T59S (p.Thr59Ser) variant of IDH2 (P48735)
T59S (p.Thr59Ser) in IDH2 (P48735) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.80 / 1. The record also includes population frequency data and structural context.
T59S (p.Thr59Ser) variant details
- p.Thr59Ser
- TOPMed rs1901037718
- gnomAD rs1901037718
- Missense
- Variant Prioritization Score for Impact Estimate 0.8
- REVEL 0.82
- CADD 26.80
- Most common in the Non-Finnish European population (allele frequency 1.5e-05)
- Structural context available