S116G (p.Ser116Gly) variant of KRT10 (Keratin, type I cytoskeletal 10)
S116G (p.Ser116Gly) in KRT10 (Keratin, type I cytoskeletal 10) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.17 / 1. The record also includes population frequency data.
S116G (p.Ser116Gly) variant details
- p.Ser116Gly
- 1000Genomes rs546321678
- ExAC rs546321678
- gnomAD rs546321678
- Missense
- Variant Prioritization Score for Impact Estimate 0.166
- REVEL 0.25
- CADD 0.00
- PolyPhen-2 0.00
- SIFT 0.39
- Most common in the 1KG:MXL population (allele frequency 0.0081)