ClinVar Miner

List of variants in gene MT-TF studied for Juvenile myopathy, encephalopathy, lactic acidosis AND stroke

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Total variants: 31
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HGVS dbSNP
NC_012920.1(MT-CYB):m.578T>C rs1603218446
NC_012920.1(MT-CYB):m.579T>C rs1603218447
NC_012920.1(MT-CYB):m.588T>C rs1603218449
NC_012920.1(MT-CYB):m.592C>T rs1603218450
NC_012920.1(MT-CYB):m.593T>C rs879123694
NC_012920.1(MT-CYB):m.595C>A rs1603218452
NC_012920.1(MT-CYB):m.595C>T rs1603218452
NC_012920.1(MT-CYB):m.595dup rs1603218451
NC_012920.1(MT-CYB):m.596T>C rs1556422474
NC_012920.1(MT-CYB):m.597C>T rs1603218453
NC_012920.1(MT-CYB):m.597_598insT rs1603218455
NC_012920.1(MT-CYB):m.603A>G rs1603218456
NC_012920.1(MT-CYB):m.606A>G rs200056066
NC_012920.1(MT-CYB):m.618T>C rs1603218460
NC_012920.1(MT-CYB):m.619T>C rs1603218462
NC_012920.1(MT-CYB):m.621A>G rs1603218463
NC_012920.1(MT-CYB):m.624C>T rs1603218465
NC_012920.1(MT-CYB):m.628C>T rs1603218467
NC_012920.1(MT-CYB):m.629T>A rs201031012
NC_012920.1(MT-CYB):m.629T>C rs201031012
NC_012920.1(MT-CYB):m.630C>T rs1603218468
NC_012920.1(MT-CYB):m.633A>G rs1603218469
NC_012920.1(MT-CYB):m.634T>A rs1603218470
NC_012920.1(MT-CYB):m.634T>C rs1603218470
NC_012920.1(MT-CYB):m.635C>T rs1603218471
NC_012920.1(MT-CYB):m.643A>G rs1603218472
NC_012920.1(MT-CYB):m.644A>G rs1556422475
NC_012920.1(MT-CYB):m.647A>G rs1569483788
m.583G>A rs118203885
m.586G>A rs387906734
m.616T>C rs387906420

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