G97S (p.Gly97Ser) variant of KRT16 (Keratin, type I cytoskeletal 16)
G97S (p.Gly97Ser) in KRT16 (Keratin, type I cytoskeletal 16) 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.
G97S (p.Gly97Ser) variant details
- p.Gly97Ser
- Ensembl rs1295347923
- Missense
- Variant Prioritization Score for Impact Estimate 0.273
- REVEL 0.28
- CADD 13.90
- PolyPhen-2 0.14
- SIFT 0.53
- Most common in the Non-Finnish European population (allele frequency 8.8e-05)
- Structural context available