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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: 12-109489917-A-G (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=12&pos=109489917&ref=A&alt=G&genome=hg38&allGenes=true"

API Response

json
{
  "message": null,
  "variants": [
    {
      "acmg_by_gene": [
        {
          "benign_score": 0,
          "criteria": [
            "PVS1",
            "PM2",
            "PP5"
          ],
          "effects": [
            "splice_acceptor_variant",
            "intron_variant"
          ],
          "gene_symbol": "UBE3B",
          "hgnc_id": 13478,
          "hgvs_c": "c.545-2A>G",
          "hgvs_p": null,
          "inheritance_mode": "AR",
          "pathogenic_score": 11,
          "score": 11,
          "transcript": "NM_130466.4",
          "verdict": "Pathogenic"
        }
      ],
      "acmg_classification": "Pathogenic",
      "acmg_criteria": "PVS1,PM2,PP5",
      "acmg_score": 11,
      "allele_count_reference_population": 0,
      "alphamissense_prediction": null,
      "alphamissense_score": null,
      "alt": "G",
      "apogee2_prediction": null,
      "apogee2_score": null,
      "bayesdelnoaf_prediction": "Pathogenic",
      "bayesdelnoaf_score": 0.33,
      "chr": "12",
      "clinvar_classification": "Pathogenic",
      "clinvar_disease": " Kaufman type,Oculocerebrofacial syndrome",
      "clinvar_review_status": "no assertion criteria provided",
      "clinvar_submissions_summary": "null",
      "computational_prediction_selected": "Pathogenic",
      "computational_score_selected": 0.33000001311302185,
      "computational_source_selected": "BayesDel_noAF",
      "consequences": [
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": 1068,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 5730,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": 3207,
          "cds_start": null,
          "consequences": [
            "splice_acceptor_variant",
            "intron_variant"
          ],
          "exon_count": 28,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "NM_130466.4",
          "gene_hgnc_id": 13478,
          "gene_symbol": "UBE3B",
          "hgvs_c": "c.545-2A>G",
          "hgvs_p": null,
          "intron_rank": 7,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": "ENST00000342494.8",
          "protein_coding": true,
          "protein_id": "NP_569733.2",
          "strand": true,
          "transcript": "NM_130466.4",
          "transcript_support_level": null
        },
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": 1068,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "protein_coding",
          "canonical": true,
          "cdna_end": null,
          "cdna_length": 5730,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": 3207,
          "cds_start": null,
          "consequences": [
            "splice_acceptor_variant",
            "intron_variant"
          ],
          "exon_count": 28,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "ENST00000342494.8",
          "gene_hgnc_id": 13478,
          "gene_symbol": "UBE3B",
          "hgvs_c": "c.545-2A>G",
          "hgvs_p": null,
          "intron_rank": 7,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": "NM_130466.4",
          "protein_coding": true,
          "protein_id": "ENSP00000340596.3",
          "strand": true,
          "transcript": "ENST00000342494.8",
          "transcript_support_level": 1
        },
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": 1068,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 5620,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": 3207,
          "cds_start": null,
          "consequences": [
            "splice_acceptor_variant",
            "intron_variant"
          ],
          "exon_count": 28,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "ENST00000434735.6",
          "gene_hgnc_id": 13478,
          "gene_symbol": "UBE3B",
          "hgvs_c": "c.545-2A>G",
          "hgvs_p": null,
          "intron_rank": 7,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000391529.2",
          "strand": true,
          "transcript": "ENST00000434735.6",
          "transcript_support_level": 1
        },
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": 870,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 2763,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": 2615,
          "cds_start": null,
          "consequences": [
            "splice_acceptor_variant",
            "intron_variant"
          ],
          "exon_count": 23,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "ENST00000539599.5",
          "gene_hgnc_id": 13478,
          "gene_symbol": "UBE3B",
          "hgvs_c": "c.545-2A>G",
          "hgvs_p": null,
          "intron_rank": 6,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000443131.1",
          "strand": true,
          "transcript": "ENST00000539599.5",
          "transcript_support_level": 1
        },
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": 244,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 1448,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": 735,
          "cds_start": null,
          "consequences": [
            "splice_acceptor_variant",
            "intron_variant"
          ],
          "exon_count": 9,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "ENST00000340074.9",
          "gene_hgnc_id": 13478,
          "gene_symbol": "UBE3B",
          "hgvs_c": "c.545-2A>G",
          "hgvs_p": null,
          "intron_rank": 7,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000342614.5",
          "strand": true,
          "transcript": "ENST00000340074.9",
          "transcript_support_level": 1
        },
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": 244,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 1120,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": 735,
          "cds_start": null,
          "consequences": [
            "splice_acceptor_variant",
            "intron_variant"
          ],
          "exon_count": 9,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "ENST00000536398.5",
          "gene_hgnc_id": 13478,
          "gene_symbol": "UBE3B",
          "hgvs_c": "c.545-2A>G",
          "hgvs_p": null,
          "intron_rank": 7,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000440585.1",
          "strand": true,
          "transcript": "ENST00000536398.5",
          "transcript_support_level": 1
        },
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": 244,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 1541,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": 735,
          "cds_start": null,
          "consequences": [
            "splice_acceptor_variant",
            "intron_variant"
          ],
          "exon_count": 9,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "ENST00000540230.5",
          "gene_hgnc_id": 13478,
          "gene_symbol": "UBE3B",
          "hgvs_c": "c.545-2A>G",
          "hgvs_p": null,
          "intron_rank": 7,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000443565.1",
          "strand": true,
          "transcript": "ENST00000540230.5",
          "transcript_support_level": 1
        },
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": null,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "nonsense_mediated_decay",
          "canonical": true,
          "cdna_end": null,
          "cdna_length": 3771,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": null,
          "cds_start": null,
          "consequences": [
            "splice_acceptor_variant",
            "intron_variant"
          ],
          "exon_count": 29,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "ENST00000449510.6",
          "gene_hgnc_id": 13478,
          "gene_symbol": "UBE3B",
          "hgvs_c": "n.545-2A>G",
          "hgvs_p": null,
          "intron_rank": 7,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": false,
          "protein_id": "ENSP00000395802.2",
          "strand": true,
          "transcript": "ENST00000449510.6",
          "transcript_support_level": 5
        },
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": 1068,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 5385,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": 3207,
          "cds_start": null,
          "consequences": [
            "splice_acceptor_variant",
            "intron_variant"
          ],
          "exon_count": 28,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "NM_183415.3",
          "gene_hgnc_id": 13478,
          "gene_symbol": "UBE3B",
          "hgvs_c": "c.545-2A>G",
          "hgvs_p": null,
          "intron_rank": 7,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "NP_904324.1",
          "strand": true,
          "transcript": "NM_183415.3",
          "transcript_support_level": null
        },
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": 1068,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 5663,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": 3207,
          "cds_start": null,
          "consequences": [
            "splice_acceptor_variant",
            "intron_variant"
          ],
          "exon_count": 29,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "ENST00000861742.1",
          "gene_hgnc_id": 13478,
          "gene_symbol": "UBE3B",
          "hgvs_c": "c.545-2A>G",
          "hgvs_p": null,
          "intron_rank": 8,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000531801.1",
          "strand": true,
          "transcript": "ENST00000861742.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": 1068,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 5630,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": 3207,
          "cds_start": null,
          "consequences": [
            "splice_acceptor_variant",
            "intron_variant"
          ],
          "exon_count": 27,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "ENST00000861743.1",
          "gene_hgnc_id": 13478,
          "gene_symbol": "UBE3B",
          "hgvs_c": "c.545-2A>G",
          "hgvs_p": null,
          "intron_rank": 6,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000531802.1",
          "strand": true,
          "transcript": "ENST00000861743.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": 1068,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 5395,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": 3207,
          "cds_start": null,
          "consequences": [
            "splice_acceptor_variant",
            "intron_variant"
          ],
          "exon_count": 28,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "ENST00000861744.1",
          "gene_hgnc_id": 13478,
          "gene_symbol": "UBE3B",
          "hgvs_c": "c.545-2A>G",
          "hgvs_p": null,
          "intron_rank": 7,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000531803.1",
          "strand": true,
          "transcript": "ENST00000861744.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": 1067,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 5402,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": 3204,
          "cds_start": null,
          "consequences": [
            "splice_acceptor_variant",
            "intron_variant"
          ],
          "exon_count": 28,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "ENST00000962216.1",
          "gene_hgnc_id": 13478,
          "gene_symbol": "UBE3B",
          "hgvs_c": "c.542-2A>G",
          "hgvs_p": null,
          "intron_rank": 7,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000632275.1",
          "strand": true,
          "transcript": "ENST00000962216.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": 1022,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 5421,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": 3069,
          "cds_start": null,
          "consequences": [
            "splice_acceptor_variant",
            "intron_variant"
          ],
          "exon_count": 26,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "ENST00000861745.1",
          "gene_hgnc_id": 13478,
          "gene_symbol": "UBE3B",
          "hgvs_c": "c.545-2A>G",
          "hgvs_p": null,
          "intron_rank": 6,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000531804.1",
          "strand": true,
          "transcript": "ENST00000861745.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": 1022,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 5596,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": 3069,
          "cds_start": null,
          "consequences": [
            "splice_acceptor_variant",
            "intron_variant"
          ],
          "exon_count": 27,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "ENST00000962217.1",
          "gene_hgnc_id": 13478,
          "gene_symbol": "UBE3B",
          "hgvs_c": "c.545-2A>G",
          "hgvs_p": null,
          "intron_rank": 7,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000632276.1",
          "strand": true,
          "transcript": "ENST00000962217.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": 247,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 3600,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": 744,
          "cds_start": null,
          "consequences": [
            "splice_acceptor_variant",
            "intron_variant"
          ],
          "exon_count": 8,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "ENST00000537063.1",
          "gene_hgnc_id": 13478,
          "gene_symbol": "UBE3B",
          "hgvs_c": "c.545-2A>G",
          "hgvs_p": null,
          "intron_rank": 7,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000437694.1",
          "strand": true,
          "transcript": "ENST00000537063.1",
          "transcript_support_level": 3
        },
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": 244,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 1466,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": 735,
          "cds_start": null,
          "consequences": [
            "splice_acceptor_variant",
            "intron_variant"
          ],
          "exon_count": 9,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "NM_001270449.2",
          "gene_hgnc_id": 13478,
          "gene_symbol": "UBE3B",
          "hgvs_c": "c.545-2A>G",
          "hgvs_p": null,
          "intron_rank": 7,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "NP_001257378.1",
          "strand": true,
          "transcript": "NM_001270449.2",
          "transcript_support_level": null
        },
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": 244,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 1121,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": 735,
          "cds_start": null,
          "consequences": [
            "splice_acceptor_variant",
            "intron_variant"
          ],
          "exon_count": 9,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "NM_001270450.2",
          "gene_hgnc_id": 13478,
          "gene_symbol": "UBE3B",
          "hgvs_c": "c.545-2A>G",
          "hgvs_p": null,
          "intron_rank": 7,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "NP_001257379.1",
          "strand": true,
          "transcript": "NM_001270450.2",
          "transcript_support_level": null
        },
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": 244,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 1133,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": 735,
          "cds_start": null,
          "consequences": [
            "splice_acceptor_variant",
            "intron_variant"
          ],
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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.