G79D (p.Gly79Asp) variant of KRT10 (Keratin, type I cytoskeletal 10)
G79D (p.Gly79Asp) in KRT10 (Keratin, type I cytoskeletal 10) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.44 / 1. The record also includes population frequency data.
G79D (p.Gly79Asp) variant details
- p.Gly79Asp
- Ensembl rs1905465737
- Missense
- Variant Prioritization Score for Impact Estimate 0.436
- REVEL 0.39
- CADD 22.90
- PolyPhen-2 0.66
- SIFT 0.01
- Most common in the African/African-American population (allele frequency 0.00041)