ClinVar Miner

List of variants in gene CACNB4 reported as 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: 13
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HGVS dbSNP
NM_000726.4(CACNB4):c.*1185T>C rs13410490
NM_000726.4(CACNB4):c.*1186G>T rs72868010
NM_000726.4(CACNB4):c.*2188del rs75297236
NM_000726.4(CACNB4):c.*3157T>A rs10497086
NM_000726.4(CACNB4):c.*3804G>C rs2344734
NM_000726.4(CACNB4):c.*442G>A rs7597215
NM_000726.4(CACNB4):c.*5029T>C rs16830412
NM_000726.4(CACNB4):c.*5385C>T rs1568673
NM_000726.4(CACNB4):c.*624del rs11291336
NM_000726.4(CACNB4):c.*890G>C rs78697588
NM_000726.4(CACNB4):c.-19-6G>T rs143675846
NM_000726.4(CACNB4):c.1239G>A (p.Leu413=) rs1805028
NM_000726.4(CACNB4):c.762T>A (p.Ile254=) rs61736804

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