S39F (p.Ser39Phe) variant of CD3E (P07766)
S39F (p.Ser39Phe) in CD3E (P07766) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.40 / 1. The record also includes population frequency data, published literature, and structural context.
S39F (p.Ser39Phe) variant details
- p.Ser39Phe
- gnomAD 11-118312630-C-T
- Missense
- Variant Prioritization Score for Impact Estimate 0.398
- REVEL 0.32
- MetaLR 0.23
- MetaSVM -0.73
- CADD 24.10
- PolyPhen-2 0.90
- SIFT 0.00
- Most common in the HGDP:MAKRANI population (allele frequency 0.023)
- Structural context available
- Literature evidence available