S9N (p.Ser9Asn) variant of IL1RN (P18510)
S9N (p.Ser9Asn) in IL1RN (P18510) 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.
S9N (p.Ser9Asn) variant details
- p.Ser9Asn
- TOPMed rs1240752552
- Missense
- Variant Prioritization Score for Impact Estimate 0.194
- REVEL 0.07
- CADD 10.40
- PolyPhen-2 0.08
- SIFT 0.09
- Most common in the East Asian population (allele frequency 2.5e-05)
- Structural context available