P39P (p.Pro39Pro) variant of LAG3 (P18627)
P39P (p.Pro39Pro) in LAG3 (P18627) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.16 / 1. The record also includes population frequency data, published literature, and structural context.
P39P (p.Pro39Pro) variant details
- p.Pro39Pro
- rs755173480
- gnomAD 12-6773250-T-C
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.161
- CADD 11.40
- Most common in the South Asian population (allele frequency 4.6e-05)
- Structural context available
- Literature evidence available