ClinVar Miner

List of variants in gene CACNA1C reported as uncertain significance by Illumina Clinical Services Laboratory,Illumina

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 98
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HGVS dbSNP
NM_000719.7(CACNA1C):c.*1473G>T rs886049221
NM_000719.7(CACNA1C):c.*1558T>A rs886049222
NM_000719.7(CACNA1C):c.*1569G>A rs886049223
NM_000719.7(CACNA1C):c.*1652_*1656GAATT[1] rs886049224
NM_000719.7(CACNA1C):c.*184G>A rs886049211
NM_000719.7(CACNA1C):c.*1911A>C rs186708407
NM_000719.7(CACNA1C):c.*1925C>T rs886049225
NM_000719.7(CACNA1C):c.*2456G>T rs142476147
NM_000719.7(CACNA1C):c.*2473G>A rs886049226
NM_000719.7(CACNA1C):c.*261G>C rs12828687
NM_000719.7(CACNA1C):c.*2651C>T rs767190987
NM_000719.7(CACNA1C):c.*267G>C rs752736296
NM_000719.7(CACNA1C):c.*2732T>G rs778220127
NM_000719.7(CACNA1C):c.*2817G>A rs555721726
NM_000719.7(CACNA1C):c.*290G>A rs749753216
NM_000719.7(CACNA1C):c.*297C>A rs886049212
NM_000719.7(CACNA1C):c.*3031T>A rs774490908
NM_000719.7(CACNA1C):c.*3042A>G rs886049227
NM_000719.7(CACNA1C):c.*3063C>G rs886049228
NM_000719.7(CACNA1C):c.*3299C>G rs886049229
NM_000719.7(CACNA1C):c.*3611C>T rs886049230
NM_000719.7(CACNA1C):c.*3722C>T rs886049231
NM_000719.7(CACNA1C):c.*3951G>C rs886049232
NM_000719.7(CACNA1C):c.*4025C>T rs886049233
NM_000719.7(CACNA1C):c.*4050G>A rs886049234
NM_000719.7(CACNA1C):c.*4134A>G rs886049235
NM_000719.7(CACNA1C):c.*4176G>T rs751166285
NM_000719.7(CACNA1C):c.*4198A>G rs886049236
NM_000719.7(CACNA1C):c.*4205C>T rs886049237
NM_000719.7(CACNA1C):c.*4226C>T rs776522592
NM_000719.7(CACNA1C):c.*4318G>A rs886049238
NM_000719.7(CACNA1C):c.*4345C>T rs886049239
NM_000719.7(CACNA1C):c.*4399T>G rs886049240
NM_000719.7(CACNA1C):c.*4410G>T rs547615657
NM_000719.7(CACNA1C):c.*4411C>T rs567401056
NM_000719.7(CACNA1C):c.*4440C>G rs886049241
NM_000719.7(CACNA1C):c.*4532G>A rs533634115
NM_000719.7(CACNA1C):c.*4598A>G rs376987352
NM_000719.7(CACNA1C):c.*5399T>C rs779194497
NM_000719.7(CACNA1C):c.*5599A>G rs886049243
NM_000719.7(CACNA1C):c.*5734G>C rs886049244
NM_000719.7(CACNA1C):c.*5811G>A rs886049245
NM_000719.7(CACNA1C):c.*5841G>A rs886049246
NM_000719.7(CACNA1C):c.*5889G>A rs886049247
NM_000719.7(CACNA1C):c.*605G>C rs886049213
NM_000719.7(CACNA1C):c.*6102G>A rs886049248
NM_000719.7(CACNA1C):c.*6281G>A rs886049249
NM_000719.7(CACNA1C):c.*630G>A rs886049214
NM_000719.7(CACNA1C):c.*6557C>G rs886049250
NM_000719.7(CACNA1C):c.*6591A>G rs886049251
NM_000719.7(CACNA1C):c.*828G>A rs886049216
NM_000719.7(CACNA1C):c.*896A>T rs886049217
NM_000719.7(CACNA1C):c.*960A>G rs886049218
NM_000719.7(CACNA1C):c.*977A>G rs886049219
NM_000719.7(CACNA1C):c.-214A>G rs886049149
NM_000719.7(CACNA1C):c.-233C>T rs886049148
NM_000719.7(CACNA1C):c.108G>A (p.Ala36=) rs781395450
NM_000719.7(CACNA1C):c.13A>C (p.Asn5His) rs886049150
NM_000719.7(CACNA1C):c.1486C>T (p.Arg496Trp) rs760888275
NM_000719.7(CACNA1C):c.1520G>A (p.Arg507His) rs768830617
NM_000719.7(CACNA1C):c.1558G>A (p.Ala520Thr) rs755167125
NM_000719.7(CACNA1C):c.1864G>A (p.Val622Ile) rs768270021
NM_000719.7(CACNA1C):c.202G>A (p.Ala68Thr) rs752000790
NM_000719.7(CACNA1C):c.2067C>T (p.Phe689=) rs112170830
NM_000719.7(CACNA1C):c.212C>T (p.Ala71Val) rs755579963
NM_000719.7(CACNA1C):c.2232A>C (p.Leu744=) rs370145265
NM_000719.7(CACNA1C):c.2391G>A (p.Gly797=) rs374857905
NM_000719.7(CACNA1C):c.2398A>C (p.Lys800Gln) rs779009338
NM_000719.7(CACNA1C):c.2813T>C (p.Ile938Thr) rs377165829
NM_000719.7(CACNA1C):c.2958C>T (p.Ile986=) rs886049203
NM_000719.7(CACNA1C):c.300G>A (p.Pro100=) rs764323907
NM_000719.7(CACNA1C):c.3201G>A (p.Ala1067=) rs758461435
NM_000719.7(CACNA1C):c.3681C>T (p.Val1227=) rs886049204
NM_000719.7(CACNA1C):c.3717+11G>A rs763622598
NM_000719.7(CACNA1C):c.3718-12C>T rs774165526
NM_000719.7(CACNA1C):c.3862G>A (p.Ala1288Thr) rs367895193
NM_000719.7(CACNA1C):c.3946-10C>T rs370630496
NM_000719.7(CACNA1C):c.4140+4G>A rs111442547
NM_000719.7(CACNA1C):c.4152A>G (p.Lys1384=) rs775331521
NM_000719.7(CACNA1C):c.4323G>A (p.Thr1441=) rs753892795
NM_000719.7(CACNA1C):c.4526+12G>C rs748926089
NM_000719.7(CACNA1C):c.4624-4G>A rs886049205
NM_000719.7(CACNA1C):c.4726+13G>A rs561365937
NM_000719.7(CACNA1C):c.4726+9G>A rs369267978
NM_000719.7(CACNA1C):c.4727-9G>A rs757966245
NM_000719.7(CACNA1C):c.4761G>A (p.Ala1587=) rs756364065
NM_000719.7(CACNA1C):c.4917T>C (p.Leu1639=) rs886049206
NM_000719.7(CACNA1C):c.5023G>A (p.Ala1675Thr) rs773930851
NM_000719.7(CACNA1C):c.537C>T (p.Ile179=) rs369673473
NM_000719.7(CACNA1C):c.5525A>C (p.Asn1842Thr) rs886049207
NM_000719.7(CACNA1C):c.5593G>A (p.Glu1865Lys) rs200231105
NM_000719.7(CACNA1C):c.567C>T (p.Ala189=) rs886049202
NM_000719.7(CACNA1C):c.5785-10G>A rs762376206
NM_000719.7(CACNA1C):c.6007G>A (p.Gly2003Arg) rs886038918
NM_000719.7(CACNA1C):c.6161A>G (p.Lys2054Arg) rs200588235
NM_000719.7(CACNA1C):c.6235_6237del (p.Asp2079del) rs886049208
NM_000719.7(CACNA1C):c.6239A>G (p.Asn2080Ser) rs886049209
NM_000719.7(CACNA1C):c.6371G>A (p.Ser2124Asn) rs886049210

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