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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: 15-28014821-G-A (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=15&pos=28014821&ref=G&alt=A&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "15",
      "pos": 28014821,
      "ref": "G",
      "alt": "A",
      "effect": "synonymous_variant",
      "transcript": "ENST00000354638.8",
      "consequences": [
        {
          "aa_ref": "I",
          "aa_alt": "I",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 9,
          "exon_rank_end": null,
          "exon_count": 24,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "OCA2",
          "gene_hgnc_id": 8101,
          "hgvs_c": "c.999C>T",
          "hgvs_p": "p.Ile333Ile",
          "transcript": "NM_000275.3",
          "protein_id": "NP_000266.2",
          "transcript_support_level": null,
          "aa_start": 333,
          "aa_end": null,
          "aa_length": 838,
          "cds_start": 999,
          "cds_end": null,
          "cds_length": 2517,
          "cdna_start": 1112,
          "cdna_end": null,
          "cdna_length": 3143,
          "mane_select": "ENST00000354638.8",
          "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": 9,
          "exon_rank_end": null,
          "exon_count": 24,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "OCA2",
          "gene_hgnc_id": 8101,
          "hgvs_c": "c.999C>T",
          "hgvs_p": "p.Ile333Ile",
          "transcript": "ENST00000354638.8",
          "protein_id": "ENSP00000346659.3",
          "transcript_support_level": 1,
          "aa_start": 333,
          "aa_end": null,
          "aa_length": 838,
          "cds_start": 999,
          "cds_end": null,
          "cds_length": 2517,
          "cdna_start": 1112,
          "cdna_end": null,
          "cdna_length": 3143,
          "mane_select": "NM_000275.3",
          "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": 9,
          "exon_rank_end": null,
          "exon_count": 23,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "OCA2",
          "gene_hgnc_id": 8101,
          "hgvs_c": "c.999C>T",
          "hgvs_p": "p.Ile333Ile",
          "transcript": "ENST00000353809.9",
          "protein_id": "ENSP00000261276.8",
          "transcript_support_level": 1,
          "aa_start": 333,
          "aa_end": null,
          "aa_length": 814,
          "cds_start": 999,
          "cds_end": null,
          "cds_length": 2445,
          "cdna_start": 1109,
          "cdna_end": null,
          "cdna_length": 3068,
          "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": 9,
          "exon_rank_end": null,
          "exon_count": 23,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "OCA2",
          "gene_hgnc_id": 8101,
          "hgvs_c": "c.999C>T",
          "hgvs_p": "p.Ile333Ile",
          "transcript": "NM_001300984.2",
          "protein_id": "NP_001287913.1",
          "transcript_support_level": null,
          "aa_start": 333,
          "aa_end": null,
          "aa_length": 814,
          "cds_start": 999,
          "cds_end": null,
          "cds_length": 2445,
          "cdna_start": 1112,
          "cdna_end": null,
          "cdna_length": 3071,
          "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": 10,
          "exon_rank_end": null,
          "exon_count": 26,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "OCA2",
          "gene_hgnc_id": 8101,
          "hgvs_c": "c.1023C>T",
          "hgvs_p": "p.Ile341Ile",
          "transcript": "XM_017022255.2",
          "protein_id": "XP_016877744.1",
          "transcript_support_level": null,
          "aa_start": 341,
          "aa_end": null,
          "aa_length": 860,
          "cds_start": 1023,
          "cds_end": null,
          "cds_length": 2583,
          "cdna_start": 2365,
          "cdna_end": null,
          "cdna_length": 4438,
          "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": 9,
          "exon_rank_end": null,
          "exon_count": 25,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "OCA2",
          "gene_hgnc_id": 8101,
          "hgvs_c": "c.999C>T",
          "hgvs_p": "p.Ile333Ile",
          "transcript": "XM_011521640.3",
          "protein_id": "XP_011519942.1",
          "transcript_support_level": null,
          "aa_start": 333,
          "aa_end": null,
          "aa_length": 852,
          "cds_start": 999,
          "cds_end": null,
          "cds_length": 2559,
          "cdna_start": 1112,
          "cdna_end": null,
          "cdna_length": 3185,
          "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": 9,
          "exon_rank_end": null,
          "exon_count": 24,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "OCA2",
          "gene_hgnc_id": 8101,
          "hgvs_c": "c.1023C>T",
          "hgvs_p": "p.Ile341Ile",
          "transcript": "XM_017022256.2",
          "protein_id": "XP_016877745.1",
          "transcript_support_level": null,
          "aa_start": 341,
          "aa_end": null,
          "aa_length": 846,
          "cds_start": 1023,
          "cds_end": null,
          "cds_length": 2541,
          "cdna_start": 3317,
          "cdna_end": null,
          "cdna_length": 5348,
          "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": 9,
          "exon_rank_end": null,
          "exon_count": 24,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "OCA2",
          "gene_hgnc_id": 8101,
          "hgvs_c": "c.1023C>T",
          "hgvs_p": "p.Ile341Ile",
          "transcript": "XM_017022257.2",
          "protein_id": "XP_016877746.1",
          "transcript_support_level": null,
          "aa_start": 341,
          "aa_end": null,
          "aa_length": 836,
          "cds_start": 1023,
          "cds_end": null,
          "cds_length": 2511,
          "cdna_start": 3318,
          "cdna_end": null,
          "cdna_length": 5319,
          "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": 9,
          "exon_rank_end": null,
          "exon_count": 24,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "OCA2",
          "gene_hgnc_id": 8101,
          "hgvs_c": "c.1023C>T",
          "hgvs_p": "p.Ile341Ile",
          "transcript": "XM_017022258.2",
          "protein_id": "XP_016877747.1",
          "transcript_support_level": null,
          "aa_start": 341,
          "aa_end": null,
          "aa_length": 835,
          "cds_start": 1023,
          "cds_end": null,
          "cds_length": 2508,
          "cdna_start": 3320,
          "cdna_end": null,
          "cdna_length": 5074,
          "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": 9,
          "exon_rank_end": null,
          "exon_count": 24,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "OCA2",
          "gene_hgnc_id": 8101,
          "hgvs_c": "c.999C>T",
          "hgvs_p": "p.Ile333Ile",
          "transcript": "XM_047432605.1",
          "protein_id": "XP_047288561.1",
          "transcript_support_level": null,
          "aa_start": 333,
          "aa_end": null,
          "aa_length": 828,
          "cds_start": 999,
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          "cds_length": 2487,
          "cdna_start": 1112,
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          "cdna_length": 3113,
          "mane_select": null,
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        },
        {
          "aa_ref": "I",
          "aa_alt": "I",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 9,
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          "exon_count": 24,
          "intron_rank": null,
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          "gene_symbol": "OCA2",
          "gene_hgnc_id": 8101,
          "hgvs_c": "c.999C>T",
          "hgvs_p": "p.Ile333Ile",
          "transcript": "XM_047432606.1",
          "protein_id": "XP_047288562.1",
          "transcript_support_level": null,
          "aa_start": 333,
          "aa_end": null,
          "aa_length": 827,
          "cds_start": 999,
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          "cds_length": 2484,
          "cdna_start": 1112,
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          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "I",
          "aa_alt": "I",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
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          ],
          "exon_rank": 9,
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          "exon_count": 23,
          "intron_rank": null,
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          "gene_symbol": "OCA2",
          "gene_hgnc_id": 8101,
          "hgvs_c": "c.1023C>T",
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          "transcript": "XM_017022259.2",
          "protein_id": "XP_016877748.1",
          "transcript_support_level": null,
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          "cds_start": 1023,
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        },
        {
          "aa_ref": "I",
          "aa_alt": "I",
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          "strand": false,
          "consequences": [
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          ],
          "exon_rank": 9,
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          "intron_rank": null,
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          "gene_symbol": "OCA2",
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          "hgvs_c": "c.1023C>T",
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          "transcript": "XM_017022260.2",
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        {
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          "protein_coding": true,
          "strand": false,
          "consequences": [
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          "intron_rank": null,
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          "gene_symbol": "OCA2",
          "gene_hgnc_id": 8101,
          "hgvs_c": "c.1023C>T",
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          "transcript": "XM_047432607.1",
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        },
        {
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          "feature": null
        },
        {
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          "strand": false,
          "consequences": [
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          ],
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          "intron_rank": null,
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          "gene_symbol": "OCA2",
          "gene_hgnc_id": 8101,
          "hgvs_c": "c.999C>T",
          "hgvs_p": "p.Ile333Ile",
          "transcript": "XM_047432609.1",
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        {
          "aa_ref": "I",
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          "intron_rank": null,
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          "gene_symbol": "OCA2",
          "gene_hgnc_id": 8101,
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          "transcript": "XM_047432610.1",
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        {
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        {
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        },
        {
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          "consequences": [
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          ],
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          "exon_count": 22,
          "intron_rank": null,
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          "gene_symbol": "OCA2",
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          "hgvs_c": "c.999C>T",
          "hgvs_p": "p.Ile333Ile",
          "transcript": "XM_047432611.1",
          "protein_id": "XP_047288567.1",
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          "cdna_length": 3005,
          "mane_select": null,
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        },
        {
          "aa_ref": "I",
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          "canonical": false,
          "protein_coding": true,
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          ],
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          "exon_count": 22,
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      ],
      "gene_symbol": "OCA2",
      "gene_hgnc_id": 8101,
      "dbsnp": "rs376454436",
      "frequency_reference_population": 0.000022305607,
      "hom_count_reference_population": 0,
      "allele_count_reference_population": 36,
      "gnomad_exomes_af": 0.0000212064,
      "gnomad_genomes_af": 0.0000328684,
      "gnomad_exomes_ac": 31,
      "gnomad_genomes_ac": 5,
      "gnomad_exomes_homalt": 0,
      "gnomad_genomes_homalt": 0,
      "gnomad_mito_homoplasmic": null,
      "gnomad_mito_heteroplasmic": null,
      "computational_score_selected": -0.7400000095367432,
      "computational_prediction_selected": "Benign",
      "computational_source_selected": "BayesDel_noAF",
      "splice_score_selected": 0.009999999776482582,
      "splice_prediction_selected": "Benign",
      "splice_source_selected": "max_spliceai",
      "revel_score": null,
      "revel_prediction": null,
      "alphamissense_score": null,
      "alphamissense_prediction": null,
      "bayesdelnoaf_score": -0.74,
      "bayesdelnoaf_prediction": "Benign",
      "phylop100way_score": -0.389,
      "phylop100way_prediction": "Benign",
      "spliceai_max_score": 0.01,
      "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": -13,
      "acmg_classification": "Benign",
      "acmg_criteria": "BP4_Strong,BP6_Very_Strong,BP7",
      "acmg_by_gene": [
        {
          "score": -13,
          "benign_score": 13,
          "pathogenic_score": 0,
          "criteria": [
            "BP4_Strong",
            "BP6_Very_Strong",
            "BP7"
          ],
          "verdict": "Benign",
          "transcript": "ENST00000354638.8",
          "gene_symbol": "OCA2",
          "hgnc_id": 8101,
          "effects": [
            "synonymous_variant"
          ],
          "inheritance_mode": "AR",
          "hgvs_c": "c.999C>T",
          "hgvs_p": "p.Ile333Ile"
        }
      ],
      "clinvar_disease": "not provided,not specified",
      "clinvar_classification": "Likely benign",
      "clinvar_review_status": "criteria provided, multiple submitters, no conflicts",
      "clinvar_submissions_summary": "LB:2",
      "phenotype_combined": "not specified|not provided",
      "pathogenicity_classification_combined": "Likely benign",
      "custom_annotations": null
    }
  ],
  "message": null
}