N38N (p.Asn38Asn) variant of CD3D (P04234)
N38N (p.Asn38Asn) in CD3D (P04234) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.10 / 1. The record also includes population frequency data, published literature, and structural context.
N38N (p.Asn38Asn) variant details
- p.Asn38Asn
- rs193284900
- gnomAD 11-118340535-A-G
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.1
- CADD 2.77
- Most common in the East Asian population (allele frequency 0.00015)
- Structural context available
- Literature evidence available