R47G (p.Arg47Gly) variant of CARD11 (Q9BXL7)
R47G (p.Arg47Gly) in CARD11 (Q9BXL7) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
R47G (p.Arg47Gly) variant details
- p.Arg47Gly
- NCI-TCGA Cosmic COSV6271
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available