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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: 14-95105111-C-G (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=14&pos=95105111&ref=C&alt=G&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "14",
      "pos": 95105111,
      "ref": "C",
      "alt": "G",
      "effect": "missense_variant",
      "transcript": "ENST00000343455.8",
      "consequences": [
        {
          "aa_ref": "D",
          "aa_alt": "H",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 20,
          "exon_rank_end": null,
          "exon_count": 27,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "DICER1",
          "gene_hgnc_id": 17098,
          "hgvs_c": "c.3229G>C",
          "hgvs_p": "p.Asp1077His",
          "transcript": "NM_177438.3",
          "protein_id": "NP_803187.1",
          "transcript_support_level": null,
          "aa_start": 1077,
          "aa_end": null,
          "aa_length": 1922,
          "cds_start": 3229,
          "cds_end": null,
          "cds_length": 5769,
          "cdna_start": 3574,
          "cdna_end": null,
          "cdna_length": 10384,
          "mane_select": "ENST00000343455.8",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "D",
          "aa_alt": "H",
          "canonical": true,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 20,
          "exon_rank_end": null,
          "exon_count": 27,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "DICER1",
          "gene_hgnc_id": 17098,
          "hgvs_c": "c.3229G>C",
          "hgvs_p": "p.Asp1077His",
          "transcript": "ENST00000343455.8",
          "protein_id": "ENSP00000343745.3",
          "transcript_support_level": 1,
          "aa_start": 1077,
          "aa_end": null,
          "aa_length": 1922,
          "cds_start": 3229,
          "cds_end": null,
          "cds_length": 5769,
          "cdna_start": 3574,
          "cdna_end": null,
          "cdna_length": 10384,
          "mane_select": "NM_177438.3",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "D",
          "aa_alt": "H",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 22,
          "exon_rank_end": null,
          "exon_count": 29,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "DICER1",
          "gene_hgnc_id": 17098,
          "hgvs_c": "c.3229G>C",
          "hgvs_p": "p.Asp1077His",
          "transcript": "ENST00000393063.6",
          "protein_id": "ENSP00000376783.1",
          "transcript_support_level": 1,
          "aa_start": 1077,
          "aa_end": null,
          "aa_length": 1922,
          "cds_start": 3229,
          "cds_end": null,
          "cds_length": 5769,
          "cdna_start": 3632,
          "cdna_end": null,
          "cdna_length": 7423,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "D",
          "aa_alt": "H",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 20,
          "exon_rank_end": null,
          "exon_count": 27,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "DICER1",
          "gene_hgnc_id": 17098,
          "hgvs_c": "c.3229G>C",
          "hgvs_p": "p.Asp1077His",
          "transcript": "ENST00000527414.5",
          "protein_id": "ENSP00000435681.1",
          "transcript_support_level": 1,
          "aa_start": 1077,
          "aa_end": null,
          "aa_length": 1922,
          "cds_start": 3229,
          "cds_end": null,
          "cds_length": 5769,
          "cdna_start": 3462,
          "cdna_end": null,
          "cdna_length": 6179,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "D",
          "aa_alt": "H",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 23,
          "exon_rank_end": null,
          "exon_count": 30,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "DICER1",
          "gene_hgnc_id": 17098,
          "hgvs_c": "c.3229G>C",
          "hgvs_p": "p.Asp1077His",
          "transcript": "ENST00000529720.2",
          "protein_id": "ENSP00000433926.2",
          "transcript_support_level": 1,
          "aa_start": 1077,
          "aa_end": null,
          "aa_length": 1922,
          "cds_start": 3229,
          "cds_end": null,
          "cds_length": 5769,
          "cdna_start": 3564,
          "cdna_end": null,
          "cdna_length": 10374,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "D",
          "aa_alt": "H",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 22,
          "exon_rank_end": null,
          "exon_count": 29,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "DICER1",
          "gene_hgnc_id": 17098,
          "hgvs_c": "c.3229G>C",
          "hgvs_p": "p.Asp1077His",
          "transcript": "ENST00000531162.7",
          "protein_id": "ENSP00000433060.3",
          "transcript_support_level": 1,
          "aa_start": 1077,
          "aa_end": null,
          "aa_length": 1922,
          "cds_start": 3229,
          "cds_end": null,
          "cds_length": 5769,
          "cdna_start": 3658,
          "cdna_end": null,
          "cdna_length": 10453,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "D",
          "aa_alt": "H",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 19,
          "exon_rank_end": null,
          "exon_count": 25,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "DICER1",
          "gene_hgnc_id": 17098,
          "hgvs_c": "c.3229G>C",
          "hgvs_p": "p.Asp1077His",
          "transcript": "ENST00000541352.5",
          "protein_id": "ENSP00000444719.1",
          "transcript_support_level": 1,
          "aa_start": 1077,
          "aa_end": null,
          "aa_length": 1829,
          "cds_start": 3229,
          "cds_end": null,
          "cds_length": 5490,
          "cdna_start": 3238,
          "cdna_end": null,
          "cdna_length": 5621,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "D",
          "aa_alt": "H",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 20,
          "exon_rank_end": null,
          "exon_count": 27,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "DICER1",
          "gene_hgnc_id": 17098,
          "hgvs_c": "c.3229G>C",
          "hgvs_p": "p.Asp1077His",
          "transcript": "NM_001271282.3",
          "protein_id": "NP_001258211.1",
          "transcript_support_level": null,
          "aa_start": 1077,
          "aa_end": null,
          "aa_length": 1922,
          "cds_start": 3229,
          "cds_end": null,
          "cds_length": 5769,
          "cdna_start": 3453,
          "cdna_end": null,
          "cdna_length": 10263,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "D",
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          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 20,
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          "exon_count": 27,
          "intron_rank": null,
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          "gene_symbol": "DICER1",
          "gene_hgnc_id": 17098,
          "hgvs_c": "c.3229G>C",
          "hgvs_p": "p.Asp1077His",
          "transcript": "NM_001291628.2",
          "protein_id": "NP_001278557.1",
          "transcript_support_level": null,
          "aa_start": 1077,
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          "cds_start": 3229,
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          "cds_length": 5769,
          "cdna_start": 3350,
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        {
          "aa_ref": "D",
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          "consequences": [
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          ],
          "exon_rank": 22,
          "exon_rank_end": null,
          "exon_count": 29,
          "intron_rank": null,
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          "gene_symbol": "DICER1",
          "gene_hgnc_id": 17098,
          "hgvs_c": "c.3229G>C",
          "hgvs_p": "p.Asp1077His",
          "transcript": "NM_001395677.1",
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      "bayesdelnoaf_score": -0.2,
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          "verdict": "Uncertain_significance",
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      "clinvar_classification": "Uncertain significance",
      "clinvar_review_status": "criteria provided, single submitter",
      "clinvar_submissions_summary": "US:1",
      "phenotype_combined": "Hereditary cancer-predisposing syndrome",
      "pathogenicity_classification_combined": "Uncertain significance",
      "custom_annotations": null
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  "message": null
}