R52W (p.Arg52Trp) variant of FSHR (P23945)
R52W (p.Arg52Trp) 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.
R52W (p.Arg52Trp) variant details
- p.Arg52Trp
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- MetaLR 0.66
- MetaSVM 0.33
- SIFT 0.19
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available