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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: 5-36608922-T-A (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=5&pos=36608922&ref=T&alt=A&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "5",
      "pos": 36608922,
      "ref": "T",
      "alt": "A",
      "effect": "intron_variant",
      "transcript": "ENST00000265113.9",
      "consequences": [
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "3_prime_UTR_variant"
          ],
          "exon_rank": 2,
          "exon_rank_end": null,
          "exon_count": 2,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SLC1A3",
          "gene_hgnc_id": 10941,
          "hgvs_c": "c.*301T>A",
          "hgvs_p": null,
          "transcript": "ENST00000512374.1",
          "protein_id": "ENSP00000506048.1",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 65,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 198,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 1096,
          "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": 10,
          "intron_rank": 2,
          "intron_rank_end": null,
          "gene_symbol": "SLC1A3",
          "gene_hgnc_id": 10941,
          "hgvs_c": "c.181+318T>A",
          "hgvs_p": null,
          "transcript": "NM_004172.5",
          "protein_id": "NP_004163.3",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 542,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 1629,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 3919,
          "mane_select": "ENST00000265113.9",
          "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": 10,
          "intron_rank": 2,
          "intron_rank_end": null,
          "gene_symbol": "SLC1A3",
          "gene_hgnc_id": 10941,
          "hgvs_c": "c.181+318T>A",
          "hgvs_p": null,
          "transcript": "ENST00000265113.9",
          "protein_id": "ENSP00000265113.4",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 542,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 1629,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 3919,
          "mane_select": "NM_004172.5",
          "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": 10,
          "intron_rank": 2,
          "intron_rank_end": null,
          "gene_symbol": "SLC1A3",
          "gene_hgnc_id": 10941,
          "hgvs_c": "c.181+318T>A",
          "hgvs_p": null,
          "transcript": "ENST00000381918.4",
          "protein_id": "ENSP00000371343.4",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 542,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 1629,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 3834,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "3_prime_UTR_variant"
          ],
          "exon_rank": 2,
          "exon_rank_end": null,
          "exon_count": 2,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SLC1A3",
          "gene_hgnc_id": 10941,
          "hgvs_c": "c.*301T>A",
          "hgvs_p": null,
          "transcript": "NM_001166696.3",
          "protein_id": "NP_001160168.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 65,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 198,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 1101,
          "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": 11,
          "intron_rank": 2,
          "intron_rank_end": null,
          "gene_symbol": "SLC1A3",
          "gene_hgnc_id": 10941,
          "hgvs_c": "c.181+318T>A",
          "hgvs_p": null,
          "transcript": "NM_001438458.1",
          "protein_id": "NP_001425387.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 589,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 1770,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 4060,
          "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": 11,
          "intron_rank": 2,
          "intron_rank_end": null,
          "gene_symbol": "SLC1A3",
          "gene_hgnc_id": 10941,
          "hgvs_c": "c.181+318T>A",
          "hgvs_p": null,
          "transcript": "ENST00000680232.1",
          "protein_id": "ENSP00000506207.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 589,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 1770,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 4194,
          "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": 11,
          "intron_rank": 3,
          "intron_rank_end": null,
          "gene_symbol": "SLC1A3",
          "gene_hgnc_id": 10941,
          "hgvs_c": "c.181+318T>A",
          "hgvs_p": null,
          "transcript": "NM_001438454.1",
          "protein_id": "NP_001425383.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 542,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 1629,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 4007,
          "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": 10,
          "intron_rank": 2,
          "intron_rank_end": null,
          "gene_symbol": "SLC1A3",
          "gene_hgnc_id": 10941,
          "hgvs_c": "c.181+318T>A",
          "hgvs_p": null,
          "transcript": "NM_001438455.1",
          "protein_id": "NP_001425384.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 542,
          "cds_start": -4,
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          "cds_length": 1629,
          "cdna_start": null,
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          "cdna_length": 3880,
          "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": 11,
          "intron_rank": 3,
          "intron_rank_end": null,
          "gene_symbol": "SLC1A3",
          "gene_hgnc_id": 10941,
          "hgvs_c": "c.181+318T>A",
          "hgvs_p": null,
          "transcript": "NM_001438456.1",
          "protein_id": "NP_001425385.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 542,
          "cds_start": -4,
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          "cds_length": 1629,
          "cdna_start": null,
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          "cdna_length": 4058,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
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          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
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          "exon_count": 10,
          "intron_rank": 2,
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          "gene_symbol": "SLC1A3",
          "gene_hgnc_id": 10941,
          "hgvs_c": "c.181+318T>A",
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          "transcript": "NM_001438457.1",
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          "transcript_support_level": null,
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          "aa_length": 542,
          "cds_start": -4,
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          "cdna_start": null,
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          "mane_select": null,
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          "biotype": null,
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        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
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          "strand": true,
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          "exon_count": 10,
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          "intron_rank_end": null,
          "gene_symbol": "SLC1A3",
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          "hgvs_c": "c.181+318T>A",
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        {
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          "gene_symbol": "SLC1A3",
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          "gene_symbol": "SLC1A3",
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        {
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          "hgvs_c": "c.181+318T>A",
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          "gene_symbol": "SLC1A3",
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        {
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        },
        {
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          ],
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          "intron_rank": 2,
          "intron_rank_end": null,
          "gene_symbol": "SLC1A3",
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          "transcript": "ENST00000681909.1",
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      "gnomad_genomes_homalt": null,
      "gnomad_mito_homoplasmic": null,
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      "computational_score_selected": -0.7300000190734863,
      "computational_prediction_selected": "Benign",
      "computational_source_selected": "BayesDel_noAF",
      "splice_score_selected": 0,
      "splice_prediction_selected": "Benign",
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      "bayesdelnoaf_score": -0.73,
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      "phylop100way_prediction": "Benign",
      "spliceai_max_score": 0,
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      "acmg_score": -2,
      "acmg_classification": "Likely_benign",
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      "acmg_by_gene": [
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          "benign_score": 4,
          "pathogenic_score": 2,
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          "verdict": "Likely_benign",
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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
}