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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: 2-58163446-CAAGA-C (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=2&pos=58163446&ref=CAAGA&alt=C&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "2",
      "pos": 58163446,
      "ref": "CAAGA",
      "alt": "C",
      "effect": "frameshift_variant",
      "transcript": "ENST00000233741.9",
      "consequences": [
        {
          "aa_ref": "FL",
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 9,
          "exon_rank_end": null,
          "exon_count": 14,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "FANCL",
          "gene_hgnc_id": 20748,
          "hgvs_c": "c.759_762delTCTT",
          "hgvs_p": "p.Phe253fs",
          "transcript": "NM_018062.4",
          "protein_id": "NP_060532.2",
          "transcript_support_level": null,
          "aa_start": 253,
          "aa_end": null,
          "aa_length": 375,
          "cds_start": 759,
          "cds_end": null,
          "cds_length": 1128,
          "cdna_start": 774,
          "cdna_end": null,
          "cdna_length": 1658,
          "mane_select": "ENST00000233741.9",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "FL",
          "aa_alt": null,
          "canonical": true,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 9,
          "exon_rank_end": null,
          "exon_count": 14,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "FANCL",
          "gene_hgnc_id": 20748,
          "hgvs_c": "c.759_762delTCTT",
          "hgvs_p": "p.Phe253fs",
          "transcript": "ENST00000233741.9",
          "protein_id": "ENSP00000233741.5",
          "transcript_support_level": 1,
          "aa_start": 253,
          "aa_end": null,
          "aa_length": 375,
          "cds_start": 759,
          "cds_end": null,
          "cds_length": 1128,
          "cdna_start": 774,
          "cdna_end": null,
          "cdna_length": 1658,
          "mane_select": "NM_018062.4",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "FL",
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 6,
          "exon_rank_end": null,
          "exon_count": 11,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "FANCL",
          "gene_hgnc_id": 20748,
          "hgvs_c": "c.582_585delTCTT",
          "hgvs_p": "p.Phe194fs",
          "transcript": "ENST00000449070.6",
          "protein_id": "ENSP00000401280.2",
          "transcript_support_level": 1,
          "aa_start": 194,
          "aa_end": null,
          "aa_length": 316,
          "cds_start": 582,
          "cds_end": null,
          "cds_length": 951,
          "cdna_start": 644,
          "cdna_end": null,
          "cdna_length": 1526,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "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": 13,
          "intron_rank": 8,
          "intron_rank_end": null,
          "gene_symbol": "FANCL",
          "gene_hgnc_id": 20748,
          "hgvs_c": "c.692-376_692-373delTCTT",
          "hgvs_p": null,
          "transcript": "ENST00000403295.8",
          "protein_id": "ENSP00000386097.3",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 347,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 1044,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 1598,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "FL",
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 10,
          "exon_rank_end": null,
          "exon_count": 14,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "FANCL",
          "gene_hgnc_id": 20748,
          "hgvs_c": "c.804_807delTCTT",
          "hgvs_p": "p.Phe268fs",
          "transcript": "NM_001438889.1",
          "protein_id": "NP_001425818.1",
          "transcript_support_level": null,
          "aa_start": 268,
          "aa_end": null,
          "aa_length": 398,
          "cds_start": 804,
          "cds_end": null,
          "cds_length": 1197,
          "cdna_start": 819,
          "cdna_end": null,
          "cdna_length": 2010,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "FL",
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 10,
          "exon_rank_end": null,
          "exon_count": 15,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "FANCL",
          "gene_hgnc_id": 20748,
          "hgvs_c": "c.819_822delTCTT",
          "hgvs_p": "p.Phe273fs",
          "transcript": "NM_001410792.1",
          "protein_id": "NP_001397721.1",
          "transcript_support_level": null,
          "aa_start": 273,
          "aa_end": null,
          "aa_length": 395,
          "cds_start": 819,
          "cds_end": null,
          "cds_length": 1188,
          "cdna_start": 834,
          "cdna_end": null,
          "cdna_length": 1718,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "FL",
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 10,
          "exon_rank_end": null,
          "exon_count": 15,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "FANCL",
          "gene_hgnc_id": 20748,
          "hgvs_c": "c.819_822delTCTT",
          "hgvs_p": "p.Phe273fs",
          "transcript": "ENST00000696326.1",
          "protein_id": "ENSP00000512562.1",
          "transcript_support_level": null,
          "aa_start": 273,
          "aa_end": null,
          "aa_length": 395,
          "cds_start": 819,
          "cds_end": null,
          "cds_length": 1188,
          "cdna_start": 881,
          "cdna_end": null,
          "cdna_length": 1680,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "FL",
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 10,
          "exon_rank_end": null,
          "exon_count": 15,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "FANCL",
          "gene_hgnc_id": 20748,
          "hgvs_c": "c.804_807delTCTT",
          "hgvs_p": "p.Phe268fs",
          "transcript": "NM_001374615.1",
          "protein_id": "NP_001361544.1",
          "transcript_support_level": null,
          "aa_start": 268,
          "aa_end": null,
          "aa_length": 390,
          "cds_start": 804,
          "cds_end": null,
          "cds_length": 1173,
          "cdna_start": 819,
          "cdna_end": null,
          "cdna_length": 1703,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "FL",
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 10,
          "exon_rank_end": null,
          "exon_count": 15,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "FANCL",
          "gene_hgnc_id": 20748,
          "hgvs_c": "c.804_807delTCTT",
          "hgvs_p": "p.Phe268fs",
          "transcript": "ENST00000427708.7",
          "protein_id": "ENSP00000400969.3",
          "transcript_support_level": 5,
          "aa_start": 268,
          "aa_end": null,
          "aa_length": 390,
          "cds_start": 804,
          "cds_end": null,
          "cds_length": 1173,
          "cdna_start": 819,
          "cdna_end": null,
          "cdna_length": 1707,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "FL",
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 9,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "FANCL",
          "gene_hgnc_id": 20748,
          "hgvs_c": "c.774_777delTCTT",
          "hgvs_p": "p.Phe258fs",
          "transcript": "NM_001438890.1",
          "protein_id": "NP_001425819.1",
          "transcript_support_level": null,
          "aa_start": 258,
          "aa_end": null,
          "aa_length": 388,
          "cds_start": 774,
          "cds_end": null,
          "cds_length": 1167,
          "cdna_start": 789,
          "cdna_end": null,
          "cdna_length": 1980,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "FL",
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 9,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "FANCL",
          "gene_hgnc_id": 20748,
          "hgvs_c": "c.759_762delTCTT",
          "hgvs_p": "p.Phe253fs",
          "transcript": "NM_001438891.1",
          "protein_id": "NP_001425820.1",
          "transcript_support_level": null,
          "aa_start": 253,
          "aa_end": null,
          "aa_length": 383,
          "cds_start": 759,
          "cds_end": null,
          "cds_length": 1152,
          "cdna_start": 774,
          "cdna_end": null,
          "cdna_length": 1965,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "FL",
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 9,
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          "exon_count": 14,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "FANCL",
          "gene_hgnc_id": 20748,
          "hgvs_c": "c.774_777delTCTT",
          "hgvs_p": "p.Phe258fs",
          "transcript": "NM_001114636.2",
          "protein_id": "NP_001108108.1",
          "transcript_support_level": null,
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          "cds_start": 774,
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          "cds_length": 1143,
          "cdna_start": 789,
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          "mane_select": null,
          "mane_plus": null,
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        },
        {
          "aa_ref": "FL",
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          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
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          ],
          "exon_rank": 9,
          "exon_rank_end": null,
          "exon_count": 14,
          "intron_rank": null,
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          "gene_symbol": "FANCL",
          "gene_hgnc_id": 20748,
          "hgvs_c": "c.774_777delTCTT",
          "hgvs_p": "p.Phe258fs",
          "transcript": "ENST00000402135.8",
          "protein_id": "ENSP00000385021.3",
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          "aa_start": 258,
          "aa_end": null,
          "aa_length": 380,
          "cds_start": 774,
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          "cdna_start": 874,
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        },
        {
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          "canonical": false,
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          "strand": false,
          "consequences": [
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          ],
          "exon_rank": 9,
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          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "FANCL",
          "gene_hgnc_id": 20748,
          "hgvs_c": "c.750_753delTCTT",
          "hgvs_p": "p.Phe250fs",
          "transcript": "ENST00000696371.1",
          "protein_id": "ENSP00000512586.1",
          "transcript_support_level": null,
          "aa_start": 250,
          "aa_end": null,
          "aa_length": 372,
          "cds_start": 750,
          "cds_end": null,
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          "cdna_start": 765,
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        },
        {
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          "gene_symbol": "FANCL",
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          "hgvs_c": "c.747_750delTCTT",
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          "transcript": "ENST00000696547.1",
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        },
        {
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          "strand": false,
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          ],
          "exon_rank": 9,
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          "exon_count": 14,
          "intron_rank": null,
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          "gene_symbol": "FANCL",
          "gene_hgnc_id": 20748,
          "hgvs_c": "c.759_762delTCTT",
          "hgvs_p": "p.Phe253fs",
          "transcript": "ENST00000696307.1",
          "protein_id": "ENSP00000512545.1",
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          "aa_start": 253,
          "aa_end": null,
          "aa_length": 370,
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          "cdna_start": 771,
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        },
        {
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          "canonical": false,
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          "consequences": [
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          "intron_rank": null,
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          "gene_symbol": "FANCL",
          "gene_hgnc_id": 20748,
          "hgvs_c": "c.735_738delTCTT",
          "hgvs_p": "p.Phe245fs",
          "transcript": "ENST00000696635.1",
          "protein_id": "ENSP00000512771.1",
          "transcript_support_level": null,
          "aa_start": 245,
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          "cds_start": 735,
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          "cdna_start": 750,
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        },
        {
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          ],
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          "gene_symbol": "FANCL",
          "gene_hgnc_id": 20748,
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        {
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          ],
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          "intron_rank": null,
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          "gene_symbol": "FANCL",
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          "hgvs_c": "c.702_705delTCTT",
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        },
        {
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          "canonical": false,
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          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "FANCL",
          "gene_hgnc_id": 20748,
          "hgvs_c": "c.759_762delTCTT",
          "hgvs_p": "p.Phe253fs",
          "transcript": "ENST00000696567.1",
          "protein_id": "ENSP00000512724.1",
          "transcript_support_level": null,
          "aa_start": 253,
          "aa_end": null,
          "aa_length": 340,
          "cds_start": 759,
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          "cdna_start": 774,
          "cdna_end": null,
          "cdna_length": 1551,
          "mane_select": null,
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          "biotype": null,
          "feature": null
        },
        {
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          "protein_coding": true,
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          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 9,
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          "exon_count": 13,
          "intron_rank": null,
          "intron_rank_end": null,
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      "computational_score_selected": null,
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      "splice_prediction_selected": "Benign",
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      "clinvar_classification": "Pathogenic/Likely pathogenic",
      "clinvar_review_status": "criteria provided, multiple submitters, no conflicts",
      "clinvar_submissions_summary": "P:1 LP:1",
      "phenotype_combined": "Fanconi anemia|Fanconi anemia complementation group L",
      "pathogenicity_classification_combined": "Pathogenic/Likely pathogenic",
      "custom_annotations": null
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  "message": null
}