P56R (p.Pro56Arg) variant of SDHB (P21912)
P56R (p.Pro56Arg) in SDHB (P21912) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
P56R (p.Pro56Arg) variant details
- p.Pro56Arg
- NCI-TCGA Cosmic COSV1009
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available