R41G (p.Arg41Gly) variant of SERPINE1 (P05121)
R41G (p.Arg41Gly) in SERPINE1 (P05121) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.44 / 1. The record also includes population frequency data and structural context.
R41G (p.Arg41Gly) variant details
- p.Arg41Gly
- 1000Genomes rs549581756
- ExAC rs549581756
- TOPMed rs549581756
- gnomAD rs549581756
- Missense
- Variant Prioritization Score for Impact Estimate 0.441
- REVEL 0.36
- CADD 25.90
- Most common in the 1KG:MSL population (allele frequency 0.0063)
- Structural context available