N25T (p.Asn25Thr) variant of ITGA6 (Integrin alpha-6)
N25T (p.Asn25Thr) in ITGA6 (Integrin alpha-6) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.63 / 1. The record also includes population frequency data, published literature, and structural context.
N25T (p.Asn25Thr) variant details
- p.Asn25Thr
- gnomAD 2-172427862-A-C
- Missense
- Variant Prioritization Score for Impact Estimate 0.628
- CADD 27.30
- PolyPhen-2 0.93
- SIFT 0.01
- Most common in the 1KG:MSL population (allele frequency 0.013)
- Structural context available
- Literature evidence available