ClinVar Miner

List of variants in gene SCN3B reported as uncertain significance for Brugada syndrome

Included ClinVar conditions (44):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 66
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HGVS dbSNP gnomAD frequency
NM_001040151.2(SCN3B):c.29T>C (p.Leu10Pro) rs121918282 0.00036
NM_001040151.2(SCN3B):c.583G>A (p.Ala195Thr) rs375755770 0.00016
NM_001040151.2(SCN3B):c.*4588T>C rs765294617 0.00006
NM_001040151.2(SCN3B):c.*2366G>A rs867302682 0.00004
NM_001040151.2(SCN3B):c.106G>A (p.Val36Met) rs147803210 0.00004
NM_001040151.2(SCN3B):c.160G>A (p.Val54Met) rs377237114 0.00004
NM_001040151.2(SCN3B):c.161T>G (p.Val54Gly) rs587777555 0.00004
NM_001040151.2(SCN3B):c.199G>A (p.Glu67Lys) rs140381249 0.00004
NM_001040151.2(SCN3B):c.416G>A (p.Arg139Gln) rs770801747 0.00004
NM_001040151.2(SCN3B):c.73G>T (p.Val25Leu) rs746954414 0.00004
NM_001040151.2(SCN3B):c.98C>T (p.Thr33Met) rs140041927 0.00004
NM_001040151.2(SCN3B):c.14A>G (p.Asn5Ser) rs369522500 0.00003
NM_001040151.2(SCN3B):c.395G>A (p.Arg132Gln) rs755967151 0.00003
NM_001040151.2(SCN3B):c.415C>T (p.Arg139Trp) rs368054375 0.00003
NM_001040151.2(SCN3B):c.232C>T (p.Arg78Trp) rs764587765 0.00002
NM_001040151.2(SCN3B):c.233G>A (p.Arg78Gln) rs375545539 0.00002
NM_001040151.2(SCN3B):c.394C>T (p.Arg132Trp) rs371558196 0.00002
NM_001040151.2(SCN3B):c.55+3A>G rs767074394 0.00002
NM_001040151.2(SCN3B):c.614A>G (p.Asn205Ser) rs781244975 0.00002
NM_001040151.2(SCN3B):c.-326C>G rs886047906 0.00001
NM_001040151.2(SCN3B):c.260C>G (p.Pro87Arg) rs371050389 0.00001
NM_001040151.2(SCN3B):c.389C>T (p.Ala130Val) rs587777556 0.00001
NM_001040151.2(SCN3B):c.392A>G (p.His131Arg) rs1457138925 0.00001
NM_001040151.2(SCN3B):c.410C>T (p.Thr137Met) rs750476444 0.00001
NM_001040151.2(SCN3B):c.584+2dup rs1265045446 0.00001
NM_001040151.2(SCN3B):c.632T>G (p.Val211Gly) rs750969469 0.00001
NC_000011.9:g.(?_123504851)_(123516478_?)dup
NM_001040151.2(SCN3B):c.*1007dup rs72553907
NM_001040151.2(SCN3B):c.*1948TATT[2] rs776449566
NM_001040151.2(SCN3B):c.*2795GAA[1] rs544984224
NM_001040151.2(SCN3B):c.*447C>A rs80017720
NM_001040151.2(SCN3B):c.-62del rs886047904
NM_001040151.2(SCN3B):c.117C>G (p.Asn39Lys)
NM_001040151.2(SCN3B):c.118C>T (p.Pro40Ser) rs762633602
NM_001040151.2(SCN3B):c.139T>A (p.Ser47Thr)
NM_001040151.2(SCN3B):c.13A>G (p.Asn5Asp)
NM_001040151.2(SCN3B):c.173C>T (p.Thr58Met)
NM_001040151.2(SCN3B):c.205G>A (p.Gly69Ser) rs1020414330
NM_001040151.2(SCN3B):c.219+2T>C rs750105827
NM_001040151.2(SCN3B):c.241C>T (p.His81Tyr)
NM_001040151.2(SCN3B):c.244C>T (p.Gln82Ter)
NM_001040151.2(SCN3B):c.256del (p.Ser86fs) rs1955806072
NM_001040151.2(SCN3B):c.272G>A (p.Arg91His)
NM_001040151.2(SCN3B):c.295G>A (p.Asp99Asn) rs753656773
NM_001040151.2(SCN3B):c.301C>A (p.Gln101Lys)
NM_001040151.2(SCN3B):c.31G>A (p.Ala11Thr) rs1955959844
NM_001040151.2(SCN3B):c.322C>T (p.Leu108Phe)
NM_001040151.2(SCN3B):c.371G>A (p.Arg124Gln)
NM_001040151.2(SCN3B):c.38T>C (p.Leu13Pro) rs1955959753
NM_001040151.2(SCN3B):c.392_397del (p.His131_Arg132del) rs2137241970
NM_001040151.2(SCN3B):c.407A>G (p.Lys136Arg)
NM_001040151.2(SCN3B):c.409ACG[1] (p.Thr138del) rs72552144
NM_001040151.2(SCN3B):c.423C>G (p.Ile141Met) rs879253730
NM_001040151.2(SCN3B):c.436A>G (p.Thr146Ala)
NM_001040151.2(SCN3B):c.446C>G (p.Ala149Gly) rs2137236047
NM_001040151.2(SCN3B):c.46A>G (p.Ile16Val) rs1306658128
NM_001040151.2(SCN3B):c.50A>G (p.Tyr17Cys)
NM_001040151.2(SCN3B):c.535T>C (p.Tyr179His)
NM_001040151.2(SCN3B):c.541T>A (p.Tyr181Asn)
NM_001040151.2(SCN3B):c.574C>G (p.Gln192Glu)
NM_001040151.2(SCN3B):c.584C>T (p.Ala195Val)
NM_001040151.2(SCN3B):c.585-1G>C
NM_001040151.2(SCN3B):c.601A>G (p.Ile201Val)
NM_001040151.2(SCN3B):c.618G>C (p.Lys206Asn)
NM_001040151.2(SCN3B):c.92C>T (p.Ser31Leu)
NM_001040151.2(SCN3B):c.95A>G (p.Glu32Gly)

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