| Gene/Event | Cancer Type | Patient | Variant | Mutation Level |
|---|---|---|---|---|
| TRIM2 | Colorectal Cancer | p004_CRC_A01 | Chr4:154216615:G>A | Private mutation |
| TRIM2 | Colorectal Cancer | p104_UC02 | p.A174T | Branch mutation |
| TRIM2 | Colorectal Cancer | p147_a09 | p.R612C | Private mutation |
| TRIM2 | Colorectal Cancer | p147_a20 | p.R502X | Private mutation |
| TRIM2 | Esophageal Squamous Cell Carcinoma | p124_ESCC012 | p.E327D | Private mutation |
| TRIM2 | Gastric Carcinoma | p106_GC01 | p.G20G | Private mutation |
| TRIM2 | Gastric Carcinoma | p106_GC02 | p.G20G | Private mutation |
| TRIM2 | Gastric Carcinoma | p106_GC03 | p.G20G | Private mutation |
| TRIM2 | Gastric Carcinoma | p106_GC06 | p.G20G | Private mutation |
| TRIM2 | Gastric Carcinoma | p106_GC09 | p.D400D | Private mutation |
| TRIM2 | Hepatocellular Carcinoma | p061_P07 | Chr4:154197271:C>A | Branch mutation |
| TRIM2 | Hepatocellular Carcinoma | p151_HCC5647 | Chr4:154217036:A>T | Trunk mutation |
| TRIM2 | Renal Cell Carcinoma | p073_RCC5 | Chr4:154236504:T>G | Branch mutation |
| TRIM2 | Urothelial Carcinoma | p031_WCM088 | p.G334G | Private mutation |