List of variants in gene MT-TR 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: 18

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HGVS	dbSNP
NC_012920.1(MT-CYB):m.10405T>C	rs1603222825
NC_012920.1(MT-CYB):m.10406G>A	rs1603222826
NC_012920.1(MT-CYB):m.10408T>C	rs1603222827
NC_012920.1(MT-CYB):m.10410T>A	rs200478835
NC_012920.1(MT-CYB):m.10410T>C	rs200478835
NC_012920.1(MT-CYB):m.10411A>G	rs1603222828
NC_012920.1(MT-CYB):m.10420A>G	rs1603222829
NC_012920.1(MT-CYB):m.10427G>A	rs1556423809
NC_012920.1(MT-CYB):m.10440T>C	rs1603222833
NC_012920.1(MT-CYB):m.10446A>G	rs1603222835
NC_012920.1(MT-CYB):m.10448T>C	rs1603222836
NC_012920.1(MT-CYB):m.10454T>C	rs878874133
NC_012920.1(MT-CYB):m.10455A>G	rs1603222840
NC_012920.1(MT-CYB):m.10456A>G	rs1603222842
NC_012920.1(MT-CYB):m.10457T>C	rs1603222845
NC_012920.1(MT-CYB):m.10460T>C	rs1603222848
NC_012920.1(MT-CYB):m.10462T>C	rs1603222850
NC_012920.1(MT-CYB):m.10463T>C	rs28358279

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