ClinVar Miner

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

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Total variants: 26
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HGVS dbSNP
NC_012920.1(MT-CYB):m.1607T>C rs1603218581
NC_012920.1(MT-CYB):m.1608G>A rs1603218582
NC_012920.1(MT-CYB):m.1617C>T rs1603218583
NC_012920.1(MT-CYB):m.1618A>G rs1603218584
NC_012920.1(MT-CYB):m.1619C>T rs1569483811
NC_012920.1(MT-CYB):m.1619_1620insT rs1603218585
NC_012920.1(MT-CYB):m.1628C>T rs1603218586
NC_012920.1(MT-CYB):m.1629A>G rs1603218587
NC_012920.1(MT-CYB):m.1630A>G rs1603218588
NC_012920.1(MT-CYB):m.1631C>T rs1603218590
NC_012920.1(MT-CYB):m.1636A>G rs1603218591
NC_012920.1(MT-CYB):m.1638T>C rs1603218592
NC_012920.1(MT-CYB):m.1640A>G rs1603218594
NC_012920.1(MT-CYB):m.1641G>A rs28416113
NC_012920.1(MT-CYB):m.1643A>G rs1603218595
NC_012920.1(MT-CYB):m.1644G>A rs587776441
NC_012920.1(MT-CYB):m.1646T>C rs1603218598
NC_012920.1(MT-CYB):m.1654T>C rs1603218602
NC_012920.1(MT-CYB):m.1656del rs1603218604
NC_012920.1(MT-CYB):m.1657C>T rs1603218606
NC_012920.1(MT-CYB):m.1658T>C rs1603218607
NC_012920.1(MT-CYB):m.1659T>C rs1603218609
NC_012920.1(MT-CYB):m.1664G>A rs200807305
NC_012920.1(MT-CYB):m.1670A>T rs1603218611
m.1606G>A rs199476143
m.1624C>T rs199476144

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