P17R (p.Pro17Arg) variant of FGFR4 (P22455)
P17R (p.Pro17Arg) in FGFR4 (P22455) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.18 / 1. The record also includes population frequency data, published literature, and structural context.
P17R (p.Pro17Arg) variant details
- p.Pro17Arg
- gnomAD 5-177089652-C-G
- Missense
- Variant Prioritization Score for Impact Estimate 0.179
- REVEL 0.09
- CADD 11.20
- PolyPhen-2 0.00
- SIFT 0.38
- Most common in the Non-Finnish European population (allele frequency 1.8e-06)
- Structural context available
- Literature evidence available