T109P (p.Thr109Pro) variant of VSIR (Q9H7M9)
T109P (p.Thr109Pro) in VSIR (Q9H7M9) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.13 / 1. The record also includes population frequency data and structural context.
T109P (p.Thr109Pro) variant details
- p.Thr109Pro
- ExAC rs759888569
- TOPMed rs759888569
- gnomAD rs759888569
- Missense
- Variant Prioritization Score for Impact Estimate 0.128
- REVEL 0.10
- CADD 13.50
- PolyPhen-2 0.30
- SIFT 0.14
- Most common in the Finnish in Finland (FIN) population (allele frequency 0.00089)
- Structural context available