E79G (p.Glu79Gly) variant of NOTCH3 (Q9UM47)
E79G (p.Glu79Gly) in NOTCH3 (Q9UM47) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
E79G (p.Glu79Gly) variant details
- p.Glu79Gly
- NCI-TCGA TCGA novel
- Ensembl rs2145443689
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available