V33G (p.Val33Gly) variant of MEFV (Pyrin)
V33G (p.Val33Gly) in MEFV (Pyrin) 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.
V33G (p.Val33Gly) variant details
- p.Val33Gly
- rs2543159777
- ClinGen CA394484765
- ClinVar RCV003443272
- Uncertain significance
- not provided
- Missense
- ClinVar: Uncertain significance (not provided)
- EBI: Variant of uncertain significance (in dbSNP:rs11466016)
- UniProt: Uncertain significance (in dbSNP:rs11466016)
- Structural context available