G65R (p.Gly65Arg) variant of KRT16 (Keratin, type I cytoskeletal 16)
G65R (p.Gly65Arg) in KRT16 (Keratin, type I cytoskeletal 16) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.58 / 1. The record also includes population frequency data and structural context.
G65R (p.Gly65Arg) variant details
- p.Gly65Arg
- ExAC rs772429436
- TOPMed rs772429436
- gnomAD rs772429436
- Missense
- Variant Prioritization Score for Impact Estimate 0.578
- REVEL 0.56
- CADD 19.40
- PolyPhen-2 0.21
- SIFT 0.06
- Most common in the Finnish in Finland (FIN) population (allele frequency 0.00091)
- Structural context available