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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-103785471-T-C (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=X&pos=103785471&ref=T&alt=C&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "X",
      "pos": 103785471,
      "ref": "T",
      "alt": "C",
      "effect": "intron_variant",
      "transcript": "NM_000533.5",
      "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": 7,
          "intron_rank": 1,
          "intron_rank_end": null,
          "gene_symbol": "PLP1",
          "gene_hgnc_id": 9086,
          "hgvs_c": "c.5-111T>C",
          "hgvs_p": null,
          "transcript": "NM_000533.5",
          "protein_id": "NP_000524.3",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 277,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 834,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": "ENST00000621218.5",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_000533.5"
        },
        {
          "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": 7,
          "intron_rank": 1,
          "intron_rank_end": null,
          "gene_symbol": "PLP1",
          "gene_hgnc_id": 9086,
          "hgvs_c": "c.5-111T>C",
          "hgvs_p": null,
          "transcript": "ENST00000621218.5",
          "protein_id": "ENSP00000484450.1",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 277,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 834,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": "NM_000533.5",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000621218.5"
        },
        {
          "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": 7,
          "intron_rank": 1,
          "intron_rank_end": null,
          "gene_symbol": "PLP1",
          "gene_hgnc_id": 9086,
          "hgvs_c": "c.5-111T>C",
          "hgvs_p": null,
          "transcript": "ENST00000619236.1",
          "protein_id": "ENSP00000477619.1",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 242,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 729,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000619236.1"
        },
        {
          "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": 8,
          "intron_rank": 1,
          "intron_rank_end": null,
          "gene_symbol": "PLP1",
          "gene_hgnc_id": 9086,
          "hgvs_c": "c.5-111T>C",
          "hgvs_p": null,
          "transcript": "ENST00000867712.1",
          "protein_id": "ENSP00000537771.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 291,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 876,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000867712.1"
        },
        {
          "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": 8,
          "intron_rank": 2,
          "intron_rank_end": null,
          "gene_symbol": "PLP1",
          "gene_hgnc_id": 9086,
          "hgvs_c": "c.5-111T>C",
          "hgvs_p": null,
          "transcript": "NM_001128834.3",
          "protein_id": "NP_001122306.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 277,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 834,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001128834.3"
        },
        {
          "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": 8,
          "intron_rank": 2,
          "intron_rank_end": null,
          "gene_symbol": "PLP1",
          "gene_hgnc_id": 9086,
          "hgvs_c": "c.5-111T>C",
          "hgvs_p": null,
          "transcript": "ENST00000612423.4",
          "protein_id": "ENSP00000481006.1",
          "transcript_support_level": 2,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 277,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 834,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000612423.4"
        },
        {
          "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": 9,
          "intron_rank": 3,
          "intron_rank_end": null,
          "gene_symbol": "PLP1",
          "gene_hgnc_id": 9086,
          "hgvs_c": "c.5-111T>C",
          "hgvs_p": null,
          "transcript": "ENST00000867699.1",
          "protein_id": "ENSP00000537758.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 277,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 834,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000867699.1"
        },
        {
          "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": 9,
          "intron_rank": 3,
          "intron_rank_end": null,
          "gene_symbol": "PLP1",
          "gene_hgnc_id": 9086,
          "hgvs_c": "c.5-111T>C",
          "hgvs_p": null,
          "transcript": "ENST00000867700.1",
          "protein_id": "ENSP00000537759.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 277,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 834,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000867700.1"
        },
        {
          "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": 9,
          "intron_rank": 3,
          "intron_rank_end": null,
          "gene_symbol": "PLP1",
          "gene_hgnc_id": 9086,
          "hgvs_c": "c.5-111T>C",
          "hgvs_p": null,
          "transcript": "ENST00000867701.1",
          "protein_id": "ENSP00000537760.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 277,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 834,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000867701.1"
        },
        {
          "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": 8,
          "intron_rank": 2,
          "intron_rank_end": null,
          "gene_symbol": "PLP1",
          "gene_hgnc_id": 9086,
          "hgvs_c": "c.5-111T>C",
          "hgvs_p": null,
          "transcript": "ENST00000867702.1",
          "protein_id": "ENSP00000537761.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 277,
          "cds_start": null,
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          "cds_length": 834,
          "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,
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          "canonical": false,
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          "strand": true,
          "consequences": [
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          ],
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          "intron_rank": 3,
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          "gene_symbol": "PLP1",
          "gene_hgnc_id": 9086,
          "hgvs_c": "c.5-111T>C",
          "hgvs_p": null,
          "transcript": "ENST00000867704.1",
          "protein_id": "ENSP00000537763.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 277,
          "cds_start": null,
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          "cds_length": 834,
          "cdna_start": null,
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          "mane_select": null,
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          "biotype": "protein_coding",
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        {
          "aa_ref": null,
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          "canonical": false,
          "protein_coding": true,
          "strand": true,
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          "gene_symbol": "PLP1",
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          "hgvs_c": "c.5-111T>C",
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          "cds_start": null,
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        {
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          "gene_symbol": "PLP1",
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          "hgvs_c": "c.5-120T>C",
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          "cds_start": null,
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        {
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          "intron_rank": 1,
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          "gene_symbol": "PLP1",
          "gene_hgnc_id": 9086,
          "hgvs_c": "c.5-111T>C",
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          "transcript": "ENST00000867710.1",
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        {
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        {
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          "gene_symbol": "PLP1",
          "gene_hgnc_id": 9086,
          "hgvs_c": "c.5-111T>C",
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          "transcript": "NM_199478.3",
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        {
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          "gene_symbol": "PLP1",
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        {
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        {
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          "intron_rank": 2,
          "intron_rank_end": null,
          "gene_symbol": "PLP1",
          "gene_hgnc_id": 9086,
          "hgvs_c": "c.5-111T>C",
          "hgvs_p": null,
          "transcript": "ENST00000867705.1",
          "protein_id": "ENSP00000537764.1",
          "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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          ],
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      "splice_source_selected": "max_spliceai",
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      "spliceai_max_score": 0,
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      "acmg_classification": "Benign",
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      "acmg_by_gene": [
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          "verdict": "Benign",
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          "effects": [
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          "inheritance_mode": "",
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        {
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            "BA1"
          ],
          "verdict": "Benign",
          "transcript": "ENST00000674162.1",
          "gene_symbol": "ENSG00000288597",
          "hgnc_id": null,
          "effects": [
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          "hgvs_c": "n.800+7210A>G",
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      "clinvar_disease": "not provided",
      "clinvar_classification": "Benign",
      "clinvar_review_status": "criteria provided, single submitter",
      "clinvar_submissions_summary": "B:1",
      "phenotype_combined": "not provided",
      "pathogenicity_classification_combined": "Benign",
      "custom_annotations": null
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  ],
  "message": null
}