L56L (p.Leu56Leu) variant of MCM2 (P49736)
L56L (p.Leu56Leu) in MCM2 (P49736) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.15 / 1. The record also includes population frequency data, published literature, and structural context.
L56L (p.Leu56Leu) variant details
- p.Leu56Leu
- rs765659379
- gnomAD 3-127599479-C-A
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.152
- CADD 10.10
- Most common in the Non-Finnish European population (allele frequency 1.8e-06)
- Structural context available
- Literature evidence available