ClinVar Miner

List of variants in gene CACNA1C reported as benign for not specified

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Gene type:
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Total variants: 82
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HGVS dbSNP
NM_000719.6(CACNA1C):c.5445-511A>G rs10774054
NM_000719.7(CACNA1C):c.1065G>A (p.Thr355=) rs757055492
NM_000719.7(CACNA1C):c.1074G>A (p.Gln358=) rs139842134
NM_000719.7(CACNA1C):c.1114-292C>T rs2238087
NM_000719.7(CACNA1C):c.1114-416G>A rs187604163
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.1391-2484C>T rs60106875
NM_000719.7(CACNA1C):c.1468G>A (p.Gly490Arg) rs121912775
NM_000719.7(CACNA1C):c.1508+15C>T rs776362233
NM_000719.7(CACNA1C):c.1674G>A (p.Thr558=) rs781180544
NM_000719.7(CACNA1C):c.171C>T (p.Asp57=) rs34419050
NM_000719.7(CACNA1C):c.1794C>T (p.Gly598=) rs116491041
NM_000719.7(CACNA1C):c.2339+18C>T rs778390407
NM_000719.7(CACNA1C):c.2339+20C>A rs201164691
NM_000719.7(CACNA1C):c.2436C>T (p.Asp812=) rs215976
NM_000719.7(CACNA1C):c.2530+13C>T rs374170716
NM_000719.7(CACNA1C):c.2530+9C>T rs587780876
NM_000719.7(CACNA1C):c.2637G>A (p.Ala879=) rs199629800
NM_000719.7(CACNA1C):c.2712C>T (p.Asn904=) rs144992959
NM_000719.7(CACNA1C):c.2793+10G>A rs587780877
NM_000719.7(CACNA1C):c.3209+12T>C rs372982213
NM_000719.7(CACNA1C):c.3387G>A (p.Thr1129=) rs188224114
NM_000719.7(CACNA1C):c.371+16C>T rs377534958
NM_000719.7(CACNA1C):c.371+17G>A rs78645318
NM_000719.7(CACNA1C):c.372-15G>A rs55792866
NM_000719.7(CACNA1C):c.375A>G (p.Pro125=) rs587780882
NM_000719.7(CACNA1C):c.3786C>T (p.Phe1262=) rs216008
NM_000719.7(CACNA1C):c.3829-614A>G rs114851656
NM_000719.7(CACNA1C):c.3912+14G>A rs372728453
NM_000719.7(CACNA1C):c.3933C>T (p.Cys1311=) rs199569953
NM_000719.7(CACNA1C):c.3948C>T (p.Asn1316=) rs150092451
NM_000719.7(CACNA1C):c.3969C>T (p.Ile1323=) rs201345843
NM_000719.7(CACNA1C):c.4038C>T (p.Ile1346=) rs56180838
NM_000719.7(CACNA1C):c.4074+14A>G rs371806132
NM_000719.7(CACNA1C):c.4170C>T (p.Thr1390=) rs587780878
NM_000719.7(CACNA1C):c.426G>A (p.Ala142=) rs546786746
NM_000719.7(CACNA1C):c.4305C>T (p.Ser1435=) rs756717724
NM_000719.7(CACNA1C):c.4317C>T (p.Asn1439=) rs183192651
NM_000719.7(CACNA1C):c.4485T>C (p.Asp1495=) rs41276710
NM_000719.7(CACNA1C):c.4527-20T>C rs587780879
NM_000719.7(CACNA1C):c.4624-8G>A rs529345041
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.478-19T>G rs571558332
NM_000719.7(CACNA1C):c.4829-7G>A rs137904817
NM_000719.7(CACNA1C):c.50-18T>C rs750923289
NM_000719.7(CACNA1C):c.5064C>T (p.Ser1688=) rs139872789
NM_000719.7(CACNA1C):c.5091+18G>A rs143343491
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.5157C>G (p.Pro1719=) rs534589273
NM_000719.7(CACNA1C):c.5214C>A (p.Gly1738=) rs199538058
NM_000719.7(CACNA1C):c.522G>A (p.Ala174=) rs1544514
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.5331C>T (p.Arg1777=) rs587780880
NM_000719.7(CACNA1C):c.5360C>T (p.Thr1787Met) rs192749597
NM_000719.7(CACNA1C):c.5361G>A (p.Thr1787=) rs1051375
NM_000719.7(CACNA1C):c.5383G>A (p.Gly1795Arg) rs111298509
NM_000719.7(CACNA1C):c.5424G>A (p.Ala1808=) rs587780881
NM_000719.7(CACNA1C):c.5444+609C>T rs760873868
NM_000719.7(CACNA1C):c.5445-584A>G rs10774053
NM_000719.7(CACNA1C):c.5445-586C>T rs10848683
NM_000719.7(CACNA1C):c.5529T>C (p.His1843=) rs371831239
NM_000719.7(CACNA1C):c.5593G>A (p.Glu1865Lys) rs200231105
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.5649G>A (p.Pro1883=) rs56270948
NM_000719.7(CACNA1C):c.5665C>T (p.Arg1889Cys) rs185788586
NM_000719.7(CACNA1C):c.5680+11C>A rs66611965
NM_000719.7(CACNA1C):c.5680+11C>T rs66611965
NM_000719.7(CACNA1C):c.5680+15C>T rs114036394
NM_000719.7(CACNA1C):c.579C>T (p.Asn193=) rs561224137
NM_000719.7(CACNA1C):c.5918G>A (p.Arg1973Gln) rs112414325
NM_000719.7(CACNA1C):c.617+17G>A rs1544515
NM_000719.7(CACNA1C):c.617+19T>C rs1544516
NM_000719.7(CACNA1C):c.618G>A (p.Gly206=) rs200602896
NM_000719.7(CACNA1C):c.6339C>T (p.Asp2113=) rs374843203
NM_000719.7(CACNA1C):c.771C>T (p.Val257=) rs112315742
NM_000719.7(CACNA1C):c.966C>T (p.His322=) rs112539787

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