ClinVar Miner

List of variants in gene SCN1B reported as likely benign for not specified

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Gene type:
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Total variants: 47
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HGVS dbSNP
NM_001037.5(SCN1B):c.*17C>T rs1057522560
NM_001037.5(SCN1B):c.*23A>G rs868601122
NM_001037.5(SCN1B):c.-26G>C rs1057520587
NM_001037.5(SCN1B):c.-27G>T rs758958222
NM_001037.5(SCN1B):c.-31G>A rs776361009
NM_001037.5(SCN1B):c.-41C>G rs1330923826
NM_001037.5(SCN1B):c.-9C>A rs66671189
NM_001037.5(SCN1B):c.192T>C (p.Thr64=) rs1057522819
NM_001037.5(SCN1B):c.207+10T>C rs1057523254
NM_001037.5(SCN1B):c.207+13C>T rs373809858
NM_001037.5(SCN1B):c.207+19C>A rs201872896
NM_001037.5(SCN1B):c.23T>C (p.Val8Ala) rs786205833
NM_001037.5(SCN1B):c.249T>C (p.Asp83=) rs1234271758
NM_001037.5(SCN1B):c.258C>T (p.Phe86=) rs751009774
NM_001037.5(SCN1B):c.273G>A (p.Val91=) rs16969926
NM_001037.5(SCN1B):c.28G>A (p.Gly10Ser) rs72552027
NM_001037.5(SCN1B):c.366C>T (p.His122=) rs761207251
NM_001037.5(SCN1B):c.396C>T (p.Tyr132=) rs181115510
NM_001037.5(SCN1B):c.41-14T>C rs778258172
NM_001037.5(SCN1B):c.412G>A (p.Val138Ile) rs72558029
NM_001037.5(SCN1B):c.414C>T (p.Val138=) rs757116018
NM_001037.5(SCN1B):c.448+111C>T rs758654948
NM_001037.5(SCN1B):c.448+189C>A rs766373298
NM_001037.5(SCN1B):c.448+193G>A rs66876876
NM_001037.5(SCN1B):c.448+278G>A rs1057521627
NM_001037.5(SCN1B):c.448+295G>T rs786205828
NM_001037.5(SCN1B):c.448+30G>A rs369058711
NM_001037.5(SCN1B):c.448+321G>A rs72558028
NM_001037.5(SCN1B):c.448+345C>T rs754815235
NM_001037.5(SCN1B):c.448+379G>T rs1555720853
NM_001037.5(SCN1B):c.448+7C>T rs748379474
NM_001037.5(SCN1B):c.448+8G>A rs200222933
NM_001037.5(SCN1B):c.449-10G>A rs1049927697
NM_001037.5(SCN1B):c.449-9C>A rs786205829
NM_001037.5(SCN1B):c.471C>T (p.Ile157=) rs765269835
NM_001037.5(SCN1B):c.5+7C>T rs28365106
NM_001037.5(SCN1B):c.501T>C (p.Ile167=) rs16969930
NM_001037.5(SCN1B):c.522C>T (p.Leu174=) rs35478147
NM_001037.5(SCN1B):c.546C>T (p.Tyr182=) rs775659068
NM_001037.5(SCN1B):c.585G>A (p.Glu195=) rs753271148
NM_001037.5(SCN1B):c.588T>C (p.Asn196=) rs77244433
NM_001037.5(SCN1B):c.591-5C>T rs1555721514
NM_001037.5(SCN1B):c.594G>A (p.Ser198=) rs112564234
NM_001037.5(SCN1B):c.6-19C>G rs1442747292
NM_001037.5(SCN1B):c.632G>A (p.Cys211Tyr) rs150721582
NM_001037.5(SCN1B):c.640G>A (p.Val214Ile) rs77106213
NM_001037.5(SCN1B):c.90C>T (p.Ala30=) rs753994622

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