A37A (p.Ala37Ala) variant of MCM2 (P49736)
A37A (p.Ala37Ala) in MCM2 (P49736) 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.
A37A (p.Ala37Ala) variant details
- p.Ala37Ala
- rs747126098
- gnomAD 3-127599422-C-T
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.291
- CADD 13.30
- Most common in the African/African-American population (allele frequency 2.4e-05)
- Structural context available
- Literature evidence available