ClinVar Miner

List of variants in gene SCN1B reported as likely benign for Cardiovascular phenotype

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Total variants: 47
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HGVS dbSNP gnomAD frequency
NM_001037.5(SCN1B):c.28G>A (p.Gly10Ser) rs72552027 0.00249
NM_001037.5(SCN1B):c.267C>T (p.Arg89=) rs140949982 0.00232
NM_001037.5(SCN1B):c.448+321G>A rs72558028 0.00173
NM_001037.5(SCN1B):c.588T>C (p.Asn196=) rs77244433 0.00117
NM_001037.5(SCN1B):c.5+7C>T rs28365106 0.00091
NM_001037.5(SCN1B):c.348G>A (p.Ser116=) rs375050816 0.00021
NM_001037.5(SCN1B):c.632G>A (p.Cys211Tyr) rs150721582 0.00021
NM_001037.5(SCN1B):c.471C>T (p.Ile157=) rs765269835 0.00014
NM_001037.5(SCN1B):c.96T>C (p.Tyr32=) rs143453040 0.00008
NM_001037.5(SCN1B):c.449-3C>A rs370937269 0.00007
NM_001037.5(SCN1B):c.415G>A (p.Val139Ile) rs560827790 0.00006
NM_001037.5(SCN1B):c.566C>T (p.Thr189Met) rs2305748 0.00006
NM_001037.5(SCN1B):c.561C>T (p.Ala187=) rs587781152 0.00005
NM_001037.5(SCN1B):c.121A>G (p.Ile41Val) rs72552028 0.00004
NM_001037.5(SCN1B):c.258C>T (p.Phe86=) rs751009774 0.00004
NM_001037.5(SCN1B):c.366C>T (p.His122=) rs761207251 0.00003
NM_001037.5(SCN1B):c.90C>T (p.Ala30=) rs753994622 0.00003
NM_001037.5(SCN1B):c.367G>A (p.Val123Ile) rs754215948 0.00002
NM_001037.5(SCN1B):c.546C>T (p.Tyr182=) rs775659068 0.00002
NM_001037.5(SCN1B):c.585G>A (p.Glu195=) rs753271148 0.00002
NM_001037.5(SCN1B):c.636G>A (p.Thr212=) rs763715229 0.00002
NM_001037.5(SCN1B):c.63C>T (p.Cys21=) rs200339565 0.00002
NM_001037.5(SCN1B):c.84C>T (p.Thr28=) rs147616219 0.00002
NM_001037.5(SCN1B):c.141C>T (p.Ser47=) rs769535020 0.00001
NM_001037.5(SCN1B):c.150C>T (p.Asn50=) rs147073518 0.00001
NM_001037.5(SCN1B):c.165C>T (p.Thr55=) rs768325106 0.00001
NM_001037.5(SCN1B):c.228G>A (p.Glu76=) rs992954476 0.00001
NM_001037.5(SCN1B):c.249T>C (p.Asp83=) rs1234271758 0.00001
NM_001037.5(SCN1B):c.255C>G (p.Arg85=) rs1060501166 0.00001
NM_001037.5(SCN1B):c.266G>A (p.Arg89His) rs138381632 0.00001
NM_001037.5(SCN1B):c.357C>T (p.Tyr119=) rs1266621411 0.00001
NM_001037.5(SCN1B):c.387C>T (p.Phe129=) rs891588693 0.00001
NM_001037.5(SCN1B):c.54C>T (p.Cys18=) rs1005312276 0.00001
NM_001037.5(SCN1B):c.594G>A (p.Ser198=) rs112564234 0.00001
NM_001037.5(SCN1B):c.640G>A (p.Val214Ile) rs77106213 0.00001
NM_001037.5(SCN1B):c.12G>A (p.Leu4=)
NM_001037.5(SCN1B):c.213G>A (p.Leu71=)
NM_001037.5(SCN1B):c.378G>A (p.Leu126=)
NM_001037.5(SCN1B):c.381C>G (p.Leu127=)
NM_001037.5(SCN1B):c.498C>T (p.Leu166=)
NM_001037.5(SCN1B):c.549G>A (p.Lys183=)
NM_001037.5(SCN1B):c.555C>T (p.Ile185=) rs1291900478
NM_001037.5(SCN1B):c.606C>G (p.Ala202=)
NM_001037.5(SCN1B):c.615T>C (p.Ser205=)
NM_001037.5(SCN1B):c.651C>T (p.Ala217=)
NM_001037.5(SCN1B):c.84C>A (p.Thr28=)
NM_001037.5(SCN1B):c.90C>A (p.Ala30=) rs753994622

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