A22G (p.Ala22Gly) variant of MSH3 (DNA mismatch repair protein Msh3)
A22G (p.Ala22Gly) in MSH3 (DNA mismatch repair protein Msh3) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as uncertain significance in the context of not provided. The available variant effect predictions contribute to a CATVariant prioritization score of 0.38 / 1. The record also includes structural context.
A22G (p.Ala22Gly) variant details
- p.Ala22Gly
- rs1749190564
- ClinGen CA360265182
- ClinVar RCV003720948
- Uncertain significance
- not provided
- Missense
- Variant Prioritization Score for Impact Estimate 0.38
- AlphaMissense 0.29
- MetaLR 0.39
- MetaSVM -0.77
- PolyPhen-2 0.02
- SIFT 0.01
- ClinVar: Uncertain significance (not provided)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available