V88M (p.Val88Met) variant of HSPG2 (P98160)
V88M (p.Val88Met) 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.
V88M (p.Val88Met) variant details
- p.Val88Met
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- REVEL 0.41
- CADD 25.60
- PolyPhen-2 1.00
- SIFT 0.00
- UniProt: Variant assessed as somatic; moderate impact.
- Population evidence available