P57T (p.Pro57Thr) variant of RAG1 (P15918)
P57T (p.Pro57Thr) in RAG1 (P15918) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.06 / 1. The record also includes population frequency data, published literature, and structural context.
P57T (p.Pro57Thr) variant details
- p.Pro57Thr
- gnomAD 11-36573473-C-A
- Missense
- Variant Prioritization Score for Impact Estimate 0.0608
- REVEL 0.05
- CADD 1.33
- PolyPhen-2 0.00
- SIFT 0.36
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available
- Literature evidence available