List of variants in gene ACADVL reported as uncertain significance by Counsyl

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: 46

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HGVS	dbSNP	gnomAD frequency
NM_000018.4(ACADVL):c.1828-4C>G	rs184559206	0.00192
NM_000018.4(ACADVL):c.1678+23C>T	rs147546456	0.00163
NM_000018.4(ACADVL):c.1894C>T (p.Arg632Cys)	rs151254520	0.00038
NM_000018.4(ACADVL):c.1533-4T>A	rs369986567	0.00026
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.205-8C>G	rs774353448	0.00007
NM_000018.4(ACADVL):c.1153C>T (p.Arg385Trp)	rs745832866	0.00004
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.1077G>A (p.Ala359=)	rs779458466	0.00002
NM_000018.4(ACADVL):c.1183-15A>G	rs765390290	0.00001
NM_000018.4(ACADVL):c.1198G>A (p.Val400Met)	rs149116708	0.00001
NM_000018.4(ACADVL):c.1360G>A (p.Asp454Asn)	rs1419606204	0.00001
NM_000018.4(ACADVL):c.1825G>A (p.Glu609Lys)	rs398123086	0.00001
NM_000018.4(ACADVL):c.227G>A (p.Gly76Glu)	rs750043368	0.00001
NM_000018.4(ACADVL):c.278-8C>T	rs1178133251	0.00001
NM_000018.4(ACADVL):c.538G>A (p.Ala180Thr)	rs727503791	0.00001
NM_000018.4(ACADVL):c.881G>A (p.Gly294Glu)	rs200573371	0.00001
NM_000018.4(ACADVL):c.1009_1011del (p.Leu337del)	rs1315330884
NM_000018.4(ACADVL):c.1019G>T (p.Gly340Val)	rs934797393
NM_000018.4(ACADVL):c.1062CAT[1] (p.Ile356del)	rs754325237
NM_000018.4(ACADVL):c.1183-2dup	rs1555528721
NM_000018.4(ACADVL):c.1328T>G (p.Met443Arg)	rs886043236
NM_000018.4(ACADVL):c.139-3C>T	rs1555527630
NM_000018.4(ACADVL):c.1430G>A (p.Cys477Tyr)	rs1555528803
NM_000018.4(ACADVL):c.1532G>C (p.Arg511Pro)	rs200771970
NM_000018.4(ACADVL):c.1617T>C (p.Ala539=)	rs1555528948
NM_000018.4(ACADVL):c.1679-5del	rs1555528999
NM_000018.4(ACADVL):c.1864C>T (p.Gln622Ter)	rs1555529172
NM_000018.4(ACADVL):c.1923G>C (p.Leu641Phe)	rs1452402269
NM_000018.4(ACADVL):c.204+5G>A	rs958328801
NM_000018.4(ACADVL):c.205-5C>G	rs768537914
NM_000018.4(ACADVL):c.230T>C (p.Met77Thr)	rs1555527718
NM_000018.4(ACADVL):c.331_339del (p.Arg111_Phe113del)	rs1555527820
NM_000018.4(ACADVL):c.439C>T (p.Pro147Ser)	rs1032857886
NM_000018.4(ACADVL):c.482C>T (p.Ala161Val)	rs796051908
NM_000018.4(ACADVL):c.535G>T (p.Gly179Trp)	rs796051909
NM_000018.4(ACADVL):c.578G>A (p.Gly193Asp)	rs1220348903
NM_000018.4(ACADVL):c.619T>C (p.Ser207Pro)	rs768975918
NM_000018.4(ACADVL):c.62+6T>C	rs1555527495
NM_000018.4(ACADVL):c.640T>G (p.Phe214Val)	rs1192969297
NM_000018.4(ACADVL):c.739A>G (p.Lys247Glu)	rs387906253
NM_000018.4(ACADVL):c.759_761del (p.Gly254del)	rs1555528346
NM_000018.4(ACADVL):c.898A>G (p.Met300Val)	rs1026112888
NM_000018.4(ACADVL):c.944T>G (p.Val315Gly)	rs1555528469

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