S199N (p.Ser199Asn) variant of STAT5B (P51692)
S199N (p.Ser199Asn) in STAT5B (P51692) 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.
S199N (p.Ser199Asn) variant details
- p.Ser199Asn
- gnomAD rs1195715633
- Missense
- Variant Prioritization Score for Impact Estimate 0.3
- REVEL 0.12
- CADD 20.20
- PolyPhen-2 0.00
- SIFT 0.33
- Most common in the Latino/Admixed American population (allele frequency 2.2e-05)
- Structural context available