List of variants reported as pathogenic for combined oxidative phosphorylation deficiency 28 by OMIM

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_001379210.1(SLC25A26):c.305C>T (p.Ala102Val)	rs869025314	0.00001
NM_001379210.1(SLC25A26):c.33+1G>A	rs781798317	0.00001
NM_001379210.1(SLC25A26):c.443T>G (p.Val148Gly)	rs869025313
NM_001379210.1(SLC25A26):c.596C>T (p.Pro199Leu)	rs869025315

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