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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: 1-35442850-T-C (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=1&pos=35442850&ref=T&alt=C&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "1",
      "pos": 35442850,
      "ref": "T",
      "alt": "C",
      "effect": "intron_variant",
      "transcript": "NM_024874.5",
      "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": 21,
          "intron_rank": 18,
          "intron_rank_end": null,
          "gene_symbol": "KIAA0319L",
          "gene_hgnc_id": 30071,
          "hgvs_c": "c.2779+56A>G",
          "hgvs_p": null,
          "transcript": "NM_024874.5",
          "protein_id": "NP_079150.3",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1049,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 3150,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 4777,
          "mane_select": "ENST00000325722.8",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_024874.5"
        },
        {
          "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": 21,
          "intron_rank": 18,
          "intron_rank_end": null,
          "gene_symbol": "KIAA0319L",
          "gene_hgnc_id": 30071,
          "hgvs_c": "c.2779+56A>G",
          "hgvs_p": null,
          "transcript": "ENST00000325722.8",
          "protein_id": "ENSP00000318406.3",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1049,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 3150,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 4777,
          "mane_select": "NM_024874.5",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000325722.8"
        },
        {
          "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": 22,
          "intron_rank": 19,
          "intron_rank_end": null,
          "gene_symbol": "KIAA0319L",
          "gene_hgnc_id": 30071,
          "hgvs_c": "c.2953+56A>G",
          "hgvs_p": null,
          "transcript": "ENST00000930788.1",
          "protein_id": "ENSP00000600847.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1107,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 3324,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 4934,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000930788.1"
        },
        {
          "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": 22,
          "intron_rank": 19,
          "intron_rank_end": null,
          "gene_symbol": "KIAA0319L",
          "gene_hgnc_id": 30071,
          "hgvs_c": "c.2908+56A>G",
          "hgvs_p": null,
          "transcript": "ENST00000961875.1",
          "protein_id": "ENSP00000631934.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1092,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 3279,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 4277,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000961875.1"
        },
        {
          "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": 22,
          "intron_rank": 19,
          "intron_rank_end": null,
          "gene_symbol": "KIAA0319L",
          "gene_hgnc_id": 30071,
          "hgvs_c": "c.2875+56A>G",
          "hgvs_p": null,
          "transcript": "ENST00000961872.1",
          "protein_id": "ENSP00000631931.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1081,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 3246,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 4271,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000961872.1"
        },
        {
          "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": 21,
          "intron_rank": 18,
          "intron_rank_end": null,
          "gene_symbol": "KIAA0319L",
          "gene_hgnc_id": 30071,
          "hgvs_c": "c.2827+56A>G",
          "hgvs_p": null,
          "transcript": "ENST00000961876.1",
          "protein_id": "ENSP00000631935.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1065,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 3198,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 4061,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000961876.1"
        },
        {
          "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": 21,
          "intron_rank": 18,
          "intron_rank_end": null,
          "gene_symbol": "KIAA0319L",
          "gene_hgnc_id": 30071,
          "hgvs_c": "c.2812+56A>G",
          "hgvs_p": null,
          "transcript": "ENST00000930786.1",
          "protein_id": "ENSP00000600845.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1060,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 3183,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 4810,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000930786.1"
        },
        {
          "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": 22,
          "intron_rank": 19,
          "intron_rank_end": null,
          "gene_symbol": "KIAA0319L",
          "gene_hgnc_id": 30071,
          "hgvs_c": "c.2812+56A>G",
          "hgvs_p": null,
          "transcript": "ENST00000961869.1",
          "protein_id": "ENSP00000631928.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1060,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 3183,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 4800,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000961869.1"
        },
        {
          "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": 21,
          "intron_rank": 18,
          "intron_rank_end": null,
          "gene_symbol": "KIAA0319L",
          "gene_hgnc_id": 30071,
          "hgvs_c": "c.2800+56A>G",
          "hgvs_p": null,
          "transcript": "ENST00000930787.1",
          "protein_id": "ENSP00000600846.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1056,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 3171,
          "cdna_start": null,
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          "cdna_length": 4795,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000930787.1"
        },
        {
          "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": 21,
          "intron_rank": 18,
          "intron_rank_end": null,
          "gene_symbol": "KIAA0319L",
          "gene_hgnc_id": 30071,
          "hgvs_c": "c.2794+56A>G",
          "hgvs_p": null,
          "transcript": "ENST00000867828.1",
          "protein_id": "ENSP00000537887.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1054,
          "cds_start": null,
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          "cdna_start": null,
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          "cdna_length": 4781,
          "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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          "exon_count": 21,
          "intron_rank": 18,
          "intron_rank_end": null,
          "gene_symbol": "KIAA0319L",
          "gene_hgnc_id": 30071,
          "hgvs_c": "c.2794+56A>G",
          "hgvs_p": null,
          "transcript": "ENST00000930783.1",
          "protein_id": "ENSP00000600842.1",
          "transcript_support_level": null,
          "aa_start": null,
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          "aa_length": 1054,
          "cds_start": null,
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          "cdna_start": null,
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          "mane_select": null,
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          "biotype": "protein_coding",
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        {
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          "canonical": false,
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          "strand": false,
          "consequences": [
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          "intron_rank": 18,
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          "protein_id": "ENSP00000631932.1",
          "transcript_support_level": null,
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        {
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        {
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          "exon_count": 21,
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          "gene_symbol": "KIAA0319L",
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          "hgvs_c": "c.2779+56A>G",
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          "transcript": "ENST00000469892.7",
          "protein_id": "ENSP00000419396.2",
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        {
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          "gene_symbol": "KIAA0319L",
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          "transcript": "ENST00000867827.1",
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        {
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          "gene_symbol": "KIAA0319L",
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          "transcript": "ENST00000867829.1",
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          "gene_symbol": "KIAA0319L",
          "gene_hgnc_id": 30071,
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          "transcript": "ENST00000930792.1",
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      "phylop100way_score": -0.514,
      "phylop100way_prediction": "Benign",
      "spliceai_max_score": 0,
      "spliceai_max_prediction": "Benign",
      "dbscsnv_ada_score": null,
      "dbscsnv_ada_prediction": null,
      "apogee2_score": null,
      "apogee2_prediction": null,
      "mitotip_score": null,
      "mitotip_prediction": null,
      "acmg_score": -12,
      "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": "NM_024874.5",
          "gene_symbol": "KIAA0319L",
          "hgnc_id": 30071,
          "effects": [
            "intron_variant"
          ],
          "inheritance_mode": "Unknown",
          "hgvs_c": "c.2779+56A>G",
          "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
}
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