List of variants in gene ACAD9 reported as likely pathogenic for Mitochondrial complex I deficiency

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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: 7

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HGVS	dbSNP	gnomAD frequency
NM_014049.5(ACAD9):c.796C>T (p.Arg266Trp)	rs753711253	0.00002
NM_014049.5(ACAD9):c.1029+1dup	rs2107657797
NM_014049.5(ACAD9):c.1240C>A (p.Arg414Ser)	rs777282696
NM_014049.5(ACAD9):c.1249C>T (p.Arg417Cys)	rs368949613
NM_014049.5(ACAD9):c.151-1_151del	rs766026673
NM_014049.5(ACAD9):c.293T>C (p.Leu98Ser)
NM_014049.5(ACAD9):c.634-1G>A

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