ClinVar Miner

List of variants in gene SCN8A reported as benign for not provided

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 85
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_001330260.2(SCN8A):c.3372+203G>C rs303809 0.87303
NM_001330260.2(SCN8A):c.3820-202A>G rs2580807 0.86280
NM_001330260.2(SCN8A):c.4796-38C>A rs303828 0.86075
NM_001330260.2(SCN8A):c.576C>T (p.Asp192=) rs4761829 0.81114
NM_001330260.2(SCN8A):c.1135-48C>T rs2291265 0.78368
NM_001330260.2(SCN8A):c.3490+20G>A rs303808 0.76481
NM_001330260.2(SCN8A):c.3372+129A>G rs303810 0.73478
NM_001330260.2(SCN8A):c.4509T>C (p.Pro1503=) rs303815 0.62374
NM_001330260.2(SCN8A):c.4419+283C>T rs303816 0.62302
NM_001330260.2(SCN8A):c.4524+56A>G rs2241855 0.15635
NM_001330260.2(SCN8A):c.3820-132G>T rs2304698 0.15474
NM_001330260.2(SCN8A):c.4524+299G>A rs2241853 0.13925
NM_001330260.2(SCN8A):c.4228-27C>T rs9943714 0.12555
NM_001330260.2(SCN8A):c.3943-208G>A rs1439791 0.12497
NM_001330260.2(SCN8A):c.4524+254T>C rs2241854 0.10978
NM_001330260.2(SCN8A):c.3820-44G>T rs752277461 0.07469
NM_001330260.2(SCN8A):c.3820-43G>T rs758243136 0.06589
NM_001330260.2(SCN8A):c.395+262T>C rs56764080 0.05648
NM_001330260.2(SCN8A):c.1636-237G>A rs74091624 0.04589
NM_001330260.2(SCN8A):c.3819+225T>C rs11836472 0.03309
NM_001330260.2(SCN8A):c.993-58A>G rs74091614 0.03307
NM_001330260.2(SCN8A):c.4419+200A>G rs58113407 0.02960
NM_001330260.2(SCN8A):c.1635+251A>G rs116880453 0.02953
NM_001330260.2(SCN8A):c.4795+49T>A rs74093917 0.02939
NM_001330260.2(SCN8A):c.3645+265A>G rs34690825 0.02740
NM_001330260.2(SCN8A):c.2901+277T>C rs74091656 0.02364
NM_001330260.2(SCN8A):c.1341+208T>C rs75757324 0.01896
NM_001330260.2(SCN8A):c.395+25T>C rs2271086 0.01584
NM_001330260.2(SCN8A):c.3076C>T (p.Arg1026Cys) rs117217073 0.01112
NM_001330260.2(SCN8A):c.3820-39C>T rs1254736818 0.00717
NM_001330260.2(SCN8A):c.4122T>A (p.Thr1374=) rs115623439 0.00531
NM_001330260.2(SCN8A):c.277-47A>G rs201794111 0.00204
NM_001330260.2(SCN8A):c.-55+12C>T rs534924909 0.00202
NM_001330260.2(SCN8A):c.2370+22C>T rs191442852 0.00171
NM_001330260.2(SCN8A):c.2901+67A>G rs536658413 0.00151
NM_001330260.2(SCN8A):c.2098A>T (p.Ile700Leu) rs187153231 0.00138
NM_001330260.2(SCN8A):c.3822C>T (p.Val1274=) rs187327463 0.00132
NM_001330260.2(SCN8A):c.2544+49A>G rs372757015 0.00130
NM_001330260.2(SCN8A):c.2132-50T>G rs200389862 0.00124
NM_001330260.2(SCN8A):c.395+44G>A rs181052973 0.00106
NM_001330260.2(SCN8A):c.706+36A>G rs189697621 0.00098
NM_001330260.2(SCN8A):c.4281+18G>A rs368432695 0.00087
NM_001330260.2(SCN8A):c.993-36T>C rs199743173 0.00085
NM_001330260.2(SCN8A):c.4796-35C>A rs149882447 0.00073
NM_001330260.2(SCN8A):c.1819G>A (p.Ala607Thr) rs367949317 0.00061
NM_001330260.2(SCN8A):c.3204C>T (p.Ser1068=) rs201045619 0.00058
NM_001330260.2(SCN8A):c.4419+22C>T rs148202722 0.00057
NM_001330260.2(SCN8A):c.1677C>T (p.His559=) rs202212399 0.00051
NM_001330260.2(SCN8A):c.3321C>T (p.Asn1107=) rs374213514 0.00050
NM_001330260.2(SCN8A):c.706+41C>G rs540984006 0.00044
NM_001330260.2(SCN8A):c.2670C>T (p.Ala890=) rs374452942 0.00035
NM_001330260.2(SCN8A):c.4764C>T (p.Phe1588=) rs200728478 0.00032
NM_001330260.2(SCN8A):c.5577C>T (p.Ser1859=) rs185667241 0.00026
NM_001330260.2(SCN8A):c.3820-7T>C rs375785915 0.00022
NM_001330260.2(SCN8A):c.5601G>A (p.Gln1867=) rs368449473 0.00022
NM_001330260.2(SCN8A):c.1135-43C>A rs181290446 0.00017
NM_001330260.2(SCN8A):c.5619C>T (p.Phe1873=) rs372752853 0.00016
NM_001330260.2(SCN8A):c.3582C>T (p.Ile1194=) rs756909923 0.00013
NM_001330260.2(SCN8A):c.3373-49G>A rs752462655 0.00009
NM_001330260.2(SCN8A):c.855C>T (p.Pro285=) rs200784857 0.00007
NM_001330260.2(SCN8A):c.615-144C>T rs192982781 0.00006
NM_001330260.2(SCN8A):c.2370+35G>A rs142420390 0.00005
NM_001330260.2(SCN8A):c.1999-4A>T rs765240974 0.00004
NM_001330260.2(SCN8A):c.5580G>A (p.Gly1860=) rs201484402 0.00003
NM_001330260.2(SCN8A):c.2073C>T (p.Tyr691=) rs146982102 0.00002
NM_001330260.2(SCN8A):c.4005C>T (p.Leu1335=) rs1030141528 0.00002
NM_001330260.2(SCN8A):c.810G>A (p.Leu270=) rs377606066 0.00002
NM_001330260.2(SCN8A):c.2131+25A>C rs571996473 0.00001
NM_001330260.2(SCN8A):c.615-291G>A rs553857771 0.00001
NM_001330260.2(SCN8A):c.888C>G (p.Gly296=) rs565852557 0.00001
NM_001330260.2(SCN8A):c.1134+324TTTTG[6] rs5798183
NM_001330260.2(SCN8A):c.1239T>C (p.Ala413=) rs2138748288
NM_001330260.2(SCN8A):c.1635+67G>A rs10783474
NM_001330260.2(SCN8A):c.1846GGCTACAGC[1] (p.616GYS[1]) rs758276968
NM_001330260.2(SCN8A):c.1999-5del rs769940455
NM_001330260.2(SCN8A):c.1999-5dup rs769940455
NM_001330260.2(SCN8A):c.2371-32A>C rs303767
NM_001330260.2(SCN8A):c.2545-7dup rs56879517
NM_001330260.2(SCN8A):c.2545-8_2545-7dup rs56879517
NM_001330260.2(SCN8A):c.2685A>G (p.Gln895=) rs528126331
NM_001330260.2(SCN8A):c.3490+258G>A rs303807
NM_001330260.2(SCN8A):c.395+243del rs59513447
NM_001330260.2(SCN8A):c.5472C>A (p.Pro1824=) rs60637
NM_001330260.2(SCN8A):c.5943GAG[1] (p.Ter1981=) rs555793953
NM_001330260.2(SCN8A):c.993-90_993-50del rs56947442

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.