List of variants reported as benign for Mitochondrial hypertrophic cardiomyopathy with lactic acidosis due to MTO1 deficiency by Labcorp Genetics (formerly Invitae), Labcorp

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Total variants: 11

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HGVS	dbSNP	gnomAD frequency
NM_012123.4(MTO1):c.1180T>C (p.Leu394=)	rs2036039	0.20359
NM_012123.4(MTO1):c.1918-7T>G	rs73452515	0.04248
NM_012123.4(MTO1):c.1894C>T (p.Leu632=)	rs117757245	0.00506
NM_012123.4(MTO1):c.1368T>C (p.Thr456=)	rs115654622	0.00454
NM_012123.4(MTO1):c.1086C>G (p.Ile362Met)	rs147329295	0.00309
NM_012123.4(MTO1):c.176G>C (p.Gly59Ala)	rs201279883	0.00085
NM_012123.4(MTO1):c.1637+16A>G	rs201990339	0.00034
NM_012123.4(MTO1):c.1059A>G (p.Leu353=)	rs201656868
NM_012123.4(MTO1):c.1785A>G (p.Gln595=)	rs147990749
NM_012123.4(MTO1):c.1917+17_1917+19del	rs760158320
NM_012123.4(MTO1):c.938+7=	rs7766570

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