List of variants in gene ACADVL reported as likely pathogenic by Women's Health and Genetics/Laboratory Corporation of America, LabCorp

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: 17

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HGVS	dbSNP	gnomAD frequency
NM_000018.4(ACADVL):c.1220G>C (p.Gly407Ala)	rs904631654	0.00011
NM_000018.4(ACADVL):c.520G>A (p.Val174Met)	rs369560930	0.00009
NM_000018.4(ACADVL):c.1076C>T (p.Ala359Val)	rs539029862	0.00003
NM_000018.4(ACADVL):c.1096C>T (p.Arg366Cys)	rs771874163	0.00003
NM_000018.4(ACADVL):c.1748C>G (p.Ser583Trp)	rs1085307648	0.00003
NM_000018.4(ACADVL):c.1077+1G>T	rs140989450	0.00001
NM_000018.4(ACADVL):c.1217A>C (p.Gln406Pro)	rs1384021857	0.00001
NM_000018.4(ACADVL):c.538G>A (p.Ala180Thr)	rs727503791	0.00001
NM_000018.4(ACADVL):c.1077_1077+1delinsCAC	rs1057516686
NM_000018.4(ACADVL):c.1113del (p.Ile373fs)	rs1057517416
NM_000018.4(ACADVL):c.1730_1733dup (p.Met578fs)	rs2071395559
NM_000018.4(ACADVL):c.1882del (p.Gln628fs)	rs1597541142
NM_000018.4(ACADVL):c.1908dup (p.Ile637fs)	rs1555529204
NM_000018.4(ACADVL):c.335del (p.Phe112fs)	rs764028320
NM_000018.4(ACADVL):c.605T>A (p.Leu202His)	rs398123090
NM_000018.4(ACADVL):c.708_709del (p.Cys237fs)	rs1555528304
NM_000018.4(ACADVL):c.932del (p.Phe311fs)	rs764488310

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