G118R (p.Gly118Arg) variant of VSIR (Q9H7M9)
G118R (p.Gly118Arg) in VSIR (Q9H7M9) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The available variant effect predictions contribute to a CATVariant prioritization score of 0.57 / 1. The record also includes population frequency data and structural context.
G118R (p.Gly118Arg) variant details
- p.Gly118Arg
- rs1312702295
- gnomAD rs1312702295
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.569
- REVEL 0.41
- CADD 25.30
- PolyPhen-2 1.00
- SIFT 0.00
- UniProt: Variant assessed as somatic; moderate impact.
- Most common in the Non-Finnish European population (allele frequency 2.7e-06)
- Structural context available