A19G (p.Ala19Gly) variant of MSH3 (DNA mismatch repair protein Msh3)
A19G (p.Ala19Gly) 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 Hereditary cancer-predisposing syndrome; not provided. The available variant effect predictions contribute to a CATVariant prioritization score of 0.19 / 1. The record also includes population frequency data, published literature, and structural context.
A19G (p.Ala19Gly) variant details
- p.Ala19Gly
- rs780785898
- ClinGen CA3327426
- ClinVar RCV001205761
- ClinVar RCV002348673
- Uncertain significance
- Hereditary cancer-predisposing syndrome; not provided
- Missense
- Variant Prioritization Score for Impact Estimate 0.185
- REVEL 0.13
- CADD 11.40
- PolyPhen-2 0.00
- SIFT 0.59
- ClinVar: Uncertain significance (Hereditary cancer-predisposing syndrome; not provided)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Most common in the Finnish in Finland (FIN) population (allele frequency 1.9e-05)
- Structural context available
- Cited in: A practice guideline from the American College of Medical Genetics and Genomics and the National Society of Genetic… (PMID 25394175)