P194L (p.Pro194Leu) variant of STAT5B (P51692)
P194L (p.Pro194Leu) in STAT5B (P51692) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The available variant effect predictions contribute to a CATVariant prioritization score of 0.36 / 1. The record also includes population frequency data and structural context.
P194L (p.Pro194Leu) variant details
- p.Pro194Leu
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.362
- REVEL 0.16
- CADD 24.50
- PolyPhen-2 0.29
- SIFT 0.03
- UniProt: Variant assessed as somatic; moderate impact.
- Most common in the Non-Finnish European population (allele frequency 1.8e-06)
- Structural context available