Entries searched:
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
First Previous Next Last  Turn to page  Goto