G102R (p.Gly102Arg) variant of KRT13 (Keratin, type I cytoskeletal 13)
G102R (p.Gly102Arg) in KRT13 (Keratin, type I cytoskeletal 13) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.61 / 1. The record also includes population frequency data and structural context.
G102R (p.Gly102Arg) variant details
- p.Gly102Arg
- TOPMed rs1905021171
- gnomAD rs1905021171
- Missense
- Variant Prioritization Score for Impact Estimate 0.611
- REVEL 0.58
- CADD 24.00
- Most common in the Non-Finnish European population (allele frequency 1.8e-06)
- Structural context available