ClinVar Miner

List of variants in gene SCN8A reported as benign

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Gene type:
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Total variants: 78
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HGVS dbSNP
NM_001330260.2(SCN8A):c.-67C>T rs374729451
NM_001330260.2(SCN8A):c.1135-48C>T rs2291265
NM_001330260.2(SCN8A):c.1215G>A (p.Leu405=) rs751093826
NM_001330260.2(SCN8A):c.1470A>G (p.Glu490=) rs187115247
NM_001330260.2(SCN8A):c.1509C>A (p.Leu503=) rs376749872
NM_001330260.2(SCN8A):c.1588C>T (p.Arg530Trp) rs761336234
NM_001330260.2(SCN8A):c.1636-237G>A rs74091624
NM_001330260.2(SCN8A):c.1677C>T (p.His559=) rs202212399
NM_001330260.2(SCN8A):c.1819G>A (p.Ala607Thr) rs367949317
NM_001330260.2(SCN8A):c.1833G>T (p.Arg611=) rs35242963
NM_001330260.2(SCN8A):c.1960G>A (p.Gly654Ser) rs905574009
NM_001330260.2(SCN8A):c.2056G>A (p.Asp686Asn) rs373073046
NM_001330260.2(SCN8A):c.2098A>T (p.Ile700Leu) rs187153231
NM_001330260.2(SCN8A):c.2118T>C (p.Asn706=) rs555404940
NM_001330260.2(SCN8A):c.2371-6A>G rs187002252
NM_001330260.2(SCN8A):c.2394G>A (p.Ala798=) rs201392695
NM_001330260.2(SCN8A):c.2475C>A (p.Val825=) rs535061303
NM_001330260.2(SCN8A):c.2632C>T (p.Leu878=) rs372582842
NM_001330260.2(SCN8A):c.2670C>T (p.Ala890=) rs374452942
NM_001330260.2(SCN8A):c.2901+277T>C rs74091656
NM_001330260.2(SCN8A):c.3076C>T (p.Arg1026Cys) rs117217073
NM_001330260.2(SCN8A):c.3148G>A (p.Gly1050Ser) rs202006479
NM_001330260.2(SCN8A):c.3150T>G (p.Gly1050=) rs552307188
NM_001330260.2(SCN8A):c.3204C>T (p.Ser1068=) rs201045619
NM_001330260.2(SCN8A):c.3321C>T (p.Asn1107=) rs374213514
NM_001330260.2(SCN8A):c.3372+129A>G rs303810
NM_001330260.2(SCN8A):c.3373-9C>T rs770747359
NM_001330260.2(SCN8A):c.3384C>A (p.Asp1128Glu) rs1444975127
NM_001330260.2(SCN8A):c.3490+258G>A rs303807
NM_001330260.2(SCN8A):c.3645+265A>G rs34690825
NM_001330260.2(SCN8A):c.3710A>G (p.Lys1237Arg) rs377197765
NM_001330260.2(SCN8A):c.3820-132G>T rs2304698
NM_001330260.2(SCN8A):c.3822C>T (p.Val1274=) rs187327463
NM_001330260.2(SCN8A):c.3942+7T>C rs757990460
NM_001330260.2(SCN8A):c.3943-208G>A rs1439791
NM_001330260.2(SCN8A):c.395+262T>C rs56764080
NM_001330260.2(SCN8A):c.3957C>T (p.Ala1319=) rs764790057
NM_001330260.2(SCN8A):c.3966C>T (p.Gly1322=) rs775267842
NM_001330260.2(SCN8A):c.4122T>A (p.Thr1374=) rs115623439
NM_001330260.2(SCN8A):c.4155A>C (p.Thr1385=) rs144424662
NM_001330260.2(SCN8A):c.4218T>C (p.Leu1406=) rs768214178
NM_001330260.2(SCN8A):c.4228-27C>T rs9943714
NM_001330260.2(SCN8A):c.4278G>A (p.Arg1426=) rs143867796
NM_001330260.2(SCN8A):c.4281+13A>G rs9943809
NM_001330260.2(SCN8A):c.4419+283C>T rs303816
NM_001330260.2(SCN8A):c.4509T>C (p.Pro1503=) rs303815
NM_001330260.2(SCN8A):c.4524+254T>C rs2241854
NM_001330260.2(SCN8A):c.4524+299G>A rs2241853
NM_001330260.2(SCN8A):c.4524+56A>G rs2241855
NM_001330260.2(SCN8A):c.4543G>A (p.Val1515Ile) rs184568764
NM_001330260.2(SCN8A):c.4764C>T (p.Phe1588=) rs200728478
NM_001330260.2(SCN8A):c.4779C>T (p.Val1593=) rs12301486
NM_001330260.2(SCN8A):c.4795+11T>C rs143139673
NM_001330260.2(SCN8A):c.4969C>T (p.Leu1657=) rs374755275
NM_001330260.2(SCN8A):c.5391C>T (p.Pro1797=) rs372155701
NM_001330260.2(SCN8A):c.5472C>A (p.Pro1824=) rs60637
NM_001330260.2(SCN8A):c.5479A>G (p.Ile1827Val) rs764115258
NM_001330260.2(SCN8A):c.5514C>T (p.Ser1838=) rs372388512
NM_001330260.2(SCN8A):c.5601G>A (p.Gln1867=) rs368449473
NM_001330260.2(SCN8A):c.576C>T (p.Asp192=) rs4761829
NM_001330260.2(SCN8A):c.5879G>A (p.Arg1960Gln) rs369346315
NM_001330260.2(SCN8A):c.5943_*2GAG[1] (p.Ter1981=) rs555793953
NM_001330260.2(SCN8A):c.615-205A>G rs773009820
NM_001330260.2(SCN8A):c.751C>T (p.Leu251=) rs200307006
NM_001330260.2(SCN8A):c.855C>T (p.Pro285=) rs200784857
NM_001330260.2(SCN8A):c.928+9C>T rs148027656
NM_001330260.2(SCN8A):c.993-90_993-50del rs56947442
NM_014191.4(SCN8A):c.*3033T>C rs172559
NM_014191.4(SCN8A):c.*4375G>A rs60928084
NM_014191.4(SCN8A):c.*457_*458AC[8] rs397974598
NM_014191.4(SCN8A):c.*811T>C rs3741705
NM_014191.4(SCN8A):c.1897C>G (p.Leu633Val)
NM_014191.4(SCN8A):c.1969T>G (p.Ser657Ala)
NM_014191.4(SCN8A):c.1998+15G>T rs375797844
NM_014191.4(SCN8A):c.2370+14_2370+15del rs768088808
NM_014191.4(SCN8A):c.3490+20G>A rs303808
NM_014191.4(SCN8A):c.4281+13A>G rs9943809
NM_014191.4(SCN8A):c.707-15A>T rs149586118

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