L198P (p.Leu198Pro) variant of STAT5B (P51692)
L198P (p.Leu198Pro) in STAT5B (P51692) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.29 / 1. The record also includes population frequency data and structural context.
L198P (p.Leu198Pro) variant details
- p.Leu198Pro
- Ensembl rs2080208358
- Missense
- Variant Prioritization Score for Impact Estimate 0.29
- REVEL 0.12
- CADD 22.90
- Most common in the Finnish in Finland (FIN) population (allele frequency 9.4e-05)
- Structural context available