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Variants in CHEK2 other than 1100delC do not make a major contribution to breast cancer susceptibility

Authors :
Schutte, A.E.M. (Mieke)
Meijers-Heijboer, E.J. (Hanne)
Easton, D.F. (Douglas)
Wasielewski, M. (Marijke)
Evans, D.G. (Gareth)
Eccles, D. (Diana)
Weber, B.L. (Barbara)
Rahman, N. (Nazneen)
Meijers, C. (Carel)
Lohman, F.
Nathanson, K.L. (Katherine)
Futreal, P.A. (Andrew)
Stratton, M.R. (Michael)
Seal, S. (Sheila)
Barfoot, R. (Rita)
Ouweland, A.M.W. (Ans) van den
Klijn, J.G.M. (Jan)
Schutte, A.E.M. (Mieke)
Meijers-Heijboer, E.J. (Hanne)
Easton, D.F. (Douglas)
Wasielewski, M. (Marijke)
Evans, D.G. (Gareth)
Eccles, D. (Diana)
Weber, B.L. (Barbara)
Rahman, N. (Nazneen)
Meijers, C. (Carel)
Lohman, F.
Nathanson, K.L. (Katherine)
Futreal, P.A. (Andrew)
Stratton, M.R. (Michael)
Seal, S. (Sheila)
Barfoot, R. (Rita)
Ouweland, A.M.W. (Ans) van den
Klijn, J.G.M. (Jan)
Publication Year :
2003

Abstract

We recently reported that a sequence variant in the cell-cycle-checkpoint kinase CHEK2 (CHEK2 1100delC) is a low-penetrance breast cancer-susceptibility allele in noncarriers of BRCA1 or BRCA2 mutations. To investigate whether other CHEK2 variants confer susceptibility to breast cancer, we screened the full CHEK2 coding sequence in BRCA1/2-negative breast cancer cases from 89 pedigrees with three or more cases of breast cancer. We identified one novel germline variant, R117G, in two separate families. To evaluate the possible association of R117G and two germline variants repor

Details

Database :
OAIster
Notes :
application/pdf, American Journal of Human Genetics, English
Publication Type :
Electronic Resource
Accession number :
edsoai.ocn929956729
Document Type :
Electronic Resource