R61S (p.Arg61Ser) variant of MCM5 (P33992)
R61S (p.Arg61Ser) in MCM5 (P33992) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.19 / 1. The record also includes population frequency data, published literature, and structural context.
R61S (p.Arg61Ser) variant details
- p.Arg61Ser
- rs1405395718
- gnomAD 22-35401410-A-C
- Missense
- Variant Prioritization Score for Impact Estimate 0.189
- CADD 0.89
- Most common in the Latino/Admixed American population (allele frequency 6.5e-05)
- Structural context available
- Literature evidence available