T38S (p.Thr38Ser) variant of PLAU (P00749)
T38S (p.Thr38Ser) in PLAU (P00749) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.30 / 1. The record also includes population frequency data, published literature, and structural context.
T38S (p.Thr38Ser) variant details
- p.Thr38Ser
- rs1414291341
- gnomAD 10-73911911-C-G
- Missense
- Variant Prioritization Score for Impact Estimate 0.301
- REVEL 0.04
- CADD 9.51
- Most common in the Latino/Admixed American population (allele frequency 2.5e-05)
- Structural context available
- Literature evidence available