Q16P (p.Gln16Pro) variant of MCM2 (P49736)
Q16P (p.Gln16Pro) in MCM2 (P49736) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.10 / 1. The record also includes population frequency data, published literature, and structural context.
Q16P (p.Gln16Pro) variant details
- p.Gln16Pro
- gnomAD 3-127599358-A-C
- Missense
- Variant Prioritization Score for Impact Estimate 0.0991
- REVEL 0.06
- MetaLR 0.05
- MetaSVM -1.05
- CADD 4.10
- PolyPhen-2 0.00
- SIFT 0.52
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available
- Literature evidence available