S17A (p.Ser17Ala) variant of SYNGAP1 (Q96PV0)
S17A (p.Ser17Ala) in SYNGAP1 (Q96PV0) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
S17A (p.Ser17Ala) variant details
- p.Ser17Ala
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available