R69G (p.Arg69Gly) variant of KRT6A (Keratin, type II cytoskeletal 6A)
R69G (p.Arg69Gly) in KRT6A (Keratin, type II cytoskeletal 6A) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.29 / 1. The record also includes population frequency data and structural context.
R69G (p.Arg69Gly) variant details
- p.Arg69Gly
- Ensembl rs1938300650
- Missense
- Variant Prioritization Score for Impact Estimate 0.285
- REVEL 0.18
- CADD 23.60
- PolyPhen-2 0.00
- SIFT 0.01
- Most common in the Finnish in Finland (FIN) population (allele frequency 0.00091)
- Structural context available