List of variants reported as uncertain significance for Mitochondrial hypertrophic cardiomyopathy with lactic acidosis due to MTO1 deficiency by Baylor Genetics

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Total variants: 9

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HGVS	dbSNP	gnomAD frequency
NM_012123.4(MTO1):c.1222A>G (p.Ile408Val)	rs149407452	0.00004
NM_012123.4(MTO1):c.82G>A (p.Asp28Asn)	rs780242649	0.00001
NM_012123.4(MTO1):c.*7A>G
NM_012123.4(MTO1):c.-4C>T
NM_012123.4(MTO1):c.1391G>T (p.Arg464Leu)	rs141970072
NM_012123.4(MTO1):c.1393A>G (p.Met465Val)	rs1000432861
NM_012123.4(MTO1):c.1637G>C (p.Arg546Thr)
NM_012123.4(MTO1):c.79A>T (p.Ser27Cys)	rs1240435216
NM_012123.4(MTO1):c.982C>T (p.Arg328Cys)

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