T49T (p.Thr49Thr) variant of MCM5 (P33992)
T49T (p.Thr49Thr) in MCM5 (P33992) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.15 / 1. The record also includes population frequency data, published literature, and structural context.
T49T (p.Thr49Thr) variant details
- p.Thr49Thr
- rs199930889
- gnomAD 22-35400585-G-T
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.153
- CADD 10.20
- Most common in the 1KG:CHB population (allele frequency 0.0049)
- Structural context available
- Literature evidence available