R40R (p.Arg40Arg) variant of MCM5 (P33992)
R40R (p.Arg40Arg) in MCM5 (P33992) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.18 / 1. The record also includes population frequency data, published literature, and structural context.
R40R (p.Arg40Arg) variant details
- p.Arg40Arg
- gnomAD 22-35400558-G-T
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.18
- CADD 13.60
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available
- Literature evidence available