P88R (p.Pro88Arg) variant of VSIR (Q9H7M9)
P88R (p.Pro88Arg) in VSIR (Q9H7M9) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.44 / 1. The record also includes population frequency data and structural context.
P88R (p.Pro88Arg) variant details
- p.Pro88Arg
- gnomAD rs1292198933
- Missense
- Variant Prioritization Score for Impact Estimate 0.442
- REVEL 0.21
- CADD 23.40
- PolyPhen-2 0.86
- SIFT 0.65
- Most common in the Finnish in Finland (FIN) population (allele frequency 1.9e-05)
- Structural context available