C39T (p.Cys39Thr) variant of POLR1D (P0DPB6)
C39T (p.Cys39Thr) in POLR1D (P0DPB6) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact in the context of in TCS2. The record also includes structural context.
C39T (p.Cys39Thr) variant details
- p.Cys39Thr
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- in TCS2
- Missense
- UniProt: Variant assessed as somatic; moderate impact. (in TCS2)
- Structural context available