List of variants in gene ACAD9 reported by CeGaT Center for Human Genetics Tuebingen

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 15

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HGVS	dbSNP	gnomAD frequency
NM_014049.5(ACAD9):c.150+87C>T	rs111805092	0.00832
NM_014049.5(ACAD9):c.988A>C (p.Lys330Gln)	rs79530903	0.00107
NM_014049.5(ACAD9):c.453+8A>G	rs199919500	0.00092
NM_014049.5(ACAD9):c.1405C>T (p.Arg469Trp)	rs139145143	0.00042
NM_014049.5(ACAD9):c.1258C>T (p.Arg420Cys)	rs202147766	0.00004
NM_014049.5(ACAD9):c.1317G>A (p.Thr439=)	rs967028824	0.00004
NM_014049.5(ACAD9):c.728C>G (p.Thr243Arg)	rs368222811	0.00003
NM_014049.5(ACAD9):c.75G>T (p.Ala25=)	rs564435799	0.00003
NM_014049.5(ACAD9):c.452A>G (p.Lys151Arg)	rs774429198	0.00002
NM_014049.5(ACAD9):c.796C>T (p.Arg266Trp)	rs753711253	0.00002
NM_014049.5(ACAD9):c.569C>T (p.Ala190Val)	rs548599849	0.00001
NM_014049.5(ACAD9):c.206A>G (p.Gln69Arg)
NM_014049.5(ACAD9):c.423C>T (p.Thr141=)
NM_014049.5(ACAD9):c.665T>C (p.Ile222Thr)	rs863223874
NM_014049.5(ACAD9):c.775C>T (p.Pro259Ser)	rs2107653892

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