P9T (p.Pro9Thr) variant of MCM6 (Q14566)
P9T (p.Pro9Thr) in MCM6 (Q14566) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.20 / 1. The record also includes population frequency data and structural context.
P9T (p.Pro9Thr) variant details
- p.Pro9Thr
- TOPMed rs1414034542
- gnomAD rs1414034542
- Missense
- Variant Prioritization Score for Impact Estimate 0.201
- REVEL 0.04
- CADD 18.80
- PolyPhen-2 0.00
- SIFT 0.11
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available