G>A",
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        },
        {
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          "gene_symbol": "LOC124906209",
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          "hgvs_c": "n.8879-3793G>A",
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          "transcript": "XR_007095796.1",
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          "cdna_length": 9018,
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      ],
      "gene_symbol": "ITPR1",
      "gene_hgnc_id": 6180,
      "dbsnp": "rs372433483",
      "frequency_reference_population": 0.000036934063,
      "hom_count_reference_population": 0,
      "allele_count_reference_population": 58,
      "gnomad_exomes_af": 0.0000345536,
      "gnomad_genomes_af": 0.0000591024,
      "gnomad_exomes_ac": 49,
      "gnomad_genomes_ac": 9,
      "gnomad_exomes_homalt": 0,
      "gnomad_genomes_homalt": 0,
      "gnomad_mito_homoplasmic": null,
      "gnomad_mito_heteroplasmic": null,
      "computational_score_selected": -0.4399999976158142,
      "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": -0.44,
      "bayesdelnoaf_prediction": "Benign",
      "phylop100way_score": -2.633,
      "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": -15,
      "acmg_classification": "Benign",
      "acmg_criteria": "BP4_Moderate,BP6_Very_Strong,BP7,BS1",
      "acmg_by_gene": [
        {
          "score": -15,
          "benign_score": 15,
          "pathogenic_score": 0,
          "criteria": [
            "BP4_Moderate",
            "BP6_Very_Strong",
            "BP7",
            "BS1"
          ],
          "verdict": "Benign",
          "transcript": "ENST00000443694.5",
          "gene_symbol": "ITPR1",
          "hgnc_id": 6180,
          "effects": [
            "synonymous_variant"
          ],
          "inheritance_mode": "AD,AR",
          "hgvs_c": "c.7965C>T",
          "hgvs_p": "p.Tyr2655Tyr"
        },
        {
          "score": -8,
          "benign_score": 10,
          "pathogenic_score": 2,
          "criteria": [
            "PM2",
            "BP4_Moderate",
            "BP6_Very_Strong"
          ],
          "verdict": "Benign",
          "transcript": "ENST00000465436.5",
          "gene_symbol": "ENSG00000235978",
          "hgnc_id": null,
          "effects": [
            "intron_variant"
          ],
          "inheritance_mode": "",
          "hgvs_c": "n.193-3793G>A",
          "hgvs_p": null
        },
        {
          "score": -8,
          "benign_score": 10,
          "pathogenic_score": 2,
          "criteria": [
            "PM2",
            "BP4_Moderate",
            "BP6_Very_Strong"
          ],
          "verdict": "Benign",
          "transcript": "XR_007095790.1",
          "gene_symbol": "LOC124906209",
          "hgnc_id": null,
          "effects": [
            "intron_variant"
          ],
          "inheritance_mode": "",
          "hgvs_c": "n.274-3793G>A",
          "hgvs_p": null
        }
      ],
      "clinvar_disease": "not provided,not specified",
      "clinvar_classification": "Benign/Likely benign",
      "clinvar_review_status": "criteria provided, multiple submitters, no conflicts",
      "clinvar_submissions_summary": "LB:1 B:1",
      "phenotype_combined": "not specified|not provided",
      "pathogenicity_classification_combined": "Benign/Likely benign",
      "custom_annotations": null
    }
  ],
  "message": null
}