L7P (p.Leu7Pro) variant of FGFR1 (P11362)
L7P (p.Leu7Pro) in FGFR1 (P11362) is a missense change. Clinical records from EBI and UniProt describe it as uncertain significance. The record also includes population frequency data and structural context.
L7P (p.Leu7Pro) variant details
- p.Leu7Pro
- 1000Genomes rs532741632
- ExAC rs532741632
- TOPMed rs532741632
- gnomAD rs532741632
- Uncertain significance
- Missense
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Population evidence available
- Structural context available