C1838979[trait identifier] AND "Computational Biology Unit, University - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 446175	NM_012140.5(SLC25A10):c.304A>T (p.Lys102Ter)	SLC25A10 (K102*)	Single nucleotide variant (nonsense)	Mitochondrial complex I deficiency +1 more	GLikely pathogenic
Select item 446176	NM_001270888.1(SLC25A10):c.[684C>T;790-37G>A]	SLC25A10 (P192S)	Single nucleotide variant (synonymous variant +2 more)	Mitochondrial complex I deficiency	GLikely pathogenic