ClinVar Miner

List of variants in gene CHRNA4 studied for not specified

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Gene type:
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Total variants: 88
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HGVS dbSNP gnomAD frequency
NM_000744.7(CHRNA4):c.1227T>C (p.Cys409=) rs2229960 0.86626
NM_000744.7(CHRNA4):c.678T>C (p.Cys226=) rs1044394 0.80763
NM_000744.7(CHRNA4):c.639T>C (p.Asp213=) rs1044393 0.78554
NM_000744.7(CHRNA4):c.1659G>A (p.Ala553=) rs1044397 0.40553
NM_000744.7(CHRNA4):c.1629C>T (p.Ser543=) rs1044396 0.40465
NM_000744.7(CHRNA4):c.1758+14A>G rs3827020 0.19437
NM_000744.7(CHRNA4):c.189C>T (p.Leu63=) rs2273506 0.09394
NM_000744.7(CHRNA4):c.1758+11C>T rs45442394 0.04350
NM_000744.7(CHRNA4):c.1759-14G>A rs45440192 0.01945
NM_000744.7(CHRNA4):c.384-11T>G rs201015514 0.00425
NM_000744.7(CHRNA4):c.1352C>T (p.Pro451Leu) rs55915440 0.00262
NM_000744.7(CHRNA4):c.1401C>T (p.Ser467=) rs45569837 0.00262
NM_000744.7(CHRNA4):c.1353G>A (p.Pro451=) rs113168860 0.00222
NM_000744.7(CHRNA4):c.1143C>T (p.Ala381=) rs75221202 0.00208
NM_000744.7(CHRNA4):c.1047G>A (p.Leu349=) rs75593857 0.00200
NM_000744.7(CHRNA4):c.1662G>A (p.Pro554=) rs121912284 0.00165
NM_000744.7(CHRNA4):c.1758+16G>A rs113109615 0.00153
NM_000744.7(CHRNA4):c.1460G>A (p.Arg487Gln) rs121912280 0.00152
NM_000744.7(CHRNA4):c.77-4G>A rs201123897 0.00141
NM_000744.7(CHRNA4):c.978C>T (p.Phe326=) rs76270730 0.00122
NM_000744.7(CHRNA4):c.384-18C>T rs200407438 0.00087
NM_000744.7(CHRNA4):c.1053C>T (p.Ile351=) rs61737042 0.00082
NM_000744.7(CHRNA4):c.1524C>T (p.Gly508=) rs56069517 0.00068
NM_000744.7(CHRNA4):c.1203G>C (p.Leu401=) rs56142348 0.00066
NM_000744.7(CHRNA4):c.876C>T (p.Ile292=) rs139694653 0.00055
NM_000744.7(CHRNA4):c.462G>A (p.Pro154=) rs121912245 0.00030
NM_000744.7(CHRNA4):c.1665C>T (p.Pro555=) rs199829902 0.00028
NM_000744.7(CHRNA4):c.1560C>T (p.Leu520=) rs142646795 0.00027
NM_000744.7(CHRNA4):c.1584G>A (p.Pro528=) rs199783192 0.00021
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.1269G>C (p.Lys423Asn) rs199916140 0.00014
NM_000744.7(CHRNA4):c.1758+9C>T rs202235637 0.00011
NM_000744.7(CHRNA4):c.1645C>T (p.Arg549Cys) rs367658654 0.00010
NM_000744.7(CHRNA4):c.1359C>T (p.His453=) rs121912276 0.00009
NM_000744.7(CHRNA4):c.729G>A (p.Pro243=) rs121912253 0.00009
NM_000744.7(CHRNA4):c.402G>A (p.Ala134=) rs201488442 0.00008
NM_000744.7(CHRNA4):c.1116C>T (p.Ile372=) rs199889002 0.00006
NM_000744.7(CHRNA4):c.1334C>T (p.Ser445Leu) rs773253903 0.00006
NM_000744.7(CHRNA4):c.1440C>T (p.Gly480=) rs749506890 0.00006
NM_000744.7(CHRNA4):c.1583C>T (p.Pro528Leu) rs201739273 0.00006
NM_000744.7(CHRNA4):c.1188C>T (p.Ser396=) rs201164674 0.00005
NM_000744.7(CHRNA4):c.1044C>T (p.Phe348=) rs199504576 0.00004
NM_000744.7(CHRNA4):c.1443C>T (p.Gly481=) rs1057522022 0.00004
NM_000744.7(CHRNA4):c.1637T>G (p.Val546Gly) rs764888239 0.00004
NM_000744.7(CHRNA4):c.1095G>A (p.Lys365=) rs773525149 0.00003
NM_000744.7(CHRNA4):c.1403T>C (p.Val468Ala) rs766778904 0.00003
NM_000744.7(CHRNA4):c.162C>T (p.Pro54=) rs776104392 0.00003
NM_000744.7(CHRNA4):c.1689C>T (p.Ala563=) rs374172256 0.00003
NM_000744.7(CHRNA4):c.411C>T (p.His137=) rs201467277 0.00003
NM_000744.7(CHRNA4):c.438C>T (p.Asp146=) rs147853603 0.00003
NM_000744.7(CHRNA4):c.442C>T (p.Arg148Trp) rs121912243 0.00003
NM_000744.7(CHRNA4):c.591C>T (p.Arg197=) rs776092779 0.00003
NM_000744.7(CHRNA4):c.1050C>T (p.Asp350=) rs751875597 0.00002
NM_000744.7(CHRNA4):c.1109G>A (p.Arg370Gln) rs121912267 0.00002
NM_000744.7(CHRNA4):c.1119G>A (p.Glu373=) rs201845913 0.00002
NM_000744.7(CHRNA4):c.1421C>G (p.Pro474Arg) rs199778549 0.00002
NM_000744.7(CHRNA4):c.1531G>T (p.Ala511Ser) rs200795334 0.00002
NM_000744.7(CHRNA4):c.1732C>T (p.Leu578=) rs199506324 0.00002
NM_000744.7(CHRNA4):c.1824C>T (p.Ile608=) rs748027182 0.00002
NM_000744.7(CHRNA4):c.384-14C>G rs202150684 0.00002
NM_000744.7(CHRNA4):c.510C>T (p.Phe170=) rs121912247 0.00002
NM_000744.7(CHRNA4):c.105C>T (p.His35=) rs199541666 0.00001
NM_000744.7(CHRNA4):c.1062C>T (p.Arg354=) rs764108665 0.00001
NM_000744.7(CHRNA4):c.1212C>T (p.Pro404=) rs764760832 0.00001
NM_000744.7(CHRNA4):c.1532C>T (p.Ala511Val) rs368476334 0.00001
NM_000744.7(CHRNA4):c.1683G>A (p.Ser561=) rs750265666 0.00001
NM_000744.7(CHRNA4):c.567C>T (p.Ile189=) rs758128052 0.00001
NM_000744.7(CHRNA4):c.570C>T (p.Asp190=) rs554282916 0.00001
NM_000744.7(CHRNA4):c.840C>T (p.Ser280=) rs776867107 0.00001
NM_000744.7(CHRNA4):c.997C>T (p.Arg333Cys) rs761631713 0.00001
NM_000744.7(CHRNA4):c.1065G>A (p.Leu355=) rs1057520889
NM_000744.7(CHRNA4):c.1158C>G (p.Pro386=) rs45564639
NM_000744.7(CHRNA4):c.1158_1160delinsGGG (p.Glu387Gly) rs796052320
NM_000744.7(CHRNA4):c.1209G>T (p.Pro403=) rs2229959
NM_000744.7(CHRNA4):c.1209_1210delinsTT (p.Pro404Ser) rs1064795858
NM_000744.7(CHRNA4):c.1220C>T (p.Ser407Phe) rs761335733
NM_000744.7(CHRNA4):c.135C>T (p.Phe45=) rs766240756
NM_000744.7(CHRNA4):c.1369G>A (p.Ala457Thr) rs753598324
NM_000744.7(CHRNA4):c.1395C>G (p.Ser465=) rs748016098
NM_000744.7(CHRNA4):c.1500C>A (p.Pro500=) rs201391859
NM_000744.7(CHRNA4):c.1564C>T (p.Pro522Ser) rs1057521949
NM_000744.7(CHRNA4):c.1726G>C (p.Asp576His) rs537904499
NM_000744.7(CHRNA4):c.1759-17G>C
NM_000744.7(CHRNA4):c.618T>C (p.Ser206=) rs1057521157
NM_000744.7(CHRNA4):c.681C>A (p.Ala227=) rs45588436
NM_000744.7(CHRNA4):c.77-5del rs1209439525
NM_000744.7(CHRNA4):c.858C>G (p.Thr286=) rs121912257

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