I78V (p.Ile78Val) variant of CD3D (P04234)
I78V (p.Ile78Val) in CD3D (P04234) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.03 / 1. The record also includes population frequency data and structural context.
I78V (p.Ile78Val) variant details
- p.Ile78Val
- ExAC rs773529981
- TOPMed rs773529981
- gnomAD rs773529981
- Missense
- Variant Prioritization Score for Impact Estimate 0.0262
- REVEL 0.00
- CADD 0.07
- PolyPhen-2 0.01
- SIFT 0.27
- Most common in the South Asian population (allele frequency 1.2e-05)
- Structural context available