D162G (p.Asp162Gly) variant of PRMT5 (O14744)
D162G (p.Asp162Gly) 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.
D162G (p.Asp162Gly) variant details
- p.Asp162Gly
- NCI-TCGA Cosmic COSV9936
- cosmic curated COSV99362
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available