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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