G69R (p.Gly69Arg) variant of CD3D (P04234)
G69R (p.Gly69Arg) in CD3D (P04234) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.58 / 1. The record also includes population frequency data and structural context.
G69R (p.Gly69Arg) variant details
- p.Gly69Arg
- gnomAD rs1188035132
- Missense
- Variant Prioritization Score for Impact Estimate 0.583
- REVEL 0.52
- CADD 24.60
- PolyPhen-2 0.48
- SIFT 0.02
- Most common in the Non-Finnish European population (allele frequency 1.8e-06)
- Structural context available