T38R (p.Thr38Arg) variant of PLAU (P00749)
T38R (p.Thr38Arg) in PLAU (P00749) 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.
T38R (p.Thr38Arg) variant details
- p.Thr38Arg
- TOPMed rs1478820563
- gnomAD rs1478820563
- Missense
- Variant Prioritization Score for Impact Estimate 0.285
- REVEL 0.31
- MetaLR 0.39
- MetaSVM -0.62
- CADD 17.10
- PolyPhen-2 0.07
- SIFT 0.03
- Most common in the Non-Finnish European population (allele frequency 1.5e-05)
- Structural context available