| Gene/Event | Cancer Type | Patient | Variant | Mutation Level |
|---|---|---|---|---|
| CENPF | Breast Cancer | p103_pat04 | Chr1:214819712:G>T | Branch mutation |
| CENPF | Breast Cancer | p143_p4 | Chr1:214795535:G>A | Branch mutation |
| CENPF | Osteosarcoma | p102_OS04 | Chr1:214816066:A>G | Branch mutation |
| CENPF | Osteosarcoma | p102_OS04 | Chr1:214816067:G>T | Branch mutation |
| CENPF | Colorectal Cancer | p034_MSU1 | Chr1:214825170:C>A | Trunk mutation |
| CENPF | Colorectal Cancer | p040_case5 | Chr1:214816655:C>T | Trunk mutation |
| CENPF | Colorectal Cancer | p069_p14 | p.A2371E | Private mutation |
| CENPF | Colorectal Cancer | p147_a09 | p.S2957G | Private mutation |
| CENPF | Esophageal Squamous Cell Carcinoma | p124_ESCC009 | p.E2627* | Trunk mutation |
| CENPF | Esophageal Squamous Cell Carcinoma | p124_ESCC027 | p.H1691Y | Private mutation |
| CENPF | Esophageal Squamous Cell Carcinoma | p128_P15 | Chr1:214818131:C>T | Private mutation |
| CENPF | Esophageal Squamous Cell Carcinoma | p139_EC0966 | p.N1961S | Trunk mutation |
| CENPF | Esophageal Squamous Cell Carcinoma | p139_EC0990 | - | Private mutation |
| CENPF | Esophageal Squamous Cell Carcinoma | p139_EC1020 | p.I1201S | Private mutation |
| CENPF | Esophageal Squamous Cell Carcinoma | p139_EC1117 | p.Q1929X | Branch mutation |
| CENPF | Esophageal Squamous Cell Carcinoma | p139_EC1155 | p.Q2532X | Private mutation |
| CENPF | Gastric Adenocarcinoma | p011_MSI-H2 | p.E2553K | Trunk mutation |
| CENPF | Glioblastoma | p070_HGG2 | Chr1:214805939:C>A | Branch mutation |
| CENPF | Glioblastoma | p113_case07 | p.S194N | Private mutation |
| CENPF | Glioblastoma | p113_case07 | p.Q1520* | Private mutation |
| CENPF | Glioblastoma | p113_case26 | p.E2918K | Private mutation |
| CENPF | Glioblastoma | p113_case36 | p.K1049N | Private mutation |
| CENPF | Glioma | p168_P18 | p.E1076K | Private mutation |
| CENPF | Intrahepatic Cholangiocarcinoma | p080_ICC892 | p.Q3046P | Private mutation |
| CENPF | Hepatocellular Carcinoma | p061_P05 | Chr1:214818930:A>T | Trunk mutation |
| CENPF | Hepatocellular Carcinoma | p157_p4 | p.N267S | Branch mutation |
| CENPF | Lung Cancer | p154_p1 | p.K1623N | Branch mutation |
| CENPF | Melanoma | p043_A | p.C1825G | Branch mutation |
| CENPF | Melanoma | p043_H | p.E249K | Private mutation |
| CENPF | Melanoma | p043_H | p.R2078K | Private mutation |
| CENPF | Prostate Cancer | p023_patient04101 | - | Private mutation |
| CENPF | Prostate Cancer | p023_patient05144 | - | Trunk mutation |
| CENPF | Clear Cell Renal Cell Carcinoma | p019_EV006 | Chr1:214818616:p.E>D | Trunk mutation |
| CENPF | Clear Cell Renal Cell Carcinoma | p019_RMH002 | Chr1:214816224:p.A>T | Branch mutation |
| CENPF | Renal Cancer | p024_GK101 | - | Trunk mutation |
| CENPF | Renal Cell Carcinoma | p073_RCC5 | Chr1:214818616:A>C | Trunk mutation |
| CENPF | Renal Cell Carcinoma | p073_RCC5 | Chr1:214781778:A>G | Branch mutation |
| CENPF | Renal Cell Carcinoma | p073_RCC8 | Chr1:214816224:G>A | Branch mutation |