C17T (p.Cys17Thr) variant of MED13L (Q71F56)
C17T (p.Cys17Thr) 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.
C17T (p.Cys17Thr) variant details
- p.Cys17Thr
- NCI-TCGA Cosmic COSV9992
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available