G26D (p.Gly26Asp) variant of KRT16 (Keratin, type I cytoskeletal 16)
G26D (p.Gly26Asp) in KRT16 (Keratin, type I cytoskeletal 16) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.46 / 1. The record also includes population frequency data and structural context.
G26D (p.Gly26Asp) variant details
- p.Gly26Asp
- gnomAD rs1377935373
- Missense
- Variant Prioritization Score for Impact Estimate 0.458
- REVEL 0.34
- CADD 22.40
- Most common in the REMAINING population (allele frequency 1.7e-05)
- Structural context available