V116M (p.Val116Met) variant of C3 (Complement C3)
V116M (p.Val116Met) in C3 (Complement C3) 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.
V116M (p.Val116Met) variant details
- p.Val116Met
- rs2512271056
- ClinGen CA403645208
- ClinVar RCV003079227
- Uncertain significance
- not provided
- Missense
- ClinVar: Uncertain significance (not provided)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available