G21C (p.Gly21Cys) variant of ITGA6 (Integrin alpha-6)
G21C (p.Gly21Cys) in ITGA6 (Integrin alpha-6) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.42 / 1. The record also includes population frequency data and structural context.
G21C (p.Gly21Cys) variant details
- p.Gly21Cys
- cosmic curated COSV99905
- Missense
- Variant Prioritization Score for Impact Estimate 0.422
- CADD 17.10
- PolyPhen-2 0.00
- SIFT 0.09
- Most common in the Finnish in Finland (FIN) population (allele frequency 0.00091)
- Structural context available