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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: 12-8930738-AGA-CGG (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=12&pos=8930738&ref=AGA&alt=CGG&genome=hg38&allGenes=true"

API Response

json
{
  "message": null,
  "variants": [
    {
      "acmg_by_gene": [
        {
          "benign_score": 0,
          "criteria": [],
          "effects": [
            "synonymous_variant"
          ],
          "gene_symbol": "PHC1",
          "hgnc_id": 3182,
          "hgvs_c": "c.916_918delAGAinsCGG",
          "hgvs_p": "p.307",
          "inheritance_mode": "AR",
          "pathogenic_score": 0,
          "score": 0,
          "transcript": "NM_004426.3",
          "verdict": "Uncertain_significance"
        }
      ],
      "acmg_classification": "Uncertain_significance",
      "acmg_criteria": "",
      "acmg_score": 0,
      "allele_count_reference_population": 0,
      "alphamissense_prediction": null,
      "alphamissense_score": null,
      "alt": "CGG",
      "apogee2_prediction": null,
      "apogee2_score": null,
      "bayesdelnoaf_prediction": null,
      "bayesdelnoaf_score": null,
      "chr": "12",
      "clinvar_classification": "",
      "clinvar_disease": "",
      "clinvar_review_status": "",
      "clinvar_submissions_summary": "",
      "computational_prediction_selected": null,
      "computational_score_selected": null,
      "computational_source_selected": null,
      "consequences": [
        {
          "aa_alt": "R",
          "aa_end": null,
          "aa_length": 1004,
          "aa_ref": "R",
          "aa_start": 306,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 5390,
          "cdna_start": 1283,
          "cds_end": null,
          "cds_length": 3015,
          "cds_start": 916,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 15,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "NM_004426.3",
          "gene_hgnc_id": 3182,
          "gene_symbol": "PHC1",
          "hgvs_c": "c.916_918delAGAinsCGG",
          "hgvs_p": "p.307",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": "ENST00000544916.6",
          "protein_coding": true,
          "protein_id": "NP_004417.2",
          "strand": true,
          "transcript": "NM_004426.3",
          "transcript_support_level": null
        },
        {
          "aa_alt": "R",
          "aa_end": null,
          "aa_length": 1004,
          "aa_ref": "R",
          "aa_start": 306,
          "biotype": "protein_coding",
          "canonical": true,
          "cdna_end": null,
          "cdna_length": 5390,
          "cdna_start": 1283,
          "cds_end": null,
          "cds_length": 3015,
          "cds_start": 916,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 15,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "ENST00000544916.6",
          "gene_hgnc_id": 3182,
          "gene_symbol": "PHC1",
          "hgvs_c": "c.916_918delAGAinsCGG",
          "hgvs_p": "p.307",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": "NM_004426.3",
          "protein_coding": true,
          "protein_id": "ENSP00000437659.1",
          "strand": true,
          "transcript": "ENST00000544916.6",
          "transcript_support_level": 1
        },
        {
          "aa_alt": "R",
          "aa_end": null,
          "aa_length": 1004,
          "aa_ref": "R",
          "aa_start": 306,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 4292,
          "cdna_start": 1248,
          "cds_end": null,
          "cds_length": 3015,
          "cds_start": 916,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 16,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "ENST00000543824.5",
          "gene_hgnc_id": 3182,
          "gene_symbol": "PHC1",
          "hgvs_c": "c.916_918delAGAinsCGG",
          "hgvs_p": "p.307",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000440674.1",
          "strand": true,
          "transcript": "ENST00000543824.5",
          "transcript_support_level": 1
        },
        {
          "aa_alt": "R",
          "aa_end": null,
          "aa_length": 959,
          "aa_ref": "R",
          "aa_start": 261,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 5033,
          "cdna_start": 926,
          "cds_end": null,
          "cds_length": 2880,
          "cds_start": 781,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 14,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "ENST00000433083.6",
          "gene_hgnc_id": 3182,
          "gene_symbol": "PHC1",
          "hgvs_c": "c.781_783delAGAinsCGG",
          "hgvs_p": "p.262",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000399194.2",
          "strand": true,
          "transcript": "ENST00000433083.6",
          "transcript_support_level": 1
        },
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": null,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "nonsense_mediated_decay",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 3869,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": null,
          "cds_start": null,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_count": 18,
          "exon_rank": 8,
          "exon_rank_end": null,
          "feature": "ENST00000540574.5",
          "gene_hgnc_id": 3182,
          "gene_symbol": "PHC1",
          "hgvs_c": "n.*285_*287delAGAinsCGG",
          "hgvs_p": null,
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": false,
          "protein_id": "ENSP00000444308.1",
          "strand": true,
          "transcript": "ENST00000540574.5",
          "transcript_support_level": 1
        },
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": null,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "nonsense_mediated_decay",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 3869,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": null,
          "cds_start": null,
          "consequences": [
            "3_prime_UTR_variant"
          ],
          "exon_count": 18,
          "exon_rank": 8,
          "exon_rank_end": null,
          "feature": "ENST00000540574.5",
          "gene_hgnc_id": 3182,
          "gene_symbol": "PHC1",
          "hgvs_c": "n.*285_*287delAGAinsCGG",
          "hgvs_p": null,
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": false,
          "protein_id": "ENSP00000444308.1",
          "strand": true,
          "transcript": "ENST00000540574.5",
          "transcript_support_level": 1
        },
        {
          "aa_alt": "R",
          "aa_end": null,
          "aa_length": 1010,
          "aa_ref": "R",
          "aa_start": 306,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 5400,
          "cdna_start": 1275,
          "cds_end": null,
          "cds_length": 3033,
          "cds_start": 916,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 15,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "ENST00000936637.1",
          "gene_hgnc_id": 3182,
          "gene_symbol": "PHC1",
          "hgvs_c": "c.916_918delAGAinsCGG",
          "hgvs_p": "p.307",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000606696.1",
          "strand": true,
          "transcript": "ENST00000936637.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "R",
          "aa_end": null,
          "aa_length": 1004,
          "aa_ref": "R",
          "aa_start": 306,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 5179,
          "cdna_start": 1072,
          "cds_end": null,
          "cds_length": 3015,
          "cds_start": 916,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 15,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "NM_001413738.1",
          "gene_hgnc_id": 3182,
          "gene_symbol": "PHC1",
          "hgvs_c": "c.916_918delAGAinsCGG",
          "hgvs_p": "p.307",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "NP_001400667.1",
          "strand": true,
          "transcript": "NM_001413738.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "R",
          "aa_end": null,
          "aa_length": 1004,
          "aa_ref": "R",
          "aa_start": 306,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 4288,
          "cdna_start": 1355,
          "cds_end": null,
          "cds_length": 3015,
          "cds_start": 916,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 14,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "ENST00000891310.1",
          "gene_hgnc_id": 3182,
          "gene_symbol": "PHC1",
          "hgvs_c": "c.916_918delAGAinsCGG",
          "hgvs_p": "p.307",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000561369.1",
          "strand": true,
          "transcript": "ENST00000891310.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "R",
          "aa_end": null,
          "aa_length": 1004,
          "aa_ref": "R",
          "aa_start": 306,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 5191,
          "cdna_start": 1084,
          "cds_end": null,
          "cds_length": 3015,
          "cds_start": 916,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 15,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "ENST00000936667.1",
          "gene_hgnc_id": 3182,
          "gene_symbol": "PHC1",
          "hgvs_c": "c.916_918delAGAinsCGG",
          "hgvs_p": "p.307",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000606726.1",
          "strand": true,
          "transcript": "ENST00000936667.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "R",
          "aa_end": null,
          "aa_length": 1004,
          "aa_ref": "R",
          "aa_start": 306,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 5361,
          "cdna_start": 1254,
          "cds_end": null,
          "cds_length": 3015,
          "cds_start": 916,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 15,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "ENST00000936668.1",
          "gene_hgnc_id": 3182,
          "gene_symbol": "PHC1",
          "hgvs_c": "c.916_918delAGAinsCGG",
          "hgvs_p": "p.307",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000606727.1",
          "strand": true,
          "transcript": "ENST00000936668.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "R",
          "aa_end": null,
          "aa_length": 1004,
          "aa_ref": "R",
          "aa_start": 306,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 5663,
          "cdna_start": 1556,
          "cds_end": null,
          "cds_length": 3015,
          "cds_start": 916,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 15,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "ENST00000936669.1",
          "gene_hgnc_id": 3182,
          "gene_symbol": "PHC1",
          "hgvs_c": "c.916_918delAGAinsCGG",
          "hgvs_p": "p.307",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000606728.1",
          "strand": true,
          "transcript": "ENST00000936669.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "R",
          "aa_end": null,
          "aa_length": 1004,
          "aa_ref": "R",
          "aa_start": 306,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 7023,
          "cdna_start": 2916,
          "cds_end": null,
          "cds_length": 3015,
          "cds_start": 916,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 15,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "ENST00000936671.1",
          "gene_hgnc_id": 3182,
          "gene_symbol": "PHC1",
          "hgvs_c": "c.916_918delAGAinsCGG",
          "hgvs_p": "p.307",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000606730.1",
          "strand": true,
          "transcript": "ENST00000936671.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "R",
          "aa_end": null,
          "aa_length": 1004,
          "aa_ref": "R",
          "aa_start": 306,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 6295,
          "cdna_start": 2188,
          "cds_end": null,
          "cds_length": 3015,
          "cds_start": 916,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 16,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "ENST00000936673.1",
          "gene_hgnc_id": 3182,
          "gene_symbol": "PHC1",
          "hgvs_c": "c.916_918delAGAinsCGG",
          "hgvs_p": "p.307",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000606732.1",
          "strand": true,
          "transcript": "ENST00000936673.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "R",
          "aa_end": null,
          "aa_length": 1004,
          "aa_ref": "R",
          "aa_start": 306,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 6168,
          "cdna_start": 2061,
          "cds_end": null,
          "cds_length": 3015,
          "cds_start": 916,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 15,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "ENST00000936675.1",
          "gene_hgnc_id": 3182,
          "gene_symbol": "PHC1",
          "hgvs_c": "c.916_918delAGAinsCGG",
          "hgvs_p": "p.307",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000606734.1",
          "strand": true,
          "transcript": "ENST00000936675.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "R",
          "aa_end": null,
          "aa_length": 1004,
          "aa_ref": "R",
          "aa_start": 306,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 5442,
          "cdna_start": 1335,
          "cds_end": null,
          "cds_length": 3015,
          "cds_start": 916,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 16,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "ENST00000936676.1",
          "gene_hgnc_id": 3182,
          "gene_symbol": "PHC1",
          "hgvs_c": "c.916_918delAGAinsCGG",
          "hgvs_p": "p.307",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000606735.1",
          "strand": true,
          "transcript": "ENST00000936676.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "R",
          "aa_end": null,
          "aa_length": 1002,
          "aa_ref": "R",
          "aa_start": 304,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 5384,
          "cdna_start": 1277,
          "cds_end": null,
          "cds_length": 3009,
          "cds_start": 910,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 15,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "NM_001413739.1",
          "gene_hgnc_id": 3182,
          "gene_symbol": "PHC1",
          "hgvs_c": "c.910_912delAGAinsCGG",
          "hgvs_p": "p.305",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "NP_001400668.1",
          "strand": true,
          "transcript": "NM_001413739.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "R",
          "aa_end": null,
          "aa_length": 1002,
          "aa_ref": "R",
          "aa_start": 298,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 5357,
          "cdna_start": 1232,
          "cds_end": null,
          "cds_length": 3009,
          "cds_start": 892,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 15,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "ENST00000936645.1",
          "gene_hgnc_id": 3182,
          "gene_symbol": "PHC1",
          "hgvs_c": "c.892_894delAGAinsCGG",
          "hgvs_p": "p.299",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000606704.1",
          "strand": true,
          "transcript": "ENST00000936645.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "R",
          "aa_end": null,
          "aa_length": 1002,
          "aa_ref": "R",
          "aa_start": 304,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 5356,
          "cdna_start": 1249,
          "cds_end": null,
          "cds_length": 3009,
          "cds_start": 910,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 15,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "ENST00000936646.1",
          "gene_hgnc_id": 3182,
          "gene_symbol": "PHC1",
          "hgvs_c": "c.910_912delAGAinsCGG",
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For research and educational, non-commercial use only. Not for clinical or diagnostic use. GeneBe does not provide medical advice. Data use for AI modeling is prohibited: if used, the cost is $0.001 per byte of downloaded uncompressed data.