R109Q (p.Arg109Gln) variant of HSPG2 (P98160)
R109Q (p.Arg109Gln) 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.
R109Q (p.Arg109Gln) variant details
- p.Arg109Gln
- rs773796176
- NCI-TCGA Cosmic COSV6593
- ExAC rs773796176
- TOPMed rs773796176
- Variant assessed as somatic; moderate impact.
- Missense
- REVEL 0.09
- CADD 19.60
- PolyPhen-2 0.01
- SIFT 0.21
- UniProt: Variant assessed as somatic; moderate impact.
- Population evidence available