L26M (p.Leu26Met) variant of ITGA6 (Integrin alpha-6)
L26M (p.Leu26Met) 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, published literature, and structural context.
L26M (p.Leu26Met) variant details
- p.Leu26Met
- gnomAD 2-172427864-T-A
- Missense
- Variant Prioritization Score for Impact Estimate 0.392
- CADD 25.00
- PolyPhen-2 1.00
- SIFT 0.00
- Most common in the HGDP:MAKRANI population (allele frequency 0.023)
- Structural context available
- Literature evidence available