F53V (p.Phe53Val) variant of FSHR (P23945)
F53V (p.Phe53Val) in FSHR (P23945) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes variant effect predictions and structural context.
F53V (p.Phe53Val) variant details
- p.Phe53Val
- NCI-TCGA TCGA novel
- Ensembl rs1572701837
- Variant assessed as somatic; moderate impact.
- Missense
- MetaLR 0.37
- MetaSVM -0.43
- SIFT 0.63
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available