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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: 8-139985033-G-C (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=8&pos=139985033&ref=G&alt=C&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "8",
      "pos": 139985033,
      "ref": "G",
      "alt": "C",
      "effect": "intron_variant",
      "transcript": "ENST00000438773.4",
      "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": 23,
          "intron_rank": 19,
          "intron_rank_end": null,
          "gene_symbol": "TRAPPC9",
          "gene_hgnc_id": 30832,
          "hgvs_c": "c.2810+3693C>G",
          "hgvs_p": null,
          "transcript": "NM_001160372.4",
          "protein_id": "NP_001153844.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1148,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 3447,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 6899,
          "mane_select": "ENST00000438773.4",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "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": 23,
          "intron_rank": 19,
          "intron_rank_end": null,
          "gene_symbol": "TRAPPC9",
          "gene_hgnc_id": 30832,
          "hgvs_c": "c.2810+3693C>G",
          "hgvs_p": null,
          "transcript": "ENST00000438773.4",
          "protein_id": "ENSP00000405060.3",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1148,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 3447,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 6899,
          "mane_select": "NM_001160372.4",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "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": 21,
          "intron_rank": 17,
          "intron_rank_end": null,
          "gene_symbol": "TRAPPC9",
          "gene_hgnc_id": 30832,
          "hgvs_c": "c.2339+3693C>G",
          "hgvs_p": null,
          "transcript": "ENST00000520857.5",
          "protein_id": "ENSP00000430116.1",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 991,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 2976,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 3693,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 12,
          "intron_rank": 8,
          "intron_rank_end": null,
          "gene_symbol": "TRAPPC9",
          "gene_hgnc_id": 30832,
          "hgvs_c": "n.1215+3693C>G",
          "hgvs_p": null,
          "transcript": "ENST00000521667.5",
          "protein_id": null,
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": null,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": null,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 2021,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "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": 24,
          "intron_rank": 20,
          "intron_rank_end": null,
          "gene_symbol": "TRAPPC9",
          "gene_hgnc_id": 30832,
          "hgvs_c": "c.2831+3693C>G",
          "hgvs_p": null,
          "transcript": "NM_001374682.1",
          "protein_id": "NP_001361611.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1155,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 3468,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 6920,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "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": 23,
          "intron_rank": 19,
          "intron_rank_end": null,
          "gene_symbol": "TRAPPC9",
          "gene_hgnc_id": 30832,
          "hgvs_c": "c.2810+3693C>G",
          "hgvs_p": null,
          "transcript": "NM_031466.8",
          "protein_id": "NP_113654.5",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1148,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 3447,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 7092,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "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": 23,
          "intron_rank": 19,
          "intron_rank_end": null,
          "gene_symbol": "TRAPPC9",
          "gene_hgnc_id": 30832,
          "hgvs_c": "c.2810+3693C>G",
          "hgvs_p": null,
          "transcript": "ENST00000648948.2",
          "protein_id": "ENSP00000498020.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1148,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 3447,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 7092,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "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": 22,
          "intron_rank": 18,
          "intron_rank_end": null,
          "gene_symbol": "TRAPPC9",
          "gene_hgnc_id": 30832,
          "hgvs_c": "c.2783+3693C>G",
          "hgvs_p": null,
          "transcript": "NM_001321646.2",
          "protein_id": "NP_001308575.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1139,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 3420,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 6872,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "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": 22,
          "intron_rank": 18,
          "intron_rank_end": null,
          "gene_symbol": "TRAPPC9",
          "gene_hgnc_id": 30832,
          "hgvs_c": "c.2699+38904C>G",
          "hgvs_p": null,
          "transcript": "NM_001374683.1",
          "protein_id": "NP_001361612.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1111,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 3336,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 6788,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "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": 22,
          "intron_rank": 18,
          "intron_rank_end": null,
          "gene_symbol": "TRAPPC9",
          "gene_hgnc_id": 30832,
          "hgvs_c": "c.2666+3693C>G",
          "hgvs_p": null,
          "transcript": "NM_001374684.1",
          "protein_id": "NP_001361613.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1100,
          "cds_start": -4,
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          "cds_length": 3303,
          "cdna_start": null,
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          "cdna_length": 6755,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
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          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
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          ],
          "exon_rank": null,
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          "exon_count": 6,
          "intron_rank": 3,
          "intron_rank_end": null,
          "gene_symbol": "TRAPPC9",
          "gene_hgnc_id": 30832,
          "hgvs_c": "n.419+3693C>G",
          "hgvs_p": null,
          "transcript": "ENST00000523777.5",
          "protein_id": null,
          "transcript_support_level": 3,
          "aa_start": null,
          "aa_end": null,
          "aa_length": null,
          "cds_start": -4,
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          "cds_length": null,
          "cdna_start": null,
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          "cdna_length": 705,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
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          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
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          ],
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          "exon_count": 5,
          "intron_rank": 2,
          "intron_rank_end": null,
          "gene_symbol": "TRAPPC9",
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          "hgvs_c": "n.236+3693C>G",
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          "transcript": "ENST00000524162.5",
          "protein_id": null,
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        },
        {
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          "consequences": [
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          "intron_rank": 18,
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          "gene_symbol": "TRAPPC9",
          "gene_hgnc_id": 30832,
          "hgvs_c": "n.2899+3693C>G",
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        {
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          "intron_rank": 18,
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          "gene_symbol": "TRAPPC9",
          "gene_hgnc_id": 30832,
          "hgvs_c": "c.3077+3693C>G",
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          "transcript": "XM_011517326.3",
          "protein_id": "XP_011515628.1",
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          "mane_select": null,
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        {
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          "intron_rank": 19,
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          "gene_symbol": "TRAPPC9",
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        {
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          "gene_symbol": "TRAPPC9",
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          "gene_symbol": "TRAPPC9",
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          "hgvs_c": "c.2783+3693C>G",
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          "gene_symbol": "TRAPPC9",
          "gene_hgnc_id": 30832,
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          "protein_id": "XP_016869383.1",
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        },
        {
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          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
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          "exon_count": 15,
          "intron_rank": 11,
          "intron_rank_end": null,
          "gene_symbol": "TRAPPC9",
          "gene_hgnc_id": 30832,
          "hgvs_c": "c.1259+3693C>G",
          "hgvs_p": null,
          "transcript": "XM_011517330.3",
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          "cds_start": -4,
          "cds_end": null,
          "cds_length": 1896,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 5456,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        }
      ],
      "gene_symbol": "TRAPPC9",
      "gene_hgnc_id": 30832,
      "dbsnp": "rs1870805",
      "frequency_reference_population": null,
      "hom_count_reference_population": 0,
      "allele_count_reference_population": 0,
      "gnomad_exomes_af": null,
      "gnomad_genomes_af": null,
      "gnomad_exomes_ac": null,
      "gnomad_genomes_ac": null,
      "gnomad_exomes_homalt": null,
      "gnomad_genomes_homalt": null,
      "gnomad_mito_homoplasmic": null,
      "gnomad_mito_heteroplasmic": null,
      "computational_score_selected": -0.8899999856948853,
      "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": -0.89,
      "bayesdelnoaf_prediction": "Benign",
      "phylop100way_score": 0.843,
      "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": -2,
      "acmg_classification": "Likely_benign",
      "acmg_criteria": "PM2,BP4_Strong",
      "acmg_by_gene": [
        {
          "score": -2,
          "benign_score": 4,
          "pathogenic_score": 2,
          "criteria": [
            "PM2",
            "BP4_Strong"
          ],
          "verdict": "Likely_benign",
          "transcript": "ENST00000438773.4",
          "gene_symbol": "TRAPPC9",
          "hgnc_id": 30832,
          "effects": [
            "intron_variant"
          ],
          "inheritance_mode": "AR",
          "hgvs_c": "c.2810+3693C>G",
          "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
}