ClinVar Miner

List of variants in gene CACNB4 reported as likely benign for not specified

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Total variants: 15
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HGVS dbSNP gnomAD frequency
NM_000726.5(CACNB4):c.1239G>A (p.Leu413=) rs1805028 0.05818
NM_000726.5(CACNB4):c.762T>A (p.Ile254=) rs61736804 0.05586
NM_000726.5(CACNB4):c.1303-3T>C rs143442080 0.00617
NM_000726.5(CACNB4):c.64-238T>G rs369342902 0.00042
NM_000726.5(CACNB4):c.*4T>C rs556761275 0.00019
NM_000726.5(CACNB4):c.1031G>A (p.Arg344Gln) rs776608168 0.00009
NM_000726.5(CACNB4):c.1020+16C>G rs778431925 0.00002
NM_000726.5(CACNB4):c.681G>A (p.Pro227=) rs1405201747 0.00002
NM_000726.5(CACNB4):c.1026A>G (p.Leu342=) rs1057521218 0.00001
NM_000726.5(CACNB4):c.315C>T (p.Gly105=) rs748422887 0.00001
NM_000726.5(CACNB4):c.222A>T (p.Arg74=) rs553682728
NM_000726.5(CACNB4):c.267+12del rs750563187
NM_000726.5(CACNB4):c.521+11A>G
NM_000726.5(CACNB4):c.618+20T>C rs1057521279
NM_000726.5(CACNB4):c.699+15T>C

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