Entries searched:
Gene/Event Cancer Type Patient Variant Mutation Level
SORD Colorectal Cancer p014_CRC2 p.G152G Private mutation
SORD Colorectal Cancer p034_MSU2 Chr15:45360405:G>A Private mutation
SORD Esophageal Squamous Cell Carcinoma p139_EC0952 p.N269T Branch mutation
SORD Glioma p168_P01 p.N269T Branch mutation
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