T42R (p.Thr42Arg) variant of CD3D (P04234)
T42R (p.Thr42Arg) in CD3D (P04234) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.09 / 1. The record also includes population frequency data and structural context.
T42R (p.Thr42Arg) variant details
- p.Thr42Arg
- ExAC rs777709761
- TOPMed rs777709761
- gnomAD rs777709761
- Missense
- Variant Prioritization Score for Impact Estimate 0.0943
- REVEL 0.12
- CADD 0.00
- PolyPhen-2 0.00
- SIFT 0.31
- Most common in the 1KG:MSL population (allele frequency 0.013)
- Structural context available