F53V (p.Phe53Val) variant of CYP17A1 (P05093)
F53V (p.Phe53Val) in CYP17A1 (P05093) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact in the context of in AH5. The record also includes structural context.
F53V (p.Phe53Val) variant details
- p.Phe53Val
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- in AH5
- Missense
- UniProt: Variant assessed as somatic; moderate impact. (in AH5)
- Structural context available