D39E (p.Asp39Glu) variant of ITGA6 (Integrin alpha-6)
D39E (p.Asp39Glu) in ITGA6 (Integrin alpha-6) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.15 / 1. The record also includes population frequency data and structural context.
D39E (p.Asp39Glu) variant details
- p.Asp39Glu
- ExAC rs776183303
- TOPMed rs776183303
- gnomAD rs776183303
- Missense
- Variant Prioritization Score for Impact Estimate 0.148
- CADD 9.46
- PolyPhen-2 0.01
- SIFT 0.97
- Most common in the HGDP:YAKUT population (allele frequency 0.04)
- Structural context available