Fig. 2From: Hereditary angioedema due to C1 inhibitor deficiency in Belarus: epidemiology, access to diagnosis and seven novel mutations in SERPING1 geneMapping of SERPING1 variants. SERPING1 variants found in Belarus patients are positioned within the gene map (exons are designated with numbered squares) by the help of arrowed lines and colours. The chromatogram relative to each variant is shown, indicating that all of them are present in heterozygosis. Variants localized in exons are indicated with the corresponding change in the translated amino acid residue, while variants localized in introns with the change on cDNA sequence. To process the data the Sequencing Analysis 5.2 software was usedBack to article page