A22T (p.Ala22Thr) variant of ITGA6 (Integrin alpha-6)
A22T (p.Ala22Thr) in ITGA6 (Integrin alpha-6) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.21 / 1. The record also includes population frequency data and structural context.
A22T (p.Ala22Thr) variant details
- p.Ala22Thr
- gnomAD rs1311063032
- Missense
- Variant Prioritization Score for Impact Estimate 0.208
- CADD 9.43
- PolyPhen-2 0.00
- SIFT 0.35
- Most common in the HGDP:FRENCH population (allele frequency 0.019)
- Structural context available