List of variants reported as uncertain significance for Fatal mitochondrial disease due to combined oxidative phosphorylation defect type 3 by Natera, Inc.

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Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_005726.6(TSFM):c.814G>C (p.Asp272His)	rs138911653	0.00030
NM_005726.6(TSFM):c.644C>T (p.Ser215Phe)	rs376562033	0.00011
NM_005726.6(TSFM):c.269G>A (p.Gly90Asp)	rs371076990	0.00004
NM_005726.6(TSFM):c.484-10G>A	rs374795252	0.00001
NM_005726.6(TSFM):c.12G>T (p.Leu4=)	rs773572404

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