G71V (p.Gly71Val) variant of KRT13 (Keratin, type I cytoskeletal 13)
G71V (p.Gly71Val) in KRT13 (Keratin, type I cytoskeletal 13) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.29 / 1. The record also includes population frequency data and structural context.
G71V (p.Gly71Val) variant details
- p.Gly71Val
- ExAC rs762086095
- TOPMed rs762086095
- gnomAD rs762086095
- Missense
- Variant Prioritization Score for Impact Estimate 0.289
- REVEL 0.32
- CADD 15.30
- PolyPhen-2 0.99
- SIFT 0.53
- Most common in the Non-Finnish European population (allele frequency 1.8e-06)
- Structural context available