List of variants in gene MT-TW studied for hereditary skeletal muscle disorder

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: 33

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HGVS	dbSNP	gnomAD frequency
NC_012920.1(MT-TW):m.5514A>G	rs1603219997
NC_012920.1(MT-TW):m.5515A>G	rs1603220000
NC_012920.1(MT-TW):m.5516A>G	rs1603220001
NC_012920.1(MT-TW):m.5521G>A	rs199474673
NC_012920.1(MT-TW):m.5524T>C	rs1603220004
NC_012920.1(MT-TW):m.5527A>G	rs1603220005
NC_012920.1(MT-TW):m.5528T>C	rs1556423004
NC_012920.1(MT-TW):m.5530C>T	rs1603220009
NC_012920.1(MT-TW):m.5532G>A	rs199474674
NC_012920.1(MT-TW):m.5536_5537insT	rs1603220010
NC_012920.1(MT-TW):m.5538G>A	rs1603220012
NC_012920.1(MT-TW):m.5539A>G	rs1603220013
NC_012920.1(MT-TW):m.5539A>T	rs1603220013
NC_012920.1(MT-TW):m.5540G>A	rs1603220014
NC_012920.1(MT-TW):m.5542C>T	rs1603220015
NC_012920.1(MT-TW):m.5543T>C	rs1603220016
NC_012920.1(MT-TW):m.5544T>C	rs1603220018
NC_012920.1(MT-TW):m.5550C>T	rs1603220019
NC_012920.1(MT-TW):m.5553T>C	rs878853053
NC_012920.1(MT-TW):m.5553T>G	rs878853053
NC_012920.1(MT-TW):m.5554C>A	rs1603220020
NC_012920.1(MT-TW):m.5557T>C	rs1603220022
NC_012920.1(MT-TW):m.5558A>G	rs370471013
NC_012920.1(MT-TW):m.5559A>G	rs1556423008
NC_012920.1(MT-TW):m.5560G>A	rs1603220026
NC_012920.1(MT-TW):m.5561T>C	rs1556423009
NC_012920.1(MT-TW):m.5563G>A	rs1603220027
NC_012920.1(MT-TW):m.5566A>G	rs1603220029
NC_012920.1(MT-TW):m.5567T>C	rs1603220030
NC_012920.1(MT-TW):m.5568A>G	rs200719361
NC_012920.1(MT-TW):m.5573A>G	rs1603220033
NC_012920.1(MT-TW):m.5575T>C	rs1603220034
m.5556G>A	rs387906736

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