S37R (p.Ser37Arg) variant of FGFR4 (P22455)
S37R (p.Ser37Arg) in FGFR4 (P22455) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.24 / 1. The record also includes population frequency data and structural context.
S37R (p.Ser37Arg) variant details
- p.Ser37Arg
- Ensembl rs2149730657
- Missense
- Variant Prioritization Score for Impact Estimate 0.245
- REVEL 0.16
- CADD 16.30
- PolyPhen-2 0.04
- SIFT 0.33
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available