A184V (p.Ala184Val) variant of STAT5B (P51692)
A184V (p.Ala184Val) in STAT5B (P51692) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.42 / 1. The record also includes population frequency data and structural context.
A184V (p.Ala184Val) variant details
- p.Ala184Val
- gnomAD rs1303688239
- Missense
- Variant Prioritization Score for Impact Estimate 0.424
- REVEL 0.20
- CADD 27.60
- PolyPhen-2 0.42
- SIFT 0.04
- Most common in the Latino/Admixed American population (allele frequency 6.5e-05)
- Structural context available