A86G (p.Ala86Gly) variant of KRT13 (Keratin, type I cytoskeletal 13)
A86G (p.Ala86Gly) in KRT13 (Keratin, type I cytoskeletal 13) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.20 / 1. The record also includes population frequency data and structural context.
A86G (p.Ala86Gly) variant details
- p.Ala86Gly
- TOPMed rs920200832
- gnomAD rs920200832
- Missense
- Variant Prioritization Score for Impact Estimate 0.199
- REVEL 0.06
- CADD 5.13
- Most common in the African/African-American population (allele frequency 0.00031)
- Structural context available