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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: 6-24547331-C-A (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=6&pos=24547331&ref=C&alt=A&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "6",
      "pos": 24547331,
      "ref": "C",
      "alt": "A",
      "effect": "missense_variant",
      "transcript": "NM_014809.4",
      "consequences": [
        {
          "aa_ref": "R",
          "aa_alt": "L",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 21,
          "exon_rank_end": null,
          "exon_count": 21,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "KIAA0319",
          "gene_hgnc_id": 21580,
          "hgvs_c": "c.3053G>T",
          "hgvs_p": "p.Arg1018Leu",
          "transcript": "NM_014809.4",
          "protein_id": "NP_055624.2",
          "transcript_support_level": null,
          "aa_start": 1018,
          "aa_end": null,
          "aa_length": 1072,
          "cds_start": 3053,
          "cds_end": null,
          "cds_length": 3219,
          "cdna_start": 3614,
          "cdna_end": null,
          "cdna_length": 6838,
          "mane_select": "ENST00000378214.8",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "L",
          "canonical": true,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 21,
          "exon_rank_end": null,
          "exon_count": 21,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "KIAA0319",
          "gene_hgnc_id": 21580,
          "hgvs_c": "c.3053G>T",
          "hgvs_p": "p.Arg1018Leu",
          "transcript": "ENST00000378214.8",
          "protein_id": "ENSP00000367459.3",
          "transcript_support_level": 1,
          "aa_start": 1018,
          "aa_end": null,
          "aa_length": 1072,
          "cds_start": 3053,
          "cds_end": null,
          "cds_length": 3219,
          "cdna_start": 3614,
          "cdna_end": null,
          "cdna_length": 6838,
          "mane_select": "NM_014809.4",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "L",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 19,
          "exon_rank_end": null,
          "exon_count": 19,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "KIAA0319",
          "gene_hgnc_id": 21580,
          "hgvs_c": "c.2870G>T",
          "hgvs_p": "p.Arg957Leu",
          "transcript": "ENST00000537886.5",
          "protein_id": "ENSP00000439700.1",
          "transcript_support_level": 1,
          "aa_start": 957,
          "aa_end": null,
          "aa_length": 1011,
          "cds_start": 2870,
          "cds_end": null,
          "cds_length": 3036,
          "cdna_start": 3395,
          "cdna_end": null,
          "cdna_length": 6622,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "L",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 17,
          "exon_rank_end": null,
          "exon_count": 17,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "KIAA0319",
          "gene_hgnc_id": 21580,
          "hgvs_c": "c.1286G>T",
          "hgvs_p": "p.Arg429Leu",
          "transcript": "ENST00000616673.4",
          "protein_id": "ENSP00000483665.1",
          "transcript_support_level": 1,
          "aa_start": 429,
          "aa_end": null,
          "aa_length": 483,
          "cds_start": 1286,
          "cds_end": null,
          "cds_length": 1452,
          "cdna_start": 2088,
          "cdna_end": null,
          "cdna_length": 5315,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "L",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 21,
          "exon_rank_end": null,
          "exon_count": 21,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "KIAA0319",
          "gene_hgnc_id": 21580,
          "hgvs_c": "c.3053G>T",
          "hgvs_p": "p.Arg1018Leu",
          "transcript": "NM_001168375.2",
          "protein_id": "NP_001161847.1",
          "transcript_support_level": null,
          "aa_start": 1018,
          "aa_end": null,
          "aa_length": 1072,
          "cds_start": 3053,
          "cds_end": null,
          "cds_length": 3219,
          "cdna_start": 3723,
          "cdna_end": null,
          "cdna_length": 6947,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "L",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 21,
          "exon_rank_end": null,
          "exon_count": 21,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "KIAA0319",
          "gene_hgnc_id": 21580,
          "hgvs_c": "c.3053G>T",
          "hgvs_p": "p.Arg1018Leu",
          "transcript": "NM_001350403.2",
          "protein_id": "NP_001337332.1",
          "transcript_support_level": null,
          "aa_start": 1018,
          "aa_end": null,
          "aa_length": 1072,
          "cds_start": 3053,
          "cds_end": null,
          "cds_length": 3219,
          "cdna_start": 3315,
          "cdna_end": null,
          "cdna_length": 6539,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "L",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 20,
          "exon_rank_end": null,
          "exon_count": 20,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "KIAA0319",
          "gene_hgnc_id": 21580,
          "hgvs_c": "c.3035G>T",
          "hgvs_p": "p.Arg1012Leu",
          "transcript": "NM_001350404.2",
          "protein_id": "NP_001337333.1",
          "transcript_support_level": null,
          "aa_start": 1012,
          "aa_end": null,
          "aa_length": 1066,
          "cds_start": 3035,
          "cds_end": null,
          "cds_length": 3201,
          "cdna_start": 3454,
          "cdna_end": null,
          "cdna_length": 6678,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "L",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 22,
          "exon_rank_end": null,
          "exon_count": 22,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "KIAA0319",
          "gene_hgnc_id": 21580,
          "hgvs_c": "c.3026G>T",
          "hgvs_p": "p.Arg1009Leu",
          "transcript": "NM_001168374.2",
          "protein_id": "NP_001161846.1",
          "transcript_support_level": null,
          "aa_start": 1009,
          "aa_end": null,
          "aa_length": 1063,
          "cds_start": 3026,
          "cds_end": null,
          "cds_length": 3192,
          "cdna_start": 3705,
          "cdna_end": null,
          "cdna_length": 6929,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "L",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 22,
          "exon_rank_end": null,
          "exon_count": 22,
          "intron_rank": null,
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          "gene_symbol": "KIAA0319",
          "gene_hgnc_id": 21580,
          "hgvs_c": "c.3026G>T",
          "hgvs_p": "p.Arg1009Leu",
          "transcript": "ENST00000535378.5",
          "protein_id": "ENSP00000442403.1",
          "transcript_support_level": 2,
          "aa_start": 1009,
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          "cds_start": 3026,
          "cds_end": null,
          "cds_length": 3192,
          "cdna_start": 3669,
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          "cdna_length": 6896,
          "mane_select": null,
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        },
        {
          "aa_ref": "R",
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          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 20,
          "exon_rank_end": null,
          "exon_count": 20,
          "intron_rank": null,
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          "gene_symbol": "KIAA0319",
          "gene_hgnc_id": 21580,
          "hgvs_c": "c.2954G>T",
          "hgvs_p": "p.Arg985Leu",
          "transcript": "NM_001350405.2",
          "protein_id": "NP_001337334.1",
          "transcript_support_level": null,
          "aa_start": 985,
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          "cds_start": 2954,
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        {
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          "intron_rank": null,
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          "gene_symbol": "KIAA0319",
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          "hgvs_c": "c.2918G>T",
          "hgvs_p": "p.Arg973Leu",
          "transcript": "NM_001168376.2",
          "protein_id": "NP_001161848.1",
          "transcript_support_level": null,
          "aa_start": 973,
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          "aa_length": 1027,
          "cds_start": 2918,
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          "cdna_start": 3563,
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          "mane_select": null,
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        {
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          "exon_count": 20,
          "intron_rank": null,
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        {
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          "gene_symbol": "KIAA0319",
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          "hgvs_c": "c.2918G>T",
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        {
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          "intron_rank": null,
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          "gene_symbol": "KIAA0319",
          "gene_hgnc_id": 21580,
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          "transcript": "NM_001168377.2",
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        {
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        {
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          "gene_symbol": "KIAA0319",
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          "transcript": "NM_001350410.2",
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        {
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          "gene_symbol": "KIAA0319",
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          "transcript": "NM_001252328.2",
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          "gene_symbol": "KIAA0319",
          "gene_hgnc_id": 21580,
          "hgvs_c": "c.2954G>T",
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          "transcript": "XM_047419603.1",
          "protein_id": "XP_047275559.1",
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        },
        {
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          "strand": false,
          "consequences": [
            "3_prime_UTR_variant"
          ],
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      ],
      "gene_symbol": "KIAA0319",
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      "dbsnp": "rs757441676",
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      "hom_count_reference_population": 0,
      "allele_count_reference_population": 0,
      "gnomad_exomes_af": null,
      "gnomad_genomes_af": null,
      "gnomad_exomes_ac": null,
      "gnomad_genomes_ac": null,
      "gnomad_exomes_homalt": null,
      "gnomad_genomes_homalt": null,
      "gnomad_mito_homoplasmic": null,
      "gnomad_mito_heteroplasmic": null,
      "computational_score_selected": 0.3084373474121094,
      "computational_prediction_selected": "Benign",
      "computational_source_selected": "MetaRNN",
      "splice_score_selected": 0.11999999731779099,
      "splice_prediction_selected": "Benign",
      "splice_source_selected": "max_spliceai",
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      "revel_prediction": "Benign",
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      "alphamissense_prediction": null,
      "bayesdelnoaf_score": -0.26,
      "bayesdelnoaf_prediction": "Benign",
      "phylop100way_score": 4.871,
      "phylop100way_prediction": "Uncertain_significance",
      "spliceai_max_score": 0.12,
      "spliceai_max_prediction": "Benign",
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      "acmg_score": 1,
      "acmg_classification": "Uncertain_significance",
      "acmg_criteria": "PM2,BP4",
      "acmg_by_gene": [
        {
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          "pathogenic_score": 2,
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            "BP4"
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          "verdict": "Uncertain_significance",
          "transcript": "NM_014809.4",
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          "hgvs_p": "p.Arg1018Leu"
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      ],
      "clinvar_disease": "",
      "clinvar_classification": "",
      "clinvar_review_status": "",
      "clinvar_submissions_summary": "",
      "phenotype_combined": null,
      "pathogenicity_classification_combined": null,
      "custom_annotations": null
    }
  ],
  "message": null
}