T52T (p.Thr52Thr) variant of MCM5 (P33992)
T52T (p.Thr52Thr) in MCM5 (P33992) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.67 / 1. The record also includes population frequency data, published literature, and structural context.
T52T (p.Thr52Thr) variant details
- p.Thr52Thr
- gnomAD 22-35400594-C-T
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.667
- CADD 12.40
- Most common in the South Asian population (allele frequency 4.7e-05)
- Structural context available
- Literature evidence available