Gene/Event |
Cancer Type |
Patient |
Variant |
Mutation Level |
PXN |
Colorectal Cancer | p004_CRC_A01 |
Chr12:120653401:C>T |
Private mutation |
PXN |
Colorectal Cancer | p155_p496 |
p.V384Afs*29 |
Private mutation |
PXN |
Esophageal Squamous Cell Carcinoma | p124_ESCC035 |
p.P326P |
Private mutation |
PXN |
Gastric Carcinoma | p106_GC11 |
p.F486F |
Private mutation |
PXN |
Glioblastoma | p070_HGG2 |
Chr12:120720084:C>A |
Private mutation |
PXN |
Glioblastoma | p113_case07 |
p.E114K |
Private mutation |
PXN |
Intrahepatic Cholangiocarcinoma | p080_ICC1370 |
p.E865K |
Private mutation |