S156L (p.Ser156Leu) variant of VSIR (Q9H7M9)
S156L (p.Ser156Leu) in VSIR (Q9H7M9) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.17 / 1. The record also includes population frequency data and structural context.
S156L (p.Ser156Leu) variant details
- p.Ser156Leu
- ESP rs147441567
- TOPMed rs147441567
- gnomAD rs147441567
- Missense
- Variant Prioritization Score for Impact Estimate 0.168
- REVEL 0.05
- CADD 11.90
- PolyPhen-2 0.00
- SIFT 0.39
- Most common in the Middle Eastern population (allele frequency 0.00018)
- Structural context available