Gene/Event |
Cancer Type |
Patient |
Variant |
Mutation Level |
ARHGAP35 |
Breast Cancer | p123_case2 |
p.D8H |
Private mutation |
ARHGAP35 |
Breast Cancer | p137_p05 |
p.A121V |
Trunk mutation |
ARHGAP35 |
Breast Cancer | p137_p05 |
p.G153R |
Private mutation |
ARHGAP35 |
Breast Cancer | p137_p20 |
p.V1095G |
Trunk mutation |
ARHGAP35 |
Osteosarcoma | p102_OS04 |
Chr19:47423542:A>C |
Branch mutation |
ARHGAP35 |
Colorectal Cancer | p034_MSU2 |
Chr19:47422054:G>A |
Trunk mutation |
ARHGAP35 |
Colorectal Cancer | p034_MSU2 |
Chr19:47423890:C>T |
Private mutation |
ARHGAP35 |
Colorectal Cancer | p104_UC02 |
p.R401W |
Branch mutation |
ARHGAP35 |
Colorectal Cancer | p104_UC02 |
p.A435V |
Branch mutation |
ARHGAP35 |
Colorectal Cancer | p104_UC06 |
p.S845T |
Branch mutation |
ARHGAP35 |
Esophageal Squamous Cell Carcinoma | p124_ESCC010 |
p.N233I |
Private mutation |
ARHGAP35 |
Esophageal Squamous Cell Carcinoma | p124_ESCC012 |
p.E1191Q |
Private mutation |
ARHGAP35 |
Esophageal Squamous Cell Carcinoma | p124_ESCC019 |
p.H72R |
Trunk mutation |
ARHGAP35 |
Esophageal Squamous Cell Carcinoma | p124_ESCC026 |
p.I1282M |
Trunk mutation |
ARHGAP35 |
Esophageal Squamous Cell Carcinoma | p124_ESCC027 |
p.N183S |
Private mutation |
ARHGAP35 |
Esophageal Squamous Cell Carcinoma | p124_ESCC029 |
p.Q103E |
Private mutation |
ARHGAP35 |
Esophageal Squamous Cell Carcinoma | p124_ESCC032 |
p.Q805* |
Trunk mutation |
ARHGAP35 |
Esophageal Squamous Cell Carcinoma | p124_ESCC035 |
p.E712K |
Private mutation |
ARHGAP35 |
Esophageal Squamous Cell Carcinoma | p128_P14 |
Chr19:47423260:C>T |
Private mutation |
ARHGAP35 |
Esophageal Squamous Cell Carcinoma | p128_P14 |
Chr19:47424117:C>T |
Private mutation |
ARHGAP35 |
Esophageal Squamous Cell Carcinoma | p128_SP27 |
Chr19:47423958:G>C |
Private mutation |
ARHGAP35 |
Esophageal Squamous Cell Carcinoma | p139_EC0988 |
p.W1242X |
Private mutation |
ARHGAP35 |
Gastric Adenocarcinoma | p011_MSI-H1 |
p.D1413D |
Branch mutation |
ARHGAP35 |
Gastric Carcinoma | p106_GC09 |
p.A435A |
Private mutation |
ARHGAP35 |
Glioblastoma | p113_case07 |
p.P107S |
Private mutation |
ARHGAP35 |
Glioma | p168_P01 |
p.G1054G |
Private mutation |
ARHGAP35 |
Glioma | p168_P18 |
p.G32E |
Private mutation |
ARHGAP35 |
Glioma | p168_P18 |
p.R688R |
Private mutation |
ARHGAP35 |
Hepato-Cholangiocarcinoma | p078_p1 |
p.R863C |
Private mutation |
ARHGAP35 |
Lung Cancer | p154_p5 |
p.E25K |
Branch mutation |
ARHGAP35 |
Melanoma | p043_H |
p.A455V |
Private mutation |
ARHGAP35 |
Melanoma | p043_H |
p.P45S |
Private mutation |
ARHGAP35 |
Ovarian Cancer | p144_AOCS065 |
p.L733V |
Private mutation |
ARHGAP35 |
Clear Cell Renal Cell Carcinoma | p025_CCCFP5 |
- |
Trunk mutation |
ARHGAP35 |
Clear Cell Renal Cell Carcinoma | p025_CCCFP5 |
- |
Branch mutation |
ARHGAP35 |
Urothelial Carcinoma | p142_p20 |
- |
Trunk mutation |