L38L (p.Leu38Leu) variant of MCM2 (P49736)
L38L (p.Leu38Leu) in MCM2 (P49736) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.16 / 1. The record also includes population frequency data, published literature, and structural context.
L38L (p.Leu38Leu) variant details
- p.Leu38Leu
- gnomAD 3-127599425-C-T
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.161
- CADD 9.60
- Most common in the Non-Finnish European population (allele frequency 1.8e-06)
- Structural context available
- Literature evidence available