R13R (p.Arg13Arg) variant of ARID2 (Q68CP9)
R13R (p.Arg13Arg) in ARID2 (Q68CP9) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.58 / 1. The record also includes population frequency data, published literature, and structural context.
R13R (p.Arg13Arg) variant details
- p.Arg13Arg
- rs2137958824
- gnomAD 12-45729875-G-A
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.579
- CADD 13.70
- Most common in the Non-Finnish European population (allele frequency 2.7e-06)
- Structural context available
- Literature evidence available