Gene/Event |
Cancer Type |
Patient |
Variant |
Mutation Level |
KCNH2 |
Breast Cancer | p111_p9-68 |
p.T722N |
Branch mutation |
KCNH2 |
Colorectal Cancer | p001_PCRC10 |
Chr7:150649763:G>A |
Trunk mutation |
KCNH2 |
Colorectal Cancer | p034_MSU3 |
Chr7:150648672:G>A |
Trunk mutation |
KCNH2 |
Colorectal Cancer | p034_MSU4 |
Chr7:150656678-150656679:TG>T |
Private mutation |
KCNH2 |
Esophageal Squamous Cell Carcinoma | p008_ESCC08 |
p.R1051G |
Trunk mutation |
KCNH2 |
Esophageal Squamous Cell Carcinoma | p124_ESCC006 |
p.R328R |
Trunk mutation |
KCNH2 |
Esophageal Squamous Cell Carcinoma | p124_ESCC012 |
p.S906* |
Branch mutation |
KCNH2 |
Esophageal Squamous Cell Carcinoma | p124_ESCC019 |
p.K21T |
Branch mutation |
KCNH2 |
Esophageal Squamous Cell Carcinoma | p124_ESCC034 |
p.F852F |
Private mutation |
KCNH2 |
Esophageal Squamous Cell Carcinoma | p128_P09 |
Chr7:150642563:G>C |
Private mutation |
KCNH2 |
Esophageal Squamous Cell Carcinoma | p128_P18 |
Chr7:150648917:G>T |
Private mutation |
KCNH2 |
Esophageal Squamous Cell Carcinoma | p128_SP09 |
Chr7:150642563:G>C |
Private mutation |
KCNH2 |
Esophageal Squamous Cell Carcinoma | p139_EC0966 |
p.L397Q |
Private mutation |
KCNH2 |
Gastric Adenocarcinoma | p011_MSI-H2 |
p.I149I |
Trunk mutation |
KCNH2 |
Gastric Adenocarcinoma | p011_MSI-H2 |
p.F173F |
Trunk mutation |
KCNH2 |
Gastric Carcinoma | p106_GC06 |
p.A490T |
Trunk mutation |
KCNH2 |
Gastric Carcinoma | p106_GC09 |
p.F686C |
Private mutation |
KCNH2 |
Glioblastoma | p113_case27 |
p.A536V |
Trunk mutation |
KCNH2 |
Hepatocellular Carcinoma | p061_P08 |
Chr7:150644882:G>T |
Branch mutation |
KCNH2 |
Lung Adenocarcinoma | p017_317ss |
Chr7:150648949:C>A |
Trunk mutation |
KCNH2 |
Lung Adenocarcinoma | p134_A014 |
p.A784fs |
Branch mutation |
KCNH2 |
Melanoma | p043_A |
p.D603N |
Trunk mutation |
KCNH2 |
Melanoma | p043_H |
p.P202S |
Private mutation |
KCNH2 |
Ovarian Cancer | p153_RJOC08 |
p.R608H |
Private mutation |
KCNH2 |
Prostate Cancer | p105_1003 |
p.R77H |
Trunk mutation |
KCNH2 |
Urothelial Carcinoma | p031_WCM077 |
p.L697L |
Private mutation |