F7L (p.Phe7Leu) variant of FGFR2 (P21802)
F7L (p.Phe7Leu) in FGFR2 (P21802) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.22 / 1. The record also includes population frequency data and structural context.
F7L (p.Phe7Leu) variant details
- p.Phe7Leu
- Ensembl rs2135485885
- Missense
- Variant Prioritization Score for Impact Estimate 0.221
- REVEL 0.15
- CADD 15.40
- PolyPhen-2 0.00
- SIFT 1.00
- Most common in the Non-Finnish European population (allele frequency 9.9e-07)
- Structural context available