ClinVar Miner

List of variants in gene AKAP9 reported as likely benign by Invitae

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Gene type:
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Total variants: 85
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HGVS dbSNP
NM_005751.4(AKAP9):c.10200G>A (p.Glu3400=) rs796565514
NM_005751.4(AKAP9):c.10221G>A (p.Glu3407=) rs200711005
NM_005751.4(AKAP9):c.10236G>A (p.Val3412=) rs878854805
NM_005751.4(AKAP9):c.10254G>C (p.Gln3418His) rs61757663
NM_005751.4(AKAP9):c.10392T>C (p.Leu3464=) rs773258039
NM_005751.4(AKAP9):c.10459G>A (p.Glu3487Lys) rs61757664
NM_005751.4(AKAP9):c.10518C>T (p.Thr3506=) rs377663331
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.1099G>A (p.Val367Met) rs138161478
NM_005751.4(AKAP9):c.1101G>A (p.Val367=) rs878854806
NM_005751.4(AKAP9):c.11157G>A (p.Lys3719=) rs1060504955
NM_005751.4(AKAP9):c.11316C>T (p.Ser3772=) rs185491437
NM_005751.4(AKAP9):c.11340T>C (p.Phe3780=) rs756185133
NM_005751.4(AKAP9):c.11580T>G (p.Gly3860=) rs756398963
NM_005751.4(AKAP9):c.126G>A (p.Thr42=) rs186969744
NM_005751.4(AKAP9):c.1623G>A (p.Arg541=) rs746045284
NM_005751.4(AKAP9):c.2349A>G (p.Glu783=) rs61757667
NM_005751.4(AKAP9):c.2609G>A (p.Cys870Tyr) rs187255726
NM_005751.4(AKAP9):c.288G>T (p.Glu96Asp) rs34953651
NM_005751.4(AKAP9):c.2945C>A (p.Ser982Tyr) rs374340343
NM_005751.4(AKAP9):c.3430T>C (p.Cys1144Arg) rs141039834
NM_005751.4(AKAP9):c.3447G>A (p.Glu1149=) rs779022140
NM_005751.4(AKAP9):c.3838-10T>C rs1426775226
NM_005751.4(AKAP9):c.3838-4A>T rs565812419
NM_005751.4(AKAP9):c.3886A>G (p.Asn1296Asp) rs753029277
NM_005751.4(AKAP9):c.4127G>C (p.Ser1376Thr) rs144372406
NM_005751.4(AKAP9):c.4143G>A (p.Pro1381=) rs754974720
NM_005751.4(AKAP9):c.4163C>T (p.Ser1388Leu) rs143565222
NM_005751.4(AKAP9):c.4190A>G (p.Gln1397Arg) rs139612565
NM_005751.4(AKAP9):c.4246-6A>T rs192046591
NM_005751.4(AKAP9):c.4259T>G (p.Phe1420Cys) rs184184931
NM_005751.4(AKAP9):c.4266G>A (p.Val1422=) rs1486993423
NM_005751.4(AKAP9):c.4302A>G (p.Lys1434=) rs1554422424
NM_005751.4(AKAP9):c.4342A>G (p.Ile1448Val) rs150379637
NM_005751.4(AKAP9):c.441A>T (p.Glu147Asp) rs185898118
NM_005751.4(AKAP9):c.4693-10A>T rs772968330
NM_005751.4(AKAP9):c.4800A>G (p.Glu1600=) rs138765069
NM_005751.4(AKAP9):c.4825_4826delinsCA (p.Arg1609Gln) rs786205707
NM_005751.4(AKAP9):c.5058+9G>C rs750169072
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.5301C>T (p.Ala1767=) rs1060504956
NM_005751.4(AKAP9):c.5369T>G (p.Val1790Gly) rs151021935
NM_005751.4(AKAP9):c.5404G>A (p.Asp1802Asn) rs142263098
NM_005751.4(AKAP9):c.5610T>C (p.His1870=) rs150332727
NM_005751.4(AKAP9):c.5725G>A (p.Ala1909Thr) rs200844952
NM_005751.4(AKAP9):c.5802T>C (p.Phe1934=) rs771217403
NM_005751.4(AKAP9):c.5907C>A (p.Ile1969=) rs1554440805
NM_005751.4(AKAP9):c.5928G>A (p.Leu1976=) rs142251048
NM_005751.4(AKAP9):c.6037G>A (p.Glu2013Lys) rs61757671
NM_005751.4(AKAP9):c.6046C>T (p.Arg2016Cys) rs376950905
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.645A>G (p.Gln215=) rs767167128
NM_005751.4(AKAP9):c.6669T>C (p.Asn2223=) rs551316515
NM_005751.4(AKAP9):c.6915G>A (p.Gln2305=) rs776992805
NM_005751.4(AKAP9):c.6966A>G (p.Glu2322=) rs878854809
NM_005751.4(AKAP9):c.6996A>G (p.Glu2332=) rs1315064294
NM_005751.4(AKAP9):c.7166A>G (p.Asp2389Gly) rs140782750
NM_005751.4(AKAP9):c.7188G>A (p.Leu2396=) rs1554450559
NM_005751.4(AKAP9):c.7208A>G (p.Glu2403Gly) rs150102469
NM_005751.4(AKAP9):c.7572C>T (p.Asp2524=) rs1004449825
NM_005751.4(AKAP9):c.7683T>C (p.Leu2561=) rs746961943
NM_005751.4(AKAP9):c.7800T>C (p.Asp2600=) rs770573236
NM_005751.4(AKAP9):c.8020-5T>C rs375175124
NM_005751.4(AKAP9):c.8052A>G (p.Glu2684=) rs878854810
NM_005751.4(AKAP9):c.8079T>C (p.Ala2693=) rs371316172
NM_005751.4(AKAP9):c.80C>T (p.Ser27Leu) rs142401936
NM_005751.4(AKAP9):c.813C>T (p.Leu271=) rs776451600
NM_005751.4(AKAP9):c.8286A>C (p.Lys2762Asn) rs144875383
NM_005751.4(AKAP9):c.8646+8G>A rs878854811
NM_005751.4(AKAP9):c.883A>G (p.Thr295Ala) rs149825027
NM_005751.4(AKAP9):c.8975C>T (p.Ser2992Leu) rs149341527
NM_005751.4(AKAP9):c.9127G>A (p.Ala3043Thr) rs138390702
NM_005751.4(AKAP9):c.9181C>T (p.Leu3061=) rs775991910
NM_005751.4(AKAP9):c.931-8T>C rs1359812106
NM_005751.4(AKAP9):c.9358+10A>T rs180926926
NM_005751.4(AKAP9):c.9359-4G>A rs983991110
NM_005751.4(AKAP9):c.9561A>G (p.Lys3187=) rs963431431
NM_005751.4(AKAP9):c.9689A>G (p.Lys3230Arg) rs192845338
NM_005751.4(AKAP9):c.9711G>T (p.Arg3237=) rs747049411
NM_005751.4(AKAP9):c.971T>C (p.Ile324Thr) rs367857951
NM_005751.4(AKAP9):c.9813C>T (p.Asn3271=) rs749572064
NM_005751.4(AKAP9):c.9915G>A (p.Glu3305=) rs878854813

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