ClinVar Miner

List of variants in gene MAFB studied for abdominal and pelvic region disorder

Included ClinVar conditions (891):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 56
Download table as spreadsheet
HGVS dbSNP
NM_005461.4(MAFB):c.*1019A>G rs545693248
NM_005461.4(MAFB):c.*1210G>A rs542788257
NM_005461.4(MAFB):c.*1212_*1213insGAGGA rs886056663
NM_005461.4(MAFB):c.*1226C>T rs886056662
NM_005461.4(MAFB):c.*1255C>T rs573637366
NM_005461.4(MAFB):c.*1314A>G rs533750110
NM_005461.4(MAFB):c.*1433A>G rs886056661
NM_005461.4(MAFB):c.*1519C>G rs185930615
NM_005461.4(MAFB):c.*1520C>G rs148352161
NM_005461.4(MAFB):c.*152G>C rs553723079
NM_005461.4(MAFB):c.*1551G>A rs886056660
NM_005461.4(MAFB):c.*155C>T rs533850442
NM_005461.4(MAFB):c.*1591T>C rs886056659
NM_005461.4(MAFB):c.*1592delT rs3215567
NM_005461.4(MAFB):c.*1592dupT rs3215567
NM_005461.4(MAFB):c.*1679C>T rs886056657
NM_005461.4(MAFB):c.*1737A>G rs532037681
NM_005461.4(MAFB):c.*1751C>T rs886056656
NM_005461.4(MAFB):c.*1787T>C rs749002713
NM_005461.4(MAFB):c.*1803C>T rs779945829
NM_005461.4(MAFB):c.*1849C>T rs3577
NM_005461.4(MAFB):c.*2008T>A rs56049320
NM_005461.4(MAFB):c.*209A>C rs886056672
NM_005461.4(MAFB):c.*229A>G rs886056671
NM_005461.4(MAFB):c.*309A>T rs886056670
NM_005461.4(MAFB):c.*30C>A rs780982442
NM_005461.4(MAFB):c.*377G>C rs886056669
NM_005461.4(MAFB):c.*410G>A rs886056668
NM_005461.4(MAFB):c.*507_*510delTGTC rs201579991
NM_005461.4(MAFB):c.*64C>T rs886056673
NM_005461.4(MAFB):c.*68G>A rs190300765
NM_005461.4(MAFB):c.*795G>T rs886056667
NM_005461.4(MAFB):c.*881G>T rs886056666
NM_005461.4(MAFB):c.*929delA rs11482617
NM_005461.4(MAFB):c.*929dupA rs11482617
NM_005461.4(MAFB):c.*976G>A rs886056664
NM_005461.4(MAFB):c.-138G>T rs755784104
NM_005461.4(MAFB):c.-171C>A rs886056676
NM_005461.4(MAFB):c.-204_-203delTG rs201369817
NM_005461.4(MAFB):c.-206T>G rs527524576
NM_005461.4(MAFB):c.-229C>T rs886056677
NM_005461.4(MAFB):c.-310G>A rs567415398
NM_005461.4(MAFB):c.-338A>G rs886056678
NM_005461.4(MAFB):c.-75C>G rs574807151
NM_005461.4(MAFB):c.-77C>G rs886056675
NM_005461.4(MAFB):c.161C>T (p.Ser54Leu) rs730880014
NM_005461.4(MAFB):c.184A>C (p.Thr62Pro) rs387907004
NM_005461.4(MAFB):c.189G>A (p.Pro63=) rs201590858
NM_005461.4(MAFB):c.208T>G (p.Ser70Ala) rs387907005
NM_005461.4(MAFB):c.209C>T (p.Ser70Leu) rs387907006
NM_005461.4(MAFB):c.211C>T (p.Pro71Ser) rs387907007
NM_005461.4(MAFB):c.212C>T (p.Pro71Leu) rs387907008
NM_005461.4(MAFB):c.253C>A (p.Leu85Met) rs377639854
NM_005461.4(MAFB):c.399C>T (p.His133=) rs762729675
NM_005461.4(MAFB):c.525C>G (p.Ser175Arg) rs886056674
NM_005461.4(MAFB):c.745C>A (p.Arg249=) rs561320614

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.