R13H (p.Arg13His) variant of VSIR (Q9H7M9)
R13H (p.Arg13His) in VSIR (Q9H7M9) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.26 / 1. The record also includes population frequency data and structural context.
R13H (p.Arg13His) variant details
- p.Arg13His
- ExAC rs751692062
- TOPMed rs751692062
- gnomAD rs751692062
- Missense
- Variant Prioritization Score for Impact Estimate 0.26
- REVEL 0.05
- CADD 21.30
- PolyPhen-2 0.00
- SIFT 0.09
- Most common in the East Asian population (allele frequency 0.00019)
- Structural context available