R13R (p.Arg13Arg) variant of WRN (Q14191)
R13R (p.Arg13Arg) in WRN (Q14191) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.39 / 1. The record also includes population frequency data, published literature, and structural context.
R13R (p.Arg13Arg) variant details
- p.Arg13Arg
- rs1812359945
- gnomAD 8-31058486-G-A
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.39
- CADD 5.12
- Most common in the Non-Finnish European population (allele frequency 1.8e-06)
- Structural context available
- Literature evidence available