G37W (p.Gly37Trp) variant of LAG3 (P18627)
G37W (p.Gly37Trp) in LAG3 (P18627) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.53 / 1. The record also includes population frequency data and structural context.
G37W (p.Gly37Trp) variant details
- p.Gly37Trp
- Ensembl rs1941862901
- Missense
- Variant Prioritization Score for Impact Estimate 0.531
- REVEL 0.33
- CADD 29.60
- PolyPhen-2 1.00
- SIFT 0.00
- Most common in the East Asian population (allele frequency 0.00018)
- Structural context available