S38S (p.Ser38Ser) variant of WRN (Q14191)
S38S (p.Ser38Ser) in WRN (Q14191) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.26 / 1. The record also includes population frequency data, published literature, and structural context.
S38S (p.Ser38Ser) variant details
- p.Ser38Ser
- rs201800431
- gnomAD 8-31059170-T-C
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.259
- CADD 10.90
- Most common in the 1KG:LWK population (allele frequency 0.0058)
- Structural context available
- Literature evidence available