A36T (p.Ala36Thr) variant of KRT14 (Keratin, type I cytoskeletal 14)
A36T (p.Ala36Thr) in KRT14 (Keratin, type I cytoskeletal 14) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.12 / 1. The record also includes population frequency data and structural context.
A36T (p.Ala36Thr) variant details
- p.Ala36Thr
- gnomAD rs1254737268
- Missense
- Variant Prioritization Score for Impact Estimate 0.124
- REVEL 0.12
- CADD 8.74
- PolyPhen-2 0.00
- SIFT 0.41
- Most common in the African/African-American population (allele frequency 3e-05)
- Structural context available