Entries searched:
Gene/Event Cancer Type Patient Variant Mutation Level
SERINC2 Colorectal Cancer p001_PCRC12 Chr1:31886735:C>T Branch mutation
SERINC2 Colorectal Cancer p040_case9 Chr1:31898175:A>G Private mutation
SERINC2 Esophageal Squamous Cell Carcinoma p128_SP25 Chr1:31897597:C>T Private mutation
SERINC2 Glioblastoma p113_case31 p.Y235H Private mutation
SERINC2 Glioma p168_P01 p.Y235Y Private mutation
SERINC2 Prostate Cancer p164_P2 p.G157C Private mutation
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