ClinVar Miner

List of variants in gene MT-CYB reported as benign for Leigh syndrome

Included ClinVar conditions (11):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 94
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HGVS dbSNP gnomAD frequency
NC_012920.1(MT-CYB):m.14750A>G rs1603224853
NC_012920.1(MT-CYB):m.14751C>T rs1603224855
NC_012920.1(MT-CYB):m.14757T>C rs1603224859
NC_012920.1(MT-CYB):m.14769A>G rs28357679
NC_012920.1(MT-CYB):m.14790A>G rs1603224887
NC_012920.1(MT-CYB):m.14793A>G rs2853504
NC_012920.1(MT-CYB):m.14798T>C rs28357681
NC_012920.1(MT-CYB):m.14861G>A rs2853505
NC_012920.1(MT-CYB):m.14862C>T rs1603224933
NC_012920.1(MT-CYB):m.14870A>G rs1603224936
NC_012920.1(MT-CYB):m.14883C>T rs1603224950
NC_012920.1(MT-CYB):m.14927A>G rs201551481
NC_012920.1(MT-CYB):m.14970A>G rs1556424510
NC_012920.1(MT-CYB):m.14978A>G rs199997767
NC_012920.1(MT-CYB):m.14979T>C rs200786872
NC_012920.1(MT-CYB):m.14990C>T rs1603225008
NC_012920.1(MT-CYB):m.15002G>A rs370448948
NC_012920.1(MT-CYB):m.15014T>C rs1603225022
NC_012920.1(MT-CYB):m.15047G>A rs1603225043
NC_012920.1(MT-CYB):m.15071T>C rs199999794
NC_012920.1(MT-CYB):m.15074T>C rs201169089
NC_012920.1(MT-CYB):m.15077G>A rs201943501
NC_012920.1(MT-CYB):m.15080A>G rs386829235
NC_012920.1(MT-CYB):m.15110G>A rs28357685
NC_012920.1(MT-CYB):m.15113A>G rs1603225089
NC_012920.1(MT-CYB):m.15119G>A rs201194402
NC_012920.1(MT-CYB):m.15164T>C rs1603225118
NC_012920.1(MT-CYB):m.15203A>G rs1603225143
NC_012920.1(MT-CYB):m.15204T>C rs28357687
NC_012920.1(MT-CYB):m.15218A>G rs2853506
NC_012920.1(MT-CYB):m.15221G>A rs1603225157
NC_012920.1(MT-CYB):m.15236A>G rs386829239
NC_012920.1(MT-CYB):m.15261G>A rs1556424551
NC_012920.1(MT-CYB):m.15263C>T rs200455825
NC_012920.1(MT-CYB):m.15272A>G rs1603225187
NC_012920.1(MT-CYB):m.15300T>C rs1556424556
NC_012920.1(MT-CYB):m.15311A>G rs35070048
NC_012920.1(MT-CYB):m.15315C>T rs879191792
NC_012920.1(MT-CYB):m.15317G>A rs2853507
NC_012920.1(MT-CYB):m.15341T>C rs1603225233
NC_012920.1(MT-CYB):m.15383T>C rs1603225252
NC_012920.1(MT-CYB):m.15386C>T rs1556424581
NC_012920.1(MT-CYB):m.15401A>G rs200521299
NC_012920.1(MT-CYB):m.15402C>T rs879163418
NC_012920.1(MT-CYB):m.15449T>C rs1603225289
NC_012920.1(MT-CYB):m.15479T>C rs202008188
NC_012920.1(MT-CYB):m.15512T>C rs879031246
NC_012920.1(MT-CYB):m.15519T>C rs200913192
NC_012920.1(MT-CYB):m.15524A>G rs1603225331
NC_012920.1(MT-CYB):m.15596G>A rs1603225369
NC_012920.1(MT-CYB):m.15617G>A rs1556424625
NC_012920.1(MT-CYB):m.15644A>G rs1603225400
NC_012920.1(MT-CYB):m.15651C>T rs1603225405
NC_012920.1(MT-CYB):m.15662A>G rs3094280
NC_012920.1(MT-CYB):m.15663T>C rs369851331
NC_012920.1(MT-CYB):m.15672T>C rs199967113
NC_012920.1(MT-CYB):m.15674T>C rs1603225419
NC_012920.1(MT-CYB):m.15692A>G rs1603225425
NC_012920.1(MT-CYB):m.15693T>C rs200975632
NC_012920.1(MT-CYB):m.15725C>T rs1603225438
NC_012920.1(MT-CYB):m.15731G>A rs1556424652
NC_012920.1(MT-CYB):m.15734G>A rs386829259
NC_012920.1(MT-CYB):m.15735C>T rs1603225446
NC_012920.1(MT-CYB):m.15746A>G rs386829260
NC_012920.1(MT-CYB):m.15747T>C rs1603225457
NC_012920.1(MT-CYB):m.15773G>A rs386829261
NC_012920.1(MT-CYB):m.15777G>A rs879182710
NC_012920.1(MT-CYB):m.15777G>C rs879182710
NC_012920.1(MT-CYB):m.15789C>T rs1556424663
NC_012920.1(MT-CYB):m.15803G>A rs1603225508
NC_012920.1(MT-CYB):m.15804T>C rs1556424669
NC_012920.1(MT-CYB):m.15813T>C rs1603225521
NC_012920.1(MT-CYB):m.15824A>G rs28357376
NC_012920.1(MT-CYB):m.15848A>G rs1057520206
NC_012920.1(MT-CYB):m.15849C>T rs202225494
NC_012920.1(MT-CYB):m.15851A>G rs3094281
NC_012920.1(MT-CYB):m.15852T>C rs1603225544
NC_012920.1(MT-CYB):m.15860A>G rs201023973
NC_012920.1(MT-CYB):m.15885C>T rs1603225562
NC_012920.1:m.15314G>A rs527236176
NC_012920.1:m.15323G>A rs527236177
NC_012920.1:m.15431G>A rs193302993
NC_012920.1:m.15452C>A rs193302994
NC_012920.1:m.15458T>C rs527236185
NC_012920.1:m.15758A>G rs527236193
NC_012920.1:m.15884G>A rs527236195
NC_012920.1:m.15884G>C rs527236195
m.14766C>T rs193302980
m.14831G>A rs199795644
m.15257G>A rs41518645
m.15287T>C rs527236044
m.15326A>G rs2853508
m.15497G>A rs199951903
m.15812G>A rs200336777

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