ClinVar Miner

List of variants in gene CHRNA4 reported as uncertain significance by GeneDx

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Total variants: 71
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HGVS dbSNP
NM_000744.6(CHRNA4):c.1012C>G (p.His338Asp) rs200069626
NM_000744.6(CHRNA4):c.1106G>A (p.Arg369Gln) rs200007766
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.1145C>T (p.Pro382Leu) rs769233762
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.1209_1210delinsTT (p.Pro404Ser) rs1064795858
NM_000744.6(CHRNA4):c.1232C>A (p.Pro411His) rs779035642
NM_000744.6(CHRNA4):c.1266C>T (p.Cys422=) rs121912274
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.1294C>T (p.Gln432Ter) rs1064793409
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.1369G>A (p.Ala457Thr) rs753598324
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.1402G>A (p.Val468Ile) rs121912278
NM_000744.6(CHRNA4):c.140G>A (p.Gly47Asp) rs764990637
NM_000744.6(CHRNA4):c.1415C>T (p.Ser472Phe) rs534477048
NM_000744.6(CHRNA4):c.1430C>T (p.Ala477Val) rs200243948
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.1459C>T (p.Arg487Trp) rs200200279
NM_000744.6(CHRNA4):c.1484G>C (p.Arg495Pro) rs549863396
NM_000744.6(CHRNA4):c.1510G>A (p.Gly504Ser) rs201244483
NM_000744.6(CHRNA4):c.1520C>T (p.Ala507Val) rs747883053
NM_000744.6(CHRNA4):c.1525G>A (p.Ala509Thr) rs142137599
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.1645C>G (p.Arg549Gly) rs367658654
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.1682C>T (p.Ser561Leu) rs199949135
NM_000744.6(CHRNA4):c.1685C>T (p.Pro562Leu) rs200750362
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.1715A>G (p.Gln572Arg) rs113794453
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.1757C>T (p.Ser586Leu) rs200644872
NM_000744.6(CHRNA4):c.1765G>A (p.Glu589Lys) rs749939383
NM_000744.6(CHRNA4):c.1792A>G (p.Ile598Val) rs1019612389
NM_000744.6(CHRNA4):c.1825G>A (p.Val609Ile) rs201168195
NM_000744.6(CHRNA4):c.1847G>T (p.Gly616Val) rs796052324
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.212C>T (p.Ala71Val) rs753677594
NM_000744.6(CHRNA4):c.274-13C>G rs1057524765
NM_000744.6(CHRNA4):c.283G>A (p.Asp95Asn) rs761317422
NM_000744.6(CHRNA4):c.358C>T (p.Arg120Trp) rs200010568
NM_000744.6(CHRNA4):c.400G>A (p.Ala134Thr) rs796052321
NM_000744.6(CHRNA4):c.442C>T (p.Arg148Trp) rs121912243
NM_000744.6(CHRNA4):c.461C>T (p.Pro154Leu) rs121912244
NM_000744.6(CHRNA4):c.479C>T (p.Ser160Phe) rs201421555
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.621C>T (p.Gly207=) rs149407396
NM_000744.6(CHRNA4):c.622G>A (p.Glu208Lys) rs771249249
NM_000744.6(CHRNA4):c.682G>A (p.Glu228Lys) rs1064795157
NM_000744.6(CHRNA4):c.692C>T (p.Pro231Leu) rs763248360
NM_000744.6(CHRNA4):c.718C>T (p.Arg240Trp) rs757030850
NM_000744.6(CHRNA4):c.816C>T (p.Gly272=) rs981113016
NM_000744.6(CHRNA4):c.88G>A (p.Val30Met) rs746557446
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.985A>G (p.Asn329Asp) rs767865433

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