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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: 10-32930080-T-G (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=10&pos=32930080&ref=T&alt=G&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "10",
      "pos": 32930080,
      "ref": "T",
      "alt": "G",
      "effect": "intron_variant",
      "transcript": "NM_033668.2",
      "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": 16,
          "intron_rank": 3,
          "intron_rank_end": null,
          "gene_symbol": "ITGB1",
          "gene_hgnc_id": 6153,
          "hgvs_c": "c.154-36A>C",
          "hgvs_p": null,
          "transcript": "NM_002211.4",
          "protein_id": "NP_002202.2",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 798,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 2397,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": "ENST00000302278.8",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_002211.4"
        },
        {
          "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": 16,
          "intron_rank": 3,
          "intron_rank_end": null,
          "gene_symbol": "ITGB1",
          "gene_hgnc_id": 6153,
          "hgvs_c": "c.154-36A>C",
          "hgvs_p": null,
          "transcript": "ENST00000302278.8",
          "protein_id": "ENSP00000303351.3",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 798,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 2397,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": "NM_002211.4",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000302278.8"
        },
        {
          "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": 16,
          "intron_rank": 3,
          "intron_rank_end": null,
          "gene_symbol": "ITGB1",
          "gene_hgnc_id": 6153,
          "hgvs_c": "c.-18-36A>C",
          "hgvs_p": null,
          "transcript": "ENST00000488427.2",
          "protein_id": "ENSP00000417508.2",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 741,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 2226,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000488427.2"
        },
        {
          "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": "ITGB1",
          "gene_hgnc_id": 6153,
          "hgvs_c": "c.154-36A>C",
          "hgvs_p": null,
          "transcript": "ENST00000966597.1",
          "protein_id": "ENSP00000636656.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 877,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 2634,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000966597.1"
        },
        {
          "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": "ITGB1",
          "gene_hgnc_id": 6153,
          "hgvs_c": "c.154-36A>C",
          "hgvs_p": null,
          "transcript": "ENST00000677310.2",
          "protein_id": "ENSP00000504508.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 825,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 2478,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000677310.2"
        },
        {
          "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": "ITGB1",
          "gene_hgnc_id": 6153,
          "hgvs_c": "c.154-36A>C",
          "hgvs_p": null,
          "transcript": "ENST00000678766.1",
          "protein_id": "ENSP00000503538.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 825,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 2478,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000678766.1"
        },
        {
          "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": "ITGB1",
          "gene_hgnc_id": 6153,
          "hgvs_c": "c.154-36A>C",
          "hgvs_p": null,
          "transcript": "ENST00000676659.1",
          "protein_id": "ENSP00000502979.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 819,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 2460,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000676659.1"
        },
        {
          "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": "ITGB1",
          "gene_hgnc_id": 6153,
          "hgvs_c": "c.178-36A>C",
          "hgvs_p": null,
          "transcript": "ENST00000474568.6",
          "protein_id": "ENSP00000420282.2",
          "transcript_support_level": 5,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 809,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 2430,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000474568.6"
        },
        {
          "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": "ITGB1",
          "gene_hgnc_id": 6153,
          "hgvs_c": "c.178-36A>C",
          "hgvs_p": null,
          "transcript": "ENST00000677363.1",
          "protein_id": "ENSP00000504791.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 809,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 2430,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000677363.1"
        },
        {
          "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": "ITGB1",
          "gene_hgnc_id": 6153,
          "hgvs_c": "c.154-36A>C",
          "hgvs_p": null,
          "transcript": "ENST00000898627.1",
          "protein_id": "ENSP00000568686.1",
          "transcript_support_level": null,
          "aa_start": null,
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          "aa_length": 809,
          "cds_start": null,
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          "cds_length": 2430,
          "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": false,
          "consequences": [
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          ],
          "exon_rank": null,
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          "intron_rank": 3,
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          "gene_symbol": "ITGB1",
          "gene_hgnc_id": 6153,
          "hgvs_c": "c.154-36A>C",
          "hgvs_p": null,
          "transcript": "ENST00000966589.1",
          "protein_id": "ENSP00000636648.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 808,
          "cds_start": null,
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          "cds_length": 2427,
          "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,
          "protein_coding": true,
          "strand": false,
          "consequences": [
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          "intron_rank": 3,
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          "gene_symbol": "ITGB1",
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          "cds_start": null,
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        {
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          "gene_symbol": "ITGB1",
          "gene_hgnc_id": 6153,
          "hgvs_c": "c.154-36A>C",
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          "transcript": "NM_033668.2",
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          "cds_start": null,
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        {
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          "intron_rank": 3,
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          "gene_symbol": "ITGB1",
          "gene_hgnc_id": 6153,
          "hgvs_c": "c.154-36A>C",
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          "transcript": "ENST00000423113.6",
          "protein_id": "ENSP00000388694.1",
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          "cds_start": null,
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        },
        {
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        {
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          "exon_count": 16,
          "intron_rank": 3,
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          "gene_symbol": "ITGB1",
          "gene_hgnc_id": 6153,
          "hgvs_c": "c.154-36A>C",
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          "protein_id": "NP_596867.1",
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        {
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          "gene_symbol": "ITGB1",
          "gene_hgnc_id": 6153,
          "hgvs_c": "c.154-36A>C",
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          "transcript": "ENST00000396033.6",
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        {
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          "gene_symbol": "ITGB1",
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        {
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          "consequences": [
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          "intron_rank": 4,
          "intron_rank_end": null,
          "gene_symbol": "ITGB1",
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          "hgvs_c": "c.154-36A>C",
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          "transcript": "ENST00000677999.1",
          "protein_id": "ENSP00000503546.1",
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          "cdna_start": null,
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          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
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        },
        {
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          ],
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      "dbsnp": "rs2256455",
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      "computational_score_selected": -0.8299999833106995,
      "computational_prediction_selected": "Benign",
      "computational_source_selected": "BayesDel_noAF",
      "splice_score_selected": 0.009999999776482582,
      "splice_prediction_selected": "Benign",
      "splice_source_selected": "max_spliceai",
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      "alphamissense_score": null,
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      "bayesdelnoaf_score": -0.83,
      "bayesdelnoaf_prediction": "Benign",
      "phylop100way_score": -0.278,
      "phylop100way_prediction": "Benign",
      "spliceai_max_score": 0.01,
      "spliceai_max_prediction": "Benign",
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      "acmg_score": -12,
      "acmg_classification": "Benign",
      "acmg_criteria": "BP4_Strong,BA1",
      "acmg_by_gene": [
        {
          "score": -12,
          "benign_score": 12,
          "pathogenic_score": 0,
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          "verdict": "Benign",
          "transcript": "NM_033668.2",
          "gene_symbol": "ITGB1",
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          "effects": [
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          "inheritance_mode": "AD",
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      ],
      "clinvar_disease": "",
      "clinvar_classification": "",
      "clinvar_review_status": "",
      "clinvar_submissions_summary": "",
      "phenotype_combined": null,
      "pathogenicity_classification_combined": null,
      "custom_annotations": null
    }
  ],
  "message": null
}