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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: 15-63597513-G-A (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=15&pos=63597513&ref=G&alt=A&genome=hg38&allGenes=true"

API Response

json
{
  "message": null,
  "variants": [
    {
      "acmg_by_gene": [
        {
          "benign_score": 4,
          "criteria": [
            "BP4_Strong"
          ],
          "effects": [
            "missense_variant"
          ],
          "gene_symbol": "FBXL22",
          "hgnc_id": 27537,
          "hgvs_c": "c.121G>A",
          "hgvs_p": "p.Asp41Asn",
          "inheritance_mode": "AR",
          "pathogenic_score": 0,
          "score": -4,
          "transcript": "NM_203373.3",
          "verdict": "Likely_benign"
        },
        {
          "benign_score": 4,
          "criteria": [
            "BP4_Strong"
          ],
          "effects": [
            "non_coding_transcript_exon_variant"
          ],
          "gene_symbol": "USP3-AS1",
          "hgnc_id": 44140,
          "hgvs_c": "n.25C>T",
          "hgvs_p": null,
          "inheritance_mode": "",
          "pathogenic_score": 0,
          "score": -4,
          "transcript": "ENST00000726078.1",
          "verdict": "Likely_benign"
        }
      ],
      "acmg_classification": "Likely_benign",
      "acmg_criteria": "BP4_Strong",
      "acmg_score": -4,
      "allele_count_reference_population": 25,
      "alphamissense_prediction": null,
      "alphamissense_score": 0.2679,
      "alt": "A",
      "apogee2_prediction": null,
      "apogee2_score": null,
      "bayesdelnoaf_prediction": "Benign",
      "bayesdelnoaf_score": -0.55,
      "chr": "15",
      "clinvar_classification": "Uncertain significance",
      "clinvar_disease": "not specified",
      "clinvar_review_status": "criteria provided, single submitter",
      "clinvar_submissions_summary": "US:1",
      "computational_prediction_selected": "Benign",
      "computational_score_selected": 0.05898371338844299,
      "computational_source_selected": "MetaRNN",
      "consequences": [
        {
          "aa_alt": "N",
          "aa_end": null,
          "aa_length": 231,
          "aa_ref": "D",
          "aa_start": 41,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 904,
          "cdna_start": 127,
          "cds_end": null,
          "cds_length": 696,
          "cds_start": 121,
          "consequences": [
            "missense_variant"
          ],
          "exon_count": 2,
          "exon_rank": 1,
          "exon_rank_end": null,
          "feature": "NM_001367807.1",
          "gene_hgnc_id": 27537,
          "gene_symbol": "FBXL22",
          "hgvs_c": "c.121G>A",
          "hgvs_p": "p.Asp41Asn",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": "ENST00000638704.2",
          "protein_coding": true,
          "protein_id": "NP_001354736.1",
          "strand": true,
          "transcript": "NM_001367807.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "N",
          "aa_end": null,
          "aa_length": 231,
          "aa_ref": "D",
          "aa_start": 41,
          "biotype": "protein_coding",
          "canonical": true,
          "cdna_end": null,
          "cdna_length": 904,
          "cdna_start": 127,
          "cds_end": null,
          "cds_length": 696,
          "cds_start": 121,
          "consequences": [
            "missense_variant"
          ],
          "exon_count": 2,
          "exon_rank": 1,
          "exon_rank_end": null,
          "feature": "ENST00000638704.2",
          "gene_hgnc_id": 27537,
          "gene_symbol": "FBXL22",
          "hgvs_c": "c.121G>A",
          "hgvs_p": "p.Asp41Asn",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": "NM_001367807.1",
          "protein_coding": true,
          "protein_id": "ENSP00000492359.1",
          "strand": true,
          "transcript": "ENST00000638704.2",
          "transcript_support_level": 2
        },
        {
          "aa_alt": "N",
          "aa_end": null,
          "aa_length": 247,
          "aa_ref": "D",
          "aa_start": 41,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 1526,
          "cdna_start": 161,
          "cds_end": null,
          "cds_length": 744,
          "cds_start": 121,
          "consequences": [
            "missense_variant"
          ],
          "exon_count": 2,
          "exon_rank": 1,
          "exon_rank_end": null,
          "feature": "ENST00000360587.2",
          "gene_hgnc_id": 27537,
          "gene_symbol": "FBXL22",
          "hgvs_c": "c.121G>A",
          "hgvs_p": "p.Asp41Asn",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000353794.3",
          "strand": true,
          "transcript": "ENST00000360587.2",
          "transcript_support_level": 1
        },
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": null,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "pseudogene",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 1784,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": null,
          "cds_start": null,
          "consequences": [
            "intron_variant"
          ],
          "exon_count": 4,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "ENST00000558831.5",
          "gene_hgnc_id": 44140,
          "gene_symbol": "USP3-AS1",
          "hgvs_c": "n.173-2727C>T",
          "hgvs_p": null,
          "intron_rank": 1,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": false,
          "protein_id": null,
          "strand": false,
          "transcript": "ENST00000558831.5",
          "transcript_support_level": 1
        },
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": null,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "pseudogene",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 1615,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": null,
          "cds_start": null,
          "consequences": [
            "intron_variant"
          ],
          "exon_count": 4,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "ENST00000559737.6",
          "gene_hgnc_id": 44140,
          "gene_symbol": "USP3-AS1",
          "hgvs_c": "n.306+1670C>T",
          "hgvs_p": null,
          "intron_rank": 2,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": false,
          "protein_id": null,
          "strand": false,
          "transcript": "ENST00000559737.6",
          "transcript_support_level": 1
        },
        {
          "aa_alt": "N",
          "aa_end": null,
          "aa_length": 247,
          "aa_ref": "D",
          "aa_start": 41,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 2496,
          "cdna_start": 127,
          "cds_end": null,
          "cds_length": 744,
          "cds_start": 121,
          "consequences": [
            "missense_variant"
          ],
          "exon_count": 2,
          "exon_rank": 1,
          "exon_rank_end": null,
          "feature": "NM_203373.3",
          "gene_hgnc_id": 27537,
          "gene_symbol": "FBXL22",
          "hgvs_c": "c.121G>A",
          "hgvs_p": "p.Asp41Asn",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "NP_976307.2",
          "strand": true,
          "transcript": "NM_203373.3",
          "transcript_support_level": null
        },
        {
          "aa_alt": "N",
          "aa_end": null,
          "aa_length": 130,
          "aa_ref": "D",
          "aa_start": 41,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 2447,
          "cdna_start": 127,
          "cds_end": null,
          "cds_length": 393,
          "cds_start": 121,
          "consequences": [
            "missense_variant"
          ],
          "exon_count": 2,
          "exon_rank": 1,
          "exon_rank_end": null,
          "feature": "NM_001367808.1",
          "gene_hgnc_id": 27537,
          "gene_symbol": "FBXL22",
          "hgvs_c": "c.121G>A",
          "hgvs_p": "p.Asp41Asn",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "NP_001354737.1",
          "strand": true,
          "transcript": "NM_001367808.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "N",
          "aa_end": null,
          "aa_length": 130,
          "aa_ref": "D",
          "aa_start": 41,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 2539,
          "cdna_start": 127,
          "cds_end": null,
          "cds_length": 393,
          "cds_start": 121,
          "consequences": [
            "missense_variant"
          ],
          "exon_count": 3,
          "exon_rank": 1,
          "exon_rank_end": null,
          "feature": "NM_001367809.1",
          "gene_hgnc_id": 27537,
          "gene_symbol": "FBXL22",
          "hgvs_c": "c.121G>A",
          "hgvs_p": "p.Asp41Asn",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "NP_001354738.1",
          "strand": true,
          "transcript": "NM_001367809.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "N",
          "aa_end": null,
          "aa_length": 130,
          "aa_ref": "D",
          "aa_start": 41,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 2443,
          "cdna_start": 123,
          "cds_end": null,
          "cds_length": 393,
          "cds_start": 121,
          "consequences": [
            "missense_variant"
          ],
          "exon_count": 2,
          "exon_rank": 1,
          "exon_rank_end": null,
          "feature": "ENST00000534939.2",
          "gene_hgnc_id": 27537,
          "gene_symbol": "FBXL22",
          "hgvs_c": "c.121G>A",
          "hgvs_p": "p.Asp41Asn",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000453697.2",
          "strand": true,
          "transcript": "ENST00000534939.2",
          "transcript_support_level": 3
        },
        {
          "aa_alt": "N",
          "aa_end": null,
          "aa_length": 142,
          "aa_ref": "D",
          "aa_start": 41,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 658,
          "cdna_start": 127,
          "cds_end": null,
          "cds_length": 429,
          "cds_start": 121,
          "consequences": [
            "missense_variant"
          ],
          "exon_count": 2,
          "exon_rank": 1,
          "exon_rank_end": null,
          "feature": "XM_047432400.1",
          "gene_hgnc_id": 27537,
          "gene_symbol": "FBXL22",
          "hgvs_c": "c.121G>A",
          "hgvs_p": "p.Asp41Asn",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "XP_047288356.1",
          "strand": true,
          "transcript": "XM_047432400.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": null,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "pseudogene",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 697,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": null,
          "cds_start": null,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_count": 4,
          "exon_rank": 1,
          "exon_rank_end": null,
          "feature": "ENST00000726078.1",
          "gene_hgnc_id": 44140,
          "gene_symbol": "USP3-AS1",
          "hgvs_c": "n.25C>T",
          "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": "ENST00000726078.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": null,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "pseudogene",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 1632,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": null,
          "cds_start": null,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_count": 3,
          "exon_rank": 1,
          "exon_rank_end": null,
          "feature": "ENST00000726079.1",
          "gene_hgnc_id": 44140,
          "gene_symbol": "USP3-AS1",
          "hgvs_c": "n.29C>T",
          "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": "ENST00000726079.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": null,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "pseudogene",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 1606,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": null,
          "cds_start": null,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_count": 3,
          "exon_rank": 1,
          "exon_rank_end": null,
          "feature": "ENST00000726080.1",
          "gene_hgnc_id": 44140,
          "gene_symbol": "USP3-AS1",
          "hgvs_c": "n.20C>T",
          "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": "ENST00000726080.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": null,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "pseudogene",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 692,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": null,
          "cds_start": null,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_count": 3,
          "exon_rank": 1,
          "exon_rank_end": null,
          "feature": "ENST00000726082.1",
          "gene_hgnc_id": 44140,
          "gene_symbol": "USP3-AS1",
          "hgvs_c": "n.32C>T",
          "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": "ENST00000726082.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": null,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "pseudogene",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 493,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": null,
          "cds_start": null,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_count": 3,
          "exon_rank": 1,
          "exon_rank_end": null,
          "feature": "ENST00000726083.1",
          "gene_hgnc_id": 44140,
          "gene_symbol": "USP3-AS1",
          "hgvs_c": "n.47C>T",
          "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": "ENST00000726083.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": null,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "pseudogene",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 890,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": null,
          "cds_start": null,
          "consequences": [
            "intron_variant"
          ],
          "exon_count": 4,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "ENST00000559861.2",
          "gene_hgnc_id": 44140,
          "gene_symbol": "USP3-AS1",
          "hgvs_c": "n.189-2727C>T",
          "hgvs_p": null,
          "intron_rank": 1,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": false,
          "protein_id": null,
          "strand": false,
          "transcript": "ENST00000559861.2",
          "transcript_support_level": 5
        },
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": null,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "pseudogene",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 552,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": null,
          "cds_start": null,
          "consequences": [
            "intron_variant"
          ],
          "exon_count": 3,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "ENST00000560622.6",
          "gene_hgnc_id": 44140,
          "gene_symbol": "USP3-AS1",
          "hgvs_c": "n.193-2727C>T",
          "hgvs_p": null,
          "intron_rank": 1,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": false,
          "protein_id": null,
          "strand": false,
          "transcript": "ENST00000560622.6",
          "transcript_support_level": 2
        },
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": null,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "pseudogene",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 2609,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": null,
          "cds_start": null,
          "consequences": [
            "intron_variant"
          ],
          "exon_count": 3,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "ENST00000560962.6",
          "gene_hgnc_id": 44140,
          "gene_symbol": "USP3-AS1",
          "hgvs_c": "n.549-2727C>T",
          "hgvs_p": null,
          "intron_rank": 1,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": false,
          "protein_id": null,
          "strand": false,
          "transcript": "ENST00000560962.6",
          "transcript_support_level": 2
        },
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": null,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "pseudogene",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 572,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": null,
          "cds_start": null,
          "consequences": [
            "intron_variant"
          ],
          "exon_count": 4,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "ENST00000561191.1",
          "gene_hgnc_id": 44140,
          "gene_symbol": "USP3-AS1",
          "hgvs_c": "n.330+1670C>T",
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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.