F9L (p.Phe9Leu) variant of FGFR1 (P11362)
F9L (p.Phe9Leu) in FGFR1 (P11362) is a missense change. Clinical records from EBI and UniProt describe it as likely benign. The record also includes structural context.
F9L (p.Phe9Leu) variant details
- p.Phe9Leu
- TOPMed rs971805245
- gnomAD rs971805245
- Likely benign
- Missense
- EBI: Likely benign
- UniProt: Likely benign
- Structural context available