G88E (p.Gly88Glu) variant of STAT5B (P51692)
G88E (p.Gly88Glu) in STAT5B (P51692) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.45 / 1. The record also includes population frequency data and structural context.
G88E (p.Gly88Glu) variant details
- p.Gly88Glu
- gnomAD rs1355612617
- Missense
- Variant Prioritization Score for Impact Estimate 0.453
- REVEL 0.25
- CADD 22.40
- PolyPhen-2 0.53
- SIFT 0.88
- Most common in the Non-Finnish European population (allele frequency 2.7e-06)
- Structural context available