E107V (p.Glu107Val) variant of HSPG2 (P98160)
E107V (p.Glu107Val) in HSPG2 (P98160) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; high impact.
E107V (p.Glu107Val) variant details
- p.Glu107Val
- NCI-TCGA TCGA novel
- Variant assessed as somatic; high impact.
- Missense
- UniProt: Variant assessed as somatic; high impact.