T39T (p.Thr39Thr) variant of MCM2 (P49736)
T39T (p.Thr39Thr) in MCM2 (P49736) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.23 / 1. The record also includes population frequency data, published literature, and structural context.
T39T (p.Thr39Thr) variant details
- p.Thr39Thr
- rs777028345
- gnomAD 3-127599428-C-T
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.232
- CADD 13.10
- Most common in the Latino/Admixed American population (allele frequency 6.5e-05)
- Structural context available
- Literature evidence available