P48P (p.Pro48Pro) variant of MCM2 (P49736)
P48P (p.Pro48Pro) in MCM2 (P49736) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.17 / 1. The record also includes population frequency data, published literature, and structural context.
P48P (p.Pro48Pro) variant details
- p.Pro48Pro
- rs761404358
- gnomAD 3-127599455-A-G
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.171
- CADD 12.80
- Most common in the Latino/Admixed American population (allele frequency 2.2e-05)
- Structural context available
- Literature evidence available