ClinVar Miner

List of variants in gene CACNA1H reported as likely benign for EIG

Included ClinVar conditions (4):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 110
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HGVS dbSNP
NM_021098.3(CACNA1H):c.1029C>T (p.Tyr343=) rs375894182
NM_021098.3(CACNA1H):c.1041C>T (p.Cys347=) rs757510335
NM_021098.3(CACNA1H):c.1047G>A (p.Ser349=) rs72552034
NM_021098.3(CACNA1H):c.1068C>T (p.Asn356=) rs369894677
NM_021098.3(CACNA1H):c.108G>C (p.Pro36=) rs28365126
NM_021098.3(CACNA1H):c.1120-5C>G rs188397970
NM_021098.3(CACNA1H):c.1129C>T (p.Leu377=) rs529122240
NM_021098.3(CACNA1H):c.1413C>G (p.Val471=) rs781240456
NM_021098.3(CACNA1H):c.1425C>T (p.Ser475=) rs60537026
NM_021098.3(CACNA1H):c.1502G>A (p.Gly501Glu) rs768197900
NM_021098.3(CACNA1H):c.1508G>A (p.Arg503His) rs201009269
NM_021098.3(CACNA1H):c.1623C>T (p.Pro541=) rs773501953
NM_021098.3(CACNA1H):c.1638C>T (p.Cys546=) rs1355615330
NM_021098.3(CACNA1H):c.1674G>A (p.Ser558=) rs777311819
NM_021098.3(CACNA1H):c.1722C>T (p.Ser574=) rs763201457
NM_021098.3(CACNA1H):c.1754C>T (p.Pro585Leu) rs372367313
NM_021098.3(CACNA1H):c.180G>C (p.Ala60=) rs749735503
NM_021098.3(CACNA1H):c.1828A>G (p.Thr610Ala) rs201449513
NM_021098.3(CACNA1H):c.1844C>T (p.Thr615Met) rs368976749
NM_021098.3(CACNA1H):c.1853C>T (p.Pro618Leu) rs60734921
NM_021098.3(CACNA1H):c.1869C>T (p.Ser623=) rs372975893
NM_021098.3(CACNA1H):c.1890C>T (p.Pro630=) rs755382298
NM_021098.3(CACNA1H):c.1983G>A (p.Pro661=) rs56875953
NM_021098.3(CACNA1H):c.2002+10C>T rs1388783364
NM_021098.3(CACNA1H):c.2103G>A (p.Pro701=) rs59906488
NM_021098.3(CACNA1H):c.2151G>A (p.Ser717=) rs200423899
NM_021098.3(CACNA1H):c.2153A>G (p.Glu718Gly) rs538923520
NM_021098.3(CACNA1H):c.2175T>G (p.Arg725=) rs1427937474
NM_021098.3(CACNA1H):c.2294A>G (p.Gln765Arg) rs372489040
NM_021098.3(CACNA1H):c.2338G>T (p.Val780Phe) rs60534546
NM_021098.3(CACNA1H):c.2484C>T (p.Ser828=) rs368916421
NM_021098.3(CACNA1H):c.2538C>T (p.Ala846=) rs748509684
NM_021098.3(CACNA1H):c.2604-4G>A rs543668710
NM_021098.3(CACNA1H):c.2604C>T (p.Ser868=) rs562148225
NM_021098.3(CACNA1H):c.270C>G (p.Arg90=) rs577235589
NM_021098.3(CACNA1H):c.2760G>T (p.Thr920=) rs776215729
NM_021098.3(CACNA1H):c.2772C>T (p.Leu924=) rs777961380
NM_021098.3(CACNA1H):c.2931C>T (p.Asn977=) rs376470846
NM_021098.3(CACNA1H):c.3114C>T (p.Phe1038=) rs374946880
NM_021098.3(CACNA1H):c.3155-4G>A rs543267343
NM_021098.3(CACNA1H):c.3163A>G (p.Met1055Val) rs563037729
NM_021098.3(CACNA1H):c.3362C>T (p.Pro1121Leu) rs200832286
NM_021098.3(CACNA1H):c.3364-3C>T rs57079020
NM_021098.3(CACNA1H):c.3408C>T (p.Gly1136=) rs61543423
NM_021098.3(CACNA1H):c.3600C>T (p.Asp1200=) rs1555515663
NM_021098.3(CACNA1H):c.3614G>A (p.Arg1205Gln) rs58594334
NM_021098.3(CACNA1H):c.3629C>T (p.Pro1210Leu) rs61319429
NM_021098.3(CACNA1H):c.3636C>A (p.Thr1212=) rs767435491
NM_021098.3(CACNA1H):c.3651C>T (p.Arg1217=) rs929083218
NM_021098.3(CACNA1H):c.366C>G (p.Pro122=) rs372041705
NM_021098.3(CACNA1H):c.3681C>T (p.Asp1227=) rs1555515806
NM_021098.3(CACNA1H):c.385G>A (p.Gly129Ser) rs187596702
NM_021098.3(CACNA1H):c.3933C>T (p.Ile1311=) rs200353061
NM_021098.3(CACNA1H):c.3970-10C>T rs377114648
NM_021098.3(CACNA1H):c.39G>A (p.Val13=) rs1306573144
NM_021098.3(CACNA1H):c.4035G>A (p.Val1345=) rs747258959
NM_021098.3(CACNA1H):c.4039-8C>T rs757467258
NM_021098.3(CACNA1H):c.4045G>A (p.Ala1349Thr) rs200400235
NM_021098.3(CACNA1H):c.4062C>T (p.Ser1354=) rs376236175
NM_021098.3(CACNA1H):c.4065C>T (p.Gly1355=) rs771718484
NM_021098.3(CACNA1H):c.4219C>T (p.Leu1407=) rs1041269521
NM_021098.3(CACNA1H):c.4224-9C>T rs1287379368
NM_021098.3(CACNA1H):c.4269G>C (p.Leu1423=) rs554182970
NM_021098.3(CACNA1H):c.4351-6C>T rs377612703
NM_021098.3(CACNA1H):c.4365G>A (p.Lys1455=) rs373587418
NM_021098.3(CACNA1H):c.4378G>A (p.Glu1460Lys) rs755817927
NM_021098.3(CACNA1H):c.4477-7C>T rs984880682
NM_021098.3(CACNA1H):c.4488G>A (p.Ser1496=) rs377112179
NM_021098.3(CACNA1H):c.4527C>T (p.Ile1509=) rs1384457303
NM_021098.3(CACNA1H):c.471C>G (p.Ala157=) rs777692032
NM_021098.3(CACNA1H):c.4758G>A (p.Arg1586=) rs200153161
NM_021098.3(CACNA1H):c.4860C>T (p.Asp1620=) rs201309183
NM_021098.3(CACNA1H):c.4881C>T (p.Ile1627=) rs576335604
NM_021098.3(CACNA1H):c.5052G>A (p.Leu1684=) rs374459574
NM_021098.3(CACNA1H):c.5127C>T (p.Ile1709=) rs1555519102
NM_021098.3(CACNA1H):c.5145C>T (p.Arg1715=) rs1182772693
NM_021098.3(CACNA1H):c.5174-5C>T rs199536335
NM_021098.3(CACNA1H):c.5382C>T (p.Phe1794=) rs567978624
NM_021098.3(CACNA1H):c.546-9C>T rs375982567
NM_021098.3(CACNA1H):c.5494C>T (p.Leu1832=) rs61732194
NM_021098.3(CACNA1H):c.5511C>T (p.Pro1837=) rs58819745
NM_021098.3(CACNA1H):c.5562G>C (p.Val1854=) rs368251427
NM_021098.3(CACNA1H):c.5634C>T (p.Ala1878=) rs373353512
NM_021098.3(CACNA1H):c.5655G>T (p.Ala1885=) rs58632975
NM_021098.3(CACNA1H):c.5887+8A>G rs1258785345
NM_021098.3(CACNA1H):c.5924C>T (p.Ser1975Phe) rs186422070
NM_021098.3(CACNA1H):c.6049-10G>A rs199547941
NM_021098.3(CACNA1H):c.6198C>T (p.Ser2066=) rs375020212
NM_021098.3(CACNA1H):c.6252G>A (p.Ala2084=) rs767753103
NM_021098.3(CACNA1H):c.6322G>A (p.Ala2108Thr) rs56930660
NM_021098.3(CACNA1H):c.6327C>T (p.Cys2109=) rs777082647
NM_021098.3(CACNA1H):c.6371C>T (p.Pro2124Leu) rs372453886
NM_021098.3(CACNA1H):c.63C>T (p.Gly21=) rs1261320353
NM_021098.3(CACNA1H):c.6441G>A (p.Pro2147=) rs759684037
NM_021098.3(CACNA1H):c.6460T>A (p.Trp2154Arg) rs767461657
NM_021098.3(CACNA1H):c.6480G>A (p.Leu2160=) rs1555520987
NM_021098.3(CACNA1H):c.6486C>T (p.Ser2162=) rs113962757
NM_021098.3(CACNA1H):c.6507G>A (p.Lys2169=) rs1555521007
NM_021098.3(CACNA1H):c.6642C>T (p.Thr2214=) rs1555521091
NM_021098.3(CACNA1H):c.6653G>A (p.Arg2218His) rs56885166
NM_021098.3(CACNA1H):c.6720C>G (p.Ala2240=) rs375725132
NM_021098.3(CACNA1H):c.6781C>T (p.Leu2261=) rs774253114
NM_021098.3(CACNA1H):c.6858C>T (p.His2286=) rs1468998569
NM_021098.3(CACNA1H):c.6943G>A (p.Gly2315Ser) rs200158741
NM_021098.3(CACNA1H):c.7026C>T (p.Thr2342=) rs745960698
NM_021098.3(CACNA1H):c.7057G>A (p.Val2353Met) rs150601404
NM_021098.3(CACNA1H):c.801C>T (p.Val267=) rs372726042
NM_021098.3(CACNA1H):c.804-4C>T rs905366458
NM_021098.3(CACNA1H):c.809A>C (p.Asn270Thr) rs200520956
NM_021098.3(CACNA1H):c.817A>T (p.Thr273Ser) rs58386301

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