No. Position Ref Alt Gene Symbol Functional Effect MITOMAP Disease Clinical Information MITOMAP Disease Clinical Status References Details
1 73 A G . . . . No References Variant Details
2 108 A G . . . . No References Variant Details
3 248 A - . . . . No References Variant Details
4 263 A G . . . . No References Variant Details
5 310 - C . . . . No References Variant Details
6 514 CA - . . . . No References Variant Details
7 750 A G . . . . No References Variant Details
8 957 C T . . . . No References Variant Details
9 992 T C . . . . No References Variant Details
10 1438 A G . . . . No References Variant Details
11 1560 T C . . . . No References Variant Details
12 2011 G T . . . . No References Variant Details
13 2706 A G . . . . No References Variant Details
14 3262 A G . . . . No References Variant Details
15 3282 A G . . . . No References Variant Details
16 3970 C T . . . . No References Variant Details
17 4051 G A MT-ND1 missense . . No References Variant Details
18 4086 C T . . . . No References Variant Details
19 4625 C T . . . . No References Variant Details
20 4769 A G . . . . No References Variant Details
21 5344 T C MT-ND2 missense . . No References Variant Details
22 5490 C A MT-ND2 missense . . No References Variant Details
23 6112 T C MT-CO1 missense . . No References Variant Details
24 6168 G T MT-CO1 missense . . No References Variant Details
25 6221 T C . . . . No References Variant Details
26 6392 T C . . . . No References Variant Details
27 6440 C A . . . . No References Variant Details
28 6570 G A MT-CO1 missense . . No References Variant Details
29 6920 C A . . . . No References Variant Details
30 6962 G A . . . . No References Variant Details
31 7028 C T . . . . No References Variant Details
32 7108 G T MT-CO1 missense . . No References Variant Details
33 7615 A G . . . . No References Variant Details
34 8149 A G . . . . No References Variant Details
35 8421 C A MT-ATP8 missense . . No References Variant Details
36 8630 A G . . . . No References Variant Details
37 8676 C A MT-ATP6 missense . . No References Variant Details
38 8681 T G MT-ATP6 missense . . No References Variant Details
39 8860 A G MT-ATP6 missense . . References (124) Variant Details
40 9053 G A MT-ATP6 missense . . References (28) Variant Details
41 9419 C A MT-CO3 missense . . No References Variant Details
42 9526 C T MT-CO3 missense . . No References Variant Details
43 9548 G A . . . . No References Variant Details
44 9589 A G MT-CO3 missense . . No References Variant Details
45 9964 A G MT-CO3 missense . . No References Variant Details
46 9985 G T MT-CO3 missense . . No References Variant Details
47 10254 G T MT-ND3 missense . . No References Variant Details
48 10310 G A . . . . No References Variant Details
49 10609 T C MT-ND4L missense Type 2 diabetes patients with underlying 3243G / LHON patient with 10663C Reported References (21) Variant Details
50 10790 T C . . . . No References Variant Details
51 11406 T A MT-ND4 missense MELAS Reported References (1) Variant Details
52 11513 C A MT-ND4 missense . . No References Variant Details
53 11719 G A . . . . No References Variant Details
54 11908 A G . . . . No References Variant Details
55 12301 G C . . . . No References Variant Details
56 12406 G A MT-ND5 missense . . References (28) Variant Details
57 12501 G C MT-ND5 missense . . No References Variant Details
58 12539 G A . . . . No References Variant Details
59 12655 T C MT-ND5 missense . . No References Variant Details
60 12684 G A . . . . No References Variant Details
61 12705 C T . . . . No References Variant Details
62 12736 G C MT-ND5 missense . . No References Variant Details
63 12763 G T MT-ND5 missense . . No References Variant Details
64 12882 C T . . . . No References Variant Details
65 12997 G A MT-ND5 missense . . References (1) Variant Details
66 13040 C A . . . . No References Variant Details
67 13072 C A MT-ND5 missense . . No References Variant Details
68 13759 G A MT-ND5 missense Possible LHON factor Reported References (39) Variant Details
69 13898 A T MT-ND5 missense . . No References Variant Details
70 13928 G C MT-ND5 missense . . References (28) Variant Details
71 14341 C T . . . . No References Variant Details
72 14766 C T MT-CYB missense . . References (113) Variant Details
73 15282 T C MT-CYB missense . . No References Variant Details
74 15299 T C . . . . No References Variant Details
75 15305 T C MT-CYB missense . . References (1) Variant Details
76 15326 A G MT-CYB missense . . References (116) Variant Details
77 15340 A G . . . . No References Variant Details
78 15503 C A MT-CYB missense . . No References Variant Details
79 15522 C A MT-CYB missense . . References (1) Variant Details
80 15643 C T . . . . No References Variant Details
81 15710 C A MT-CYB missense . . No References Variant Details
82 16108 C T . . . . No References Variant Details
83 16129 G A . . . . No References Variant Details
84 16162 A G . . . . No References Variant Details
85 16172 T C . . . . No References Variant Details
86 16304 T C . . . . No References Variant Details
87 16311 T C . . . . No References Variant Details
88 16359 T C . . . . No References Variant Details
89 16519 T C . . . . No References Variant Details
No. Position Ref Alt Gene Symbol Functional Effect MITOMAP Disease Clinical Information MITOMAP Disease Clinical Status References Details