T79T (p.Thr79Thr) variant of RAG2 (P55895)
T79T (p.Thr79Thr) in RAG2 (P55895) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.12 / 1. The record also includes population frequency data, published literature, and structural context.
T79T (p.Thr79Thr) variant details
- p.Thr79Thr
- gnomAD 11-36593932-T-C
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.117
- CADD 5.15
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available
- Literature evidence available