p.Thr47 Gln51delinsLys variant of LAG3 (P18627)
p.Thr47 Gln51delinsLys in LAG3 (P18627) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.19 / 1. The record also includes population frequency data, published literature, and structural context.
p.Thr47 Gln51delinsLys variant details
- rs773617171
- gnomAD 12-6773272-ACAATC
- Inframe Deletion
- Variant Prioritization Score for Impact Estimate 0.185
- CADD 14.80
- Most common in the Non-Finnish European population (allele frequency 1.5e-05)
- Structural context available
- Literature evidence available