D39N (p.Asp39Asn) variant of ITGA6 (Integrin alpha-6)
D39N (p.Asp39Asn) in ITGA6 (Integrin alpha-6) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.70 / 1. The record also includes population frequency data, published literature, and structural context.
D39N (p.Asp39Asn) variant details
- p.Asp39Asn
- gnomAD 2-172427903-G-A
- Missense
- Variant Prioritization Score for Impact Estimate 0.696
- CADD 23.70
- PolyPhen-2 0.04
- SIFT 0.08
- Population evidence available
- Structural context available
- Literature evidence available