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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: 12-22494922-G-T (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=12&pos=22494922&ref=G&alt=T&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "12",
      "pos": 22494922,
      "ref": "G",
      "alt": "T",
      "effect": "intron_variant",
      "transcript": "ENST00000446597.6",
      "consequences": [
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 27,
          "intron_rank": 10,
          "intron_rank_end": null,
          "gene_symbol": "C2CD5",
          "gene_hgnc_id": 29062,
          "hgvs_c": "c.1148-1585C>A",
          "hgvs_p": null,
          "transcript": "NM_001286176.2",
          "protein_id": "NP_001273105.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1051,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 3156,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 4585,
          "mane_select": "ENST00000446597.6",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": true,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 27,
          "intron_rank": 10,
          "intron_rank_end": null,
          "gene_symbol": "C2CD5",
          "gene_hgnc_id": 29062,
          "hgvs_c": "c.1148-1585C>A",
          "hgvs_p": null,
          "transcript": "ENST00000446597.6",
          "protein_id": "ENSP00000388756.1",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1051,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 3156,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 4585,
          "mane_select": "NM_001286176.2",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 28,
          "intron_rank": 11,
          "intron_rank_end": null,
          "gene_symbol": "C2CD5",
          "gene_hgnc_id": 29062,
          "hgvs_c": "c.1154-1585C>A",
          "hgvs_p": null,
          "transcript": "ENST00000536386.5",
          "protein_id": "ENSP00000439392.1",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1053,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 3162,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 3496,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 27,
          "intron_rank": 10,
          "intron_rank_end": null,
          "gene_symbol": "C2CD5",
          "gene_hgnc_id": 29062,
          "hgvs_c": "c.1121-1585C>A",
          "hgvs_p": null,
          "transcript": "ENST00000396028.6",
          "protein_id": "ENSP00000379345.2",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1042,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 3129,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 3463,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 25,
          "intron_rank": 10,
          "intron_rank_end": null,
          "gene_symbol": "C2CD5",
          "gene_hgnc_id": 29062,
          "hgvs_c": "c.1148-1585C>A",
          "hgvs_p": null,
          "transcript": "ENST00000333957.8",
          "protein_id": "ENSP00000334229.4",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1000,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 3003,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 4436,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 28,
          "intron_rank": 11,
          "intron_rank_end": null,
          "gene_symbol": "C2CD5",
          "gene_hgnc_id": 29062,
          "hgvs_c": "c.1340-1585C>A",
          "hgvs_p": null,
          "transcript": "NM_001385322.1",
          "protein_id": "NP_001372251.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1115,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 3348,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 4777,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 28,
          "intron_rank": 11,
          "intron_rank_end": null,
          "gene_symbol": "C2CD5",
          "gene_hgnc_id": 29062,
          "hgvs_c": "c.1187-1585C>A",
          "hgvs_p": null,
          "transcript": "NM_001385323.1",
          "protein_id": "NP_001372252.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1064,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 3195,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 4624,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 28,
          "intron_rank": 11,
          "intron_rank_end": null,
          "gene_symbol": "C2CD5",
          "gene_hgnc_id": 29062,
          "hgvs_c": "c.1187-1585C>A",
          "hgvs_p": null,
          "transcript": "NM_001286175.2",
          "protein_id": "NP_001273104.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1054,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 3165,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 4594,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 28,
          "intron_rank": 11,
          "intron_rank_end": null,
          "gene_symbol": "C2CD5",
          "gene_hgnc_id": 29062,
          "hgvs_c": "c.1187-1585C>A",
          "hgvs_p": null,
          "transcript": "ENST00000545552.5",
          "protein_id": "ENSP00000443204.1",
          "transcript_support_level": 2,
          "aa_start": null,
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          "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": false,
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          "strand": false,
          "consequences": [
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          ],
          "exon_rank": null,
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          "exon_count": 28,
          "intron_rank": 11,
          "intron_rank_end": null,
          "gene_symbol": "C2CD5",
          "gene_hgnc_id": 29062,
          "hgvs_c": "c.1154-1585C>A",
          "hgvs_p": null,
          "transcript": "NM_001286173.2",
          "protein_id": "NP_001273102.1",
          "transcript_support_level": null,
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          "cdna_length": 4591,
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        {
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          "exon_count": 24,
          "intron_rank": 9,
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          "gene_symbol": "C2CD5",
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      "splice_prediction_selected": "Benign",
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      "bayesdelnoaf_score": -0.88,
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      "phylop100way_prediction": "Benign",
      "spliceai_max_score": 0.01,
      "spliceai_max_prediction": "Benign",
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      "acmg_classification": "Benign",
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      "acmg_by_gene": [
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          "verdict": "Benign",
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          "verdict": "Benign",
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          "gene_symbol": "C2CD5-AS1",
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          "effects": [
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          "inheritance_mode": "",
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      "clinvar_disease": "",
      "clinvar_classification": "",
      "clinvar_review_status": "",
      "clinvar_submissions_summary": "",
      "phenotype_combined": null,
      "pathogenicity_classification_combined": null,
      "custom_annotations": null
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  ],
  "message": null
}