ClinVar Miner

List of variants in gene CACNA1C reported as likely benign for Cardiovascular phenotype

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Total variants: 66
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HGVS dbSNP
NM_000719.6(CACNA1C):c.1074G>A (p.Gln358=) rs139842134
NM_000719.6(CACNA1C):c.1176G>T (p.Gly392=) rs1051360
NM_000719.6(CACNA1C):c.1290A>G (p.Leu430=) rs886038927
NM_000719.6(CACNA1C):c.1332C>T (p.Ala444=) rs202027411
NM_000719.6(CACNA1C):c.1359C>T (p.Asp453=) rs200330469
NM_000719.6(CACNA1C):c.1419C>T (p.Ser473=) rs368065584
NM_000719.6(CACNA1C):c.1524G>A (p.Arg508=) rs377431864
NM_000719.6(CACNA1C):c.1635C>T (p.His545=) rs1171966123
NM_000719.6(CACNA1C):c.1704G>A (p.Thr568=) rs770625734
NM_000719.6(CACNA1C):c.1794C>T (p.Gly598=) rs116491041
NM_000719.6(CACNA1C):c.1953C>T (p.Ile651=) rs762656408
NM_000719.6(CACNA1C):c.2280G>A (p.Glu760=) rs141633456
NM_000719.6(CACNA1C):c.2427C>T (p.Ile809=) rs886038904
NM_000719.6(CACNA1C):c.2760G>A (p.Glu920=) rs1156871556
NM_000719.6(CACNA1C):c.2766G>A (p.Pro922=) rs184684058
NM_000719.6(CACNA1C):c.2988C>T (p.Ile996=) rs886039065
NM_000719.6(CACNA1C):c.3201G>A (p.Ala1067=) rs758461435
NM_000719.6(CACNA1C):c.3234C>T (p.Asp1078=) rs111606207
NM_000719.6(CACNA1C):c.3531C>T (p.Tyr1177=) rs754527651
NM_000719.6(CACNA1C):c.3642C>T (p.Tyr1214=) rs56394008
NM_000719.6(CACNA1C):c.3654C>T (p.Ser1218=) rs776884902
NM_000719.6(CACNA1C):c.3723C>T (p.Tyr1241=) rs377686760
NM_000719.6(CACNA1C):c.3736C>T (p.Leu1246=) rs763674076
NM_000719.6(CACNA1C):c.375A>G (p.Pro125=) rs587780882
NM_000719.6(CACNA1C):c.3780C>A (p.Gly1260=) rs201258230
NM_000719.6(CACNA1C):c.3948C>T (p.Asn1316=) rs150092451
NM_000719.6(CACNA1C):c.4122C>T (p.Tyr1374=) rs146868811
NM_000719.6(CACNA1C):c.4140+4G>A rs111442547
NM_000719.6(CACNA1C):c.4242C>T (p.Thr1414=) rs773062528
NM_000719.6(CACNA1C):c.4317C>T (p.Asn1439=) rs183192651
NM_000719.6(CACNA1C):c.459C>T (p.Asn153=) rs367638447
NM_000719.6(CACNA1C):c.4659C>T (p.Asp1553=) rs563090568
NM_000719.6(CACNA1C):c.4761G>A (p.Ala1587=) rs756364065
NM_000719.6(CACNA1C):c.486G>A (p.Val162=) rs1555599597
NM_000719.6(CACNA1C):c.5022C>T (p.Thr1674=) rs372300407
NM_000719.6(CACNA1C):c.5148C>T (p.Ser1716=) rs371262001
NM_000719.6(CACNA1C):c.5199G>A (p.Ala1733=) rs200638007
NM_000719.6(CACNA1C):c.5214C>A (p.Gly1738=) rs199538058
NM_000719.6(CACNA1C):c.5214C>T (p.Gly1738=) rs199538058
NM_000719.6(CACNA1C):c.5235C>T (p.His1745=) rs201861473
NM_000719.6(CACNA1C):c.5283C>T (p.Thr1761=) rs747358417
NM_000719.6(CACNA1C):c.537C>T (p.Ile179=) rs369673473
NM_000719.6(CACNA1C):c.5391C>G (p.Pro1797=) rs376124689
NM_000719.6(CACNA1C):c.5424G>A (p.Ala1808=) rs587780881
NM_000719.6(CACNA1C):c.5451C>T (p.His1817=) rs113239186
NM_000719.6(CACNA1C):c.5478G>A (p.Ala1826=) rs200283756
NM_000719.6(CACNA1C):c.5499G>A (p.Gln1833=) rs886039095
NM_000719.6(CACNA1C):c.5529T>C (p.His1843=) rs371831239
NM_000719.6(CACNA1C):c.5593G>A (p.Glu1865Lys) rs200231105
NM_000719.6(CACNA1C):c.5658T>C (p.Gly1886=) rs769766334
NM_000719.6(CACNA1C):c.5747A>G (p.Gln1916Arg) rs186867242
NM_000719.6(CACNA1C):c.5865A>C (p.Pro1955=) rs199621004
NM_000719.6(CACNA1C):c.5898A>C (p.Pro1966=) rs886038778
NM_000719.6(CACNA1C):c.5905G>A (p.Val1969Ile) rs748408098
NM_000719.6(CACNA1C):c.6000C>T (p.Pro2000=) rs772160508
NM_000719.6(CACNA1C):c.6006C>T (p.Gly2002=) rs373253192
NM_000719.6(CACNA1C):c.6213A>T (p.Ile2071=) rs778147251
NM_000719.6(CACNA1C):c.6234C>T (p.Ala2078=) rs774966357
NM_000719.6(CACNA1C):c.6342G>A (p.Ala2114=) rs368073321
NM_000719.6(CACNA1C):c.6344G>C (p.Gly2115Ala) rs199694744
NM_000719.6(CACNA1C):c.6348T>C (p.Cys2116=) rs1556335598
NM_000719.6(CACNA1C):c.666C>T (p.Asn222=) rs527741368
NM_000719.6(CACNA1C):c.720C>T (p.Arg240=) rs527755968
NM_000719.6(CACNA1C):c.724C>T (p.Leu242=) rs200800133
NM_000719.6(CACNA1C):c.966C>T (p.His322=) rs112539787
NM_000719.6(CACNA1C):c.984C>T (p.Asn328=) rs374050127

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