S36N (p.Ser36Asn) variant of STAT6 (P42226)
S36N (p.Ser36Asn) in STAT6 (P42226) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.20 / 1. The record also includes population frequency data and structural context.
S36N (p.Ser36Asn) variant details
- p.Ser36Asn
- ESP rs368611496
- ExAC rs368611496
- TOPMed rs368611496
- gnomAD rs368611496
- Missense
- Variant Prioritization Score for Impact Estimate 0.2
- REVEL 0.07
- CADD 6.84
- PolyPhen-2 0.00
- SIFT 1.00
- Most common in the Non-Finnish European population (allele frequency 1.5e-05)
- Structural context available