F28V (p.Phe28Val) variant of MSH3 (DNA mismatch repair protein Msh3)
F28V (p.Phe28Val) 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 record also includes structural context.
F28V (p.Phe28Val) variant details
- p.Phe28Val
- rs2546709932
- ClinGen CA360265237
- ClinVar RCV003690358
- Uncertain significance
- Hereditary cancer-predisposing syndrome; not provided
- Missense
- ClinVar: Uncertain significance (Hereditary cancer-predisposing syndrome; not provided)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available