Gene/Event |
Cancer Type |
Patient |
Variant |
Mutation Level |
RNFT2 |
Colorectal Cancer | p004_CRC_A01 |
Chr12:117178943:G>A |
Private mutation |
RNFT2 |
Colorectal Cancer | p034_MSU2 |
Chr12:117271640:G>A |
Trunk mutation |
RNFT2 |
Esophageal Squamous Cell Carcinoma | p124_ESCC023 |
- |
Private mutation |
RNFT2 |
Esophageal Squamous Cell Carcinoma | p128_SP28 |
Chr12:117178320:G>C |
Private mutation |
RNFT2 |
Esophageal Squamous Cell Carcinoma | p139_EC1117 |
p.A106T |
Branch mutation |
RNFT2 |
Esophageal Squamous Cell Carcinoma | p139_EC1125 |
- |
Private mutation |
RNFT2 |
Gastric Carcinoma | p106_GC07 |
p.E210V |
Private mutation |
RNFT2 |
Glioblastoma | p113_case08 |
p.A266T |
Private mutation |
RNFT2 |
Medulloblastoma | p072_MB6 |
Chr12:117289603:A>G |
Branch mutation |
RNFT2 |
Medulloblastoma | p072_MB6 |
Chr12:117289776:G>T |
Private mutation |
RNFT2 |
Urothelial Carcinoma | p031_WCM088 |
p.G374R |
Private mutation |