H62Y (p.His62Tyr) variant of MCM5 (P33992)
H62Y (p.His62Tyr) in MCM5 (P33992) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.11 / 1. The record also includes population frequency data, published literature, and structural context.
H62Y (p.His62Tyr) variant details
- p.His62Tyr
- gnomAD 22-35401393-C-T
- Missense
- Variant Prioritization Score for Impact Estimate 0.105
- CADD 3.49
- Most common in the African/African-American population (allele frequency 0.00012)
- Structural context available
- Literature evidence available