Entries searched:
Gene/Event Cancer Type Patient Variant Mutation Level
RALYL Colorectal Cancer p001_PCRC12 Chr8:85618200:C>T Private mutation
RALYL Colorectal Cancer p155_p252 p.F37L Private mutation
RALYL Esophageal Squamous Cell Carcinoma p124_ESCC005 p.T30K Private mutation
RALYL Esophageal Squamous Cell Carcinoma p128_SP10 Chr8:85800006:G>T Private mutation
RALYL Esophageal Squamous Cell Carcinoma p128_SP27 Chr8:85785527:G>A Private mutation
RALYL Glioma p168_P01 p.G50E Private mutation
RALYL Hepatocellular Carcinoma p151_HCC8213 Chr8:85441553:A>T Trunk mutation
RALYL Melanoma p043_B p.G56S Trunk mutation
RALYL Ovarian Serous Carcinomas p006_OSC3 p.A53A Private mutation
RALYL Prostate Cancer p105_1009 p.L254L Branch mutation
RALYL Prostate Cancer p105_1015 p.Y155F Branch mutation
RALYL Urothelial Carcinoma p142_p10 - Trunk mutation
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