G61G (p.Gly61Gly) variant of MCM2 (P49736)
G61G (p.Gly61Gly) 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.
G61G (p.Gly61Gly) variant details
- p.Gly61Gly
- rs1430580053
- gnomAD 3-127599494-G-T
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.149
- CADD 9.62
- Most common in the Non-Finnish European population (allele frequency 2.9e-05)
- Structural context available
- Literature evidence available