ClinVar Miner

List of variants in gene AKAP9 reported as benign for Long QT syndrome

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Gene type:
ClinVar version:
Total variants: 86
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HGVS dbSNP gnomAD frequency
NM_005751.5(AKAP9):c.8935C>T (p.Pro2979Ser) rs1063242 0.99690
NM_005751.5(AKAP9):c.3075C>T (p.Thr1025=) rs1989779 0.90157
NM_005751.5(AKAP9):c.5163-20G>A rs9785013 0.46162
NM_005751.5(AKAP9):c.4004_4006dup (p.Lys1335_Leu1336insGln) rs10644111 0.45670
NM_005751.5(AKAP9):c.10426A>C (p.Arg3476=) rs1063243 0.42386
NM_005751.5(AKAP9):c.8665C>T (p.Leu2889=) rs10228334 0.42044
NM_005751.5(AKAP9):c.3504A>G (p.Glu1168=) rs13245393 0.42036
NM_005751.5(AKAP9):c.1389G>T (p.Met463Ile) rs6964587 0.41920
NM_005751.5(AKAP9):c.6945+8C>T rs733957 0.40759
NM_005751.5(AKAP9):c.5778C>T (p.Gly1926=) rs10236397 0.40488
NM_005751.5(AKAP9):c.8375A>G (p.Asn2792Ser) rs6960867 0.33817
NM_005751.5(AKAP9):c.9145C>T (p.Leu3049=) rs28927678 0.33792
NM_005751.5(AKAP9):c.7451A>G (p.Lys2484Arg) rs35759833 0.09968
NM_005751.5(AKAP9):c.4199T>C (p.Met1400Thr) rs73407505 0.03644
NM_005751.5(AKAP9):c.3318+13C>A rs73403768 0.03055
NM_005751.5(AKAP9):c.2782T>C (p.Leu928=) rs34370932 0.01563
NM_005751.5(AKAP9):c.10608-15G>C rs112467497 0.01552
NM_005751.5(AKAP9):c.10331A>G (p.Gln3444Arg) rs34956633 0.01509
NM_005751.5(AKAP9):c.1301G>A (p.Arg434Gln) rs60031334 0.01237
NM_005751.5(AKAP9):c.10840A>G (p.Met3614Val) rs34327395 0.00921
NM_005751.5(AKAP9):c.4841G>A (p.Arg1614Gln) rs2230768 0.00849
NM_005751.5(AKAP9):c.139C>T (p.His47Tyr) rs35669569 0.00775
NM_005751.5(AKAP9):c.9929G>A (p.Arg3310Gln) rs78351282 0.00735
NM_005751.5(AKAP9):c.3827G>A (p.Arg1276Gln) rs146797353 0.00635
NM_005751.5(AKAP9):c.11331-11A>T rs115270109 0.00611
NM_005751.5(AKAP9):c.9092A>G (p.Gln3031Arg) rs61757673 0.00583
NM_005751.5(AKAP9):c.8485G>A (p.Glu2829Lys) rs149946443 0.00303
NM_005751.5(AKAP9):c.2425A>G (p.Ile809Val) rs144615758 0.00298
NM_005751.5(AKAP9):c.7275G>A (p.Gln2425=) rs61757672 0.00298
NM_005751.5(AKAP9):c.10858A>G (p.Ile3620Val) rs142729919 0.00296
NM_005751.5(AKAP9):c.9648A>G (p.Lys3216=) rs146710448 0.00289
NM_005751.5(AKAP9):c.6134A>G (p.Asn2045Ser) rs139963188 0.00279
NM_005751.5(AKAP9):c.1053A>G (p.Lys351=) rs368967178 0.00263
NM_005751.5(AKAP9):c.4519G>C (p.Asp1507His) rs34086871 0.00262
NM_005751.5(AKAP9):c.7638A>G (p.Ile2546Met) rs144662445 0.00253
NM_005751.5(AKAP9):c.6556T>C (p.Ser2186Pro) rs76177450 0.00250
NM_005751.5(AKAP9):c.1372G>C (p.Ala458Pro) rs143894795 0.00241
NM_005751.5(AKAP9):c.11098-13T>G rs76709221 0.00235
NM_005751.5(AKAP9):c.11225G>C (p.Arg3742Pro) rs34101758 0.00217
NM_005751.5(AKAP9):c.510G>C (p.Glu170Asp) rs144888041 0.00212
NM_005751.5(AKAP9):c.6331-8T>C rs186211000 0.00210
NM_005751.5(AKAP9):c.5978-4A>G rs147494754 0.00175
NM_005751.5(AKAP9):c.5428A>G (p.Met1810Val) rs115624293 0.00167
NM_005751.5(AKAP9):c.11273G>A (p.Arg3758His) rs141856443 0.00158
NM_005751.5(AKAP9):c.10197T>C (p.Thr3399=) rs143627839 0.00148
NM_005751.5(AKAP9):c.11300C>T (p.Ser3767Leu) rs149979685 0.00148
NM_005751.5(AKAP9):c.1536C>T (p.Leu512=) rs61757665 0.00146
NM_005751.5(AKAP9):c.6921A>G (p.Gln2307=) rs141156177 0.00136
NM_005751.5(AKAP9):c.3624T>C (p.Ser1208=) rs142610139 0.00118
NM_005751.5(AKAP9):c.6249C>T (p.Phe2083=) rs139770404 0.00113
NM_005751.5(AKAP9):c.10767G>A (p.Leu3589=) rs56198613 0.00111
NM_005751.5(AKAP9):c.9358+11T>C rs199714035 0.00101
NM_005751.5(AKAP9):c.6508-20A>T rs374874284 0.00079
NM_005751.5(AKAP9):c.6696A>G (p.Gln2232=) rs147194783 0.00065
NM_005751.5(AKAP9):c.3223T>C (p.Leu1075=) rs143712699 0.00064
NM_005751.5(AKAP9):c.10118C>A (p.Ser3373Tyr) rs140470576 0.00061
NM_005751.5(AKAP9):c.1737T>G (p.Ser579=) rs138049714 0.00061
NM_005751.5(AKAP9):c.10845G>A (p.Lys3615=) rs138739292 0.00054
NM_005751.5(AKAP9):c.3072G>C (p.Val1024=) rs151038875 0.00043
NM_005751.5(AKAP9):c.6918G>A (p.Gln2306=) rs188264356 0.00041
NM_005751.5(AKAP9):c.81G>A (p.Ser27=) rs145936668 0.00039
NM_005751.5(AKAP9):c.3580G>A (p.Ala1194Thr) rs139965373 0.00035
NM_005751.5(AKAP9):c.4164G>A (p.Ser1388=) rs146831402 0.00034
NM_005751.5(AKAP9):c.4825A>C (p.Arg1609=) rs143473598 0.00033
NM_005751.5(AKAP9):c.9214-6T>C rs377532409 0.00033
NM_005751.5(AKAP9):c.948A>G (p.Val316=) rs767404316 0.00031
NM_005751.5(AKAP9):c.2589G>A (p.Glu863=) rs147158224 0.00029
NM_005751.5(AKAP9):c.11135G>A (p.Arg3712Gln) rs186148498 0.00026
NM_005751.5(AKAP9):c.5895G>A (p.Glu1965=) rs138928104 0.00024
NM_005751.5(AKAP9):c.3246A>G (p.Ser1082=) rs760173622 0.00021
NM_005751.5(AKAP9):c.9763A>G (p.Arg3255Gly) rs201048693 0.00018
NM_005751.5(AKAP9):c.3193A>G (p.Ser1065Gly) rs185594755 0.00016
NM_005751.5(AKAP9):c.11714T>C (p.Met3905Thr) rs77447750 0.00014
NM_005751.5(AKAP9):c.1575T>C (p.Ala525=) rs374455304 0.00006
NM_005751.5(AKAP9):c.2477T>C (p.Ile826Thr) rs534185372 0.00006
NM_005751.5(AKAP9):c.7221A>G (p.Glu2407=) rs779280501 0.00006
NM_005751.5(AKAP9):c.11330+7A>G rs781216766 0.00004
NM_005751.5(AKAP9):c.4440G>T (p.Val1480=) rs768773867 0.00003
NM_005751.5(AKAP9):c.6330+19T>C rs376744370 0.00003
NM_005751.5(AKAP9):c.11416+23del
NM_005751.5(AKAP9):c.1242C>T (p.Phe414=) rs200250245
NM_005751.5(AKAP9):c.4245+13del rs779223487
NM_005751.5(AKAP9):c.4918-10dup rs755283199
NM_005751.5(AKAP9):c.7773A>C (p.Gln2591His) rs553800160
NM_005751.5(AKAP9):c.931-8dup
NM_005751.5(AKAP9):c.9358+10A>G rs180926926

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