ClinVar Miner

List of variants in gene AKAP9 reported by Biesecker Lab/Clinical Genomics Section,National Institutes of Health

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Gene type:
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Total variants: 66
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HGVS dbSNP
NM_005751.4(AKAP9):c.10118C>A (p.Ser3373Tyr) rs140470576
NM_005751.4(AKAP9):c.10249C>T (p.Arg3417Cys) rs146495719
NM_005751.4(AKAP9):c.10254G>C (p.Gln3418His) rs61757663
NM_005751.4(AKAP9):c.10331A>G (p.Gln3444Arg) rs34956633
NM_005751.4(AKAP9):c.10459G>A (p.Glu3487Lys) rs61757664
NM_005751.4(AKAP9):c.10523G>A (p.Cys3508Tyr) rs750007670
NM_005751.4(AKAP9):c.10664A>T (p.Asp3555Val) rs139046510
NM_005751.4(AKAP9):c.10672A>G (p.Ile3558Val) rs144054367
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.11135G>A (p.Arg3712Gln) rs186148498
NM_005751.4(AKAP9):c.11225G>C (p.Arg3742Pro) rs34101758
NM_005751.4(AKAP9):c.11229G>A (p.Met3743Ile) rs143306820
NM_005751.4(AKAP9):c.11230G>T (p.Gly3744Trp) rs200327385
NM_005751.4(AKAP9):c.11273G>A (p.Arg3758His) rs141856443
NM_005751.4(AKAP9):c.11362G>C (p.Val3788Leu) rs199527737
NM_005751.4(AKAP9):c.1158A>T (p.Lys386Asn) rs142673316
NM_005751.4(AKAP9):c.11714T>C (p.Met3905Thr) rs77447750
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.1685A>G (p.His562Arg) rs145033147
NM_005751.4(AKAP9):c.1742C>A (p.Ser581Tyr) rs786205260
NM_005751.4(AKAP9):c.2230G>A (p.Glu744Lys) rs202091548
NM_005751.4(AKAP9):c.2425A>G (p.Ile809Val) rs144615758
NM_005751.4(AKAP9):c.2581T>C (p.Tyr861His) rs61757557
NM_005751.4(AKAP9):c.3580G>A (p.Ala1194Thr) rs139965373
NM_005751.4(AKAP9):c.3827G>A (p.Arg1276Gln) rs146797353
NM_005751.4(AKAP9):c.389C>G (p.Pro130Arg) rs200518712
NM_005751.4(AKAP9):c.3950T>C (p.Ile1317Thr) rs199773513
NM_005751.4(AKAP9):c.4156G>T (p.Val1386Phe) rs762293635
NM_005751.4(AKAP9):c.4190A>G (p.Gln1397Arg) rs139612565
NM_005751.4(AKAP9):c.4199T>C (p.Met1400Thr) rs73407505
NM_005751.4(AKAP9):c.4342A>G (p.Ile1448Val) rs150379637
NM_005751.4(AKAP9):c.4519G>C (p.Asp1507His) rs34086871
NM_005751.4(AKAP9):c.4841G>A (p.Arg1614Gln) rs2230768
NM_005751.4(AKAP9):c.510G>C (p.Glu170Asp) rs144888041
NM_005751.4(AKAP9):c.5234T>C (p.Val1745Ala) rs201632145
NM_005751.4(AKAP9):c.5246T>C (p.Ile1749Thr) rs150016098
NM_005751.4(AKAP9):c.5369T>G (p.Val1790Gly) rs151021935
NM_005751.4(AKAP9):c.5534A>G (p.Asn1845Ser) rs786205261
NM_005751.4(AKAP9):c.5543C>G (p.Ser1848Cys) rs189083857
NM_005751.4(AKAP9):c.5636T>C (p.Met1879Thr) rs776979647
NM_005751.4(AKAP9):c.5827G>T (p.Asp1943Tyr) rs201144675
NM_005751.4(AKAP9):c.6037G>A (p.Glu2013Lys) rs61757671
NM_005751.4(AKAP9):c.610G>A (p.Asp204Asn) rs148920964
NM_005751.4(AKAP9):c.6176A>G (p.Glu2059Gly) rs73226383
NM_005751.4(AKAP9):c.6556T>C (p.Ser2186Pro) rs76177450
NM_005751.4(AKAP9):c.7451A>G (p.Lys2484Arg) rs35759833
NM_005751.4(AKAP9):c.7488T>G (p.Asn2496Lys) rs201977551
NM_005751.4(AKAP9):c.7773A>C (p.Gln2591His) rs553800160
NM_005751.4(AKAP9):c.80C>T (p.Ser27Leu) rs142401936
NM_005751.4(AKAP9):c.8286A>C (p.Lys2762Asn) rs144875383
NM_005751.4(AKAP9):c.8375A>G (p.Asn2792Ser) rs6960867
NM_005751.4(AKAP9):c.8894A>G (p.Tyr2965Cys) rs201958512
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.9577A>G (p.Arg3193Gly) rs199762211
NM_005751.4(AKAP9):c.971T>C (p.Ile324Thr) rs367857951
NM_005751.4(AKAP9):c.9763A>G (p.Arg3255Gly) rs201048693
NM_005751.4(AKAP9):c.9830T>C (p.Ile3277Thr) rs144021475
NM_005751.4(AKAP9):c.9929G>A (p.Arg3310Gln) rs78351282
NM_147185.3(AKAP9):c.4004_4006dup (p.Leu1336_Glu1337insGln) rs10644111
NM_147185.3(AKAP9):c.7897_7899AAG[1] (p.Lys2634del) rs786205262

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