| Gene/Event | Cancer Type | Patient | Variant | Mutation Level |
|---|---|---|---|---|
| H1FNT | Breast Cancer | p143_p5 | Chr12:48723500:C>T | Branch mutation |
| H1FNT | Esophageal Squamous Cell Carcinoma | p124_ESCC029 | p.A99V | Branch mutation |
| H1FNT | Esophageal Squamous Cell Carcinoma | p139_EC1111 | p.R59T | Branch mutation |
| H1FNT | Gastric Carcinoma | p106_GC09 | p.R185S | Private mutation |
| H1FNT | Intrahepatic Cholangiocarcinoma | p080_ICC1239 | p.P227Q | Private mutation |
| H1FNT | Melanoma | p043_F | p.R84Q | Trunk mutation |
| H1FNT | Ovarian Cancer | p144_AOCS034 | p.T147P | Private mutation |
| H1FNT | Urothelial Carcinoma | p031_WCM088 | p.G17G | Private mutation |
| H1FNT | Urothelial Carcinoma | p031_WCM117 | p.E215K | Private mutation |