Q41H (p.Gln41His) variant of LAG3 (P18627)
Q41H (p.Gln41His) in LAG3 (P18627) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.09 / 1. The record also includes population frequency data, published literature, and structural context.
Q41H (p.Gln41His) variant details
- p.Gln41His
- gnomAD 12-6773256-G-C
- Missense
- Variant Prioritization Score for Impact Estimate 0.0922
- REVEL 0.04
- CADD 14.70
- PolyPhen-2 0.01
- SIFT 0.16
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available
- Literature evidence available