ClinVar Miner

List of variants in gene SCN1B studied for not provided

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Total variants: 76
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HGVS dbSNP
NM_001037.5(SCN1B):c.-226C>T
NM_001037.5(SCN1B):c.-9C>A rs66671189
NM_001037.5(SCN1B):c.108del (p.Phe36fs) rs1064794589
NM_001037.5(SCN1B):c.134G>A (p.Arg45His) rs180943300
NM_001037.5(SCN1B):c.136C>T (p.Arg46Cys) rs371646049
NM_001037.5(SCN1B):c.13C>A (p.Leu5Met) rs1064796847
NM_001037.5(SCN1B):c.141C>T (p.Ser47=)
NM_001037.5(SCN1B):c.168G>C (p.Glu56Asp) rs886043547
NM_001037.5(SCN1B):c.196G>T (p.Glu66Ter) rs1193962006
NM_001037.5(SCN1B):c.1A>C (p.Met1Leu) rs1375857363
NM_001037.5(SCN1B):c.207+55G>A
NM_001037.5(SCN1B):c.208-136del
NM_001037.5(SCN1B):c.208-320T>C
NM_001037.5(SCN1B):c.214C>T (p.Arg72Cys) rs746782800
NM_001037.5(SCN1B):c.22G>C (p.Val8Leu) rs786205832
NM_001037.5(SCN1B):c.248A>T (p.Asp83Val) rs1057524601
NM_001037.5(SCN1B):c.254G>A (p.Arg85His) rs16969925
NM_001037.5(SCN1B):c.266G>A (p.Arg89His) rs138381632
NM_001037.5(SCN1B):c.267C>T (p.Arg89=) rs140949982
NM_001037.5(SCN1B):c.268G>A (p.Val90Met) rs778461222
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.347del (p.Ser116fs) rs794727487
NM_001037.5(SCN1B):c.352G>T (p.Asp118Tyr) rs761925369
NM_001037.5(SCN1B):c.363C>G (p.Cys121Trp) rs104894718
NM_001037.5(SCN1B):c.367G>A (p.Val123Ile) rs754215948
NM_001037.5(SCN1B):c.374G>A (p.Arg125His) rs759839781
NM_001037.5(SCN1B):c.38T>C (p.Leu13Pro) rs786205834
NM_001037.5(SCN1B):c.396C>G (p.Tyr132Ter) rs181115510
NM_001037.5(SCN1B):c.396C>T (p.Tyr132=) rs181115510
NM_001037.5(SCN1B):c.40+15G>A
NM_001037.5(SCN1B):c.40+9G>A
NM_001037.5(SCN1B):c.405C>G (p.Asn135Lys) rs372630267
NM_001037.5(SCN1B):c.41-239T>G
NM_001037.5(SCN1B):c.41-313T>A
NM_001037.5(SCN1B):c.41-3C>T rs1064796801
NM_001037.5(SCN1B):c.412G>A (p.Val138Ile) rs72558029
NM_001037.5(SCN1B):c.429C>T (p.His143=)
NM_001037.5(SCN1B):c.448+100G>T rs779658201
NM_001037.5(SCN1B):c.448+103C>T rs372041274
NM_001037.5(SCN1B):c.448+10G>C rs959703607
NM_001037.5(SCN1B):c.448+112G>A rs72558026
NM_001037.5(SCN1B):c.448+126G>T rs746419159
NM_001037.5(SCN1B):c.448+135del rs761070541
NM_001037.5(SCN1B):c.448+144A>G rs763402433
NM_001037.5(SCN1B):c.448+193G>A rs66876876
NM_001037.5(SCN1B):c.448+217C>T rs1085307597
NM_001037.5(SCN1B):c.448+337G>A rs369032304
NM_001037.5(SCN1B):c.448+354G>A rs752552401
NM_001037.5(SCN1B):c.448+45G>A rs762453360
NM_001037.5(SCN1B):c.448+4_448+12del rs1322172446
NM_001037.5(SCN1B):c.448+610T>C
NM_001037.5(SCN1B):c.448+679A>C
NM_001037.5(SCN1B):c.448+88G>A rs267607028
NM_001037.5(SCN1B):c.448+8G>C rs200222933
NM_001037.5(SCN1B):c.449-1G>A rs786205835
NM_001037.5(SCN1B):c.449C>T (p.Ala150Val) rs1131691415
NM_001037.5(SCN1B):c.457G>A (p.Asp153Asn) rs72550247
NM_001037.5(SCN1B):c.465A>G (p.Ala155=)
NM_001037.5(SCN1B):c.472G>A (p.Val158Met) rs138450474
NM_001037.5(SCN1B):c.477delinsATGATGGATG (p.Glu160_Ile161insTer) rs1131691338
NM_001037.5(SCN1B):c.508T>C (p.Leu170=) rs748491132
NM_001037.5(SCN1B):c.508T>G (p.Leu170Val) rs748491132
NM_001037.5(SCN1B):c.561C>T (p.Ala187=) rs587781152
NM_001037.5(SCN1B):c.590+1G>A rs112767703
NM_001037.5(SCN1B):c.590C>T (p.Ala197Val) rs554201948
NM_001037.5(SCN1B):c.615dup (p.Glu206Ter) rs1555721523
NM_001037.5(SCN1B):c.621C>T (p.Ser207=) rs1378669075
NM_001037.5(SCN1B):c.627G>C (p.Glu209Asp) rs745580499
NM_001037.5(SCN1B):c.630C>A (p.Asn210Lys) rs786205836
NM_001037.5(SCN1B):c.632G>A (p.Cys211Tyr) rs150721582
NM_001037.5(SCN1B):c.638G>A (p.Gly213Asp) rs201209882
NM_001037.5(SCN1B):c.644del (p.Gln215fs) rs1555721533
NM_001037.5(SCN1B):c.73G>A (p.Asp25Asn) rs786205837
NM_001037.5(SCN1B):c.82A>G (p.Thr28Ala) rs786205838
NM_001037.5(SCN1B):c.85G>C (p.Glu29Gln) rs767384862

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