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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: 10-109886389-A-G (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=10&pos=109886389&ref=A&alt=G&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "10",
      "pos": 109886389,
      "ref": "A",
      "alt": "G",
      "effect": "intron_variant",
      "transcript": "ENST00000502935.6",
      "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": 21,
          "intron_rank": 7,
          "intron_rank_end": null,
          "gene_symbol": "XPNPEP1",
          "gene_hgnc_id": 12822,
          "hgvs_c": "c.653-48T>C",
          "hgvs_p": null,
          "transcript": "NM_020383.4",
          "protein_id": "NP_065116.3",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 666,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 2001,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 2497,
          "mane_select": "ENST00000502935.6",
          "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": 21,
          "intron_rank": 7,
          "intron_rank_end": null,
          "gene_symbol": "XPNPEP1",
          "gene_hgnc_id": 12822,
          "hgvs_c": "c.653-48T>C",
          "hgvs_p": null,
          "transcript": "ENST00000502935.6",
          "protein_id": "ENSP00000421566.1",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 666,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 2001,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 2497,
          "mane_select": "NM_020383.4",
          "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": 20,
          "intron_rank": 7,
          "intron_rank_end": null,
          "gene_symbol": "XPNPEP1",
          "gene_hgnc_id": 12822,
          "hgvs_c": "c.653-48T>C",
          "hgvs_p": null,
          "transcript": "ENST00000322238.12",
          "protein_id": "ENSP00000324011.8",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 642,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 1929,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 2467,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 17,
          "intron_rank": 4,
          "intron_rank_end": null,
          "gene_symbol": "XPNPEP1",
          "gene_hgnc_id": 12822,
          "hgvs_c": "n.428-48T>C",
          "hgvs_p": null,
          "transcript": "ENST00000488118.6",
          "protein_id": null,
          "transcript_support_level": 1,
          "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": 4384,
          "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": 22,
          "intron_rank": 7,
          "intron_rank_end": null,
          "gene_symbol": "XPNPEP1",
          "gene_hgnc_id": 12822,
          "hgvs_c": "c.653-48T>C",
          "hgvs_p": null,
          "transcript": "NM_001324133.2",
          "protein_id": "NP_001311062.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 695,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 2088,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 2555,
          "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": 21,
          "intron_rank": 7,
          "intron_rank_end": null,
          "gene_symbol": "XPNPEP1",
          "gene_hgnc_id": 12822,
          "hgvs_c": "c.638-48T>C",
          "hgvs_p": null,
          "transcript": "NM_001324136.1",
          "protein_id": "NP_001311065.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 661,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 1986,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 2754,
          "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": 20,
          "intron_rank": 7,
          "intron_rank_end": null,
          "gene_symbol": "XPNPEP1",
          "gene_hgnc_id": 12822,
          "hgvs_c": "c.653-48T>C",
          "hgvs_p": null,
          "transcript": "NM_001324135.2",
          "protein_id": "NP_001311064.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 649,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 1950,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 2446,
          "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": 20,
          "intron_rank": 7,
          "intron_rank_end": null,
          "gene_symbol": "XPNPEP1",
          "gene_hgnc_id": 12822,
          "hgvs_c": "c.653-48T>C",
          "hgvs_p": null,
          "transcript": "NM_001167604.2",
          "protein_id": "NP_001161076.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 642,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 1929,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 2425,
          "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": 20,
          "intron_rank": 6,
          "intron_rank_end": null,
          "gene_symbol": "XPNPEP1",
          "gene_hgnc_id": 12822,
          "hgvs_c": "c.524-48T>C",
          "hgvs_p": null,
          "transcript": "NM_001324132.2",
          "protein_id": "NP_001311061.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 623,
          "cds_start": -4,
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          "cds_length": 1872,
          "cdna_start": null,
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          "cdna_length": 2408,
          "mane_select": null,
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          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
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          "exon_count": 19,
          "intron_rank": 5,
          "intron_rank_end": null,
          "gene_symbol": "XPNPEP1",
          "gene_hgnc_id": 12822,
          "hgvs_c": "c.311-48T>C",
          "hgvs_p": null,
          "transcript": "NM_001324128.2",
          "protein_id": "NP_001311057.1",
          "transcript_support_level": null,
          "aa_start": null,
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          "aa_length": 552,
          "cds_start": -4,
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          "cds_length": 1659,
          "cdna_start": null,
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          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
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        },
        {
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          "canonical": false,
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          "consequences": [
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          "intron_rank": 5,
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          "gene_symbol": "XPNPEP1",
          "gene_hgnc_id": 12822,
          "hgvs_c": "c.311-48T>C",
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          "cds_start": -4,
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        {
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          "canonical": false,
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          "consequences": [
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          "intron_rank": 8,
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          "gene_symbol": "XPNPEP1",
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          "hgvs_c": "c.311-48T>C",
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        {
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          "hgvs_c": "c.524-48T>C",
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        {
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          "gene_symbol": "XPNPEP1",
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        {
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          ],
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          "intron_rank": 4,
          "intron_rank_end": null,
          "gene_symbol": "XPNPEP1",
          "gene_hgnc_id": 12822,
          "hgvs_c": "n.439-48T>C",
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          "transcript": "ENST00000505255.5",
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      "clinvar_disease": "",
      "clinvar_classification": "",
      "clinvar_review_status": "",
      "clinvar_submissions_summary": "",
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      "custom_annotations": null
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  "message": null
}