ClinVar Miner

List of variants in gene MT-TT reported as benign for Juvenile myopathy, encephalopathy, lactic acidosis AND stroke

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Gene type:
ClinVar version:
Total variants: 36
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HGVS dbSNP
NC_012920.1(MT-CYB):m.15889T>C rs199833246
NC_012920.1(MT-CYB):m.15891C>T rs1556424681
NC_012920.1(MT-CYB):m.15892T>C rs1556424683
NC_012920.1(MT-CYB):m.15894G>A rs1569484752
NC_012920.1(MT-CYB):m.15900T>C rs878927456
NC_012920.1(MT-CYB):m.15902A>G rs1556424685
NC_012920.1(MT-CYB):m.15903A>G rs1603225580
NC_012920.1(MT-CYB):m.15904C>T rs35788393
NC_012920.1(MT-CYB):m.15905T>C rs879126276
NC_012920.1(MT-CYB):m.15907A>G rs41383248
NC_012920.1(MT-CYB):m.15908T>C rs386829266
NC_012920.1(MT-CYB):m.15913C>T rs1603225584
NC_012920.1(MT-CYB):m.15914A>G rs1603225587
NC_012920.1(MT-CYB):m.15916T>C rs1603225591
NC_012920.1(MT-CYB):m.15924A>G rs193303001
NC_012920.1(MT-CYB):m.15926C>T rs1603225597
NC_012920.1(MT-CYB):m.15929A>G rs878866272
NC_012920.1(MT-CYB):m.15930G>A rs41441949
NC_012920.1(MT-CYB):m.15932T>C rs527236199
NC_012920.1(MT-CYB):m.15935A>G rs1556424699
NC_012920.1(MT-CYB):m.15936A>T rs1556424701
NC_012920.1(MT-CYB):m.15937A>G rs1603225605
NC_012920.1(MT-CYB):m.15938C>T rs200572753
NC_012920.1(MT-CYB):m.15939C>T rs878981265
NC_012920.1(MT-CYB):m.15940T>C rs879197567
NC_012920.1(MT-CYB):m.15941T>C rs193303003
NC_012920.1(MT-CYB):m.15942T>C rs28535186
NC_012920.1(MT-CYB):m.15944del rs1603225607
NC_012920.1(MT-CYB):m.15944dup rs1603225607
NC_012920.1(MT-CYB):m.15946C>T rs202014122
NC_012920.1(MT-CYB):m.15947A>G rs1556424708
NC_012920.1(MT-CYB):m.15949G>A rs1603225611
NC_012920.1(MT-CYB):m.15951A>G rs199993959
NC_012920.1:m.15927G>A rs193303002
NC_012920.1:m.15928G>A rs527236198
NC_012920.1:m.15943T>C rs527236200

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