Table 1.

Common homoplasmic mutations, identified in the study.

Position	Gene/Region	Character (m, missense; s, synonymous), for mutations in protein genes	Name	Sum in general	Sum in controls	Sum in atherosclerotic patients
73	Noncoding	–	m.73A>G	36	22	14
146	Noncoding	–	m.146T>C	4	3	1
152	Noncoding	–	m.152T>C	9	4	5
185	Noncoding	–	m.185G>A	5	4	1
195	Noncoding	–	m.195T>C	9	6	3
204	Noncoding	–	m.204T>C	4	1	3
228	Noncoding	–	m.228G>A	5	3	2
263	Noncoding	–	m.263A>G	58	29	29
462	Noncoding	–	m.462C>T	4	3	1
489	Noncoding	–	m.489T>C	7	5	2
709	RNR1	–	m.709G>A	9	6	3
750	RNR1	–	m.750A>G	56	27	29
930	RNR1	–	m.930G>A	3	3	0
1438	RNR1	–	m.1438A>G	52	27	25
1811	RNR2	–	m.1811A>G	8	6	2
1888	RNR2	–	m.1888G>A	7	5	2
2706	RNR2	–	m.2706A>G	35	20	15
3010	RNR2	–	m.3010G>A	13	5	8
3107	RNR2	–	m.3107delN	57	29	28
3197	RNR2	–	m.3197T>C	5	2	3
4216	ND1	m	m.4216T>C	13	9	4
4769	ND2	s	m.4769A>G	56	28	28
4917	ND2	m	m.4917A>G	8	5	3
5147	ND2	s	m.5147G>A	3	3	0
7028	COX1	s	m.7028C>T	37	22	15
8251	COX2	s	m.8251G>A	5	1	4
8697	ATP6	s	m.8697G>A	7	5	2
8860	ATP6	m	m.8860A>G	58	29	29
10398	ND3	m	m.10398A>G	12	7	5
10463	TRNR	–	m.10463T>C	8	5	3
11251	ND4	s	m.11251A>G	13	9	4
11467	ND4	s	m.11467A>G	14	9	5
11719	ND4	s	m.11719G>A	33	19	14
11812	ND4	s	m.11812A>G	5	4	1
12308	TRNL2	–	m.12308A>G	14	9	5
12372	ND5	s	m.12372G>A	14	9	5
12612	ND5	s	m.12612A>G	6	4	2
12705	ND5	s	m.12705C>T	6	2	4
13368	ND5	s	m.13368G>A	8	5	3
13617	ND5	s	m.13617T>C	5	2	3
13708	ND5	m	m.13708G>A	7	5	2
14233	ND6	s	m.14233A>G	6	5	1
14766	CYTB	m	m.14766C>T	34	20	14
14798	CYTB	m	m.14798T>C	5	4	1
14905	CYTB	s	m.14905G>A	9	6	3
15326	CYTB	m	m.15326A>G	58	29	29
15452	CYTB	m	m.15452C>A	13	9	4
15607	CYTB	s	m.15607A>G	6	4	2
15928	TRNT	–	m.15928G>A	7	5	2
16069	Noncoding	–	m.16069C>T	6	4	2
16126	Noncoding	–	m.16126T>C	12	9	3
16223	Noncoding	–	m.16223C>T	7	3	4
16256	Noncoding	–	m.16256C>T	5	3	2
16270	Noncoding	–	m.16270C>T	5	2	3
16294	Noncoding	–	m.16294C>T	9	6	3
16296	Noncoding	–	m.16296C>T	5	4	1
16304	Noncoding	–	m.16304T>C	5	3	2
16311	Noncoding	–	m.16311T>C	7	3	4
16519	Noncoding	–	m.16519T>C	29	15	14