List of variants in gene MT-TG studied for MELAS syndrome

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-TG):m.10003T>C	rs1603222620
NC_012920.1(MT-TG):m.10005A>G	rs1603222621
NC_012920.1(MT-TG):m.10005A>T	rs1603222621
NC_012920.1(MT-TG):m.10006A>G	rs1603222622
NC_012920.1(MT-TG):m.10007T>C	rs201906571
NC_012920.1(MT-TG):m.10008A>G	rs1603222626
NC_012920.1(MT-TG):m.10013C>T	rs1603222627
NC_012920.1(MT-TG):m.10014G>A	rs1603222629
NC_012920.1(MT-TG):m.10015T>C	rs28374827
NC_012920.1(MT-TG):m.10018A>G	rs1556423757
NC_012920.1(MT-TG):m.10020T>C	rs1603222636
NC_012920.1(MT-TG):m.10027T>C	rs1603222638
NC_012920.1(MT-TG):m.10029A>G	rs1603222639
NC_012920.1(MT-TG):m.10031T>C	rs200048690
NC_012920.1(MT-TG):m.10034T>C	rs41347846
NC_012920.1(MT-TG):m.10040C>T	rs1603222642
NC_012920.1(MT-TG):m.10042A>G	rs1603222643
NC_012920.1(MT-TG):m.10043del	rs1603222645
NC_012920.1(MT-TG):m.10044A>G	rs41362547
NC_012920.1(MT-TG):m.10045T>C	rs1603222648
NC_012920.1(MT-TG):m.10046T>C	rs876661357
NC_012920.1(MT-TG):m.10048A>G	rs878957961
NC_012920.1(MT-TG):m.10055A>G	rs1603222653
NC_012920.1(MT-TG):m.9991A>G	rs1603222612
NC_012920.1(MT-TG):m.9993T>C	rs1603222613
NC_012920.1(MT-TG):m.9995T>C	rs1603222616
NC_012920.1(MT-TG):m.9996T>C	rs1556423755
NC_012920.1(MT-TG):m.9997T>A	rs121434475

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