S9G (p.Ser9Gly) variant of IL1RN (P18510)
S9G (p.Ser9Gly) in IL1RN (P18510) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.04 / 1. The record also includes population frequency data and structural context.
S9G (p.Ser9Gly) variant details
- p.Ser9Gly
- 1000Genomes rs199841275
- ESP rs199841275
- ExAC rs199841275
- TOPMed rs199841275
- Missense
- Variant Prioritization Score for Impact Estimate 0.037
- REVEL 0.01
- CADD 3.28
- PolyPhen-2 0.00
- SIFT 0.24
- Most common in the 1KG:LWK population (allele frequency 0.0058)
- Structural context available