F38F (p.Phe38Phe) variant of MCM5 (P33992)
F38F (p.Phe38Phe) in MCM5 (P33992) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.39 / 1. The record also includes population frequency data, published literature, and structural context.
F38F (p.Phe38Phe) variant details
- p.Phe38Phe
- rs1447168504
- gnomAD 22-35400552-C-T
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.386
- CADD 15.50
- Most common in the Non-Finnish European population (allele frequency 1.5e-05)
- Structural context available
- Literature evidence available