Gene/Event |
Cancer Type |
Patient |
Variant |
Mutation Level |
NOP2 |
Colorectal Cancer | p155_p493 |
p.L738S |
Private mutation |
NOP2 |
Esophageal Squamous Cell Carcinoma | p124_ESCC024 |
p.K503N |
Trunk mutation |
NOP2 |
Esophageal Squamous Cell Carcinoma | p124_ESCC029 |
p.V226fs |
Private mutation |
NOP2 |
Esophageal Squamous Cell Carcinoma | p128_P05 |
Chr12:6670908:G>A |
Private mutation |
NOP2 |
Esophageal Squamous Cell Carcinoma | p128_P06 |
Chr12:6666450:G>C |
Private mutation |
NOP2 |
Esophageal Squamous Cell Carcinoma | p128_P09 |
Chr12:6675320:G>A |
Private mutation |
NOP2 |
Esophageal Squamous Cell Carcinoma | p128_SP09 |
Chr12:6675320:G>A |
Private mutation |
NOP2 |
Lung Adenocarcinoma | p017_317ss |
Chr12:6670061:G>A |
Branch mutation |
NOP2 |
Clear Cell Renal Cell Carcinoma | p019_EV007 |
Chr12:6677069:p.D>Y |
Branch mutation |
NOP2 |
Renal Cell Carcinoma | p073_RCC6 |
Chr12:6677069:C>A |
Branch mutation |
NOP2 |
Urothelial Carcinoma | p031_WCM249 |
p.E188E |
Branch mutation |