| Gene/Event | Cancer Type | Patient | Variant | Mutation Level |
|---|---|---|---|---|
| GLTSCR1 | Breast Cancer | p111_p8-82 | p.Q681X | Private mutation |
| GLTSCR1 | Breast Cancer | p143_p5 | Chr19:48179121:A>G | Private mutation |
| GLTSCR1 | Colorectal Cancer | p001_PCRC10 | Chr19:48197810:C>T | Trunk mutation |
| GLTSCR1 | Colorectal Cancer | p001_PCRC12 | Chr19:48198671:C>T | Branch mutation |
| GLTSCR1 | Colorectal Cancer | p034_MSU1 | Chr19:48197890-48197891:AC>A | Private mutation |
| GLTSCR1 | Colorectal Cancer | p034_MSU4 | Chr19:48183557:C>T | Private mutation |
| GLTSCR1 | Colorectal Cancer | p034_MSU4 | Chr19:48205549:G>A | Private mutation |
| GLTSCR1 | Colorectal Cancer | p040_case9 | Chr19:48198197:C>G | Private mutation |
| GLTSCR1 | Colorectal Cancer | p104_UC02 | p.S525R | Branch mutation |
| GLTSCR1 | Colorectal Cancer | p155_p494 | p.S412L | Private mutation |
| GLTSCR1 | Esophageal Squamous Cell Carcinoma | p124_ESCC012 | p.A296T | Trunk mutation |
| GLTSCR1 | Esophageal Squamous Cell Carcinoma | p124_ESCC018 | p.S305F | Trunk mutation |
| GLTSCR1 | Esophageal Squamous Cell Carcinoma | p128_P03 | Chr19:48202314:C>T | Private mutation |
| GLTSCR1 | Esophageal Squamous Cell Carcinoma | p139_EC1020 | p.Q395X | Private mutation |
| GLTSCR1 | Gastric Adenocarcinoma | p011_MSI-H1 | - | Branch mutation |
| GLTSCR1 | Gastric Carcinoma | p106_GC04 | p.T1325T | Private mutation |
| GLTSCR1 | Glioblastoma | p113_case07 | p.A1214T | Private mutation |
| GLTSCR1 | Glioblastoma | p113_case28 | p.P980S | Private mutation |
| GLTSCR1 | Lung Adenocarcinoma | p017_330 | Chr19:48205166:G>A | Trunk mutation |
| GLTSCR1 | Lung Adenocarcinoma | p083_X330 | - | Trunk mutation |
| GLTSCR1 | Melanoma | p043_H | p.P940L | Private mutation |
| GLTSCR1 | Prostate Cancer | p023_patient04101 | - | Private mutation |
| GLTSCR1 | Urothelial Carcinoma | p031_WCM077 | p.T1498T | Branch mutation |
| GLTSCR1 | Urothelial Carcinoma | p031_WCM088 | p.T902A | Trunk mutation |
| GLTSCR1 | Urothelial Carcinoma | p031_WCM117 | p.P478L | Branch mutation |