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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: 20-62238609-C-T (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=20&pos=62238609&ref=C&alt=T&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "20",
      "pos": 62238609,
      "ref": "C",
      "alt": "T",
      "effect": "intron_variant",
      "transcript": "NM_144498.4",
      "consequences": [
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 14,
          "intron_rank": 1,
          "intron_rank_end": null,
          "gene_symbol": "OSBPL2",
          "gene_hgnc_id": 15761,
          "hgvs_c": "c.-129+12C>T",
          "hgvs_p": null,
          "transcript": "NM_144498.4",
          "protein_id": "NP_653081.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 480,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1443,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": "ENST00000313733.9",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_144498.4"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": true,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 14,
          "intron_rank": 1,
          "intron_rank_end": null,
          "gene_symbol": "OSBPL2",
          "gene_hgnc_id": 15761,
          "hgvs_c": "c.-129+12C>T",
          "hgvs_p": null,
          "transcript": "ENST00000313733.9",
          "protein_id": "ENSP00000316649.3",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 480,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1443,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": "NM_144498.4",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000313733.9"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 14,
          "intron_rank": 1,
          "intron_rank_end": null,
          "gene_symbol": "OSBPL2",
          "gene_hgnc_id": 15761,
          "hgvs_c": "c.-129+12C>T",
          "hgvs_p": null,
          "transcript": "ENST00000358053.3",
          "protein_id": "ENSP00000350755.2",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 468,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1407,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000358053.3"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "5_prime_UTR_variant"
          ],
          "exon_rank": 1,
          "exon_rank_end": null,
          "exon_count": 14,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "OSBPL2",
          "gene_hgnc_id": 15761,
          "hgvs_c": "c.-585C>T",
          "hgvs_p": null,
          "transcript": "ENST00000917729.1",
          "protein_id": "ENSP00000587788.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 480,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1443,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000917729.1"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "5_prime_UTR_variant"
          ],
          "exon_rank": 1,
          "exon_rank_end": null,
          "exon_count": 14,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "OSBPL2",
          "gene_hgnc_id": 15761,
          "hgvs_c": "c.-581C>T",
          "hgvs_p": null,
          "transcript": "ENST00000917730.1",
          "protein_id": "ENSP00000587789.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 480,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1443,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000917730.1"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 14,
          "intron_rank": 1,
          "intron_rank_end": null,
          "gene_symbol": "OSBPL2",
          "gene_hgnc_id": 15761,
          "hgvs_c": "c.-129+12C>T",
          "hgvs_p": null,
          "transcript": "ENST00000865094.1",
          "protein_id": "ENSP00000535153.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 528,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1587,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000865094.1"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 15,
          "intron_rank": 1,
          "intron_rank_end": null,
          "gene_symbol": "OSBPL2",
          "gene_hgnc_id": 15761,
          "hgvs_c": "c.-243+12C>T",
          "hgvs_p": null,
          "transcript": "ENST00000643412.1",
          "protein_id": "ENSP00000494549.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 480,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1443,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000643412.1"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 15,
          "intron_rank": 1,
          "intron_rank_end": null,
          "gene_symbol": "OSBPL2",
          "gene_hgnc_id": 15761,
          "hgvs_c": "c.-526+12C>T",
          "hgvs_p": null,
          "transcript": "ENST00000865092.1",
          "protein_id": "ENSP00000535151.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 480,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1443,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000865092.1"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 16,
          "intron_rank": 1,
          "intron_rank_end": null,
          "gene_symbol": "OSBPL2",
          "gene_hgnc_id": 15761,
          "hgvs_c": "c.-633+12C>T",
          "hgvs_p": null,
          "transcript": "ENST00000958290.1",
          "protein_id": "ENSP00000628349.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 480,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1443,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000958290.1"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 14,
          "intron_rank": 1,
          "intron_rank_end": null,
          "gene_symbol": "OSBPL2",
          "gene_hgnc_id": 15761,
          "hgvs_c": "c.-129+12C>T",
          "hgvs_p": null,
          "transcript": "ENST00000865091.1",
          "protein_id": "ENSP00000535150.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 470,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1413,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000865091.1"
        },
        {
          "aa_ref": null,
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          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
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          "exon_count": 14,
          "intron_rank": 1,
          "intron_rank_end": null,
          "gene_symbol": "OSBPL2",
          "gene_hgnc_id": 15761,
          "hgvs_c": "c.-129+12C>T",
          "hgvs_p": null,
          "transcript": "NM_014835.5",
          "protein_id": "NP_055650.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 468,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1407,
          "cdna_start": null,
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          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_014835.5"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
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          ],
          "exon_rank": null,
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          "exon_count": 14,
          "intron_rank": 1,
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          "gene_symbol": "OSBPL2",
          "gene_hgnc_id": 15761,
          "hgvs_c": "c.-129+3246C>T",
          "hgvs_p": null,
          "transcript": "ENST00000958289.1",
          "protein_id": "ENSP00000628348.1",
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          "cds_start": null,
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          "cdna_start": null,
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          "biotype": "protein_coding",
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        },
        {
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          "consequences": [
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          "intron_rank": 1,
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          "gene_symbol": "OSBPL2",
          "gene_hgnc_id": 15761,
          "hgvs_c": "c.-129+12C>T",
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          "transcript": "ENST00000865093.1",
          "protein_id": "ENSP00000535152.1",
          "transcript_support_level": null,
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          "cds_start": null,
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          "cdna_start": null,
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          "biotype": "protein_coding",
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        },
        {
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          "canonical": false,
          "protein_coding": true,
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          ],
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          "exon_count": 13,
          "intron_rank": 1,
          "intron_rank_end": null,
          "gene_symbol": "OSBPL2",
          "gene_hgnc_id": 15761,
          "hgvs_c": "c.-60+12C>T",
          "hgvs_p": null,
          "transcript": "ENST00000644702.1",
          "protein_id": "ENSP00000494264.1",
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          "cds_start": null,
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        {
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          "gene_symbol": "OSBPL2",
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          "hgvs_c": "c.-129+12C>T",
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          "biotype": "protein_coding",
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        },
        {
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          "canonical": false,
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          "intron_rank": 1,
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          "gene_symbol": "OSBPL2",
          "gene_hgnc_id": 15761,
          "hgvs_c": "c.-185+12C>T",
          "hgvs_p": null,
          "transcript": "ENST00000644775.1",
          "protein_id": "ENSP00000495955.1",
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          "aa_length": 413,
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        {
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          "exon_count": 15,
          "intron_rank": 1,
          "intron_rank_end": null,
          "gene_symbol": "OSBPL2",
          "gene_hgnc_id": 15761,
          "hgvs_c": "c.-495+12C>T",
          "hgvs_p": null,
          "transcript": "NM_001363878.2",
          "protein_id": "NP_001350807.1",
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          "aa_length": 388,
          "cds_start": null,
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        {
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          "gene_symbol": "OSBPL2",
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          "transcript": "ENST00000645442.1",
          "protein_id": "ENSP00000494921.1",
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        },
        {
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          ],
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          "gene_symbol": "OSBPL2",
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          "hgvs_c": "c.-350+12C>T",
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          "transcript": "NM_001278649.3",
          "protein_id": "NP_001265578.1",
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          "biotype": "protein_coding",
          "feature": "NM_001278649.3"
        },
        {
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          "canonical": false,
          "protein_coding": true,
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          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
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          "exon_count": 13,
          "intron_rank": 1,
          "intron_rank_end": null,
          "gene_symbol": "OSBPL2",
          "gene_hgnc_id": 15761,
          "hgvs_c": "c.-405+12C>T",
          "hgvs_p": null,
          "transcript": "ENST00000439951.6",
          "protein_id": "ENSP00000397602.2",
          "transcript_support_level": 5,
          "aa_start": null,
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          "aa_length": 370,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1113,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000439951.6"
        },
        {
          "aa_ref": null,
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          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
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          "feature": "ENST00000646968.1"
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      ],
      "gene_symbol": "OSBPL2",
      "gene_hgnc_id": 15761,
      "dbsnp": "rs60622969",
      "frequency_reference_population": 0.3721766,
      "hom_count_reference_population": 11618,
      "allele_count_reference_population": 55100,
      "gnomad_exomes_af": 0.4,
      "gnomad_genomes_af": 0.372171,
      "gnomad_exomes_ac": 12,
      "gnomad_genomes_ac": 55088,
      "gnomad_exomes_homalt": 1,
      "gnomad_genomes_homalt": 11617,
      "gnomad_mito_homoplasmic": null,
      "gnomad_mito_heteroplasmic": null,
      "computational_score_selected": -0.75,
      "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": -0.75,
      "bayesdelnoaf_prediction": "Benign",
      "phylop100way_score": 0.362,
      "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": -20,
      "acmg_classification": "Benign",
      "acmg_criteria": "BP4_Strong,BP6_Very_Strong,BA1",
      "acmg_by_gene": [
        {
          "score": -20,
          "benign_score": 20,
          "pathogenic_score": 0,
          "criteria": [
            "BP4_Strong",
            "BP6_Very_Strong",
            "BA1"
          ],
          "verdict": "Benign",
          "transcript": "NM_144498.4",
          "gene_symbol": "OSBPL2",
          "hgnc_id": 15761,
          "effects": [
            "intron_variant"
          ],
          "inheritance_mode": "AD",
          "hgvs_c": "c.-129+12C>T",
          "hgvs_p": null
        }
      ],
      "clinvar_disease": "not provided,not specified",
      "clinvar_classification": "Benign",
      "clinvar_review_status": "criteria provided, multiple submitters, no conflicts",
      "clinvar_submissions_summary": "B:2",
      "phenotype_combined": "not specified|not provided",
      "pathogenicity_classification_combined": "Benign",
      "custom_annotations": null
    }
  ],
  "message": null
}