R18R (p.Arg18Arg) variant of MCM2 (P49736)
R18R (p.Arg18Arg) in MCM2 (P49736) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.14 / 1. The record also includes population frequency data, published literature, and structural context.
R18R (p.Arg18Arg) variant details
- p.Arg18Arg
- rs751073432
- gnomAD 3-127599365-G-T
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.141
- CADD 8.56
- Most common in the Non-Finnish European population (allele frequency 1.5e-05)
- Structural context available
- Literature evidence available