P38L (p.Pro38Leu) variant of FGFR2 (P21802)
P38L (p.Pro38Leu) in FGFR2 (P21802) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.52 / 1. The record also includes population frequency data and structural context.
P38L (p.Pro38Leu) variant details
- p.Pro38Leu
- gnomAD rs1248875226
- Missense
- Variant Prioritization Score for Impact Estimate 0.517
- REVEL 0.41
- CADD 26.90
- PolyPhen-2 0.01
- SIFT 0.03
- Most common in the Non-Finnish European population (allele frequency 5e-05)
- Structural context available