List of variants in gene ACADVL reported as uncertain significance for not specified

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: 36

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HGVS	dbSNP	gnomAD frequency
NM_000018.4(ACADVL):c.1844G>A (p.Arg615Gln)	rs148584617	0.00244
NM_000018.4(ACADVL):c.818G>C (p.Gly273Ala)	rs150149784	0.00124
NM_000018.4(ACADVL):c.1567G>A (p.Gly523Arg)	rs139425622	0.00066
NM_000018.4(ACADVL):c.1591C>T (p.Arg531Trp)	rs146379816	0.00039
NM_000018.4(ACADVL):c.1894C>T (p.Arg632Cys)	rs151254520	0.00038
NM_000018.4(ACADVL):c.1273G>A (p.Ala425Thr)	rs138834083	0.00009
NM_000018.4(ACADVL):c.1733T>C (p.Met578Thr)	rs375806217	0.00009
NM_000018.4(ACADVL):c.1803G>A (p.Met601Ile)	rs201462718	0.00009
NM_000018.4(ACADVL):c.1434G>A (p.Met478Ile)	rs775537775	0.00006
NM_000018.4(ACADVL):c.760G>A (p.Gly254Ser)	rs765423779	0.00005
NM_000018.4(ACADVL):c.1931G>A (p.Arg644Gln)	rs774762384	0.00003
NM_000018.4(ACADVL):c.1024T>C (p.Phe342Leu)	rs1356652354	0.00002
NM_000018.4(ACADVL):c.709T>C (p.Cys237Arg)	rs1189763523	0.00002
NM_000018.4(ACADVL):c.1001T>G (p.Met334Arg)	rs398123079	0.00001
NM_000018.4(ACADVL):c.1052C>A (p.Thr351Asn)	rs796051911	0.00001
NM_000018.4(ACADVL):c.1064T>C (p.Ile355Thr)	rs1351976589	0.00001
NM_000018.4(ACADVL):c.1182+3G>T	rs376281637	0.00001
NM_000018.4(ACADVL):c.1375C>T (p.Arg459Trp)	rs766742117	0.00001
NM_000018.4(ACADVL):c.1540G>A (p.Gly514Arg)	rs370282954	0.00001
NM_000018.4(ACADVL):c.1552G>A (p.Gly518Ser)	rs374507980	0.00001
NM_000018.4(ACADVL):c.1678+4A>T	rs1057518417	0.00001
NM_000018.4(ACADVL):c.227G>A (p.Gly76Glu)	rs750043368	0.00001
NM_000018.4(ACADVL):c.628A>C (p.Thr210Pro)	rs775400380	0.00001
NM_000018.4(ACADVL):c.725C>T (p.Thr242Ile)	rs769631635	0.00001
NM_000018.4(ACADVL):c.853G>C (p.Glu285Gln)	rs202216257	0.00001
NM_000018.4(ACADVL):c.907A>G (p.Lys303Glu)	rs369149696	0.00001
NM_000018.4(ACADVL):c.950T>C (p.Val317Ala)	rs398123095	0.00001
NM_000018.4(ACADVL):c.1062CAT[1] (p.Ile356del)	rs754325237
NM_000018.4(ACADVL):c.1183-7A>G	rs750441118
NM_000018.4(ACADVL):c.215C>T (p.Ser72Phe)	rs1161495077
NM_000018.4(ACADVL):c.495G>T (p.Glu165Asp)	rs370169077
NM_000018.4(ACADVL):c.513C>G (p.Asp171Glu)	rs2071227581
NM_000018.4(ACADVL):c.535G>T (p.Gly179Trp)	rs796051909
NM_000018.4(ACADVL):c.736A>G (p.Ser246Gly)	rs1555528320
NM_000018.4(ACADVL):c.753-11T>G	rs1555528341
NM_000018.4(ACADVL):c.756T>A (p.Asn252Lys)	rs143233413

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