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Figure 3 | SpringerPlus

Figure 3

From: Role of the single nucleotide polymorphism rs7903146 of TCF7L2 in inducing nonsense-mediated decay

Figure 3

Sequence of part of intron 4 around the C/T SNP rs7903146. Both genotypes the C and the T variant are shown: the C and T nucleotides of the SNP are shown in capital and bold. Possible stop codons which if inserted could mediate NMD are in grey, possible 5′ (ag) and 3′ (gt) splice sites for the hypothesized extra exon are double underlined (possible exon includes nucleotides from ag to gt), possible ESE are underlined in the C variant and possible ESS are in italic in the T variant.

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