D146H (p.Asp146His) variant of GNAQ (P50148)
D146H (p.Asp146His) 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.
D146H (p.Asp146His) variant details
- p.Asp146His
- NCI-TCGA Cosmic COSV5412
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available