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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: 5-69366309-G-A (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=5&pos=69366309&ref=G&alt=A&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "5",
      "pos": 69366309,
      "ref": "G",
      "alt": "A",
      "effect": "intron_variant",
      "transcript": "ENST00000217893.10",
      "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": 3,
          "intron_rank": 2,
          "intron_rank_end": null,
          "gene_symbol": "TAF9",
          "gene_hgnc_id": 11542,
          "hgvs_c": "c.-18+194C>T",
          "hgvs_p": null,
          "transcript": "NM_003187.5",
          "protein_id": "NP_003178.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 264,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 795,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 1163,
          "mane_select": "ENST00000217893.10",
          "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": 3,
          "intron_rank": 2,
          "intron_rank_end": null,
          "gene_symbol": "TAF9",
          "gene_hgnc_id": 11542,
          "hgvs_c": "c.-18+194C>T",
          "hgvs_p": null,
          "transcript": "ENST00000217893.10",
          "protein_id": "ENSP00000217893.7",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 264,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 795,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 1163,
          "mane_select": "NM_003187.5",
          "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": 5,
          "intron_rank": 2,
          "intron_rank_end": null,
          "gene_symbol": "AK6",
          "gene_hgnc_id": 49151,
          "hgvs_c": "c.121+194C>T",
          "hgvs_p": null,
          "transcript": "NM_016283.5",
          "protein_id": "NP_057367.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 172,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 519,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 1626,
          "mane_select": "ENST00000380822.9",
          "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": 5,
          "intron_rank": 2,
          "intron_rank_end": null,
          "gene_symbol": "AK6",
          "gene_hgnc_id": 49151,
          "hgvs_c": "c.121+194C>T",
          "hgvs_p": null,
          "transcript": "ENST00000380822.9",
          "protein_id": "ENSP00000370201.4",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 172,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 519,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 1626,
          "mane_select": "NM_016283.5",
          "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": 3,
          "intron_rank": 2,
          "intron_rank_end": null,
          "gene_symbol": "TAF9",
          "gene_hgnc_id": 11542,
          "hgvs_c": "c.-18+194C>T",
          "hgvs_p": null,
          "transcript": "ENST00000506736.2",
          "protein_id": "ENSP00000421873.1",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 264,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 795,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 1180,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 2,
          "exon_rank_end": null,
          "exon_count": 2,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TAF9",
          "gene_hgnc_id": 11542,
          "hgvs_c": "n.357C>T",
          "hgvs_p": null,
          "transcript": "ENST00000685776.1",
          "protein_id": null,
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": null,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": null,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 4640,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 2,
          "exon_rank_end": null,
          "exon_count": 2,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TAF9",
          "gene_hgnc_id": 11542,
          "hgvs_c": "n.343C>T",
          "hgvs_p": null,
          "transcript": "ENST00000686157.1",
          "protein_id": null,
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": null,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": null,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 1818,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 2,
          "exon_rank_end": null,
          "exon_count": 2,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TAF9",
          "gene_hgnc_id": 11542,
          "hgvs_c": "n.640C>T",
          "hgvs_p": null,
          "transcript": "ENST00000693538.1",
          "protein_id": null,
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": null,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": null,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 2165,
          "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": 3,
          "intron_rank": 2,
          "intron_rank_end": null,
          "gene_symbol": "TAF9",
          "gene_hgnc_id": 11542,
          "hgvs_c": "c.-18+194C>T",
          "hgvs_p": null,
          "transcript": "NM_001015892.2",
          "protein_id": "NP_001015892.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 264,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 795,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 1273,
          "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": 3,
          "intron_rank": 2,
          "intron_rank_end": null,
          "gene_symbol": "TAF9",
          "gene_hgnc_id": 11542,
          "hgvs_c": "c.-18+194C>T",
          "hgvs_p": null,
          "transcript": "ENST00000328663.8",
          "protein_id": "ENSP00000370193.1",
          "transcript_support_level": 2,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 264,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 795,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 1461,
          "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": 3,
          "intron_rank": 2,
          "intron_rank_end": null,
          "gene_symbol": "TAF9",
          "gene_hgnc_id": 11542,
          "hgvs_c": "c.-18+194C>T",
          "hgvs_p": null,
          "transcript": "ENST00000503245.6",
          "protein_id": "ENSP00000425944.4",
          "transcript_support_level": 5,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 264,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 795,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 1168,
          "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": 4,
          "intron_rank": 3,
          "intron_rank_end": null,
          "gene_symbol": "TAF9",
          "gene_hgnc_id": 11542,
          "hgvs_c": "c.-18+194C>T",
          "hgvs_p": null,
          "transcript": "ENST00000504109.6",
          "protein_id": "ENSP00000426283.2",
          "transcript_support_level": 3,
          "aa_start": null,
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          "aa_length": 264,
          "cds_start": -4,
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          "cdna_start": null,
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          "cdna_length": 1339,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
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        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
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          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 3,
          "intron_rank": 2,
          "intron_rank_end": null,
          "gene_symbol": "TAF9",
          "gene_hgnc_id": 11542,
          "hgvs_c": "c.-18+194C>T",
          "hgvs_p": null,
          "transcript": "ENST00000508954.4",
          "protein_id": "ENSP00000427617.4",
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          "aa_length": 264,
          "cds_start": -4,
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          "cdna_start": null,
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          "cdna_length": 1705,
          "mane_select": null,
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          "feature": null
        },
        {
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          "canonical": false,
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          "strand": false,
          "consequences": [
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          ],
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          "intron_rank": 2,
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          "gene_symbol": "TAF9",
          "gene_hgnc_id": 11542,
          "hgvs_c": "c.-18+194C>T",
          "hgvs_p": null,
          "transcript": "ENST00000509462.6",
          "protein_id": "ENSP00000427343.4",
          "transcript_support_level": 2,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 264,
          "cds_start": -4,
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          "cdna_start": null,
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          "cdna_length": 1057,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
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          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
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          ],
          "exon_rank": null,
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          "exon_count": 3,
          "intron_rank": 2,
          "intron_rank_end": null,
          "gene_symbol": "TAF9",
          "gene_hgnc_id": 11542,
          "hgvs_c": "c.-18+194C>T",
          "hgvs_p": null,
          "transcript": "ENST00000512152.6",
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        {
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          "canonical": false,
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          "consequences": [
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          ],
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          "gene_symbol": "TAF9",
          "gene_hgnc_id": 11542,
          "hgvs_c": "c.-18+194C>T",
          "hgvs_p": null,
          "transcript": "ENST00000687836.1",
          "protein_id": "ENSP00000509753.1",
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          "cds_start": -4,
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          "cdna_start": null,
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          "cdna_length": 1193,
          "mane_select": null,
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          "feature": null
        },
        {
          "aa_ref": null,
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          "canonical": false,
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          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
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          "exon_count": 4,
          "intron_rank": 3,
          "intron_rank_end": null,
          "gene_symbol": "TAF9",
          "gene_hgnc_id": 11542,
          "hgvs_c": "c.-18+194C>T",
          "hgvs_p": null,
          "transcript": "ENST00000688968.1",
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          "cdna_start": null,
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          "mane_select": null,
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          "biotype": null,
          "feature": null
        },
        {
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          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 3,
          "intron_rank": 2,
          "intron_rank_end": null,
          "gene_symbol": "TAF9",
          "gene_hgnc_id": 11542,
          "hgvs_c": "c.-18+194C>T",
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          "transcript": "ENST00000689249.1",
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        {
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          ],
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          "exon_count": 3,
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          "gene_symbol": "TAF9",
          "gene_hgnc_id": 11542,
          "hgvs_c": "c.-18+194C>T",
          "hgvs_p": null,
          "transcript": "ENST00000690749.1",
          "protein_id": "ENSP00000510605.1",
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        },
        {
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          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
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          "intron_rank": 2,
          "intron_rank_end": null,
          "gene_symbol": "TAF9",
          "gene_hgnc_id": 11542,
          "hgvs_c": "c.-18+194C>T",
          "hgvs_p": null,
          "transcript": "ENST00000691076.1",
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          "cdna_start": null,
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          "cdna_length": 1348,
          "mane_select": null,
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          "biotype": null,
          "feature": null
        },
        {
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          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 3,
          "intron_rank": 2,
          "intron_rank_end": null,
          "gene_symbol": "TAF9",
          "gene_hgnc_id": 11542,
          "hgvs_c": "c.-18+194C>T",
          "hgvs_p": null,
          "transcript": "ENST00000691515.1",
          "protein_id": "ENSP00000509452.1",
          "transcript_support_level": null,
          "aa_start": null,
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          "cdna_start": null,
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          "verdict": "Benign",
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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
}