Entries searched:
Gene/Event
Cancer Type
Patient
Variant
Mutation Level
FAM89B
Colorectal Cancer
p155_p494
p.R82R
Private mutation
FAM89B
Esophageal Squamous Cell Carcinoma
p128_SP19
Chr11:65340380:G>A
Private mutation
FAM89B
Melanoma
p043_H
p.A69V
Private mutation
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