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Egyptian Journal of Medical Human Genetics
Fig. 1 | Egyptian Journal of Medical Human Genetics

Fig. 1

From: Mutational analysis of phospholipase C epsilon 1 gene in Egyptian children with steroid-resistant nephrotic syndrome

Fig. 1

The chromatograms of obtained variants from direct sequencing and visually inspected by Finch TV. each variant called according to HGVS criteria and ordered in ascending manner from exon 9 to exon 27, where A designate the exon 9 non sense SNP B designate the exon 12 missense SNP C designate the exon 15 missense SNP D designate the exon 19 heterozygous missense SNP E designate the exon 19 homozygous missense SNP. F designate the intronic SNP in exon 19. G designate the non sense SNP in exon 27. H designate the intronic SNP in exon 27; Each vertical rectangle mark the location of SNP and each codon change leading to amino acid change designated by upper line with the codon and its relative amino acid

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