Entries searched:
Gene/Event Cancer Type Patient Variant Mutation Level
RNFT2 Colorectal Cancer p004_CRC_A01 Chr12:117178943:G>A Private mutation
RNFT2 Colorectal Cancer p034_MSU2 Chr12:117271640:G>A Trunk mutation
RNFT2 Esophageal Squamous Cell Carcinoma p124_ESCC023 - Private mutation
RNFT2 Esophageal Squamous Cell Carcinoma p128_SP28 Chr12:117178320:G>C Private mutation
RNFT2 Esophageal Squamous Cell Carcinoma p139_EC1117 p.A106T Branch mutation
RNFT2 Esophageal Squamous Cell Carcinoma p139_EC1125 - Private mutation
RNFT2 Gastric Carcinoma p106_GC07 p.E210V Private mutation
RNFT2 Glioblastoma p113_case08 p.A266T Private mutation
RNFT2 Medulloblastoma p072_MB6 Chr12:117289603:A>G Branch mutation
RNFT2 Medulloblastoma p072_MB6 Chr12:117289776:G>T Private mutation
RNFT2 Urothelial Carcinoma p031_WCM088 p.G374R Private mutation
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