G38E (p.Gly38Glu) variant of KRT14 (Keratin, type I cytoskeletal 14)
G38E (p.Gly38Glu) in KRT14 (Keratin, type I cytoskeletal 14) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.61 / 1. The record also includes population frequency data and structural context.
G38E (p.Gly38Glu) variant details
- p.Gly38Glu
- ExAC rs765150501
- TOPMed rs765150501
- gnomAD rs765150501
- Missense
- Variant Prioritization Score for Impact Estimate 0.612
- REVEL 0.56
- CADD 23.60
- PolyPhen-2 0.52
- SIFT 0.00
- Most common in the Latino/Admixed American population (allele frequency 6.5e-05)
- Structural context available