V28M (p.Val28Met) variant of FGFR4 (P22455)
V28M (p.Val28Met) 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 and structural context.
V28M (p.Val28Met) variant details
- p.Val28Met
- TOPMed rs979979470
- gnomAD rs979979470
- Missense
- Variant Prioritization Score for Impact Estimate 0.169
- REVEL 0.15
- CADD 13.40
- PolyPhen-2 0.00
- SIFT 0.26
- Most common in the South Asian population (allele frequency 1.2e-05)
- Structural context available