P39S (p.Pro39Ser) variant of FGFR2 (P21802)
P39S (p.Pro39Ser) in FGFR2 (P21802) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.40 / 1. The record also includes population frequency data and structural context.
P39S (p.Pro39Ser) variant details
- p.Pro39Ser
- gnomAD rs1488994705
- Missense
- Variant Prioritization Score for Impact Estimate 0.398
- REVEL 0.29
- CADD 20.90
- PolyPhen-2 0.01
- SIFT 0.19
- Most common in the Ashkenazi Jewish population (allele frequency 5.1e-05)
- Structural context available