P47A (p.Pro47Ala) variant of IL10RA (Q13651)
P47A (p.Pro47Ala) in IL10RA (Q13651) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.37 / 1. The record also includes population frequency data and structural context.
P47A (p.Pro47Ala) variant details
- p.Pro47Ala
- gnomAD rs2058001692
- Missense
- Variant Prioritization Score for Impact Estimate 0.372
- REVEL 0.41
- MetaLR 0.39
- MetaSVM -0.63
- CADD 13.40
- PolyPhen-2 0.27
- SIFT 0.04
- Most common in the Finnish in Finland (FIN) population (allele frequency 9.4e-05)
- Structural context available