S36T (p.Ser36Thr) variant of PLAT (P00750)
S36T (p.Ser36Thr) in PLAT (P00750) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.34 / 1. The record also includes population frequency data and structural context.
S36T (p.Ser36Thr) variant details
- p.Ser36Thr
- TOPMed rs1396290576
- gnomAD rs1396290576
- Missense
- Variant Prioritization Score for Impact Estimate 0.336
- REVEL 0.30
- CADD 21.60
- PolyPhen-2 0.20
- SIFT 0.16
- Most common in the East Asian population (allele frequency 0.00019)
- Structural context available