Skip to main content
. 2022 Jan 16;23(2):952. doi: 10.3390/ijms23020952

Table 1.

List of mtDNA mutations associated with CAD.

Mutation Gene Other Notes References
Mt5568 (A > G) tRNATrp Iranian CAD Patients [34]
Mt5711 (T > A) tRNAAsn
Mt5725 (T > G) tRNAAsn
Mt12308 (A > G) tRNALeu (CUN)
Mt16089 (T > C) D-loop TG Association with CVD risk factors in Chinese Han CAD patients [35]
Mt16145 (G > A) D-loop TG; LVEF
Mt16089 (T > C) D-loop PC
Mt14178 (T > C) MT-ND6 TC
Mt215 (A > G) D-loop LDLC
Mt8231 (C > A) MT-CO2 Iranian CAD Patients [36]
Mt8376 (T > A) MT-ATP8
Mt15928 (G > A) tRNAThr
Mt5628 (T > C) tRNAAla Chinese CAD patients [37]
Mt681 (T > C) 12S rRNA
Mt5592 (A > G) tRNAAla
mtDNA4977 Deletion Alone or in combination with LTL associated with recurrent MACEs and all-cause mortality in Caucasian CAD patients [38]
Associated with MACEs and all-cause mortality in Italian CAD patients [39]
In combination with low folate level associated with high CAD risk among Chinese diabetic patients [40]
Mt15910 (C > T) tRNAThr Han Chinese patients withLHON, signs of maternally inherited CHD [41]