ClinVar Miner

List of variants in gene CACNA1C reported as likely benign for not provided

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Total variants: 39
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HGVS dbSNP
GRCh37/hg19 12p13.33(chr12:2235940-2382140)x1
NM_000719.7(CACNA1C):c.109G>A (p.Gly37Arg) rs34534613
NM_000719.7(CACNA1C):c.1113+78C>T
NM_000719.7(CACNA1C):c.1114-145A>G
NM_000719.7(CACNA1C):c.1114-438T>G
NM_000719.7(CACNA1C):c.1114-587G>A
NM_000719.7(CACNA1C):c.1217+154G>C
NM_000719.7(CACNA1C):c.1218-66G>A
NM_000719.7(CACNA1C):c.1468G>A (p.Gly490Arg) rs121912775
NM_000719.7(CACNA1C):c.1482-177A>G
NM_000719.7(CACNA1C):c.1482-296C>G
NM_000719.7(CACNA1C):c.1669+54G>A
NM_000719.7(CACNA1C):c.1686C>T (p.Ala562=)
NM_000719.7(CACNA1C):c.2103+190A>G
NM_000719.7(CACNA1C):c.2565C>T (p.Val855=) rs760390307
NM_000719.7(CACNA1C):c.2663+188C>T
NM_000719.7(CACNA1C):c.2663+79C>T
NM_000719.7(CACNA1C):c.2853+438C>T
NM_000719.7(CACNA1C):c.3559-17C>T
NM_000719.7(CACNA1C):c.371+121C>T
NM_000719.7(CACNA1C):c.3718-131C>T
NM_000719.7(CACNA1C):c.3718-216G>A
NM_000719.7(CACNA1C):c.3945+212C>T
NM_000719.7(CACNA1C):c.4074+153G>A
NM_000719.7(CACNA1C):c.4527-151C>T
NM_000719.7(CACNA1C):c.4527-67C>T
NM_000719.7(CACNA1C):c.4727-190G>A
NM_000719.7(CACNA1C):c.4956+13G>A
NM_000719.7(CACNA1C):c.5150C>G (p.Ala1717Gly) rs201492706
NM_000719.7(CACNA1C):c.5445-841_5445-840insCTC
NM_000719.7(CACNA1C):c.5451C>T (p.His1817=) rs113239186
NM_000719.7(CACNA1C):c.5665C>T (p.Arg1889Cys) rs185788586
NM_000719.7(CACNA1C):c.5784+199G>A
NM_000719.7(CACNA1C):c.5918G>A (p.Arg1973Gln) rs112414325
NM_000719.7(CACNA1C):c.615G>A (p.Val205=)
NM_000719.7(CACNA1C):c.758-38G>A
NM_000719.7(CACNA1C):c.810C>T (p.His270=)
NM_000719.7(CACNA1C):c.911T>C (p.Ile304Thr) rs201756421
NM_000719.7(CACNA1C):c.917-20T>C

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