G16V (p.Gly16Val) variant of FGFR4 (P22455)
G16V (p.Gly16Val) in FGFR4 (P22455) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.21 / 1. The record also includes population frequency data and structural context.
G16V (p.Gly16Val) variant details
- p.Gly16Val
- TOPMed rs1784280548
- gnomAD rs1784280548
- Missense
- Variant Prioritization Score for Impact Estimate 0.208
- REVEL 0.17
- CADD 6.42
- PolyPhen-2 0.06
- SIFT 0.43
- Most common in the REMAINING population (allele frequency 0.00048)
- Structural context available