ClinVar Miner

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

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Gene type:
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Total variants: 106
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HGVS dbSNP gnomAD frequency
NM_000719.7(CACNA1C):c.1114-292C>T rs2238087 0.06609
NM_000719.7(CACNA1C):c.5649G>A (p.Pro1883=) rs56270948 0.01676
NM_000719.7(CACNA1C):c.109G>A (p.Gly37Arg) rs34534613 0.00346
NM_000719.7(CACNA1C):c.2449C>T (p.Pro817Ser) rs112532048 0.00279
NM_000719.7(CACNA1C):c.5665C>T (p.Arg1889Cys) rs185788586 0.00182
NM_001167623.2(CACNA1C):c.3883A>G (p.Ile1295Val) rs114851656 0.00169
NM_000719.7(CACNA1C):c.3642C>T (p.Tyr1214=) rs56394008 0.00096
NM_000719.7(CACNA1C):c.5451C>T (p.His1817=) rs113239186 0.00063
NM_000719.7(CACNA1C):c.5091+17C>T rs375537358 0.00051
NM_000719.7(CACNA1C):c.5150C>G (p.Ala1717Gly) rs201492706 0.00048
NM_000719.7(CACNA1C):c.1468G>A (p.Gly490Arg) rs121912775 0.00036
NM_000719.7(CACNA1C):c.5639G>A (p.Arg1880Gln) rs182208896 0.00036
NM_000719.7(CACNA1C):c.5885G>A (p.Arg1962Gln) rs199776761 0.00026
NM_000719.7(CACNA1C):c.3747C>T (p.Ile1249=) rs370576211 0.00025
NM_000719.7(CACNA1C):c.5119G>A (p.Val1707Ile) rs147896322 0.00016
NM_000719.7(CACNA1C):c.5143C>A (p.Arg1715=) rs373996684 0.00016
NM_000719.7(CACNA1C):c.202G>A (p.Ala68Thr) rs752000790 0.00014
NM_000719.7(CACNA1C):c.4829-8C>T rs370969487 0.00013
NM_000719.7(CACNA1C):c.5444+610G>A rs371574216 0.00012
NM_000719.7(CACNA1C):c.1332C>T (p.Ala444=) rs202027411 0.00009
NM_000719.7(CACNA1C):c.5444+719G>A rs765829807 0.00009
NM_000719.7(CACNA1C):c.5550G>A (p.Glu1850=) rs367783859 0.00009
NM_000719.7(CACNA1C):c.135C>G (p.Thr45=) rs749123185 0.00007
NM_000719.7(CACNA1C):c.2232A>C (p.Leu744=) rs370145265 0.00007
NM_000719.7(CACNA1C):c.6011G>T (p.Gly2004Val) rs374991642 0.00007
NM_000719.7(CACNA1C):c.1896-18C>A rs1056995890 0.00006
NM_000719.7(CACNA1C):c.2461-3T>C rs918755208 0.00006
NM_000719.7(CACNA1C):c.6342G>A (p.Ala2114=) rs368073321 0.00006
NM_000719.7(CACNA1C):c.990G>A (p.Thr330=) rs371837699 0.00005
NM_000719.7(CACNA1C):c.-28C>T rs989994685 0.00004
NM_000719.7(CACNA1C):c.1481+16G>A rs369604192 0.00004
NM_000719.7(CACNA1C):c.5181G>A (p.Pro1727=) rs370149297 0.00004
NM_000719.7(CACNA1C):c.5226G>A (p.Ser1742=) rs368281620 0.00004
NM_000719.7(CACNA1C):c.5737G>A (p.Asp1913Asn) rs181502604 0.00004
NM_000719.7(CACNA1C):c.1467C>T (p.Cys489=) rs781074075 0.00003
NM_000719.7(CACNA1C):c.1669+15C>T rs774122237 0.00003
NM_000719.7(CACNA1C):c.2961-5C>T rs781703710 0.00003
NM_000719.7(CACNA1C):c.4050G>A (p.Leu1350=) rs371640459 0.00003
NM_000719.7(CACNA1C):c.4956+16C>T rs781417944 0.00003
NM_000719.7(CACNA1C):c.5098G>A (p.Gly1700Ser) rs761966966 0.00003
NM_000719.7(CACNA1C):c.5493G>A (p.Thr1831=) rs368046891 0.00003
NM_000719.7(CACNA1C):c.1689G>C (p.Leu563=) rs372908090 0.00002
NM_000719.7(CACNA1C):c.2634C>T (p.Ser878=) rs752800134 0.00002
NM_000719.7(CACNA1C):c.3789C>A (p.Thr1263=) rs765393806 0.00002
NM_000719.7(CACNA1C):c.4074+19C>T rs779341594 0.00002
NM_000719.7(CACNA1C):c.408C>T (p.Ala136=) rs769295096 0.00002
NM_000719.7(CACNA1C):c.5445-17dup rs752372266 0.00002
NM_000719.7(CACNA1C):c.6234C>T (p.Ala2078=) rs774966357 0.00002
NM_000719.7(CACNA1C):c.-27T>G rs776331800 0.00001
NM_000719.7(CACNA1C):c.1114-417C>T rs746270394 0.00001
NM_000719.7(CACNA1C):c.1356G>A (p.Glu452=) rs1257737700 0.00001
NM_000719.7(CACNA1C):c.1508+16G>A rs1358258790 0.00001
NM_000719.7(CACNA1C):c.1716C>T (p.Leu572=) rs745728974 0.00001
NM_000719.7(CACNA1C):c.1800C>T (p.Ile600=) rs1057523219 0.00001
NM_000719.7(CACNA1C):c.1806G>A (p.Glu602=) rs775181288 0.00001
NM_000719.7(CACNA1C):c.225A>C (p.Thr75=) rs756361032 0.00001
NM_000719.7(CACNA1C):c.2664-11C>G rs767514995 0.00001
NM_000719.7(CACNA1C):c.2854-10C>G rs767334396 0.00001
NM_000719.7(CACNA1C):c.3111C>T (p.Thr1037=) rs1057520903 0.00001
NM_000719.7(CACNA1C):c.3157-16G>C rs770629047 0.00001
NM_000719.7(CACNA1C):c.3498C>T (p.Ile1166=) rs201147949 0.00001
NM_000719.7(CACNA1C):c.3723C>T (p.Tyr1241=) rs377686760 0.00001
NM_000719.7(CACNA1C):c.3978C>T (p.Thr1326=) rs1022346720 0.00001
NM_000719.7(CACNA1C):c.4232+16C>A rs757493608 0.00001
NM_000719.7(CACNA1C):c.4782G>A (p.Lys1594=) rs1336965329 0.00001
NM_000719.7(CACNA1C):c.5338C>T (p.Arg1780Cys) rs371760034 0.00001
NM_000719.7(CACNA1C):c.5883C>T (p.Ser1961=) rs1291974001 0.00001
NM_000719.7(CACNA1C):c.5929G>A (p.Val1977Ile) rs786205741 0.00001
NM_000719.7(CACNA1C):c.6050T>C (p.Met2017Thr) rs786205742 0.00001
NM_000719.7(CACNA1C):c.6279C>T (p.Ala2093=) rs768208850 0.00001
NM_000719.7(CACNA1C):c.672C>T (p.Leu224=) rs868024886 0.00001
NM_000719.7(CACNA1C):c.75C>T (p.Pro25=) rs773869181 0.00001
NM_001167623.2(CACNA1C):c.1122C>T (p.Asp374=) rs374268470 0.00001
NM_000719.7(CACNA1C):c.1114-292C>G rs2238087
NM_000719.7(CACNA1C):c.1217+11C>T rs886038364
NM_000719.7(CACNA1C):c.135C>A (p.Thr45=) rs749123185
NM_000719.7(CACNA1C):c.1391-17C>G rs1057524174
NM_000719.7(CACNA1C):c.1482-15C>T rs1057521702
NM_000719.7(CACNA1C):c.1508+14dup rs1428591728
NM_000719.7(CACNA1C):c.1508+20C>T rs1471165180
NM_000719.7(CACNA1C):c.1815G>A (p.Leu605=) rs1555800189
NM_000719.7(CACNA1C):c.1851C>T (p.Ser617=) rs371654949
NM_000719.7(CACNA1C):c.2229C>T (p.Ile743=) rs759734767
NM_000719.7(CACNA1C):c.2331G>A (p.Lys777=) rs1555833118
NM_000719.7(CACNA1C):c.2339+20C>T rs201164691
NM_000719.7(CACNA1C):c.2794-5del rs1555860850
NM_000719.7(CACNA1C):c.3087C>A (p.Ile1029=) rs151211423
NM_000719.7(CACNA1C):c.3648C>T (p.Val1216=) rs1057521327
NM_000719.7(CACNA1C):c.3718-14C>G rs1555888662
NM_000719.7(CACNA1C):c.3822A>G (p.Lys1274=) rs1057524175
NM_000719.7(CACNA1C):c.3939C>T (p.Pro1313=) rs2094569738
NM_000719.7(CACNA1C):c.3946-45C>A rs201551454
NM_000719.7(CACNA1C):c.3946-46C>T rs112919597
NM_000719.7(CACNA1C):c.4141-20C>A rs934540211
NM_000719.7(CACNA1C):c.4232+18T>G rs779157902
NM_000719.7(CACNA1C):c.4527-7C>T rs1057522340
NM_000719.7(CACNA1C):c.4623+20A>G rs1440822075
NM_000719.7(CACNA1C):c.4726+13G>A rs561365937
NM_000719.7(CACNA1C):c.4860C>A (p.Ala1620=) rs1057522559
NM_000719.7(CACNA1C):c.4957-12C>T rs1556045982
NM_000719.7(CACNA1C):c.5016T>C (p.Asp1672=) rs778856101
NM_000719.7(CACNA1C):c.50G>A (p.Gly17Asp) rs747083495
NM_000719.7(CACNA1C):c.5145G>A (p.Arg1715=) rs761205516
NM_000719.7(CACNA1C):c.5444+618C>T rs1057520958
NM_000719.7(CACNA1C):c.6307G>T (p.Ala2103Ser) rs193922616
NM_000719.7(CACNA1C):c.757+14G>A rs753042094

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