V37M (p.Val37Met) variant of KRT13 (Keratin, type I cytoskeletal 13)
V37M (p.Val37Met) in KRT13 (Keratin, type I cytoskeletal 13) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.32 / 1. The record also includes population frequency data and structural context.
V37M (p.Val37Met) variant details
- p.Val37Met
- ExAC rs764706490
- gnomAD rs764706490
- Missense
- Variant Prioritization Score for Impact Estimate 0.32
- REVEL 0.18
- CADD 21.20
- PolyPhen-2 0.36
- SIFT 0.11
- Most common in the HGDP:MAKRANI population (allele frequency 0.023)
- Structural context available