ClinVar Miner

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

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Total variants: 28
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HGVS dbSNP
NC_012920.1(MT-CYB):m.10003T>C rs1603222620
NC_012920.1(MT-CYB):m.10005A>G rs1603222621
NC_012920.1(MT-CYB):m.10005A>T rs1603222621
NC_012920.1(MT-CYB):m.10006A>G rs1603222622
NC_012920.1(MT-CYB):m.10007T>C rs201906571
NC_012920.1(MT-CYB):m.10008A>G rs1603222626
NC_012920.1(MT-CYB):m.10013C>T rs1603222627
NC_012920.1(MT-CYB):m.10014G>A rs1603222629
NC_012920.1(MT-CYB):m.10015T>C rs28374827
NC_012920.1(MT-CYB):m.10020T>C rs1603222636
NC_012920.1(MT-CYB):m.10027T>C rs1603222638
NC_012920.1(MT-CYB):m.10029A>G rs1603222639
NC_012920.1(MT-CYB):m.10031T>C rs200048690
NC_012920.1(MT-CYB):m.10034T>C rs41347846
NC_012920.1(MT-CYB):m.10040C>T rs1603222642
NC_012920.1(MT-CYB):m.10042A>G rs1603222643
NC_012920.1(MT-CYB):m.10043del rs1603222645
NC_012920.1(MT-CYB):m.10045T>C rs1603222648
NC_012920.1(MT-CYB):m.10048A>G rs878957961
NC_012920.1(MT-CYB):m.10055A>G rs1603222653
NC_012920.1(MT-CYB):m.9991A>G rs1603222612
NC_012920.1(MT-CYB):m.9993T>C rs1603222613
NC_012920.1(MT-CYB):m.9995T>C rs1603222616
NC_012920.1(MT-CYB):m.9996T>C rs1556423755
NC_012920.1(MT-CYB):m.9997T>A rs121434475
NC_012920.1:m.10018A>G rs1556423757
NC_012920.1:m.10046T>C rs876661357
m.10044A>G rs41362547

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