A11T (p.Ala11Thr) variant of MCM6 (Q14566)
A11T (p.Ala11Thr) in MCM6 (Q14566) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.17 / 1. The record also includes population frequency data and structural context.
A11T (p.Ala11Thr) variant details
- p.Ala11Thr
- ExAC rs753887287
- gnomAD rs753887287
- Missense
- Variant Prioritization Score for Impact Estimate 0.166
- REVEL 0.13
- CADD 12.60
- PolyPhen-2 0.00
- SIFT 0.18
- Most common in the South Asian population (allele frequency 1.2e-05)
- Structural context available