| Gene/Event | Cancer Type | Patient | Variant | Mutation Level |
|---|---|---|---|---|
| LNX2 | Colorectal Cancer | p040_case9 | Chr13:28143253:G>A | Branch mutation |
| LNX2 | Esophageal Squamous Cell Carcinoma | p128_P12 | Chr13:28143356:T>G | Private mutation |
| LNX2 | Esophageal Squamous Cell Carcinoma | p139_EC0949 | p.D600N | Branch mutation |
| LNX2 | Gastric Carcinoma | p106_GC09 | p.G184G | Private mutation |
| LNX2 | Glioblastoma | p113_case07 | p.G348D | Private mutation |
| LNX2 | Glioblastoma | p113_case07 | p.A195V | Private mutation |
| LNX2 | Glioblastoma | p113_case24 | p.V261L | Trunk mutation |
| LNX2 | Melanoma | p043_G | p.R143W | Trunk mutation |
| LNX2 | Prostate Cancer | p164_P1 | p.S198P | Branch mutation |
| LNX2 | Prostate Cancer | p164_P2 | p.S198P | Private mutation |
| LNX2 | Renal Cell Carcinoma | p073_RCC1 | Chr13:28155586:C>T | Private mutation |
| LNX2 | Urothelial Carcinoma | p031_WCM077 | p.R675R | Branch mutation |