ClinVar Miner

List of variants in gene CACNA1C reported as benign by Invitae

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Total variants: 55
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HGVS dbSNP
NM_000719.7(CACNA1C):c.1002C>T (p.Pro334=) rs112002520
NM_000719.7(CACNA1C):c.1074G>A (p.Gln358=) rs139842134
NM_000719.7(CACNA1C):c.109G>A (p.Gly37Arg) rs34534613
NM_000719.7(CACNA1C):c.1176G>T (p.Gly392=) rs1051360
NM_000719.7(CACNA1C):c.1359C>T (p.Asp453=) rs200330469
NM_000719.7(CACNA1C):c.1669+10G>A rs576194052
NM_000719.7(CACNA1C):c.1707A>G (p.Ala569=) rs375534041
NM_000719.7(CACNA1C):c.171C>T (p.Asp57=) rs34419050
NM_000719.7(CACNA1C):c.1734G>A (p.Leu578=) rs150692845
NM_000719.7(CACNA1C):c.1794C>T (p.Gly598=) rs116491041
NM_000719.7(CACNA1C):c.213G>A (p.Ala71=) rs113869350
NM_000719.7(CACNA1C):c.2449C>T (p.Pro817Ser) rs112532048
NM_000719.7(CACNA1C):c.2712C>T (p.Asn904=) rs144992959
NM_000719.7(CACNA1C):c.2766G>A (p.Pro922=) rs184684058
NM_000719.7(CACNA1C):c.3049-10C>T rs186741807
NM_000719.7(CACNA1C):c.3075C>T (p.Ala1025=) rs375813950
NM_000719.7(CACNA1C):c.3114G>C (p.Leu1038=) rs114139824
NM_000719.7(CACNA1C):c.3234C>T (p.Asp1078=) rs111606207
NM_000719.7(CACNA1C):c.3387G>A (p.Thr1129=) rs188224114
NM_000719.7(CACNA1C):c.340C>A (p.Arg114=) rs758229132
NM_000719.7(CACNA1C):c.3642C>T (p.Tyr1214=) rs56394008
NM_000719.7(CACNA1C):c.3780C>A (p.Gly1260=) rs201258230
NM_000719.7(CACNA1C):c.3948C>T (p.Asn1316=) rs150092451
NM_000719.7(CACNA1C):c.4038C>T (p.Ile1346=) rs56180838
NM_000719.7(CACNA1C):c.4485T>C (p.Asp1495=) rs41276710
NM_000719.7(CACNA1C):c.4611C>T (p.Arg1537=) rs372702466
NM_000719.7(CACNA1C):c.4624-9C>T rs377568567
NM_000719.7(CACNA1C):c.4659C>T (p.Asp1553=) rs563090568
NM_000719.7(CACNA1C):c.4726+9G>A rs369267978
NM_000719.7(CACNA1C):c.4829-7G>A rs137904817
NM_000719.7(CACNA1C):c.5064C>T (p.Ser1688=) rs139872789
NM_000719.7(CACNA1C):c.5097C>T (p.Ala1699=) rs113595214
NM_000719.7(CACNA1C):c.5139C>T (p.Asp1713=) rs115216455
NM_000719.7(CACNA1C):c.5199G>A (p.Ala1733=) rs200638007
NM_000719.7(CACNA1C):c.5214C>A (p.Gly1738=) rs199538058
NM_000719.7(CACNA1C):c.5214C>T (p.Gly1738=) rs199538058
NM_000719.7(CACNA1C):c.5235C>T (p.His1745=) rs201861473
NM_000719.7(CACNA1C):c.5292C>T (p.Asn1764=) rs72552065
NM_000719.7(CACNA1C):c.5360C>T (p.Thr1787Met) rs192749597
NM_000719.7(CACNA1C):c.5383G>A (p.Gly1795Arg) rs111298509
NM_000719.7(CACNA1C):c.5391C>G (p.Pro1797=) rs376124689
NM_000719.7(CACNA1C):c.5478G>A (p.Ala1826=) rs200283756
NM_000719.7(CACNA1C):c.5604A>G (p.Gln1868=) rs11062316
NM_000719.7(CACNA1C):c.5609C>T (p.Thr1870Met) rs201777030
NM_000719.7(CACNA1C):c.5639G>A (p.Arg1880Gln) rs182208896
NM_000719.7(CACNA1C):c.5649G>A (p.Pro1883=) rs56270948
NM_000719.7(CACNA1C):c.5665C>T (p.Arg1889Cys) rs185788586
NM_000719.7(CACNA1C):c.5706A>G (p.Glu1902=) rs537002656
NM_000719.7(CACNA1C):c.5918G>A (p.Arg1973Gln) rs112414325
NM_000719.7(CACNA1C):c.6342G>A (p.Ala2114=) rs368073321
NM_000719.7(CACNA1C):c.724C>T (p.Leu242=) rs200800133
NM_000719.7(CACNA1C):c.771C>T (p.Val257=) rs112315742
NM_000719.7(CACNA1C):c.960G>A (p.Thr320=) rs553958501
NM_000719.7(CACNA1C):c.966C>T (p.His322=) rs112539787
NM_000719.7(CACNA1C):c.984C>T (p.Asn328=) rs374050127

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