F97S (p.Phe97Ser) variant of STAT2 (P52630)
F97S (p.Phe97Ser) in STAT2 (P52630) 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.
F97S (p.Phe97Ser) variant details
- p.Phe97Ser
- ESP rs142832877
- ExAC rs142832877
- TOPMed rs142832877
- gnomAD rs142832877
- Missense
- Variant Prioritization Score for Impact Estimate 0.303
- REVEL 0.27
- CADD 20.60
- PolyPhen-2 0.28
- SIFT 0.02
- Most common in the African/African-American population (allele frequency 3e-05)
- Structural context available