G38V (p.Gly38Val) variant of ITGA6 (Integrin alpha-6)
G38V (p.Gly38Val) in ITGA6 (Integrin alpha-6) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.79 / 1. The record also includes population frequency data, published literature, and structural context.
G38V (p.Gly38Val) variant details
- p.Gly38Val
- gnomAD 2-172427901-G-T
- Missense
- Variant Prioritization Score for Impact Estimate 0.79
- CADD 31.00
- PolyPhen-2 1.00
- SIFT 0.00
- Population evidence available
- Structural context available
- Literature evidence available