G68A (p.Gly68Ala) variant of KRT2 (P35908)
G68A (p.Gly68Ala) in KRT2 (P35908) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.40 / 1. The record also includes population frequency data and structural context.
G68A (p.Gly68Ala) variant details
- p.Gly68Ala
- ExAC rs756077444
- TOPMed rs756077444
- gnomAD rs756077444
- Missense
- Variant Prioritization Score for Impact Estimate 0.395
- REVEL 0.28
- CADD 21.90
- PolyPhen-2 0.11
- SIFT 0.00
- Most common in the REMAINING population (allele frequency 0.00048)
- Structural context available