R56W (p.Arg56Trp) variant of MCM3 (P25205)
R56W (p.Arg56Trp) in MCM3 (P25205) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.69 / 1. The record also includes population frequency data.
R56W (p.Arg56Trp) variant details
- p.Arg56Trp
- gnomAD rs1421302254
- Missense
- Variant Prioritization Score for Impact Estimate 0.69
- CADD 32.00
- PolyPhen-2 0.88
- SIFT 0.01
- Most common in the South Asian population (allele frequency 1.2e-05)