List of variants in gene MT-CO1 reported as benign for Leigh syndrome

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 47

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HGVS	dbSNP	gnomAD frequency
NC_012920.1(MT-CO1):m.5910G>A	rs1603220177
NC_012920.1(MT-CO1):m.5911C>T	rs879227822
NC_012920.1(MT-CO1):m.5913G>A	rs201617272
NC_012920.1(MT-CO1):m.5973G>A	rs1556423059
NC_012920.1(MT-CO1):m.5979G>A	rs1556423060
NC_012920.1(MT-CO1):m.5985G>A	rs386828982
NC_012920.1(MT-CO1):m.6018G>A	rs1603220225
NC_012920.1(MT-CO1):m.6040A>G	rs1556423072
NC_012920.1(MT-CO1):m.6150G>A	rs879053914
NC_012920.1(MT-CO1):m.6228C>T	rs1603220332
NC_012920.1(MT-CO1):m.6237C>A	rs1603220344
NC_012920.1(MT-CO1):m.6249G>A	rs1556423095
NC_012920.1(MT-CO1):m.6253T>C	rs200165736
NC_012920.1(MT-CO1):m.6261G>A	rs201262114
NC_012920.1(MT-CO1):m.6267G>A	rs202216551
NC_012920.1(MT-CO1):m.6285G>A	rs878947044
NC_012920.1(MT-CO1):m.6340C>T	rs1603220429
NC_012920.1(MT-CO1):m.6345T>C	rs1556423121
NC_012920.1(MT-CO1):m.6366G>A	rs370673798
NC_012920.1(MT-CO1):m.6366G>C	rs370673798
NC_012920.1(MT-CO1):m.6456G>A	rs1603220483
NC_012920.1(MT-CO1):m.6465G>A	rs28414181
NC_012920.1(MT-CO1):m.6546C>T	rs1603220531
NC_012920.1(MT-CO1):m.6570G>T	rs386828988
NC_012920.1(MT-CO1):m.6663A>G	rs200784106
NC_012920.1(MT-CO1):m.6723G>A	rs1603220595
NC_012920.1(MT-CO1):m.6852G>A	rs1603220651
NC_012920.1(MT-CO1):m.6891A>G	rs879091068
NC_012920.1(MT-CO1):m.6915G>A	rs1603220687
NC_012920.1(MT-CO1):m.7080T>C	rs1556423226
NC_012920.1(MT-CO1):m.7119G>A	rs1556423235
NC_012920.1(MT-CO1):m.7146A>G	rs372136420
NC_012920.1(MT-CO1):m.7150T>C	rs1603220803
NC_012920.1(MT-CO1):m.7158A>G	rs878887002
NC_012920.1(MT-CO1):m.7245A>G	rs1556423253
NC_012920.1(MT-CO1):m.7257A>G	rs1603220854
NC_012920.1(MT-CO1):m.7258T>C	rs1556423260
NC_012920.1(MT-CO1):m.7269G>A	rs386829004
NC_012920.1(MT-CO1):m.7270T>C	rs879002867
NC_012920.1(MT-CO1):m.7278T>C	rs1556423264
NC_012920.1(MT-CO1):m.7299A>G	rs879071265
NC_012920.1(MT-CO1):m.7309T>C	rs1556423267
NC_012920.1(MT-CO1):m.7356G>A	rs1556423271
NC_012920.1(MT-CO1):m.7389T>C	rs9783095
NC_012920.1(MT-CO1):m.7419G>A	rs1603220951
m.6480G>A	rs199476128
m.6489C>A	rs28461189

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