Gene/Event |
Cancer Type |
Patient |
Variant |
Mutation Level |
NPFFR2 |
Colorectal Cancer | p001_PCRC10 |
Chr4:72897736:G>A |
Trunk mutation |
NPFFR2 |
Colorectal Cancer | p001_PCRC13 |
Chr4:73013583:T>A |
Private mutation |
NPFFR2 |
Colorectal Cancer | p040_case7 |
Chr4:73003775:C>T |
Private mutation |
NPFFR2 |
Colorectal Cancer | p104_UC02 |
p.T200N |
Branch mutation |
NPFFR2 |
Colorectal Cancer | p155_p337 |
p.T218M |
Private mutation |
NPFFR2 |
Colorectal Cancer | p155_p492 |
p.G342G |
Private mutation |
NPFFR2 |
Esophageal Squamous Cell Carcinoma | p008_ESCC03 |
p.K25M |
Branch mutation |
NPFFR2 |
Esophageal Squamous Cell Carcinoma | p124_ESCC027 |
p.S20* |
Private mutation |
NPFFR2 |
Esophageal Squamous Cell Carcinoma | p128_P02 |
Chr4:73012767:C>A |
Trunk mutation |
NPFFR2 |
Esophageal Squamous Cell Carcinoma | p128_P14 |
Chr4:72994621:G>A |
Private mutation |
NPFFR2 |
Glioblastoma | p113_case15 |
p.R458Efs*10 |
Private mutation |
NPFFR2 |
Glioma | p168_P18 |
p.A22T |
Private mutation |
NPFFR2 |
Hepatocellular Carcinoma | p151_HCC5647 |
Chr4:73003854:T>C |
Trunk mutation |
NPFFR2 |
Renal Cell Carcinoma | p073_RCC3 |
Chr4:73003675:C>A |
Private mutation |