A38T (p.Ala38Thr) variant of LAG3 (P18627)
A38T (p.Ala38Thr) in LAG3 (P18627) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.17 / 1. The record also includes population frequency data and structural context.
A38T (p.Ala38Thr) variant details
- p.Ala38Thr
- ExAC rs751673910
- gnomAD rs751673910
- Missense
- Variant Prioritization Score for Impact Estimate 0.17
- REVEL 0.05
- CADD 23.00
- PolyPhen-2 0.67
- SIFT 0.15
- Most common in the South Asian population (allele frequency 2.3e-05)
- Structural context available