| Gene/Event | Cancer Type | Patient | Variant | Mutation Level |
|---|---|---|---|---|
| INVS | Colorectal Cancer | p004_CRC_A04 | Chr9:103014761:G>T | Private mutation |
| INVS | Colorectal Cancer | p034_MSU1 | Chr9:103062934:C>CA | Private mutation |
| INVS | Esophageal Squamous Cell Carcinoma | p124_ESCC014 | - | Private mutation |
| INVS | Esophageal Squamous Cell Carcinoma | p128_SP21 | Chr9:103054619:G>C | Private mutation |
| INVS | Gastric Carcinoma | p106_GC03 | p.R815Q | Private mutation |
| INVS | Gastric Carcinoma | p106_GC07 | p.T223T | Private mutation |
| INVS | Gastric Carcinoma | p106_GC09 | p.A926T | Private mutation |
| INVS | Gastric Carcinoma | p106_GC09 | p.E970G | Private mutation |
| INVS | Gastric Carcinoma | p106_GC09 | p.A919A | Private mutation |
| INVS | Glioblastoma | p113_case08 | p.Q887* | Private mutation |
| INVS | Medulloblastoma | p072_MB6 | Chr9:103027355:C>G | Branch mutation |
| INVS | Medulloblastoma | p072_MB6 | Chr9:103027356:C>T | Branch mutation |
| INVS | Medulloblastoma | p072_MB6 | Chr9:103027003:T>A | Private mutation |
| INVS | Melanoma | p043_A | p.E780K | Trunk mutation |
| INVS | Melanoma | p043_F | p.R832Q | Trunk mutation |