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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: 17-41755804-G-A (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=17&pos=41755804&ref=G&alt=A&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "17",
      "pos": 41755804,
      "ref": "G",
      "alt": "A",
      "effect": "synonymous_variant",
      "transcript": "ENST00000393931.8",
      "consequences": [
        {
          "aa_ref": "I",
          "aa_alt": "I",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 14,
          "exon_rank_end": null,
          "exon_count": 14,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "JUP",
          "gene_hgnc_id": 6207,
          "hgvs_c": "c.2178C>T",
          "hgvs_p": "p.Ile726Ile",
          "transcript": "NM_002230.4",
          "protein_id": "NP_002221.1",
          "transcript_support_level": null,
          "aa_start": 726,
          "aa_end": null,
          "aa_length": 745,
          "cds_start": 2178,
          "cds_end": null,
          "cds_length": 2238,
          "cdna_start": 2310,
          "cdna_end": null,
          "cdna_length": 3505,
          "mane_select": "ENST00000393931.8",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "I",
          "aa_alt": "I",
          "canonical": true,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 14,
          "exon_rank_end": null,
          "exon_count": 14,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "JUP",
          "gene_hgnc_id": 6207,
          "hgvs_c": "c.2178C>T",
          "hgvs_p": "p.Ile726Ile",
          "transcript": "ENST00000393931.8",
          "protein_id": "ENSP00000377508.3",
          "transcript_support_level": 1,
          "aa_start": 726,
          "aa_end": null,
          "aa_length": 745,
          "cds_start": 2178,
          "cds_end": null,
          "cds_length": 2238,
          "cdna_start": 2310,
          "cdna_end": null,
          "cdna_length": 3505,
          "mane_select": "NM_002230.4",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "I",
          "aa_alt": "I",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 14,
          "exon_rank_end": null,
          "exon_count": 15,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "JUP",
          "gene_hgnc_id": 6207,
          "hgvs_c": "c.2178C>T",
          "hgvs_p": "p.Ile726Ile",
          "transcript": "ENST00000310706.9",
          "protein_id": "ENSP00000311113.5",
          "transcript_support_level": 1,
          "aa_start": 726,
          "aa_end": null,
          "aa_length": 745,
          "cds_start": 2178,
          "cds_end": null,
          "cds_length": 2238,
          "cdna_start": 2297,
          "cdna_end": null,
          "cdna_length": 3200,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "I",
          "aa_alt": "I",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 14,
          "exon_rank_end": null,
          "exon_count": 14,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "JUP",
          "gene_hgnc_id": 6207,
          "hgvs_c": "c.2178C>T",
          "hgvs_p": "p.Ile726Ile",
          "transcript": "NM_001352773.2",
          "protein_id": "NP_001339702.1",
          "transcript_support_level": null,
          "aa_start": 726,
          "aa_end": null,
          "aa_length": 745,
          "cds_start": 2178,
          "cds_end": null,
          "cds_length": 2238,
          "cdna_start": 2332,
          "cdna_end": null,
          "cdna_length": 3527,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "I",
          "aa_alt": "I",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 14,
          "exon_rank_end": null,
          "exon_count": 15,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "JUP",
          "gene_hgnc_id": 6207,
          "hgvs_c": "c.2178C>T",
          "hgvs_p": "p.Ile726Ile",
          "transcript": "NM_001352774.2",
          "protein_id": "NP_001339703.1",
          "transcript_support_level": null,
          "aa_start": 726,
          "aa_end": null,
          "aa_length": 745,
          "cds_start": 2178,
          "cds_end": null,
          "cds_length": 2238,
          "cdna_start": 2307,
          "cdna_end": null,
          "cdna_length": 3205,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "I",
          "aa_alt": "I",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 14,
          "exon_rank_end": null,
          "exon_count": 15,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "JUP",
          "gene_hgnc_id": 6207,
          "hgvs_c": "c.2178C>T",
          "hgvs_p": "p.Ile726Ile",
          "transcript": "NM_001352775.2",
          "protein_id": "NP_001339704.1",
          "transcript_support_level": null,
          "aa_start": 726,
          "aa_end": null,
          "aa_length": 745,
          "cds_start": 2178,
          "cds_end": null,
          "cds_length": 2238,
          "cdna_start": 2329,
          "cdna_end": null,
          "cdna_length": 3227,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "I",
          "aa_alt": "I",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 15,
          "exon_rank_end": null,
          "exon_count": 16,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "JUP",
          "gene_hgnc_id": 6207,
          "hgvs_c": "c.2178C>T",
          "hgvs_p": "p.Ile726Ile",
          "transcript": "NM_001352776.2",
          "protein_id": "NP_001339705.1",
          "transcript_support_level": null,
          "aa_start": 726,
          "aa_end": null,
          "aa_length": 745,
          "cds_start": 2178,
          "cds_end": null,
          "cds_length": 2238,
          "cdna_start": 2419,
          "cdna_end": null,
          "cdna_length": 3317,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "I",
          "aa_alt": "I",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 14,
          "exon_rank_end": null,
          "exon_count": 15,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "JUP",
          "gene_hgnc_id": 6207,
          "hgvs_c": "c.2178C>T",
          "hgvs_p": "p.Ile726Ile",
          "transcript": "NM_001352777.2",
          "protein_id": "NP_001339706.1",
          "transcript_support_level": null,
          "aa_start": 726,
          "aa_end": null,
          "aa_length": 745,
          "cds_start": 2178,
          "cds_end": null,
          "cds_length": 2238,
          "cdna_start": 2260,
          "cdna_end": null,
          "cdna_length": 3158,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "I",
          "aa_alt": "I",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 14,
          "exon_rank_end": null,
          "exon_count": 15,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "JUP",
          "gene_hgnc_id": 6207,
          "hgvs_c": "c.2178C>T",
          "hgvs_p": "p.Ile726Ile",
          "transcript": "NM_021991.4",
          "protein_id": "NP_068831.1",
          "transcript_support_level": null,
          "aa_start": 726,
          "aa_end": null,
          "aa_length": 745,
          "cds_start": 2178,
          "cds_end": null,
          "cds_length": 2238,
          "cdna_start": 2310,
          "cdna_end": null,
          "cdna_length": 3208,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "I",
          "aa_alt": "I",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 14,
          "exon_rank_end": null,
          "exon_count": 15,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "JUP",
          "gene_hgnc_id": 6207,
          "hgvs_c": "c.2178C>T",
          "hgvs_p": "p.Ile726Ile",
          "transcript": "ENST00000393930.5",
          "protein_id": "ENSP00000377507.1",
          "transcript_support_level": 5,
          "aa_start": 726,
          "aa_end": null,
          "aa_length": 745,
          "cds_start": 2178,
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          "cds_length": 2238,
          "cdna_start": 2395,
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          "mane_select": null,
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        },
        {
          "aa_ref": "I",
          "aa_alt": "I",
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          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 15,
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          "intron_rank": null,
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          "gene_symbol": "JUP",
          "gene_hgnc_id": 6207,
          "hgvs_c": "c.2229C>T",
          "hgvs_p": "p.Ile743Ile",
          "transcript": "XM_047435934.1",
          "protein_id": "XP_047291890.1",
          "transcript_support_level": null,
          "aa_start": 743,
          "aa_end": null,
          "aa_length": 762,
          "cds_start": 2229,
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          "cds_length": 2289,
          "cdna_start": 2690,
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          "mane_select": null,
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        },
        {
          "aa_ref": "I",
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          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
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          "exon_count": 15,
          "intron_rank": null,
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          "gene_symbol": "JUP",
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        {
          "aa_ref": "I",
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          "gene_symbol": "JUP",
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        {
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          "strand": false,
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          "gene_symbol": "JUP",
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          "hgvs_c": "c.2178C>T",
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          "transcript": "XM_006721874.4",
          "protein_id": "XP_006721937.1",
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        },
        {
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        {
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          "gene_symbol": "JUP",
          "gene_hgnc_id": 6207,
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          "transcript": "XM_011524758.2",
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        {
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        {
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        {
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          "gene_symbol": "JUP",
          "gene_hgnc_id": 6207,
          "hgvs_c": "c.2178C>T",
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          "transcript": "XM_047435940.1",
          "protein_id": "XP_047291896.1",
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        },
        {
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          "strand": false,
          "consequences": [
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          ],
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          "exon_count": 15,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "JUP",
          "gene_hgnc_id": 6207,
          "hgvs_c": "c.2178C>T",
          "hgvs_p": "p.Ile726Ile",
          "transcript": "XM_047435941.1",
          "protein_id": "XP_047291897.1",
          "transcript_support_level": null,
          "aa_start": 726,
          "aa_end": null,
          "aa_length": 745,
          "cds_start": 2178,
          "cds_end": null,
          "cds_length": 2238,
          "cdna_start": 4182,
          "cdna_end": null,
          "cdna_length": 5080,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "I",
          "aa_alt": "I",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 14,
          "exon_rank_end": null,
          "exon_count": 15,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "JUP",
          "gene_hgnc_id": 6207,
          "hgvs_c": "c.2178C>T",
          "hgvs_p": "p.Ile726Ile",
          "transcript": "XM_047435942.1",
          "protein_id": "XP_047291898.1",
          "transcript_support_level": null,
          "aa_start": 726,
          "aa_end": null,
          "aa_length": 745,
          "cds_start": 2178,
          "cds_end": null,
          "cds_length": 2238,
          "cdna_start": 2277,
          "cdna_end": null,
          "cdna_length": 3175,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        }
      ],
      "gene_symbol": "JUP",
      "gene_hgnc_id": 6207,
      "dbsnp": "rs141295561",
      "frequency_reference_population": 0.00032545425,
      "hom_count_reference_population": 0,
      "allele_count_reference_population": 525,
      "gnomad_exomes_af": 0.000340903,
      "gnomad_genomes_af": 0.000177275,
      "gnomad_exomes_ac": 498,
      "gnomad_genomes_ac": 27,
      "gnomad_exomes_homalt": 0,
      "gnomad_genomes_homalt": 0,
      "gnomad_mito_homoplasmic": null,
      "gnomad_mito_heteroplasmic": null,
      "computational_score_selected": -0.6299999952316284,
      "computational_prediction_selected": "Benign",
      "computational_source_selected": "BayesDel_noAF",
      "splice_score_selected": 0,
      "splice_prediction_selected": "Benign",
      "splice_source_selected": "max_spliceai",
      "revel_score": null,
      "revel_prediction": null,
      "alphamissense_score": null,
      "alphamissense_prediction": null,
      "bayesdelnoaf_score": -0.63,
      "bayesdelnoaf_prediction": "Benign",
      "phylop100way_score": -3.938,
      "phylop100way_prediction": "Benign",
      "spliceai_max_score": 0,
      "spliceai_max_prediction": "Benign",
      "dbscsnv_ada_score": null,
      "dbscsnv_ada_prediction": null,
      "apogee2_score": null,
      "apogee2_prediction": null,
      "mitotip_score": null,
      "mitotip_prediction": null,
      "acmg_score": -10,
      "acmg_classification": "Benign",
      "acmg_criteria": "BP4_Strong,BP6,BP7,BS1",
      "acmg_by_gene": [
        {
          "score": -10,
          "benign_score": 10,
          "pathogenic_score": 0,
          "criteria": [
            "BP4_Strong",
            "BP6",
            "BP7",
            "BS1"
          ],
          "verdict": "Benign",
          "transcript": "ENST00000393931.8",
          "gene_symbol": "JUP",
          "hgnc_id": 6207,
          "effects": [
            "synonymous_variant"
          ],
          "inheritance_mode": "AR,AD",
          "hgvs_c": "c.2178C>T",
          "hgvs_p": "p.Ile726Ile"
        }
      ],
      "clinvar_disease": "Arrhythmogenic right ventricular dysplasia 12,Cardiomyopathy,Cardiovascular phenotype,JUP-related disorder,Naxos disease,not specified",
      "clinvar_classification": "Conflicting classifications of pathogenicity",
      "clinvar_review_status": "criteria provided, conflicting classifications",
      "clinvar_submissions_summary": "US:2 LB:5 B:2",
      "phenotype_combined": "not specified|Arrhythmogenic right ventricular dysplasia 12;Naxos disease|Cardiovascular phenotype|Arrhythmogenic right ventricular dysplasia 12|Naxos disease|JUP-related disorder|Cardiomyopathy",
      "pathogenicity_classification_combined": "Conflicting classifications of pathogenicity",
      "custom_annotations": null
    }
  ],
  "message": null
}