ClinVar Miner

List of variants in gene SCN1B reported as benign

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Total variants: 38
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HGVS dbSNP
NM_001037.5(SCN1B):c.*76G>T
NM_001037.5(SCN1B):c.-40C>G rs587781150
NM_001037.5(SCN1B):c.-9C>A rs66671189
NM_001037.5(SCN1B):c.207+14G>A rs16969924
NM_001037.5(SCN1B):c.207+7G>A rs374588869
NM_001037.5(SCN1B):c.208-14C>T rs72550272
NM_001037.5(SCN1B):c.208-320T>C
NM_001037.5(SCN1B):c.267C>T (p.Arg89=) rs140949982
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.40+15G>T rs72556351
NM_001037.5(SCN1B):c.40+6T>C rs587781151
NM_001037.5(SCN1B):c.41-239T>G
NM_001037.5(SCN1B):c.41-313T>A
NM_001037.5(SCN1B):c.412G>A (p.Val138Ile) rs72558029
NM_001037.5(SCN1B):c.448+112G>A rs72558026
NM_001037.5(SCN1B):c.448+167C>G rs529053826
NM_001037.5(SCN1B):c.448+181T>C rs55742440
NM_001037.5(SCN1B):c.448+193G>A rs66876876
NM_001037.5(SCN1B):c.448+230C>T rs769132369
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+314C>A rs373295182
NM_001037.5(SCN1B):c.448+321G>A rs72558028
NM_001037.5(SCN1B):c.448+610T>C
NM_001037.5(SCN1B):c.448+679A>C
NM_001037.5(SCN1B):c.448+8G>C rs200222933
NM_001037.5(SCN1B):c.492T>C (p.Tyr164=) rs535042320
NM_001037.5(SCN1B):c.501T>C (p.Ile167=) rs16969930
NM_001037.5(SCN1B):c.561C>T (p.Ala187=) rs587781152
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.63C>T (p.Cys21=) rs200339565
NM_199037.3(SCN1B):c.749G>C (p.Arg250Thr) rs67486287

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