N91K (p.Asn91Lys) variant of VSIR (Q9H7M9)
N91K (p.Asn91Lys) in VSIR (Q9H7M9) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.34 / 1. The record also includes population frequency data and structural context.
N91K (p.Asn91Lys) variant details
- p.Asn91Lys
- gnomAD rs1242057967
- Missense
- Variant Prioritization Score for Impact Estimate 0.344
- REVEL 0.21
- CADD 25.90
- PolyPhen-2 1.00
- SIFT 0.00
- Most common in the East Asian population (allele frequency 2.5e-05)
- Structural context available