A21V (p.Ala21Val) variant of FGFR2 (P21802)
A21V (p.Ala21Val) in FGFR2 (P21802) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.50 / 1. The record also includes population frequency data and structural context.
A21V (p.Ala21Val) variant details
- p.Ala21Val
- ExAC rs773358865
- gnomAD rs773358865
- Missense
- Variant Prioritization Score for Impact Estimate 0.503
- REVEL 0.31
- CADD 26.00
- PolyPhen-2 0.57
- SIFT 0.02
- Most common in the Non-Finnish European population (allele frequency 9.9e-07)
- Structural context available