R59G (p.Arg59Gly) variant of FGFR4 (P22455)
R59G (p.Arg59Gly) in FGFR4 (P22455) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.28 / 1. The record also includes population frequency data and structural context.
R59G (p.Arg59Gly) variant details
- p.Arg59Gly
- cosmic curated COSV52810
- 1000Genomes rs200344385
- ESP rs200344385
- ExAC rs200344385
- Missense
- Variant Prioritization Score for Impact Estimate 0.275
- REVEL 0.28
- CADD 14.30
- PolyPhen-2 0.04
- SIFT 0.38
- Population evidence available
- Structural context available