T98S (p.Thr98Ser) variant of STAT6 (P42226)
T98S (p.Thr98Ser) 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.
T98S (p.Thr98Ser) variant details
- p.Thr98Ser
- TOPMed rs937605959
- gnomAD rs937605959
- Missense
- Variant Prioritization Score for Impact Estimate 0.304
- REVEL 0.10
- CADD 17.90
- PolyPhen-2 0.09
- SIFT 0.14
- Most common in the African/African-American population (allele frequency 7.2e-05)
- Structural context available