S13R (p.Ser13Arg) variant of MCM2 (P49736)
S13R (p.Ser13Arg) in MCM2 (P49736) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as uncertain significance in the context of not provided. The record also includes structural context.
S13R (p.Ser13Arg) variant details
- p.Ser13Arg
- rs1201891506
- ClinGen CA354380156
- ClinVar RCV002639932
- Uncertain significance
- not provided
- Missense
- ClinVar: Uncertain significance (not provided)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available