S161N (p.Ser161Asn) variant of STAT6 (P42226)
S161N (p.Ser161Asn) in STAT6 (P42226) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.22 / 1. The record also includes population frequency data, published literature, and structural context.
S161N (p.Ser161Asn) variant details
- p.Ser161Asn
- rs1438998075
- gnomAD 12-57097133-C-T
- Missense
- Variant Prioritization Score for Impact Estimate 0.219
- CADD 8.58
- Most common in the Non-Finnish European population (allele frequency 1.9e-06)
- Structural context available
- Literature evidence available