F38V (p.Phe38Val) variant of IL10RA (Q13651)
F38V (p.Phe38Val) in IL10RA (Q13651) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.49 / 1. The record also includes population frequency data, published literature, and structural context.
F38V (p.Phe38Val) variant details
- p.Phe38Val
- gnomAD 11-117988426-T-G
- Missense
- Variant Prioritization Score for Impact Estimate 0.489
- REVEL 0.51
- MetaLR 0.31
- MetaSVM -0.49
- CADD 25.80
- PolyPhen-2 0.46
- SIFT 0.01
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available
- Literature evidence available