S39N (p.Ser39Asn) variant of MCM6 (Q14566)
S39N (p.Ser39Asn) in MCM6 (Q14566) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.15 / 1. The record also includes population frequency data and structural context.
S39N (p.Ser39Asn) variant details
- p.Ser39Asn
- Ensembl rs1009736928
- Missense
- Variant Prioritization Score for Impact Estimate 0.15
- REVEL 0.06
- CADD 14.60
- PolyPhen-2 0.00
- SIFT 0.46
- Most common in the REMAINING population (allele frequency 5e-05)
- Structural context available