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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: 10-27994945-T-C (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=10&pos=27994945&ref=T&alt=C&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "10",
      "pos": 27994945,
      "ref": "T",
      "alt": "C",
      "effect": "synonymous_variant",
      "transcript": "ENST00000305242.10",
      "consequences": [
        {
          "aa_ref": "S",
          "aa_alt": "S",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 2,
          "exon_rank_end": null,
          "exon_count": 20,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ODAD2",
          "gene_hgnc_id": 25583,
          "hgvs_c": "c.198A>G",
          "hgvs_p": "p.Ser66Ser",
          "transcript": "NM_018076.5",
          "protein_id": "NP_060546.2",
          "transcript_support_level": null,
          "aa_start": 66,
          "aa_end": null,
          "aa_length": 1044,
          "cds_start": 198,
          "cds_end": null,
          "cds_length": 3135,
          "cdna_start": 322,
          "cdna_end": null,
          "cdna_length": 3603,
          "mane_select": "ENST00000305242.10",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "S",
          "aa_alt": "S",
          "canonical": true,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 2,
          "exon_rank_end": null,
          "exon_count": 20,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ODAD2",
          "gene_hgnc_id": 25583,
          "hgvs_c": "c.198A>G",
          "hgvs_p": "p.Ser66Ser",
          "transcript": "ENST00000305242.10",
          "protein_id": "ENSP00000306410.5",
          "transcript_support_level": 1,
          "aa_start": 66,
          "aa_end": null,
          "aa_length": 1044,
          "cds_start": 198,
          "cds_end": null,
          "cds_length": 3135,
          "cdna_start": 322,
          "cdna_end": null,
          "cdna_length": 3603,
          "mane_select": "NM_018076.5",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "S",
          "aa_alt": "S",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 2,
          "exon_rank_end": null,
          "exon_count": 20,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ODAD2",
          "gene_hgnc_id": 25583,
          "hgvs_c": "c.198A>G",
          "hgvs_p": "p.Ser66Ser",
          "transcript": "NM_001290020.2",
          "protein_id": "NP_001276949.1",
          "transcript_support_level": null,
          "aa_start": 66,
          "aa_end": null,
          "aa_length": 1044,
          "cds_start": 198,
          "cds_end": null,
          "cds_length": 3135,
          "cdna_start": 331,
          "cdna_end": null,
          "cdna_length": 3612,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "S",
          "aa_alt": "S",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 2,
          "exon_rank_end": null,
          "exon_count": 20,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ODAD2",
          "gene_hgnc_id": 25583,
          "hgvs_c": "c.198A>G",
          "hgvs_p": "p.Ser66Ser",
          "transcript": "ENST00000673439.1",
          "protein_id": "ENSP00000500782.1",
          "transcript_support_level": null,
          "aa_start": 66,
          "aa_end": null,
          "aa_length": 1044,
          "cds_start": 198,
          "cds_end": null,
          "cds_length": 3135,
          "cdna_start": 296,
          "cdna_end": null,
          "cdna_length": 3486,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "S",
          "aa_alt": "S",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 3,
          "exon_rank_end": null,
          "exon_count": 4,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ODAD2",
          "gene_hgnc_id": 25583,
          "hgvs_c": "c.198A>G",
          "hgvs_p": "p.Ser66Ser",
          "transcript": "ENST00000486279.2",
          "protein_id": "ENSP00000473438.2",
          "transcript_support_level": 5,
          "aa_start": 66,
          "aa_end": null,
          "aa_length": 96,
          "cds_start": 198,
          "cds_end": null,
          "cds_length": 293,
          "cdna_start": 335,
          "cdna_end": null,
          "cdna_length": 430,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "S",
          "aa_alt": "S",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 2,
          "exon_rank_end": null,
          "exon_count": 22,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ODAD2",
          "gene_hgnc_id": 25583,
          "hgvs_c": "c.198A>G",
          "hgvs_p": "p.Ser66Ser",
          "transcript": "XM_024448049.2",
          "protein_id": "XP_024303817.1",
          "transcript_support_level": null,
          "aa_start": 66,
          "aa_end": null,
          "aa_length": 1107,
          "cds_start": 198,
          "cds_end": null,
          "cds_length": 3324,
          "cdna_start": 331,
          "cdna_end": null,
          "cdna_length": 3801,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "S",
          "aa_alt": "S",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 3,
          "exon_rank_end": null,
          "exon_count": 23,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ODAD2",
          "gene_hgnc_id": 25583,
          "hgvs_c": "c.198A>G",
          "hgvs_p": "p.Ser66Ser",
          "transcript": "XM_024448050.2",
          "protein_id": "XP_024303818.1",
          "transcript_support_level": null,
          "aa_start": 66,
          "aa_end": null,
          "aa_length": 1107,
          "cds_start": 198,
          "cds_end": null,
          "cds_length": 3324,
          "cdna_start": 748,
          "cdna_end": null,
          "cdna_length": 4218,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "S",
          "aa_alt": "S",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 2,
          "exon_rank_end": null,
          "exon_count": 22,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ODAD2",
          "gene_hgnc_id": 25583,
          "hgvs_c": "c.198A>G",
          "hgvs_p": "p.Ser66Ser",
          "transcript": "XM_024448051.2",
          "protein_id": "XP_024303819.1",
          "transcript_support_level": null,
          "aa_start": 66,
          "aa_end": null,
          "aa_length": 1107,
          "cds_start": 198,
          "cds_end": null,
          "cds_length": 3324,
          "cdna_start": 322,
          "cdna_end": null,
          "cdna_length": 3792,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "S",
          "aa_alt": "S",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 2,
          "exon_rank_end": null,
          "exon_count": 22,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ODAD2",
          "gene_hgnc_id": 25583,
          "hgvs_c": "c.198A>G",
          "hgvs_p": "p.Ser66Ser",
          "transcript": "XM_024448052.2",
          "protein_id": "XP_024303820.1",
          "transcript_support_level": null,
          "aa_start": 66,
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          "aa_length": 1107,
          "cds_start": 198,
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          "cdna_start": 413,
          "cdna_end": null,
          "cdna_length": 3883,
          "mane_select": null,
          "mane_plus": null,
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          "feature": null
        },
        {
          "aa_ref": "S",
          "aa_alt": "S",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 2,
          "exon_rank_end": null,
          "exon_count": 21,
          "intron_rank": null,
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          "gene_symbol": "ODAD2",
          "gene_hgnc_id": 25583,
          "hgvs_c": "c.198A>G",
          "hgvs_p": "p.Ser66Ser",
          "transcript": "XM_024448053.2",
          "protein_id": "XP_024303821.1",
          "transcript_support_level": null,
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          "cds_start": 198,
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          "cdna_start": 331,
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        {
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          "hgvs_p": "p.Ser66Ser",
          "transcript": "XM_011519527.2",
          "protein_id": "XP_011517829.1",
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          "mane_select": null,
          "mane_plus": null,
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        },
        {
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          "aa_alt": "S",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
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          ],
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          "intron_rank": null,
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          "gene_symbol": "ODAD2",
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        {
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          "intron_rank": null,
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          "gene_symbol": "ODAD2",
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          "hgvs_c": "c.198A>G",
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          "transcript": "XM_047425403.1",
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        {
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        {
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        {
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        {
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          "gene_symbol": "ODAD2",
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        },
        {
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          "protein_coding": true,
          "strand": false,
          "consequences": [
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          ],
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          "hgvs_c": "c.198A>G",
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        {
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          "gene_symbol": "ODAD2",
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          "transcript": "XM_047425414.1",
          "protein_id": "XP_047281370.1",
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        },
        {
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          "exon_count": 3,
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          "gene_symbol": "LOC112268060",
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          "hgvs_c": "n.171-123T>C",
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          "transcript": "XR_002957065.1",
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        }
      ],
      "gene_symbol": "ODAD2",
      "gene_hgnc_id": 25583,
      "dbsnp": "rs143338979",
      "frequency_reference_population": 0.000006569784,
      "hom_count_reference_population": 0,
      "allele_count_reference_population": 1,
      "gnomad_exomes_af": null,
      "gnomad_genomes_af": 0.00000656978,
      "gnomad_exomes_ac": null,
      "gnomad_genomes_ac": 1,
      "gnomad_exomes_homalt": null,
      "gnomad_genomes_homalt": 0,
      "gnomad_mito_homoplasmic": null,
      "gnomad_mito_heteroplasmic": null,
      "computational_score_selected": -0.5600000023841858,
      "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": -0.56,
      "bayesdelnoaf_prediction": "Benign",
      "phylop100way_score": 0.833,
      "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": -3,
      "acmg_classification": "Likely_benign",
      "acmg_criteria": "PM2,BP4_Strong,BP7",
      "acmg_by_gene": [
        {
          "score": -3,
          "benign_score": 5,
          "pathogenic_score": 2,
          "criteria": [
            "PM2",
            "BP4_Strong",
            "BP7"
          ],
          "verdict": "Likely_benign",
          "transcript": "ENST00000305242.10",
          "gene_symbol": "ODAD2",
          "hgnc_id": 25583,
          "effects": [
            "synonymous_variant"
          ],
          "inheritance_mode": "AD,AR",
          "hgvs_c": "c.198A>G",
          "hgvs_p": "p.Ser66Ser"
        },
        {
          "score": -2,
          "benign_score": 4,
          "pathogenic_score": 2,
          "criteria": [
            "PM2",
            "BP4_Strong"
          ],
          "verdict": "Likely_benign",
          "transcript": "XR_002957065.1",
          "gene_symbol": "LOC112268060",
          "hgnc_id": null,
          "effects": [
            "intron_variant"
          ],
          "inheritance_mode": "",
          "hgvs_c": "n.171-123T>C",
          "hgvs_p": null
        }
      ],
      "clinvar_disease": "",
      "clinvar_classification": "",
      "clinvar_review_status": "",
      "clinvar_submissions_summary": "",
      "phenotype_combined": null,
      "pathogenicity_classification_combined": null,
      "custom_annotations": null
    }
  ],
  "message": null
}