Gene/Event |
Cancer Type |
Patient |
Variant |
Mutation Level |
ARHGAP39 |
Osteosarcoma | p102_OS04 |
Chr8:145772742:C>T |
Branch mutation |
ARHGAP39 |
Colorectal Cancer | p034_MSU4 |
Chr8:145773629:G>C |
Private mutation |
ARHGAP39 |
Colorectal Cancer | p040_case4 |
Chr8:145772883:G>A |
Branch mutation |
ARHGAP39 |
Esophageal Squamous Cell Carcinoma | p008_ESCC07 |
p.Q107H |
Trunk mutation |
ARHGAP39 |
Esophageal Squamous Cell Carcinoma | p124_ESCC002 |
p.Q376H |
Private mutation |
ARHGAP39 |
Esophageal Squamous Cell Carcinoma | p124_ESCC011 |
p.E32D |
Trunk mutation |
ARHGAP39 |
Esophageal Squamous Cell Carcinoma | p124_ESCC012 |
p.S500F |
Branch mutation |
ARHGAP39 |
Esophageal Squamous Cell Carcinoma | p124_ESCC012 |
p.W617C |
Private mutation |
ARHGAP39 |
Esophageal Squamous Cell Carcinoma | p124_ESCC023 |
p.C744Y |
Private mutation |
ARHGAP39 |
Esophageal Squamous Cell Carcinoma | p139_EC1110 |
p.F710L |
Branch mutation |
ARHGAP39 |
Gastric Adenocarcinoma | p011_MSI-H2 |
p.D1022D |
Trunk mutation |
ARHGAP39 |
Gastric Carcinoma | p106_GC09 |
p.R212C |
Private mutation |
ARHGAP39 |
Glioblastoma | p113_case07 |
p.E1094K |
Private mutation |
ARHGAP39 |
Glioma | p168_P18 |
p.K880K |
Private mutation |
ARHGAP39 |
Small Cell Lung Carcinoma | p100_p4 |
Chr8:145772716:T>C |
Trunk mutation |
ARHGAP39 |
Melanoma | p043_H |
p.V733M |
Branch mutation |
ARHGAP39 |
Clear Cell Renal Cell Carcinoma | p019_RK26 |
Chr8:145771055:p.K>T |
Branch mutation |
ARHGAP39 |
Renal Cell Carcinoma | p073_RCC5 |
Chr8:145830896:T>C |
Branch mutation |
ARHGAP39 |
Renal Cell Carcinoma | p073_RCC7 |
Chr8:145771055:T>G |
Branch mutation |