S122F (p.Ser122Phe) variant of GNAQ (P50148)
S122F (p.Ser122Phe) in GNAQ (P50148) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
S122F (p.Ser122Phe) variant details
- p.Ser122Phe
- NCI-TCGA Cosmic COSV5410
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available