A22G (p.Ala22Gly) variant of ITGA6 (Integrin alpha-6)
A22G (p.Ala22Gly) in ITGA6 (Integrin alpha-6) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.39 / 1. The record also includes population frequency data and structural context.
A22G (p.Ala22Gly) variant details
- p.Ala22Gly
- TOPMed rs1179548249
- gnomAD rs1179548249
- Missense
- Variant Prioritization Score for Impact Estimate 0.385
- CADD 19.20
- PolyPhen-2 0.00
- SIFT 0.32
- Most common in the Non-Finnish European population (allele frequency 2.9e-05)
- Structural context available