[Figure 8]: Sequence walker analysis of the genomic sequence of human NF2 near the beginning of exon 5 with three closely located distinct mutations. All give the same transcript modification, a deletion of 20 bp, using the weak to very weak site at wt +20 bp. In addition, mutation agTA -> atTA (IVS5-1 g>t) gives an exon using the slightly stronger acceptor at wt + 5 bp.
[Figure 8A]: WT sequence near the beginning of exon 5, showing the strong acceptor along with the confirmed ( --- > exon.