F38I (p.Phe38Ile) variant of IL10RA (Q13651)
F38I (p.Phe38Ile) in IL10RA (Q13651) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.41 / 1. The record also includes population frequency data and structural context.
F38I (p.Phe38Ile) variant details
- p.Phe38Ile
- gnomAD rs1483446748
- Missense
- Variant Prioritization Score for Impact Estimate 0.415
- REVEL 0.39
- MetaLR 0.23
- MetaSVM -0.66
- CADD 22.80
- PolyPhen-2 0.08
- SIFT 0.13
- Most common in the Non-Finnish European population (allele frequency 1.1e-05)
- Structural context available