Gene/Event |
Cancer Type |
Patient |
Variant |
Mutation Level |
H1FNT |
Breast Cancer | p143_p5 |
Chr12:48723500:C>T |
Branch mutation |
H1FNT |
Esophageal Squamous Cell Carcinoma | p124_ESCC029 |
p.A99V |
Branch mutation |
H1FNT |
Esophageal Squamous Cell Carcinoma | p139_EC1111 |
p.R59T |
Branch mutation |
H1FNT |
Gastric Carcinoma | p106_GC09 |
p.R185S |
Private mutation |
H1FNT |
Intrahepatic Cholangiocarcinoma | p080_ICC1239 |
p.P227Q |
Private mutation |
H1FNT |
Melanoma | p043_F |
p.R84Q |
Trunk mutation |
H1FNT |
Ovarian Cancer | p144_AOCS034 |
p.T147P |
Private mutation |
H1FNT |
Urothelial Carcinoma | p031_WCM088 |
p.G17G |
Private mutation |
H1FNT |
Urothelial Carcinoma | p031_WCM117 |
p.E215K |
Private mutation |