Gene/Event | Cancer Type | Patient | Variant | Mutation Level |
---|---|---|---|---|
CLVS2 | Colorectal Cancer | p155_p494 | p.R59R | Private mutation |
CLVS2 | Esophageal Squamous Cell Carcinoma | p124_ESCC036 | p.A193V | Private mutation |
CLVS2 | Gastric Carcinoma | p106_GC06 | Splice sites | Trunk mutation |
CLVS2 | Gastric Carcinoma | p106_GC14 | p.P42P | Private mutation |
CLVS2 | Glioblastoma | p113_case09 | p.T49M | Branch mutation |
CLVS2 | Glioma | p168_P18 | p.R17R | Private mutation |
CLVS2 | Medulloblastoma | p072_MB6 | Chr6:123369847:G>A | Private mutation |
CLVS2 | Melanoma | p043_F | p.R138H | Trunk mutation |
CLVS2 | Melanoma | p043_F | p.N166S | Trunk mutation |
CLVS2 | Urothelial Carcinoma | p031_WCM259 | p.L326L | Private mutation |