ClinVar Miner

List of variants in gene CACNA1C reported as likely benign for History of neurodevelopmental disorder

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Total variants: 29
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HGVS dbSNP
NM_000719.7(CACNA1C):c.1176G>T (p.Gly392=) rs1051360
NM_000719.7(CACNA1C):c.1359C>T (p.Asp453=) rs200330469
NM_000719.7(CACNA1C):c.1524G>A (p.Arg508=) rs377431864
NM_000719.7(CACNA1C):c.1557C>A (p.Ala519=) rs186720824
NM_000719.7(CACNA1C):c.1686C>T (p.Ala562=)
NM_000719.7(CACNA1C):c.1734G>A (p.Leu578=) rs150692845
NM_000719.7(CACNA1C):c.1782C>T (p.Phe594=)
NM_000719.7(CACNA1C):c.1794C>T (p.Gly598=) rs116491041
NM_000719.7(CACNA1C):c.2067C>T (p.Phe689=) rs112170830
NM_000719.7(CACNA1C):c.2412T>A (p.Ile804=) rs1568589524
NM_000719.7(CACNA1C):c.2542_2544GAG[2] (p.Glu850del) rs575583988
NM_000719.7(CACNA1C):c.2766G>A (p.Pro922=) rs184684058
NM_000719.7(CACNA1C):c.3234C>T (p.Asp1078=) rs111606207
NM_000719.7(CACNA1C):c.3372C>T (p.Ser1124=)
NM_000719.7(CACNA1C):c.3567C>T (p.Cys1189=) rs202058956
NM_000719.7(CACNA1C):c.3642C>T (p.Tyr1214=) rs56394008
NM_000719.7(CACNA1C):c.3780C>A (p.Gly1260=) rs201258230
NM_000719.7(CACNA1C):c.3789C>T (p.Thr1263=)
NM_000719.7(CACNA1C):c.4563C>T (p.Leu1521=) rs1569144723
NM_000719.7(CACNA1C):c.4611C>T (p.Arg1537=) rs372702466
NM_000719.7(CACNA1C):c.5214C>A (p.Gly1738=) rs199538058
NM_000719.7(CACNA1C):c.5451C>T (p.His1817=) rs113239186
NM_000719.7(CACNA1C):c.5478G>A (p.Ala1826=) rs200283756
NM_000719.7(CACNA1C):c.5593G>A (p.Glu1865Lys) rs200231105
NM_000719.7(CACNA1C):c.5639G>A (p.Arg1880Gln) rs182208896
NM_000719.7(CACNA1C):c.5747A>G (p.Gln1916Arg) rs186867242
NM_000719.7(CACNA1C):c.6087C>T (p.Phe2029=)
NM_000719.7(CACNA1C):c.966C>T (p.His322=) rs112539787
NM_000719.7(CACNA1C):c.984C>T (p.Asn328=) rs374050127

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