ClinVar Miner

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

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Total variants: 31
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HGVS dbSNP
NC_012920.1(MT-CYB):m.5514A>G rs1603219997
NC_012920.1(MT-CYB):m.5515A>G rs1603220000
NC_012920.1(MT-CYB):m.5516A>G rs1603220001
NC_012920.1(MT-CYB):m.5524T>C rs1603220004
NC_012920.1(MT-CYB):m.5527A>G rs1603220005
NC_012920.1(MT-CYB):m.5528T>C rs1556423004
NC_012920.1(MT-CYB):m.5530C>T rs1603220009
NC_012920.1(MT-CYB):m.5536_5537insT rs1603220010
NC_012920.1(MT-CYB):m.5538G>A rs1603220012
NC_012920.1(MT-CYB):m.5539A>G rs1603220013
NC_012920.1(MT-CYB):m.5539A>T rs1603220013
NC_012920.1(MT-CYB):m.5540G>A rs1603220014
NC_012920.1(MT-CYB):m.5542C>T rs1603220015
NC_012920.1(MT-CYB):m.5543T>C rs1603220016
NC_012920.1(MT-CYB):m.5544T>C rs1603220018
NC_012920.1(MT-CYB):m.5550C>T rs1603220019
NC_012920.1(MT-CYB):m.5553T>C rs878853053
NC_012920.1(MT-CYB):m.5553T>G rs878853053
NC_012920.1(MT-CYB):m.5554C>A rs1603220020
NC_012920.1(MT-CYB):m.5557T>C rs1603220022
NC_012920.1(MT-CYB):m.5558A>G rs370471013
NC_012920.1(MT-CYB):m.5560G>A rs1603220026
NC_012920.1(MT-CYB):m.5563G>A rs1603220027
NC_012920.1(MT-CYB):m.5566A>G rs1603220029
NC_012920.1(MT-CYB):m.5567T>C rs1603220030
NC_012920.1(MT-CYB):m.5568A>G rs200719361
NC_012920.1(MT-CYB):m.5573A>G rs1603220033
NC_012920.1(MT-CYB):m.5575T>C rs1603220034
NC_012920.1:m.5559A>G rs1556423008
NC_012920.1:m.5561T>C rs1556423009
m.5521G>A rs199474673

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