S132R (p.Ser132Arg) variant of STAT5B (P51692)
S132R (p.Ser132Arg) in STAT5B (P51692) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.13 / 1. The record also includes population frequency data and structural context.
S132R (p.Ser132Arg) variant details
- p.Ser132Arg
- ExAC rs770921312
- TOPMed rs770921312
- gnomAD rs770921312
- Missense
- Variant Prioritization Score for Impact Estimate 0.13
- REVEL 0.12
- CADD 7.35
- Most common in the African/African-American population (allele frequency 2.4e-05)
- Structural context available