R58T (p.Arg58Thr) variant of LAG3 (P18627)
R58T (p.Arg58Thr) in LAG3 (P18627) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.31 / 1. The record also includes population frequency data and structural context.
R58T (p.Arg58Thr) variant details
- p.Arg58Thr
- TOPMed rs1264184775
- gnomAD rs1264184775
- Missense
- Variant Prioritization Score for Impact Estimate 0.311
- REVEL 0.07
- CADD 13.70
- Most common in the African/African-American population (allele frequency 4.8e-05)
- Structural context available