Gene/Event |
Cancer Type |
Patient |
Variant |
Mutation Level |
PDGFRB |
Breast Cancer | p111_p1-69 |
c.G530A |
Trunk mutation |
PDGFRB |
Breast Cancer | p137_p06 |
p.R496H |
Trunk mutation |
PDGFRB |
Breast Cancer | p143_p5 |
Chr5:149512424:A>G |
Private mutation |
PDGFRB |
Colorectal Cancer | p001_PCRC16 |
Chr5:149500544:G>A |
Private mutation |
PDGFRB |
Colorectal Cancer | p104_UC06 |
p.C291C |
Branch mutation |
PDGFRB |
Esophageal Squamous Cell Carcinoma | p124_ESCC011 |
p.H499Y |
Private mutation |
PDGFRB |
Esophageal Squamous Cell Carcinoma | p124_ESCC012 |
p.E404K |
Private mutation |
PDGFRB |
Esophageal Squamous Cell Carcinoma | p124_ESCC029 |
p.C149S |
Private mutation |
PDGFRB |
Esophageal Squamous Cell Carcinoma | p128_P25 |
Chr5:149509423:G>A |
Private mutation |
PDGFRB |
Gastric Carcinoma | p106_GC09 |
p.R604C |
Private mutation |
PDGFRB |
Glioblastoma | p113_case25 |
p.G675V |
Private mutation |
PDGFRB |
Glioblastoma | p113_case36 |
p.A74T |
Private mutation |
PDGFRB |
Glioma | p168_P90 |
p.E341Q |
Trunk mutation |
PDGFRB |
Lung Adenocarcinoma | p017_472 |
Chr5:149497486:C>T |
Branch mutation |
PDGFRB |
Lung Cancer | p028_RJLC2 |
p.R922H |
Private mutation |
PDGFRB |
Small Cell Lung Carcinoma | p100_p4 |
Chr5:149514330:T>C |
Trunk mutation |
PDGFRB |
Non-Small Cell Lung Cancer | p107_P007 |
p.S712R |
Branch mutation |
PDGFRB |
Non-Small Cell Lung Cancer | p138_p017 |
p.P725R |
Branch mutation |
PDGFRB |
Non-Small Cell Lung Cancer | p148_p01 |
p.K707E |
Trunk mutation |
PDGFRB |
Non-Small Cell Lung Cancer | p148_p13 |
p.Q613H |
Trunk mutation |
PDGFRB |
Non-Small Cell Lung Cancer | p163_P017 |
p.P725R |
Branch mutation |
PDGFRB |
Melanoma | p043_F |
p.R987W |
Trunk mutation |
PDGFRB |
Melanoma | p135_p10 |
Chr5:149499682:A>G |
Trunk mutation |
PDGFRB |
Melanoma | p135_p11 |
Chr5:149502718:C>T |
Trunk mutation |
PDGFRB |
Oropharyngeal Squamous Cell Carcinoma | p062_case |
Chr5:149512490:C>T |
Trunk mutation |
PDGFRB |
Ovarian Cancer | p052_Case2 |
p.R208K |
Branch mutation |
PDGFRB |
Thyroid Cancer | p081_p1 |
p.N666K |
Private mutation |