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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: 19-11575171-T-TG (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=19&pos=11575171&ref=T&alt=TG&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "19",
      "pos": 11575171,
      "ref": "T",
      "alt": "TG",
      "effect": "frameshift_variant",
      "transcript": "ENST00000648477.1",
      "consequences": [
        {
          "aa_ref": "R",
          "aa_alt": "R?",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 5,
          "exon_rank_end": null,
          "exon_count": 5,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ACP5",
          "gene_hgnc_id": 124,
          "hgvs_c": "c.816dupC",
          "hgvs_p": "p.Lys273fs",
          "transcript": "NM_001611.5",
          "protein_id": "NP_001602.1",
          "transcript_support_level": null,
          "aa_start": 272,
          "aa_end": null,
          "aa_length": 325,
          "cds_start": 816,
          "cds_end": null,
          "cds_length": 978,
          "cdna_start": 869,
          "cdna_end": null,
          "cdna_length": 1381,
          "mane_select": "ENST00000648477.1",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "R?",
          "canonical": true,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 5,
          "exon_rank_end": null,
          "exon_count": 5,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ACP5",
          "gene_hgnc_id": 124,
          "hgvs_c": "c.816dupC",
          "hgvs_p": "p.Lys273fs",
          "transcript": "ENST00000648477.1",
          "protein_id": "ENSP00000496973.1",
          "transcript_support_level": null,
          "aa_start": 272,
          "aa_end": null,
          "aa_length": 325,
          "cds_start": 816,
          "cds_end": null,
          "cds_length": 978,
          "cdna_start": 869,
          "cdna_end": null,
          "cdna_length": 1381,
          "mane_select": "NM_001611.5",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "R?",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 7,
          "exon_rank_end": null,
          "exon_count": 7,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ACP5",
          "gene_hgnc_id": 124,
          "hgvs_c": "c.816dupC",
          "hgvs_p": "p.Lys273fs",
          "transcript": "ENST00000218758.10",
          "protein_id": "ENSP00000218758.4",
          "transcript_support_level": 1,
          "aa_start": 272,
          "aa_end": null,
          "aa_length": 325,
          "cds_start": 816,
          "cds_end": null,
          "cds_length": 978,
          "cdna_start": 1240,
          "cdna_end": null,
          "cdna_length": 1752,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "R?",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 6,
          "exon_rank_end": null,
          "exon_count": 6,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ACP5",
          "gene_hgnc_id": 124,
          "hgvs_c": "c.816dupC",
          "hgvs_p": "p.Lys273fs",
          "transcript": "NM_001111034.3",
          "protein_id": "NP_001104504.1",
          "transcript_support_level": null,
          "aa_start": 272,
          "aa_end": null,
          "aa_length": 325,
          "cds_start": 816,
          "cds_end": null,
          "cds_length": 978,
          "cdna_start": 1059,
          "cdna_end": null,
          "cdna_length": 1571,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "R?",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 7,
          "exon_rank_end": null,
          "exon_count": 7,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ACP5",
          "gene_hgnc_id": 124,
          "hgvs_c": "c.816dupC",
          "hgvs_p": "p.Lys273fs",
          "transcript": "NM_001111035.3",
          "protein_id": "NP_001104505.1",
          "transcript_support_level": null,
          "aa_start": 272,
          "aa_end": null,
          "aa_length": 325,
          "cds_start": 816,
          "cds_end": null,
          "cds_length": 978,
          "cdna_start": 1108,
          "cdna_end": null,
          "cdna_length": 1620,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "R?",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 6,
          "exon_rank_end": null,
          "exon_count": 6,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ACP5",
          "gene_hgnc_id": 124,
          "hgvs_c": "c.816dupC",
          "hgvs_p": "p.Lys273fs",
          "transcript": "NM_001111036.3",
          "protein_id": "NP_001104506.1",
          "transcript_support_level": null,
          "aa_start": 272,
          "aa_end": null,
          "aa_length": 325,
          "cds_start": 816,
          "cds_end": null,
          "cds_length": 978,
          "cdna_start": 1035,
          "cdna_end": null,
          "cdna_length": 1547,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "R?",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 6,
          "exon_rank_end": null,
          "exon_count": 6,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ACP5",
          "gene_hgnc_id": 124,
          "hgvs_c": "c.816dupC",
          "hgvs_p": "p.Lys273fs",
          "transcript": "NM_001322023.2",
          "protein_id": "NP_001308952.1",
          "transcript_support_level": null,
          "aa_start": 272,
          "aa_end": null,
          "aa_length": 325,
          "cds_start": 816,
          "cds_end": null,
          "cds_length": 978,
          "cdna_start": 1137,
          "cdna_end": null,
          "cdna_length": 1649,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "R?",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 7,
          "exon_rank_end": null,
          "exon_count": 7,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ACP5",
          "gene_hgnc_id": 124,
          "hgvs_c": "c.816dupC",
          "hgvs_p": "p.Lys273fs",
          "transcript": "NM_001439233.1",
          "protein_id": "NP_001426162.1",
          "transcript_support_level": null,
          "aa_start": 272,
          "aa_end": null,
          "aa_length": 325,
          "cds_start": 816,
          "cds_end": null,
          "cds_length": 978,
          "cdna_start": 1215,
          "cdna_end": null,
          "cdna_length": 1727,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "R?",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 7,
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          "exon_count": 7,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ACP5",
          "gene_hgnc_id": 124,
          "hgvs_c": "c.816dupC",
          "hgvs_p": "p.Lys273fs",
          "transcript": "NM_001439234.1",
          "protein_id": "NP_001426163.1",
          "transcript_support_level": null,
          "aa_start": 272,
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          "cds_start": 816,
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          "cdna_start": 1213,
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          "mane_select": null,
          "mane_plus": null,
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          "feature": null
        },
        {
          "aa_ref": "R",
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          "canonical": false,
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          "strand": false,
          "consequences": [
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          "exon_rank": 8,
          "exon_rank_end": null,
          "exon_count": 8,
          "intron_rank": null,
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          "gene_symbol": "ACP5",
          "gene_hgnc_id": 124,
          "hgvs_c": "c.816dupC",
          "hgvs_p": "p.Lys273fs",
          "transcript": "NM_001439235.1",
          "protein_id": "NP_001426164.1",
          "transcript_support_level": null,
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          "cds_start": 816,
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          "cdna_start": 1279,
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          "mane_select": null,
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        {
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          "gene_symbol": "ACP5",
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          "cds_start": 816,
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        },
        {
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          "consequences": [
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          "intron_rank": null,
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          "gene_symbol": "ACP5",
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        {
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          "hgvs_c": "c.816dupC",
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          "gene_symbol": "ACP5",
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          "transcript": "ENST00000590832.2",
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        {
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          "gene_symbol": "ACP5",
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        {
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          "gene_symbol": "ACP5",
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        {
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        {
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          "gene_symbol": "ACP5",
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      "gnomad_genomes_ac": null,
      "gnomad_exomes_homalt": 0,
      "gnomad_genomes_homalt": null,
      "gnomad_mito_homoplasmic": null,
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      "computational_score_selected": null,
      "computational_prediction_selected": null,
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      "splice_score_selected": 0,
      "splice_prediction_selected": "Benign",
      "splice_source_selected": "max_spliceai",
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      "alphamissense_score": null,
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      "bayesdelnoaf_score": null,
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      "phylop100way_score": 0.159,
      "phylop100way_prediction": "Benign",
      "spliceai_max_score": 0,
      "spliceai_max_prediction": "Benign",
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      "acmg_criteria": "PVS1_Strong,PM2,PP5",
      "acmg_by_gene": [
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            "PM2",
            "PP5"
          ],
          "verdict": "Likely_pathogenic",
          "transcript": "ENST00000648477.1",
          "gene_symbol": "ACP5",
          "hgnc_id": 124,
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        {
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          "benign_score": 0,
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            "PP5"
          ],
          "verdict": "Uncertain_significance",
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          "gene_symbol": "ZNF627",
          "hgnc_id": 30570,
          "effects": [
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          ],
          "inheritance_mode": "AR",
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        {
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            "PP5"
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          "verdict": "Uncertain_significance",
          "transcript": "XR_007067140.1",
          "gene_symbol": "LOC124904638",
          "hgnc_id": null,
          "effects": [
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          ],
          "inheritance_mode": "",
          "hgvs_c": "n.-78_-77insG",
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      ],
      "clinvar_disease": "Spondyloenchondrodysplasia with immune dysregulation",
      "clinvar_classification": "Pathogenic",
      "clinvar_review_status": "no assertion criteria provided",
      "clinvar_submissions_summary": "null",
      "phenotype_combined": "Spondyloenchondrodysplasia with immune dysregulation",
      "pathogenicity_classification_combined": "Pathogenic",
      "custom_annotations": null
    }
  ],
  "message": null
}