ClinVar Miner

List of variants in gene MT-TK 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.8298T>C rs1603221389
NC_012920.1(MT-CYB):m.8299G>A rs1603221391
NC_012920.1(MT-CYB):m.8300T>C rs1603221393
NC_012920.1(MT-CYB):m.8301A>G rs1603221396
NC_012920.1(MT-CYB):m.8308A>G rs879081228
NC_012920.1(MT-CYB):m.8311T>A rs371589230
NC_012920.1(MT-CYB):m.8311T>C rs371589230
NC_012920.1(MT-CYB):m.8315A>G rs1603221400
NC_012920.1(MT-CYB):m.8319A>G rs1603221401
NC_012920.1(MT-CYB):m.8331A>G rs1603221403
NC_012920.1(MT-CYB):m.8337T>C rs1603221405
NC_012920.1(MT-CYB):m.8338A>G rs1603221407
NC_012920.1(MT-CYB):m.8340_8341insT rs1603221409
NC_012920.1(MT-CYB):m.8343A>G rs1603221411
NC_012920.1(MT-CYB):m.8345C>T rs1603221413
NC_012920.1(MT-CYB):m.8346C>A rs1603221415
NC_012920.1(MT-CYB):m.8347A>G rs1603221417
NC_012920.1(MT-CYB):m.8348A>G rs1556423430
NC_012920.1(MT-CYB):m.8349C>T rs1603221418
NC_012920.1(MT-CYB):m.8350A>G rs1603221419
NC_012920.1(MT-CYB):m.8358A>G rs1603221421
NC_012920.1(MT-CYB):m.8360A>G rs1603221422
NC_012920.1(MT-CYB):m.8362T>G rs1603221423
NC_012920.1(MT-CYB):m.8364A>T rs1603221428
m.8296A>G rs118192102
m.8344A>G rs118192098
m.8356T>C rs118192099
m.8363G>A rs118192100

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