A37T (p.Ala37Thr) variant of MCM2 (P49736)
A37T (p.Ala37Thr) in MCM2 (P49736) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.31 / 1. The record also includes population frequency data, published literature, and structural context.
A37T (p.Ala37Thr) variant details
- p.Ala37Thr
- gnomAD 3-127599420-G-A
- Missense
- Variant Prioritization Score for Impact Estimate 0.31
- REVEL 0.16
- MetaLR 0.08
- MetaSVM -1.07
- CADD 22.80
- PolyPhen-2 0.01
- SIFT 0.12
- Most common in the Finnish in Finland (FIN) population (allele frequency 1.9e-05)
- Structural context available
- Literature evidence available