Gene/Event |
Cancer Type |
Patient |
Variant |
Mutation Level |
DENND2A |
Breast Cancer | p143_p5 |
Chr7:140269464:C>A |
Trunk mutation |
DENND2A |
Breast Cancer | p143_p5 |
Chr7:140255509:C>T |
Private mutation |
DENND2A |
Colorectal Cancer | p001_PCRC05 |
Chr7:140273661:A>C |
Private mutation |
DENND2A |
Colorectal Cancer | p034_MSU1 |
Chr7:140218540-140218541:TA>T |
Private mutation |
DENND2A |
Colorectal Cancer | p034_MSU2 |
Chr7:140221700:G>A |
Private mutation |
DENND2A |
Colorectal Cancer | p034_MSU4 |
Chr7:140218540-140218542:TAA>T |
Private mutation |
DENND2A |
Esophageal Squamous Cell Carcinoma | p124_ESCC027 |
p.R143P |
Branch mutation |
DENND2A |
Esophageal Squamous Cell Carcinoma | p124_ESCC035 |
p.G658G |
Private mutation |
DENND2A |
Esophageal Squamous Cell Carcinoma | p124_ESCC035 |
p.I557I |
Private mutation |
DENND2A |
Esophageal Squamous Cell Carcinoma | p139_EC0990 |
p.V217D |
Private mutation |
DENND2A |
Gastric Adenocarcinoma | p011_MSI-H1 |
- |
Trunk mutation |
DENND2A |
Glioblastoma | p113_case14 |
p.D351E |
Private mutation |
DENND2A |
Glioma | p168_P01 |
p.E527E |
Branch mutation |
DENND2A |
Lung Adenocarcinoma | p017_330 |
Chr7:140223187:T>A |
Private mutation |
DENND2A |
Lung Adenocarcinoma | p017_317ss |
Chr7:140244299:C>T |
Trunk mutation |
DENND2A |
Lung Adenocarcinoma | p017_317ss |
Chr7:140301619:G>T |
Trunk mutation |
DENND2A |
Lung Adenocarcinoma | p083_X330 |
- |
Private mutation |
DENND2A |
Melanoma | p043_F |
p.P778L |
Trunk mutation |
DENND2A |
Melanoma | p043_H |
p.T228I |
Private mutation |
DENND2A |
Ovarian Serous Carcinomas | p006_OSC3 |
p.R976P |
Branch mutation |
DENND2A |
Ovarian Cancer | p144_AOCS137 |
p.R100K |
Private mutation |
DENND2A |
Prostate Cancer | p105_1027 |
p.V117I |
Branch mutation |
DENND2A |
Renal Cell Carcinoma | p073_RCC5 |
Chr7:140301180:T>C |
Trunk mutation |
DENND2A |
Renal Cell Carcinoma | p073_RCC5 |
Chr7:140285288:T>G |
Branch mutation |
DENND2A |
Urothelial Carcinoma | p031_WCM088 |
p.V135M |
Private mutation |
DENND2A |
Urothelial Carcinoma | p031_WCM233 |
p.V539M |
Private mutation |