T79K (p.Thr79Lys) variant of RAG2 (P55895)
T79K (p.Thr79Lys) in RAG2 (P55895) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.18 / 1. The record also includes population frequency data, published literature, and structural context.
T79K (p.Thr79Lys) variant details
- p.Thr79Lys
- gnomAD 11-36593933-G-T
- Missense
- Variant Prioritization Score for Impact Estimate 0.178
- REVEL 0.19
- CADD 4.98
- PolyPhen-2 0.04
- SIFT 0.72
- Most common in the Non-Finnish European population (allele frequency 1.8e-06)
- Structural context available
- Literature evidence available