ClinVar Miner

List of variants in gene CHRNA4 reported as likely benign by Invitae

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Gene type:
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Total variants: 101
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HGVS dbSNP
NM_000744.6(CHRNA4):c.1158C>T (p.Pro386=) rs45564639
NM_000744.6(CHRNA4):c.1194C>T (p.Thr398=) rs752592838
NM_000744.6(CHRNA4):c.1209G>A (p.Pro403=) rs2229959
NM_000744.6(CHRNA4):c.1221C>T (p.Ser407=) rs1601473794
NM_000744.6(CHRNA4):c.1278C>T (p.Ser426=) rs202169925
NM_000744.6(CHRNA4):c.1337C>T (p.Pro446Leu) rs769897766
NM_000744.6(CHRNA4):c.1395C>T (p.Ser465=) rs748016098
NM_000744.6(CHRNA4):c.147C>T (p.Asn49=) rs201484306
NM_000744.6(CHRNA4):c.1758+9C>T rs202235637
NM_000744.6(CHRNA4):c.1779C>T (p.Tyr593=) rs201347598
NM_000744.6(CHRNA4):c.198C>T (p.Phe66=) rs201018244
NM_000744.6(CHRNA4):c.327C>T (p.Thr109=) rs200741415
NM_000744.6(CHRNA4):c.369C>T (p.Ile123=) rs1334588457
NM_000744.6(CHRNA4):c.384-8C>G rs369806756
NM_000744.6(CHRNA4):c.384-9C>T rs199992800
NM_000744.6(CHRNA4):c.414G>A (p.Leu138=) rs769287364
NM_000744.6(CHRNA4):c.669C>T (p.Tyr223=) rs79068736
NM_000744.6(CHRNA4):c.77-10C>T rs200490160
NM_000744.6(CHRNA4):c.77-5C>T rs200082259
NM_000744.6(CHRNA4):c.77-5del rs1209439525
NM_000744.6(CHRNA4):c.787C>T (p.Leu263=) rs76830527
NM_000744.6(CHRNA4):c.801G>A (p.Leu267=) rs747762347
NM_000744.6(CHRNA4):c.957G>A (p.Leu319=) rs761872673
NM_000744.6(CHRNA4):c.95C>A (p.Thr32Asn) rs200601170
NM_000744.6(CHRNA4):c.987C>T (p.Asn329=) rs572366184
NM_000744.7(CHRNA4):c.1006C>T (p.Arg336Cys) rs56175056
NM_000744.7(CHRNA4):c.1010C>T (p.Thr337Met) rs201673381
NM_000744.7(CHRNA4):c.1012C>G (p.His338Asp) rs200069626
NM_000744.7(CHRNA4):c.1033C>T (p.Arg345Cys) rs142260793
NM_000744.7(CHRNA4):c.105C>T (p.His35=) rs199541666
NM_000744.7(CHRNA4):c.1062C>T (p.Arg354=) rs764108665
NM_000744.7(CHRNA4):c.1083G>A (p.Pro361=) rs202140852
NM_000744.7(CHRNA4):c.1104C>T (p.Cys368=) rs202166947
NM_000744.7(CHRNA4):c.1108C>T (p.Arg370Trp) rs76378652
NM_000744.7(CHRNA4):c.1109G>A (p.Arg370Gln) rs121912267
NM_000744.7(CHRNA4):c.1148G>A (p.Arg383His) rs762374374
NM_000744.7(CHRNA4):c.1160A>G (p.Glu387Gly) rs45604738
NM_000744.7(CHRNA4):c.1188C>T (p.Ser396=) rs201164674
NM_000744.7(CHRNA4):c.1227_1228inv (p.Val410Ile)
NM_000744.7(CHRNA4):c.1245G>A (p.Pro415=) rs200164578
NM_000744.7(CHRNA4):c.1266C>T (p.Cys422=) rs121912274
NM_000744.7(CHRNA4):c.1273C>T (p.Pro425Ser) rs764808511
NM_000744.7(CHRNA4):c.1283A>T (p.Gln428Leu) rs560507450
NM_000744.7(CHRNA4):c.1300C>A (p.Pro434Thr) rs545104411
NM_000744.7(CHRNA4):c.1316A>C (p.Lys439Thr) rs796052318
NM_000744.7(CHRNA4):c.1318G>C (p.Ala440Pro)
NM_000744.7(CHRNA4):c.132C>T (p.Leu44=) rs1555840462
NM_000744.7(CHRNA4):c.1334C>T (p.Ser445Leu) rs773253903
NM_000744.7(CHRNA4):c.1359C>T (p.His453=) rs121912276
NM_000744.7(CHRNA4):c.1376G>A (p.Gly459Glu) rs753201154
NM_000744.7(CHRNA4):c.1403T>C (p.Val468Ala) rs766778904
NM_000744.7(CHRNA4):c.1417A>G (p.Ser473Gly) rs1555837484
NM_000744.7(CHRNA4):c.1420C>T (p.Pro474Ser) rs773450609
NM_000744.7(CHRNA4):c.1430C>T (p.Ala477Val) rs200243948
NM_000744.7(CHRNA4):c.1440C>T (p.Gly480=) rs749506890
NM_000744.7(CHRNA4):c.1441G>A (p.Gly481Ser) rs111969225
NM_000744.7(CHRNA4):c.1454G>A (p.Arg485Gln) rs755416498
NM_000744.7(CHRNA4):c.1484G>C (p.Arg495Pro) rs549863396
NM_000744.7(CHRNA4):c.1494C>T (p.Ala498=) rs137860047
NM_000744.7(CHRNA4):c.1495G>A (p.Ala499Thr) rs150336658
NM_000744.7(CHRNA4):c.1527C>T (p.Ala509=) rs758693290
NM_000744.7(CHRNA4):c.1531G>T (p.Ala511Ser) rs200795334
NM_000744.7(CHRNA4):c.1551G>A (p.Ser517=) rs201441215
NM_000744.7(CHRNA4):c.1584G>A (p.Pro528=) rs199783192
NM_000744.7(CHRNA4):c.1634C>T (p.Thr545Met) rs121912282
NM_000744.7(CHRNA4):c.1635G>A (p.Thr545=) rs121912283
NM_000744.7(CHRNA4):c.1645C>T (p.Arg549Cys) rs367658654
NM_000744.7(CHRNA4):c.1658C>T (p.Ala553Val) rs762808071
NM_000744.7(CHRNA4):c.1661C>T (p.Pro554Leu) rs56000199
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>T (p.Ala567Val) rs76895198
NM_000744.7(CHRNA4):c.1711G>A (p.Val571Ile) rs121912285
NM_000744.7(CHRNA4):c.1715A>G (p.Gln572Arg) rs113794453
NM_000744.7(CHRNA4):c.1726G>C (p.Asp576His) rs537904499
NM_000744.7(CHRNA4):c.1757C>T (p.Ser586Leu) rs200644872
NM_000744.7(CHRNA4):c.177G>A (p.Ser59=) rs138295365
NM_000744.7(CHRNA4):c.1824C>T (p.Ile608=) rs748027182
NM_000744.7(CHRNA4):c.1860G>A (p.Pro620=) rs202203317
NM_000744.7(CHRNA4):c.1867C>T (p.Leu623=) rs878854142
NM_000744.7(CHRNA4):c.225C>T (p.Asp75=) rs113080067
NM_000744.7(CHRNA4):c.274G>C (p.Glu92Gln) rs146651027
NM_000744.7(CHRNA4):c.345C>T (p.Ser115=) rs201033859
NM_000744.7(CHRNA4):c.372C>T (p.Val124=) rs201386851
NM_000744.7(CHRNA4):c.438C>T (p.Asp146=) rs147853603
NM_000744.7(CHRNA4):c.501C>T (p.Phe167=) rs374602963
NM_000744.7(CHRNA4):c.510C>T (p.Phe170=) rs121912247
NM_000744.7(CHRNA4):c.537C>T (p.Phe179=) rs747499031
NM_000744.7(CHRNA4):c.552C>T (p.Tyr184=) rs112301452
NM_000744.7(CHRNA4):c.560C>G (p.Ala187Gly) rs200197645
NM_000744.7(CHRNA4):c.591C>T (p.Arg197=) rs776092779
NM_000744.7(CHRNA4):c.712G>A (p.Val238Ile) rs745790876
NM_000744.7(CHRNA4):c.729G>A (p.Pro243=) rs121912253
NM_000744.7(CHRNA4):c.777C>T (p.Cys259=) rs1555837947
NM_000744.7(CHRNA4):c.858C>T (p.Thr286=) rs121912257
NM_000744.7(CHRNA4):c.879C>T (p.Thr293=) rs371527699
NM_000744.7(CHRNA4):c.900A>G (p.Ser300=) rs878854143
NM_000744.7(CHRNA4):c.912A>G (p.Pro304=) rs1041716120
NM_000744.7(CHRNA4):c.963C>T (p.Ile321=) rs121912261
NM_000744.7(CHRNA4):c.964G>A (p.Val322Ile) rs779790555
NM_000744.7(CHRNA4):c.99G>C (p.Arg33=) rs539718301

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