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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: 11-9033742-C-T (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=11&pos=9033742&ref=C&alt=T&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "11",
      "pos": 9033742,
      "ref": "C",
      "alt": "T",
      "effect": "missense_variant",
      "transcript": "ENST00000649792.2",
      "consequences": [
        {
          "aa_ref": "C",
          "aa_alt": "Y",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 17,
          "exon_rank_end": null,
          "exon_count": 23,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SCUBE2",
          "gene_hgnc_id": 30425,
          "hgvs_c": "c.2057G>A",
          "hgvs_p": "p.Cys686Tyr",
          "transcript": "NM_001367977.2",
          "protein_id": "NP_001354906.1",
          "transcript_support_level": null,
          "aa_start": 686,
          "aa_end": null,
          "aa_length": 1028,
          "cds_start": 2057,
          "cds_end": null,
          "cds_length": 3087,
          "cdna_start": 2128,
          "cdna_end": null,
          "cdna_length": 4727,
          "mane_select": "ENST00000649792.2",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "C",
          "aa_alt": "Y",
          "canonical": true,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 17,
          "exon_rank_end": null,
          "exon_count": 23,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SCUBE2",
          "gene_hgnc_id": 30425,
          "hgvs_c": "c.2057G>A",
          "hgvs_p": "p.Cys686Tyr",
          "transcript": "ENST00000649792.2",
          "protein_id": "ENSP00000497523.1",
          "transcript_support_level": null,
          "aa_start": 686,
          "aa_end": null,
          "aa_length": 1028,
          "cds_start": 2057,
          "cds_end": null,
          "cds_length": 3087,
          "cdna_start": 2128,
          "cdna_end": null,
          "cdna_length": 4727,
          "mane_select": "NM_001367977.2",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "C",
          "aa_alt": "Y",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 13,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SCUBE2",
          "gene_hgnc_id": 30425,
          "hgvs_c": "c.1592G>A",
          "hgvs_p": "p.Cys531Tyr",
          "transcript": "ENST00000450649.6",
          "protein_id": "ENSP00000415187.2",
          "transcript_support_level": 1,
          "aa_start": 531,
          "aa_end": null,
          "aa_length": 807,
          "cds_start": 1592,
          "cds_end": null,
          "cds_length": 2424,
          "cdna_start": 1610,
          "cdna_end": null,
          "cdna_length": 2912,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "C",
          "aa_alt": "Y",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 16,
          "exon_rank_end": null,
          "exon_count": 22,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SCUBE2",
          "gene_hgnc_id": 30425,
          "hgvs_c": "c.1970G>A",
          "hgvs_p": "p.Cys657Tyr",
          "transcript": "NM_001330199.3",
          "protein_id": "NP_001317128.1",
          "transcript_support_level": null,
          "aa_start": 657,
          "aa_end": null,
          "aa_length": 999,
          "cds_start": 1970,
          "cds_end": null,
          "cds_length": 3000,
          "cdna_start": 2041,
          "cdna_end": null,
          "cdna_length": 4640,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "C",
          "aa_alt": "Y",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 16,
          "exon_rank_end": null,
          "exon_count": 22,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SCUBE2",
          "gene_hgnc_id": 30425,
          "hgvs_c": "c.1970G>A",
          "hgvs_p": "p.Cys657Tyr",
          "transcript": "ENST00000309263.7",
          "protein_id": "ENSP00000310658.3",
          "transcript_support_level": 5,
          "aa_start": 657,
          "aa_end": null,
          "aa_length": 999,
          "cds_start": 1970,
          "cds_end": null,
          "cds_length": 3000,
          "cdna_start": 2043,
          "cdna_end": null,
          "cdna_length": 3727,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "C",
          "aa_alt": "Y",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 13,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SCUBE2",
          "gene_hgnc_id": 30425,
          "hgvs_c": "c.1592G>A",
          "hgvs_p": "p.Cys531Tyr",
          "transcript": "NM_001170690.3",
          "protein_id": "NP_001164161.1",
          "transcript_support_level": null,
          "aa_start": 531,
          "aa_end": null,
          "aa_length": 807,
          "cds_start": 1592,
          "cds_end": null,
          "cds_length": 2424,
          "cdna_start": 1663,
          "cdna_end": null,
          "cdna_length": 4064,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "C",
          "aa_alt": "Y",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 16,
          "exon_rank_end": null,
          "exon_count": 22,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SCUBE2",
          "gene_hgnc_id": 30425,
          "hgvs_c": "c.1934G>A",
          "hgvs_p": "p.Cys645Tyr",
          "transcript": "XM_005253034.5",
          "protein_id": "XP_005253091.2",
          "transcript_support_level": null,
          "aa_start": 645,
          "aa_end": null,
          "aa_length": 987,
          "cds_start": 1934,
          "cds_end": null,
          "cds_length": 2964,
          "cdna_start": 2005,
          "cdna_end": null,
          "cdna_length": 4604,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "C",
          "aa_alt": "Y",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 17,
          "exon_rank_end": null,
          "exon_count": 22,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SCUBE2",
          "gene_hgnc_id": 30425,
          "hgvs_c": "c.2057G>A",
          "hgvs_p": "p.Cys686Tyr",
          "transcript": "XM_011520246.3",
          "protein_id": "XP_011518548.1",
          "transcript_support_level": null,
          "aa_start": 686,
          "aa_end": null,
          "aa_length": 962,
          "cds_start": 2057,
          "cds_end": null,
          "cds_length": 2889,
          "cdna_start": 2128,
          "cdna_end": null,
          "cdna_length": 4529,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "C",
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          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 15,
          "exon_rank_end": null,
          "exon_count": 21,
          "intron_rank": null,
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          "gene_symbol": "SCUBE2",
          "gene_hgnc_id": 30425,
          "hgvs_c": "c.1853G>A",
          "hgvs_p": "p.Cys618Tyr",
          "transcript": "XM_011520247.3",
          "protein_id": "XP_011518549.1",
          "transcript_support_level": null,
          "aa_start": 618,
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          "aa_length": 960,
          "cds_start": 1853,
          "cds_end": null,
          "cds_length": 2883,
          "cdna_start": 1924,
          "cdna_end": null,
          "cdna_length": 4523,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
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        },
        {
          "aa_ref": "C",
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          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 15,
          "exon_rank_end": null,
          "exon_count": 21,
          "intron_rank": null,
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          "gene_symbol": "SCUBE2",
          "gene_hgnc_id": 30425,
          "hgvs_c": "c.1847G>A",
          "hgvs_p": "p.Cys616Tyr",
          "transcript": "XM_017018080.2",
          "protein_id": "XP_016873569.1",
          "transcript_support_level": null,
          "aa_start": 616,
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          "aa_length": 958,
          "cds_start": 1847,
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        {
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          "consequences": [
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          "gene_symbol": "SCUBE2",
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          "hgvs_c": "c.2057G>A",
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        {
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          "intron_rank": null,
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          "gene_symbol": "SCUBE2",
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        {
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        {
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          "gene_symbol": "SCUBE2",
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          "hgvs_c": "c.1934G>A",
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          "transcript": "XM_047427356.1",
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        {
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        {
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          "gene_symbol": "SCUBE2",
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        {
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          "gene_symbol": "SCUBE2",
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          "hgvs_c": "c.1853G>A",
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          "transcript": "XM_047427363.1",
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        {
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          ],
          "verdict": "Likely_pathogenic",
          "transcript": "ENST00000649792.2",
          "gene_symbol": "SCUBE2",
          "hgnc_id": 30425,
          "effects": [
            "missense_variant"
          ],
          "inheritance_mode": "AR",
          "hgvs_c": "c.2057G>A",
          "hgvs_p": "p.Cys686Tyr"
        },
        {
          "score": 8,
          "benign_score": 0,
          "pathogenic_score": 8,
          "criteria": [
            "PM2",
            "PP3_Strong",
            "PP5_Moderate"
          ],
          "verdict": "Likely_pathogenic",
          "transcript": "ENST00000531592.1",
          "gene_symbol": "NRIP3-DT",
          "hgnc_id": 55524,
          "effects": [
            "intron_variant"
          ],
          "inheritance_mode": "",
          "hgvs_c": "n.514+3404C>T",
          "hgvs_p": null
        }
      ],
      "clinvar_disease": "Cerebral arteriovenous malformation",
      "clinvar_classification": "Likely pathogenic",
      "clinvar_review_status": "criteria provided, single submitter",
      "clinvar_submissions_summary": "LP:1",
      "phenotype_combined": "Cerebral arteriovenous malformation",
      "pathogenicity_classification_combined": "Likely pathogenic",
      "custom_annotations": null
    }
  ],
  "message": null
}