S68N (p.Ser68Asn) variant of KRT9 (Keratin, type I cytoskeletal 9)
S68N (p.Ser68Asn) in KRT9 (Keratin, type I cytoskeletal 9) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.18 / 1. The record also includes population frequency data and structural context.
S68N (p.Ser68Asn) variant details
- p.Ser68Asn
- ESP rs369258653
- ExAC rs369258653
- TOPMed rs369258653
- gnomAD rs369258653
- Missense
- Variant Prioritization Score for Impact Estimate 0.184
- REVEL 0.18
- CADD 2.24
- PolyPhen-2 0.03
- SIFT 0.19
- Most common in the HGDP:YAKUT population (allele frequency 0.04)
- Structural context available