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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: 10-77838130-A-G (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=10&pos=77838130&ref=A&alt=G&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "10",
      "pos": 77838130,
      "ref": "A",
      "alt": "G",
      "effect": "intron_variant",
      "transcript": "NM_004747.4",
      "consequences": [
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 32,
          "intron_rank": 7,
          "intron_rank_end": null,
          "gene_symbol": "DLG5",
          "gene_hgnc_id": 2904,
          "hgvs_c": "c.1438-2208T>C",
          "hgvs_p": null,
          "transcript": "NM_004747.4",
          "protein_id": "NP_004738.3",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1919,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 5760,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": "ENST00000372391.7",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_004747.4"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": true,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 32,
          "intron_rank": 7,
          "intron_rank_end": null,
          "gene_symbol": "DLG5",
          "gene_hgnc_id": 2904,
          "hgvs_c": "c.1438-2208T>C",
          "hgvs_p": null,
          "transcript": "ENST00000372391.7",
          "protein_id": "ENSP00000361467.2",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1919,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 5760,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": "NM_004747.4",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000372391.7"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 32,
          "intron_rank": 7,
          "intron_rank_end": null,
          "gene_symbol": "DLG5",
          "gene_hgnc_id": 2904,
          "hgvs_c": "c.1426-2208T>C",
          "hgvs_p": null,
          "transcript": "ENST00000928380.1",
          "protein_id": "ENSP00000598439.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1915,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 5748,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000928380.1"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 31,
          "intron_rank": 7,
          "intron_rank_end": null,
          "gene_symbol": "DLG5",
          "gene_hgnc_id": 2904,
          "hgvs_c": "c.1438-2208T>C",
          "hgvs_p": null,
          "transcript": "ENST00000928379.1",
          "protein_id": "ENSP00000598438.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1888,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 5667,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000928379.1"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 30,
          "intron_rank": 7,
          "intron_rank_end": null,
          "gene_symbol": "DLG5",
          "gene_hgnc_id": 2904,
          "hgvs_c": "c.1438-2208T>C",
          "hgvs_p": null,
          "transcript": "ENST00000962015.1",
          "protein_id": "ENSP00000632074.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1548,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 4647,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000962015.1"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 32,
          "intron_rank": 7,
          "intron_rank_end": null,
          "gene_symbol": "DLG5",
          "gene_hgnc_id": 2904,
          "hgvs_c": "c.1426-2208T>C",
          "hgvs_p": null,
          "transcript": "XM_005270276.5",
          "protein_id": "XP_005270333.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1915,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 5748,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "XM_005270276.5"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 32,
          "intron_rank": 7,
          "intron_rank_end": null,
          "gene_symbol": "DLG5",
          "gene_hgnc_id": 2904,
          "hgvs_c": "c.1261-2208T>C",
          "hgvs_p": null,
          "transcript": "XM_011540341.4",
          "protein_id": "XP_011538643.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1860,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 5583,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "XM_011540341.4"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 32,
          "intron_rank": 7,
          "intron_rank_end": null,
          "gene_symbol": "DLG5",
          "gene_hgnc_id": 2904,
          "hgvs_c": "c.1168-2208T>C",
          "hgvs_p": null,
          "transcript": "XM_011540342.2",
          "protein_id": "XP_011538644.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1829,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 5490,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "XM_011540342.2"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
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          "exon_count": 32,
          "intron_rank": 7,
          "intron_rank_end": null,
          "gene_symbol": "DLG5",
          "gene_hgnc_id": 2904,
          "hgvs_c": "c.1156-2208T>C",
          "hgvs_p": null,
          "transcript": "XM_017016913.2",
          "protein_id": "XP_016872402.1",
          "transcript_support_level": null,
          "aa_start": null,
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          "aa_length": 1825,
          "cds_start": null,
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          "cds_length": 5478,
          "cdna_start": null,
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          "mane_select": null,
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          "biotype": "protein_coding",
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        },
        {
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          "canonical": false,
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          "strand": false,
          "consequences": [
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          ],
          "exon_rank": null,
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          "exon_count": 32,
          "intron_rank": 7,
          "intron_rank_end": null,
          "gene_symbol": "DLG5",
          "gene_hgnc_id": 2904,
          "hgvs_c": "c.1108-2208T>C",
          "hgvs_p": null,
          "transcript": "XM_017016914.2",
          "protein_id": "XP_016872403.1",
          "transcript_support_level": null,
          "aa_start": null,
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          "aa_length": 1809,
          "cds_start": null,
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          "cdna_start": null,
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        {
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          "intron_rank": 7,
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          "gene_symbol": "DLG5",
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          "hgvs_c": "c.1108-2208T>C",
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          "transcript": "XM_047425998.1",
          "protein_id": "XP_047281954.1",
          "transcript_support_level": null,
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          "cds_start": null,
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        {
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        {
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          "gene_symbol": "DLG5",
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        {
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          "intron_rank": 7,
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          "gene_symbol": "DLG5",
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          "gene_symbol": "DLG5",
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          "hgvs_c": "c.1438-2208T>C",
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          "transcript": "XM_047426002.1",
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        {
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          "biotype": "retained_intron",
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      ],
      "gene_symbol": "DLG5",
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      "dbsnp": "rs1270912",
      "frequency_reference_population": 0.7294359,
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      "gnomad_exomes_af": null,
      "gnomad_genomes_af": 0.729436,
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      "gnomad_genomes_ac": 110972,
      "gnomad_exomes_homalt": null,
      "gnomad_genomes_homalt": 41186,
      "gnomad_mito_homoplasmic": null,
      "gnomad_mito_heteroplasmic": null,
      "computational_score_selected": -0.8299999833106995,
      "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": -0.83,
      "bayesdelnoaf_prediction": "Benign",
      "phylop100way_score": -1.174,
      "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": -12,
      "acmg_classification": "Benign",
      "acmg_criteria": "BP4_Strong,BA1",
      "acmg_by_gene": [
        {
          "score": -12,
          "benign_score": 12,
          "pathogenic_score": 0,
          "criteria": [
            "BP4_Strong",
            "BA1"
          ],
          "verdict": "Benign",
          "transcript": "NM_004747.4",
          "gene_symbol": "DLG5",
          "hgnc_id": 2904,
          "effects": [
            "intron_variant"
          ],
          "inheritance_mode": "AD,AR",
          "hgvs_c": "c.1438-2208T>C",
          "hgvs_p": null
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      ],
      "clinvar_disease": "",
      "clinvar_classification": "",
      "clinvar_review_status": "",
      "clinvar_submissions_summary": "",
      "phenotype_combined": null,
      "pathogenicity_classification_combined": null,
      "custom_annotations": null
    }
  ],
  "message": null
}