ClinVar Miner

List of variants reported as benign for 3-hydroxyacyl-CoA dehydrogenase deficiency

Included ClinVar conditions (7):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 48
Download table as spreadsheet
HGVS dbSNP
NM_000182.5(HADHA):c.*202G>A rs7260
NM_000182.5(HADHA):c.*302G>A rs1049987
NM_000182.5(HADHA):c.*331T>C
NM_000182.5(HADHA):c.*510A>T rs13432453
NM_000182.5(HADHA):c.*561C>T
NM_000182.5(HADHA):c.1072C>A (p.Gln358Lys) rs2229420
NM_000182.5(HADHA):c.1284C>T (p.Asn428=) rs199535840
NM_000182.5(HADHA):c.1392+10G>A rs60085478
NM_000182.5(HADHA):c.1620+11G>C rs112236946
NM_000182.5(HADHA):c.1690-6G>A rs111662358
NM_000182.5(HADHA):c.1843A>G (p.Asn615Asp) rs61731155
NM_000182.5(HADHA):c.1981C>T (p.Leu661=) rs142348718
NM_000182.5(HADHA):c.2060T>C (p.Met687Thr) rs149632783
NM_000182.5(HADHA):c.474C>T (p.Tyr158=) rs11552518
NM_000182.5(HADHA):c.573+8dup rs112196218
NM_000182.5(HADHA):c.68-10T>G rs144414842
NM_000183.3(HADHB):c.*136G>C rs1056471
NM_000183.3(HADHB):c.*196A>G rs7586822
NM_000183.3(HADHB):c.*351C>G rs7575987
NM_000183.3(HADHB):c.*486G>A rs7601689
NM_000183.3(HADHB):c.*52A>G rs183649494
NM_000183.3(HADHB):c.1014-14A>G rs17528590
NM_000183.3(HADHB):c.1149+4A>T rs2303893
NM_000183.3(HADHB):c.135G>A (p.Thr45=) rs574464531
NM_000183.3(HADHB):c.1371G>A (p.Ala457=) rs72851542
NM_000183.3(HADHB):c.246A>G (p.Ala82=) rs151302743
NM_000183.3(HADHB):c.5_7dup (p.Thr2dup) rs3839049
NM_000183.3(HADHB):c.780C>T (p.Leu260=) rs7607527
NM_000183.3(HADHB):c.812-5A>T rs72851534
NM_000183.3(HADHB):c.825T>C (p.Val275=) rs1056389
NM_000183.3(HADHB):c.830A>G (p.Lys277Arg) rs57969630
NM_000183.3(HADHB):c.891C>T (p.Ile297=) rs56902571
NM_000183.3(HADHB):c.900C>T (p.Tyr300=) rs144093705
NM_000183.3(HADHB):c.966G>A (p.Ala322=) rs7572240
NM_001184705.2(HADH):c.-102G>A rs182097151
NM_001184705.2(HADH):c.-193G>A rs10017687
NM_001184705.2(HADH):c.-65G>A rs28703310
NM_001184705.2(HADH):c.-71C>T rs760202
NM_001281512.1(HADHB):c.-201G>A rs3806516
NM_001331027.1(HADH):c.*818A>G rs17511319
NM_005327.5(HADH):c.*109T>A rs221347
NM_005327.5(HADH):c.-38T>C rs17550794
NM_005327.5(HADH):c.257= (p.Leu86=) rs4956145
NM_005327.5(HADH):c.636+13G>A rs17511214
NM_005327.5(HADH):c.662G>A (p.Arg221His) rs76476980
NM_005327.5(HADH):c.881A>G (p.Asn294Ser) rs36030668
NM_005327.7(HADH):c.*514A>G
NM_005327.7(HADH):c.133-15C>T

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.