I149S (p.Ile149Ser) variant of WWTR1 (Q9GZV5)
I149S (p.Ile149Ser) in WWTR1 (Q9GZV5) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; high impact. The record also includes structural context.
I149S (p.Ile149Ser) variant details
- p.Ile149Ser
- NCI-TCGA TCGA novel
- Variant assessed as somatic; high impact.
- Missense
- UniProt: Variant assessed as somatic; high impact.
- Structural context available