G89A (p.Gly89Ala) variant of MED13L (Q71F56)
G89A (p.Gly89Ala) 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.
G89A (p.Gly89Ala) variant details
- p.Gly89Ala
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available