G67D (p.Gly67Asp) variant of KRT13 (Keratin, type I cytoskeletal 13)
G67D (p.Gly67Asp) in KRT13 (Keratin, type I cytoskeletal 13) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.18 / 1. The record also includes population frequency data and structural context.
G67D (p.Gly67Asp) variant details
- p.Gly67Asp
- TOPMed rs1288521318
- gnomAD rs1288521318
- Missense
- Variant Prioritization Score for Impact Estimate 0.179
- REVEL 0.15
- CADD 12.10
- Most common in the Non-Finnish European population (allele frequency 2.9e-05)
- Structural context available