E122D (p.Glu122Asp) variant of HSPG2 (P98160)
E122D (p.Glu122Asp) in HSPG2 (P98160) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes variant effect predictions and population frequency data.
E122D (p.Glu122Asp) variant details
- p.Glu122Asp
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- CADD 15.60
- UniProt: Variant assessed as somatic; moderate impact.
- Population evidence available