V47G (p.Val47Gly) variant of FGFR4 (P22455)
V47G (p.Val47Gly) in FGFR4 (P22455) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.55 / 1. The record also includes population frequency data and structural context.
V47G (p.Val47Gly) variant details
- p.Val47Gly
- Ensembl rs2149730721
- Missense
- Variant Prioritization Score for Impact Estimate 0.546
- REVEL 0.50
- CADD 23.80
- PolyPhen-2 0.46
- SIFT 0.02
- Most common in the Non-Finnish European population (allele frequency 1.8e-06)
- Structural context available