ClinVar Miner

List of variants in gene CACNB4 reported as uncertain significance for adolescent-onset epilepsy syndrome

Included ClinVar conditions (80):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 44
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HGVS dbSNP
NM_000726.4(CACNB4):c.*1501del rs886054963
NM_000726.4(CACNB4):c.*1501dup rs886054963
NM_000726.4(CACNB4):c.*151del rs79470866
NM_000726.4(CACNB4):c.*151dup rs79470866
NM_000726.4(CACNB4):c.*1520del rs374745796
NM_000726.4(CACNB4):c.*1635T>C rs886054962
NM_000726.4(CACNB4):c.*1785G>A rs886054961
NM_000726.4(CACNB4):c.*1811C>A rs886054960
NM_000726.4(CACNB4):c.*1826A>G rs886054959
NM_000726.4(CACNB4):c.*1931T>C rs886054958
NM_000726.4(CACNB4):c.*1937T>G rs758893086
NM_000726.4(CACNB4):c.*1952C>A rs764877003
NM_000726.4(CACNB4):c.*2542G>A rs886054957
NM_000726.4(CACNB4):c.*2924T>C rs886054956
NM_000726.4(CACNB4):c.*3387C>G rs886054955
NM_000726.4(CACNB4):c.*3688G>A rs886054954
NM_000726.4(CACNB4):c.*4081G>A rs148903851
NM_000726.4(CACNB4):c.*4145T>C rs781255950
NM_000726.4(CACNB4):c.*442_*443del rs886054966
NM_000726.4(CACNB4):c.*454del rs879114509
NM_000726.4(CACNB4):c.*454dup rs879114509
NM_000726.4(CACNB4):c.*4569A>G rs778742650
NM_000726.4(CACNB4):c.*4845T>C rs886054953
NM_000726.4(CACNB4):c.*4919G>A rs763593694
NM_000726.4(CACNB4):c.*5022A>G rs548177540
NM_000726.4(CACNB4):c.*5122C>T rs187940787
NM_000726.4(CACNB4):c.*5418T>C rs886054952
NM_000726.4(CACNB4):c.*5487T>C rs111700454
NM_000726.4(CACNB4):c.*5589+406dup rs886054949
NM_000726.4(CACNB4):c.*5863T>G rs886054951
NM_000726.4(CACNB4):c.*592T>C rs779110885
NM_000726.4(CACNB4):c.*5977G>T rs886054950
NM_000726.4(CACNB4):c.*624A>T rs755272601
NM_000726.4(CACNB4):c.*737C>T rs558590558
NM_000726.4(CACNB4):c.*795T>G rs766545084
NM_000726.4(CACNB4):c.-57G>T rs886054971
NM_000726.4(CACNB4):c.1278T>C (p.Tyr426=) rs376015337
NM_000726.4(CACNB4):c.187G>C (p.Asp63His) rs886054969
NM_000726.4(CACNB4):c.337G>T (p.Val113Phe) rs886054968
NM_000726.4(CACNB4):c.44C>G (p.Pro15Arg) rs200662010
NM_000726.4(CACNB4):c.5C>T (p.Ser2Phe) rs200092211
NM_000726.4(CACNB4):c.64-4C>T rs886054970
NM_000726.4(CACNB4):c.642T>C (p.Asp214=) rs886054967
NM_000726.4(CACNB4):c.91A>C (p.Ser31Arg) rs773391545

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