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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: 12-42469464-C-T (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=12&pos=42469464&ref=C&alt=T&genome=hg38&allGenes=true"

API Response

json
{
  "message": null,
  "variants": [
    {
      "acmg_by_gene": [
        {
          "benign_score": 20,
          "criteria": [
            "BP4_Strong",
            "BP6_Very_Strong",
            "BA1"
          ],
          "effects": [
            "missense_variant"
          ],
          "gene_symbol": "PRICKLE1",
          "hgnc_id": 17019,
          "hgvs_c": "c.370G>A",
          "hgvs_p": "p.Ala124Thr",
          "inheritance_mode": "AR,AD",
          "pathogenic_score": 0,
          "score": -20,
          "transcript": "NM_153026.3",
          "verdict": "Benign"
        }
      ],
      "acmg_classification": "Benign",
      "acmg_criteria": "BP4_Strong,BP6_Very_Strong,BA1",
      "acmg_score": -20,
      "allele_count_reference_population": 10918,
      "alphamissense_prediction": null,
      "alphamissense_score": 0.0732,
      "alt": "T",
      "apogee2_prediction": null,
      "apogee2_score": null,
      "bayesdelnoaf_prediction": "Benign",
      "bayesdelnoaf_score": -0.36,
      "chr": "12",
      "clinvar_classification": "Benign",
      "clinvar_disease": " 1B, progressive myoclonic,Epilepsy,Self-limited epilepsy with centrotemporal spikes,not provided,not specified",
      "clinvar_review_status": "criteria provided, multiple submitters, no conflicts",
      "clinvar_submissions_summary": "B:6",
      "computational_prediction_selected": "Benign",
      "computational_score_selected": 0.0016219019889831543,
      "computational_source_selected": "MetaRNN",
      "consequences": [
        {
          "aa_alt": "T",
          "aa_end": null,
          "aa_length": 831,
          "aa_ref": "A",
          "aa_start": 124,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 5878,
          "cdna_start": 700,
          "cds_end": null,
          "cds_length": 2496,
          "cds_start": 370,
          "consequences": [
            "missense_variant"
          ],
          "exon_count": 8,
          "exon_rank": 4,
          "exon_rank_end": null,
          "feature": "NM_153026.3",
          "gene_hgnc_id": 17019,
          "gene_symbol": "PRICKLE1",
          "hgvs_c": "c.370G>A",
          "hgvs_p": "p.Ala124Thr",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": "ENST00000345127.9",
          "protein_coding": true,
          "protein_id": "NP_694571.2",
          "strand": false,
          "transcript": "NM_153026.3",
          "transcript_support_level": null
        },
        {
          "aa_alt": "T",
          "aa_end": null,
          "aa_length": 831,
          "aa_ref": "A",
          "aa_start": 124,
          "biotype": "protein_coding",
          "canonical": true,
          "cdna_end": null,
          "cdna_length": 5878,
          "cdna_start": 700,
          "cds_end": null,
          "cds_length": 2496,
          "cds_start": 370,
          "consequences": [
            "missense_variant"
          ],
          "exon_count": 8,
          "exon_rank": 4,
          "exon_rank_end": null,
          "feature": "ENST00000345127.9",
          "gene_hgnc_id": 17019,
          "gene_symbol": "PRICKLE1",
          "hgvs_c": "c.370G>A",
          "hgvs_p": "p.Ala124Thr",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": "NM_153026.3",
          "protein_coding": true,
          "protein_id": "ENSP00000345064.3",
          "strand": false,
          "transcript": "ENST00000345127.9",
          "transcript_support_level": 1
        },
        {
          "aa_alt": "T",
          "aa_end": null,
          "aa_length": 831,
          "aa_ref": "A",
          "aa_start": 124,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 5836,
          "cdna_start": 658,
          "cds_end": null,
          "cds_length": 2496,
          "cds_start": 370,
          "consequences": [
            "missense_variant"
          ],
          "exon_count": 8,
          "exon_rank": 4,
          "exon_rank_end": null,
          "feature": "NM_001144881.2",
          "gene_hgnc_id": 17019,
          "gene_symbol": "PRICKLE1",
          "hgvs_c": "c.370G>A",
          "hgvs_p": "p.Ala124Thr",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "NP_001138353.1",
          "strand": false,
          "transcript": "NM_001144881.2",
          "transcript_support_level": null
        },
        {
          "aa_alt": "T",
          "aa_end": null,
          "aa_length": 831,
          "aa_ref": "A",
          "aa_start": 124,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 5849,
          "cdna_start": 671,
          "cds_end": null,
          "cds_length": 2496,
          "cds_start": 370,
          "consequences": [
            "missense_variant"
          ],
          "exon_count": 8,
          "exon_rank": 4,
          "exon_rank_end": null,
          "feature": "NM_001144882.2",
          "gene_hgnc_id": 17019,
          "gene_symbol": "PRICKLE1",
          "hgvs_c": "c.370G>A",
          "hgvs_p": "p.Ala124Thr",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "NP_001138354.1",
          "strand": false,
          "transcript": "NM_001144882.2",
          "transcript_support_level": null
        },
        {
          "aa_alt": "T",
          "aa_end": null,
          "aa_length": 831,
          "aa_ref": "A",
          "aa_start": 124,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 5846,
          "cdna_start": 668,
          "cds_end": null,
          "cds_length": 2496,
          "cds_start": 370,
          "consequences": [
            "missense_variant"
          ],
          "exon_count": 8,
          "exon_rank": 4,
          "exon_rank_end": null,
          "feature": "NM_001144883.2",
          "gene_hgnc_id": 17019,
          "gene_symbol": "PRICKLE1",
          "hgvs_c": "c.370G>A",
          "hgvs_p": "p.Ala124Thr",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "NP_001138355.1",
          "strand": false,
          "transcript": "NM_001144883.2",
          "transcript_support_level": null
        },
        {
          "aa_alt": "T",
          "aa_end": null,
          "aa_length": 831,
          "aa_ref": "A",
          "aa_start": 124,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 4075,
          "cdna_start": 500,
          "cds_end": null,
          "cds_length": 2496,
          "cds_start": 370,
          "consequences": [
            "missense_variant"
          ],
          "exon_count": 8,
          "exon_rank": 4,
          "exon_rank_end": null,
          "feature": "ENST00000445766.7",
          "gene_hgnc_id": 17019,
          "gene_symbol": "PRICKLE1",
          "hgvs_c": "c.370G>A",
          "hgvs_p": "p.Ala124Thr",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000398947.2",
          "strand": false,
          "transcript": "ENST00000445766.7",
          "transcript_support_level": 5
        },
        {
          "aa_alt": "T",
          "aa_end": null,
          "aa_length": 831,
          "aa_ref": "A",
          "aa_start": 124,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 4277,
          "cdna_start": 714,
          "cds_end": null,
          "cds_length": 2496,
          "cds_start": 370,
          "consequences": [
            "missense_variant"
          ],
          "exon_count": 9,
          "exon_rank": 5,
          "exon_rank_end": null,
          "feature": "ENST00000455697.6",
          "gene_hgnc_id": 17019,
          "gene_symbol": "PRICKLE1",
          "hgvs_c": "c.370G>A",
          "hgvs_p": "p.Ala124Thr",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000401060.1",
          "strand": false,
          "transcript": "ENST00000455697.6",
          "transcript_support_level": 5
        },
        {
          "aa_alt": "T",
          "aa_end": null,
          "aa_length": 831,
          "aa_ref": "A",
          "aa_start": 124,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 3635,
          "cdna_start": 651,
          "cds_end": null,
          "cds_length": 2496,
          "cds_start": 370,
          "consequences": [
            "missense_variant"
          ],
          "exon_count": 8,
          "exon_rank": 4,
          "exon_rank_end": null,
          "feature": "ENST00000548696.6",
          "gene_hgnc_id": 17019,
          "gene_symbol": "PRICKLE1",
          "hgvs_c": "c.370G>A",
          "hgvs_p": "p.Ala124Thr",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000448359.1",
          "strand": false,
          "transcript": "ENST00000548696.6",
          "transcript_support_level": 2
        },
        {
          "aa_alt": "T",
          "aa_end": null,
          "aa_length": 831,
          "aa_ref": "A",
          "aa_start": 124,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 3311,
          "cdna_start": 656,
          "cds_end": null,
          "cds_length": 2496,
          "cds_start": 370,
          "consequences": [
            "missense_variant"
          ],
          "exon_count": 8,
          "exon_rank": 4,
          "exon_rank_end": null,
          "feature": "ENST00000552240.6",
          "gene_hgnc_id": 17019,
          "gene_symbol": "PRICKLE1",
          "hgvs_c": "c.370G>A",
          "hgvs_p": "p.Ala124Thr",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000449819.1",
          "strand": false,
          "transcript": "ENST00000552240.6",
          "transcript_support_level": 5
        },
        {
          "aa_alt": "T",
          "aa_end": null,
          "aa_length": 831,
          "aa_ref": "A",
          "aa_start": 124,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 3341,
          "cdna_start": 671,
          "cds_end": null,
          "cds_length": 2496,
          "cds_start": 370,
          "consequences": [
            "missense_variant"
          ],
          "exon_count": 8,
          "exon_rank": 4,
          "exon_rank_end": null,
          "feature": "ENST00000639566.1",
          "gene_hgnc_id": 17019,
          "gene_symbol": "PRICKLE1",
          "hgvs_c": "c.370G>A",
          "hgvs_p": "p.Ala124Thr",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000492332.1",
          "strand": false,
          "transcript": "ENST00000639566.1",
          "transcript_support_level": 5
        },
        {
          "aa_alt": "T",
          "aa_end": null,
          "aa_length": 831,
          "aa_ref": "A",
          "aa_start": 124,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 5761,
          "cdna_start": 589,
          "cds_end": null,
          "cds_length": 2496,
          "cds_start": 370,
          "consequences": [
            "missense_variant"
          ],
          "exon_count": 8,
          "exon_rank": 4,
          "exon_rank_end": null,
          "feature": "ENST00000639589.1",
          "gene_hgnc_id": 17019,
          "gene_symbol": "PRICKLE1",
          "hgvs_c": "c.370G>A",
          "hgvs_p": "p.Ala124Thr",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000491051.1",
          "strand": false,
          "transcript": "ENST00000639589.1",
          "transcript_support_level": 5
        },
        {
          "aa_alt": "T",
          "aa_end": null,
          "aa_length": 831,
          "aa_ref": "A",
          "aa_start": 124,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 3803,
          "cdna_start": 697,
          "cds_end": null,
          "cds_length": 2496,
          "cds_start": 370,
          "consequences": [
            "missense_variant"
          ],
          "exon_count": 8,
          "exon_rank": 4,
          "exon_rank_end": null,
          "feature": "ENST00000639958.1",
          "gene_hgnc_id": 17019,
          "gene_symbol": "PRICKLE1",
          "hgvs_c": "c.370G>A",
          "hgvs_p": "p.Ala124Thr",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000492644.1",
          "strand": false,
          "transcript": "ENST00000639958.1",
          "transcript_support_level": 5
        },
        {
          "aa_alt": "T",
          "aa_end": null,
          "aa_length": 831,
          "aa_ref": "A",
          "aa_start": 124,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 3778,
          "cdna_start": 668,
          "cds_end": null,
          "cds_length": 2496,
          "cds_start": 370,
          "consequences": [
            "missense_variant"
          ],
          "exon_count": 9,
          "exon_rank": 5,
          "exon_rank_end": null,
          "feature": "ENST00000640055.1",
          "gene_hgnc_id": 17019,
          "gene_symbol": "PRICKLE1",
          "hgvs_c": "c.370G>A",
          "hgvs_p": "p.Ala124Thr",
          "intron_rank": null,
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          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000492763.1",
          "strand": false,
          "transcript": "ENST00000640055.1",
          "transcript_support_level": 5
        },
        {
          "aa_alt": "T",
          "aa_end": null,
          "aa_length": 831,
          "aa_ref": "A",
          "aa_start": 124,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 4278,
          "cdna_start": 715,
          "cds_end": null,
          "cds_length": 2496,
          "cds_start": 370,
          "consequences": [
            "missense_variant"
          ],
          "exon_count": 8,
          "exon_rank": 4,
          "exon_rank_end": null,
          "feature": "ENST00000640132.1",
          "gene_hgnc_id": 17019,
          "gene_symbol": "PRICKLE1",
          "hgvs_c": "c.370G>A",
          "hgvs_p": "p.Ala124Thr",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000491228.1",
          "strand": false,
          "transcript": "ENST00000640132.1",
          "transcript_support_level": 2
        },
        {
          "aa_alt": "T",
          "aa_end": null,
          "aa_length": 831,
          "aa_ref": "A",
          "aa_start": 124,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 3674,
          "cdna_start": 989,
          "cds_end": null,
          "cds_length": 2496,
          "cds_start": 370,
          "consequences": [
            "missense_variant"
          ],
          "exon_count": 9,
          "exon_rank": 5,
          "exon_rank_end": null,
          "feature": "ENST00000899955.1",
          "gene_hgnc_id": 17019,
          "gene_symbol": "PRICKLE1",
          "hgvs_c": "c.370G>A",
          "hgvs_p": "p.Ala124Thr",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000570014.1",
          "strand": false,
          "transcript": "ENST00000899955.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "T",
          "aa_end": null,
          "aa_length": 831,
          "aa_ref": "A",
          "aa_start": 124,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 4280,
          "cdna_start": 701,
          "cds_end": null,
          "cds_length": 2496,
          "cds_start": 370,
          "consequences": [
            "missense_variant"
          ],
          "exon_count": 8,
          "exon_rank": 4,
          "exon_rank_end": null,
          "feature": "ENST00000899957.1",
          "gene_hgnc_id": 17019,
          "gene_symbol": "PRICKLE1",
          "hgvs_c": "c.370G>A",
          "hgvs_p": "p.Ala124Thr",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000570016.1",
          "strand": false,
          "transcript": "ENST00000899957.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "T",
          "aa_end": null,
          "aa_length": 831,
          "aa_ref": "A",
          "aa_start": 124,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 3163,
          "cdna_start": 478,
          "cds_end": null,
          "cds_length": 2496,
          "cds_start": 370,
          "consequences": [
            "missense_variant"
          ],
          "exon_count": 8,
          "exon_rank": 4,
          "exon_rank_end": null,
          "feature": "ENST00000899959.1",
          "gene_hgnc_id": 17019,
          "gene_symbol": "PRICKLE1",
          "hgvs_c": "c.370G>A",
          "hgvs_p": "p.Ala124Thr",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000570018.1",
          "strand": false,
          "transcript": "ENST00000899959.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "T",
          "aa_end": null,
          "aa_length": 831,
          "aa_ref": "A",
          "aa_start": 124,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 3398,
          "cdna_start": 713,
          "cds_end": null,
          "cds_length": 2496,
          "cds_start": 370,
          "consequences": [
            "missense_variant"
          ],
          "exon_count": 9,
          "exon_rank": 5,
          "exon_rank_end": null,
          "feature": "ENST00000899960.1",
          "gene_hgnc_id": 17019,
          "gene_symbol": "PRICKLE1",
          "hgvs_c": "c.370G>A",
          "hgvs_p": "p.Ala124Thr",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000570019.1",
          "strand": false,
          "transcript": "ENST00000899960.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "T",
          "aa_end": null,
          "aa_length": 831,
          "aa_ref": "A",
          "aa_start": 124,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 3139,
          "cdna_start": 454,
          "cds_end": null,
          "cds_length": 2496,
          "cds_start": 370,
          "consequences": [
            "missense_variant"
          ],
          "exon_count": 8,
          "exon_rank": 4,
          "exon_rank_end": null,
          "feature": "ENST00000899961.1",
          "gene_hgnc_id": 17019,
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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.