D58E (p.Asp58Glu) variant of HSPG2 (P98160)
D58E (p.Asp58Glu) in HSPG2 (P98160) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; high impact.
D58E (p.Asp58Glu) variant details
- p.Asp58Glu
- NCI-TCGA TCGA novel
- Variant assessed as somatic; high impact.
- Missense
- UniProt: Variant assessed as somatic; high impact.