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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: 16-56499883-CGA-GCT (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=16&pos=56499883&ref=CGA&alt=GCT&genome=hg38&allGenes=true"

API Response

json
{
  "message": null,
  "variants": [
    {
      "acmg_by_gene": [
        {
          "benign_score": 0,
          "criteria": [],
          "effects": [
            "synonymous_variant"
          ],
          "gene_symbol": "BBS2",
          "hgnc_id": 967,
          "hgvs_c": "c.1420_1422delTCGinsAGC",
          "hgvs_p": "p.475",
          "inheritance_mode": "AR,AD",
          "pathogenic_score": 0,
          "score": 0,
          "transcript": "NM_031885.5",
          "verdict": "Uncertain_significance"
        },
        {
          "benign_score": 0,
          "criteria": [],
          "effects": [
            "non_coding_transcript_exon_variant"
          ],
          "gene_symbol": "ENSG00000288725",
          "hgnc_id": null,
          "hgvs_c": "n.340_342delTCGinsAGC",
          "hgvs_p": null,
          "inheritance_mode": "",
          "pathogenic_score": 0,
          "score": 0,
          "transcript": "ENST00000684388.1",
          "verdict": "Uncertain_significance"
        }
      ],
      "acmg_classification": "Uncertain_significance",
      "acmg_criteria": "",
      "acmg_score": 0,
      "allele_count_reference_population": 0,
      "alphamissense_prediction": null,
      "alphamissense_score": null,
      "alt": "GCT",
      "apogee2_prediction": null,
      "apogee2_score": null,
      "bayesdelnoaf_prediction": null,
      "bayesdelnoaf_score": null,
      "chr": "16",
      "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": "S",
          "aa_end": null,
          "aa_length": 721,
          "aa_ref": "S",
          "aa_start": 474,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 2704,
          "cdna_start": 1584,
          "cds_end": null,
          "cds_length": 2166,
          "cds_start": 1420,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 17,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "NM_031885.5",
          "gene_hgnc_id": 967,
          "gene_symbol": "BBS2",
          "hgvs_c": "c.1420_1422delTCGinsAGC",
          "hgvs_p": "p.475",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": "ENST00000245157.11",
          "protein_coding": true,
          "protein_id": "NP_114091.4",
          "strand": false,
          "transcript": "NM_031885.5",
          "transcript_support_level": null
        },
        {
          "aa_alt": "S",
          "aa_end": null,
          "aa_length": 721,
          "aa_ref": "S",
          "aa_start": 474,
          "biotype": "protein_coding",
          "canonical": true,
          "cdna_end": null,
          "cdna_length": 2704,
          "cdna_start": 1584,
          "cds_end": null,
          "cds_length": 2166,
          "cds_start": 1420,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 17,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "ENST00000245157.11",
          "gene_hgnc_id": 967,
          "gene_symbol": "BBS2",
          "hgvs_c": "c.1420_1422delTCGinsAGC",
          "hgvs_p": "p.475",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": "NM_031885.5",
          "protein_coding": true,
          "protein_id": "ENSP00000245157.5",
          "strand": false,
          "transcript": "ENST00000245157.11",
          "transcript_support_level": 1
        },
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": null,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "retained_intron",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 6109,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": null,
          "cds_start": null,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_count": 12,
          "exon_rank": 8,
          "exon_rank_end": null,
          "feature": "ENST00000565781.6",
          "gene_hgnc_id": 967,
          "gene_symbol": "BBS2",
          "hgvs_c": "n.3742_3744delTCGinsAGC",
          "hgvs_p": null,
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": false,
          "protein_id": null,
          "strand": false,
          "transcript": "ENST00000565781.6",
          "transcript_support_level": 1
        },
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": null,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "nonsense_mediated_decay",
          "canonical": true,
          "cdna_end": null,
          "cdna_length": 3810,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": null,
          "cds_start": null,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_count": 14,
          "exon_rank": 3,
          "exon_rank_end": null,
          "feature": "ENST00000684388.1",
          "gene_hgnc_id": null,
          "gene_symbol": "ENSG00000288725",
          "hgvs_c": "n.340_342delTCGinsAGC",
          "hgvs_p": null,
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": false,
          "protein_id": "ENSP00000507647.1",
          "strand": false,
          "transcript": "ENST00000684388.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "S",
          "aa_end": null,
          "aa_length": 736,
          "aa_ref": "S",
          "aa_start": 474,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 2828,
          "cdna_start": 1635,
          "cds_end": null,
          "cds_length": 2211,
          "cds_start": 1420,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 17,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "ENST00000682188.1",
          "gene_hgnc_id": 967,
          "gene_symbol": "BBS2",
          "hgvs_c": "c.1420_1422delTCGinsAGC",
          "hgvs_p": "p.475",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000507655.1",
          "strand": false,
          "transcript": "ENST00000682188.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "S",
          "aa_end": null,
          "aa_length": 721,
          "aa_ref": "S",
          "aa_start": 474,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 2540,
          "cdna_start": 1584,
          "cds_end": null,
          "cds_length": 2166,
          "cds_start": 1420,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 18,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "NM_001377456.1",
          "gene_hgnc_id": 967,
          "gene_symbol": "BBS2",
          "hgvs_c": "c.1420_1422delTCGinsAGC",
          "hgvs_p": "p.475",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "NP_001364385.1",
          "strand": false,
          "transcript": "NM_001377456.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "S",
          "aa_end": null,
          "aa_length": 721,
          "aa_ref": "S",
          "aa_start": 474,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 2572,
          "cdna_start": 1563,
          "cds_end": null,
          "cds_length": 2166,
          "cds_start": 1420,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 18,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "ENST00000682047.1",
          "gene_hgnc_id": 967,
          "gene_symbol": "BBS2",
          "hgvs_c": "c.1420_1422delTCGinsAGC",
          "hgvs_p": "p.475",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000507699.1",
          "strand": false,
          "transcript": "ENST00000682047.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "S",
          "aa_end": null,
          "aa_length": 721,
          "aa_ref": "S",
          "aa_start": 474,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 2935,
          "cdna_start": 1584,
          "cds_end": null,
          "cds_length": 2166,
          "cds_start": 1420,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 18,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "ENST00000682205.1",
          "gene_hgnc_id": 967,
          "gene_symbol": "BBS2",
          "hgvs_c": "c.1420_1422delTCGinsAGC",
          "hgvs_p": "p.475",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000508377.1",
          "strand": false,
          "transcript": "ENST00000682205.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "S",
          "aa_end": null,
          "aa_length": 721,
          "aa_ref": "S",
          "aa_start": 474,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 3688,
          "cdna_start": 1609,
          "cds_end": null,
          "cds_length": 2166,
          "cds_start": 1420,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 18,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "ENST00000682470.1",
          "gene_hgnc_id": 967,
          "gene_symbol": "BBS2",
          "hgvs_c": "c.1420_1422delTCGinsAGC",
          "hgvs_p": "p.475",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000507654.1",
          "strand": false,
          "transcript": "ENST00000682470.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "S",
          "aa_end": null,
          "aa_length": 721,
          "aa_ref": "S",
          "aa_start": 474,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 2540,
          "cdna_start": 1584,
          "cds_end": null,
          "cds_length": 2166,
          "cds_start": 1420,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 18,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "ENST00000682855.1",
          "gene_hgnc_id": 967,
          "gene_symbol": "BBS2",
          "hgvs_c": "c.1420_1422delTCGinsAGC",
          "hgvs_p": "p.475",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000507027.1",
          "strand": false,
          "transcript": "ENST00000682855.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "S",
          "aa_end": null,
          "aa_length": 721,
          "aa_ref": "S",
          "aa_start": 474,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 3868,
          "cdna_start": 1558,
          "cds_end": null,
          "cds_length": 2166,
          "cds_start": 1420,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 18,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "ENST00000854960.1",
          "gene_hgnc_id": 967,
          "gene_symbol": "BBS2",
          "hgvs_c": "c.1420_1422delTCGinsAGC",
          "hgvs_p": "p.475",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000525019.1",
          "strand": false,
          "transcript": "ENST00000854960.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "S",
          "aa_end": null,
          "aa_length": 717,
          "aa_ref": "S",
          "aa_start": 474,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 2725,
          "cdna_start": 1583,
          "cds_end": null,
          "cds_length": 2154,
          "cds_start": 1420,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 17,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "ENST00000966325.1",
          "gene_hgnc_id": 967,
          "gene_symbol": "BBS2",
          "hgvs_c": "c.1420_1422delTCGinsAGC",
          "hgvs_p": "p.475",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000636384.1",
          "strand": false,
          "transcript": "ENST00000966325.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "S",
          "aa_end": null,
          "aa_length": 710,
          "aa_ref": "S",
          "aa_start": 463,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 2634,
          "cdna_start": 1515,
          "cds_end": null,
          "cds_length": 2133,
          "cds_start": 1387,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 17,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "ENST00000854962.1",
          "gene_hgnc_id": 967,
          "gene_symbol": "BBS2",
          "hgvs_c": "c.1387_1389delTCGinsAGC",
          "hgvs_p": "p.464",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000525021.1",
          "strand": false,
          "transcript": "ENST00000854962.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "S",
          "aa_end": null,
          "aa_length": 709,
          "aa_ref": "S",
          "aa_start": 462,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 2693,
          "cdna_start": 1573,
          "cds_end": null,
          "cds_length": 2130,
          "cds_start": 1384,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 17,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "ENST00000854961.1",
          "gene_hgnc_id": 967,
          "gene_symbol": "BBS2",
          "hgvs_c": "c.1384_1386delTCGinsAGC",
          "hgvs_p": "p.463",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000525020.1",
          "strand": false,
          "transcript": "ENST00000854961.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "S",
          "aa_end": null,
          "aa_length": 705,
          "aa_ref": "S",
          "aa_start": 458,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 2735,
          "cdna_start": 1587,
          "cds_end": null,
          "cds_length": 2118,
          "cds_start": 1372,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 17,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "ENST00000683858.1",
          "gene_hgnc_id": 967,
          "gene_symbol": "BBS2",
          "hgvs_c": "c.1372_1374delTCGinsAGC",
          "hgvs_p": "p.459",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000507657.1",
          "strand": false,
          "transcript": "ENST00000683858.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "S",
          "aa_end": null,
          "aa_length": 698,
          "aa_ref": "S",
          "aa_start": 451,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 2510,
          "cdna_start": 1540,
          "cds_end": null,
          "cds_length": 2097,
          "cds_start": 1351,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 18,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "ENST00000923962.1",
          "gene_hgnc_id": 967,
          "gene_symbol": "BBS2",
          "hgvs_c": "c.1351_1353delTCGinsAGC",
          "hgvs_p": "p.452",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000594021.1",
          "strand": false,
          "transcript": "ENST00000923962.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "S",
          "aa_end": null,
          "aa_length": 698,
          "aa_ref": "S",
          "aa_start": 451,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 2706,
          "cdna_start": 1546,
          "cds_end": null,
          "cds_length": 2097,
          "cds_start": 1351,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 17,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "ENST00000923963.1",
          "gene_hgnc_id": 967,
          "gene_symbol": "BBS2",
          "hgvs_c": "c.1351_1353delTCGinsAGC",
          "hgvs_p": "p.452",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000594022.1",
          "strand": false,
          "transcript": "ENST00000923963.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "S",
          "aa_end": null,
          "aa_length": 696,
          "aa_ref": "S",
          "aa_start": 449,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 2998,
          "cdna_start": 1530,
          "cds_end": null,
          "cds_length": 2091,
          "cds_start": 1345,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 19,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "ENST00000682930.1",
          "gene_hgnc_id": 967,
          "gene_symbol": "BBS2",
          "hgvs_c": "c.1345_1347delTCGinsAGC",
          "hgvs_p": "p.450",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000507981.1",
          "strand": false,
          "transcript": "ENST00000682930.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "S",
          "aa_end": null,
          "aa_length": 686,
          "aa_ref": "S",
          "aa_start": 439,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 2671,
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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.