| Gene/Event | Cancer Type | Patient | Variant | Mutation Level |
|---|---|---|---|---|
| ARHGAP28 | Colorectal Cancer | p040_case2 | Chr18:6837201:G>T | Trunk mutation |
| ARHGAP28 | Esophageal Squamous Cell Carcinoma | p124_ESCC033 | p.S291F | Private mutation |
| ARHGAP28 | Gastric Carcinoma | p106_GC08 | Splice sites | Trunk mutation |
| ARHGAP28 | Glioma | p168_P01 | p.L491L | Private mutation |
| ARHGAP28 | Medulloblastoma | p072_MB6 | Chr18:6890403:C>A | Private mutation |
| ARHGAP28 | Melanoma | p043_F | p.R91Q | Trunk mutation |
| ARHGAP28 | Melanoma | p043_F | p.R515G | Trunk mutation |
| ARHGAP28 | Urothelial Carcinoma | p142_p19 | - | Private mutation |