ClinVar Miner

List of variants in gene SCN8A reported as uncertain significance by Illumina Clinical Services Laboratory,Illumina

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Gene type:
ClinVar version:
Total variants: 55
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HGVS dbSNP
NM_014191.4(SCN8A):c.*128C>T rs531602660
NM_014191.4(SCN8A):c.*1317C>T rs886049592
NM_014191.4(SCN8A):c.*1803C>G rs886049593
NM_014191.4(SCN8A):c.*2303T>C rs886049594
NM_014191.4(SCN8A):c.*2401T>G rs763119399
NM_014191.4(SCN8A):c.*243T>A rs886049586
NM_014191.4(SCN8A):c.*2484C>T rs886049595
NM_014191.4(SCN8A):c.*2662T>C rs760569392
NM_014191.4(SCN8A):c.*2832A>T rs886049596
NM_014191.4(SCN8A):c.*3047T>C rs561570521
NM_014191.4(SCN8A):c.*336T>A rs886049587
NM_014191.4(SCN8A):c.*3749G>T rs781671258
NM_014191.4(SCN8A):c.*3802G>A rs886049598
NM_014191.4(SCN8A):c.*3835T>C rs886049599
NM_014191.4(SCN8A):c.*395C>T rs779857857
NM_014191.4(SCN8A):c.*4077T>C rs886049600
NM_014191.4(SCN8A):c.*4150C>A rs886049601
NM_014191.4(SCN8A):c.*4174A>G rs537437117
NM_014191.4(SCN8A):c.*4196G>A rs774353077
NM_014191.4(SCN8A):c.*4223C>T rs886049602
NM_014191.4(SCN8A):c.*4311C>G rs886049603
NM_014191.4(SCN8A):c.*460C>T rs886049588
NM_014191.4(SCN8A):c.*4785_*4786TG[10] rs371717199
NM_014191.4(SCN8A):c.*4785_*4786TG[11] rs371717199
NM_014191.4(SCN8A):c.*4785_*4786TG[7] rs371717199
NM_014191.4(SCN8A):c.*4785_*4786TG[8] rs371717199
NM_014191.4(SCN8A):c.*5271G>C rs569034973
NM_014191.4(SCN8A):c.*559T>C rs886049589
NM_014191.4(SCN8A):c.*708A>T rs886049590
NM_014191.4(SCN8A):c.*791A>G rs886049591
NM_014191.4(SCN8A):c.*884A>C rs527789517
NM_014191.4(SCN8A):c.*965A>G rs552654863
NM_014191.4(SCN8A):c.-102G>C rs886049579
NM_014191.4(SCN8A):c.-157A>G rs886049578
NM_014191.4(SCN8A):c.-67C>T rs374729451
NM_014191.4(SCN8A):c.-95G>A rs886049580
NM_014191.4(SCN8A):c.1173C>T (p.Phe391=) rs886049582
NM_014191.4(SCN8A):c.1977C>T (p.Ile659=) rs886049583
NM_014191.4(SCN8A):c.2432A>G (p.Tyr811Cys) rs886049584
NM_014191.4(SCN8A):c.2508C>T (p.Asp836=) rs772945312
NM_014191.4(SCN8A):c.2901+13T>A rs375198486
NM_014191.4(SCN8A):c.3060G>C (p.Gln1020His) rs528718802
NM_014191.4(SCN8A):c.3158T>G (p.Ile1053Ser) rs587780453
NM_014191.4(SCN8A):c.340A>G (p.Ile114Val) rs527246057
NM_014191.4(SCN8A):c.3423A>G (p.Pro1141=) rs376102810
NM_014191.4(SCN8A):c.3442G>A (p.Val1148Met) rs536452913
NM_014191.4(SCN8A):c.3480C>T (p.Cys1160=) rs760251864
NM_014191.4(SCN8A):c.3491-12C>T rs369532655
NM_014191.4(SCN8A):c.402T>C (p.Phe134=) rs559668426
NM_014191.4(SCN8A):c.4134G>T (p.Lys1378Asn) rs752899010
NM_014191.4(SCN8A):c.4141G>C (p.Glu1381Gln) rs886049585
NM_014191.4(SCN8A):c.4542C>T (p.Ile1514=) rs370105734
NM_014191.4(SCN8A):c.564C>G (p.Thr188=) rs886049581
NM_014191.4(SCN8A):c.5795G>C (p.Arg1932Pro) rs371766742
NM_014191.4(SCN8A):c.751C>T (p.Leu251=) rs200307006

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