ClinVar Miner

List of variants in gene LOC110121288, SCN10A studied for Brugada syndrome

Included ClinVar conditions (25):
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Gene type:
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Total variants: 30
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HGVS dbSNP
NM_006514.3(SCN10A):c.2814C>T (p.Phe938=) rs200870389
NM_006514.3(SCN10A):c.2816C>T (p.Pro939Leu) rs202174472
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.2842G>C (p.Val948Leu) 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.2940C>G (p.Pro980=) rs1192005964
NM_006514.3(SCN10A):c.2972C>T (p.Pro991Leu) rs138413438
NM_006514.3(SCN10A):c.2988T>C (p.Ser996=) rs375913659
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.3133C>A (p.Pro1045Thr) rs73062575
NM_006514.3(SCN10A):c.3138G>A (p.Arg1046=) rs371613636
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)
NM_006514.3(SCN10A):c.3237C>T (p.Asp1079=) rs745921364
NM_006514.3(SCN10A):c.3238G>A (p.Asp1080Asn) rs376528831
NM_006514.3(SCN10A):c.3255G>A (p.Glu1085=) rs143610297
NM_006514.3(SCN10A):c.3289A>C (p.Ile1097Leu) rs1397301108
NM_006514.3(SCN10A):c.3291C>G (p.Ile1097Met) rs148041371
NM_006514.3(SCN10A):c.3340T>C (p.Cys1114Arg)
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.3440G>A (p.Arg1147His) rs375926577
NM_006514.3(SCN10A):c.3482T>C (p.Met1161Thr) rs200713724
NM_006514.3(SCN10A):c.3507+10G>A rs767411176

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