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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: 16-723892-G-A (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=16&pos=723892&ref=G&alt=A&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "16",
      "pos": 723892,
      "ref": "G",
      "alt": "A",
      "effect": "synonymous_variant",
      "transcript": "ENST00000345165.10",
      "consequences": [
        {
          "aa_ref": "P",
          "aa_alt": "P",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 11,
          "exon_rank_end": null,
          "exon_count": 14,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CCDC78",
          "gene_hgnc_id": 14153,
          "hgvs_c": "c.1098C>T",
          "hgvs_p": "p.Pro366Pro",
          "transcript": "NM_001378030.1",
          "protein_id": "NP_001364959.1",
          "transcript_support_level": null,
          "aa_start": 366,
          "aa_end": null,
          "aa_length": 470,
          "cds_start": 1098,
          "cds_end": null,
          "cds_length": 1413,
          "cdna_start": 1174,
          "cdna_end": null,
          "cdna_length": 1585,
          "mane_select": "ENST00000345165.10",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "P",
          "aa_alt": "P",
          "canonical": true,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 11,
          "exon_rank_end": null,
          "exon_count": 14,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CCDC78",
          "gene_hgnc_id": 14153,
          "hgvs_c": "c.1098C>T",
          "hgvs_p": "p.Pro366Pro",
          "transcript": "ENST00000345165.10",
          "protein_id": "ENSP00000316851.5",
          "transcript_support_level": 5,
          "aa_start": 366,
          "aa_end": null,
          "aa_length": 470,
          "cds_start": 1098,
          "cds_end": null,
          "cds_length": 1413,
          "cdna_start": 1174,
          "cdna_end": null,
          "cdna_length": 1585,
          "mane_select": "NM_001378030.1",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "P",
          "aa_alt": "P",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 11,
          "exon_rank_end": null,
          "exon_count": 14,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CCDC78",
          "gene_hgnc_id": 14153,
          "hgvs_c": "c.1098C>T",
          "hgvs_p": "p.Pro366Pro",
          "transcript": "ENST00000293889.10",
          "protein_id": "ENSP00000293889.6",
          "transcript_support_level": 1,
          "aa_start": 366,
          "aa_end": null,
          "aa_length": 438,
          "cds_start": 1098,
          "cds_end": null,
          "cds_length": 1317,
          "cdna_start": 1204,
          "cdna_end": null,
          "cdna_length": 1611,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "P",
          "aa_alt": "P",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 11,
          "exon_rank_end": null,
          "exon_count": 14,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CCDC78",
          "gene_hgnc_id": 14153,
          "hgvs_c": "c.1098C>T",
          "hgvs_p": "p.Pro366Pro",
          "transcript": "NM_001031737.3",
          "protein_id": "NP_001026907.2",
          "transcript_support_level": null,
          "aa_start": 366,
          "aa_end": null,
          "aa_length": 438,
          "cds_start": 1098,
          "cds_end": null,
          "cds_length": 1317,
          "cdna_start": 1174,
          "cdna_end": null,
          "cdna_length": 1581,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "P",
          "aa_alt": "P",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 7,
          "exon_rank_end": null,
          "exon_count": 10,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CCDC78",
          "gene_hgnc_id": 14153,
          "hgvs_c": "c.531C>T",
          "hgvs_p": "p.Pro177Pro",
          "transcript": "NM_001378033.1",
          "protein_id": "NP_001364962.1",
          "transcript_support_level": null,
          "aa_start": 177,
          "aa_end": null,
          "aa_length": 281,
          "cds_start": 531,
          "cds_end": null,
          "cds_length": 846,
          "cdna_start": 848,
          "cdna_end": null,
          "cdna_length": 1259,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "P",
          "aa_alt": "P",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 7,
          "exon_rank_end": null,
          "exon_count": 9,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CCDC78",
          "gene_hgnc_id": 14153,
          "hgvs_c": "c.1545C>T",
          "hgvs_p": "p.Pro515Pro",
          "transcript": "XM_011522356.2",
          "protein_id": "XP_011520658.1",
          "transcript_support_level": null,
          "aa_start": 515,
          "aa_end": null,
          "aa_length": 643,
          "cds_start": 1545,
          "cds_end": null,
          "cds_length": 1932,
          "cdna_start": 1621,
          "cdna_end": null,
          "cdna_length": 2104,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "P",
          "aa_alt": "P",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 9,
          "exon_rank_end": null,
          "exon_count": 11,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CCDC78",
          "gene_hgnc_id": 14153,
          "hgvs_c": "c.1533C>T",
          "hgvs_p": "p.Pro511Pro",
          "transcript": "XM_011522357.2",
          "protein_id": "XP_011520659.1",
          "transcript_support_level": null,
          "aa_start": 511,
          "aa_end": null,
          "aa_length": 639,
          "cds_start": 1533,
          "cds_end": null,
          "cds_length": 1920,
          "cdna_start": 1609,
          "cdna_end": null,
          "cdna_length": 2092,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "P",
          "aa_alt": "P",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 7,
          "exon_rank_end": null,
          "exon_count": 9,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CCDC78",
          "gene_hgnc_id": 14153,
          "hgvs_c": "c.1545C>T",
          "hgvs_p": "p.Pro515Pro",
          "transcript": "XM_011522358.3",
          "protein_id": "XP_011520660.1",
          "transcript_support_level": null,
          "aa_start": 515,
          "aa_end": null,
          "aa_length": 635,
          "cds_start": 1545,
          "cds_end": null,
          "cds_length": 1908,
          "cdna_start": 1621,
          "cdna_end": null,
          "cdna_length": 2080,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "P",
          "aa_alt": "P",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 7,
          "exon_rank_end": null,
          "exon_count": 9,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CCDC78",
          "gene_hgnc_id": 14153,
          "hgvs_c": "c.1512C>T",
          "hgvs_p": "p.Pro504Pro",
          "transcript": "XM_011522359.2",
          "protein_id": "XP_011520661.1",
          "transcript_support_level": null,
          "aa_start": 504,
          "aa_end": null,
          "aa_length": 632,
          "cds_start": 1512,
          "cds_end": null,
          "cds_length": 1899,
          "cdna_start": 1588,
          "cdna_end": null,
          "cdna_length": 2071,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "P",
          "aa_alt": "P",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 9,
          "exon_rank_end": null,
          "exon_count": 11,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CCDC78",
          "gene_hgnc_id": 14153,
          "hgvs_c": "c.1500C>T",
          "hgvs_p": "p.Pro500Pro",
          "transcript": "XM_011522360.2",
          "protein_id": "XP_011520662.1",
          "transcript_support_level": null,
          "aa_start": 500,
          "aa_end": null,
          "aa_length": 628,
          "cds_start": 1500,
          "cds_end": null,
          "cds_length": 1887,
          "cdna_start": 1576,
          "cdna_end": null,
          "cdna_length": 2059,
          "mane_select": null,
          "mane_plus": null,
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        },
        {
          "aa_ref": "P",
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          "protein_coding": true,
          "strand": false,
          "consequences": [
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          ],
          "exon_rank": 7,
          "exon_rank_end": null,
          "exon_count": 10,
          "intron_rank": null,
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          "gene_symbol": "CCDC78",
          "gene_hgnc_id": 14153,
          "hgvs_c": "c.1545C>T",
          "hgvs_p": "p.Pro515Pro",
          "transcript": "XM_011522361.2",
          "protein_id": "XP_011520663.1",
          "transcript_support_level": null,
          "aa_start": 515,
          "aa_end": null,
          "aa_length": 619,
          "cds_start": 1545,
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          "cdna_start": 1621,
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          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "P",
          "aa_alt": "P",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 7,
          "exon_rank_end": null,
          "exon_count": 10,
          "intron_rank": null,
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          "gene_symbol": "CCDC78",
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          "hgvs_c": "c.1545C>T",
          "hgvs_p": "p.Pro515Pro",
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        {
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          "strand": false,
          "consequences": [
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          ],
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          "intron_rank": null,
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          "gene_symbol": "CCDC78",
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          "hgvs_c": "c.1545C>T",
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          "transcript": "XM_011522362.2",
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        {
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          "protein_coding": true,
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          ],
          "exon_rank": 7,
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          "gene_symbol": "CCDC78",
          "gene_hgnc_id": 14153,
          "hgvs_c": "c.1545C>T",
          "hgvs_p": "p.Pro515Pro",
          "transcript": "XM_011522363.2",
          "protein_id": "XP_011520665.1",
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        {
          "aa_ref": "P",
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          ],
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        {
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          "protein_coding": true,
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          ],
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          "intron_rank": null,
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          "gene_symbol": "CCDC78",
          "gene_hgnc_id": 14153,
          "hgvs_c": "c.1332C>T",
          "hgvs_p": "p.Pro444Pro",
          "transcript": "XM_011522365.2",
          "protein_id": "XP_011520667.1",
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        {
          "aa_ref": "P",
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          "canonical": false,
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          "strand": false,
          "consequences": [
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          ],
          "exon_rank": 8,
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          "intron_rank": null,
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          "gene_symbol": "CCDC78",
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          "hgvs_c": "c.1323C>T",
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          "transcript": "XM_011522366.2",
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        {
          "aa_ref": "P",
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        {
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          "gene_symbol": "CCDC78",
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          "hgvs_c": "c.1320C>T",
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        },
        {
          "aa_ref": "P",
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          "protein_coding": true,
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          "consequences": [
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          ],
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          "intron_rank": null,
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          "gene_symbol": "CCDC78",
          "gene_hgnc_id": 14153,
          "hgvs_c": "c.1164C>T",
          "hgvs_p": "p.Pro388Pro",
          "transcript": "XM_011522367.2",
          "protein_id": "XP_011520669.1",
          "transcript_support_level": null,
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          "cdna_start": 1240,
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          "mane_select": null,
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          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "P",
          "aa_alt": "P",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 9,
          "exon_rank_end": null,
          "exon_count": 11,
          "intron_rank": null,
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          "gene_symbol": "CCDC78",
          "gene_hgnc_id": 14153,
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      "gnomad_genomes_af": 0.000997781,
      "gnomad_exomes_ac": 1548,
      "gnomad_genomes_ac": 152,
      "gnomad_exomes_homalt": 3,
      "gnomad_genomes_homalt": 1,
      "gnomad_mito_homoplasmic": null,
      "gnomad_mito_heteroplasmic": null,
      "computational_score_selected": 0.028999999165534973,
      "computational_prediction_selected": "Benign",
      "computational_source_selected": "REVEL",
      "splice_score_selected": 0.07999999821186066,
      "splice_prediction_selected": "Benign",
      "splice_source_selected": "max_spliceai",
      "revel_score": 0.029,
      "revel_prediction": "Benign",
      "alphamissense_score": null,
      "alphamissense_prediction": null,
      "bayesdelnoaf_score": -0.88,
      "bayesdelnoaf_prediction": "Benign",
      "phylop100way_score": -0.441,
      "phylop100way_prediction": "Benign",
      "spliceai_max_score": 0.08,
      "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": -9,
      "acmg_classification": "Benign",
      "acmg_criteria": "BP4_Moderate,BP6_Moderate,BP7,BS2",
      "acmg_by_gene": [
        {
          "score": -9,
          "benign_score": 9,
          "pathogenic_score": 0,
          "criteria": [
            "BP4_Moderate",
            "BP6_Moderate",
            "BP7",
            "BS2"
          ],
          "verdict": "Benign",
          "transcript": "ENST00000345165.10",
          "gene_symbol": "CCDC78",
          "hgnc_id": 14153,
          "effects": [
            "synonymous_variant"
          ],
          "inheritance_mode": "AD",
          "hgvs_c": "c.1098C>T",
          "hgvs_p": "p.Pro366Pro"
        }
      ],
      "clinvar_disease": "Congenital myopathy with internal nuclei and atypical cores",
      "clinvar_classification": "Benign",
      "clinvar_review_status": "criteria provided, single submitter",
      "clinvar_submissions_summary": "B:1",
      "phenotype_combined": "Congenital myopathy with internal nuclei and atypical cores",
      "pathogenicity_classification_combined": "Benign",
      "custom_annotations": null
    }
  ],
  "message": null
}