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Figure 4 | BMC Medical Genetics

Figure 4

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

Figure 4

Schematic presentation of haplotypes in mtDNA haplogroup U5a1. Red nodes, patients with epilepsy (N = 9); white nodes, Finnish population controls (N = 19); grey nodes, sequences found in HmtDB database (N = 66). Inside the nodes, patients identified by numbers; population controls by numbers C1 - C21 [19], database controls by numbers D1 – D66. Only discriminant variants for the four haplotypes are shown. CRS, the revised Cambridge Reference Sequence [GenBank: NC_012920]. Unless marked otherwise, variants are transitions. GenBank accession for database controls; D1 - D3: AY339528, AY339529, EF657601; D4 – D24: GU296581, GU296583, GU296594, GU296558, HM852852, GU459066, HM852873, DQ489510, GQ160809, GU296652, GU296636, GU296601, GU296595, EU597527, EU698951, GQ368895, GU206811, EU523128, DQ904330, DQ826448, EF657412; D25 - D29: AY339523, DQ112838, EF397754, HM490393, JN604831; D30 - D66: AY339524, AY339525, AY339526, AY339527, EF657616, EF363686, EF177408, EU215455, GU391321, GQ214520, HM246245, HM229344, GU122993, HM144108, HM142902, GU296650, GU296635, GU296634, GU296626, GU296615, GU296613, GU296605, GU296602, GU296597, GU296596, GU296580, GU296574, GU296548, GU797137, EU007851, EU124886, AM260578, AM260577, AM260576, AM260573, AM260572, HM765474.

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BMC Medical Genetics

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