ClinVar Miner

List of variants in gene AKAP9 reported as uncertain significance for not provided

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Gene type:
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Total variants: 98
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HGVS dbSNP gnomAD frequency
NM_005751.5(AKAP9):c.510G>C (p.Glu170Asp) rs144888041 0.00212
NM_005751.5(AKAP9):c.6037G>A (p.Glu2013Lys) rs61757671 0.00142
NM_005751.5(AKAP9):c.10767G>A (p.Leu3589=) rs56198613 0.00111
NM_005751.5(AKAP9):c.8286A>C (p.Lys2762Asn) rs144875383 0.00093
NM_005751.5(AKAP9):c.3580G>A (p.Ala1194Thr) rs139965373 0.00035
NM_005751.5(AKAP9):c.4826G>A (p.Arg1609Lys) rs148146011 0.00026
NM_005751.5(AKAP9):c.7488T>G (p.Asn2496Lys) rs201977551 0.00025
NM_005751.5(AKAP9):c.8677G>C (p.Asp2893His) rs142573103 0.00025
NM_005751.5(AKAP9):c.11714T>C (p.Met3905Thr) rs77447750 0.00014
NM_005751.5(AKAP9):c.2311G>A (p.Ala771Thr) rs148267537 0.00013
NM_005751.5(AKAP9):c.1334T>C (p.Ile445Thr) rs147302252 0.00011
NM_005751.5(AKAP9):c.9970G>A (p.Ala3324Thr) rs182048899 0.00010
NM_005751.5(AKAP9):c.109A>G (p.Lys37Glu) rs752156538 0.00006
NM_005751.5(AKAP9):c.1396C>T (p.Arg466Trp) rs373876340 0.00006
NM_005751.5(AKAP9):c.3793G>A (p.Glu1265Lys) rs1424485718 0.00006
NM_005751.5(AKAP9):c.9244C>T (p.Leu3082Phe) rs377611430 0.00006
NM_005751.5(AKAP9):c.3994G>C (p.Glu1332Gln) rs774110970 0.00005
NM_005751.5(AKAP9):c.2575G>A (p.Val859Ile) rs751606673 0.00004
NM_005751.5(AKAP9):c.4840C>T (p.Arg1614Trp) rs772669837 0.00004
NM_005751.5(AKAP9):c.5251C>T (p.Arg1751Cys) rs144269839 0.00004
NM_005751.5(AKAP9):c.5543C>G (p.Ser1848Cys) rs189083857 0.00004
NM_005751.5(AKAP9):c.7675A>C (p.Ile2559Leu) rs757278868 0.00004
NM_005751.5(AKAP9):c.1685A>G (p.His562Arg) rs145033147 0.00003
NM_005751.5(AKAP9):c.5180C>T (p.Ala1727Val) rs369047678 0.00003
NM_005751.5(AKAP9):c.9577A>G (p.Arg3193Gly) rs199762211 0.00003
NM_005751.5(AKAP9):c.9830T>C (p.Ile3277Thr) rs144021475 0.00003
NM_005751.5(AKAP9):c.6046C>T (p.Arg2016Cys) rs376950905 0.00002
NM_005751.5(AKAP9):c.10523G>A (p.Cys3508Tyr) rs750007670 0.00001
NM_005751.5(AKAP9):c.1074A>T (p.Leu358Phe) rs1346719880 0.00001
NM_005751.5(AKAP9):c.10774A>C (p.Asn3592His) rs751653287 0.00001
NM_005751.5(AKAP9):c.11348G>A (p.Arg3783Gln) rs143967328 0.00001
NM_005751.5(AKAP9):c.1859C>A (p.Ala620Asp) rs774013935 0.00001
NM_005751.5(AKAP9):c.2370G>A (p.Met790Ile) rs1298504605 0.00001
NM_005751.5(AKAP9):c.257C>G (p.Thr86Ser) rs768859701 0.00001
NM_005751.5(AKAP9):c.389C>G (p.Pro130Arg) rs200518712 0.00001
NM_005751.5(AKAP9):c.3950T>C (p.Ile1317Thr) rs199773513 0.00001
NM_005751.5(AKAP9):c.4156G>T (p.Val1386Phe) rs762293635 0.00001
NM_005751.5(AKAP9):c.460C>A (p.Pro154Thr) rs746612786 0.00001
NM_005751.5(AKAP9):c.4672A>G (p.Thr1558Ala) rs746815931 0.00001
NM_005751.5(AKAP9):c.4709C>T (p.Ser1570Leu) rs121908566 0.00001
NM_005751.5(AKAP9):c.4765G>A (p.Asp1589Asn) rs371957004 0.00001
NM_005751.5(AKAP9):c.4814C>T (p.Thr1605Met) rs777627168 0.00001
NM_005751.5(AKAP9):c.4832C>T (p.Ala1611Val) rs1430748591 0.00001
NM_005751.5(AKAP9):c.4837A>G (p.Met1613Val) rs193922723 0.00001
NM_005751.5(AKAP9):c.5505A>G (p.Ile1835Met) rs1057521238 0.00001
NM_005751.5(AKAP9):c.5636T>C (p.Met1879Thr) rs776979647 0.00001
NM_005751.5(AKAP9):c.5767G>A (p.Val1923Ile) rs755463664 0.00001
NM_005751.5(AKAP9):c.6188A>G (p.Glu2063Gly) rs778681643 0.00001
NM_005751.5(AKAP9):c.61C>T (p.Arg21Ter) rs1060503553 0.00001
NM_005751.5(AKAP9):c.6916C>T (p.Gln2306Ter) rs899419546 0.00001
NM_005751.5(AKAP9):c.7555T>C (p.Tyr2519His) rs752977579 0.00001
NM_005751.5(AKAP9):c.7783G>T (p.Asp2595Tyr) rs754949903 0.00001
NM_005751.5(AKAP9):c.8585A>G (p.Gln2862Arg) rs752618658 0.00001
NM_005751.5(AKAP9):c.9040C>T (p.Gln3014Ter) rs1285403296 0.00001
NM_005751.5(AKAP9):c.9317T>C (p.Ile3106Thr) rs747304560 0.00001
NM_005751.5(AKAP9):c.9881G>A (p.Arg3294Gln) rs752685614 0.00001
NC_000007.14:g.91973711_91973719del rs1381647167
NM_005751.5(AKAP9):c.10223T>A (p.Leu3408His)
NM_005751.5(AKAP9):c.10801C>T (p.Gln3601Ter) rs2130907246
NM_005751.5(AKAP9):c.10892dup (p.Asp3631fs) rs2130907490
NM_005751.5(AKAP9):c.11012C>T (p.Ala3671Val) rs1359148155
NM_005751.5(AKAP9):c.11189A>G (p.Gln3730Arg) rs372297197
NM_005751.5(AKAP9):c.11366_11367del (p.Thr3789fs) rs1818404612
NM_005751.5(AKAP9):c.11525C>T (p.Ser3842Phe) rs936516286
NM_005751.5(AKAP9):c.1394C>T (p.Thr465Ile)
NM_005751.5(AKAP9):c.1655C>T (p.Ala552Val) rs1359715379
NM_005751.5(AKAP9):c.1742C>A (p.Ser581Tyr) rs786205260
NM_005751.5(AKAP9):c.185G>A (p.Cys62Tyr) rs1433559893
NM_005751.5(AKAP9):c.1870_1871del (p.Arg624fs) rs754882162
NM_005751.5(AKAP9):c.3381T>G (p.His1127Gln) rs746651292
NM_005751.5(AKAP9):c.352-1G>A rs2130633941
NM_005751.5(AKAP9):c.3643A>C (p.Thr1215Pro) rs1801485947
NM_005751.5(AKAP9):c.3952+2T>G rs1388639878
NM_005751.5(AKAP9):c.4090G>C (p.Glu1364Gln) rs1802542345
NM_005751.5(AKAP9):c.4360G>A (p.Ala1454Thr) rs760328706
NM_005751.5(AKAP9):c.4825_4826delinsCA (p.Arg1609Gln) rs786205707
NM_005751.5(AKAP9):c.4858C>T (p.Arg1620Ter) rs551980172
NM_005751.5(AKAP9):c.4882G>A (p.Glu1628Lys)
NM_005751.5(AKAP9):c.4903A>G (p.Arg1635Gly)
NM_005751.5(AKAP9):c.5233G>C (p.Val1745Leu) rs1060503578
NM_005751.5(AKAP9):c.5234T>C (p.Val1745Ala) rs201632145
NM_005751.5(AKAP9):c.5534A>G (p.Asn1845Ser) rs786205261
NM_005751.5(AKAP9):c.5827G>T (p.Asp1943Tyr) rs201144675
NM_005751.5(AKAP9):c.643CAA[1] (p.Gln216del)
NM_005751.5(AKAP9):c.6613-10_6614del rs1584446954
NM_005751.5(AKAP9):c.6762del (p.Phe2254fs) rs1486680667
NM_005751.5(AKAP9):c.7519A>G (p.Thr2507Ala) rs2130862031
NM_005751.5(AKAP9):c.7773A>C (p.Gln2591His) rs553800160
NM_005751.5(AKAP9):c.7777del (p.Arg2593fs) rs2130862600
NM_005751.5(AKAP9):c.7921AAG[1] (p.Lys2642del) rs786205262
NM_005751.5(AKAP9):c.7955del (p.Gly2652fs) rs1370153980
NM_005751.5(AKAP9):c.835del (p.Glu279fs) rs2130646435
NM_005751.5(AKAP9):c.8631T>G (p.Cys2877Trp) rs1563113459
NM_005751.5(AKAP9):c.8782C>T (p.Arg2928Ter) rs746403215
NM_005751.5(AKAP9):c.8833-1G>A rs2130875407
NM_005751.5(AKAP9):c.8894A>G (p.Tyr2965Cys) rs201958512
NM_005751.5(AKAP9):c.9536T>A (p.Leu3179His) rs2130892060
NM_005751.5(AKAP9):c.9991G>A (p.Gly3331Ser)

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