V76I (p.Val76Ile) variant of KRT17 (Keratin, type I cytoskeletal 17)
V76I (p.Val76Ile) in KRT17 (Keratin, type I cytoskeletal 17) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.19 / 1. The record also includes population frequency data and structural context.
V76I (p.Val76Ile) variant details
- p.Val76Ile
- gnomAD rs1329150569
- Missense
- Variant Prioritization Score for Impact Estimate 0.185
- REVEL 0.10
- CADD 5.20
- PolyPhen-2 0.00
- SIFT 0.41
- Most common in the African/African-American population (allele frequency 0.00041)
- Structural context available