G86A (p.Gly86Ala) variant of KRT14 (Keratin, type I cytoskeletal 14)
G86A (p.Gly86Ala) in KRT14 (Keratin, type I cytoskeletal 14) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.24 / 1. The record also includes population frequency data and structural context.
G86A (p.Gly86Ala) variant details
- p.Gly86Ala
- TOPMed rs1463244515
- gnomAD rs1463244515
- Missense
- Variant Prioritization Score for Impact Estimate 0.245
- REVEL 0.26
- CADD 8.65
- PolyPhen-2 0.00
- SIFT 0.08
- Most common in the Non-Finnish European population (allele frequency 1.5e-05)
- Structural context available