P88T (p.Pro88Thr) variant of PRMT5 (O14744)
P88T (p.Pro88Thr) 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.
P88T (p.Pro88Thr) variant details
- p.Pro88Thr
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available