C37F (p.Cys37Phe) variant of CD3D (P04234)
C37F (p.Cys37Phe) in CD3D (P04234) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.57 / 1. The record also includes population frequency data, published literature, and structural context.
C37F (p.Cys37Phe) variant details
- p.Cys37Phe
- gnomAD 11-118340539-C-A
- Missense
- Variant Prioritization Score for Impact Estimate 0.572
- REVEL 0.57
- CADD 22.80
- PolyPhen-2 0.98
- SIFT 0.00
- Most common in the 1KG:CLM population (allele frequency 0.0053)
- Structural context available
- Literature evidence available