G29G (p.Gly29Gly) variant of MCM2 (P49736)
G29G (p.Gly29Gly) in MCM2 (P49736) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.38 / 1. The record also includes population frequency data, published literature, and structural context.
G29G (p.Gly29Gly) variant details
- p.Gly29Gly
- gnomAD 3-127599398-C-T
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.384
- CADD 13.30
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available
- Literature evidence available