Gene/Event |
Cancer Type |
Patient |
Variant |
Mutation Level |
NLGN2 |
Colorectal Cancer | p034_MSU1 |
Chr17:7311965:G>A |
Private mutation |
NLGN2 |
Colorectal Cancer | p034_MSU1 |
Chr17:7320506-7320507:TC>T |
Private mutation |
NLGN2 |
Colorectal Cancer | p155_p496 |
p.T674T |
Private mutation |
NLGN2 |
Esophageal Squamous Cell Carcinoma | p124_ESCC021 |
p.A162E |
Private mutation |
NLGN2 |
Esophageal Squamous Cell Carcinoma | p124_ESCC037 |
p.L728M |
Private mutation |
NLGN2 |
Esophageal Squamous Cell Carcinoma | p124_ESCC037 |
p.I691I |
Private mutation |
NLGN2 |
Esophageal Squamous Cell Carcinoma | p124_ESCC037 |
p.P737L |
Private mutation |
NLGN2 |
Gastric Adenocarcinoma | p011_MSI-H2 |
p.G381G |
Trunk mutation |
NLGN2 |
Glioblastoma | p113_case07 |
p.G385E |
Private mutation |
NLGN2 |
Melanoma | p043_F |
p.P26S |
Trunk mutation |
NLGN2 |
Melanoma | p043_F |
p.P814L |
Trunk mutation |
NLGN2 |
Urothelial Carcinoma | p031_WCM077 |
p.R159L |
Private mutation |