E55R (p.Glu55Arg) variant of TGFB2 (P61812)
E55R (p.Glu55Arg) in TGFB2 (P61812) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; high impact. The record also includes structural context.
E55R (p.Glu55Arg) variant details
- p.Glu55Arg
- NCI-TCGA TCGA novel
- Variant assessed as somatic; high impact.
- Missense
- UniProt: Variant assessed as somatic; high impact.
- Structural context available