G16G (p.Gly16Gly) variant of MCM5 (P33992)
G16G (p.Gly16Gly) in MCM5 (P33992) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.17 / 1. The record also includes population frequency data, published literature, and structural context.
G16G (p.Gly16Gly) variant details
- p.Gly16Gly
- gnomAD 22-35400486-G-C
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.171
- CADD 12.80
- Most common in the REMAINING population (allele frequency 1.7e-05)
- Structural context available
- Literature evidence available