G28D (p.Gly28Asp) variant of KRT13 (Keratin, type I cytoskeletal 13)
G28D (p.Gly28Asp) in KRT13 (Keratin, type I cytoskeletal 13) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.12 / 1. The record also includes population frequency data and structural context.
G28D (p.Gly28Asp) variant details
- p.Gly28Asp
- ExAC rs780999432
- Missense
- Variant Prioritization Score for Impact Estimate 0.122
- REVEL 0.06
- CADD 13.30
- PolyPhen-2 0.01
- SIFT 0.05
- Most common in the Non-Finnish European population (allele frequency 1.8e-06)
- Structural context available