Gene/Event |
Cancer Type |
Patient |
Variant |
Mutation Level |
HEMGN |
Osteosarcoma | p102_OS06 |
Chr9:100692755:T>A |
Branch mutation |
HEMGN |
Colorectal Cancer | p040_case9 |
Chr9:100700516:A>C |
Branch mutation |
HEMGN |
Esophageal Squamous Cell Carcinoma | p124_ESCC012 |
p.Q259E |
Private mutation |
HEMGN |
Esophageal Squamous Cell Carcinoma | p128_P09 |
Chr9:100692761:G>A |
Private mutation |
HEMGN |
Esophageal Squamous Cell Carcinoma | p128_SP09 |
Chr9:100692761:G>A |
Private mutation |
HEMGN |
Glioma | p168_P18 |
p.Q442X |
Private mutation |
HEMGN |
Glioma | p168_P18 |
p.P215S |
Private mutation |
HEMGN |
Melanoma | p043_H |
p.P18S |
Private mutation |