C44W (p.Cys44Trp) variant of LAG3 (P18627)
C44W (p.Cys44Trp) in LAG3 (P18627) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.46 / 1. The record also includes population frequency data and structural context.
C44W (p.Cys44Trp) variant details
- p.Cys44Trp
- TOPMed rs1941863286
- gnomAD rs1941863286
- Missense
- Variant Prioritization Score for Impact Estimate 0.456
- REVEL 0.47
- CADD 25.70
- Most common in the Non-Finnish European population (allele frequency 1.5e-05)
- Structural context available