| Gene/Event | Cancer Type | Patient | Variant | Mutation Level |
|---|---|---|---|---|
| ADAM12 | Breast Cancer | p123_case9 | p.S499N | Trunk mutation |
| ADAM12 | Breast Cancer | p143_p5 | Chr10:127705845:T>G | Private mutation |
| ADAM12 | Colorectal Cancer | p014_CRC3 | p.F739C | Branch mutation |
| ADAM12 | Colorectal Cancer | p034_MSS4 | Chr10:128018997:T>G | Private mutation |
| ADAM12 | Colorectal Cancer | p040_case9 | Chr10:127824205:C>T | Trunk mutation |
| ADAM12 | Colorectal Cancer | p155_p493 | p.K238E | Private mutation |
| ADAM12 | Esophageal Squamous Cell Carcinoma | p124_ESCC025 | p.C464C | Trunk mutation |
| ADAM12 | Esophageal Squamous Cell Carcinoma | p124_ESCC031 | p.S566W | Branch mutation |
| ADAM12 | Esophageal Squamous Cell Carcinoma | p128_SP19 | Chr10:127843815:C>G | Private mutation |
| ADAM12 | Esophageal Squamous Cell Carcinoma | p128_SP19 | Chr10:127705849:G>A | Private mutation |
| ADAM12 | Esophageal Squamous Cell Carcinoma | p128_SP28 | Chr10:127730754:G>A | Private mutation |
| ADAM12 | Gastric Adenocarcinoma | p011_MSI-H2 | p.N505N | Trunk mutation |
| ADAM12 | Gastric Carcinoma | p106_GC14 | p.P457P | Private mutation |
| ADAM12 | Gastric Carcinoma | p106_GC15 | p.N802N | Trunk mutation |
| ADAM12 | Glioblastoma | p113_case01 | p.G48R | Trunk mutation |
| ADAM12 | Glioblastoma | p113_case14 | p.G48R | Trunk mutation |
| ADAM12 | Glioblastoma | p113_case16 | p.G48R | Trunk mutation |
| ADAM12 | Glioblastoma | p113_case21 | p.G48R | Trunk mutation |
| ADAM12 | Glioblastoma | p113_case26 | p.G48R | Trunk mutation |
| ADAM12 | Glioblastoma | p113_case29 | p.G48R | Trunk mutation |
| ADAM12 | Glioblastoma | p113_case32 | p.G48R | Trunk mutation |
| ADAM12 | Glioblastoma | p113_case36 | p.G48R | Trunk mutation |
| ADAM12 | Glioma | p168_P01 | p.V133V | Private mutation |
| ADAM12 | Melanoma | p135_p10 | Chr10:127967521:C>T | Trunk mutation |
| ADAM12 | Renal Cancer | p018_patient2 | Chr10:127737976:G>A | Private mutation |
| ADAM12 | Clear Cell Renal Cell Carcinoma | p019_EV002 | Chr10:127737976:p.R>Q | Private mutation |