Gene/Event |
Cancer Type |
Patient |
Variant |
Mutation Level |
PCNT |
Osteosarcoma | p102_OS08 |
Chr21:47766653:G>A:c.367-4G>A |
Private mutation |
PCNT |
Colorectal Cancer | p034_MSU1 |
Chr21:47809304:C>T |
Trunk mutation |
PCNT |
Colorectal Cancer | p034_MSU1 |
Chr21:47808750:C>T |
Private mutation |
PCNT |
Colorectal Cancer | p034_MSU3 |
Chr21:47851449:C>T |
Trunk mutation |
PCNT |
Colorectal Cancer | p034_MSU4 |
Chr21:47773220:T>C |
Private mutation |
PCNT |
Colorectal Cancer | p038_N |
- |
Branch mutation |
PCNT |
Colorectal Cancer | p147_a06 |
p.L2871M |
Trunk mutation |
PCNT |
Colorectal Cancer | p147_a20 |
p.R2561H |
Trunk mutation |
PCNT |
Esophageal Squamous Cell Carcinoma | p008_ESCC09 |
p.G229S |
Private mutation |
PCNT |
Esophageal Squamous Cell Carcinoma | p124_ESCC009 |
p.E1538fs |
Private mutation |
PCNT |
Esophageal Squamous Cell Carcinoma | p124_ESCC012 |
p.D1851N |
Branch mutation |
PCNT |
Esophageal Squamous Cell Carcinoma | p124_ESCC012 |
p.Q1645Q |
Private mutation |
PCNT |
Esophageal Squamous Cell Carcinoma | p124_ESCC021 |
p.R1949T |
Branch mutation |
PCNT |
Esophageal Squamous Cell Carcinoma | p124_ESCC022 |
p.L459L |
Branch mutation |
PCNT |
Esophageal Squamous Cell Carcinoma | p124_ESCC022 |
p.K460* |
Branch mutation |
PCNT |
Esophageal Squamous Cell Carcinoma | p124_ESCC022 |
p.Q381H |
Private mutation |
PCNT |
Esophageal Squamous Cell Carcinoma | p124_ESCC022 |
p.L2077L |
Private mutation |
PCNT |
Esophageal Squamous Cell Carcinoma | p124_ESCC027 |
p.T275M |
Private mutation |
PCNT |
Esophageal Squamous Cell Carcinoma | p128_P04 |
Chr21:47836251:A>T |
Branch mutation |
PCNT |
Esophageal Squamous Cell Carcinoma | p128_SP14 |
Chr21:47860971:C>T |
Trunk mutation |
PCNT |
Gastric Adenocarcinoma | p011_MSI-H1 |
p.H2541Y |
Private mutation |
PCNT |
Gastric Adenocarcinoma | p011_MSI-H2 |
- |
Trunk mutation |
PCNT |
Gastric Carcinoma | p106_GC07 |
p.E730K |
Private mutation |
PCNT |
Glioblastoma | p070_HGG3 |
Chr21:47860641:G>C |
Private mutation |
PCNT |
Glioblastoma | p113_case09 |
p.K1682Nfs*23 |
Private mutation |
PCNT |
Glioblastoma | p113_case26 |
p.P2377S |
Private mutation |
PCNT |
Glioma | p168_P01 |
p.L226L |
Branch mutation |
PCNT |
Intrahepatic Cholangiocarcinoma | p080_ICC892 |
p.A1816D |
Branch mutation |
PCNT |
Hepatocellular Carcinoma | p151_HCC6690 |
Chr21:47769657:C>G |
Trunk mutation |
PCNT |
Lung Adenocarcinoma | p134_A022 |
p.H190L |
Trunk mutation |
PCNT |
Lung Cancer | p154_p5 |
p.T1036I |
Private mutation |
PCNT |
Medulloblastoma | p072_MB6 |
Chr21:47819274:T>G |
Branch mutation |
PCNT |
Medulloblastoma | p072_MB6 |
Chr21:47855723:A>G |
Branch mutation |
PCNT |
Melanoma | p043_F |
p.E2633K |
Trunk mutation |
PCNT |
Ovarian Cancer | p153_RJOC07 |
p.S2417G |
Trunk mutation |
PCNT |
Pancreatic Cancer | p054_Pa01 |
- |
Trunk mutation |
PCNT |
Prostate Cancer | p164_P1 |
p.G586E |
Branch mutation |
PCNT |
Prostate Cancer | p164_P1 |
p.Q2541H |
Branch mutation |
PCNT |
Prostate Cancer | p164_P1 |
p.Q2674R |
Branch mutation |
PCNT |
Prostate Cancer | p164_P2 |
p.Q2541H |
Trunk mutation |
PCNT |
Prostate Cancer | p164_P2 |
p.G586E |
Branch mutation |
PCNT |
Prostate Cancer | p164_P2 |
p.Q2674R |
Branch mutation |
PCNT |
Prostate Cancer | p164_P2 |
p.I1521V |
Private mutation |
PCNT |
Renal Cell Carcinoma | p073_RCC3 |
Chr21:47847702:G>A |
Private mutation |
PCNT |
Urothelial Carcinoma | p031_WCM088 |
p.E302K |
Private mutation |
PCNT |
Urothelial Carcinoma | p142_p36 |
- |
Private mutation |