G137D (p.Gly137Asp) variant of PLAT (P00750)
G137D (p.Gly137Asp) in PLAT (P00750) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.83 / 1. The record also includes population frequency data and structural context.
G137D (p.Gly137Asp) variant details
- p.Gly137Asp
- TOPMed rs1406253336
- gnomAD rs1406253336
- Missense
- Variant Prioritization Score for Impact Estimate 0.83
- REVEL 0.88
- CADD 24.40
- PolyPhen-2 1.00
- SIFT 0.00
- Most common in the East Asian population (allele frequency 5e-05)
- Structural context available