S36T (p.Ser36Thr) variant of KRT9 (Keratin, type I cytoskeletal 9)
S36T (p.Ser36Thr) in KRT9 (Keratin, type I cytoskeletal 9) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.27 / 1. The record also includes population frequency data and structural context.
S36T (p.Ser36Thr) variant details
- p.Ser36Thr
- gnomAD rs1452186640
- Missense
- Variant Prioritization Score for Impact Estimate 0.269
- REVEL 0.18
- CADD 13.20
- PolyPhen-2 0.31
- SIFT 0.11
- Most common in the HGDP:MAKRANI population (allele frequency 0.023)
- Structural context available