ClinVar Miner

List of variants in gene AKAP9 reported as benign

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Gene type:
ClinVar version:
Total variants: 117
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HGVS dbSNP
GRCh37/hg19 7q21.2(chr7:91572749-91691565)x3
GRCh37/hg19 7q21.2(chr7:91572749-91700267)x3
GRCh37/hg19 7q21.2(chr7:91575417-91691565)x3
GRCh37/hg19 7q21.2(chr7:91575417-91694743)x3
GRCh37/hg19 7q21.2(chr7:91707197-91719608)x0
NC_000007.14:g.92071328_92071329del
NM_005751.4(AKAP9):c.-285C>T
NM_005751.4(AKAP9):c.10118C>A (p.Ser3373Tyr) rs140470576
NM_005751.4(AKAP9):c.10197T>C (p.Thr3399=) rs143627839
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.1053A>G (p.Lys351=) rs368967178
NM_005751.4(AKAP9):c.10608-38G>A
NM_005751.4(AKAP9):c.10767G>A (p.Leu3589=) rs56198613
NM_005751.4(AKAP9):c.10840A>G (p.Met3614Val) rs34327395
NM_005751.4(AKAP9):c.10845G>A (p.Lys3615=) rs138739292
NM_005751.4(AKAP9):c.10858A>G (p.Ile3620Val) rs142729919
NM_005751.4(AKAP9):c.11097+221A>T
NM_005751.4(AKAP9):c.11135G>A (p.Arg3712Gln) rs186148498
NM_005751.4(AKAP9):c.11225G>C (p.Arg3742Pro) rs34101758
NM_005751.4(AKAP9):c.11273G>A (p.Arg3758His) rs141856443
NM_005751.4(AKAP9):c.11300C>T (p.Ser3767Leu) rs149979685
NM_005751.4(AKAP9):c.11416+222A>G
NM_005751.4(AKAP9):c.11417-143T>G
NM_005751.4(AKAP9):c.11417-301C>G
NM_005751.4(AKAP9):c.11546+138A>G
NM_005751.4(AKAP9):c.11546+185C>T
NM_005751.4(AKAP9):c.11546+321T>C
NM_005751.4(AKAP9):c.11546+58T>A
NM_005751.4(AKAP9):c.11714T>C (p.Met3905Thr) rs77447750
NM_005751.4(AKAP9):c.1242C>T (p.Phe414=) rs200250245
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.1737T>G (p.Ser579=) rs138049714
NM_005751.4(AKAP9):c.2425A>G (p.Ile809Val) rs144615758
NM_005751.4(AKAP9):c.2589G>A (p.Glu863=) rs147158224
NM_005751.4(AKAP9):c.2782T>C (p.Leu928=) rs34370932
NM_005751.4(AKAP9):c.3072G>C (p.Val1024=) rs151038875
NM_005751.4(AKAP9):c.3075C>T (p.Thr1025=) rs1989779
NM_005751.4(AKAP9):c.3193A>G (p.Ser1065Gly) rs185594755
NM_005751.4(AKAP9):c.3223T>C (p.Leu1075=) rs143712699
NM_005751.4(AKAP9):c.3246A>G (p.Ser1082=) rs760173622
NM_005751.4(AKAP9):c.3504A>G (p.Glu1168=) rs13245393
NM_005751.4(AKAP9):c.3533-161G>T
NM_005751.4(AKAP9):c.3580G>A (p.Ala1194Thr) rs139965373
NM_005751.4(AKAP9):c.3613-178A>G
NM_005751.4(AKAP9):c.3613-291G>C
NM_005751.4(AKAP9):c.3624T>C (p.Ser1208=) rs142610139
NM_005751.4(AKAP9):c.3752-133C>T
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.4149-59C>G
NM_005751.4(AKAP9):c.4164G>A (p.Ser1388=) rs146831402
NM_005751.4(AKAP9):c.4199T>C (p.Met1400Thr) rs73407505
NM_005751.4(AKAP9):c.4338+193G>C
NM_005751.4(AKAP9):c.4339-41T>G
NM_005751.4(AKAP9):c.4519G>C (p.Asp1507His) rs34086871
NM_005751.4(AKAP9):c.4692+279G>A
NM_005751.4(AKAP9):c.4693-11del rs71292989
NM_005751.4(AKAP9):c.4693-180G>A
NM_005751.4(AKAP9):c.48+154C>A
NM_005751.4(AKAP9):c.4841G>A (p.Arg1614Gln) rs2230768
NM_005751.4(AKAP9):c.49-21G>A
NM_005751.4(AKAP9):c.5058+12T>G rs373705132
NM_005751.4(AKAP9):c.5059-129C>A
NM_005751.4(AKAP9):c.510G>C (p.Glu170Asp) rs144888041
NM_005751.4(AKAP9):c.5162+318G>A
NM_005751.4(AKAP9):c.5163-20G>A rs9785013
NM_005751.4(AKAP9):c.5246T>C (p.Ile1749Thr) rs150016098
NM_005751.4(AKAP9):c.5283T>C (p.Ser1761=) rs776345336
NM_005751.4(AKAP9):c.5368+280T>C
NM_005751.4(AKAP9):c.5369-244dup
NM_005751.4(AKAP9):c.5428A>G (p.Met1810Val) rs115624293
NM_005751.4(AKAP9):c.5602-117A>G
NM_005751.4(AKAP9):c.576+307G>A
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.5977+146G>T
NM_005751.4(AKAP9):c.5978-4A>G rs147494754
NM_005751.4(AKAP9):c.6134A>G (p.Asn2045Ser) rs139963188
NM_005751.4(AKAP9):c.6249C>T (p.Phe2083=) rs139770404
NM_005751.4(AKAP9):c.6331-8T>C rs186211000
NM_005751.4(AKAP9):c.6507+259G>A
NM_005751.4(AKAP9):c.6508-239C>T
NM_005751.4(AKAP9):c.6508-312A>C
NM_005751.4(AKAP9):c.6556T>C (p.Ser2186Pro) rs76177450
NM_005751.4(AKAP9):c.6696A>G (p.Gln2232=) rs147194783
NM_005751.4(AKAP9):c.6765+303C>G
NM_005751.4(AKAP9):c.6921A>G (p.Gln2307=) rs141156177
NM_005751.4(AKAP9):c.6945+8C>T rs733957
NM_005751.4(AKAP9):c.6946-174T>C
NM_005751.4(AKAP9):c.7221A>G (p.Glu2407=) rs779280501
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.747A>G (p.Glu249=) rs78515732
NM_005751.4(AKAP9):c.7638A>G (p.Ile2546Met) rs144662445
NM_005751.4(AKAP9):c.7773A>C (p.Gln2591His) rs553800160
NM_005751.4(AKAP9):c.8020-45A>G
NM_005751.4(AKAP9):c.80C>T (p.Ser27Leu) rs142401936
NM_005751.4(AKAP9):c.8375A>G (p.Asn2792Ser) rs6960867
NM_005751.4(AKAP9):c.8485G>A (p.Glu2829Lys) rs149946443
NM_005751.4(AKAP9):c.8665C>T (p.Leu2889=) rs10228334
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.9145C>T (p.Leu3049=) rs28927678
NM_005751.4(AKAP9):c.931-161G>C
NM_005751.4(AKAP9):c.931-178T>G
NM_005751.4(AKAP9):c.9358+10A>G rs180926926
NM_005751.4(AKAP9):c.948A>G (p.Val316=) rs767404316
NM_005751.4(AKAP9):c.9648A>G (p.Lys3216=) rs146710448
NM_005751.4(AKAP9):c.9729+266G>A
NM_005751.4(AKAP9):c.9730-309G>C
NM_005751.4(AKAP9):c.9763A>G (p.Arg3255Gly) rs201048693
NM_005751.4(AKAP9):c.9929G>A (p.Arg3310Gln) rs78351282

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