G69C (p.Gly69Cys) variant of KRT10 (Keratin, type I cytoskeletal 10)
G69C (p.Gly69Cys) in KRT10 (Keratin, type I cytoskeletal 10) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.34 / 1. The record also includes population frequency data.
G69C (p.Gly69Cys) variant details
- p.Gly69Cys
- TOPMed rs1323745980
- gnomAD rs1323745980
- Missense
- Variant Prioritization Score for Impact Estimate 0.339
- REVEL 0.31
- CADD 23.00
- Most common in the African/African-American population (allele frequency 0.00012)