G98A (p.Gly98Ala) variant of KRT14 (Keratin, type I cytoskeletal 14)
G98A (p.Gly98Ala) 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.
G98A (p.Gly98Ala) variant details
- p.Gly98Ala
- gnomAD rs1476741932
- Missense
- Variant Prioritization Score for Impact Estimate 0.244
- REVEL 0.37
- CADD 3.47
- PolyPhen-2 0.00
- SIFT 0.08
- Most common in the South Asian population (allele frequency 8.1e-05)
- Structural context available