T79I (p.Thr79Ile) variant of RAG2 (P55895)
T79I (p.Thr79Ile) in RAG2 (P55895) 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.
T79I (p.Thr79Ile) variant details
- p.Thr79Ile
- gnomAD 11-36593933-G-A
- Missense
- Variant Prioritization Score for Impact Estimate 0.188
- REVEL 0.20
- CADD 7.28
- PolyPhen-2 0.00
- SIFT 0.26
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available
- Literature evidence available