T37M (p.Thr37Met) variant of VSIR (Q9H7M9)
T37M (p.Thr37Met) in VSIR (Q9H7M9) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.32 / 1. The record also includes population frequency data and structural context.
T37M (p.Thr37Met) variant details
- p.Thr37Met
- ExAC rs199678615
- TOPMed rs199678615
- gnomAD rs199678615
- Missense
- Variant Prioritization Score for Impact Estimate 0.322
- REVEL 0.11
- CADD 25.10
- PolyPhen-2 0.90
- SIFT 0.01
- Most common in the HGDP:SHE population (allele frequency 0.056)
- Structural context available