Entries searched:
Gene/Event Cancer Type Patient Variant Mutation Level
FAM57B Colorectal Cancer p001_PCRC13 Chr16:30036618:G>A Private mutation
FAM57B Colorectal Cancer p034_MSU2 Chr16:30040796:C>T Private mutation
FAM57B Esophageal Squamous Cell Carcinoma p124_ESCC031 p.V167V Branch mutation
FAM57B Glioblastoma p113_case14 p.D88N Private mutation
FAM57B Melanoma p043_A p.H136Y Trunk mutation
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