S33P (p.Ser33Pro) variant of HSPG2 (P98160)
S33P (p.Ser33Pro) in HSPG2 (P98160) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact.
S33P (p.Ser33Pro) variant details
- p.Ser33Pro
- NCI-TCGA Cosmic COSV6597
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.