Table 1.

Mitochondrial DNA Variation Detection

Position[i] Base change[ii] Gene[iii] Amino acid change[iv] Position[i] Base change[ii] Gene[iii] Amino acid change[iv]
 185G → ACTRL8473T → CATP8Syn
 188A → GCTRL10876A → GND4Syn
 217T → CCTRL11251A → GND4Syn
 228G → ACTRL11467A → GND4Syn
 462C → TCTRL12612A → GND5Syn
 489T → CCTRL13708G → AND5Ala → Thr
 508A → GCTRL14798T → CCTYBPhe → Leu
 514CAC → CCTRL15907A → GCTRL
1811A → G16S16051A → GCTRL
3010G → A16S16069C → TCTRL
3720A → G* ND1Syn16092T → CCTRL
3849G → A* ND1Syn16126T → CCTRL
4553T → C* ND2Syn16129G → CCTRL
4736T → C* ND2Syn16183A → CCTRL
5390A → GND2Syn16189T → CCTRL
5426T → C* ND2Syn16291C → A* CTRL
6045C → TCOISyn16362T → CCTRL
6152T → CCOISyn16366C → TCTRL

[i] Position in the Anderson reference sequence (Anderson et al. 1981).

[ii] Arrow direction indicates base change from the Anderson reference sequence; asterisk indicates novel polymorphism.

[iii] Gene name abbreviations: CTRL, control region; 16S, 16S rRNA; ND, NADH dehydrogenase; ATP, ATP synthase; CO, cytochrome oxidase; Cytb, cytochrome b.

[iv] Abbreviations: —, non-coding; Syn, synonymous mutation.