ClinVar Miner

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

Included ClinVar conditions (88):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 13
Download table as spreadsheet
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.-25G>T rs143675846
NM_000726.4(CACNB4):c.1239G>A (p.Leu413=) rs1805028
NM_000726.4(CACNB4):c.762T>A (p.Ile254=) rs61736804

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.