A21G (p.Ala21Gly) variant of VIM (Vimentin)
A21G (p.Ala21Gly) in VIM (Vimentin) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.22 / 1. The record also includes population frequency data and structural context.
A21G (p.Ala21Gly) variant details
- p.Ala21Gly
- ExAC rs776383614
- gnomAD rs776383614
- Missense
- Variant Prioritization Score for Impact Estimate 0.22
- REVEL 0.25
- CADD 15.60
- PolyPhen-2 0.00
- SIFT 0.50
- Most common in the Non-Finnish European population (allele frequency 1.5e-05)
- Structural context available