Gene/Event |
Cancer Type |
Patient |
Variant |
Mutation Level |
MAGEL2 |
Breast Cancer | p143_p5 |
Chr15:23891009:C>T |
Private mutation |
MAGEL2 |
Colorectal Cancer | p034_MSU3 |
Chr15:23889835:G>A |
Private mutation |
MAGEL2 |
Colorectal Cancer | p040_case1 |
Chr15:23892614:A>C |
Private mutation |
MAGEL2 |
Colorectal Cancer | p040_case9 |
Chr15:23892219:G>- |
Private mutation |
MAGEL2 |
Colorectal Cancer | p104_UC06 |
p.K760T |
Private mutation |
MAGEL2 |
Esophageal Squamous Cell Carcinoma | p128_P01 |
Chr15:23890754:A>G |
Private mutation |
MAGEL2 |
Esophageal Squamous Cell Carcinoma | p128_SP14 |
Chr15:23891107:C>T |
Private mutation |
MAGEL2 |
Esophageal Squamous Cell Carcinoma | p139_EC0961 |
p.P33L |
Private mutation |
MAGEL2 |
Esophageal Squamous Cell Carcinoma | p139_EC1125 |
p.R881H |
Branch mutation |
MAGEL2 |
Gastric Adenocarcinoma | p011_MSS3 |
p.R410H |
Branch mutation |
MAGEL2 |
Gastric Carcinoma | p106_GC01 |
p.P185L |
Private mutation |
MAGEL2 |
Gastric Carcinoma | p106_GC15 |
p.P838P |
Trunk mutation |
MAGEL2 |
Hepato-Cholangiocarcinoma | p078_p6 |
p.R445C |
Private mutation |
MAGEL2 |
Intrahepatic Cholangiocarcinoma | p080_ICC1239 |
p.K1068T |
Private mutation |
MAGEL2 |
Hepatocellular Carcinoma | p151_HCC6690 |
Chr15:23891664:A>T |
Trunk mutation |
MAGEL2 |
Hepatocellular Carcinoma | p151_HCC8257 |
Chr15:23892096:G>T |
Private mutation |
MAGEL2 |
Hepatocellular Carcinoma | p158_pa |
Chr15:23891689:C>T |
Branch mutation |
MAGEL2 |
Lung Adenocarcinoma | p017_356 |
Chr15:23891038:G>C |
Trunk mutation |
MAGEL2 |
Lung Adenocarcinoma | p083_X356 |
- |
Trunk mutation |
MAGEL2 |
Non-Small Cell Lung Cancer | p107_P021 |
p.A190G |
Private mutation |
MAGEL2 |
Melanoma | p043_A |
p.P204L |
Trunk mutation |
MAGEL2 |
Melanoma | p043_A |
p.G166E |
Trunk mutation |
MAGEL2 |
Melanoma | p043_F |
p.P154L |
Trunk mutation |
MAGEL2 |
Melanoma | p043_F |
p.P184L |
Trunk mutation |
MAGEL2 |
Melanoma | p043_H |
p.P595S |
Private mutation |
MAGEL2 |
Melanoma | p043_H |
p.P358L |
Private mutation |
MAGEL2 |
Ovarian Cancer | p153_RJOC08 |
p.R501Q |
Private mutation |