T9I (p.Thr9Ile) variant of KRT14 (Keratin, type I cytoskeletal 14)
T9I (p.Thr9Ile) in KRT14 (Keratin, type I cytoskeletal 14) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.42 / 1. The record also includes population frequency data and structural context.
T9I (p.Thr9Ile) variant details
- p.Thr9Ile
- gnomAD rs1410997626
- Missense
- Variant Prioritization Score for Impact Estimate 0.419
- REVEL 0.28
- CADD 22.80
- PolyPhen-2 0.01
- SIFT 0.01
- Most common in the Finnish in Finland (FIN) population (allele frequency 2e-05)
- Structural context available