Q183H (p.Gln183His) variant of STAT5B (P51692)
Q183H (p.Gln183His) in STAT5B (P51692) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.39 / 1. The record also includes population frequency data and structural context.
Q183H (p.Gln183His) variant details
- p.Gln183His
- gnomAD rs1459499647
- Missense
- Variant Prioritization Score for Impact Estimate 0.393
- REVEL 0.40
- CADD 23.90
- PolyPhen-2 0.92
- SIFT 0.00
- Most common in the South Asian population (allele frequency 1.2e-05)
- Structural context available