P53L (p.Pro53Leu) variant of TGFB2 (P61812)
P53L (p.Pro53Leu) in TGFB2 (P61812) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes population frequency data and structural context.
P53L (p.Pro53Leu) variant details
- p.Pro53Leu
- rs745960678
- ExAC rs745960678
- gnomAD rs745960678
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Population evidence available
- Structural context available