C33W (p.Cys33Trp) variant of U2AF1 (Q01081)
C33W (p.Cys33Trp) in U2AF1 (Q01081) is a missense change. Clinical records from EBI and UniProt describe it as benign. The record also includes structural context.
C33W (p.Cys33Trp) variant details
- p.Cys33Trp
- ESP rs139959814
- ExAC rs139959814
- gnomAD rs139959814
- Benign
- Missense
- EBI: Benign
- UniProt: Benign
- Structural context available