F51F (p.Phe51Phe) variant of MCM5 (P33992)
F51F (p.Phe51Phe) in MCM5 (P33992) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.46 / 1. The record also includes population frequency data, published literature, and structural context.
F51F (p.Phe51Phe) variant details
- p.Phe51Phe
- rs376131731
- gnomAD 22-35400591-C-T
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.458
- CADD 14.90
- Most common in the REMAINING population (allele frequency 5e-05)
- Structural context available
- Literature evidence available