| Gene/Event | Cancer Type | Patient | Variant | Mutation Level |
|---|---|---|---|---|
| BOC | Breast Cancer | p123_case3 | p.P446P | Trunk mutation |
| BOC | Colorectal Cancer | p001_PCRC03 | Chr3:113004270:C>T | Trunk mutation |
| BOC | Colorectal Cancer | p001_PCRC05 | Chr3:112991379:T>C | Private mutation |
| BOC | Colorectal Cancer | p034_MSU1 | Chr3:112999459:C>T | Trunk mutation |
| BOC | Colorectal Cancer | p034_MSU2 | Chr3:113005674:C>T | Trunk mutation |
| BOC | Colorectal Cancer | p155_p493 | p.A112V | Private mutation |
| BOC | Esophageal Squamous Cell Carcinoma | p008_ESCC03 | p.E1092K | Branch mutation |
| BOC | Esophageal Squamous Cell Carcinoma | p128_P02 | Chr3:112998817:G>A | Private mutation |
| BOC | Gastric Adenocarcinoma | p011_MSI-H2 | p.Q915H | Trunk mutation |
| BOC | Gastric Adenocarcinoma | p011_MSI-H2 | p.I241I | Trunk mutation |
| BOC | Gastric Adenocarcinoma | p011_MSI-H2 | p.P335P | Trunk mutation |
| BOC | Anaplastic Astrocytoma | p070_HGG1 | Chr3:112987277:C>A | Private mutation |
| BOC | Glioblastoma | p113_case26 | p.A190V | Private mutation |
| BOC | Hepatocellular Carcinoma | p151_HCC6952 | Chr3:112969420:C>G | Trunk mutation |
| BOC | Acute Myeloid Leukemia | p114_AML40 | p.G747 | Trunk mutation |
| BOC | Lung Adenocarcinoma | p017_317ss | Chr3:112987253:C>T | Trunk mutation |
| BOC | Squamous Cell Lung Carcinoma | p100_p2 | Chr3:112989729:C>G | Private mutation |
| BOC | Melanoma | p043_H | p.R602C | Private mutation |
| BOC | Melanoma | p043_H | p.V847M | Private mutation |
| BOC | Melanoma | p135_p10 | Chr3:112969664:C>T | Trunk mutation |
| BOC | Prostate Cancer | p164_P1 | p.P913S | Branch mutation |
| BOC | Renal Cell Carcinoma | p073_RCC1 | Chr3:113004342:C>A | Branch mutation |
| BOC | Urothelial Carcinoma | p031_WCM088 | Chr3:112935113:G>C | Private mutation |
| BOC | Urothelial Carcinoma | p031_WCM117 | p.C956* | Private mutation |
| BOC | Urothelial Carcinoma | p031_WCM249 | p.C956* | Private mutation |
| BOC | Urothelial Carcinoma | p142_p36 | - | Private mutation |