ClinVar Miner

List of variants in gene ACOX1 reported as benign for central nervous system disorder

Included ClinVar conditions (2498):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 42
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HGVS dbSNP gnomAD frequency
NM_004035.7(ACOX1):c.936C>G (p.Ile312Met) rs1135640 0.53769
NM_004035.7(ACOX1):c.658+45A>G rs10852766 0.53593
NM_004035.7(ACOX1):c.*679T>C rs3682 0.48163
NM_004035.7(ACOX1):c.1936-100C>T rs2666003 0.46197
NM_004035.7(ACOX1):c.*3872G>A rs2608880 0.46181
NM_004035.7(ACOX1):c.1729-58A>C rs2666005 0.24335
NM_004035.7(ACOX1):c.*5164A>G rs3643 0.21826
NM_004035.7(ACOX1):c.*4490A>G rs7212287 0.12568
NM_004035.7(ACOX1):c.1729-31T>G rs12051891 0.12344
NM_004035.7(ACOX1):c.*4444G>A rs7207656 0.12341
NM_004035.7(ACOX1):c.*874C>T rs12430 0.11066
NM_004035.7(ACOX1):c.1320T>C (p.Asp440=) rs8065946 0.06791
NM_004035.7(ACOX1):c.*2771A>C rs9915973 0.06790
NM_004035.7(ACOX1):c.*633G>C rs71382188 0.05233
NM_004035.7(ACOX1):c.*5124A>G rs73355712 0.03353
NM_004035.7(ACOX1):c.*4296C>A rs79900384 0.03254
NM_004035.7(ACOX1):c.110-20G>T rs9914319 0.01969
NM_004035.7(ACOX1):c.*3943C>T rs16968333 0.01823
NM_004035.7(ACOX1):c.*474G>A rs115919790 0.01800
NM_004035.7(ACOX1):c.591G>A (p.Gly197=) rs75808808 0.01720
NM_004035.7(ACOX1):c.1771C>T (p.Arg591Cys) rs35629489 0.00908
NM_004035.7(ACOX1):c.921G>A (p.Arg307=) rs79677613 0.00869
NM_004035.7(ACOX1):c.*654A>G rs1057921 0.00854
NM_004035.7(ACOX1):c.*4585C>T rs145992742 0.00708
NM_004035.7(ACOX1):c.1520T>C (p.Ile507Thr) rs77139740 0.00707
NM_004035.7(ACOX1):c.*1977C>T rs141097660 0.00683
NM_004035.7(ACOX1):c.80C>T (p.Pro27Leu) rs145082938 0.00672
NM_004035.7(ACOX1):c.1794G>T (p.Leu598=) rs79605652 0.00571
NM_004035.7(ACOX1):c.*2977C>T rs73997670 0.00432
NM_004035.7(ACOX1):c.1302C>T (p.Phe434=) rs144742319 0.00404
NM_004035.7(ACOX1):c.954A>G (p.Glu318=) rs16968343 0.00404
NM_004035.7(ACOX1):c.804G>A (p.Pro268=) rs114057990 0.00205
NM_004035.7(ACOX1):c.1368C>T (p.Asn456=) rs151255626 0.00147
NM_004035.7(ACOX1):c.1478+13T>C rs199908120 0.00059
NM_004035.7(ACOX1):c.*3228T>G rs142553986 0.00049
NM_004035.7(ACOX1):c.1695T>C (p.Tyr565=) rs774049893 0.00014
NM_004035.7(ACOX1):c.1584+11G>A rs185329691 0.00012
NM_004035.7(ACOX1):c.1068C>T (p.Asn356=) rs374533122 0.00003
NM_004035.7(ACOX1):c.867T>C (p.Ala289=) rs370001667 0.00002
NM_004035.7(ACOX1):c.945-14del
NM_004035.7(ACOX1):c.945-20del
NM_004035.7(ACOX1):c.945-20dup

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