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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: X-45089792-C-T (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=X&pos=45089792&ref=C&alt=T&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "X",
      "pos": 45089792,
      "ref": "C",
      "alt": "T",
      "effect": "missense_variant",
      "transcript": "ENST00000611820.5",
      "consequences": [
        {
          "aa_ref": "L",
          "aa_alt": "F",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 26,
          "exon_rank_end": null,
          "exon_count": 30,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "KDM6A",
          "gene_hgnc_id": 12637,
          "hgvs_c": "c.3754C>T",
          "hgvs_p": "p.Leu1252Phe",
          "transcript": "NM_001291415.2",
          "protein_id": "NP_001278344.1",
          "transcript_support_level": null,
          "aa_start": 1252,
          "aa_end": null,
          "aa_length": 1453,
          "cds_start": 3754,
          "cds_end": null,
          "cds_length": 4362,
          "cdna_start": 4118,
          "cdna_end": null,
          "cdna_length": 6094,
          "mane_select": "ENST00000611820.5",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "L",
          "aa_alt": "F",
          "canonical": true,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 26,
          "exon_rank_end": null,
          "exon_count": 30,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "KDM6A",
          "gene_hgnc_id": 12637,
          "hgvs_c": "c.3754C>T",
          "hgvs_p": "p.Leu1252Phe",
          "transcript": "ENST00000611820.5",
          "protein_id": "ENSP00000483595.2",
          "transcript_support_level": 1,
          "aa_start": 1252,
          "aa_end": null,
          "aa_length": 1453,
          "cds_start": 3754,
          "cds_end": null,
          "cds_length": 4362,
          "cdna_start": 4118,
          "cdna_end": null,
          "cdna_length": 6094,
          "mane_select": "NM_001291415.2",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "L",
          "aa_alt": "F",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 25,
          "exon_rank_end": null,
          "exon_count": 29,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "KDM6A",
          "gene_hgnc_id": 12637,
          "hgvs_c": "c.3619C>T",
          "hgvs_p": "p.Leu1207Phe",
          "transcript": "ENST00000382899.9",
          "protein_id": "ENSP00000372355.6",
          "transcript_support_level": 1,
          "aa_start": 1207,
          "aa_end": null,
          "aa_length": 1408,
          "cds_start": 3619,
          "cds_end": null,
          "cds_length": 4227,
          "cdna_start": 3983,
          "cdna_end": null,
          "cdna_length": 5778,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "L",
          "aa_alt": "F",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 25,
          "exon_rank_end": null,
          "exon_count": 29,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "KDM6A",
          "gene_hgnc_id": 12637,
          "hgvs_c": "c.3598C>T",
          "hgvs_p": "p.Leu1200Phe",
          "transcript": "ENST00000377967.9",
          "protein_id": "ENSP00000367203.4",
          "transcript_support_level": 1,
          "aa_start": 1200,
          "aa_end": null,
          "aa_length": 1401,
          "cds_start": 3598,
          "cds_end": null,
          "cds_length": 4206,
          "cdna_start": 3962,
          "cdna_end": null,
          "cdna_length": 5761,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "L",
          "aa_alt": "F",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 24,
          "exon_rank_end": null,
          "exon_count": 28,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "KDM6A",
          "gene_hgnc_id": 12637,
          "hgvs_c": "c.3463C>T",
          "hgvs_p": "p.Leu1155Phe",
          "transcript": "ENST00000536777.6",
          "protein_id": "ENSP00000437405.3",
          "transcript_support_level": 1,
          "aa_start": 1155,
          "aa_end": null,
          "aa_length": 1356,
          "cds_start": 3463,
          "cds_end": null,
          "cds_length": 4071,
          "cdna_start": 3827,
          "cdna_end": null,
          "cdna_length": 5622,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "L",
          "aa_alt": "F",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 23,
          "exon_rank_end": null,
          "exon_count": 27,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "KDM6A",
          "gene_hgnc_id": 12637,
          "hgvs_c": "c.3361C>T",
          "hgvs_p": "p.Leu1121Phe",
          "transcript": "ENST00000543216.6",
          "protein_id": "ENSP00000443078.3",
          "transcript_support_level": 1,
          "aa_start": 1121,
          "aa_end": null,
          "aa_length": 1322,
          "cds_start": 3361,
          "cds_end": null,
          "cds_length": 3969,
          "cdna_start": 3725,
          "cdna_end": null,
          "cdna_length": 5520,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "L",
          "aa_alt": "F",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 26,
          "exon_rank_end": null,
          "exon_count": 31,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "KDM6A",
          "gene_hgnc_id": 12637,
          "hgvs_c": "c.3754C>T",
          "hgvs_p": "p.Leu1252Phe",
          "transcript": "NM_001419809.1",
          "protein_id": "NP_001406738.1",
          "transcript_support_level": null,
          "aa_start": 1252,
          "aa_end": null,
          "aa_length": 1489,
          "cds_start": 3754,
          "cds_end": null,
          "cds_length": 4470,
          "cdna_start": 4118,
          "cdna_end": null,
          "cdna_length": 6202,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "L",
          "aa_alt": "F",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 25,
          "exon_rank_end": null,
          "exon_count": 30,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "KDM6A",
          "gene_hgnc_id": 12637,
          "hgvs_c": "c.3652C>T",
          "hgvs_p": "p.Leu1218Phe",
          "transcript": "NM_001419810.1",
          "protein_id": "NP_001406739.1",
          "transcript_support_level": null,
          "aa_start": 1218,
          "aa_end": null,
          "aa_length": 1455,
          "cds_start": 3652,
          "cds_end": null,
          "cds_length": 4368,
          "cdna_start": 4016,
          "cdna_end": null,
          "cdna_length": 6100,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "L",
          "aa_alt": "F",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 25,
          "exon_rank_end": null,
          "exon_count": 30,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "KDM6A",
          "gene_hgnc_id": 12637,
          "hgvs_c": "c.3619C>T",
          "hgvs_p": "p.Leu1207Phe",
          "transcript": "NM_001419811.1",
          "protein_id": "NP_001406740.1",
          "transcript_support_level": null,
          "aa_start": 1207,
          "aa_end": null,
          "aa_length": 1444,
          "cds_start": 3619,
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          "cdna_start": 3983,
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          "mane_select": null,
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          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "L",
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          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 25,
          "exon_rank_end": null,
          "exon_count": 30,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "KDM6A",
          "gene_hgnc_id": 12637,
          "hgvs_c": "c.3598C>T",
          "hgvs_p": "p.Leu1200Phe",
          "transcript": "NM_001419812.1",
          "protein_id": "NP_001406741.1",
          "transcript_support_level": null,
          "aa_start": 1200,
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          "cds_start": 3598,
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        {
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          "exon_count": 30,
          "intron_rank": null,
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          "gene_symbol": "KDM6A",
          "gene_hgnc_id": 12637,
          "hgvs_c": "c.3676C>T",
          "hgvs_p": "p.Leu1226Phe",
          "transcript": "ENST00000674586.1",
          "protein_id": "ENSP00000502660.1",
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        {
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        {
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          "gene_symbol": "KDM6A",
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          "transcript": "NM_001291416.2",
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        {
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          "intron_rank": null,
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          "gene_symbol": "KDM6A",
          "gene_hgnc_id": 12637,
          "hgvs_c": "c.3496C>T",
          "hgvs_p": "p.Leu1166Phe",
          "transcript": "NM_001419814.1",
          "protein_id": "NP_001406743.1",
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        {
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        {
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          "intron_rank": null,
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          "gene_symbol": "KDM6A",
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          "hgvs_c": "c.3517C>T",
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          "gene_symbol": "KDM6A",
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          "transcript": "NM_001410742.1",
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          "exon_count": 28,
          "intron_rank": null,
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          "gene_symbol": "KDM6A",
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          "hgvs_c": "c.3463C>T",
          "hgvs_p": "p.Leu1155Phe",
          "transcript": "NM_001291417.2",
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        {
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      "clinvar_submissions_summary": "LP:1",
      "phenotype_combined": "Kabuki syndrome 2",
      "pathogenicity_classification_combined": "Likely pathogenic",
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  "message": null
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