ClinVar Miner

List of variants in gene SCN8A reported as likely benign by Illumina Clinical Services Laboratory,Illumina

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 46
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HGVS dbSNP
NM_014191.4(SCN8A):c.*1149T>C rs570715105
NM_014191.4(SCN8A):c.*1199T>C rs181144372
NM_014191.4(SCN8A):c.*1405C>T rs141823772
NM_014191.4(SCN8A):c.*1468T>C rs11829893
NM_014191.4(SCN8A):c.*1559G>A rs73299772
NM_014191.4(SCN8A):c.*1742T>G rs535755337
NM_014191.4(SCN8A):c.*1881A>T rs117540380
NM_014191.4(SCN8A):c.*2067T>G rs59570241
NM_014191.4(SCN8A):c.*2235_*2236del rs556349961
NM_014191.4(SCN8A):c.*2361T>C rs145994509
NM_014191.4(SCN8A):c.*2497A>T rs190395161
NM_014191.4(SCN8A):c.*2651C>T rs76675503
NM_014191.4(SCN8A):c.*2825T>A rs74092804
NM_014191.4(SCN8A):c.*2826A>T rs11833203
NM_014191.4(SCN8A):c.*2908C>T rs570197791
NM_014191.4(SCN8A):c.*3114_*3118TATAA[1] rs149334030
NM_014191.4(SCN8A):c.*324G>A rs185269212
NM_014191.4(SCN8A):c.*3494G>C rs190760531
NM_014191.4(SCN8A):c.*3706del rs560775301
NM_014191.4(SCN8A):c.*3717T>G rs147574884
NM_014191.4(SCN8A):c.*3914_*3917dup rs370929972
NM_014191.4(SCN8A):c.*4277_*4278TC[2] rs368023390
NM_014191.4(SCN8A):c.*434T>C rs146762782
NM_014191.4(SCN8A):c.*4399T>G rs117916312
NM_014191.4(SCN8A):c.*4412G>A rs546954995
NM_014191.4(SCN8A):c.*4470T>C rs151295158
NM_014191.4(SCN8A):c.*4953T>C rs150461009
NM_014191.4(SCN8A):c.*5189C>A rs115534804
NM_014191.4(SCN8A):c.*628G>A rs576031194
NM_014191.4(SCN8A):c.*762C>T rs3741706
NM_014191.4(SCN8A):c.*774T>C rs563030320
NM_014191.4(SCN8A):c.*925T>C rs188422745
NM_014191.4(SCN8A):c.1677C>T (p.His559=) rs202212399
NM_014191.4(SCN8A):c.1833G>T (p.Arg611=) rs35242963
NM_014191.4(SCN8A):c.2098A>T (p.Ile700Leu) rs187153231
NM_014191.4(SCN8A):c.2371-6A>G rs187002252
NM_014191.4(SCN8A):c.2475C>A (p.Val825=) rs535061303
NM_014191.4(SCN8A):c.2685A>G (p.Gln895=) rs528126331
NM_014191.4(SCN8A):c.3076C>T (p.Arg1026Cys) rs117217073
NM_014191.4(SCN8A):c.3822C>T (p.Val1274=) rs187327463
NM_014191.4(SCN8A):c.3942+7T>C rs757990460
NM_014191.4(SCN8A):c.4122T>A (p.Thr1374=) rs115623439
NM_014191.4(SCN8A):c.4779C>T (p.Val1593=) rs12301486
NM_014191.4(SCN8A):c.4795+11T>C rs143139673
NM_014191.4(SCN8A):c.5943_*2GAG[1] (p.Ter1981=) rs555793953
NM_014191.4(SCN8A):c.855C>T (p.Pro285=) rs200784857

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