ClinVar Miner

List of variants in gene SCN3A reported as uncertain significance by GeneDx

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Gene type:
ClinVar version:
Total variants: 162
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HGVS dbSNP gnomAD frequency
NM_006922.4(SCN3A):c.1381-3C>T rs756980047 0.00006
NM_006922.4(SCN3A):c.5881A>T (p.Ser1961Cys) rs184544899 0.00006
NM_006922.4(SCN3A):c.1070G>A (p.Arg357Gln) rs774195502 0.00005
NM_006922.4(SCN3A):c.2698G>A (p.Gly900Ser) rs749586926 0.00004
NM_006922.4(SCN3A):c.5696A>T (p.Gln1899Leu) rs950595171 0.00004
NM_006922.4(SCN3A):c.3478G>A (p.Glu1160Lys) rs377632429 0.00003
NM_006922.4(SCN3A):c.3494C>T (p.Pro1165Leu) rs563038965 0.00003
NM_006922.4(SCN3A):c.2078T>C (p.Met693Thr) rs1244798421 0.00002
NM_006922.4(SCN3A):c.4117T>C (p.Phe1373Leu) rs977221211 0.00002
NM_006922.4(SCN3A):c.1103C>G (p.Thr368Ser) rs769077073 0.00001
NM_006922.4(SCN3A):c.152C>T (p.Pro51Leu) rs1399602856 0.00001
NM_006922.4(SCN3A):c.1855G>A (p.Glu619Lys) rs577018955 0.00001
NM_006922.4(SCN3A):c.1859G>A (p.Arg620Gln) rs369720053 0.00001
NM_006922.4(SCN3A):c.1861C>T (p.Arg621Cys) rs1416035110 0.00001
NM_006922.4(SCN3A):c.2255T>C (p.Leu752Pro) rs1221758679 0.00001
NM_006922.4(SCN3A):c.2351T>C (p.Met784Thr) rs1458545066 0.00001
NM_006922.4(SCN3A):c.2411C>T (p.Thr804Ile) rs1428022575 0.00001
NM_006922.4(SCN3A):c.2606A>G (p.Asn869Ser) rs139866701 0.00001
NM_006922.4(SCN3A):c.3986T>G (p.Val1329Gly) rs1685414246 0.00001
NM_006922.4(SCN3A):c.4121A>T (p.Asp1374Val) rs377507565 0.00001
NM_006922.4(SCN3A):c.4331T>C (p.Met1444Thr) rs371715608 0.00001
NM_006922.4(SCN3A):c.4535C>A (p.Ala1512Glu) rs1279700412 0.00001
NM_006922.4(SCN3A):c.4780T>C (p.Phe1594Leu) rs947813427 0.00001
NM_006922.4(SCN3A):c.5228A>G (p.Asn1743Ser) rs1685063887 0.00001
NM_006922.4(SCN3A):c.5424A>G (p.Ile1808Met) rs535637931 0.00001
NM_006922.4(SCN3A):c.5813T>C (p.Leu1938Ser) rs1304082055 0.00001
NM_006922.4(SCN3A):c.85G>A (p.Ala29Thr) rs1690456258 0.00001
NM_006922.4(SCN3A):c.1066G>C (p.Gly356Arg) rs2105866774
NM_006922.4(SCN3A):c.1084G>A (p.Gly362Ser) rs1688989882
NM_006922.4(SCN3A):c.1094G>A (p.Ser365Asn) rs766043781
NM_006922.4(SCN3A):c.1136T>C (p.Leu379Pro)
NM_006922.4(SCN3A):c.1155G>A (p.Trp385Ter) rs1553535422
NM_006922.4(SCN3A):c.1201A>G (p.Met401Val) rs2105861870
NM_006922.4(SCN3A):c.1207T>G (p.Phe403Val) rs1688904462
NM_006922.4(SCN3A):c.1220T>C (p.Val407Ala)
NM_006922.4(SCN3A):c.1234T>C (p.Ser412Pro)
NM_006922.4(SCN3A):c.125A>G (p.Asp42Gly)
NM_006922.4(SCN3A):c.1336C>A (p.Gln446Lys)
NM_006922.4(SCN3A):c.1372G>A (p.Glu458Lys)
NM_006922.4(SCN3A):c.1436G>C (p.Gly479Ala) rs1688388372
NM_006922.4(SCN3A):c.1451G>C (p.Ser484Thr)
NM_006922.4(SCN3A):c.1493A>G (p.Glu498Gly)
NM_006922.4(SCN3A):c.1556A>G (p.Glu519Gly)
NM_006922.4(SCN3A):c.1559_1562del (p.Arg520fs) rs1688374063
NM_006922.4(SCN3A):c.1560A>T (p.Arg520Ser)
NM_006922.4(SCN3A):c.1563C>G (p.Asp521Glu)
NM_006922.4(SCN3A):c.1625A>G (p.Asp542Gly)
NM_006922.4(SCN3A):c.1632C>G (p.Asn544Lys)
NM_006922.4(SCN3A):c.1637T>G (p.Leu546Arg)
NM_006922.4(SCN3A):c.1661C>T (p.Ser554Phe)
NM_006922.4(SCN3A):c.1664C>T (p.Pro555Leu)
NM_006922.4(SCN3A):c.1682G>A (p.Ser561Asn)
NM_006922.4(SCN3A):c.1685T>A (p.Ile562Asn)
NM_006922.4(SCN3A):c.1726A>G (p.Ser576Gly) rs1687976841
NM_006922.4(SCN3A):c.1756G>T (p.Asp586Tyr) rs2105812313
NM_006922.4(SCN3A):c.1827del (p.Ser610fs)
NM_006922.4(SCN3A):c.1843C>A (p.His615Asn)
NM_006922.4(SCN3A):c.2024C>A (p.Thr675Asn)
NM_006922.4(SCN3A):c.2032G>A (p.Glu678Lys) rs1553527564
NM_006922.4(SCN3A):c.2066A>C (p.Tyr689Ser)
NM_006922.4(SCN3A):c.2176T>C (p.Cys726Arg) rs1235837313
NM_006922.4(SCN3A):c.217G>A (p.Val73Met) rs915992958
NM_006922.4(SCN3A):c.2186G>A (p.Cys729Tyr)
NM_006922.4(SCN3A):c.2213T>C (p.Leu738Ser)
NM_006922.4(SCN3A):c.2260A>G (p.Asn754Asp)
NM_006922.4(SCN3A):c.2321C>A (p.Thr774Asn)
NM_006922.4(SCN3A):c.2329A>G (p.Met777Val) rs746866750
NM_006922.4(SCN3A):c.2368A>T (p.Ser790Cys)
NM_006922.4(SCN3A):c.2656A>C (p.Thr886Pro) rs2105772668
NM_006922.4(SCN3A):c.2702T>A (p.Met901Lys) rs983605439
NM_006922.4(SCN3A):c.2702T>C (p.Met901Thr) rs983605439
NM_006922.4(SCN3A):c.2713G>C (p.Gly905Arg)
NM_006922.4(SCN3A):c.2747A>G (p.Asn916Ser)
NM_006922.4(SCN3A):c.2754C>G (p.Asp918Glu) rs1687224167
NM_006922.4(SCN3A):c.2780A>G (p.Asn927Ser)
NM_006922.4(SCN3A):c.2791C>T (p.His931Tyr) rs2105772102
NM_006922.4(SCN3A):c.2902A>C (p.Met968Leu)
NM_006922.4(SCN3A):c.2996A>G (p.Asn999Ser) rs2105763978
NM_006922.4(SCN3A):c.3001_3002delinsCA (p.Met1001Gln)
NM_006922.4(SCN3A):c.3017T>C (p.Ile1006Thr)
NM_006922.4(SCN3A):c.3023T>C (p.Val1008Ala)
NM_006922.4(SCN3A):c.3107_3112del (p.Val1036_Ile1037del)
NM_006922.4(SCN3A):c.3197A>G (p.Asp1066Gly)
NM_006922.4(SCN3A):c.3239T>C (p.Val1080Ala)
NM_006922.4(SCN3A):c.3260A>G (p.Glu1087Gly) rs1018039184
NM_006922.4(SCN3A):c.3265G>C (p.Asp1089His) rs1574158109
NM_006922.4(SCN3A):c.3268T>G (p.Tyr1090Asp) rs780784373
NM_006922.4(SCN3A):c.3287A>C (p.Asn1096Thr)
NM_006922.4(SCN3A):c.3350C>A (p.Thr1117Asn) rs767706892
NM_006922.4(SCN3A):c.3365G>A (p.Ser1122Asn)
NM_006922.4(SCN3A):c.3377T>C (p.Leu1126Pro)
NM_006922.4(SCN3A):c.3384A>C (p.Glu1128Asp)
NM_006922.4(SCN3A):c.3412T>G (p.Ser1138Ala)
NM_006922.4(SCN3A):c.3420A>C (p.Glu1140Asp) rs1686330793
NM_006922.4(SCN3A):c.3424A>C (p.Ser1142Arg)
NM_006922.4(SCN3A):c.3435T>G (p.Asp1145Glu) rs1686329652
NM_006922.4(SCN3A):c.347C>A (p.Pro116His) rs2105910555
NM_006922.4(SCN3A):c.3507T>A (p.Phe1169Leu)
NM_006922.4(SCN3A):c.3559G>C (p.Gly1187Arg)
NM_006922.4(SCN3A):c.3593C>A (p.Thr1198Asn)
NM_006922.4(SCN3A):c.3628A>T (p.Thr1210Ser)
NM_006922.4(SCN3A):c.3629C>T (p.Thr1210Ile) rs2105710443
NM_006922.4(SCN3A):c.3631T>C (p.Phe1211Leu) rs2105710435
NM_006922.4(SCN3A):c.3632T>C (p.Phe1211Ser) rs2105710420
NM_006922.4(SCN3A):c.3678A>T (p.Glu1226Asp)
NM_006922.4(SCN3A):c.3724T>C (p.Tyr1242His) rs1348671298
NM_006922.4(SCN3A):c.3734A>C (p.Lys1245Thr)
NM_006922.4(SCN3A):c.3750A>G (p.Ile1250Met) rs1179208168
NM_006922.4(SCN3A):c.3795A>C (p.Gln1265His) rs1553519903
NM_006922.4(SCN3A):c.3874C>T (p.Leu1292Phe) rs1553518639
NM_006922.4(SCN3A):c.3892G>C (p.Gly1298Arg) rs375050462
NM_006922.4(SCN3A):c.3920G>C (p.Arg1307Thr) rs2105659949
NM_006922.4(SCN3A):c.3979G>C (p.Ala1327Pro)
NM_006922.4(SCN3A):c.4178G>A (p.Trp1393Ter)
NM_006922.4(SCN3A):c.4239+2dup rs1553518222
NM_006922.4(SCN3A):c.4239+6T>A
NM_006922.4(SCN3A):c.4289G>A (p.Arg1430Gln)
NM_006922.4(SCN3A):c.4345_4346dup (p.Ile1450fs)
NM_006922.4(SCN3A):c.4362del (p.Phe1454fs) rs2105640828
NM_006922.4(SCN3A):c.4455G>C (p.Met1485Ile)
NM_006922.4(SCN3A):c.4486A>G (p.Met1496Val)
NM_006922.4(SCN3A):c.4526C>G (p.Pro1509Arg) rs1685257527
NM_006922.4(SCN3A):c.4564T>A (p.Phe1522Ile)
NM_006922.4(SCN3A):c.4616A>G (p.Asn1539Ser) rs2105627166
NM_006922.4(SCN3A):c.4742G>A (p.Arg1581Lys) rs2105626390
NM_006922.4(SCN3A):c.4754T>A (p.Phe1585Tyr)
NM_006922.4(SCN3A):c.4768A>G (p.Asn1590Asp)
NM_006922.4(SCN3A):c.4792A>T (p.Ile1598Phe)
NM_006922.4(SCN3A):c.4799C>T (p.Ser1600Phe)
NM_006922.4(SCN3A):c.4883T>C (p.Ile1628Thr)
NM_006922.4(SCN3A):c.4912G>A (p.Ala1638Thr)
NM_006922.4(SCN3A):c.4939G>A (p.Ala1647Thr)
NM_006922.4(SCN3A):c.5027A>T (p.Asn1676Ile)
NM_006922.4(SCN3A):c.5065A>G (p.Met1689Val)
NM_006922.4(SCN3A):c.5097G>T (p.Met1699Ile)
NM_006922.4(SCN3A):c.5183C>T (p.Pro1728Leu)
NM_006922.4(SCN3A):c.5254G>A (p.Val1752Ile) rs2105619881
NM_006922.4(SCN3A):c.5302G>A (p.Ala1768Thr) rs1323737106
NM_006922.4(SCN3A):c.5303C>T (p.Ala1768Val)
NM_006922.4(SCN3A):c.5423T>C (p.Ile1808Thr) rs1685054282
NM_006922.4(SCN3A):c.5491A>G (p.Lys1831Glu)
NM_006922.4(SCN3A):c.5508C>T (p.Ala1836=) rs2105618821
NM_006922.4(SCN3A):c.5551G>A (p.Asp1851Asn)
NM_006922.4(SCN3A):c.5563G>C (p.Ala1855Pro)
NM_006922.4(SCN3A):c.5576G>A (p.Arg1859His) rs778995406
NM_006922.4(SCN3A):c.5591G>T (p.Ser1864Ile) rs1085307836
NM_006922.4(SCN3A):c.5606C>T (p.Ala1869Val) rs2105618194
NM_006922.4(SCN3A):c.5627A>T (p.Asp1876Val)
NM_006922.4(SCN3A):c.5684T>C (p.Leu1895Ser)
NM_006922.4(SCN3A):c.5792C>T (p.Ala1931Val)
NM_006922.4(SCN3A):c.5834T>C (p.Ile1945Thr) rs2105616234
NM_006922.4(SCN3A):c.5852G>A (p.Gly1951Glu)
NM_006922.4(SCN3A):c.5873C>G (p.Thr1958Arg)
NM_006922.4(SCN3A):c.593T>C (p.Ile198Thr)
NM_006922.4(SCN3A):c.5970C>G (p.Ser1990Arg)
NM_006922.4(SCN3A):c.5983G>A (p.Val1995Ile) rs2105615122
NM_006922.4(SCN3A):c.5989G>T (p.Glu1997Ter)
NM_006922.4(SCN3A):c.726G>T (p.Gln242His)
NM_006922.4(SCN3A):c.781T>A (p.Phe261Ile) rs774900155
NM_006922.4(SCN3A):c.809T>C (p.Met270Thr) rs2105890332
NM_006922.4(SCN3A):c.967+1G>A
NM_006922.4(SCN3A):c.989G>A (p.Gly330Glu) rs1689457079

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