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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: 9-89338609-G-A (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=9&pos=89338609&ref=G&alt=A&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "9",
      "pos": 89338609,
      "ref": "G",
      "alt": "A",
      "effect": "intron_variant",
      "transcript": "NM_024077.5",
      "consequences": [
        {
          "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": 17,
          "intron_rank": 8,
          "intron_rank_end": null,
          "gene_symbol": "SECISBP2",
          "gene_hgnc_id": 30972,
          "hgvs_c": "c.1212+29G>A",
          "hgvs_p": null,
          "transcript": "NM_024077.5",
          "protein_id": "NP_076982.3",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 854,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 2565,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": "ENST00000375807.8",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_024077.5"
        },
        {
          "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": 17,
          "intron_rank": 8,
          "intron_rank_end": null,
          "gene_symbol": "SECISBP2",
          "gene_hgnc_id": 30972,
          "hgvs_c": "c.1212+29G>A",
          "hgvs_p": null,
          "transcript": "ENST00000375807.8",
          "protein_id": "ENSP00000364965.3",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 854,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 2565,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": "NM_024077.5",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000375807.8"
        },
        {
          "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": 17,
          "intron_rank": 8,
          "intron_rank_end": null,
          "gene_symbol": "SECISBP2",
          "gene_hgnc_id": 30972,
          "hgvs_c": "c.993+29G>A",
          "hgvs_p": null,
          "transcript": "ENST00000339901.8",
          "protein_id": "ENSP00000364959.3",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 781,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 2346,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000339901.8"
        },
        {
          "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": 18,
          "intron_rank": 8,
          "intron_rank_end": null,
          "gene_symbol": "SECISBP2",
          "gene_hgnc_id": 30972,
          "hgvs_c": "c.1212+29G>A",
          "hgvs_p": null,
          "transcript": "ENST00000960321.1",
          "protein_id": "ENSP00000630380.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 854,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 2565,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000960321.1"
        },
        {
          "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": 17,
          "intron_rank": 8,
          "intron_rank_end": null,
          "gene_symbol": "SECISBP2",
          "gene_hgnc_id": 30972,
          "hgvs_c": "c.1209+29G>A",
          "hgvs_p": null,
          "transcript": "NM_001282688.2",
          "protein_id": "NP_001269617.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 853,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 2562,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001282688.2"
        },
        {
          "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": 17,
          "intron_rank": 8,
          "intron_rank_end": null,
          "gene_symbol": "SECISBP2",
          "gene_hgnc_id": 30972,
          "hgvs_c": "c.1209+29G>A",
          "hgvs_p": null,
          "transcript": "ENST00000936002.1",
          "protein_id": "ENSP00000606061.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 853,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 2562,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000936002.1"
        },
        {
          "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": 17,
          "intron_rank": 8,
          "intron_rank_end": null,
          "gene_symbol": "SECISBP2",
          "gene_hgnc_id": 30972,
          "hgvs_c": "c.1212+29G>A",
          "hgvs_p": null,
          "transcript": "ENST00000858961.1",
          "protein_id": "ENSP00000529020.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 852,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 2559,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000858961.1"
        },
        {
          "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": 16,
          "intron_rank": 8,
          "intron_rank_end": null,
          "gene_symbol": "SECISBP2",
          "gene_hgnc_id": 30972,
          "hgvs_c": "c.1212+29G>A",
          "hgvs_p": null,
          "transcript": "ENST00000858959.1",
          "protein_id": "ENSP00000529018.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 824,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 2475,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000858959.1"
        },
        {
          "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": 17,
          "intron_rank": 8,
          "intron_rank_end": null,
          "gene_symbol": "SECISBP2",
          "gene_hgnc_id": 30972,
          "hgvs_c": "c.1098+29G>A",
          "hgvs_p": null,
          "transcript": "NM_001354697.2",
          "protein_id": "NP_001341626.1",
          "transcript_support_level": null,
          "aa_start": null,
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          "aa_length": 816,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 2451,
          "cdna_start": null,
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          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001354697.2"
        },
        {
          "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": 17,
          "intron_rank": 8,
          "intron_rank_end": null,
          "gene_symbol": "SECISBP2",
          "gene_hgnc_id": 30972,
          "hgvs_c": "c.1095+29G>A",
          "hgvs_p": null,
          "transcript": "NM_001354696.2",
          "protein_id": "NP_001341625.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 815,
          "cds_start": null,
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          "cdna_start": null,
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          "biotype": "protein_coding",
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        {
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          "canonical": false,
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          "intron_rank": 8,
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          "gene_symbol": "SECISBP2",
          "gene_hgnc_id": 30972,
          "hgvs_c": "c.1095+29G>A",
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          "transcript": "ENST00000858958.1",
          "protein_id": "ENSP00000529017.1",
          "transcript_support_level": null,
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          "aa_length": 815,
          "cds_start": null,
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          "cdna_start": null,
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          "mane_select": null,
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        {
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        {
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        {
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          "gene_symbol": "SECISBP2",
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        {
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          "gene_symbol": "SECISBP2",
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          "intron_rank_end": null,
          "gene_symbol": "SECISBP2",
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          "hgvs_c": "c.993+29G>A",
          "hgvs_p": null,
          "transcript": "NM_001282689.2",
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      "gnomad_exomes_af": 6.87624e-7,
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      "computational_score_selected": -0.8700000047683716,
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      "computational_source_selected": "BayesDel_noAF",
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      "phylop100way_prediction": "Benign",
      "spliceai_max_score": 0.84,
      "spliceai_max_prediction": "Pathogenic",
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      "acmg_score": 5,
      "acmg_classification": "Uncertain_significance",
      "acmg_criteria": "PM2,PP3_Moderate,PP5",
      "acmg_by_gene": [
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          "verdict": "Uncertain_significance",
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      "clinvar_disease": " abnormal 1,Thyroid hormone metabolism",
      "clinvar_classification": "Pathogenic",
      "clinvar_review_status": "no assertion criteria provided",
      "clinvar_submissions_summary": "null",
      "phenotype_combined": "Thyroid hormone metabolism, abnormal 1",
      "pathogenicity_classification_combined": "Pathogenic",
      "custom_annotations": null
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  ],
  "message": null
}