S39F (p.Ser39Phe) variant of SMARCA2 (P51531)
S39F (p.Ser39Phe) in SMARCA2 (P51531) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
S39F (p.Ser39Phe) variant details
- p.Ser39Phe
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available