TY - JOUR
T1 - Haplotype and phenotype analysis of six recurrent BRCA1 mutations in 61 families
T2 - Results of an international study
AU - Neuhausen, Susan L.
AU - Mazoyer, Sylvie
AU - Friedman, Lori
AU - Stratton, Michael
AU - Offit, Ken
AU - Caligo, Adelaide
AU - Tomlinson, Gail
AU - Cannon-Albright, Lisa
AU - Bishop, Tim
AU - Kelsell, David
AU - Solomon, Ellen
AU - Weber, Barbara
AU - Couch, Fergus
AU - Struewing, Jeffery
AU - Tonin, Patricia
AU - Durocher, Francine
AU - Narod, Steven
AU - Skolnick, Mark H.
AU - Lenoir, Gilbert
AU - Serova, Olga
AU - Ponder, Bruce
AU - Stoppa-Lyonnet, Dominique
AU - Easton, Douglas
AU - King, Mary Claire
AU - Goldgar, David E.
PY - 1996
Y1 - 1996
N2 - Several BRCA1 mutations have now been found to occur in geographically diverse breast and ovarian cancer families. To investigate mutation origin and mutation-specific phenotypes due to BRCA1, we constructed a haplotype of nine polymorphic markers within or immediately flanking the BRCA1 locus in a set of 61 breast/ovarian cancer families selected for having one of six recurrent BRCA1 mutations. Tests of both mutations and family-specific differences in age at diagnosis were not significant. A comparison of the six mutations in the relative proportions of cases of breast and ovarian cancer was suggestive of an effect (P = .069), with 57% of women presumed affected because of the 1294 del 40 BRCA1 mutation having ovarian cancer, compared with 14% of affected women with the splice-site mutation in intron 5 of BRCA1. For the BRCA1 mutations studied here, the individual mutations are estimated to have arisen 9-170 generations ago. In general, a high degree of haplotype conservation across the region was observed, with haplotype differences most often due to mutations in the short-tandem-repeat markers, although some likely instances of recombination also were observed. For several of the instances, there was evidence for multiple, independent, BRCA1 mutational events.
AB - Several BRCA1 mutations have now been found to occur in geographically diverse breast and ovarian cancer families. To investigate mutation origin and mutation-specific phenotypes due to BRCA1, we constructed a haplotype of nine polymorphic markers within or immediately flanking the BRCA1 locus in a set of 61 breast/ovarian cancer families selected for having one of six recurrent BRCA1 mutations. Tests of both mutations and family-specific differences in age at diagnosis were not significant. A comparison of the six mutations in the relative proportions of cases of breast and ovarian cancer was suggestive of an effect (P = .069), with 57% of women presumed affected because of the 1294 del 40 BRCA1 mutation having ovarian cancer, compared with 14% of affected women with the splice-site mutation in intron 5 of BRCA1. For the BRCA1 mutations studied here, the individual mutations are estimated to have arisen 9-170 generations ago. In general, a high degree of haplotype conservation across the region was observed, with haplotype differences most often due to mutations in the short-tandem-repeat markers, although some likely instances of recombination also were observed. For several of the instances, there was evidence for multiple, independent, BRCA1 mutational events.
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M3 - Article
C2 - 8571953
AN - SCOPUS:19144362921
SN - 0002-9297
VL - 58
SP - 271
EP - 280
JO - American journal of human genetics
JF - American journal of human genetics
IS - 2
ER -