ClinVar Miner

List of variants in gene combination LOC110121288, SCN10A reported as uncertain significance for Brugada syndrome

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Total variants: 16
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NM_006514.3(SCN10A):c.2833C>T (p.Pro945Ser) rs372907454
NM_006514.3(SCN10A):c.2842G>A (p.Val948Met) rs145694222
NM_006514.3(SCN10A):c.2854C>G (p.Pro952Ala) rs370880796
NM_006514.3(SCN10A):c.2902del (p.Arg968fs) rs1553616744
NM_006514.3(SCN10A):c.3061C>T (p.Gln1021Ter) rs751252167
NM_006514.3(SCN10A):c.3070G>A (p.Val1024Met) rs201106879
NM_006514.3(SCN10A):c.3151G>A (p.Gly1051Arg) rs374447261
NM_006514.3(SCN10A):c.3170T>G (p.Leu1057Arg) rs1559424975
NM_006514.3(SCN10A):c.3191C>T (p.Thr1064Met) rs774803610
NM_006514.3(SCN10A):c.3289A>C (p.Ile1097Leu) rs1397301108
NM_006514.3(SCN10A):c.3340T>C (p.Cys1114Arg) rs771127702
NM_006514.3(SCN10A):c.3355T>A (p.Cys1119Ser) rs1450059546
NM_006514.3(SCN10A):c.3361C>T (p.Arg1121Cys) rs146965005
NM_006514.3(SCN10A):c.3374G>C (p.Cys1125Ser)
NM_006514.3(SCN10A):c.3417G>C (p.Trp1139Cys) rs143744796
NM_006514.3(SCN10A):c.3482T>C (p.Met1161Thr) rs200713724

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