ClinVar Miner

List of variants in gene CHRNA4 reported as uncertain significance

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 174
Download table as spreadsheet
HGVS dbSNP
NM_000744.6(CHRNA4):c.1006C>T (p.Arg336Cys) rs56175056
NM_000744.6(CHRNA4):c.1007G>A (p.Arg336His) rs281865068
NM_000744.6(CHRNA4):c.1010C>T (p.Thr337Met)
NM_000744.6(CHRNA4):c.1012C>G (p.His338Asp) rs200069626
NM_000744.6(CHRNA4):c.1033C>T (p.Arg345Cys) rs142260793
NM_000744.6(CHRNA4):c.1057C>A (p.Pro353Thr) rs201052218
NM_000744.6(CHRNA4):c.1060C>T (p.Arg354Cys) rs758534439
NM_000744.6(CHRNA4):c.1075A>T (p.Lys359Ter) rs1555837732
NM_000744.6(CHRNA4):c.1087G>A (p.Val363Met) rs121912266
NM_000744.6(CHRNA4):c.1106G>A (p.Arg369Gln) rs200007766
NM_000744.6(CHRNA4):c.1108C>T (p.Arg370Trp) rs76378652
NM_000744.6(CHRNA4):c.1117G>A (p.Glu373Lys) rs1064794565
NM_000744.6(CHRNA4):c.1138A>G (p.Ser380Gly) rs187372416
NM_000744.6(CHRNA4):c.1139G>A (p.Ser380Asn)
NM_000744.6(CHRNA4):c.1144C>T (p.Pro382Ser) rs1568809115
NM_000744.6(CHRNA4):c.1145C>T (p.Pro382Leu) rs769233762
NM_000744.6(CHRNA4):c.1148G>A (p.Arg383His) rs762374374
NM_000744.6(CHRNA4):c.1158_1160delinsGGG (p.Glu387Gly) rs796052320
NM_000744.6(CHRNA4):c.1161G>C (p.Glu387Asp) rs1064795592
NM_000744.6(CHRNA4):c.1178dup (p.Ala394fs) rs1435638963
NM_000744.6(CHRNA4):c.1196A>G (p.Gln399Arg) rs781131183
NM_000744.6(CHRNA4):c.1203G>C (p.Leu401=) rs56142348
NM_000744.6(CHRNA4):c.1209_1210delinsTT (p.Pro404Ser) rs1064795858
NM_000744.6(CHRNA4):c.1214C>T (p.Ser405Leu) rs1568808891
NM_000744.6(CHRNA4):c.1220C>T (p.Ser407Phe) rs761335733
NM_000744.6(CHRNA4):c.1227_1228inv (p.Val410Ile)
NM_000744.6(CHRNA4):c.1228G>A (p.Val410Ile) rs121912272
NM_000744.6(CHRNA4):c.1232C>A (p.Pro411His) rs779035642
NM_000744.6(CHRNA4):c.1245G>A (p.Pro415=) rs200164578
NM_000744.6(CHRNA4):c.1265G>A (p.Cys422Tyr) rs121912273
NM_000744.6(CHRNA4):c.1266C>T (p.Cys422=) rs121912274
NM_000744.6(CHRNA4):c.1269G>C (p.Lys423Asn) rs199916140
NM_000744.6(CHRNA4):c.1273C>T (p.Pro425Ser) rs764808511
NM_000744.6(CHRNA4):c.1277C>T (p.Ser426Phe) rs1064794408
NM_000744.6(CHRNA4):c.1283A>T (p.Gln428Leu)
NM_000744.6(CHRNA4):c.1294C>T (p.Gln432Ter) rs1064793409
NM_000744.6(CHRNA4):c.1300C>A (p.Pro434Thr)
NM_000744.6(CHRNA4):c.1300C>T (p.Pro434Ser)
NM_000744.6(CHRNA4):c.1316A>C (p.Lys439Thr) rs796052318
NM_000744.6(CHRNA4):c.1327C>G (p.His443Asp) rs796052319
NM_000744.6(CHRNA4):c.1354C>T (p.Pro452Ser) rs199914663
NM_000744.6(CHRNA4):c.1360G>A (p.Gly454Ser) rs78306886
NM_000744.6(CHRNA4):c.1369G>A (p.Ala457Thr) rs753598324
NM_000744.6(CHRNA4):c.1369G>C (p.Ala457Pro)
NM_000744.6(CHRNA4):c.1373C>T (p.Pro458Leu) rs121912277
NM_000744.6(CHRNA4):c.1376G>A (p.Gly459Glu) rs753201154
NM_000744.6(CHRNA4):c.1385A>C (p.Lys462Thr) rs1568808487
NM_000744.6(CHRNA4):c.138C>T (p.Ser46=) rs200705061
NM_000744.6(CHRNA4):c.1402G>A (p.Val468Ile) rs121912278
NM_000744.6(CHRNA4):c.140G>A (p.Gly47Asp) rs764990637
NM_000744.6(CHRNA4):c.1412T>C (p.Met471Thr) rs1317529556
NM_000744.6(CHRNA4):c.1415C>T (p.Ser472Phe) rs534477048
NM_000744.6(CHRNA4):c.1417A>G (p.Ser473Gly) rs1555837484
NM_000744.6(CHRNA4):c.1420C>T (p.Pro474Ser) rs773450609
NM_000744.6(CHRNA4):c.1425C>T (p.Gly475=) rs121912279
NM_000744.6(CHRNA4):c.1430C>T (p.Ala477Val) rs200243948
NM_000744.6(CHRNA4):c.1441G>A (p.Gly481Ser) rs111969225
NM_000744.6(CHRNA4):c.1447C>T (p.Arg483Trp)
NM_000744.6(CHRNA4):c.1448G>A (p.Arg483Gln) rs55855125
NM_000744.6(CHRNA4):c.144_146CAA[1] (p.Asn49del) rs780385531
NM_000744.6(CHRNA4):c.1454G>A (p.Arg485Gln) rs755416498
NM_000744.6(CHRNA4):c.1459C>T (p.Arg487Trp) rs200200279
NM_000744.6(CHRNA4):c.1460G>A (p.Arg487Gln) rs121912280
NM_000744.6(CHRNA4):c.1484G>C (p.Arg495Pro) rs549863396
NM_000744.6(CHRNA4):c.1494C>T (p.Ala498=) rs137860047
NM_000744.6(CHRNA4):c.1495G>A (p.Ala499Thr) rs150336658
NM_000744.6(CHRNA4):c.1510G>A (p.Gly504Ser) rs201244483
NM_000744.6(CHRNA4):c.1517C>A (p.Ala506Asp) rs1317311176
NM_000744.6(CHRNA4):c.1520C>T (p.Ala507Val) rs747883053
NM_000744.6(CHRNA4):c.1522G>A (p.Gly508Ser)
NM_000744.6(CHRNA4):c.1525G>A (p.Ala509Thr) rs142137599
NM_000744.6(CHRNA4):c.1535C>G (p.Ser512Cys)
NM_000744.6(CHRNA4):c.1537C>T (p.Arg513Cys)
NM_000744.6(CHRNA4):c.1538G>A (p.Arg513His) rs868845088
NM_000744.6(CHRNA4):c.1560C>T (p.Leu520=) rs142646795
NM_000744.6(CHRNA4):c.1576C>T (p.Pro526Ser) rs1064795533
NM_000744.6(CHRNA4):c.1583C>T (p.Pro528Leu) rs201739273
NM_000744.6(CHRNA4):c.1609C>T (p.Pro537Ser) rs758895760
NM_000744.6(CHRNA4):c.1625C>T (p.Pro542Leu) rs121912281
NM_000744.6(CHRNA4):c.1634C>T (p.Thr545Met) rs121912282
NM_000744.6(CHRNA4):c.1635G>A (p.Thr545=) rs121912283
NM_000744.6(CHRNA4):c.1637T>G (p.Val546Gly) rs764888239
NM_000744.6(CHRNA4):c.1645C>G (p.Arg549Gly) rs367658654
NM_000744.6(CHRNA4):c.1653C>A (p.Thr551=) rs886043995
NM_000744.6(CHRNA4):c.1663C>T (p.Pro555Ser)
NM_000744.6(CHRNA4):c.1667C>G (p.Pro556Arg) rs77345643
NM_000744.6(CHRNA4):c.1667C>T (p.Pro556Leu) rs77345643
NM_000744.6(CHRNA4):c.1670A>C (p.His557Pro) rs1282336623
NM_000744.6(CHRNA4):c.1682C>T (p.Ser561Leu) rs199949135
NM_000744.6(CHRNA4):c.1685C>T (p.Pro562Leu) rs200750362
NM_000744.6(CHRNA4):c.1697G>A (p.Arg566Gln) rs200810080
NM_000744.6(CHRNA4):c.1700C>G (p.Ala567Gly) rs76895198
NM_000744.6(CHRNA4):c.1700C>T (p.Ala567Val) rs76895198
NM_000744.6(CHRNA4):c.1711G>A (p.Val571Ile) rs121912285
NM_000744.6(CHRNA4):c.1715A>G (p.Gln572Arg) rs113794453
NM_000744.6(CHRNA4):c.1721T>C (p.Ile574Thr)
NM_000744.6(CHRNA4):c.1726G>A (p.Asp576Asn) rs537904499
NM_000744.6(CHRNA4):c.1726G>C (p.Asp576His) rs537904499
NM_000744.6(CHRNA4):c.1738G>A (p.Ala580Thr) rs1064795265
NM_000744.6(CHRNA4):c.1746_1747CA[1] (p.Thr583fs) rs772170088
NM_000744.6(CHRNA4):c.1757C>T (p.Ser586Leu) rs200644872
NM_000744.6(CHRNA4):c.1765G>A (p.Glu589Lys) rs749939383
NM_000744.6(CHRNA4):c.176C>T (p.Ser59Leu)
NM_000744.6(CHRNA4):c.1792A>G (p.Ile598Val) rs1019612389
NM_000744.6(CHRNA4):c.180C>G (p.Asp60Glu) rs112051150
NM_000744.6(CHRNA4):c.181G>T (p.Val61Leu) rs150451372
NM_000744.6(CHRNA4):c.1825G>A (p.Val609Ile) rs201168195
NM_000744.6(CHRNA4):c.1842G>A (p.Thr614=) rs727503871
NM_000744.6(CHRNA4):c.1847G>T (p.Gly616Val) rs796052324
NM_000744.6(CHRNA4):c.1854C>G (p.Phe618Leu) rs1568805215
NM_000744.6(CHRNA4):c.1859C>T (p.Pro620Leu) rs754340834
NM_000744.6(CHRNA4):c.1861C>A (p.Pro621Thr) rs199852690
NM_000744.6(CHRNA4):c.193C>T (p.Arg65Cys) rs748440038
NM_000744.6(CHRNA4):c.199G>A (p.Gly67Ser) rs750325388
NM_000744.6(CHRNA4):c.200G>A (p.Gly67Asp) rs1568819500
NM_000744.6(CHRNA4):c.211G>A (p.Ala71Thr) rs200527878
NM_000744.6(CHRNA4):c.212C>T (p.Ala71Val) rs753677594
NM_000744.6(CHRNA4):c.229-10G>A
NM_000744.6(CHRNA4):c.229-10G>T
NM_000744.6(CHRNA4):c.229G>A (p.Asp77Asn) rs1204737071
NM_000744.6(CHRNA4):c.254C>T (p.Thr85Met) rs199699339
NM_000744.6(CHRNA4):c.274-13C>G rs1057524765
NM_000744.6(CHRNA4):c.274G>C (p.Glu92Gln) rs146651027
NM_000744.6(CHRNA4):c.283G>A (p.Asp95Asn) rs761317422
NM_000744.6(CHRNA4):c.301G>A (p.Asp101Asn)
NM_000744.6(CHRNA4):c.358C>T (p.Arg120Trp) rs200010568
NM_000744.6(CHRNA4):c.362C>T (p.Pro121Leu)
NM_000744.6(CHRNA4):c.373C>T (p.Leu125Phe) rs1568816521
NM_000744.6(CHRNA4):c.400G>A (p.Ala134Thr) rs796052321
NM_000744.6(CHRNA4):c.412C>T (p.Leu138=) rs372063405
NM_000744.6(CHRNA4):c.413T>A (p.Leu138Gln) rs1379403896
NM_000744.6(CHRNA4):c.442C>T (p.Arg148Trp) rs121912243
NM_000744.6(CHRNA4):c.448C>T (p.Gln150Ter)
NM_000744.6(CHRNA4):c.461C>T (p.Pro154Leu) rs121912244
NM_000744.6(CHRNA4):c.466A>G (p.Ile156Val) rs754895704
NM_000744.6(CHRNA4):c.479C>T (p.Ser160Phe) rs201421555
NM_000744.6(CHRNA4):c.493G>A (p.Val165Ile) rs762764855
NM_000744.6(CHRNA4):c.496A>T (p.Thr166Ser) rs1568810867
NM_000744.6(CHRNA4):c.506C>G (p.Pro169Arg) rs199519224
NM_000744.6(CHRNA4):c.521A>G (p.Asn174Ser) rs796052316
NM_000744.6(CHRNA4):c.560C>G (p.Ala187Gly) rs200197645
NM_000744.6(CHRNA4):c.589C>T (p.Arg197Cys)
NM_000744.6(CHRNA4):c.590G>A (p.Arg197His)
NM_000744.6(CHRNA4):c.621C>T (p.Gly207=) rs149407396
NM_000744.6(CHRNA4):c.622G>A (p.Glu208Lys) rs771249249
NM_000744.6(CHRNA4):c.640G>A (p.Ala214Thr)
NM_000744.6(CHRNA4):c.678_679inv (p.Ala227Thr)
NM_000744.6(CHRNA4):c.681C>A (p.Ala227=) rs45588436
NM_000744.6(CHRNA4):c.682G>A (p.Glu228Lys) rs1064795157
NM_000744.6(CHRNA4):c.683A>T (p.Glu228Val) rs1568810474
NM_000744.6(CHRNA4):c.692C>T (p.Pro231Leu) rs763248360
NM_000744.6(CHRNA4):c.712G>A (p.Val238Ile)
NM_000744.6(CHRNA4):c.718C>T (p.Arg240Trp) rs757030850
NM_000744.6(CHRNA4):c.727C>A (p.Pro243Thr) rs1568810345
NM_000744.6(CHRNA4):c.729G>A (p.Pro243=) rs121912253
NM_000744.6(CHRNA4):c.758C>T (p.Pro253Leu) rs747083728
NM_000744.6(CHRNA4):c.77-4G>A rs201123897
NM_000744.6(CHRNA4):c.77C>T (p.Ala26Val)
NM_000744.6(CHRNA4):c.799C>T (p.Leu267=) rs121912256
NM_000744.6(CHRNA4):c.816C>T (p.Gly272=) rs981113016
NM_000744.6(CHRNA4):c.839C>G (p.Ser280Cys)
NM_000744.6(CHRNA4):c.841G>A (p.Val281Met)
NM_000744.6(CHRNA4):c.844C>G (p.Leu282Val)
NM_000744.6(CHRNA4):c.868C>T (p.Leu290=) rs762952445
NM_000744.6(CHRNA4):c.880G>A (p.Glu294Lys) rs201654194
NM_000744.6(CHRNA4):c.88G>A (p.Val30Met) rs746557446
NM_000744.6(CHRNA4):c.904dup (p.Val302fs) rs1568809897
NM_000744.6(CHRNA4):c.919G>A (p.Gly307Ser) rs764586079
NM_000744.6(CHRNA4):c.961A>G (p.Ile321Val) rs375340441
NM_000744.6(CHRNA4):c.964G>A (p.Val322Ile) rs779790555
NM_000744.6(CHRNA4):c.967A>G (p.Ile323Val)
NM_000744.6(CHRNA4):c.971C>T (p.Thr324Met)
NM_000744.6(CHRNA4):c.985A>G (p.Asn329Asp) rs767865433
NM_000744.6(CHRNA4):c.98G>C (p.Arg33Pro)

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.