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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: 9-6978321-A-G (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=9&pos=6978321&ref=A&alt=G&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "9",
      "pos": 6978321,
      "ref": "A",
      "alt": "G",
      "effect": "intron_variant",
      "transcript": "ENST00000381309.8",
      "consequences": [
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 22,
          "intron_rank": 8,
          "intron_rank_end": null,
          "gene_symbol": "KDM4C",
          "gene_hgnc_id": 17071,
          "hgvs_c": "c.922-2604A>G",
          "hgvs_p": null,
          "transcript": "NM_015061.6",
          "protein_id": "NP_055876.2",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1056,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 3171,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 4338,
          "mane_select": "ENST00000381309.8",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": true,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 22,
          "intron_rank": 8,
          "intron_rank_end": null,
          "gene_symbol": "KDM4C",
          "gene_hgnc_id": 17071,
          "hgvs_c": "c.922-2604A>G",
          "hgvs_p": null,
          "transcript": "ENST00000381309.8",
          "protein_id": "ENSP00000370710.3",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1056,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 3171,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 4338,
          "mane_select": "NM_015061.6",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": 8,
          "intron_rank_end": null,
          "gene_symbol": "KDM4C",
          "gene_hgnc_id": 17071,
          "hgvs_c": "c.922-2604A>G",
          "hgvs_p": null,
          "transcript": "ENST00000536108.7",
          "protein_id": "ENSP00000440656.4",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 813,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 2442,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 3406,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 23,
          "intron_rank": 8,
          "intron_rank_end": null,
          "gene_symbol": "KDM4C",
          "gene_hgnc_id": 17071,
          "hgvs_c": "c.922-2604A>G",
          "hgvs_p": null,
          "transcript": "NM_001353997.3",
          "protein_id": "NP_001340926.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1089,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 3270,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 4437,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 21,
          "intron_rank": 8,
          "intron_rank_end": null,
          "gene_symbol": "KDM4C",
          "gene_hgnc_id": 17071,
          "hgvs_c": "c.922-2604A>G",
          "hgvs_p": null,
          "transcript": "ENST00000381306.7",
          "protein_id": "ENSP00000370707.3",
          "transcript_support_level": 2,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1047,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 3144,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 4601,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 22,
          "intron_rank": 8,
          "intron_rank_end": null,
          "gene_symbol": "KDM4C",
          "gene_hgnc_id": 17071,
          "hgvs_c": "c.922-2604A>G",
          "hgvs_p": null,
          "transcript": "NM_001304339.4",
          "protein_id": "NP_001291268.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1023,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 3072,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 4331,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": 8,
          "intron_rank_end": null,
          "gene_symbol": "KDM4C",
          "gene_hgnc_id": 17071,
          "hgvs_c": "c.988-2604A>G",
          "hgvs_p": null,
          "transcript": "NM_001146696.2",
          "protein_id": "NP_001140168.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 835,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 2508,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 3406,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": 8,
          "intron_rank_end": null,
          "gene_symbol": "KDM4C",
          "gene_hgnc_id": 17071,
          "hgvs_c": "c.922-2604A>G",
          "hgvs_p": null,
          "transcript": "NM_001146695.4",
          "protein_id": "NP_001140167.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 813,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 2442,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 3502,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": 8,
          "intron_rank_end": null,
          "gene_symbol": "KDM4C",
          "gene_hgnc_id": 17071,
          "hgvs_c": "c.922-2604A>G",
          "hgvs_p": null,
          "transcript": "ENST00000543771.5",
          "protein_id": "ENSP00000445427.1",
          "transcript_support_level": 2,
          "aa_start": null,
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          "aa_length": 813,
          "cds_start": -4,
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          "cds_length": 2442,
          "cdna_start": null,
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          "cdna_length": 3332,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
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          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
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          ],
          "exon_rank": null,
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          "exon_count": 20,
          "intron_rank": 7,
          "intron_rank_end": null,
          "gene_symbol": "KDM4C",
          "gene_hgnc_id": 17071,
          "hgvs_c": "c.379-2604A>G",
          "hgvs_p": null,
          "transcript": "NM_001304340.4",
          "protein_id": "NP_001291269.1",
          "transcript_support_level": null,
          "aa_start": null,
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          "aa_length": 801,
          "cds_start": -4,
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          "cdna_start": null,
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          "cdna_length": 3940,
          "mane_select": null,
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        {
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          "gene_symbol": "KDM4C",
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          "transcript": "NM_001353998.3",
          "protein_id": "NP_001340927.1",
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          "cdna_start": null,
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          "mane_select": null,
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          "feature": null
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          "intron_rank": 1,
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          "gene_symbol": "KDM4C",
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          "gene_symbol": "KDM4C",
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          "transcript": "NM_001354000.3",
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          "gene_symbol": "KDM4C",
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          "transcript": "ENST00000438023.5",
          "protein_id": "ENSP00000404756.1",
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          "intron_rank": 3,
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          "gene_symbol": "ENSG00000224972",
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          "transcript": "ENST00000445708.1",
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        {
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          "gene_symbol": "KDM4C",
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          "gene_symbol": "KDM4C",
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        {
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          ],
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          "exon_count": 23,
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          "intron_rank_end": null,
          "gene_symbol": "KDM4C",
          "gene_hgnc_id": 17071,
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      "acmg_classification": "Benign",
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          "verdict": "Benign",
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          "verdict": "Benign",
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          "gene_symbol": "ENSG00000224972",
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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
}