Gene/Event |
Cancer Type |
Patient |
Variant |
Mutation Level |
USP29 |
Colorectal Cancer | p034_MSU3 |
Chr19:57641918:C>T |
Trunk mutation |
USP29 |
Colorectal Cancer | p040_case7 |
Chr19:57641832:C>A |
Private mutation |
USP29 |
Colorectal Cancer | p040_case7 |
Chr19:57641833:C>A |
Private mutation |
USP29 |
Esophageal Squamous Cell Carcinoma | p124_ESCC012 |
p.L184L |
Private mutation |
USP29 |
Esophageal Squamous Cell Carcinoma | p124_ESCC031 |
p.E732K |
Private mutation |
USP29 |
Esophageal Squamous Cell Carcinoma | p124_ESCC035 |
p.R513L |
Trunk mutation |
USP29 |
Esophageal Squamous Cell Carcinoma | p139_EC1125 |
p.L4V |
Private mutation |
USP29 |
Gastric Adenocarcinoma | p011_MSI-H1 |
p.K808N |
Trunk mutation |
USP29 |
Gastric Carcinoma | p106_GC15 |
p.T132T |
Private mutation |
USP29 |
Gastric Carcinoma | p106_GC15 |
p.L200L |
Private mutation |
USP29 |
Glioblastoma | p113_case03 |
p.V701I |
Trunk mutation |
USP29 |
Hepatocellular Carcinoma | p061_P10 |
Chr19:57641344:T>A |
Trunk mutation |
USP29 |
Hepatocellular Carcinoma | p151_HCC5647 |
Chr19:57640280:C>A |
Trunk mutation |
USP29 |
Melanoma | p043_F |
p.Q52* |
Trunk mutation |
USP29 |
Melanoma | p043_F |
p.P466L |
Trunk mutation |
USP29 |
Melanoma | p135_p04 |
Chr19:57642499:C>T |
Trunk mutation |
USP29 |
Melanoma | p135_p05 |
Chr19:57642485:G>A |
Trunk mutation |
USP29 |
Melanoma | p135_p08 |
Chr19:57641061:G>A |
Trunk mutation |
USP29 |
Melanoma | p135_p08 |
Chr19:57641738:C>T |
Private mutation |
USP29 |
Melanoma | p135_p11 |
Chr19:57640074:C>T |
Trunk mutation |
USP29 |
Melanoma | p135_p15 |
Chr19:57642163:G>A |
Trunk mutation |
USP29 |
Melanoma | p135_p25 |
Chr19:57642077:C>T |
Trunk mutation |
USP29 |
Renal Cell Carcinoma | p073_RCC1 |
Chr19:57640603:A>G |
Private mutation |