G41R (p.Gly41Arg) variant of KRT10 (Keratin, type I cytoskeletal 10)
G41R (p.Gly41Arg) in KRT10 (Keratin, type I cytoskeletal 10) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.30 / 1. The record also includes population frequency data.
G41R (p.Gly41Arg) variant details
- p.Gly41Arg
- gnomAD rs1348226953
- Missense
- Variant Prioritization Score for Impact Estimate 0.297
- REVEL 0.37
- CADD 13.30
- Most common in the African/African-American population (allele frequency 4.8e-05)