L108M (p.Leu108Met) variant of FSHR (P23945)
L108M (p.Leu108Met) 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.
L108M (p.Leu108Met) variant details
- p.Leu108Met
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available