S16N (p.Ser16Asn) variant of KRT10 (Keratin, type I cytoskeletal 10)
S16N (p.Ser16Asn) in KRT10 (Keratin, type I cytoskeletal 10) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.40 / 1. The record also includes population frequency data.
S16N (p.Ser16Asn) variant details
- p.Ser16Asn
- ESP rs146957992
- ExAC rs146957992
- TOPMed rs146957992
- gnomAD rs146957992
- Missense
- Variant Prioritization Score for Impact Estimate 0.402
- REVEL 0.27
- CADD 16.60
- PolyPhen-2 0.15
- SIFT 0.00
- Most common in the East Asian population (allele frequency 2.5e-05)