I62T (p.Ile62Thr) variant of GNAQ (P50148)
I62T (p.Ile62Thr) 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.
I62T (p.Ile62Thr) variant details
- p.Ile62Thr
- NCI-TCGA Cosmic COSV5410
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available