ClinVar Miner

List of variants in gene SCN1B studied for not specified

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Gene type:
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Total variants: 84
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HGVS dbSNP
NM_001037.5(SCN1B):c.*13G>A rs1555721564
NM_001037.5(SCN1B):c.*17C>T rs1057522560
NM_001037.5(SCN1B):c.*23A>G rs868601122
NM_001037.5(SCN1B):c.*76G>T
NM_001037.5(SCN1B):c.-1C>T rs1057518527
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.-40C>G rs587781150
NM_001037.5(SCN1B):c.-41C>G rs1330923826
NM_001037.5(SCN1B):c.-9C>A rs66671189
NM_001037.5(SCN1B):c.121A>G (p.Ile41Val) rs72552028
NM_001037.5(SCN1B):c.133C>T (p.Arg45Cys) rs757554677
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+14G>A rs16969924
NM_001037.5(SCN1B):c.207+19C>A rs201872896
NM_001037.5(SCN1B):c.207+7G>A rs374588869
NM_001037.5(SCN1B):c.208-14C>T rs72550272
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.267C>T (p.Arg89=) rs140949982
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.300C>T (p.Asp100=) rs16969927
NM_001037.5(SCN1B):c.348G>A (p.Ser116=) rs375050816
NM_001037.5(SCN1B):c.351C>T (p.Gly117=) rs3746255
NM_001037.5(SCN1B):c.366C>T (p.His122=) rs761207251
NM_001037.5(SCN1B):c.38T>C (p.Leu13Pro) rs786205834
NM_001037.5(SCN1B):c.396C>T (p.Tyr132=) rs181115510
NM_001037.5(SCN1B):c.40+15G>T rs72556351
NM_001037.5(SCN1B):c.40+6T>C rs587781151
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+112G>A rs72558026
NM_001037.5(SCN1B):c.448+129G>T rs1060499899
NM_001037.5(SCN1B):c.448+167C>G rs529053826
NM_001037.5(SCN1B):c.448+181T>C rs55742440
NM_001037.5(SCN1B):c.448+189C>A rs766373298
NM_001037.5(SCN1B):c.448+193G>A rs66876876
NM_001037.5(SCN1B):c.448+199G>A rs946927516
NM_001037.5(SCN1B):c.448+225C>T rs369588692
NM_001037.5(SCN1B):c.448+230C>T rs769132369
NM_001037.5(SCN1B):c.448+278G>A rs1057521627
NM_001037.5(SCN1B):c.448+295G>T rs786205828
NM_001037.5(SCN1B):c.448+296C>A rs67701503
NM_001037.5(SCN1B):c.448+29C>T rs186759145
NM_001037.5(SCN1B):c.448+301G>A rs67486287
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.448+8G>C rs200222933
NM_001037.5(SCN1B):c.449-10G>A rs1049927697
NM_001037.5(SCN1B):c.449-3C>A rs370937269
NM_001037.5(SCN1B):c.449-9C>A rs786205829
NM_001037.5(SCN1B):c.457G>A (p.Asp153Asn) rs72550247
NM_001037.5(SCN1B):c.471C>T (p.Ile157=) rs765269835
NM_001037.5(SCN1B):c.492T>C (p.Tyr164=) rs535042320
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.561C>T (p.Ala187=) rs587781152
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.590+16G>A rs201053958
NM_001037.5(SCN1B):c.591-14C>A rs28365109
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.63C>T (p.Cys21=) rs200339565
NM_001037.5(SCN1B):c.640G>A (p.Val214Ile) rs77106213
NM_001037.5(SCN1B):c.67del (p.Glu23fs) rs1060499898
NM_001037.5(SCN1B):c.90C>T (p.Ala30=) rs753994622
NM_199037.3(SCN1B):c.749G>C (p.Arg250Thr) rs67486287
NM_199037.3(SCN1B):c.751G>A (p.Val251Ile) rs193922728

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