V14M (p.Val14Met) variant of FGFR4 (P22455)
V14M (p.Val14Met) in FGFR4 (P22455) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.18 / 1. The record also includes population frequency data and structural context.
V14M (p.Val14Met) variant details
- p.Val14Met
- ExAC rs768529489
- gnomAD rs768529489
- Missense
- Variant Prioritization Score for Impact Estimate 0.18
- REVEL 0.12
- CADD 9.97
- PolyPhen-2 0.06
- SIFT 0.08
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available