ClinVar Miner

List of variants studied for Brugada syndrome 3

Included ClinVar conditions (3):
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Total variants: 17
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NM_000719.7(CACNA1C):c.116C>T (p.Ala39Val) rs121912776
NM_000719.7(CACNA1C):c.1468G>A (p.Gly490Arg) rs121912775
NM_000719.7(CACNA1C):c.200G>A (p.Ser67Asn)
NM_000719.7(CACNA1C):c.2T>C (p.Met1Thr) rs761378545
NM_000719.7(CACNA1C):c.3679G>A (p.Val1227Ile) rs373124557
NM_000719.7(CACNA1C):c.4436T>C (p.Phe1479Ser)
NM_000719.7(CACNA1C):c.5098G>A (p.Gly1700Ser) rs761966966
NM_000719.7(CACNA1C):c.5120T>C (p.Val1707Ala) rs531161884
NM_000719.7(CACNA1C):c.5456G>A (p.Arg1819Gln) rs764212214
NM_000719.7(CACNA1C):c.5731G>C (p.Gly1911Arg) rs374528680
NM_000719.7(CACNA1C):c.6001G>A (p.Gly2001Ser) rs552478740
NM_000719.7(CACNA1C):c.6011G>T (p.Gly2004Val) rs374991642
NM_000719.7(CACNA1C):c.6040G>A (p.Val2014Ile) rs199473660
NM_000719.7(CACNA1C):c.65G>T (p.Ser22Ile) rs769703001
NM_000719.7(CACNA1C):c.694G>C (p.Asp232His)
NM_000719.7(CACNA1C):c.722T>C (p.Val241Ala)
NM_000719.7(CACNA1C):c.98A>G (p.Asn33Ser) rs535608443

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