T51N (p.Thr51Asn) variant of KRT17 (Keratin, type I cytoskeletal 17)
T51N (p.Thr51Asn) in KRT17 (Keratin, type I cytoskeletal 17) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.34 / 1. The record also includes population frequency data and structural context.
T51N (p.Thr51Asn) variant details
- p.Thr51Asn
- TOPMed rs1482978208
- gnomAD rs1482978208
- Missense
- Variant Prioritization Score for Impact Estimate 0.339
- REVEL 0.17
- CADD 2.58
- PolyPhen-2 0.00
- SIFT 0.30
- Most common in the East Asian population (allele frequency 2.5e-05)
- Structural context available