S42F (p.Ser42Phe) variant of FSHR (P23945)
S42F (p.Ser42Phe) 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.
S42F (p.Ser42Phe) variant details
- p.Ser42Phe
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- MetaLR 0.88
- MetaSVM 0.75
- SIFT 0.47
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available