ClinVar Miner

List of variants in gene CACNB4 reported as likely benign for adolescent-onset epilepsy syndrome

Included ClinVar conditions (80):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 49
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HGVS dbSNP
NM_000726.4(CACNB4):c.*1009C>T rs367723727
NM_000726.4(CACNB4):c.*1093T>C rs142139235
NM_000726.4(CACNB4):c.*1110C>A rs147608603
NM_000726.4(CACNB4):c.*1284T>G rs112989362
NM_000726.4(CACNB4):c.*1459T>C rs114958916
NM_000726.4(CACNB4):c.*1656T>C rs62174451
NM_000726.4(CACNB4):c.*1814G>A rs181447432
NM_000726.4(CACNB4):c.*1909C>T rs113319414
NM_000726.4(CACNB4):c.*1910_*1911del rs372743707
NM_000726.4(CACNB4):c.*1942T>C rs139629003
NM_000726.4(CACNB4):c.*2163G>A rs80306085
NM_000726.4(CACNB4):c.*2188T>G rs548234328
NM_000726.4(CACNB4):c.*2210A>G rs114341631
NM_000726.4(CACNB4):c.*2391T>G rs143821304
NM_000726.4(CACNB4):c.*2695G>T rs74894311
NM_000726.4(CACNB4):c.*2729G>A rs144329745
NM_000726.4(CACNB4):c.*2778A>C rs114659375
NM_000726.4(CACNB4):c.*2837A>G rs138327808
NM_000726.4(CACNB4):c.*2885T>C rs116457978
NM_000726.4(CACNB4):c.*3475A>T rs567549082
NM_000726.4(CACNB4):c.*3668T>C rs543493236
NM_000726.4(CACNB4):c.*4131A>G rs373381936
NM_000726.4(CACNB4):c.*443A>G rs538829019
NM_000726.4(CACNB4):c.*4570T>C rs549017506
NM_000726.4(CACNB4):c.*4771G>A rs80248494
NM_000726.4(CACNB4):c.*4773A>G rs113408437
NM_000726.4(CACNB4):c.*4969G>A rs537140595
NM_000726.4(CACNB4):c.*4976T>C rs191424720
NM_000726.4(CACNB4):c.*4T>C rs556761275
NM_000726.4(CACNB4):c.*528A>T rs111999910
NM_000726.4(CACNB4):c.*5372T>C rs150406641
NM_000726.4(CACNB4):c.*5433A>G rs563567053
NM_000726.4(CACNB4):c.*5562A>G rs192309143
NM_000726.4(CACNB4):c.*5622C>T rs187012852
NM_000726.4(CACNB4):c.*5855A>C rs118093432
NM_000726.4(CACNB4):c.*6140G>T rs74944346
NM_000726.4(CACNB4):c.*6183A>G rs185830609
NM_000726.4(CACNB4):c.*787del rs560958457
NM_000726.4(CACNB4):c.*865G>A rs75365487
NM_000726.4(CACNB4):c.-70G>A rs183873853
NM_000726.4(CACNB4):c.1303-3T>C rs143442080
NM_000726.4(CACNB4):c.1413G>A (p.Arg471=) rs1805029
NM_000726.4(CACNB4):c.177G>A (p.Pro59=) rs552093496
NM_000726.4(CACNB4):c.311G>T (p.Cys104Phe) rs1805031
NM_000726.4(CACNB4):c.44C>G (p.Pro15Arg) rs200662010
NM_000726.4(CACNB4):c.521+9C>T rs747291810
NM_000726.4(CACNB4):c.599-15G>A rs41270209
NM_000726.4(CACNB4):c.5C>T (p.Ser2Phe) rs200092211
NM_000726.4(CACNB4):c.8C>T (p.Ser3Phe) rs542973906

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