C9W (p.Cys9Trp) variant of FGFR2 (P21802)
C9W (p.Cys9Trp) in FGFR2 (P21802) is a missense change. Clinical records from EBI and UniProt describe it as likely benign. The record also includes structural context.
C9W (p.Cys9Trp) variant details
- p.Cys9Trp
- gnomAD rs1863033887
- Likely benign
- Missense
- EBI: Likely benign
- UniProt: Likely benign
- Structural context available