Quantifying prediction of pathogenicity for within-codon concordance (PM5) using 7541 functional classifications of BRCA1 and MSH2 missense variants.
Genetics In Medicine : Official Journal Of The American College Of Medical Genetics
Loong, Lucy L; Cubuk, Cankut C; Choi, Subin S; Allen, Sophie S; Torr, Beth B; Garrett, Alice A; Loveday, Chey C; Durkie, Miranda M; Callaway, Alison A; Burghel, George J GJ; Drummond, James J; Robinson, Rachel R; Berry, Ian R IR; Wallace, Andrew A; Eccles, Diana M DM; Tischkowitz, Marc M; Ellard, Sian S; Ware, James S JS; Hanson, Helen H; Turnbull, Clare C; ,
Publication Date: 2022-03
Variant appearance in text: MSH2: 1654A>C; Thr552Pro
Molecular analysis of hereditary nonpolyposis colorectal cancer in the United States: high mutation detection rate among clinically selected families and characterization of an American founder genomic deletion of the MSH2 gene.
American Journal Of Human Genetics
Wagner, Anja A; Barrows, Alicia A; Wijnen, Juul Th JT; van der Klift, Heleen H; Franken, Patrick F PF; Verkuijlen, Paul P; Nakagawa, Hidewaki H; Geugien, Marjan M; Jaghmohan-Changur, Shantie S; Breukel, Cor C; Meijers-Heijboer, Hanne H; Morreau, Hans H; van Puijenbroek, Marjo M; Burn, John J; Coronel, Stephany S; Kinarski, Yulia Y; Okimoto, Ross R; Watson, Patrice P; Lynch, Jane F JF; de la Chapelle, Albert A; Lynch, Henry T HT; Fodde, Riccardo R