A37G (p.Ala37Gly) variant of IL1RN (P18510)
A37G (p.Ala37Gly) in IL1RN (P18510) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.11 / 1. The record also includes population frequency data, published literature, and structural context.
A37G (p.Ala37Gly) variant details
- p.Ala37Gly
- rs775797091
- gnomAD 2-113120117-C-G
- Missense
- Variant Prioritization Score for Impact Estimate 0.114
- MetaLR 0.05
- MetaSVM -1.04
- CADD 0.05
- SIFT 0.43
- Most common in the REMAINING population (allele frequency 1.7e-05)
- Structural context available
- Literature evidence available