G109S (p.Gly109Ser) variant of KRT16 (Keratin, type I cytoskeletal 16)
G109S (p.Gly109Ser) in KRT16 (Keratin, type I cytoskeletal 16) 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.
G109S (p.Gly109Ser) variant details
- p.Gly109Ser
- TOPMed rs1244335082
- gnomAD rs1244335082
- Missense
- Variant Prioritization Score for Impact Estimate 0.212
- REVEL 0.14
- CADD 10.40
- PolyPhen-2 0.00
- SIFT 0.46
- Most common in the Finnish in Finland (FIN) population (allele frequency 0.00019)
- Structural context available