S9F (p.Ser9Phe) variant of KRT9 (Keratin, type I cytoskeletal 9)
S9F (p.Ser9Phe) in KRT9 (Keratin, type I cytoskeletal 9) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.30 / 1. The record also includes population frequency data and structural context.
S9F (p.Ser9Phe) variant details
- p.Ser9Phe
- ExAC rs776856368
- gnomAD rs776856368
- Missense
- Variant Prioritization Score for Impact Estimate 0.304
- REVEL 0.32
- CADD 19.90
- PolyPhen-2 0.73
- SIFT 0.00
- Most common in the African/African-American population (allele frequency 0.00012)
- Structural context available