W4L (p.Trp4Leu) variant of FGFR2 (P21802)
W4L (p.Trp4Leu) in FGFR2 (P21802) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.53 / 1. The record also includes population frequency data and structural context.
W4L (p.Trp4Leu) variant details
- p.Trp4Leu
- gnomAD rs1863039134
- Missense
- Variant Prioritization Score for Impact Estimate 0.53
- REVEL 0.45
- CADD 22.50
- Most common in the Ashkenazi Jewish population (allele frequency 7.7e-05)
- Structural context available