S14G (p.Ser14Gly) variant of KRT9 (Keratin, type I cytoskeletal 9)
S14G (p.Ser14Gly) in KRT9 (Keratin, type I cytoskeletal 9) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.13 / 1. The record also includes population frequency data and structural context.
S14G (p.Ser14Gly) variant details
- p.Ser14Gly
- gnomAD rs1907106567
- Missense
- Variant Prioritization Score for Impact Estimate 0.131
- REVEL 0.17
- CADD 3.93
- PolyPhen-2 0.00
- SIFT 0.15
- Most common in the Non-Finnish European population (allele frequency 2.9e-05)
- Structural context available