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Figure 1 | BMC Medical Genetics

Figure 1

From: High frequency of the IVS2-2A>G DNA sequence variation in SLC26A5, encoding the cochlear motor protein prestin, precludes its involvement in hereditary hearing loss

Figure 1

Potential alternate splicing of intron 2 of SLC26A5 containing the IVS2-2A>G variant. Alternative splice acceptor sites in intron 2 of SLC26A5 having a confidence score above 0.99 out of a maximum possible score of 1.00 are shown. Numbering of intron 2 begins at the +1 position. Dotted lines above the gene drawing show potential alternately spliced gene products. The solid line below the gene drawing shows the wild type splice donor and acceptor sites that join exon 2 to exon 3.

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BMC Medical Genetics

ISSN: 1471-2350

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