ClinVar Miner

List of variants in gene CHRNA4 reported as benign by GeneDx

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 103
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HGVS dbSNP gnomAD frequency
NM_000744.7(CHRNA4):c.384-313G>A rs6011772 0.88372
NM_000744.7(CHRNA4):c.77-250T>G rs45457196 0.87373
NM_000744.7(CHRNA4):c.384-232A>G rs55781913 0.86919
NM_000744.7(CHRNA4):c.228+26A>G rs6090384 0.86813
NM_000744.7(CHRNA4):c.1227T>C (p.Cys409=) rs2229960 0.86626
NM_000744.7(CHRNA4):c.1759-309A>G rs6090380 0.86161
NM_000744.7(CHRNA4):c.77-196A>G rs6011789 0.83001
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.384-117A>G rs13041103 0.76965
NM_000744.7(CHRNA4):c.384-177T>C rs77439870 0.73657
NM_000744.7(CHRNA4):c.384-196G>A rs8124039 0.65349
NM_000744.7(CHRNA4):c.384-184A>G rs8115455 0.47965
NM_000744.7(CHRNA4):c.384-202A>C rs8115495 0.44902
NM_000744.7(CHRNA4):c.384-166G>A rs77645330 0.44095
NM_000744.7(CHRNA4):c.384-159del rs763902315 0.40556
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.384-189C>T rs78581196 0.37912
NM_000744.7(CHRNA4):c.384-209_384-208insAC rs1555838328 0.28349
NM_000744.7(CHRNA4):c.384-171T>C rs55658831 0.27399
NM_000744.7(CHRNA4):c.384-201T>C rs59145036 0.27213
NM_000744.7(CHRNA4):c.384-135_384-134insCGTGGGCATGGGTGTGGATGTGGGCGTGGGACGTGGG rs1568811491 0.21653
NM_000744.7(CHRNA4):c.1758+14A>G rs3827020 0.19437
NM_000744.7(CHRNA4):c.229-294C>T rs2273504 0.19175
NM_000744.7(CHRNA4):c.77-90C>T rs3818204 0.18011
NM_000744.7(CHRNA4):c.384-133G>A rs55731226 0.17787
NM_000744.7(CHRNA4):c.384-211T>G rs866354873 0.15974
NM_000744.7(CHRNA4):c.384-213C>T rs79124348 0.11212
NM_000744.7(CHRNA4):c.189C>T (p.Leu63=) rs2273506 0.09394
NM_000744.7(CHRNA4):c.228+317C>G rs6011788 0.09393
NM_000744.7(CHRNA4):c.228+22G>A rs2273505 0.09385
NM_000744.7(CHRNA4):c.384-157A>G rs8115452 0.06354
NM_000744.7(CHRNA4):c.1758+191C>T rs114426220 0.06197
NM_000744.7(CHRNA4):c.384-23C>T rs56151028 0.04930
NM_000744.7(CHRNA4):c.384-159A>G rs78401560 0.04537
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.*255C>T rs187153060 0.00222
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.*218T>G rs192006981 0.00114
NM_000744.7(CHRNA4):c.1160A>G (p.Glu387Gly) rs45604738 0.00088
NM_000744.7(CHRNA4):c.1053C>T (p.Ile351=) rs61737042 0.00082
NM_000744.7(CHRNA4):c.1108C>T (p.Arg370Trp) rs76378652 0.00080
NM_000744.7(CHRNA4):c.*301C>T rs201041492 0.00071
NM_000744.7(CHRNA4):c.1441G>A (p.Gly481Ser) rs111969225 0.00070
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.228+41G>A rs199714054 0.00056
NM_000744.7(CHRNA4):c.*217C>G rs200987079 0.00050
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.1550C>T (p.Ser517Leu) rs45622132 0.00026
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.1359C>T (p.His453=) rs121912276 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.492C>T (p.Asp164=) rs200259564 0.00005
NM_000744.7(CHRNA4):c.1138A>G (p.Ser380Gly) rs187372416 0.00004
NM_000744.7(CHRNA4):c.828G>A (p.Thr276=) rs2234932 0.00004
NM_000744.7(CHRNA4):c.1095G>A (p.Lys365=) rs773525149 0.00003
NM_000744.7(CHRNA4):c.510C>T (p.Phe170=) rs121912247 0.00002
NM_000744.7(CHRNA4):c.*114C>T rs201354711 0.00001
NM_000744.7(CHRNA4):c.*144G>C rs199879109
NM_000744.7(CHRNA4):c.*252C>T rs113458361
NM_000744.7(CHRNA4):c.1158C>G (p.Pro386=) rs45564639
NM_000744.7(CHRNA4):c.1209G>T (p.Pro403=) rs2229959
NM_000744.7(CHRNA4):c.1758+192G>C rs3899053
NM_000744.7(CHRNA4):c.384-142dup rs11483691
NM_000744.7(CHRNA4):c.384-153A>C rs370897210
NM_000744.7(CHRNA4):c.384-161_384-160insGACGT rs879502414
NM_000744.7(CHRNA4):c.384-172A>C rs374263187
NM_000744.7(CHRNA4):c.384-172_384-171insCGTGGGGCGTGGGCGTGGC rs1555838260
NM_000744.7(CHRNA4):c.384-172_384-171insCGTGGGGCGTGGGCGTGGCTGTGGGCGTGGGGCGTGGC rs1555838260
NM_000744.7(CHRNA4):c.384-183C>T rs372826141
NM_000744.7(CHRNA4):c.384-195C>T rs1395104048
NM_000744.7(CHRNA4):c.384-206_384-205insGACGGGGGCA rs879688121
NM_000744.7(CHRNA4):c.384-208_384-207insCATGGA rs1232189431
NM_000744.7(CHRNA4):c.681C>A (p.Ala227=) rs45588436
NM_000744.7(CHRNA4):c.77-169_77-168del rs67528285
NM_000744.7(CHRNA4):c.77-170G>C rs13044665
NM_000744.7(CHRNA4):c.77-186CA[7] rs1296560500
NM_000744.7(CHRNA4):c.77-186_77-185insCGCA rs1555840750
NM_000744.7(CHRNA4):c.77-186_77-185insGCGC rs11472697
NM_000744.7(CHRNA4):c.77-187_77-186dup rs11472697
NM_000744.7(CHRNA4):c.77-207_77-206insCACACACACACAGCGCACGCCCGG rs1555840815
NM_000744.7(CHRNA4):c.77-215_77-214insTACACAGCGCACGCCCGG rs1268419860
NM_000744.7(CHRNA4):c.77-230CA[11] rs57641753
NM_000744.7(CHRNA4):c.77-230CA[17] rs57641753
NM_000744.7(CHRNA4):c.77-230CA[20] rs57641753
NM_000744.7(CHRNA4):c.77-230CA[21] rs57641753

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