List of variants in gene MT-TK 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: 29

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HGVS	dbSNP	gnomAD frequency
NC_012920.1(MT-TK):m.8296A>G	rs118192102
NC_012920.1(MT-TK):m.8298T>C	rs1603221389
NC_012920.1(MT-TK):m.8299G>A	rs1603221391
NC_012920.1(MT-TK):m.8300T>C	rs1603221393
NC_012920.1(MT-TK):m.8301A>G	rs1603221396
NC_012920.1(MT-TK):m.8308A>G	rs879081228
NC_012920.1(MT-TK):m.8311T>A	rs371589230
NC_012920.1(MT-TK):m.8311T>C	rs371589230
NC_012920.1(MT-TK):m.8315A>G	rs1603221400
NC_012920.1(MT-TK):m.8316T>C	rs2521961625
NC_012920.1(MT-TK):m.8319A>G	rs1603221401
NC_012920.1(MT-TK):m.8331A>G	rs1603221403
NC_012920.1(MT-TK):m.8337T>C	rs1603221405
NC_012920.1(MT-TK):m.8338A>G	rs1603221407
NC_012920.1(MT-TK):m.8340_8341insT	rs1603221409
NC_012920.1(MT-TK):m.8343A>G	rs1603221411
NC_012920.1(MT-TK):m.8344A>G	rs118192098
NC_012920.1(MT-TK):m.8345C>T	rs1603221413
NC_012920.1(MT-TK):m.8346C>A	rs1603221415
NC_012920.1(MT-TK):m.8347A>G	rs1603221417
NC_012920.1(MT-TK):m.8348A>G	rs1556423430
NC_012920.1(MT-TK):m.8349C>T	rs1603221418
NC_012920.1(MT-TK):m.8350A>G	rs1603221419
NC_012920.1(MT-TK):m.8356T>C	rs118192099
NC_012920.1(MT-TK):m.8358A>G	rs1603221421
NC_012920.1(MT-TK):m.8360A>G	rs1603221422
NC_012920.1(MT-TK):m.8362T>G	rs1603221423
NC_012920.1(MT-TK):m.8363G>A	rs118192100
NC_012920.1(MT-TK):m.8364A>T	rs1603221428

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