ClinVar Miner

List of variants in gene CACNA1A reported as uncertain significance by Athena Diagnostics Inc

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Total variants: 62
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HGVS dbSNP
NM_001127221.1(CACNA1A):c.*264G>A rs1442777428
NM_001127221.1(CACNA1A):c.*401G>A rs768129470
NM_001127221.1(CACNA1A):c.*409G>C
NM_001127221.1(CACNA1A):c.*452G>A rs1568416040
NM_001127221.1(CACNA1A):c.*503G>A rs1052515747
NM_001127221.1(CACNA1A):c.*621G>A
NM_001127221.1(CACNA1A):c.*648C>G
NM_001127221.1(CACNA1A):c.1199-9C>T rs529977616
NM_001127221.1(CACNA1A):c.1270A>T (p.Thr424Ser) rs1555766588
NM_001127221.1(CACNA1A):c.1364G>A (p.Arg455Gln) rs561858384
NM_001127221.1(CACNA1A):c.1537G>C (p.Glu513Gln)
NM_001127221.1(CACNA1A):c.1672G>T (p.Val558Phe) rs1568519134
NM_001127221.1(CACNA1A):c.1909G>C (p.Gly637Arg)
NM_001127221.1(CACNA1A):c.2091G>A (p.Leu697=) rs908321451
NM_001127221.1(CACNA1A):c.2107+6C>T rs372970603
NM_001127221.1(CACNA1A):c.2268C>T (p.Asn756=) rs1382705855
NM_001127221.1(CACNA1A):c.2283-5T>A rs1555756483
NM_001127221.1(CACNA1A):c.2365G>A (p.Ala789Thr) rs1568509752
NM_001127221.1(CACNA1A):c.2394G>A (p.Met798Ile) rs370746809
NM_001127221.1(CACNA1A):c.2504A>C (p.Asn835Thr)
NM_001127221.1(CACNA1A):c.2695G>C (p.Gly899Arg)
NM_001127221.1(CACNA1A):c.2710C>T (p.His904Tyr)
NM_001127221.1(CACNA1A):c.2815G>C (p.Gly939Arg) rs771423362
NM_001127221.1(CACNA1A):c.2836G>A (p.Gly946Arg) rs527593196
NM_001127221.1(CACNA1A):c.2893C>T (p.Pro965Ser) rs1383144531
NM_001127221.1(CACNA1A):c.3112G>A (p.Val1038Ile)
NM_001127221.1(CACNA1A):c.3132C>A (p.Asn1044Lys) rs1187232740
NM_001127221.1(CACNA1A):c.3170G>A (p.Arg1057His) rs200850308
NM_001127221.1(CACNA1A):c.3178C>T (p.Pro1060Ser)
NM_001127221.1(CACNA1A):c.3386C>T (p.Pro1129Leu) rs754208553
NM_001127221.1(CACNA1A):c.3439G>A (p.Val1147Ile) rs376365775
NM_001127221.1(CACNA1A):c.3535C>A (p.Leu1179Ile)
NM_001127221.1(CACNA1A):c.3538A>C (p.Asn1180His) rs964526144
NM_001127221.1(CACNA1A):c.3609_3611GGA[3] (p.Glu1207del) rs750826355
NM_001127221.1(CACNA1A):c.3914A>C (p.Gln1305Pro) rs755279579
NM_001127221.1(CACNA1A):c.3949G>A (p.Asp1317Asn) rs1568485068
NM_001127221.1(CACNA1A):c.4093-9A>T rs369269870
NM_001127221.1(CACNA1A):c.4202G>A (p.Gly1401Glu) rs1555745111
NM_001127221.1(CACNA1A):c.4253G>A (p.Arg1418Gln) rs1568471977
NM_001127221.1(CACNA1A):c.4451G>T (p.Arg1484Leu) rs1271930393
NM_001127221.1(CACNA1A):c.4696C>T (p.Pro1566Ser) rs1353824164
NM_001127221.1(CACNA1A):c.4810G>A (p.Val1604Ile) rs943715197
NM_001127221.1(CACNA1A):c.5000G>A (p.Arg1667Gln) rs1568447650
NM_001127221.1(CACNA1A):c.5160C>T (p.Asp1720=) rs758409135
NM_001127221.1(CACNA1A):c.5628+1173G>A rs1568439088
NM_001127221.1(CACNA1A):c.5743G>A (p.Asp1915Asn)
NM_001127221.1(CACNA1A):c.578C>T (p.Thr193Met) rs1365721398
NM_001127221.1(CACNA1A):c.6016G>A (p.Ala2006Thr) rs374063403
NM_001127221.1(CACNA1A):c.6047G>A (p.Gly2016Glu)
NM_001127221.1(CACNA1A):c.6058G>T (p.Ala2020Ser) rs1393616835
NM_001127221.1(CACNA1A):c.6080A>G (p.Glu2027Gly)
NM_001127221.1(CACNA1A):c.6128C>T (p.Thr2043Met) rs563345694
NM_001127221.1(CACNA1A):c.6193-3C>A rs368480650
NM_001127221.1(CACNA1A):c.6213G>A (p.Met2071Ile) rs1555731738
NM_001127221.1(CACNA1A):c.622G>A (p.Gly208Arg) rs1568581246
NM_001127221.1(CACNA1A):c.6269G>A (p.Arg2090Gln)
NM_001127221.1(CACNA1A):c.631+4C>T rs1568581241
NM_001127221.1(CACNA1A):c.6403C>T (p.Arg2135Cys) rs121908235
NM_001127221.1(CACNA1A):c.6434C>T (p.Pro2145Leu) rs750077868
NM_001127221.1(CACNA1A):c.643G>A (p.Val215Ile) rs1555774867
NM_001127221.1(CACNA1A):c.6517G>T (p.Asp2173Tyr) rs370289732
NM_001127221.1(CACNA1A):c.889G>A (p.Gly297Arg) rs1168625480

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