Gene/Event |
Cancer Type |
Patient |
Variant |
Mutation Level |
PLXNB2 |
Breast Cancer | p143_p5 |
Chr22:50717121:C>G |
Trunk mutation |
PLXNB2 |
Breast Cancer | p143_p5 |
Chr22:50728906:G>A |
Private mutation |
PLXNB2 |
Colorectal Cancer | p001_PCRC16 |
Chr22:50727511:C>T |
Trunk mutation |
PLXNB2 |
Colorectal Cancer | p004_CRC_A01 |
Chr22:50727973:G>A |
Private mutation |
PLXNB2 |
Colorectal Cancer | p034_MSU2 |
Chr22:50728647:G>A |
Trunk mutation |
PLXNB2 |
Colorectal Cancer | p104_UC03 |
p.W1689C |
Private mutation |
PLXNB2 |
Colorectal Cancer | p104_UC07 |
p.F1100L |
Branch mutation |
PLXNB2 |
Colorectal Cancer | p155_p251 |
p.F723L |
Private mutation |
PLXNB2 |
Esophageal Squamous Cell Carcinoma | p124_ESCC012 |
p.V949V |
Branch mutation |
PLXNB2 |
Esophageal Squamous Cell Carcinoma | p124_ESCC012 |
p.I1019I |
Branch mutation |
PLXNB2 |
Esophageal Squamous Cell Carcinoma | p124_ESCC012 |
p.L1119V |
Branch mutation |
PLXNB2 |
Esophageal Squamous Cell Carcinoma | p124_ESCC026 |
p.R23fs |
Trunk mutation |
PLXNB2 |
Esophageal Squamous Cell Carcinoma | p124_ESCC029 |
p.V1467V |
Branch mutation |
PLXNB2 |
Esophageal Squamous Cell Carcinoma | p124_ESCC031 |
p.G139R |
Trunk mutation |
PLXNB2 |
Esophageal Squamous Cell Carcinoma | p124_ESCC036 |
p.E1398Q |
Private mutation |
PLXNB2 |
Esophageal Squamous Cell Carcinoma | p128_P11 |
Chr22:50714204:C>T |
Private mutation |
PLXNB2 |
Esophageal Squamous Cell Carcinoma | p128_P21 |
Chr22:50727947:C>T |
Private mutation |
PLXNB2 |
Esophageal Squamous Cell Carcinoma | p128_P24 |
Chr22:50720419:C>A |
Branch mutation |
PLXNB2 |
Esophageal Squamous Cell Carcinoma | p128_SP28 |
Chr22:50728774:G>A |
Private mutation |
PLXNB2 |
Esophageal Squamous Cell Carcinoma | p139_EC1125 |
p.V51M |
Branch mutation |
PLXNB2 |
Esophageal Squamous Cell Carcinoma | p139_EC1134 |
p.S1009N |
Private mutation |
PLXNB2 |
Gastric Adenocarcinoma | p011_MSI-H2 |
p.N759D |
Trunk mutation |
PLXNB2 |
Gastric Adenocarcinoma | p011_MSI-H2 |
p.Q1036Q |
Trunk mutation |
PLXNB2 |
Gastric Carcinoma | p106_GC04 |
p.E1619K |
Private mutation |
PLXNB2 |
Gastric Carcinoma | p106_GC07 |
p.L11P |
Private mutation |
PLXNB2 |
Gastric Carcinoma | p106_GC09 |
p.Y1755C |
Private mutation |
PLXNB2 |
Gastric Carcinoma | p106_GC13 |
p.R241W |
Private mutation |
PLXNB2 |
Glioblastoma | p113_case07 |
p.G829D |
Private mutation |
PLXNB2 |
Glioblastoma | p113_case14 |
p.T679P |
Private mutation |
PLXNB2 |
Glioblastoma | p113_case16 |
p.N802D |
Trunk mutation |
PLXNB2 |
Glioblastoma | p113_case21 |
p.N802D |
Trunk mutation |
PLXNB2 |
Glioblastoma | p113_case37 |
p.N802D |
Trunk mutation |
PLXNB2 |
Intrahepatic Cholangiocarcinoma | p080_ICC772 |
p.R857Q |
Private mutation |
PLXNB2 |
Hepatocellular Carcinoma | p029_case |
- |
Branch mutation |
PLXNB2 |
Hepatocellular Carcinoma | p151_HCC5647 |
Chr22:50717305:T>A |
Trunk mutation |
PLXNB2 |
Melanoma | p043_H |
p.P105S |
Private mutation |
PLXNB2 |
Melanoma | p043_H |
p.A534V |
Private mutation |
PLXNB2 |
Prostate Cancer | p116_PS352 |
c.1098_1098delinsCG |
Private mutation |
PLXNB2 |
Prostate Cancer | p117_PrCa14 |
- |
Private mutation |
PLXNB2 |
Prostate Cancer | p164_P2 |
p.H1370R |
Private mutation |
PLXNB2 |
Prostate Cancer | p164_P2 |
p.K318E |
Private mutation |
PLXNB2 |
Syndromic Neuroendocrine Carcinoma | p127_C4 |
p.I82V |
Private mutation |
PLXNB2 |
Renal Cell Carcinoma | p073_RCC3 |
Chr22:50724369:G>A |
Private mutation |
PLXNB2 |
Urothelial Carcinoma | p142_p10 |
- |
Trunk mutation |
PLXNB2 |
Urothelial Carcinoma | p142_p21 |
- |
Private mutation |