G91S (p.Gly91Ser) variant of KRT16 (Keratin, type I cytoskeletal 16)
G91S (p.Gly91Ser) in KRT16 (Keratin, type I cytoskeletal 16) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.38 / 1. The record also includes population frequency data and structural context.
G91S (p.Gly91Ser) variant details
- p.Gly91Ser
- TOPMed rs1285683912
- gnomAD rs1285683912
- Missense
- Variant Prioritization Score for Impact Estimate 0.379
- REVEL 0.36
- CADD 13.30
- PolyPhen-2 0.26
- SIFT 0.34
- Most common in the Non-Finnish European population (allele frequency 2.9e-05)
- Structural context available