Gene/Event |
Cancer Type |
Patient |
Variant |
Mutation Level |
PHOX2B |
Colorectal Cancer | p040_case2 |
Chr4:41747783:G>A |
Private mutation |
PHOX2B |
Colorectal Cancer | p104_CD01 |
p.G276G |
Private mutation |
PHOX2B |
Colorectal Cancer | p104_UC02 |
p.A274S |
Branch mutation |
PHOX2B |
Esophageal Squamous Cell Carcinoma | p008_ESCC04 |
p.A253T |
Branch mutation |
PHOX2B |
Esophageal Squamous Cell Carcinoma | p008_ESCC08 |
p.A256A |
Branch mutation |
PHOX2B |
Glioblastoma | p113_case09 |
p.R154H |
Branch mutation |
PHOX2B |
Glioma | p168_P18 |
p.A79T |
Private mutation |
PHOX2B |
Melanoma | p043_D |
p.G222E |
Trunk mutation |
PHOX2B |
Melanoma | p043_H |
p.P218L |
Private mutation |
PHOX2B |
Melanoma | p135_p11 |
Chr4:41749426:G>A |
Trunk mutation |
PHOX2B |
Ovarian Cancer | p144_AOCS139 |
p.P224Q |
Private mutation |
PHOX2B |
Clear Cell Renal Cell Carcinoma | p013_patient2 |
p.G20V |
Private mutation |
PHOX2B |
Renal Cell Carcinoma | p073_RCC5 |
Chr4:41749629:A>C |
Branch mutation |