Q13H (p.Gln13His) variant of LAG3 (P18627)
Q13H (p.Gln13His) in LAG3 (P18627) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.06 / 1. The record also includes population frequency data and structural context.
Q13H (p.Gln13His) variant details
- p.Gln13His
- gnomAD rs1322282282
- Missense
- Variant Prioritization Score for Impact Estimate 0.0616
- REVEL 0.06
- CADD 2.88
- PolyPhen-2 0.00
- SIFT 0.03
- Most common in the REMAINING population (allele frequency 1.7e-05)
- Structural context available