E97D (p.Glu97Asp) variant of PRMT5 (O14744)
E97D (p.Glu97Asp) 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.
E97D (p.Glu97Asp) variant details
- p.Glu97Asp
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available