R68P (p.Arg68Pro) variant of CD3D (P04234)
R68P (p.Arg68Pro) in CD3D (P04234) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.39 / 1. The record also includes population frequency data, published literature, and structural context.
R68P (p.Arg68Pro) variant details
- p.Arg68Pro
- gnomAD 11-118340446-C-G
- Missense
- Variant Prioritization Score for Impact Estimate 0.389
- REVEL 0.30
- CADD 24.00
- PolyPhen-2 0.98
- SIFT 0.00
- Most common in the REMAINING population (allele frequency 0.00048)
- Structural context available
- Literature evidence available