A138V (p.Ala138Val) variant of RPA1 (P27694)
A138V (p.Ala138Val) in RPA1 (P27694) is a missense change. Clinical records from ClinVar and UniProt describe it as uncertain significance in the context of not specified. The record also includes population frequency data.
A138V (p.Ala138Val) variant details
- p.Ala138Val
- TOPMed rs1913411066
- gnomAD rs1913411066
- Uncertain significance
- not specified
- Missense
- ClinVar: Uncertain significance (not specified)
- UniProt: Uncertain significance
- Population evidence available