G16R (p.Gly16Arg) variant of PLAT (P00750)
G16R (p.Gly16Arg) in PLAT (P00750) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.52 / 1. The record also includes population frequency data and structural context.
G16R (p.Gly16Arg) variant details
- p.Gly16Arg
- TOPMed rs1015144994
- gnomAD rs1015144994
- Missense
- Variant Prioritization Score for Impact Estimate 0.524
- REVEL 0.48
- CADD 23.00
- PolyPhen-2 0.99
- SIFT 0.04
- Most common in the Non-Finnish European population (allele frequency 1.5e-05)
- Structural context available