Gene/Event |
Cancer Type |
Patient |
Variant |
Mutation Level |
USP54 |
Breast Cancer | p143_p1 |
Chr10:75276339:C>T |
Branch mutation |
USP54 |
Colorectal Cancer | p034_MSU4 |
Chr10:75302839:C>A |
Private mutation |
USP54 |
Colorectal Cancer | p104_UC02 |
p.A78T |
Branch mutation |
USP54 |
Colorectal Cancer | p104_UC06 |
p.S73C |
Branch mutation |
USP54 |
Colorectal Cancer | p146_CR108 |
p.H1205N |
Private mutation |
USP54 |
Colorectal Cancer | p147_a16 |
p.E1028V |
Private mutation |
USP54 |
Esophageal Squamous Cell Carcinoma | p124_ESCC010 |
p.S1620* |
Private mutation |
USP54 |
Esophageal Squamous Cell Carcinoma | p124_ESCC012 |
p.S1425* |
Branch mutation |
USP54 |
Mixed Adenoneuroendocrine Carcinoma | p125_M9 |
Chr10:75277207:C>A |
Branch mutation |
USP54 |
Esophageal Squamous Cell Carcinoma | p128_P08 |
Chr10:75302838:G>A |
Private mutation |
USP54 |
Esophageal Squamous Cell Carcinoma | p128_SP08 |
Chr10:75302838:G>A |
Private mutation |
USP54 |
Anaplastic Astrocytoma | p070_HGG1 |
Chr10:75264764:C>A |
Private mutation |
USP54 |
Glioblastoma | p113_case07 |
p.P1613L |
Private mutation |
USP54 |
Glioblastoma | p113_case08 |
p.A147V |
Private mutation |
USP54 |
Glioblastoma | p113_case27 |
p.D676G |
Private mutation |
USP54 |
Glioma | p168_P90 |
p.A821G |
Private mutation |
USP54 |
Intrahepatic Cholangiocarcinoma | p080_ICC1239 |
p.A833S |
Private mutation |
USP54 |
Intrahepatic Cholangiocarcinoma | p159_Pat4 |
p.S1154R |
Trunk mutation |
USP54 |
Lung Adenocarcinoma | p017_330 |
Chr10:75277490:C>T |
Trunk mutation |
USP54 |
Lung Adenocarcinoma | p017_317ss |
Chr10:75276616:G>C |
Trunk mutation |
USP54 |
Melanoma | p043_F |
p.K579E |
Trunk mutation |
USP54 |
Melanoma | p135_p25 |
Chr10:75279693:A>G |
Trunk mutation |
USP54 |
Ovarian Cancer | p144_AOCS092 |
p.Y96S |
Trunk mutation |
USP54 |
Ovarian Cancer | p153_RJOC10 |
p.T1292M |
Private mutation |
USP54 |
Renal Cancer | p024_RK36 |
- |
Private mutation |
USP54 |
Renal Cell Carcinoma | p073_RCC5 |
Chr10:75286613:T>C |
Branch mutation |
USP54 |
Urothelial Carcinoma | p031_WCM249 |
p.A1570A |
Private mutation |