List of variants reported as uncertain significance for combined oxidative phosphorylation deficiency by Genome-Nilou Lab

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Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_024996.7(GFM1):c.1383C>T (p.Asn461=)	rs774976760	0.00004
NM_024996.7(GFM1):c.344A>G (p.Asn115Ser)	rs779253646	0.00002
NM_005726.6(TSFM):c.231+1GT[6]	rs762424912
NM_005726.6(TSFM):c.830del (p.Gly277fs)	rs1190369642
NM_024996.7(GFM1):c.1384G>T (p.Asp462Tyr)	rs200244667

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