S73G (p.Ser73Gly) variant of PLAT (P00750)
S73G (p.Ser73Gly) in PLAT (P00750) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.07 / 1. The record also includes population frequency data and structural context.
S73G (p.Ser73Gly) variant details
- p.Ser73Gly
- TOPMed rs1182273420
- gnomAD rs1182273420
- Missense
- Variant Prioritization Score for Impact Estimate 0.0675
- REVEL 0.07
- CADD 0.29
- PolyPhen-2 0.00
- SIFT 0.69
- Most common in the African/African-American population (allele frequency 4.8e-05)
- Structural context available