C178T (p.Cys178Thr) variant of MED13L (Q71F56)
C178T (p.Cys178Thr) in MED13L (Q71F56) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
C178T (p.Cys178Thr) variant details
- p.Cys178Thr
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available