Y98D (p.Tyr98Asp) variant of KRT10 (Keratin, type I cytoskeletal 10)
Y98D (p.Tyr98Asp) in KRT10 (Keratin, type I cytoskeletal 10) 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.
Y98D (p.Tyr98Asp) variant details
- p.Tyr98Asp
- gnomAD rs1905461015
- Missense
- Variant Prioritization Score for Impact Estimate 0.387
- REVEL 0.32
- CADD 15.00
- PolyPhen-2 0.23
- SIFT 0.19
- Most common in the African/African-American population (allele frequency 0.00041)