Journal article

Frequency of the ATM IVS10-6T→G variant in Australian multiple-case breast cancer families

GJ Lindeman, M Hiew, JE Visvader, J Leary, M Field, CL Gaff, RMK Gardner, K Trainor, G Cheetham, G Suthers, J Kirk

Breast Cancer Research | BIOMED CENTRAL LTD | Published : 2004

Abstract

Background: Germline mutations in the genes BRCA1 and BRCA2 account for only a proportion of hereditary breast cancer, suggesting that additional genes contribute to hereditary breast cancer. Recently a heterozygous variant in the ataxia–telangiectasia mutated (ATM) gene, IVS10-6T→G, was reported by an Australian multiple-case breast cancer family cohort study (the Kathleen Cuningham Foundation Consortium for Research into Familial Breast Cancer) to confer a substantial breast cancer risk. Although this variant can result in a truncated ATM product, its clinical significance as a high-penetrance breast cancer allele or its role as a low-penetrance risk-modifier is controversial. Methods: We ..

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