ClinVar Miner

List of variants in gene CACNA1C reported as likely benign for Long QT syndrome

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 137
Download table as spreadsheet
HGVS dbSNP
NM_000719.7(CACNA1C):c.1032C>G (p.Thr344=) rs760916463
NM_000719.7(CACNA1C):c.1125C>T (p.Ala375=) rs1131652
NM_000719.7(CACNA1C):c.132C>T (p.Pro44=) rs770183452
NM_000719.7(CACNA1C):c.1332C>T (p.Ala444=) rs202027411
NM_000719.7(CACNA1C):c.1341C>T (p.Ile447=) rs377643814
NM_000719.7(CACNA1C):c.135C>G (p.Thr45=) rs749123185
NM_000719.7(CACNA1C):c.1419C>T (p.Ser473=) rs368065584
NM_000719.7(CACNA1C):c.1428C>T (p.Thr476=) rs750843602
NM_000719.7(CACNA1C):c.1467C>T (p.Cys489=) rs781074075
NM_000719.7(CACNA1C):c.1468G>A (p.Gly490Arg) rs121912775
NM_000719.7(CACNA1C):c.1479G>A (p.Leu493=) rs1555775201
NM_000719.7(CACNA1C):c.1491C>T (p.Ile497=) rs750329281
NM_000719.7(CACNA1C):c.1524G>A (p.Arg508=) rs377431864
NM_000719.7(CACNA1C):c.153G>A (p.Ser51=) rs563315606
NM_000719.7(CACNA1C):c.1734G>C (p.Leu578=) rs150692845
NM_000719.7(CACNA1C):c.1749C>T (p.Tyr583=) rs375155518
NM_000719.7(CACNA1C):c.1783G>A (p.Val595Ile) rs201392574
NM_000719.7(CACNA1C):c.1839A>C (p.Pro613=) rs1060504922
NM_000719.7(CACNA1C):c.1872G>A (p.Leu624=) rs202227691
NM_000719.7(CACNA1C):c.1895+7G>A rs767905628
NM_000719.7(CACNA1C):c.1953C>T (p.Ile651=) rs762656408
NM_000719.7(CACNA1C):c.1965C>T (p.Leu655=) rs775843731
NM_000719.7(CACNA1C):c.1983C>T (p.Phe661=) rs1555825459
NM_000719.7(CACNA1C):c.1989C>T (p.Ile663=) rs1453566638
NM_000719.7(CACNA1C):c.198C>G (p.Gly66=) rs1060504919
NM_000719.7(CACNA1C):c.2067C>T (p.Phe689=) rs112170830
NM_000719.7(CACNA1C):c.2220A>G (p.Gly740=) rs940854113
NM_000719.7(CACNA1C):c.2232A>C (p.Leu744=) rs370145265
NM_000719.7(CACNA1C):c.2280G>A (p.Glu760=) rs141633456
NM_000719.7(CACNA1C):c.2339+7C>G rs748481639
NM_000719.7(CACNA1C):c.2340-4C>G rs1157833396
NM_000719.7(CACNA1C):c.234C>T (p.Ser78=) rs1060504924
NM_000719.7(CACNA1C):c.2382G>A (p.Pro794=) rs371978680
NM_000719.7(CACNA1C):c.2391G>A (p.Gly797=) rs374857905
NM_000719.7(CACNA1C):c.2542_2544GAG[2] (p.Glu850del) rs575583988
NM_000719.7(CACNA1C):c.2565C>T (p.Val855=) rs760390307
NM_000719.7(CACNA1C):c.2619C>T (p.Pro873=) rs374481837
NM_000719.7(CACNA1C):c.2637G>A (p.Ala879=) rs199629800
NM_000719.7(CACNA1C):c.2664-6G>A rs374269485
NM_000719.7(CACNA1C):c.2700G>A (p.Thr900=) rs200717140
NM_000719.7(CACNA1C):c.2854-4G>A rs113929946
NM_000719.7(CACNA1C):c.3060G>A (p.Gln1020=) rs115017320
NM_000719.7(CACNA1C):c.3081G>A (p.Arg1027=) rs746010296
NM_000719.7(CACNA1C):c.3157-7C>T rs759274364
NM_000719.7(CACNA1C):c.3201G>A (p.Ala1067=) rs758461435
NM_000719.7(CACNA1C):c.3201G>C (p.Ala1067=) rs758461435
NM_000719.7(CACNA1C):c.3240G>A (p.Glu1080=) rs1555882488
NM_000719.7(CACNA1C):c.3246C>T (p.Asp1082=) rs370662635
NM_000719.7(CACNA1C):c.3363G>A (p.Leu1121=) rs778991232
NM_000719.7(CACNA1C):c.3459C>T (p.Ile1153=) rs374850501
NM_000719.7(CACNA1C):c.3492C>T (p.Phe1164=) rs757106180
NM_000719.7(CACNA1C):c.3558+10dup rs1555884916
NM_000719.7(CACNA1C):c.3567C>T (p.Cys1189=) rs202058956
NM_000719.7(CACNA1C):c.3654C>T (p.Ser1218=) rs776884902
NM_000719.7(CACNA1C):c.372-9C>G rs367763190
NM_000719.7(CACNA1C):c.3723C>T (p.Tyr1241=) rs377686760
NM_000719.7(CACNA1C):c.375A>G (p.Pro125=) rs587780882
NM_000719.7(CACNA1C):c.3762C>T (p.Leu1254=) rs781762504
NM_000719.7(CACNA1C):c.3933C>T (p.Cys1311=) rs199569953
NM_000719.7(CACNA1C):c.3946-10C>T rs370630496
NM_000719.7(CACNA1C):c.3946-7G>A rs1060504923
NM_000719.7(CACNA1C):c.3969C>T (p.Ile1323=) rs201345843
NM_000719.7(CACNA1C):c.3988C>T (p.Leu1330=) rs1455874684
NM_000719.7(CACNA1C):c.4068C>T (p.Ser1356=) rs765091519
NM_000719.7(CACNA1C):c.4075-4C>A rs369044605
NM_000719.7(CACNA1C):c.4122C>T (p.Tyr1374=) rs146868811
NM_000719.7(CACNA1C):c.4128G>A (p.Val1376=) rs377173101
NM_000719.7(CACNA1C):c.4141-4C>T rs745757052
NM_000719.7(CACNA1C):c.4233-6C>A rs1377204108
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.4323G>A (p.Thr1441=) rs753892795
NM_000719.7(CACNA1C):c.4380C>T (p.Tyr1460=) rs747654175
NM_000719.7(CACNA1C):c.4389T>C (p.Cys1463=) rs1060504918
NM_000719.7(CACNA1C):c.4533T>C (p.Arg1511=) rs1060504920
NM_000719.7(CACNA1C):c.456C>T (p.Ser152=) rs776532518
NM_000719.7(CACNA1C):c.459C>T (p.Asn153=) rs367638447
NM_000719.7(CACNA1C):c.4641C>T (p.Asn1547=) rs202194703
NM_000719.7(CACNA1C):c.4704G>A (p.Thr1568=) rs377050884
NM_000719.7(CACNA1C):c.4727-10C>T rs749903718
NM_000719.7(CACNA1C):c.4727-9G>A rs757966245
NM_000719.7(CACNA1C):c.477+8C>T rs763228787
NM_000719.7(CACNA1C):c.478-6T>G rs769218160
NM_000719.7(CACNA1C):c.4941C>T (p.Asn1647=) rs773832706
NM_000719.7(CACNA1C):c.4944G>A (p.Ala1648=) rs200330326
NM_000719.7(CACNA1C):c.5022C>T (p.Thr1674=) rs372300407
NM_000719.7(CACNA1C):c.5034G>A (p.Glu1678=) rs863224373
NM_000719.7(CACNA1C):c.5109C>T (p.Phe1703=) rs767569416
NM_000719.7(CACNA1C):c.5119G>A (p.Val1707Ile) rs147896322
NM_000719.7(CACNA1C):c.5136C>T (p.Ser1712=) rs780871697
NM_000719.7(CACNA1C):c.5143C>A (p.Arg1715=) rs373996684
NM_000719.7(CACNA1C):c.5148C>T (p.Ser1716=) rs371262001
NM_000719.7(CACNA1C):c.5149G>A (p.Ala1717Thr) rs200865354
NM_000719.7(CACNA1C):c.5150C>G (p.Ala1717Gly) rs201492706
NM_000719.7(CACNA1C):c.5157C>G (p.Pro1719=) rs534589273
NM_000719.7(CACNA1C):c.5217C>T (p.Asp1739=) rs864622139
NM_000719.7(CACNA1C):c.5250C>T (p.Asp1750=) rs1231791018
NM_000719.7(CACNA1C):c.5277G>A (p.Ser1759=) rs371931644
NM_000719.7(CACNA1C):c.5346C>T (p.Ala1782=) rs369254461
NM_000719.7(CACNA1C):c.537C>T (p.Ile179=) rs369673473
NM_000719.7(CACNA1C):c.5442C>T (p.Asn1814=) rs1051978823
NM_000719.7(CACNA1C):c.5444+719G>A rs765829807
NM_000719.7(CACNA1C):c.5451C>T (p.His1817=) rs113239186
NM_000719.7(CACNA1C):c.5493G>A (p.Thr1831=) rs368046891
NM_000719.7(CACNA1C):c.5529T>C (p.His1843=) rs371831239
NM_000719.7(CACNA1C):c.5550G>A (p.Glu1850=) rs367783859
NM_000719.7(CACNA1C):c.570C>T (p.Tyr190=) rs372770722
NM_000719.7(CACNA1C):c.5785-5C>T rs750451768
NM_000719.7(CACNA1C):c.579C>T (p.Asn193=) rs561224137
NM_000719.7(CACNA1C):c.5841A>G (p.Ser1947=) rs1056550014
NM_000719.7(CACNA1C):c.5895C>T (p.Pro1965=) rs200227029
NM_000719.7(CACNA1C):c.5917C>A (p.Arg1973=) rs774402582
NM_000719.7(CACNA1C):c.5997C>G (p.Thr1999=) rs1291561787
NM_000719.7(CACNA1C):c.6039C>T (p.Pro2013=) rs780157730
NM_000719.7(CACNA1C):c.6040G>A (p.Val2014Ile) rs199473660
NM_000719.7(CACNA1C):c.6057C>T (p.Pro2019=) rs1556311718
NM_000719.7(CACNA1C):c.6090C>T (p.His2030=) rs750835120
NM_000719.7(CACNA1C):c.6096T>C (p.Ser2032=) rs530955089
NM_000719.7(CACNA1C):c.6111G>A (p.Val2037=) rs758922114
NM_000719.7(CACNA1C):c.615G>T (p.Val205=) rs747320984
NM_000719.7(CACNA1C):c.618G>A (p.Gly206=) rs200602896
NM_000719.7(CACNA1C):c.6234C>T (p.Ala2078=) rs774966357
NM_000719.7(CACNA1C):c.6270C>A (p.Pro2090=) rs1060504921
NM_000719.7(CACNA1C):c.6272A>G (p.Asn2091Ser) rs201090446
NM_000719.7(CACNA1C):c.6276C>A (p.Gly2092=) rs1556333950
NM_000719.7(CACNA1C):c.6339C>T (p.Asp2113=) rs374843203
NM_000719.7(CACNA1C):c.6344G>C (p.Gly2115Ala) rs199694744
NM_000719.7(CACNA1C):c.6388G>A (p.Asp2130Asn) rs199473392
NM_000719.7(CACNA1C):c.705G>A (p.Ala235=) rs775314673
NM_000719.7(CACNA1C):c.714C>G (p.Ala238=) rs561293967
NM_000719.7(CACNA1C):c.828G>A (p.Leu276=) rs540934161
NM_000719.7(CACNA1C):c.846C>T (p.Tyr282=) rs200847105
NM_000719.7(CACNA1C):c.906G>A (p.Glu302=) rs367860917
NM_000719.7(CACNA1C):c.911T>C (p.Ile304Thr) rs201756421
NM_000719.7(CACNA1C):c.927A>G (p.Ala309=) rs369079645
NM_000719.7(CACNA1C):c.951G>A (p.Ala317=) rs373875149

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.