V47I (p.Val47Ile) variant of FGFR4 (P22455)
V47I (p.Val47Ile) in FGFR4 (P22455) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.08 / 1. The record also includes population frequency data and structural context.
V47I (p.Val47Ile) variant details
- p.Val47Ile
- Ensembl rs2149730716
- Missense
- Variant Prioritization Score for Impact Estimate 0.0801
- REVEL 0.04
- CADD 5.58
- PolyPhen-2 0.05
- SIFT 0.15
- Most common in the Latino/Admixed American population (allele frequency 2.2e-05)
- Structural context available