ClinVar Miner

List of variants in gene CHRNA4 reported as uncertain significance for not provided

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Total variants: 144
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HGVS dbSNP gnomAD frequency
NM_000744.7(CHRNA4):c.77-4G>A rs201123897 0.00141
NM_000744.7(CHRNA4):c.1108C>T (p.Arg370Trp) rs76378652 0.00080
NM_000744.7(CHRNA4):c.1441G>A (p.Gly481Ser) rs111969225 0.00070
NM_000744.7(CHRNA4):c.1203G>C (p.Leu401=) rs56142348 0.00066
NM_000744.7(CHRNA4):c.1006C>T (p.Arg336Cys) rs56175056 0.00045
NM_000744.7(CHRNA4):c.1560C>T (p.Leu520=) rs142646795 0.00027
NM_000744.7(CHRNA4):c.1635G>A (p.Thr545=) rs121912283 0.00021
NM_000744.7(CHRNA4):c.1448G>A (p.Arg483Gln) rs55855125 0.00016
NM_000744.7(CHRNA4):c.1360G>A (p.Gly454Ser) rs78306886 0.00014
NM_000744.7(CHRNA4):c.1373C>T (p.Pro458Leu) rs121912277 0.00013
NM_000744.7(CHRNA4):c.1459C>T (p.Arg487Trp) rs200200279 0.00013
NM_000744.7(CHRNA4):c.1715A>G (p.Gln572Arg) rs113794453 0.00011
NM_000744.7(CHRNA4):c.589C>T (p.Arg197Cys) rs144716263 0.00011
NM_000744.7(CHRNA4):c.1316A>C (p.Lys439Thr) rs796052318 0.00009
NM_000744.7(CHRNA4):c.729G>A (p.Pro243=) rs121912253 0.00009
NM_000744.7(CHRNA4):c.1510G>A (p.Gly504Ser) rs201244483 0.00008
NM_000744.7(CHRNA4):c.1106G>A (p.Arg369Gln) rs200007766 0.00007
NM_000744.7(CHRNA4):c.1494C>T (p.Ala498=) rs137860047 0.00007
NM_000744.7(CHRNA4):c.1266C>T (p.Cys422=) rs121912274 0.00006
NM_000744.7(CHRNA4):c.1430C>T (p.Ala477Val) rs200243948 0.00006
NM_000744.7(CHRNA4):c.1454G>A (p.Arg485Gln) rs755416498 0.00006
NM_000744.7(CHRNA4):c.1609C>T (p.Pro537Ser) rs758895760 0.00006
NM_000744.7(CHRNA4):c.461C>T (p.Pro154Leu) rs121912244 0.00006
NM_000744.7(CHRNA4):c.1525G>A (p.Ala509Thr) rs142137599 0.00005
NM_000744.7(CHRNA4):c.1483C>T (p.Arg495Ter) rs765379481 0.00004
NM_000744.7(CHRNA4):c.1637T>G (p.Val546Gly) rs764888239 0.00004
NM_000744.7(CHRNA4):c.1682C>T (p.Ser561Leu) rs199949135 0.00004
NM_000744.7(CHRNA4):c.1757C>T (p.Ser586Leu) rs200644872 0.00004
NM_000744.7(CHRNA4):c.514C>T (p.Gln172Ter) rs112748821 0.00004
NM_000744.7(CHRNA4):c.692C>T (p.Pro231Leu) rs763248360 0.00004
NM_000744.7(CHRNA4):c.1327C>G (p.His443Asp) rs796052319 0.00003
NM_000744.7(CHRNA4):c.1742A>G (p.Glu581Gly) rs767165466 0.00003
NM_000744.7(CHRNA4):c.442C>T (p.Arg148Trp) rs121912243 0.00003
NM_000744.7(CHRNA4):c.1082C>T (p.Pro361Leu) rs267606048 0.00002
NM_000744.7(CHRNA4):c.1109G>A (p.Arg370Gln) rs121912267 0.00002
NM_000744.7(CHRNA4):c.1685C>T (p.Pro562Leu) rs200750362 0.00002
NM_000744.7(CHRNA4):c.961A>G (p.Ile321Val) rs375340441 0.00002
NM_000744.7(CHRNA4):c.971C>T (p.Thr324Met) rs531615515 0.00002
NM_000744.7(CHRNA4):c.1034G>T (p.Arg345Leu) rs200666489 0.00001
NM_000744.7(CHRNA4):c.1060C>T (p.Arg354Cys) rs758534439 0.00001
NM_000744.7(CHRNA4):c.1117G>A (p.Glu373Lys) rs1064794565 0.00001
NM_000744.7(CHRNA4):c.1145C>T (p.Pro382Leu) rs769233762 0.00001
NM_000744.7(CHRNA4):c.1159G>A (p.Glu387Lys) rs534229205 0.00001
NM_000744.7(CHRNA4):c.1232C>A (p.Pro411His) rs779035642 0.00001
NM_000744.7(CHRNA4):c.1252C>T (p.Pro418Ser) rs1412148347 0.00001
NM_000744.7(CHRNA4):c.1273C>T (p.Pro425Ser) rs764808511 0.00001
NM_000744.7(CHRNA4):c.1277C>T (p.Ser426Phe) rs1064794408 0.00001
NM_000744.7(CHRNA4):c.1354C>T (p.Pro452Ser) rs199914663 0.00001
NM_000744.7(CHRNA4):c.140G>A (p.Gly47Asp) rs764990637 0.00001
NM_000744.7(CHRNA4):c.1426G>A (p.Glu476Lys) rs201420419 0.00001
NM_000744.7(CHRNA4):c.1495G>A (p.Ala499Thr) rs150336658 0.00001
NM_000744.7(CHRNA4):c.1576C>T (p.Pro526Ser) rs1064795533 0.00001
NM_000744.7(CHRNA4):c.1630G>A (p.Ala544Thr) rs540705031 0.00001
NM_000744.7(CHRNA4):c.1634C>T (p.Thr545Met) rs121912282 0.00001
NM_000744.7(CHRNA4):c.1670A>C (p.His557Pro) rs1282336623 0.00001
NM_000744.7(CHRNA4):c.1696C>T (p.Arg566Trp) rs201674914 0.00001
NM_000744.7(CHRNA4):c.1721T>C (p.Ile574Thr) rs139657121 0.00001
NM_000744.7(CHRNA4):c.1741G>A (p.Glu581Lys) rs752289948 0.00001
NM_000744.7(CHRNA4):c.1765G>A (p.Glu589Lys) rs749939383 0.00001
NM_000744.7(CHRNA4):c.176C>T (p.Ser59Leu) rs775143571 0.00001
NM_000744.7(CHRNA4):c.1842G>A (p.Thr614=) rs727503871 0.00001
NM_000744.7(CHRNA4):c.1859C>T (p.Pro620Leu) rs754340834 0.00001
NM_000744.7(CHRNA4):c.199G>A (p.Gly67Ser) rs750325388 0.00001
NM_000744.7(CHRNA4):c.212C>T (p.Ala71Val) rs753677594 0.00001
NM_000744.7(CHRNA4):c.226G>A (p.Val76Met) rs201115841 0.00001
NM_000744.7(CHRNA4):c.391G>A (p.Gly131Arg) rs759269817 0.00001
NM_000744.7(CHRNA4):c.400G>A (p.Ala134Thr) rs796052321 0.00001
NM_000744.7(CHRNA4):c.412C>T (p.Leu138=) rs372063405 0.00001
NM_000744.7(CHRNA4):c.479C>T (p.Ser160Phe) rs201421555 0.00001
NM_000744.7(CHRNA4):c.621C>T (p.Gly207=) rs149407396 0.00001
NM_000744.7(CHRNA4):c.673T>G (p.Cys225Gly) rs1263987235 0.00001
NM_000744.7(CHRNA4):c.718C>T (p.Arg240Trp) rs757030850 0.00001
NM_000744.7(CHRNA4):c.758C>T (p.Pro253Leu) rs747083728 0.00001
NM_000744.7(CHRNA4):c.778C>A (p.Leu260Ile) rs770780958 0.00001
NM_000744.7(CHRNA4):c.784G>A (p.Val262Met) rs150082508 0.00001
NM_000744.7(CHRNA4):c.859G>A (p.Val287Ile) rs772253190 0.00001
NM_000744.7(CHRNA4):c.868C>T (p.Leu290=) rs762952445 0.00001
NM_000744.7(CHRNA4):c.88G>A (p.Val30Met) rs746557446 0.00001
NM_000744.7(CHRNA4):c.985A>G (p.Asn329Asp) rs767865433 0.00001
NM_000744.7(CHRNA4):c.986A>G (p.Asn329Ser) rs201046441 0.00001
NM_000744.7(CHRNA4):c.1046T>C (p.Leu349Pro)
NM_000744.7(CHRNA4):c.1078C>T (p.Arg360Trp) rs759167480
NM_000744.7(CHRNA4):c.1161G>C (p.Glu387Asp) rs1064795592
NM_000744.7(CHRNA4):c.116G>A (p.Arg39Gln) rs1412355004
NM_000744.7(CHRNA4):c.1208_1209delinsT (p.Pro403fs) rs2068566927
NM_000744.7(CHRNA4):c.1223T>C (p.Phe408Ser)
NM_000744.7(CHRNA4):c.1227_1228inv (p.Val410Ile)
NM_000744.7(CHRNA4):c.1243C>T (p.Pro415Ser) rs2123470966
NM_000744.7(CHRNA4):c.1294C>T (p.Gln432Ter) rs1064793409
NM_000744.7(CHRNA4):c.1352C>G (p.Pro451Arg)
NM_000744.7(CHRNA4):c.1361G>A (p.Gly454Asp)
NM_000744.7(CHRNA4):c.144CAA[1] (p.Asn49del) rs780385531
NM_000744.7(CHRNA4):c.1466T>G (p.Ile489Ser) rs377087067
NM_000744.7(CHRNA4):c.1490A>G (p.Asp497Gly)
NM_000744.7(CHRNA4):c.1517C>A (p.Ala506Asp) rs1317311176
NM_000744.7(CHRNA4):c.1517C>G (p.Ala506Gly)
NM_000744.7(CHRNA4):c.1523_1525dup (p.Gly508dup) rs2068557278
NM_000744.7(CHRNA4):c.1645C>G (p.Arg549Gly) rs367658654
NM_000744.7(CHRNA4):c.1653C>A (p.Thr551=) rs886043995
NM_000744.7(CHRNA4):c.1658_1659delinsTA (p.Ala553Val) rs2123469840
NM_000744.7(CHRNA4):c.1663C>T (p.Pro555Ser) rs757510859
NM_000744.7(CHRNA4):c.1666C>A (p.Pro556Thr)
NM_000744.7(CHRNA4):c.1667C>G (p.Pro556Arg) rs77345643
NM_000744.7(CHRNA4):c.1667C>T (p.Pro556Leu) rs77345643
NM_000744.7(CHRNA4):c.1700C>G (p.Ala567Gly) rs76895198
NM_000744.7(CHRNA4):c.1700C>T (p.Ala567Val) rs76895198
NM_000744.7(CHRNA4):c.170A>G (p.Asn57Ser) rs2145408343
NM_000744.7(CHRNA4):c.1728C>A (p.Asp576Glu)
NM_000744.7(CHRNA4):c.1738G>A (p.Ala580Thr) rs1064795265
NM_000744.7(CHRNA4):c.1792A>G (p.Ile598Val) rs1019612389
NM_000744.7(CHRNA4):c.1814T>A (p.Met605Lys) rs2123463759
NM_000744.7(CHRNA4):c.1841C>T (p.Thr614Met)
NM_000744.7(CHRNA4):c.1847G>T (p.Gly616Val) rs796052324
NM_000744.7(CHRNA4):c.409C>T (p.His137Tyr)
NM_000744.7(CHRNA4):c.410A>G (p.His137Arg) rs1380488577
NM_000744.7(CHRNA4):c.448C>A (p.Gln150Lys) rs200747769
NM_000744.7(CHRNA4):c.458C>T (p.Pro153Leu)
NM_000744.7(CHRNA4):c.466A>G (p.Ile156Val) rs754895704
NM_000744.7(CHRNA4):c.476G>A (p.Ser159Asn) rs2068587768
NM_000744.7(CHRNA4):c.506C>G (p.Pro169Arg) rs199519224
NM_000744.7(CHRNA4):c.511G>A (p.Asp171Asn) rs1352017376
NM_000744.7(CHRNA4):c.521A>G (p.Asn174Ser) rs796052316
NM_000744.7(CHRNA4):c.581T>C (p.Met194Thr) rs2068585706
NM_000744.7(CHRNA4):c.592G>A (p.Val198Met)
NM_000744.7(CHRNA4):c.622G>A (p.Glu208Lys) rs771249249
NM_000744.7(CHRNA4):c.632T>C (p.Ile211Thr)
NM_000744.7(CHRNA4):c.639_640inv (p.Ala214Thr)
NM_000744.7(CHRNA4):c.661A>G (p.Arg221Gly)
NM_000744.7(CHRNA4):c.681C>A (p.Ala227=) rs45588436
NM_000744.7(CHRNA4):c.682G>A (p.Glu228Lys) rs1064795157
NM_000744.7(CHRNA4):c.711C>G (p.Phe237Leu)
NM_000744.7(CHRNA4):c.722G>A (p.Arg241Gln)
NM_000744.7(CHRNA4):c.727C>G (p.Pro243Ala) rs1568810345
NM_000744.7(CHRNA4):c.731T>C (p.Leu244Pro) rs2123472530
NM_000744.7(CHRNA4):c.806C>G (p.Ser269Cys) rs2123472338
NM_000744.7(CHRNA4):c.816C>T (p.Gly272=) rs981113016
NM_000744.7(CHRNA4):c.81C>A (p.Ser27Arg) rs1211831892
NM_000744.7(CHRNA4):c.825C>G (p.Ile275Met)
NM_000744.7(CHRNA4):c.904dup (p.Val302fs) rs1568809897
NM_000744.7(CHRNA4):c.919G>A (p.Gly307Ser) rs764586079
NM_000744.7(CHRNA4):c.934T>C (p.Phe312Leu) rs2123472007
NM_000744.7(CHRNA4):c.939C>T (p.Thr313=)
NM_000744.7(CHRNA4):c.959C>A (p.Ser320Tyr) rs776272483
NM_000744.7(CHRNA4):c.98G>C (p.Arg33Pro) rs201575409

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