List of variants in gene ACADS reported as likely benign 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
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 9

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HGVS	dbSNP	gnomAD frequency
NM_000017.4(ACADS):c.522C>T (p.Gly174=)	rs143925225	0.00169
NM_000017.4(ACADS):c.654A>C (p.Pro218=)	rs149430391	0.00075
NM_000017.4(ACADS):c.327C>T (p.Cys109=)	rs144083614	0.00007
NM_000017.4(ACADS):c.147C>G (p.Ala49=)	rs202193021	0.00004
NM_000017.4(ACADS):c.900C>T (p.Phe300=)	rs150980955	0.00003
NM_000017.4(ACADS):c.228G>A (p.Gly76=)
NM_000017.4(ACADS):c.249C>T (p.Asp83=)
NM_000017.4(ACADS):c.267C>T (p.Gly89=)
NM_000017.4(ACADS):c.286C>T (p.Leu96=)

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