Gene/Event |
Cancer Type |
Patient |
Variant |
Mutation Level |
LPHN2 |
Colorectal Cancer | p034_MSU1 |
Chr1:82409338:G>A |
Trunk mutation |
LPHN2 |
Colorectal Cancer | p034_MSU2 |
Chr1:82436133:T>C |
Private mutation |
LPHN2 |
Colorectal Cancer | p034_MSU3 |
Chr1:82416119:C>T |
Trunk mutation |
LPHN2 |
Esophageal Squamous Cell Carcinoma | p124_ESCC015 |
p.T139N |
Branch mutation |
LPHN2 |
Esophageal Squamous Cell Carcinoma | p128_P03 |
Chr1:82456243:C>G |
Private mutation |
LPHN2 |
Esophageal Squamous Cell Carcinoma | p128_SP03 |
Chr1:82456243:C>G |
Private mutation |
LPHN2 |
Gastric Adenocarcinoma | p011_MSS1 |
p.P52P |
Branch mutation |
LPHN2 |
Gastric Adenocarcinoma | p011_MSI-H1 |
p.S687S |
Trunk mutation |
LPHN2 |
Gastric Adenocarcinoma | p011_MSI-H2 |
p.S1239G |
Trunk mutation |
LPHN2 |
Gastric Adenocarcinoma | p011_MSI-H2 |
p.S1255N |
Trunk mutation |
LPHN2 |
Gastric Adenocarcinoma | p011_MSI-H2 |
p.D574D |
Trunk mutation |
LPHN2 |
Glioblastoma | p113_case02 |
p.E1241G |
Private mutation |
LPHN2 |
Glioblastoma | p113_case07 |
p.T1300I |
Private mutation |
LPHN2 |
Glioma | p168_P01 |
p.F884F |
Branch mutation |
LPHN2 |
Glioma | p168_P18 |
p.A911V |
Private mutation |
LPHN2 |
Lung Adenocarcinoma | p017_499s |
Chr1:81967559:G>T |
Trunk mutation |
LPHN2 |
Non-Small Cell Lung Cancer | p107_P007 |
- |
Branch mutation |
LPHN2 |
Non-Small Cell Lung Cancer | p107_P016 |
p.Q712L |
Branch mutation |
LPHN2 |
Melanoma | p043_A |
p.R206Q |
Trunk mutation |
LPHN2 |
Melanoma | p043_F |
p.M285I |
Trunk mutation |
LPHN2 |
Melanoma | p043_F |
p.P757S |
Trunk mutation |
LPHN2 |
Melanoma | p043_G |
p.S1138F |
Trunk mutation |
LPHN2 |
Melanoma | p043_H |
p.V954D |
Branch mutation |
LPHN2 |
Melanoma | p135_p05 |
Chr1:82456533:C>T |
Trunk mutation |
LPHN2 |
Melanoma | p135_p27 |
Chr1:82408826:G>A |
Trunk mutation |
LPHN2 |
Renal Cancer | p018_patient2 |
Chr1:82409438:C>G |
Private mutation |
LPHN2 |
Clear Cell Renal Cell Carcinoma | p019_EV002 |
Chr1:82409438:p.P>A |
Private mutation |
LPHN2 |
Renal Cell Carcinoma | p073_RCC2 |
Chr1:82409438:C>G |
Private mutation |
LPHN2 |
Urothelial Carcinoma | p031_WCM088 |
p.Q596Q |
Branch mutation |
LPHN2 |
Urothelial Carcinoma | p031_WCM117 |
p.W258* |
Branch mutation |