S69G (p.Ser69Gly) variant of LAG3 (P18627)
S69G (p.Ser69Gly) in LAG3 (P18627) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.21 / 1. The record also includes population frequency data and structural context.
S69G (p.Ser69Gly) variant details
- p.Ser69Gly
- gnomAD rs1187624530
- Missense
- Variant Prioritization Score for Impact Estimate 0.214
- REVEL 0.03
- CADD 24.50
- PolyPhen-2 0.17
- SIFT 0.15
- Most common in the REMAINING population (allele frequency 1.7e-05)
- Structural context available