ClinVar Miner

List of variants in gene AKAP9 studied for not specified

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Gene type:
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Total variants: 75
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HGVS dbSNP
NM_005751.4(AKAP9):c.10118C>G (p.Ser3373Cys) rs140470576
NM_005751.4(AKAP9):c.10254G>C (p.Gln3418His) rs61757663
NM_005751.4(AKAP9):c.10319T>C (p.Met3440Thr) rs751924200
NM_005751.4(AKAP9):c.10331A>G (p.Gln3444Arg) rs34956633
NM_005751.4(AKAP9):c.10426A>C (p.Arg3476=) rs1063243
NM_005751.4(AKAP9):c.10495A>G (p.Ile3499Val) rs756721657
NM_005751.4(AKAP9):c.10526A>G (p.Asn3509Ser) rs786205711
NM_005751.4(AKAP9):c.10664A>T (p.Asp3555Val) rs139046510
NM_005751.4(AKAP9):c.10840A>G (p.Met3614Val) rs34327395
NM_005751.4(AKAP9):c.10858A>G (p.Ile3620Val) rs142729919
NM_005751.4(AKAP9):c.1099G>A (p.Val367Met) rs138161478
NM_005751.4(AKAP9):c.11225G>C (p.Arg3742Pro) rs34101758
NM_005751.4(AKAP9):c.11519T>C (p.Ile3840Thr) rs145675748
NM_005751.4(AKAP9):c.1158A>T (p.Lys386Asn) rs142673316
NM_005751.4(AKAP9):c.119G>A (p.Arg40Lys) rs755408339
NM_005751.4(AKAP9):c.1223A>G (p.Asn408Ser) rs761210281
NM_005751.4(AKAP9):c.1288T>A (p.Leu430Ile) rs756987149
NM_005751.4(AKAP9):c.1289T>A (p.Leu430Ter) rs778556625
NM_005751.4(AKAP9):c.1301G>A (p.Arg434Gln) rs60031334
NM_005751.4(AKAP9):c.1372G>C (p.Ala458Pro) rs143894795
NM_005751.4(AKAP9):c.1389G>T (p.Met463Ile) rs6964587
NM_005751.4(AKAP9):c.139C>T (p.His47Tyr) rs35669569
NM_005751.4(AKAP9):c.1536C>T (p.Leu512=) rs61757665
NM_005751.4(AKAP9):c.1538A>G (p.Lys513Arg) rs786205713
NM_005751.4(AKAP9):c.158A>G (p.His53Arg) rs142125596
NM_005751.4(AKAP9):c.1651A>G (p.Ile551Val) rs140664656
NM_005751.4(AKAP9):c.235C>T (p.Pro79Ser) rs768026366
NM_005751.4(AKAP9):c.2425A>G (p.Ile809Val) rs144615758
NM_005751.4(AKAP9):c.2477T>C (p.Ile826Thr) rs534185372
NM_005751.4(AKAP9):c.288G>T (p.Glu96Asp) rs34953651
NM_005751.4(AKAP9):c.289C>G (p.Gln97Glu) rs786205712
NM_005751.4(AKAP9):c.2945C>A (p.Ser982Tyr) rs374340343
NM_005751.4(AKAP9):c.3075C>T (p.Thr1025=) rs1989779
NM_005751.4(AKAP9):c.3504A>G (p.Glu1168=) rs13245393
NM_005751.4(AKAP9):c.3827G>A (p.Arg1276Gln) rs146797353
NM_005751.4(AKAP9):c.4004_4006dup (p.Leu1336_Glu1337insGln) rs10644111
NM_005751.4(AKAP9):c.4127G>C (p.Ser1376Thr) rs144372406
NM_005751.4(AKAP9):c.4195A>G (p.Thr1399Ala) rs757261572
NM_005751.4(AKAP9):c.4199T>C (p.Met1400Thr) rs73407505
NM_005751.4(AKAP9):c.4519G>C (p.Asp1507His) rs34086871
NM_005751.4(AKAP9):c.4800A>G (p.Glu1600=) rs138765069
NM_005751.4(AKAP9):c.4814C>T (p.Thr1605Met) rs777627168
NM_005751.4(AKAP9):c.4837A>G (p.Met1613Val) rs193922723
NM_005751.4(AKAP9):c.4841G>A (p.Arg1614Gln) rs2230768
NM_005751.4(AKAP9):c.4872A>G (p.Glu1624=) rs570384292
NM_005751.4(AKAP9):c.4917+14del rs765796287
NM_005751.4(AKAP9):c.4917+3A>C rs200730225
NM_005751.4(AKAP9):c.4927A>C (p.Ile1643Leu) rs141990258
NM_005751.4(AKAP9):c.4985C>T (p.Ala1662Val) rs149244653
NM_005751.4(AKAP9):c.5058+12T>G rs373705132
NM_005751.4(AKAP9):c.5117A>G (p.Asp1706Gly) rs139468199
NM_005751.4(AKAP9):c.5163-20G>A rs9785013
NM_005751.4(AKAP9):c.5246T>C (p.Ile1749Thr) rs150016098
NM_005751.4(AKAP9):c.5284A>G (p.Lys1762Glu) rs568626378
NM_005751.4(AKAP9):c.5369T>G (p.Val1790Gly) rs151021935
NM_005751.4(AKAP9):c.5778C>T (p.Gly1926=) rs10236397
NM_005751.4(AKAP9):c.5830A>G (p.Ile1944Val) rs587780849
NM_005751.4(AKAP9):c.6945+8C>T rs733957
NM_005751.4(AKAP9):c.6974G>A (p.Arg2325Lys) rs786205708
NM_005751.4(AKAP9):c.7275G>A (p.Gln2425=) rs61757672
NM_005751.4(AKAP9):c.7451A>G (p.Lys2484Arg) rs35759833
NM_005751.4(AKAP9):c.7638A>G (p.Ile2546Met) rs144662445
NM_005751.4(AKAP9):c.80C>T (p.Ser27Leu) rs142401936
NM_005751.4(AKAP9):c.8189A>G (p.Gln2730Arg) rs80191629
NM_005751.4(AKAP9):c.8207T>G (p.Val2736Gly) rs769936861
NM_005751.4(AKAP9):c.8221G>T (p.Ala2741Ser) rs368001901
NM_005751.4(AKAP9):c.8375A>G (p.Asn2792Ser) rs6960867
NM_005751.4(AKAP9):c.8656A>G (p.Ile2886Val) rs143283097
NM_005751.4(AKAP9):c.8665C>T (p.Leu2889=) rs10228334
NM_005751.4(AKAP9):c.8912A>G (p.His2971Arg) rs786205710
NM_005751.4(AKAP9):c.8935C>T (p.Pro2979Ser) rs1063242
NM_005751.4(AKAP9):c.9092A>G (p.Gln3031Arg) rs61757673
NM_005751.4(AKAP9):c.9112C>T (p.Arg3038Cys) rs753467156
NM_005751.4(AKAP9):c.9145C>T (p.Leu3049=) rs28927678
NM_005751.4(AKAP9):c.9214-6T>C rs377532409

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