S37N (p.Ser37Asn) variant of FGFR4 (P22455)
S37N (p.Ser37Asn) 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.
S37N (p.Ser37Asn) variant details
- p.Ser37Asn
- gnomAD 5-177090408-G-A
- Missense
- Variant Prioritization Score for Impact Estimate 0.205
- REVEL 0.14
- CADD 12.70
- PolyPhen-2 0.01
- SIFT 0.27
- Population evidence available
- Structural context available
- Literature evidence available