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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: 7-148815031-A-G (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=7&pos=148815031&ref=A&alt=G&genome=hg38&allGenes=true"API Response
json
{
  "variants": [
    {
      "chr": "7",
      "pos": 148815031,
      "ref": "A",
      "alt": "G",
      "effect": "missense_variant",
      "transcript": "ENST00000320356.7",
      "consequences": [
        {
          "aa_ref": "S",
          "aa_alt": "P",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 14,
          "exon_rank_end": null,
          "exon_count": 20,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "EZH2",
          "gene_hgnc_id": 3527,
          "hgvs_c": "c.1555T>C",
          "hgvs_p": "p.Ser519Pro",
          "transcript": "NM_004456.5",
          "protein_id": "NP_004447.2",
          "transcript_support_level": null,
          "aa_start": 519,
          "aa_end": null,
          "aa_length": 751,
          "cds_start": 1555,
          "cds_end": null,
          "cds_length": 2256,
          "cdna_start": 1690,
          "cdna_end": null,
          "cdna_length": 2654,
          "mane_select": "ENST00000320356.7",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "S",
          "aa_alt": "P",
          "canonical": true,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 14,
          "exon_rank_end": null,
          "exon_count": 20,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "EZH2",
          "gene_hgnc_id": 3527,
          "hgvs_c": "c.1555T>C",
          "hgvs_p": "p.Ser519Pro",
          "transcript": "ENST00000320356.7",
          "protein_id": "ENSP00000320147.2",
          "transcript_support_level": 1,
          "aa_start": 519,
          "aa_end": null,
          "aa_length": 751,
          "cds_start": 1555,
          "cds_end": null,
          "cds_length": 2256,
          "cdna_start": 1690,
          "cdna_end": null,
          "cdna_length": 2654,
          "mane_select": "NM_004456.5",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "S",
          "aa_alt": "P",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 14,
          "exon_rank_end": null,
          "exon_count": 20,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "EZH2",
          "gene_hgnc_id": 3527,
          "hgvs_c": "c.1540T>C",
          "hgvs_p": "p.Ser514Pro",
          "transcript": "ENST00000460911.5",
          "protein_id": "ENSP00000419711.1",
          "transcript_support_level": 1,
          "aa_start": 514,
          "aa_end": null,
          "aa_length": 746,
          "cds_start": 1540,
          "cds_end": null,
          "cds_length": 2241,
          "cdna_start": 1629,
          "cdna_end": null,
          "cdna_length": 2591,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "S",
          "aa_alt": "P",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 13,
          "exon_rank_end": null,
          "exon_count": 19,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "EZH2",
          "gene_hgnc_id": 3527,
          "hgvs_c": "c.1423T>C",
          "hgvs_p": "p.Ser475Pro",
          "transcript": "ENST00000350995.6",
          "protein_id": "ENSP00000223193.2",
          "transcript_support_level": 1,
          "aa_start": 475,
          "aa_end": null,
          "aa_length": 707,
          "cds_start": 1423,
          "cds_end": null,
          "cds_length": 2124,
          "cdna_start": 1515,
          "cdna_end": null,
          "cdna_length": 2477,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "S",
          "aa_alt": "P",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 14,
          "exon_rank_end": null,
          "exon_count": 20,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "EZH2",
          "gene_hgnc_id": 3527,
          "hgvs_c": "c.1540T>C",
          "hgvs_p": "p.Ser514Pro",
          "transcript": "NM_001203247.2",
          "protein_id": "NP_001190176.1",
          "transcript_support_level": null,
          "aa_start": 514,
          "aa_end": null,
          "aa_length": 746,
          "cds_start": 1540,
          "cds_end": null,
          "cds_length": 2241,
          "cdna_start": 1675,
          "cdna_end": null,
          "cdna_length": 2639,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "S",
          "aa_alt": "P",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 14,
          "exon_rank_end": null,
          "exon_count": 20,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "EZH2",
          "gene_hgnc_id": 3527,
          "hgvs_c": "c.1513T>C",
          "hgvs_p": "p.Ser505Pro",
          "transcript": "NM_001203248.2",
          "protein_id": "NP_001190177.1",
          "transcript_support_level": null,
          "aa_start": 505,
          "aa_end": null,
          "aa_length": 737,
          "cds_start": 1513,
          "cds_end": null,
          "cds_length": 2214,
          "cdna_start": 1648,
          "cdna_end": null,
          "cdna_length": 2612,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "S",
          "aa_alt": "P",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 14,
          "exon_rank_end": null,
          "exon_count": 20,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "EZH2",
          "gene_hgnc_id": 3527,
          "hgvs_c": "c.1513T>C",
          "hgvs_p": "p.Ser505Pro",
          "transcript": "ENST00000483967.5",
          "protein_id": "ENSP00000419856.1",
          "transcript_support_level": 2,
          "aa_start": 505,
          "aa_end": null,
          "aa_length": 737,
          "cds_start": 1513,
          "cds_end": null,
          "cds_length": 2214,
          "cdna_start": 1644,
          "cdna_end": null,
          "cdna_length": 2466,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "S",
          "aa_alt": "P",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 13,
          "exon_rank_end": null,
          "exon_count": 19,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "EZH2",
          "gene_hgnc_id": 3527,
          "hgvs_c": "c.1423T>C",
          "hgvs_p": "p.Ser475Pro",
          "transcript": "NM_152998.3",
          "protein_id": "NP_694543.1",
          "transcript_support_level": null,
          "aa_start": 475,
          "aa_end": null,
          "aa_length": 707,
          "cds_start": 1423,
          "cds_end": null,
          "cds_length": 2124,
          "cdna_start": 1558,
          "cdna_end": null,
          "cdna_length": 2522,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "S",
          "aa_alt": "P",
          "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": "EZH2",
          "gene_hgnc_id": 3527,
          "hgvs_c": "c.1579T>C",
          "hgvs_p": "p.Ser527Pro",
          "transcript": "XM_011515883.3",
          "protein_id": "XP_011514185.1",
          "transcript_support_level": null,
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        {
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          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
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          "exon_count": 20,
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          "gene_symbol": "EZH2",
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          "hgvs_c": "c.1579T>C",
          "hgvs_p": "p.Ser527Pro",
          "transcript": "XM_017011817.3",
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        {
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        {
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          "strand": false,
          "consequences": [
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          "intron_rank": null,
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        {
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          "strand": false,
          "consequences": [
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          "intron_rank": null,
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          "gene_symbol": "EZH2",
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          "hgvs_c": "c.1555T>C",
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        {
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        {
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          "strand": false,
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          ],
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          "gene_symbol": "EZH2",
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          "hgvs_c": "c.1540T>C",
          "hgvs_p": "p.Ser514Pro",
          "transcript": "XM_047419992.1",
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        {
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          "gene_symbol": "EZH2",
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          ],
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        },
        {
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          "protein_coding": true,
          "strand": false,
          "consequences": [
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          ],
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          "intron_rank": null,
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          "gene_symbol": "EZH2",
          "gene_hgnc_id": 3527,
          "hgvs_c": "c.1531T>C",
          "hgvs_p": "p.Ser511Pro",
          "transcript": "XM_047419995.1",
          "protein_id": "XP_047275951.1",
          "transcript_support_level": null,
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        },
        {
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          "protein_coding": true,
          "strand": false,
          "consequences": [
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          ],
          "exon_rank": 14,
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          "exon_count": 20,
          "intron_rank": null,
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      "dbsnp": "rs747009766",
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      "allele_count_reference_population": 44,
      "gnomad_exomes_af": 0.0000273677,
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      "gnomad_exomes_ac": 40,
      "gnomad_genomes_ac": 4,
      "gnomad_exomes_homalt": 0,
      "gnomad_genomes_homalt": 0,
      "gnomad_mito_homoplasmic": null,
      "gnomad_mito_heteroplasmic": null,
      "computational_score_selected": 0.5479501485824585,
      "computational_prediction_selected": "Uncertain_significance",
      "computational_source_selected": "MetaRNN",
      "splice_score_selected": 0.07000000029802322,
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      "splice_source_selected": "max_spliceai",
      "revel_score": 0.769,
      "revel_prediction": "Pathogenic",
      "alphamissense_score": 0.2398,
      "alphamissense_prediction": null,
      "bayesdelnoaf_score": 0.29,
      "bayesdelnoaf_prediction": "Pathogenic",
      "phylop100way_score": 8.893,
      "phylop100way_prediction": "Pathogenic",
      "spliceai_max_score": 0.07,
      "spliceai_max_prediction": "Benign",
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      "acmg_score": -9,
      "acmg_classification": "Benign",
      "acmg_criteria": "BP6,BS1,BS2",
      "acmg_by_gene": [
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          "benign_score": 9,
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          "verdict": "Benign",
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      "clinvar_disease": "EZH2-related disorder,Inborn genetic diseases,Weaver syndrome",
      "clinvar_classification": "Conflicting classifications of pathogenicity",
      "clinvar_review_status": "criteria provided, conflicting classifications",
      "clinvar_submissions_summary": "US:1 LB:1",
      "phenotype_combined": "Weaver syndrome|Inborn genetic diseases|EZH2-related disorder",
      "pathogenicity_classification_combined": "Conflicting classifications of pathogenicity",
      "custom_annotations": null
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  ],
  "message": null
}