S76W (p.Ser76Trp) variant of VSIR (Q9H7M9)
S76W (p.Ser76Trp) in VSIR (Q9H7M9) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.19 / 1. The record also includes population frequency data and structural context.
S76W (p.Ser76Trp) variant details
- p.Ser76Trp
- 1000Genomes rs572650329
- ExAC rs572650329
- TOPMed rs572650329
- gnomAD rs572650329
- Missense
- Variant Prioritization Score for Impact Estimate 0.186
- REVEL 0.09
- CADD 24.60
- PolyPhen-2 0.89
- SIFT 0.00
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available