List of variants in gene TSFM reported as likely benign for combined oxidative phosphorylation deficiency

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

Total variants: 10

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HGVS	dbSNP	gnomAD frequency
NM_005726.6(TSFM):c.232-19T>G	rs112348190	0.00291
NM_005726.6(TSFM):c.69T>A (p.Leu23=)	rs147317818	0.00086
NM_005726.6(TSFM):c.539G>C (p.Gly180Ala)	rs138534976	0.00045
NM_005726.6(TSFM):c.726G>A (p.Thr242=)	rs140461538	0.00019
NM_005726.6(TSFM):c.644C>T (p.Ser215Phe)	rs376562033	0.00011
NM_005726.6(TSFM):c.885C>T (p.Thr295=)	rs750718644	0.00004
NM_005726.6(TSFM):c.10C>T (p.Leu4=)	rs765871977	0.00003
NM_005726.6(TSFM):c.816C>T (p.Asp272=)	rs183575246	0.00003
NM_005726.6(TSFM):c.271T>G (p.Trp91Gly)	rs542571914	0.00001
NM_005726.6(TSFM):c.408G>A (p.Leu136=)	rs144109380

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