G47R (p.Gly47Arg) variant of VSIR (Q9H7M9)
G47R (p.Gly47Arg) in VSIR (Q9H7M9) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.71 / 1. The record also includes population frequency data and structural context.
G47R (p.Gly47Arg) variant details
- p.Gly47Arg
- ExAC rs772806957
- gnomAD rs772806957
- Missense
- Variant Prioritization Score for Impact Estimate 0.715
- REVEL 0.78
- CADD 26.70
- PolyPhen-2 0.99
- SIFT 0.00
- Most common in the Middle Eastern population (allele frequency 0.00017)
- Structural context available