G37E (p.Gly37Glu) variant of KRT16 (Keratin, type I cytoskeletal 16)
G37E (p.Gly37Glu) in KRT16 (Keratin, type I cytoskeletal 16) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.43 / 1. The record also includes population frequency data and structural context.
G37E (p.Gly37Glu) variant details
- p.Gly37Glu
- ExAC rs762970825
- gnomAD rs762970825
- Missense
- Variant Prioritization Score for Impact Estimate 0.435
- REVEL 0.36
- CADD 15.00
- PolyPhen-2 0.35
- SIFT 0.07
- Most common in the REMAINING population (allele frequency 0.00048)
- Structural context available