ClinVar Miner

List of variants in gene CACNA1C reported as uncertain significance for not specified

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Total variants: 21
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HGVS dbSNP
NM_000719.7(CACNA1C):c.130C>G (p.Pro44Ala) rs1057518456
NM_000719.7(CACNA1C):c.1468G>A (p.Gly490Arg) rs121912775
NM_000719.7(CACNA1C):c.1487G>A (p.Arg496Gln) rs369255950
NM_000719.7(CACNA1C):c.154T>C (p.Trp52Arg) rs786205765
NM_000719.7(CACNA1C):c.1673C>T (p.Thr558Met) rs572234918
NM_000719.7(CACNA1C):c.2311_2313GAG[1] (p.Glu772del) rs786205770
NM_000719.7(CACNA1C):c.2517C>A (p.Asn839Lys) rs774002530
NM_000719.7(CACNA1C):c.3061T>G (p.Cys1021Gly) rs1057518301
NM_000719.7(CACNA1C):c.3367C>T (p.Arg1123Cys) rs1057518445
NM_000719.7(CACNA1C):c.3679G>A (p.Val1227Ile) rs373124557
NM_000719.7(CACNA1C):c.4782G>A (p.Lys1594=) rs1336965329
NM_000719.7(CACNA1C):c.4942G>A (p.Ala1648Thr) rs370432385
NM_000719.7(CACNA1C):c.5145G>A (p.Arg1715=) rs761205516
NM_000719.7(CACNA1C):c.5717G>A (p.Arg1906Gln) rs758166168
NM_000719.7(CACNA1C):c.5883C>T (p.Ser1961=) rs1291974001
NM_000719.7(CACNA1C):c.5918G>A (p.Arg1973Gln) rs112414325
NM_000719.7(CACNA1C):c.6019G>A (p.Ala2007Thr) rs750411964
NM_000719.7(CACNA1C):c.6040G>A (p.Val2014Ile) rs199473660
NM_000719.7(CACNA1C):c.6329dup (p.Glu2111fs) rs771708175
NM_000719.7(CACNA1C):c.911T>C (p.Ile304Thr) rs201756421
NM_000719.7(CACNA1C):c.990G>A (p.Thr330=) rs371837699

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