"PreventionGenetics, part of Exact Sciences"[submitter] AND "SLC25A26" - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3045209	NM_001379210.1(SLC25A26):c.42G>A (p.Gly14=)	SLC25A26	Single nucleotide variant (synonymous variant +3 more)	SLC25A26-related disorder	GLikely benign
Select item 1317386	NM_001379210.1(SLC25A26):c.45A>G (p.Val15=)	SLC25A26	Single nucleotide variant (5 prime UTR variant +2 more)	SLC25A26-related disorder +1 more	GLikely benign
Select item 683883	NM_001379210.1(SLC25A26):c.122G>A (p.Ser41Asn)	SLC25A26 (S41N)	Single nucleotide variant (5 prime UTR variant +2 more)	Combined oxidative phosphorylation deficiency 28 +2 more	GBenign
Select item 3054590	NM_001379210.1(SLC25A26):c.156C>T (p.Gly52=)	SLC25A26	Single nucleotide variant (synonymous variant +3 more)	SLC25A26-related disorder	GLikely benign
Select item 672596	NM_001379210.1(SLC25A26):c.252A>G (p.Ser84=)	SLC25A26	Single nucleotide variant (5 prime UTR variant +2 more)	SLC25A26-related disorder +1 more	GBenign
Select item 2175441	NM_001379210.1(SLC25A26):c.568+6A>C	SLC25A26	Single nucleotide variant (intron variant)	not provided +1 more	GConflicting classifications of pathogenicity

ClinVar