R86H (p.Arg86His) variant of VSIR (Q9H7M9)
R86H (p.Arg86His) 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 0.12 / 1. The record also includes population frequency data and structural context.
R86H (p.Arg86His) variant details
- p.Arg86His
- rs746223877
- ExAC rs746223877
- TOPMed rs746223877
- gnomAD rs746223877
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.119
- REVEL 0.02
- CADD 17.00
- PolyPhen-2 0.03
- SIFT 0.22
- UniProt: Variant assessed as somatic; moderate impact.
- Most common in the REMAINING population (allele frequency 5e-05)
- Structural context available