S77G (p.Ser77Gly) variant of SMARCE1 (Q969G3)
S77G (p.Ser77Gly) in SMARCE1 (Q969G3) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
S77G (p.Ser77Gly) variant details
- p.Ser77Gly
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available