P154L (p.Pro154Leu) variant of KRT13 (Keratin, type I cytoskeletal 13)
P154L (p.Pro154Leu) in KRT13 (Keratin, type I cytoskeletal 13) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.16 / 1. The record also includes population frequency data and structural context.
P154L (p.Pro154Leu) variant details
- p.Pro154Leu
- TOPMed rs1165181435
- gnomAD rs1165181435
- Missense
- Variant Prioritization Score for Impact Estimate 0.158
- REVEL 0.20
- CADD 1.95
- Most common in the African/African-American population (allele frequency 2.4e-05)
- Structural context available