G67D (p.Gly67Asp) variant of KRT16 (Keratin, type I cytoskeletal 16)
G67D (p.Gly67Asp) in KRT16 (Keratin, type I cytoskeletal 16) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.57 / 1. The record also includes population frequency data and structural context.
G67D (p.Gly67Asp) variant details
- p.Gly67Asp
- TOPMed rs1373417012
- gnomAD rs1373417012
- Missense
- Variant Prioritization Score for Impact Estimate 0.569
- REVEL 0.46
- CADD 21.60
- PolyPhen-2 0.33
- SIFT 0.03
- Most common in the REMAINING population (allele frequency 0.00048)
- Structural context available