S35T (p.Ser35Thr) variant of KRT3 (Keratin, type II cytoskeletal 3)
S35T (p.Ser35Thr) in KRT3 (Keratin, type II cytoskeletal 3) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.18 / 1. The record also includes population frequency data and structural context.
S35T (p.Ser35Thr) variant details
- p.Ser35Thr
- gnomAD rs1301994725
- Missense
- Variant Prioritization Score for Impact Estimate 0.176
- REVEL 0.17
- CADD 0.05
- Most common in the South Asian population (allele frequency 1.2e-05)
- Structural context available