D67G (p.Asp67Gly) variant of RAG1 (P15918)
D67G (p.Asp67Gly) in RAG1 (P15918) 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.
D67G (p.Asp67Gly) variant details
- p.Asp67Gly
- gnomAD 11-36573504-A-G
- Missense
- Variant Prioritization Score for Impact Estimate 0.176
- REVEL 0.09
- CADD 17.90
- PolyPhen-2 0.05
- SIFT 0.22
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available
- Literature evidence available