S50W (p.Ser50Trp) variant of GNAQ (P50148)
S50W (p.Ser50Trp) in GNAQ (P50148) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; high impact. The record also includes structural context.
S50W (p.Ser50Trp) variant details
- p.Ser50Trp
- NCI-TCGA TCGA novel
- Variant assessed as somatic; high impact.
- Missense
- UniProt: Variant assessed as somatic; high impact.
- Structural context available