V41M (p.Val41Met) variant of KRT8 (Keratin, type II cytoskeletal 8)
V41M (p.Val41Met) in KRT8 (Keratin, type II cytoskeletal 8) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.59 / 1. The record also includes population frequency data.
V41M (p.Val41Met) variant details
- p.Val41Met
- gnomAD rs1267862887
- Missense
- Variant Prioritization Score for Impact Estimate 0.59
- CADD 15.50
- Most common in the 1KG:CLM population (allele frequency 0.0053)