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

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 28

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HGVS	dbSNP	gnomAD frequency
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
NC_012920.1(MT-ND1):m.1616A>G	rs2124591018
NC_012920.1(MT-TV):m.1642G>A	rs2124591032
m.1606G>A	rs199476143
m.1624C>T	rs199476144

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