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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: 6-42299264-G-T (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=6&pos=42299264&ref=G&alt=T&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "6",
      "pos": 42299264,
      "ref": "G",
      "alt": "T",
      "effect": "intron_variant",
      "transcript": "NM_001297573.2",
      "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": 18,
          "intron_rank": 4,
          "intron_rank_end": null,
          "gene_symbol": "TRERF1",
          "gene_hgnc_id": 18273,
          "hgvs_c": "c.-259+1374C>A",
          "hgvs_p": null,
          "transcript": "NM_001395490.1",
          "protein_id": "NP_001382419.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1212,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 3639,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": "ENST00000695948.1",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001395490.1"
        },
        {
          "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": 18,
          "intron_rank": 4,
          "intron_rank_end": null,
          "gene_symbol": "TRERF1",
          "gene_hgnc_id": 18273,
          "hgvs_c": "c.-259+1374C>A",
          "hgvs_p": null,
          "transcript": "ENST00000695948.1",
          "protein_id": "ENSP00000512293.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1212,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 3639,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": "NM_001395490.1",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000695948.1"
        },
        {
          "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": 18,
          "intron_rank": 4,
          "intron_rank_end": null,
          "gene_symbol": "TRERF1",
          "gene_hgnc_id": 18273,
          "hgvs_c": "c.-259+1374C>A",
          "hgvs_p": null,
          "transcript": "ENST00000541110.5",
          "protein_id": "ENSP00000439689.1",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1220,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 3663,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000541110.5"
        },
        {
          "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": 18,
          "intron_rank": 4,
          "intron_rank_end": null,
          "gene_symbol": "TRERF1",
          "gene_hgnc_id": 18273,
          "hgvs_c": "c.-259+1374C>A",
          "hgvs_p": null,
          "transcript": "ENST00000372922.8",
          "protein_id": "ENSP00000362013.4",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1200,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 3603,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000372922.8"
        },
        {
          "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": 18,
          "intron_rank": 4,
          "intron_rank_end": null,
          "gene_symbol": "TRERF1",
          "gene_hgnc_id": 18273,
          "hgvs_c": "n.-259+1374C>A",
          "hgvs_p": null,
          "transcript": "ENST00000372917.9",
          "protein_id": "ENSP00000362008.6",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": null,
          "cds_start": null,
          "cds_end": null,
          "cds_length": null,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "nonsense_mediated_decay",
          "feature": "ENST00000372917.9"
        },
        {
          "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": 18,
          "intron_rank": 4,
          "intron_rank_end": null,
          "gene_symbol": "TRERF1",
          "gene_hgnc_id": 18273,
          "hgvs_c": "c.-259+1374C>A",
          "hgvs_p": null,
          "transcript": "ENST00000934154.1",
          "protein_id": "ENSP00000604213.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1232,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 3699,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000934154.1"
        },
        {
          "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": 19,
          "intron_rank": 5,
          "intron_rank_end": null,
          "gene_symbol": "TRERF1",
          "gene_hgnc_id": 18273,
          "hgvs_c": "c.-259+1374C>A",
          "hgvs_p": null,
          "transcript": "ENST00000934164.1",
          "protein_id": "ENSP00000604223.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1232,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 3699,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000934164.1"
        },
        {
          "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": 18,
          "intron_rank": 4,
          "intron_rank_end": null,
          "gene_symbol": "TRERF1",
          "gene_hgnc_id": 18273,
          "hgvs_c": "c.-259+1374C>A",
          "hgvs_p": null,
          "transcript": "ENST00000934166.1",
          "protein_id": "ENSP00000604225.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1232,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 3699,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000934166.1"
        },
        {
          "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": 18,
          "intron_rank": 4,
          "intron_rank_end": null,
          "gene_symbol": "TRERF1",
          "gene_hgnc_id": 18273,
          "hgvs_c": "c.-259+1374C>A",
          "hgvs_p": null,
          "transcript": "ENST00000934174.1",
          "protein_id": "ENSP00000604233.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1232,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 3699,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000934174.1"
        },
        {
          "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": 18,
          "intron_rank": 4,
          "intron_rank_end": null,
          "gene_symbol": "TRERF1",
          "gene_hgnc_id": 18273,
          "hgvs_c": "c.-259+1374C>A",
          "hgvs_p": null,
          "transcript": "ENST00000934177.1",
          "protein_id": "ENSP00000604236.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1232,
          "cds_start": null,
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          "cds_length": 3699,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000934177.1"
        },
        {
          "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": 19,
          "intron_rank": 4,
          "intron_rank_end": null,
          "gene_symbol": "TRERF1",
          "gene_hgnc_id": 18273,
          "hgvs_c": "c.-381+1374C>A",
          "hgvs_p": null,
          "transcript": "ENST00000934179.1",
          "protein_id": "ENSP00000604238.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1232,
          "cds_start": null,
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          "cds_length": 3699,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000934179.1"
        },
        {
          "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": 17,
          "intron_rank": 3,
          "intron_rank_end": null,
          "gene_symbol": "TRERF1",
          "gene_hgnc_id": 18273,
          "hgvs_c": "c.-259+1374C>A",
          "hgvs_p": null,
          "transcript": "ENST00000934183.1",
          "protein_id": "ENSP00000604242.1",
          "transcript_support_level": null,
          "aa_start": null,
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          "aa_length": 1232,
          "cds_start": null,
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          "cdna_start": null,
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          "cdna_length": null,
          "mane_select": null,
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          "biotype": "protein_coding",
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        {
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          "canonical": false,
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          "intron_rank": 4,
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          "gene_symbol": "TRERF1",
          "gene_hgnc_id": 18273,
          "hgvs_c": "c.-259+1374C>A",
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          "transcript": "NM_001297573.2",
          "protein_id": "NP_001284502.1",
          "transcript_support_level": null,
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          "mane_select": null,
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          "biotype": "protein_coding",
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        },
        {
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          "strand": false,
          "consequences": [
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          ],
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          "exon_count": 18,
          "intron_rank": 4,
          "intron_rank_end": null,
          "gene_symbol": "TRERF1",
          "gene_hgnc_id": 18273,
          "hgvs_c": "c.-259+1374C>A",
          "hgvs_p": null,
          "transcript": "ENST00000934155.1",
          "protein_id": "ENSP00000604214.1",
          "transcript_support_level": null,
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        {
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          "transcript": "ENST00000934156.1",
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          "biotype": "protein_coding",
          "feature": "ENST00000934156.1"
        },
        {
          "aa_ref": null,
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          "canonical": false,
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          "strand": false,
          "consequences": [
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          ],
          "exon_rank": null,
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          "exon_count": 18,
          "intron_rank": 4,
          "intron_rank_end": null,
          "gene_symbol": "TRERF1",
          "gene_hgnc_id": 18273,
          "hgvs_c": "c.-259+1374C>A",
          "hgvs_p": null,
          "transcript": "ENST00000934158.1",
          "protein_id": "ENSP00000604217.1",
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          "biotype": "protein_coding",
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        {
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          ],
          "exon_rank": null,
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          "exon_count": 17,
          "intron_rank": 3,
          "intron_rank_end": null,
          "gene_symbol": "TRERF1",
          "gene_hgnc_id": 18273,
          "hgvs_c": "c.-259+1374C>A",
          "hgvs_p": null,
          "transcript": "ENST00000934160.1",
          "protein_id": "ENSP00000604219.1",
          "transcript_support_level": null,
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        {
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          "hgvs_c": "c.-259+1374C>A",
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        {
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        },
        {
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          "strand": false,
          "consequences": [
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          ],
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          "exon_count": 18,
          "intron_rank": 4,
          "intron_rank_end": null,
          "gene_symbol": "TRERF1",
          "gene_hgnc_id": 18273,
          "hgvs_c": "c.-259+1374C>A",
          "hgvs_p": null,
          "transcript": "ENST00000934165.1",
          "protein_id": "ENSP00000604224.1",
          "transcript_support_level": null,
          "aa_start": null,
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          "cds_start": null,
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        },
        {
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      "acmg_classification": "Likely_benign",
      "acmg_criteria": "PM2,BP4_Strong",
      "acmg_by_gene": [
        {
          "score": -2,
          "benign_score": 4,
          "pathogenic_score": 2,
          "criteria": [
            "PM2",
            "BP4_Strong"
          ],
          "verdict": "Likely_benign",
          "transcript": "NM_001297573.2",
          "gene_symbol": "TRERF1",
          "hgnc_id": 18273,
          "effects": [
            "intron_variant"
          ],
          "inheritance_mode": "AR",
          "hgvs_c": "c.-259+1374C>A",
          "hgvs_p": null
        }
      ],
      "clinvar_disease": "",
      "clinvar_classification": "",
      "clinvar_review_status": "",
      "clinvar_submissions_summary": "",
      "phenotype_combined": null,
      "pathogenicity_classification_combined": null,
      "custom_annotations": null
    }
  ],
  "message": null
}