N74H (p.Asn74His) variant of CD3D (P04234)
N74H (p.Asn74His) 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, published literature, and structural context.
N74H (p.Asn74His) variant details
- p.Asn74His
- gnomAD 11-118340429-T-G
- Missense
- Variant Prioritization Score for Impact Estimate 0.0342
- REVEL 0.02
- CADD 0.47
- PolyPhen-2 0.00
- SIFT 0.13
- Most common in the Finnish in Finland (FIN) population (allele frequency 0.00019)
- Structural context available
- Literature evidence available