N38S (p.Asn38Ser) variant of CD3D (P04234)
N38S (p.Asn38Ser) in CD3D (P04234) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.38 / 1. The record also includes population frequency data and structural context.
N38S (p.Asn38Ser) variant details
- p.Asn38Ser
- ExAC rs771000136
- gnomAD rs771000136
- Missense
- Variant Prioritization Score for Impact Estimate 0.378
- REVEL 0.22
- CADD 15.40
- PolyPhen-2 0.27
- SIFT 0.03
- Most common in the 1KG:CLM population (allele frequency 0.0053)
- Structural context available