S17A (p.Ser17Ala) variant of CD3D (P04234)
S17A (p.Ser17Ala) in CD3D (P04234) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.13 / 1. The record also includes population frequency data, published literature, and structural context.
S17A (p.Ser17Ala) variant details
- p.Ser17Ala
- rs1417615347
- gnomAD 11-118340903-A-C
- Missense
- Variant Prioritization Score for Impact Estimate 0.133
- CADD 7.46
- Most common in the Non-Finnish European population (allele frequency 1.8e-06)
- Structural context available
- Literature evidence available