R49C (p.Arg49Cys) variant of PRMT5 (O14744)
R49C (p.Arg49Cys) in PRMT5 (O14744) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
R49C (p.Arg49Cys) variant details
- p.Arg49Cys
- NCI-TCGA Cosmic COSV5354
- cosmic curated COSV53545
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available