G66R (p.Gly66Arg) variant of HSPG2 (P98160)
G66R (p.Gly66Arg) in HSPG2 (P98160) is a missense change. Clinical records from ClinVar and UniProt describe it as uncertain significance in the context of not provided. The record also includes variant effect predictions and population frequency data.
G66R (p.Gly66Arg) variant details
- p.Gly66Arg
- gnomAD rs1321699592
- Uncertain significance
- not provided
- Missense
- REVEL 0.33
- CADD 22.60
- PolyPhen-2 0.19
- SIFT 0.00
- ClinVar: Uncertain significance (not provided)
- UniProt: Uncertain significance
- Population evidence available