Entries searched:
Gene/Event Cancer Type Patient Variant Mutation Level
FAM168B Colorectal Cancer p001_PCRC16 Chr2:131813174:G>A Private mutation
FAM168B Colorectal Cancer p104_UC01 p.P96A Branch mutation
FAM168B Colorectal Cancer p155_p495 p.V84A Private mutation
FAM168B Anaplastic Astrocytoma p070_HGG1 Chr2:131829630:C>T Private mutation
FAM168B Glioblastoma p070_HGG2 Chr2:131829401:C>A Branch mutation
FAM168B Hepatocellular Carcinoma p151_HCC6690 Chr2:131812953:G>A Private mutation
FAM168B Non-Small Cell Lung Cancer p107_P024 p.P35T Branch mutation
FAM168B Renal Cell Carcinoma p073_RCC9 Chr2:131805714:A>G Trunk mutation
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