Q89R (p.Gln89Arg) variant of STAT6 (P42226)
Q89R (p.Gln89Arg) in STAT6 (P42226) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.30 / 1. The record also includes population frequency data and structural context.
Q89R (p.Gln89Arg) variant details
- p.Gln89Arg
- gnomAD rs1483954081
- Missense
- Variant Prioritization Score for Impact Estimate 0.295
- REVEL 0.09
- CADD 20.30
- PolyPhen-2 0.04
- SIFT 0.49
- Most common in the Finnish in Finland (FIN) population (allele frequency 1.9e-05)
- Structural context available