Gene/Event |
Cancer Type |
Patient |
Variant |
Mutation Level |
INO80 |
Osteosarcoma | p112_OS1101 |
p.A275V |
Branch mutation |
INO80 |
Colorectal Cancer | p034_MSU1 |
Chr15:41297826:C>T |
Private mutation |
INO80 |
Colorectal Cancer | p104_UC01 |
p.A1476V |
Branch mutation |
INO80 |
Esophageal Squamous Cell Carcinoma | p124_ESCC012 |
p.S97F |
Trunk mutation |
INO80 |
Esophageal Squamous Cell Carcinoma | p124_ESCC022 |
p.E52* |
Private mutation |
INO80 |
Esophageal Squamous Cell Carcinoma | p124_ESCC030 |
p.K453K |
Branch mutation |
INO80 |
Esophageal Squamous Cell Carcinoma | p128_P01 |
Chr15:41379870:A>G |
Private mutation |
INO80 |
Glioma | p168_P01 |
p.T263I |
Private mutation |
INO80 |
Hepatocellular Carcinoma | p061_P03 |
Chr15:41272481:T>A |
Trunk mutation |
INO80 |
Hepatocellular Carcinoma | p061_P09 |
Chr15:41276415:T>C |
Trunk mutation |
INO80 |
Hepatocellular Carcinoma | p158_pa |
Chr15:41308142:C>-A |
Branch mutation |
INO80 |
Medulloblastoma | p072_MB6 |
Chr15:41455833:G>T |
Branch mutation |
INO80 |
Medulloblastoma | p072_MB6 |
Chr15:41455898:G>C |
Branch mutation |
INO80 |
Medulloblastoma | p072_MB6 |
Chr15:41339766:T>C |
Private mutation |
INO80 |
Melanoma | p043_A |
p.D1195N |
Trunk mutation |
INO80 |
Melanoma | p043_F |
p.P241S |
Trunk mutation |
INO80 |
Urothelial Carcinoma | p031_WCM168 |
p.E83K |
Branch mutation |