D18D (p.Asp18Asp) variant of MCM5 (P33992)
D18D (p.Asp18Asp) in MCM5 (P33992) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.29 / 1. The record also includes population frequency data, published literature, and structural context.
D18D (p.Asp18Asp) variant details
- p.Asp18Asp
- rs1260649916
- gnomAD 22-35400492-C-T
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.294
- CADD 12.40
- Most common in the East Asian population (allele frequency 0.00019)
- Structural context available
- Literature evidence available