P145S (p.Pro145Ser) variant of KRT13 (Keratin, type I cytoskeletal 13)
P145S (p.Pro145Ser) in KRT13 (Keratin, type I cytoskeletal 13) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.47 / 1. The record also includes population frequency data and structural context.
P145S (p.Pro145Ser) variant details
- p.Pro145Ser
- cosmic curated COSV10455
- TOPMed rs1905013716
- gnomAD rs1905013716
- Missense
- Variant Prioritization Score for Impact Estimate 0.467
- REVEL 0.27
- CADD 23.50
- Most common in the REMAINING population (allele frequency 0.00048)
- Structural context available