ClinVar Miner

List of variants in gene CACNA1H reported as likely benign for Idiopathic generalized epilepsy; Hyperaldosteronism, familial, type IV

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Total variants: 47
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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.1068C>T (p.Asn356=) rs369894677
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.1638C>T (p.Cys546=) rs1355615330
NM_021098.3(CACNA1H):c.1983G>A (p.Pro661=) rs56875953
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.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.2772C>T (p.Leu924=) rs777961380
NM_021098.3(CACNA1H):c.3114C>T (p.Phe1038=) rs374946880
NM_021098.3(CACNA1H):c.3636C>A (p.Thr1212=) rs767435491
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.3933C>T (p.Ile1311=) rs200353061
NM_021098.3(CACNA1H):c.3970-10C>T rs377114648
NM_021098.3(CACNA1H):c.4035G>A (p.Val1345=) rs747258959
NM_021098.3(CACNA1H):c.4045G>A (p.Ala1349Thr) rs200400235
NM_021098.3(CACNA1H):c.4219C>T (p.Leu1407=) rs1041269521
NM_021098.3(CACNA1H):c.4224-9C>T rs1287379368
NM_021098.3(CACNA1H):c.4351-6C>T rs377612703
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.4881C>T (p.Ile1627=) rs576335604
NM_021098.3(CACNA1H):c.5052G>A (p.Leu1684=) rs374459574
NM_021098.3(CACNA1H):c.5145C>T (p.Arg1715=) rs1182772693
NM_021098.3(CACNA1H):c.5174-5C>T rs199536335
NM_021098.3(CACNA1H):c.5511C>T (p.Pro1837=) rs58819745
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.6327C>T (p.Cys2109=) rs777082647
NM_021098.3(CACNA1H):c.63C>T (p.Gly21=) rs1261320353
NM_021098.3(CACNA1H):c.6480G>A (p.Leu2160=) rs1555520987
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.6858C>T (p.His2286=) rs1468998569
NM_021098.3(CACNA1H):c.7026C>T (p.Thr2342=) rs745960698
NM_021098.3(CACNA1H):c.801C>T (p.Val267=) rs372726042
NM_021098.3(CACNA1H):c.804-4C>T rs905366458

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