Entries searched:

Gene/Event	Cancer Type	Patient	Variant	Mutation Level
TRIM42	Colorectal Cancer	p034_MSU1	Chr3:140397089:C>T	Private mutation
TRIM42	Colorectal Cancer	p040_case3	Chr3:140401359:T>C	Branch mutation
TRIM42	Colorectal Cancer	p155_p252	p.R151W	Private mutation
TRIM42	Esophageal Squamous Cell Carcinoma	p124_ESCC012	p.E47K	Private mutation
TRIM42	Esophageal Squamous Cell Carcinoma	p124_ESCC023	p.E178D	Private mutation
TRIM42	Esophageal Squamous Cell Carcinoma	p124_ESCC029	p.E59V	Private mutation
TRIM42	Esophageal Squamous Cell Carcinoma	p124_ESCC031	p.R377T	Trunk mutation
TRIM42	Esophageal Squamous Cell Carcinoma	p124_ESCC034	p.R535L	Branch mutation
TRIM42	Esophageal Squamous Cell Carcinoma	p124_ESCC035	p.E207E	Private mutation
TRIM42	Esophageal Squamous Cell Carcinoma	p128_P08	Chr3:140409851:G>A	Private mutation
TRIM42	Esophageal Squamous Cell Carcinoma	p139_EC0990	p.G501R	Private mutation
TRIM42	Esophageal Squamous Cell Carcinoma	p139_EC1110	p.I682M	Private mutation
TRIM42	Esophageal Squamous Cell Carcinoma	p139_EC1110	p.V475M	Private mutation
TRIM42	Gastric Adenocarcinoma	p011_MSS3	p.R48W	Private mutation
TRIM42	Gastric Adenocarcinoma	p011_MSI-H2	p.R297H	Private mutation
TRIM42	Gastric Carcinoma	p106_GC05	p.V510M	Trunk mutation
TRIM42	Gastric Carcinoma	p106_GC09	p.H211Q	Private mutation
TRIM42	Gastric Carcinoma	p106_GC15	p.K226R	Private mutation
TRIM42	Intrahepatic Cholangiocarcinoma	p159_Pat1	p.R97C	Trunk mutation
TRIM42	Melanoma	p043_H	p.D192N	Private mutation
TRIM42	Melanoma	p135_p10	Chr3:140401756:C>T	Trunk mutation
TRIM42	Melanoma	p135_p25	Chr3:140406642:G>A	Trunk mutation
TRIM42	Ovarian Cancer	p144_AOCS139	p.P606A	Private mutation
TRIM42	Prostate Cancer	p164_P1	p.V475M	Branch mutation
TRIM42	Urothelial Carcinoma	p031_WCM088	p.V497A	Private mutation

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