P67T (p.Pro67Thr) variant of LAG3 (P18627)
P67T (p.Pro67Thr) in LAG3 (P18627) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.34 / 1. The record also includes population frequency data and structural context.
P67T (p.Pro67Thr) variant details
- p.Pro67Thr
- ESP rs149722682
- ExAC rs149722682
- TOPMed rs149722682
- gnomAD rs149722682
- Missense
- Variant Prioritization Score for Impact Estimate 0.339
- REVEL 0.05
- CADD 23.30
- PolyPhen-2 0.11
- SIFT 0.00
- Most common in the Finnish in Finland (FIN) population (allele frequency 0.00028)
- Structural context available