Gene/Event |
Cancer Type |
Patient |
Variant |
Mutation Level |
NUP88 |
Colorectal Cancer | p004_CRC_A01 |
Chr17:5294876:C>T |
Private mutation |
NUP88 |
Colorectal Cancer | p040_case9 |
Chr17:5314096:G>A |
Trunk mutation |
NUP88 |
Colorectal Cancer | p104_UC01 |
p.V223A |
Branch mutation |
NUP88 |
Colorectal Cancer | p147_a21 |
p.W140R |
Private mutation |
NUP88 |
Esophageal Squamous Cell Carcinoma | p124_ESCC035 |
p.VNCR153del |
Private mutation |
NUP88 |
Esophageal Squamous Cell Carcinoma | p128_P25 |
Chr17:5290945:C>G |
Private mutation |
NUP88 |
Esophageal Squamous Cell Carcinoma | p128_SP07 |
Chr17:5302899:C>G |
Private mutation |
NUP88 |
Esophageal Squamous Cell Carcinoma | p128_SP23 |
Chr17:5290988:T>C |
Private mutation |
NUP88 |
Esophageal Squamous Cell Carcinoma | p139_EC1000 |
p.W492C |
Private mutation |
NUP88 |
Intrahepatic Cholangiocarcinoma | p159_Pat4 |
p.K600EfsX21 |
Trunk mutation |
NUP88 |
Hepatocellular Carcinoma | p061_P02 |
Chr17:5290040:A>G |
Branch mutation |
NUP88 |
Urothelial Carcinoma | p142_p33 |
- |
Private mutation |