P17H (p.Pro17His) variant of FGFR4 (P22455)
P17H (p.Pro17His) in FGFR4 (P22455) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.20 / 1. The record also includes population frequency data, published literature, and structural context.
P17H (p.Pro17His) variant details
- p.Pro17His
- gnomAD 5-177089652-C-A
- Missense
- Variant Prioritization Score for Impact Estimate 0.199
- REVEL 0.12
- CADD 13.30
- PolyPhen-2 0.04
- SIFT 0.12
- Most common in the REMAINING population (allele frequency 1.7e-05)
- Structural context available
- Literature evidence available