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Figure 3 | BMC Medical Genetics

Figure 3

From: Mitochondrial DNA variant m.15218A > G in Finnish epilepsy patients who have maternal relatives with epilepsy, sensorineural hearing impairment or diabetes mellitus

Figure 3

Number of nonsynonymous variants predicted to be pathogenic or benign in 79 patients with epilepsy. Pathogenicity predictions were carried out on 52 nonsynonymous mtDNA mutations in 79 patients with epilepsy by using PolyPhen-2, SIFT BLink and PMut analyses. Gray bar, number of variants predicted to be benign; black bar, number of variants predicted to be pathogenic.

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BMC Medical Genetics

ISSN: 1471-2350

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