P42P (p.Pro42Pro) variant of MCM2 (P49736)
P42P (p.Pro42Pro) in MCM2 (P49736) 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.
P42P (p.Pro42Pro) variant details
- p.Pro42Pro
- rs140680894
- gnomAD 3-127599437-T-A
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.153
- CADD 10.20
- Most common in the Latino/Admixed American population (allele frequency 2.2e-05)
- Structural context available
- Literature evidence available