L18F (p.Leu18Phe) variant of FGFR1 (P11362)
L18F (p.Leu18Phe) in FGFR1 (P11362) is a missense change. The record also includes structural context.
L18F (p.Leu18Phe) variant details
- p.Leu18Phe
- ExAC rs771549051
- TOPMed rs771549051
- gnomAD rs771549051
- Missense
- Structural context available