V39I (p.Val39Ile) variant of WRN (Q14191)
V39I (p.Val39Ile) in WRN (Q14191) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.17 / 1. The record also includes population frequency data and structural context.
V39I (p.Val39Ile) variant details
- p.Val39Ile
- gnomAD rs1238761248
- Missense
- Variant Prioritization Score for Impact Estimate 0.171
- REVEL 0.06
- CADD 17.20
- PolyPhen-2 0.00
- SIFT 0.22
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available