D137A (p.Asp137Ala) variant of STAT1 (P42224)
D137A (p.Asp137Ala) in STAT1 (P42224) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.33 / 1. The record also includes population frequency data and structural context.
D137A (p.Asp137Ala) variant details
- p.Asp137Ala
- ExAC rs749245387
- TOPMed rs749245387
- gnomAD rs749245387
- Missense
- Variant Prioritization Score for Impact Estimate 0.327
- REVEL 0.13
- CADD 24.00
- PolyPhen-2 0.07
- SIFT 0.02
- Most common in the Finnish in Finland (FIN) population (allele frequency 9.4e-05)
- Structural context available