G77R (p.Gly77Arg) variant of HSPG2 (P98160)
G77R (p.Gly77Arg) 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.
G77R (p.Gly77Arg) variant details
- p.Gly77Arg
- rs1033676362
- NCI-TCGA Cosmic COSV1010
- TOPMed rs1033676362
- gnomAD rs1033676362
- Variant assessed as somatic; moderate impact.
- Missense
- REVEL 0.23
- CADD 22.10
- PolyPhen-2 0.29
- SIFT 0.01
- UniProt: Variant assessed as somatic; moderate impact.
- Population evidence available