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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: 3-4814565-A-G (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=3&pos=4814565&ref=A&alt=G&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "3",
      "pos": 4814565,
      "ref": "A",
      "alt": "G",
      "effect": "splice_region_variant,intron_variant",
      "transcript": "ENST00000443694.5",
      "consequences": [
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 62,
          "intron_rank": 58,
          "intron_rank_end": null,
          "gene_symbol": "ITPR1",
          "gene_hgnc_id": 6180,
          "hgvs_c": "c.7701+3A>G",
          "hgvs_p": null,
          "transcript": "NM_001378452.1",
          "protein_id": "NP_001365381.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 2758,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 8277,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 9908,
          "mane_select": "ENST00000649015.2",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": true,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 62,
          "intron_rank": 58,
          "intron_rank_end": null,
          "gene_symbol": "ITPR1",
          "gene_hgnc_id": 6180,
          "hgvs_c": "c.7701+3A>G",
          "hgvs_p": null,
          "transcript": "ENST00000649015.2",
          "protein_id": "ENSP00000497605.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 2758,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 8277,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 9908,
          "mane_select": "NM_001378452.1",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": true,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 62,
          "intron_rank": 58,
          "intron_rank_end": null,
          "gene_symbol": "ITPR1",
          "gene_hgnc_id": 6180,
          "hgvs_c": "c.7677+3A>G",
          "hgvs_p": null,
          "transcript": "ENST00000354582.12",
          "protein_id": "ENSP00000346595.8",
          "transcript_support_level": 5,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 2750,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 8253,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 9876,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": true,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 62,
          "intron_rank": 58,
          "intron_rank_end": null,
          "gene_symbol": "ITPR1",
          "gene_hgnc_id": 6180,
          "hgvs_c": "c.7674+3A>G",
          "hgvs_p": null,
          "transcript": "ENST00000648266.1",
          "protein_id": "ENSP00000498014.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 2749,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 8250,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 9767,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": true,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 61,
          "intron_rank": 57,
          "intron_rank_end": null,
          "gene_symbol": "ITPR1",
          "gene_hgnc_id": 6180,
          "hgvs_c": "c.7659+3A>G",
          "hgvs_p": null,
          "transcript": "ENST00000650294.1",
          "protein_id": "ENSP00000498056.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 2744,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 8235,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 9353,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": true,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 61,
          "intron_rank": 57,
          "intron_rank_end": null,
          "gene_symbol": "ITPR1",
          "gene_hgnc_id": 6180,
          "hgvs_c": "c.7656+3A>G",
          "hgvs_p": null,
          "transcript": "ENST00000443694.5",
          "protein_id": "ENSP00000401671.2",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 2743,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 8232,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 9647,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": true,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 59,
          "intron_rank": 55,
          "intron_rank_end": null,
          "gene_symbol": "ITPR1",
          "gene_hgnc_id": 6180,
          "hgvs_c": "c.7629+3A>G",
          "hgvs_p": null,
          "transcript": "ENST00000648309.1",
          "protein_id": "ENSP00000497026.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 2734,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 8205,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 9311,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": true,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 59,
          "intron_rank": 55,
          "intron_rank_end": null,
          "gene_symbol": "ITPR1",
          "gene_hgnc_id": 6180,
          "hgvs_c": "c.7557+3A>G",
          "hgvs_p": null,
          "transcript": "ENST00000357086.10",
          "protein_id": "ENSP00000349597.4",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 2710,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 8133,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 9767,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": true,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 58,
          "intron_rank": 54,
          "intron_rank_end": null,
          "gene_symbol": "ITPR1",
          "gene_hgnc_id": 6180,
          "hgvs_c": "c.7512+3A>G",
          "hgvs_p": null,
          "transcript": "ENST00000456211.8",
          "protein_id": "ENSP00000397885.2",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 2695,
          "cds_start": -4,
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          "cds_length": 8088,
          "cdna_start": null,
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          "cdna_length": 9506,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": true,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 42,
          "intron_rank": 38,
          "intron_rank_end": null,
          "gene_symbol": "ITPR1",
          "gene_hgnc_id": 6180,
          "hgvs_c": "c.5463+3A>G",
          "hgvs_p": null,
          "transcript": "ENST00000648038.1",
          "protein_id": "ENSP00000497872.1",
          "transcript_support_level": null,
          "aa_start": null,
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          "aa_length": 2012,
          "cds_start": -4,
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          "cdna_start": null,
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          "mane_select": null,
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        {
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          "canonical": true,
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          "exon_rank_end": null,
          "exon_count": 39,
          "intron_rank": 35,
          "intron_rank_end": null,
          "gene_symbol": "ITPR1",
          "gene_hgnc_id": 6180,
          "hgvs_c": "c.4878+3A>G",
          "hgvs_p": null,
          "transcript": "ENST00000648431.1",
          "protein_id": "ENSP00000498149.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1817,
          "cds_start": -4,
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          "cdna_start": null,
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          "mane_select": null,
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        {
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          "canonical": true,
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          "strand": true,
          "consequences": [
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          ],
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          "intron_rank": 35,
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          "cds_start": -4,
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          "mane_select": null,
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        {
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          ],
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          "intron_rank": 16,
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          "gene_symbol": "ITPR1",
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          "transcript": "ENST00000544951.6",
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        {
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          "consequences": [
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          ],
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          "exon_rank_end": null,
          "exon_count": 61,
          "intron_rank": 57,
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          "gene_symbol": "ITPR1",
          "gene_hgnc_id": 6180,
          "hgvs_c": "c.7656+3A>G",
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          "transcript": "NM_001168272.2",
          "protein_id": "NP_001161744.1",
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          ],
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          "gene_symbol": "ITPR1",
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          "transcript": "NM_001099952.4",
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          "mane_select": null,
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          "feature": null
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        {
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          "consequences": [
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            "intron_variant"
          ],
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          "exon_count": 58,
          "intron_rank": 54,
          "intron_rank_end": null,
          "gene_symbol": "ITPR1",
          "gene_hgnc_id": 6180,
          "hgvs_c": "c.7512+3A>G",
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          "transcript": "NM_002222.7",
          "protein_id": "NP_002213.5",
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        {
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          "canonical": false,
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          "consequences": [
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            "intron_variant"
          ],
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          "exon_count": 34,
          "intron_rank": 30,
          "intron_rank_end": null,
          "gene_symbol": "ITPR1",
          "gene_hgnc_id": 6180,
          "hgvs_c": "c.4068+3A>G",
          "hgvs_p": null,
          "transcript": "ENST00000648016.1",
          "protein_id": "ENSP00000496893.1",
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          "gene_symbol": "ITPR1",
          "gene_hgnc_id": 6180,
          "hgvs_c": "c.33+3A>G",
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        {
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          "gene_symbol": "ITPR1",
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          "transcript": "ENST00000648390.1",
          "protein_id": "ENSP00000497404.1",
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          "feature": null
        },
        {
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          "protein_coding": false,
          "strand": true,
          "consequences": [
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            "intron_variant"
          ],
          "exon_rank": null,
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          "exon_count": 61,
          "intron_rank": 57,
          "intron_rank_end": null,
          "gene_symbol": "ITPR1",
          "gene_hgnc_id": 6180,
          "hgvs_c": "n.*2705+3A>G",
          "hgvs_p": null,
          "transcript": "ENST00000302640.13",
          "protein_id": "ENSP00000306253.9",
          "transcript_support_level": 5,
          "aa_start": null,
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          "cds_length": null,
          "cdna_start": null,
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          "biotype": null,
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        {
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          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
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      ],
      "gene_symbol": "ITPR1",
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      "computational_score_selected": -0.6100000143051147,
      "computational_prediction_selected": "Benign",
      "computational_source_selected": "BayesDel_noAF",
      "splice_score_selected": 0.6359999775886536,
      "splice_prediction_selected": "Benign",
      "splice_source_selected": "dbscSNV1_RF",
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      "revel_prediction": null,
      "alphamissense_score": null,
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      "bayesdelnoaf_score": -0.61,
      "bayesdelnoaf_prediction": "Benign",
      "phylop100way_score": 2.459,
      "phylop100way_prediction": "Benign",
      "spliceai_max_score": 0,
      "spliceai_max_prediction": "Benign",
      "dbscsnv_ada_score": 0.666976738832884,
      "dbscsnv_ada_prediction": "Benign",
      "apogee2_score": null,
      "apogee2_prediction": null,
      "mitotip_score": null,
      "mitotip_prediction": null,
      "acmg_score": -20,
      "acmg_classification": "Benign",
      "acmg_criteria": "BP4_Strong,BP6_Very_Strong,BS1,BS2",
      "acmg_by_gene": [
        {
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          "benign_score": 20,
          "pathogenic_score": 0,
          "criteria": [
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            "BP6_Very_Strong",
            "BS1",
            "BS2"
          ],
          "verdict": "Benign",
          "transcript": "ENST00000443694.5",
          "gene_symbol": "ITPR1",
          "hgnc_id": 6180,
          "effects": [
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            "intron_variant"
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          "inheritance_mode": "AD,AR",
          "hgvs_c": "c.7656+3A>G",
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        },
        {
          "score": -16,
          "benign_score": 16,
          "pathogenic_score": 0,
          "criteria": [
            "BP4_Strong",
            "BP6_Very_Strong",
            "BS2"
          ],
          "verdict": "Benign",
          "transcript": "ENST00000465436.5",
          "gene_symbol": "ENSG00000235978",
          "hgnc_id": null,
          "effects": [
            "intron_variant"
          ],
          "inheritance_mode": "",
          "hgvs_c": "n.193-134T>C",
          "hgvs_p": null
        },
        {
          "score": -16,
          "benign_score": 16,
          "pathogenic_score": 0,
          "criteria": [
            "BP4_Strong",
            "BP6_Very_Strong",
            "BS2"
          ],
          "verdict": "Benign",
          "transcript": "XR_007095790.1",
          "gene_symbol": "LOC124906209",
          "hgnc_id": null,
          "effects": [
            "intron_variant"
          ],
          "inheritance_mode": "",
          "hgvs_c": "n.274-134T>C",
          "hgvs_p": null
        }
      ],
      "clinvar_disease": "Autosomal dominant cerebellar ataxia,Gillespie syndrome,ITPR1-related disorder,not provided",
      "clinvar_classification": "Benign/Likely benign",
      "clinvar_review_status": "criteria provided, multiple submitters, no conflicts",
      "clinvar_submissions_summary": "LB:2 B:3",
      "phenotype_combined": "not provided|Autosomal dominant cerebellar ataxia|ITPR1-related disorder|Gillespie syndrome",
      "pathogenicity_classification_combined": "Benign/Likely benign",
      "custom_annotations": null
    }
  ],
  "message": null
}