R46S (p.Arg46Ser) variant of FSHR (P23945)
R46S (p.Arg46Ser) in FSHR (P23945) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
R46S (p.Arg46Ser) variant details
- p.Arg46Ser
- NCI-TCGA Cosmic COSV1004
- cosmic curated COSV10043
- TOPMed rs1673166650
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available