Entries searched:
Gene/Event Cancer Type Patient Variant Mutation Level
FAM181B Colorectal Cancer p001_PCRC08 Chr11:82443444:C>T Private mutation
FAM181B Colorectal Cancer p040_case9 Chr11:82443998:G>A Private mutation
FAM181B Esophageal Squamous Cell Carcinoma p124_ESCC014 p.P386P Branch mutation
FAM181B Gastric Adenocarcinoma p011_MSS2 p.S87L Private mutation
FAM181B Ovarian Cancer p144_AOCS034 p.G24A Trunk mutation
FAM181B Renal Cell Carcinoma p073_RCC4 Chr11:82517094:C>T Branch mutation
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