A37V (p.Ala37Val) variant of IL1RN (P18510)
A37V (p.Ala37Val) in IL1RN (P18510) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.12 / 1. The record also includes population frequency data, published literature, and structural context.
A37V (p.Ala37Val) variant details
- p.Ala37Val
- gnomAD 2-113120117-C-T
- Missense
- Variant Prioritization Score for Impact Estimate 0.116
- MetaLR 0.05
- MetaSVM -1.03
- CADD 0.82
- SIFT 0.31
- Most common in the Non-Finnish European population (allele frequency 4.5e-06)
- Structural context available
- Literature evidence available