V19M (p.Val19Met) variant of CD3D (P04234)
V19M (p.Val19Met) in CD3D (P04234) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.36 / 1. The record also includes population frequency data, published literature, and structural context.
V19M (p.Val19Met) variant details
- p.Val19Met
- gnomAD 11-118340870-C-T
- Missense
- Variant Prioritization Score for Impact Estimate 0.358
- CADD 6.39
- Most common in the REMAINING population (allele frequency 0.00048)
- Structural context available
- Literature evidence available