Q79K (p.Gln79Lys) variant of FSHR (P23945)
Q79K (p.Gln79Lys) 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.
Q79K (p.Gln79Lys) variant details
- p.Gln79Lys
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available