| Gene/Event | Cancer Type | Patient | Variant | Mutation Level |
|---|---|---|---|---|
| HMCN2 | Breast Cancer | p143_p4 | Chr9:133272928:C>T | Private mutation |
| HMCN2 | Colorectal Cancer | p001_PCRC03 | Chr9:133301277:C>T | Private mutation |
| HMCN2 | Colorectal Cancer | p001_PCRC08 | Chr9:133048496:C>T | Private mutation |
| HMCN2 | Colorectal Cancer | p155_p493 | p.I556N | Private mutation |
| HMCN2 | Esophageal Squamous Cell Carcinoma | p124_ESCC012 | p.N91N | Private mutation |
| HMCN2 | Esophageal Squamous Cell Carcinoma | p139_EC0990 | - | Private mutation |
| HMCN2 | Intrahepatic Cholangiocarcinoma | p080_ICC772 | p.I3174T | Private mutation |
| HMCN2 | Intrahepatic Cholangiocarcinoma | p080_ICC880 | p.P2806T | Branch mutation |
| HMCN2 | Intrahepatic Cholangiocarcinoma | p080_ICC892 | p.P2806T | Branch mutation |
| HMCN2 | Intrahepatic Cholangiocarcinoma | p080_ICC1239 | p.P2806T | Branch mutation |
| HMCN2 | Intrahepatic Cholangiocarcinoma | p080_ICC1969 | p.V148M | Private mutation |
| HMCN2 | Ovarian Cancer | p144_AOCS064 | - | Private mutation |
| HMCN2 | Urothelial Carcinoma | p031_WCM088 | p.G466S | Private mutation |