M14T (p.Met14Thr) variant of KRT14 (Keratin, type I cytoskeletal 14)
M14T (p.Met14Thr) in KRT14 (Keratin, type I cytoskeletal 14) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.33 / 1. The record also includes population frequency data and structural context.
M14T (p.Met14Thr) variant details
- p.Met14Thr
- gnomAD rs1166730746
- Missense
- Variant Prioritization Score for Impact Estimate 0.334
- REVEL 0.23
- CADD 21.80
- PolyPhen-2 0.00
- SIFT 0.18
- Most common in the Non-Finnish European population (allele frequency 9.1e-07)
- Structural context available