S41N (p.Ser41Asn) variant of MCM3 (P25205)
S41N (p.Ser41Asn) in MCM3 (P25205) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.49 / 1. The record also includes population frequency data.
S41N (p.Ser41Asn) variant details
- p.Ser41Asn
- gnomAD rs1295485082
- Missense
- Variant Prioritization Score for Impact Estimate 0.486
- CADD 17.70
- PolyPhen-2 0.00
- SIFT 1.00
- Most common in the Non-Finnish European population (allele frequency 2.7e-06)