C18W (p.Cys18Trp) variant of CHEK2 (O96017)
C18W (p.Cys18Trp) in CHEK2 (O96017) is a missense change. Clinical records from EBI and UniProt describe it as likely benign. The record also includes structural context.
C18W (p.Cys18Trp) variant details
- p.Cys18Trp
- gnomAD rs1057523962
- Likely benign
- Missense
- EBI: Likely benign
- UniProt: Likely benign
- Structural context available