T47A (p.Thr47Ala) variant of CD3D (P04234)
T47A (p.Thr47Ala) in CD3D (P04234) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.30 / 1. The record also includes population frequency data, published literature, and structural context.
T47A (p.Thr47Ala) variant details
- p.Thr47Ala
- gnomAD 11-118340510-T-C
- Missense
- Variant Prioritization Score for Impact Estimate 0.302
- REVEL 0.29
- CADD 15.60
- PolyPhen-2 0.19
- SIFT 0.15
- Most common in the REMAINING population (allele frequency 0.00048)
- Structural context available
- Literature evidence available