G65D (p.Gly65Asp) variant of KRT9 (Keratin, type I cytoskeletal 9)
G65D (p.Gly65Asp) in KRT9 (Keratin, type I cytoskeletal 9) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.42 / 1. The record also includes population frequency data and structural context.
G65D (p.Gly65Asp) variant details
- p.Gly65Asp
- gnomAD rs1470857969
- Missense
- Variant Prioritization Score for Impact Estimate 0.418
- REVEL 0.44
- CADD 18.90
- PolyPhen-2 0.82
- SIFT 0.00
- Most common in the HGDP:YAKUT population (allele frequency 0.04)
- Structural context available