V29I (p.Val29Ile) variant of KRT13 (Keratin, type I cytoskeletal 13)
V29I (p.Val29Ile) in KRT13 (Keratin, type I cytoskeletal 13) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.10 / 1. The record also includes population frequency data and structural context.
V29I (p.Val29Ile) variant details
- p.Val29Ile
- gnomAD rs1157169159
- Missense
- Variant Prioritization Score for Impact Estimate 0.0978
- REVEL 0.12
- CADD 0.54
- PolyPhen-2 0.00
- SIFT 0.53
- Most common in the REMAINING population (allele frequency 0.00048)
- Structural context available