ClinVar Miner

List of variants in gene combination SCN1A, SCN9A studied for not specified

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Total variants: 98
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HGVS dbSNP gnomAD frequency
NM_001365536.1(SCN9A):c.4774+16T>A rs10180721 0.89276
NM_001365536.1(SCN9A):c.3481T>C (p.Trp1161Arg) rs6746030 0.87930
NM_001365536.1(SCN9A):c.1287T>A (p.Arg429=) rs6747673 0.56670
NM_001365536.1(SCN9A):c.2105-14C>T rs6432893 0.56480
NM_001365536.1(SCN9A):c.1266A>G (p.Glu422=) rs13402180 0.38348
NM_001365536.1(SCN9A):c.1119T>C (p.Ala373=) rs13414203 0.38341
NM_001365536.1(SCN9A):c.2105-15G>A rs4525717 0.12980
NM_001365536.1(SCN9A):c.3802-4A>G rs75230218 0.06754
NM_001365536.1(SCN9A):c.4812G>T (p.Val1604=) rs149207258 0.06646
NM_001365536.1(SCN9A):c.1469G>A (p.Ser490Asn) rs58022607 0.04393
NM_001365536.1(SCN9A):c.1155G>T (p.Val385=) rs58465962 0.04390
NM_001365536.1(SCN9A):c.5756A>G (p.Asp1919Gly) rs3750904 0.02756
NM_001365536.1(SCN9A):c.3802-8T>C rs76550960 0.02262
NM_001365536.1(SCN9A):c.3362G>A (p.Arg1121Gln) rs74401238 0.02210
NM_001365536.1(SCN9A):c.2827A>C (p.Met943Leu) rs12478318 0.01339
NM_001365536.1(SCN9A):c.3004G>T (p.Val1002Leu) rs4369876 0.01322
NM_001365536.1(SCN9A):c.3767A>G (p.Asn1256Ser) rs141268327 0.00496
NM_001365536.1(SCN9A):c.2517+6C>T rs145316463 0.00460
NM_001365536.1(SCN9A):c.1398C>T (p.Ser466=) rs201531206 0.00386
NM_001365536.1(SCN9A):c.2190G>C (p.Trp730Cys) rs202055175 0.00341
NM_001365536.1(SCN9A):c.5779C>T (p.Leu1927Phe) rs111558968 0.00315
NM_001365536.1(SCN9A):c.3361C>T (p.Arg1121Trp) rs190664764 0.00304
NM_001365536.1(SCN9A):c.2248A>G (p.Ile750Val) rs182650126 0.00278
NM_001365536.1(SCN9A):c.4356C>T (p.Phe1452=) rs201145311 0.00263
NM_001365536.1(SCN9A):c.3506A>C (p.Asn1169Thr) rs151241025 0.00216
NM_001365536.1(SCN9A):c.1997A>G (p.Lys666Arg) rs121908919 0.00180
NM_001365536.1(SCN9A):c.3832C>G (p.Leu1278Val) rs180922748 0.00174
NM_001365536.1(SCN9A):c.4645T>C (p.Trp1549Arg) rs202084411 0.00173
NM_001365536.1(SCN9A):c.4314C>T (p.Val1438=) rs188336294 0.00171
NM_001365536.1(SCN9A):c.3675C>A (p.Ile1225=) rs77144869 0.00141
NM_001365536.1(SCN9A):c.3509T>C (p.Ile1170Thr) rs73019664 0.00128
NM_001365536.1(SCN9A):c.5791G>C (p.Asp1931His) rs200410805 0.00121
NM_001365536.1(SCN9A):c.2409T>C (p.Tyr803=) rs142219317 0.00106
NM_001365536.1(SCN9A):c.1326G>A (p.Ala442=) rs200065104 0.00102
NM_001365536.1(SCN9A):c.3195C>T (p.Ser1065=) rs111674454 0.00099
NM_001365536.1(SCN9A):c.2766C>T (p.Arg922=) rs199653503 0.00096
NM_001365536.1(SCN9A):c.3020G>A (p.Arg1007His) rs188145203 0.00077
NM_001365536.1(SCN9A):c.4315G>A (p.Val1439Ile) rs149346064 0.00061
NM_001365536.1(SCN9A):c.2392A>G (p.Met798Val) rs149707354 0.00056
NM_001365536.1(SCN9A):c.3002A>G (p.Tyr1001Cys) rs199692186 0.00056
NM_001365536.1(SCN9A):c.3402G>T (p.Leu1134Phe) rs200160858 0.00052
NM_001365536.1(SCN9A):c.4923T>C (p.Leu1641=) rs199550149 0.00041
NM_001365536.1(SCN9A):c.4399-14G>T rs112927502 0.00038
NM_001365536.1(SCN9A):c.4399-17_4399-16insA rs569037217 0.00030
NM_001365536.1(SCN9A):c.2192T>A (p.Ile731Lys) rs200945460 0.00019
NM_001365536.1(SCN9A):c.2344-20A>T rs199905079 0.00018
NM_001365536.1(SCN9A):c.1177C>T (p.Leu393=) rs184773311 0.00017
NM_001365536.1(SCN9A):c.1110G>A (p.Thr370=) rs202002028 0.00016
NM_001365536.1(SCN9A):c.3573C>T (p.His1191=) rs375710841 0.00016
NM_001365536.1(SCN9A):c.1675G>A (p.Gly559Ser) rs201569378 0.00013
NM_001365536.1(SCN9A):c.3207C>T (p.His1069=) rs200689065 0.00010
NM_001365536.1(SCN9A):c.965+13T>C rs772337722 0.00010
NM_001365536.1(SCN9A):c.5711G>A (p.Arg1904His) rs79805025 0.00009
NM_001365536.1(SCN9A):c.2634C>T (p.Phe878=) rs188678956 0.00007
NM_001365536.1(SCN9A):c.3538A>G (p.Asn1180Asp) rs750269576 0.00007
NM_001365536.1(SCN9A):c.3802-13del rs747729984 0.00007
NM_001365536.1(SCN9A):c.3944T>C (p.Ile1315Thr) rs202235611 0.00007
NM_001365536.1(SCN9A):c.5945A>T (p.Asp1982Val) rs199822303 0.00006
NM_001365536.1(SCN9A):c.1975-8T>A rs752961542 0.00005
NM_001365536.1(SCN9A):c.4148A>G (p.Lys1383Arg) rs779536952 0.00005
NM_001365536.1(SCN9A):c.1150G>A (p.Val384Ile) rs200973534 0.00004
NM_001365536.1(SCN9A):c.1714G>A (p.Asp572Asn) rs747040987 0.00004
NM_001365536.1(SCN9A):c.3271A>G (p.Ile1091Val) rs202212176 0.00004
NM_001365536.1(SCN9A):c.3540C>T (p.Asn1180=) rs766241126 0.00003
NM_001365536.1(SCN9A):c.4629G>A (p.Met1543Ile) rs200328637 0.00003
NM_001365536.1(SCN9A):c.966-8G>A rs199942413 0.00003
NM_001365536.1(SCN9A):c.1602+15G>T rs201987507 0.00002
NM_001365536.1(SCN9A):c.1107+7A>G rs199623041 0.00001
NM_001365536.1(SCN9A):c.2253C>T (p.Thr751=) rs751536693 0.00001
NM_001365536.1(SCN9A):c.2521C>T (p.Arg841Ter) rs780673293 0.00001
NM_001365536.1(SCN9A):c.2566A>G (p.Ile856Val) rs1218485798 0.00001
NM_001365536.1(SCN9A):c.2712G>A (p.Thr904=) rs200494981 0.00001
NM_001365536.1(SCN9A):c.3036A>G (p.Lys1012=) rs200375962 0.00001
NM_001365536.1(SCN9A):c.3807T>A (p.Ser1269=) rs1272510761 0.00001
NM_001365536.1(SCN9A):c.4261-3T>C rs773953311 0.00001
NM_001365536.1(SCN9A):c.5858C>T (p.Thr1953Ile) rs1222885641 0.00001
NM_001365536.1(SCN9A):c.5954A>G (p.Glu1985Gly) rs755850299 0.00001
NM_001365536.1(SCN9A):c.990T>C (p.Cys330=) rs1384436013 0.00001
NM_001365536.1(SCN9A):c.1828C>A (p.Pro610Thr) rs41268673
NM_001365536.1(SCN9A):c.1975-3del rs35888674
NM_001365536.1(SCN9A):c.1975-3dup rs35888674
NM_001365536.1(SCN9A):c.1999A>G (p.Lys667Glu) rs775090142
NM_001365536.1(SCN9A):c.2420G>T (p.Gly807Val) rs1553488264
NM_001365536.1(SCN9A):c.2644G>C (p.Val882Leu) rs1553487882
NM_001365536.1(SCN9A):c.2874+11_2874+13delinsTT rs1553487749
NM_001365536.1(SCN9A):c.2875-18C>T rs1553486847
NM_001365536.1(SCN9A):c.3003T>C (p.Tyr1001=) rs886038521
NM_001365536.1(SCN9A):c.3351+15T>C rs763278343
NM_001365536.1(SCN9A):c.3834T>G (p.Leu1278=) rs1553480111
NM_001365536.1(SCN9A):c.3925-10T>C
NM_001365536.1(SCN9A):c.4141C>A (p.Arg1381=) rs748159444
NM_001365536.1(SCN9A):c.4184G>A (p.Gly1395Asp) rs764682998
NM_001365536.1(SCN9A):c.4207G>T (p.Ala1403Ser)
NM_001365536.1(SCN9A):c.4399-10_4399-7del rs77944059
NM_001365536.1(SCN9A):c.4932_4935del (p.Phe1645fs)
NM_001365536.1(SCN9A):c.5030A>T (p.Asp1677Val) rs1553473210
NM_001365536.1(SCN9A):c.5444T>C (p.Ile1815Thr)
NM_001365536.1(SCN9A):c.965+18T>C rs1553492740

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