G26S (p.Gly26Ser) variant of KRT9 (Keratin, type I cytoskeletal 9)
G26S (p.Gly26Ser) in KRT9 (Keratin, type I cytoskeletal 9) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.21 / 1. The record also includes population frequency data and structural context.
G26S (p.Gly26Ser) variant details
- p.Gly26Ser
- gnomAD rs1310435573
- Missense
- Variant Prioritization Score for Impact Estimate 0.208
- REVEL 0.18
- CADD 6.34
- PolyPhen-2 0.01
- SIFT 0.31
- Most common in the South Asian population (allele frequency 1.2e-05)
- Structural context available