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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: 3-194413757-A-G (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=3&pos=194413757&ref=A&alt=G&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "3",
      "pos": 194413757,
      "ref": "A",
      "alt": "G",
      "effect": "splice_donor_variant,intron_variant",
      "transcript": "NM_001367549.1",
      "consequences": [
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_donor_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 34,
          "intron_rank": 32,
          "intron_rank_end": null,
          "gene_symbol": "ATP13A3",
          "gene_hgnc_id": 24113,
          "hgvs_c": "c.3483+2T>C",
          "hgvs_p": null,
          "transcript": "NM_001367549.1",
          "protein_id": "NP_001354478.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1256,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 3771,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": "ENST00000645319.2",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001367549.1"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": true,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_donor_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 34,
          "intron_rank": 32,
          "intron_rank_end": null,
          "gene_symbol": "ATP13A3",
          "gene_hgnc_id": 24113,
          "hgvs_c": "c.3483+2T>C",
          "hgvs_p": null,
          "transcript": "ENST00000645319.2",
          "protein_id": "ENSP00000494937.2",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1256,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 3771,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": "NM_001367549.1",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000645319.2"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "splice_donor_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": 11,
          "intron_rank_end": null,
          "gene_symbol": "ATP13A3",
          "gene_hgnc_id": 24113,
          "hgvs_c": "n.1329+2T>C",
          "hgvs_p": null,
          "transcript": "ENST00000429136.7",
          "protein_id": null,
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": null,
          "cds_start": null,
          "cds_end": null,
          "cds_length": null,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "retained_intron",
          "feature": "ENST00000429136.7"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "splice_donor_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 4,
          "intron_rank": 2,
          "intron_rank_end": null,
          "gene_symbol": "ATP13A3",
          "gene_hgnc_id": 24113,
          "hgvs_c": "n.587+2T>C",
          "hgvs_p": null,
          "transcript": "ENST00000461660.2",
          "protein_id": null,
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": null,
          "cds_start": null,
          "cds_end": null,
          "cds_length": null,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "retained_intron",
          "feature": "ENST00000461660.2"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_donor_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 35,
          "intron_rank": 33,
          "intron_rank_end": null,
          "gene_symbol": "ATP13A3",
          "gene_hgnc_id": 24113,
          "hgvs_c": "c.3600+2T>C",
          "hgvs_p": null,
          "transcript": "ENST00000963858.1",
          "protein_id": "ENSP00000633917.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1295,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 3888,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000963858.1"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_donor_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 34,
          "intron_rank": 32,
          "intron_rank_end": null,
          "gene_symbol": "ATP13A3",
          "gene_hgnc_id": 24113,
          "hgvs_c": "c.3600+2T>C",
          "hgvs_p": null,
          "transcript": "ENST00000963862.1",
          "protein_id": "ENSP00000633921.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1295,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 3888,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000963862.1"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_donor_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 33,
          "intron_rank": 31,
          "intron_rank_end": null,
          "gene_symbol": "ATP13A3",
          "gene_hgnc_id": 24113,
          "hgvs_c": "c.3483+2T>C",
          "hgvs_p": null,
          "transcript": "ENST00000856972.1",
          "protein_id": "ENSP00000527031.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1256,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 3771,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000856972.1"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_donor_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 34,
          "intron_rank": 32,
          "intron_rank_end": null,
          "gene_symbol": "ATP13A3",
          "gene_hgnc_id": 24113,
          "hgvs_c": "c.3483+2T>C",
          "hgvs_p": null,
          "transcript": "ENST00000856973.1",
          "protein_id": "ENSP00000527032.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1256,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 3771,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000856973.1"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_donor_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 34,
          "intron_rank": 32,
          "intron_rank_end": null,
          "gene_symbol": "ATP13A3",
          "gene_hgnc_id": 24113,
          "hgvs_c": "c.3483+2T>C",
          "hgvs_p": null,
          "transcript": "ENST00000856974.1",
          "protein_id": "ENSP00000527033.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1256,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 3771,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000856974.1"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_donor_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 33,
          "intron_rank": 31,
          "intron_rank_end": null,
          "gene_symbol": "ATP13A3",
          "gene_hgnc_id": 24113,
          "hgvs_c": "c.3483+2T>C",
          "hgvs_p": null,
          "transcript": "ENST00000856975.1",
          "protein_id": "ENSP00000527034.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1256,
          "cds_start": null,
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          "cds_length": 3771,
          "cdna_start": null,
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          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000856975.1"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_donor_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 33,
          "intron_rank": 31,
          "intron_rank_end": null,
          "gene_symbol": "ATP13A3",
          "gene_hgnc_id": 24113,
          "hgvs_c": "c.3483+2T>C",
          "hgvs_p": null,
          "transcript": "ENST00000920215.1",
          "protein_id": "ENSP00000590274.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1256,
          "cds_start": null,
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          "cds_length": 3771,
          "cdna_start": null,
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          "mane_select": null,
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          "biotype": "protein_coding",
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        {
          "aa_ref": null,
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          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
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            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 35,
          "intron_rank": 33,
          "intron_rank_end": null,
          "gene_symbol": "ATP13A3",
          "gene_hgnc_id": 24113,
          "hgvs_c": "c.3483+2T>C",
          "hgvs_p": null,
          "transcript": "ENST00000920218.1",
          "protein_id": "ENSP00000590277.1",
          "transcript_support_level": null,
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          "cds_start": null,
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          "mane_select": null,
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          "biotype": "protein_coding",
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        },
        {
          "aa_ref": null,
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          "canonical": false,
          "protein_coding": true,
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          "consequences": [
            "splice_donor_variant",
            "intron_variant"
          ],
          "exon_rank": null,
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          "intron_rank": 31,
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          "gene_symbol": "ATP13A3",
          "gene_hgnc_id": 24113,
          "hgvs_c": "c.3483+2T>C",
          "hgvs_p": null,
          "transcript": "ENST00000963861.1",
          "protein_id": "ENSP00000633920.1",
          "transcript_support_level": null,
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          "cdna_start": null,
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          "cdna_length": null,
          "mane_select": null,
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          "biotype": "protein_coding",
          "feature": "ENST00000963861.1"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_donor_variant",
            "intron_variant"
          ],
          "exon_rank": null,
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          "exon_count": 33,
          "intron_rank": 31,
          "intron_rank_end": null,
          "gene_symbol": "ATP13A3",
          "gene_hgnc_id": 24113,
          "hgvs_c": "c.3420+2T>C",
          "hgvs_p": null,
          "transcript": "ENST00000963860.1",
          "protein_id": "ENSP00000633919.1",
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          "strand": false,
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            "intron_variant"
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          "intron_rank": 31,
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          "gene_symbol": "ATP13A3",
          "gene_hgnc_id": 24113,
          "hgvs_c": "c.3402+2T>C",
          "hgvs_p": null,
          "transcript": "NM_001374836.1",
          "protein_id": "NP_001361765.1",
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          "aa_length": 1229,
          "cds_start": null,
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          "cds_length": 3690,
          "cdna_start": null,
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          "feature": "NM_001374836.1"
        },
        {
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          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
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          ],
          "exon_rank": null,
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          "exon_count": 33,
          "intron_rank": 31,
          "intron_rank_end": null,
          "gene_symbol": "ATP13A3",
          "gene_hgnc_id": 24113,
          "hgvs_c": "c.3402+2T>C",
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          "transcript": "ENST00000920212.1",
          "protein_id": "ENSP00000590271.1",
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        },
        {
          "aa_ref": null,
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          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_donor_variant",
            "intron_variant"
          ],
          "exon_rank": null,
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          "exon_count": 32,
          "intron_rank": 30,
          "intron_rank_end": null,
          "gene_symbol": "ATP13A3",
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          "hgvs_c": "c.3402+2T>C",
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          "transcript": "ENST00000963864.1",
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        {
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          ],
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          "exon_count": 33,
          "intron_rank": 32,
          "intron_rank_end": null,
          "gene_symbol": "ATP13A3",
          "gene_hgnc_id": 24113,
          "hgvs_c": "c.3483+2T>C",
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          "transcript": "NM_001437993.1",
          "protein_id": "NP_001424922.1",
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          "biotype": "protein_coding",
          "feature": "NM_001437993.1"
        },
        {
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          "consequences": [
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            "intron_variant"
          ],
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          "exon_count": 32,
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          "gene_symbol": "ATP13A3",
          "gene_hgnc_id": 24113,
          "hgvs_c": "c.3483+2T>C",
          "hgvs_p": null,
          "transcript": "NM_024524.4",
          "protein_id": "NP_078800.3",
          "transcript_support_level": null,
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          "aa_length": 1226,
          "cds_start": null,
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          "cdna_start": null,
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          "cdna_length": null,
          "mane_select": null,
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          "biotype": "protein_coding",
          "feature": "NM_024524.4"
        },
        {
          "aa_ref": null,
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          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_donor_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 32,
          "intron_rank": 31,
          "intron_rank_end": null,
          "gene_symbol": "ATP13A3",
          "gene_hgnc_id": 24113,
          "hgvs_c": "c.3483+2T>C",
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          "feature": "NR_164667.1"
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      ],
      "gene_symbol": "ATP13A3",
      "gene_hgnc_id": 24113,
      "dbsnp": "rs1715607975",
      "frequency_reference_population": null,
      "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": 0.20000000298023224,
      "computational_prediction_selected": "Pathogenic",
      "computational_source_selected": "BayesDel_noAF",
      "splice_score_selected": 0.7459999918937683,
      "splice_prediction_selected": "Pathogenic",
      "splice_source_selected": "dbscSNV1_RF",
      "revel_score": null,
      "revel_prediction": null,
      "alphamissense_score": null,
      "alphamissense_prediction": null,
      "bayesdelnoaf_score": 0.2,
      "bayesdelnoaf_prediction": "Pathogenic",
      "phylop100way_score": 7.573,
      "phylop100way_prediction": "Pathogenic",
      "spliceai_max_score": 0.82,
      "spliceai_max_prediction": "Pathogenic",
      "dbscsnv_ada_score": 0.965904012078529,
      "dbscsnv_ada_prediction": "Pathogenic",
      "apogee2_score": null,
      "apogee2_prediction": null,
      "mitotip_score": null,
      "mitotip_prediction": null,
      "acmg_score": 4,
      "acmg_classification": "Uncertain_significance",
      "acmg_criteria": "PVS1_Moderate,PM2",
      "acmg_by_gene": [
        {
          "score": 4,
          "benign_score": 0,
          "pathogenic_score": 4,
          "criteria": [
            "PVS1_Moderate",
            "PM2"
          ],
          "verdict": "Uncertain_significance",
          "transcript": "NM_001367549.1",
          "gene_symbol": "ATP13A3",
          "hgnc_id": 24113,
          "effects": [
            "splice_donor_variant",
            "intron_variant"
          ],
          "inheritance_mode": "SD",
          "hgvs_c": "c.3483+2T>C",
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      ],
      "clinvar_disease": "not provided",
      "clinvar_classification": "Uncertain significance",
      "clinvar_review_status": "criteria provided, single submitter",
      "clinvar_submissions_summary": "US:1",
      "phenotype_combined": "not provided",
      "pathogenicity_classification_combined": "Uncertain significance",
      "custom_annotations": null
    }
  ],
  "message": null
}