V14A (p.Val14Ala) variant of FGFR4 (P22455)
V14A (p.Val14Ala) in FGFR4 (P22455) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.17 / 1. The record also includes population frequency data, published literature, and structural context.
V14A (p.Val14Ala) variant details
- p.Val14Ala
- gnomAD 5-177089643-T-C
- Missense
- Variant Prioritization Score for Impact Estimate 0.169
- REVEL 0.23
- CADD 3.52
- PolyPhen-2 0.00
- SIFT 0.33
- Most common in the REMAINING population (allele frequency 1.7e-05)
- Structural context available
- Literature evidence available