Predicting the Most Deleterious Missense Nonsynonymous Single-Nucleotide Polymorphisms of Hennekam Syndrome-Causing CCBE1 Gene, In Silico Analysis

<div>Amino acid alignment of human CCBE1 (UniProt ID: Q6UXH8) along with its homologues in phylogenetically close species in ABWGB and Q3MI99. Solid horizontal bars indicate conserved sequence motifs, and residues with asterisk (<sup>∗</sup>) mark indicate evolutionary conserved amino acids. The amino acid identities were colored according the Clustal color scheme, and the conservation index at each alignment position was provided by Jalview.</div>

The Scientific World Journal

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Figure 4: Predicting the Most Deleterious Missense Nonsynonymous Single-Nucleotide Polymorphisms of Hennekam Syndrome-Causing CCBE1 Gene, In Silico Analysis 

Figure 4 | Predicting the Most Deleterious Missense Nonsynonymous Single-Nucleotide Polymorphisms of Hennekam Syndrome-Causing CCBE1 Gene, In Silico Analysis 