G38S (p.Gly38Ser) variant of KRT4 (Keratin, type II cytoskeletal 4)
G38S (p.Gly38Ser) in KRT4 (Keratin, type II cytoskeletal 4) 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.
G38S (p.Gly38Ser) variant details
- p.Gly38Ser
- gnomAD rs1427716418
- Missense
- Variant Prioritization Score for Impact Estimate 0.471
- REVEL 0.47
- CADD 19.90
- PolyPhen-2 0.88
- SIFT 0.26
- Most common in the REMAINING population (allele frequency 1.7e-05)
- Structural context available