A37T (p.Ala37Thr) variant of IL1RN (P18510)
A37T (p.Ala37Thr) in IL1RN (P18510) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.43 / 1. The record also includes population frequency data, published literature, and structural context.
A37T (p.Ala37Thr) variant details
- p.Ala37Thr
- rs1226009223
- gnomAD 2-113118022-G-A
- Missense
- Variant Prioritization Score for Impact Estimate 0.434
- MetaLR 0.08
- MetaSVM -1.02
- CADD 19.00
- SIFT 0.22
- Most common in the Non-Finnish European population (allele frequency 3.6e-06)
- Structural context available
- Literature evidence available