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. 2022 Jun 22;10:919996. doi: 10.3389/fped.2022.919996

Figure 3.

Figure 3

(A) Chromatogram of Sanger sequencing showing the c.1212A>G p.Val404Ile in 10 unrelated patients SCN1A gene from the cohort of 25 epileptic sporadic patients. The green oval is showing the change in the base pair in mutant and while type sequence. (B) Protein alignment of different species was done to show the highly conserved amino acid variants p.Val404Ile SCN1A gene highlighted in all species.