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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: 14-103395856-G-A (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=14&pos=103395856&ref=G&alt=A&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "14",
      "pos": 103395856,
      "ref": "G",
      "alt": "A",
      "effect": "intron_variant",
      "transcript": "ENST00000429436.7",
      "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": 1,
          "intron_rank_end": null,
          "gene_symbol": "MARK3",
          "gene_hgnc_id": 6897,
          "hgvs_c": "c.52-9220G>A",
          "hgvs_p": null,
          "transcript": "NM_001128918.3",
          "protein_id": "NP_001122390.2",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 753,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 2262,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 3481,
          "mane_select": "ENST00000429436.7",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "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": 1,
          "intron_rank_end": null,
          "gene_symbol": "MARK3",
          "gene_hgnc_id": 6897,
          "hgvs_c": "c.52-9220G>A",
          "hgvs_p": null,
          "transcript": "ENST00000429436.7",
          "protein_id": "ENSP00000411397.2",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 753,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 2262,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 3481,
          "mane_select": "NM_001128918.3",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "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": 1,
          "intron_rank_end": null,
          "gene_symbol": "MARK3",
          "gene_hgnc_id": 6897,
          "hgvs_c": "c.52-9220G>A",
          "hgvs_p": null,
          "transcript": "ENST00000556744.2",
          "protein_id": "ENSP00000451623.2",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 789,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 2370,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 3578,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "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": 17,
          "intron_rank": 1,
          "intron_rank_end": null,
          "gene_symbol": "MARK3",
          "gene_hgnc_id": 6897,
          "hgvs_c": "c.52-9220G>A",
          "hgvs_p": null,
          "transcript": "ENST00000416682.6",
          "protein_id": "ENSP00000408092.2",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 752,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 2259,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 2969,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "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": 17,
          "intron_rank": 1,
          "intron_rank_end": null,
          "gene_symbol": "MARK3",
          "gene_hgnc_id": 6897,
          "hgvs_c": "c.52-9220G>A",
          "hgvs_p": null,
          "transcript": "ENST00000553942.5",
          "protein_id": "ENSP00000450772.1",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 744,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 2235,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 2298,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "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": 1,
          "intron_rank_end": null,
          "gene_symbol": "MARK3",
          "gene_hgnc_id": 6897,
          "hgvs_c": "c.52-9220G>A",
          "hgvs_p": null,
          "transcript": "ENST00000303622.13",
          "protein_id": "ENSP00000303698.9",
          "transcript_support_level": 1,
          "aa_start": null,
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          "aa_length": 729,
          "cds_start": -4,
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          "cds_length": 2190,
          "cdna_start": null,
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          "cdna_length": 3283,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
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          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
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          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 16,
          "intron_rank": 1,
          "intron_rank_end": null,
          "gene_symbol": "MARK3",
          "gene_hgnc_id": 6897,
          "hgvs_c": "c.52-9220G>A",
          "hgvs_p": null,
          "transcript": "ENST00000216288.11",
          "protein_id": "ENSP00000216288.7",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 713,
          "cds_start": -4,
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          "cds_length": 2142,
          "cdna_start": null,
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          "cdna_length": 2911,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
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          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 16,
          "intron_rank": 1,
          "intron_rank_end": null,
          "gene_symbol": "MARK3",
          "gene_hgnc_id": 6897,
          "hgvs_c": "c.52-9220G>A",
          "hgvs_p": null,
          "transcript": "ENST00000440884.7",
          "protein_id": "ENSP00000402104.3",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 659,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 1980,
          "cdna_start": null,
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          "cdna_length": 2643,
          "mane_select": null,
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          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
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          "canonical": false,
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          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
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          "exon_count": 8,
          "intron_rank": 1,
          "intron_rank_end": null,
          "gene_symbol": "MARK3",
          "gene_hgnc_id": 6897,
          "hgvs_c": "n.667-9220G>A",
          "hgvs_p": null,
          "transcript": "ENST00000558223.6",
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        {
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          "gene_symbol": "MARK3",
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          "hgvs_c": "c.52-9220G>A",
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          "transcript": "ENST00000678179.1",
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      "acmg_classification": "Benign",
      "acmg_criteria": "BP4_Strong,BA1",
      "acmg_by_gene": [
        {
          "score": -12,
          "benign_score": 12,
          "pathogenic_score": 0,
          "criteria": [
            "BP4_Strong",
            "BA1"
          ],
          "verdict": "Benign",
          "transcript": "ENST00000429436.7",
          "gene_symbol": "MARK3",
          "hgnc_id": 6897,
          "effects": [
            "intron_variant"
          ],
          "inheritance_mode": "Unknown,AR",
          "hgvs_c": "c.52-9220G>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
}