List of variants in gene MT-TP studied for congenital myopathy

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: 19

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HGVS	dbSNP	gnomAD frequency
NC_012920.1(MT-TP):m.15965A>G	rs199474700
NC_012920.1(MT-TP):m.15967G>A	rs199474701
NC_012920.1(MT-TP):m.15968T>C	rs1603225617
NC_012920.1(MT-TP):m.15970T>C	rs375213730
NC_012920.1(MT-TP):m.15976T>C	rs1603225620
NC_012920.1(MT-TP):m.15977C>T	rs1556424716
NC_012920.1(MT-TP):m.15978C>T	rs201041059
NC_012920.1(MT-TP):m.15983T>C	rs1603225623
NC_012920.1(MT-TP):m.15984T>C	rs1603225624
NC_012920.1(MT-TP):m.15992A>T	rs1556424718
NC_012920.1(MT-TP):m.15994A>G	rs1603225627
NC_012920.1(MT-TP):m.15995G>A	rs1603225630
NC_012920.1(MT-TP):m.16002T>C	rs1603225633
NC_012920.1(MT-TP):m.16003T>C	rs1603225634
NC_012920.1(MT-TP):m.16011A>G	rs1603225635
NC_012920.1(MT-TP):m.16013A>G	rs1603225636
NC_012920.1(MT-TP):m.16017T>C	rs201864830
NC_012920.1(MT-TP):m.16018_16032dup	rs1603225639
NC_012920.1(MT-TP):m.16021C>T	rs1603225641

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