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BRCA2 c.5946delT (6174delT) — Mutation du fondateur juif Ashkenazi

Vue déterministe de l'entité source de la LJAM. L'autorité clinique demeure avec les ID de la source cités et l'état d'approbation de l ́examinateur.

IDBIO-BRCA2-ASHKENAZI-FOUNDER-6174DELT
TypeBiomarqueur
Alias
BRCA2 6174delTBRCA2 6174delT mutation fondatriceBRCA2 c.5946delTBRCA2 c.5946delT (6174delT) — засновницька мутація ашкеназіc.5946del
Étatreviewed 2026-05-18 | pending_clinical_signoff
MaladiesAucune déclaration
SourcesSRC-NCCN-GENETIC-FAMILIAL-BREAST-OVARIAN-2025

Données biomarqueurs

Type de biomarqueurgene_mutation
Détails de la mutation{"exon": "11", "functional_impact": "loss_of_function", "gene": "BRCA2", "gene_hugo_id": "HGNC:1101", "hgvs_coding": "c.5946delT", "hgvs_protein": "p.Ser1982ArgfsTer22", "variant_type": "frameshift deletion"}
Biomarqueurs connexesBIO-BRCA1-BRCA2-GERMLINE

Notes

Third of three Ashkenazi Jewish founder mutations (combined carrier frequency ~2.5% in AJ; ~1.5% for this BRCA2 variant alone in some cohorts). Single-T deletion in exon 11 causing frameshift and premature termination in the DNA-binding domain region — abolishes RAD51-mediated homologous-recombination repair. Modern HGVS notation c.5946delT; legacy notation 6174delT (older mRNA-numbering convention). Lifetime cancer risks consistent with BRCA2 average: breast ~50-60%, ovarian ~15-20%, male breast ~6-8%, pancreas ~5-7%, prostate ~20-25%. Higher pancreas risk than BRCA1 — CAPS-Consortium pancreatic surveillance (annual MRI/MRCP or EUS from age 50 or 10 years before youngest PDAC in family) applies to BRCA2 carriers with PDAC family history. Same breast/ovarian surveillance and risk-reduction protocols as other BRCA2 pathogenic variants (annual MRI from 25-30, RRSO 40-45). NCCN 2025 endorses population-wide AJ founder-panel testing. STUB pending two-Co-Lead signoff.

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