S141N (p.Ser141Asn) variant of VSIR (Q9H7M9)
S141N (p.Ser141Asn) in VSIR (Q9H7M9) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.15 / 1. The record also includes population frequency data and structural context.
S141N (p.Ser141Asn) variant details
- p.Ser141Asn
- TOPMed rs530354809
- Missense
- Variant Prioritization Score for Impact Estimate 0.147
- REVEL 0.12
- CADD 9.78
- PolyPhen-2 0.01
- SIFT 0.22
- Most common in the Non-Finnish European population (allele frequency 4.5e-06)
- Structural context available