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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-111216599-C-G (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=X&pos=111216599&ref=C&alt=G&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "X",
      "pos": 111216599,
      "ref": "C",
      "alt": "G",
      "effect": "intron_variant",
      "transcript": "NM_001128168.3",
      "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": 18,
          "intron_rank": 17,
          "intron_rank_end": null,
          "gene_symbol": "PAK3",
          "gene_hgnc_id": 8592,
          "hgvs_c": "c.1545+41C>G",
          "hgvs_p": null,
          "transcript": "NM_002578.5",
          "protein_id": "NP_002569.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 544,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1635,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": "ENST00000372007.10",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_002578.5"
        },
        {
          "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": 18,
          "intron_rank": 17,
          "intron_rank_end": null,
          "gene_symbol": "PAK3",
          "gene_hgnc_id": 8592,
          "hgvs_c": "c.1545+41C>G",
          "hgvs_p": null,
          "transcript": "ENST00000372007.10",
          "protein_id": "ENSP00000361077.4",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 544,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1635,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": "NM_002578.5",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000372007.10"
        },
        {
          "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": 16,
          "intron_rank": 15,
          "intron_rank_end": null,
          "gene_symbol": "PAK3",
          "gene_hgnc_id": 8592,
          "hgvs_c": "c.1653+41C>G",
          "hgvs_p": null,
          "transcript": "ENST00000360648.8",
          "protein_id": "ENSP00000353864.4",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 580,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1743,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000360648.8"
        },
        {
          "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": 15,
          "intron_rank": 14,
          "intron_rank_end": null,
          "gene_symbol": "PAK3",
          "gene_hgnc_id": 8592,
          "hgvs_c": "c.1608+41C>G",
          "hgvs_p": null,
          "transcript": "ENST00000417227.5",
          "protein_id": "ENSP00000389172.1",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 565,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1698,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000417227.5"
        },
        {
          "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": 15,
          "intron_rank": 14,
          "intron_rank_end": null,
          "gene_symbol": "PAK3",
          "gene_hgnc_id": 8592,
          "hgvs_c": "c.1590+41C>G",
          "hgvs_p": null,
          "transcript": "ENST00000262836.6",
          "protein_id": "ENSP00000262836.4",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 559,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1680,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000262836.6"
        },
        {
          "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": 16,
          "intron_rank": 15,
          "intron_rank_end": null,
          "gene_symbol": "PAK3",
          "gene_hgnc_id": 8592,
          "hgvs_c": "c.1545+41C>G",
          "hgvs_p": null,
          "transcript": "ENST00000446737.5",
          "protein_id": "ENSP00000410853.1",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 544,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1635,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000446737.5"
        },
        {
          "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": 20,
          "intron_rank": 19,
          "intron_rank_end": null,
          "gene_symbol": "PAK3",
          "gene_hgnc_id": 8592,
          "hgvs_c": "c.1653+41C>G",
          "hgvs_p": null,
          "transcript": "NM_001128168.3",
          "protein_id": "NP_001121640.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 580,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1743,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001128168.3"
        },
        {
          "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": 20,
          "intron_rank": 19,
          "intron_rank_end": null,
          "gene_symbol": "PAK3",
          "gene_hgnc_id": 8592,
          "hgvs_c": "c.1653+41C>G",
          "hgvs_p": null,
          "transcript": "ENST00000518291.6",
          "protein_id": "ENSP00000428921.1",
          "transcript_support_level": 5,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 580,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1743,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000518291.6"
        },
        {
          "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": 15,
          "intron_rank": 14,
          "intron_rank_end": null,
          "gene_symbol": "PAK3",
          "gene_hgnc_id": 8592,
          "hgvs_c": "c.1608+41C>G",
          "hgvs_p": null,
          "transcript": "NM_001128172.2",
          "protein_id": "NP_001121644.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 565,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1698,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001128172.2"
        },
        {
          "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": 19,
          "intron_rank": 18,
          "intron_rank_end": null,
          "gene_symbol": "PAK3",
          "gene_hgnc_id": 8592,
          "hgvs_c": "c.1608+41C>G",
          "hgvs_p": null,
          "transcript": "ENST00000519681.5",
          "protein_id": "ENSP00000429113.1",
          "transcript_support_level": 5,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 565,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1698,
          "cdna_start": null,
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          "cdna_length": null,
          "mane_select": null,
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          "biotype": "protein_coding",
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        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
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          "intron_rank": 18,
          "intron_rank_end": null,
          "gene_symbol": "PAK3",
          "gene_hgnc_id": 8592,
          "hgvs_c": "c.1590+41C>G",
          "hgvs_p": null,
          "transcript": "NM_001128173.3",
          "protein_id": "NP_001121645.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 559,
          "cds_start": null,
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          "cds_length": 1680,
          "cdna_start": null,
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          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001128173.3"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
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          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": 17,
          "intron_rank_end": null,
          "gene_symbol": "PAK3",
          "gene_hgnc_id": 8592,
          "hgvs_c": "c.1590+41C>G",
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          "transcript": "NM_001324327.2",
          "protein_id": "NP_001311256.1",
          "transcript_support_level": null,
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          "aa_length": 559,
          "cds_start": null,
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          "mane_select": null,
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        {
          "aa_ref": null,
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          ],
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          "gene_symbol": "PAK3",
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          "hgvs_c": "c.1590+41C>G",
          "hgvs_p": null,
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          "protein_id": "NP_001311257.1",
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          "cds_start": null,
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        {
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          "exon_count": 19,
          "intron_rank": 18,
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          "gene_symbol": "PAK3",
          "gene_hgnc_id": 8592,
          "hgvs_c": "c.1590+41C>G",
          "hgvs_p": null,
          "transcript": "NM_001324329.2",
          "protein_id": "NP_001311258.1",
          "transcript_support_level": null,
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          "cds_start": null,
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          "cdna_start": null,
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        },
        {
          "aa_ref": null,
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          "gene_symbol": "PAK3",
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        {
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          "exon_count": 19,
          "intron_rank": 18,
          "intron_rank_end": null,
          "gene_symbol": "PAK3",
          "gene_hgnc_id": 8592,
          "hgvs_c": "c.1590+41C>G",
          "hgvs_p": null,
          "transcript": "ENST00000372010.5",
          "protein_id": "ENSP00000361080.1",
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          "biotype": "protein_coding",
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        {
          "aa_ref": null,
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          "canonical": false,
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          "intron_rank_end": null,
          "gene_symbol": "PAK3",
          "gene_hgnc_id": 8592,
          "hgvs_c": "c.1545+41C>G",
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          "transcript": "NM_001128166.3",
          "protein_id": "NP_001121638.1",
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        {
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          "gene_symbol": "PAK3",
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          "transcript": "NM_001324325.2",
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        },
        {
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          "consequences": [
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          ],
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          "exon_count": 16,
          "intron_rank": 15,
          "intron_rank_end": null,
          "gene_symbol": "PAK3",
          "gene_hgnc_id": 8592,
          "hgvs_c": "c.1545+41C>G",
          "hgvs_p": null,
          "transcript": "NM_001324326.2",
          "protein_id": "NP_001311255.1",
          "transcript_support_level": null,
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          "cdna_start": null,
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          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001324326.2"
        },
        {
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          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 16,
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          "verdict": "Benign",
          "transcript": "NM_001128168.3",
          "gene_symbol": "PAK3",
          "hgnc_id": 8592,
          "effects": [
            "intron_variant"
          ],
          "inheritance_mode": "XL",
          "hgvs_c": "c.1653+41C>G",
          "hgvs_p": null
        }
      ],
      "clinvar_disease": "not provided",
      "clinvar_classification": "Benign",
      "clinvar_review_status": "criteria provided, multiple submitters, no conflicts",
      "clinvar_submissions_summary": "B:2",
      "phenotype_combined": "not provided",
      "pathogenicity_classification_combined": "Benign",
      "custom_annotations": null
    }
  ],
  "message": null
}