P18L (p.Pro18Leu) variant of FGFR4 (P22455)
P18L (p.Pro18Leu) in FGFR4 (P22455) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.23 / 1. The record also includes population frequency data and structural context.
P18L (p.Pro18Leu) variant details
- p.Pro18Leu
- Ensembl rs2149729712
- Missense
- Variant Prioritization Score for Impact Estimate 0.227
- REVEL 0.16
- CADD 19.30
- PolyPhen-2 0.00
- SIFT 0.07
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available