R37W (p.Arg37Trp) variant of MCM3 (P25205)
R37W (p.Arg37Trp) in MCM3 (P25205) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.51 / 1. The record also includes population frequency data.
R37W (p.Arg37Trp) variant details
- p.Arg37Trp
- ExAC rs778529414
- gnomAD rs778529414
- Missense
- Variant Prioritization Score for Impact Estimate 0.512
- CADD 26.80
- PolyPhen-2 0.68
- SIFT 0.01
- Most common in the South Asian population (allele frequency 5.8e-05)