ClinVar Miner

List of variants in gene AKAP9 reported as likely benign for not specified

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Gene type:
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Total variants: 63
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HGVS dbSNP gnomAD frequency
NM_005751.5(AKAP9):c.8375A>G (p.Asn2792Ser) rs6960867 0.33817
NM_005751.5(AKAP9):c.7451A>G (p.Lys2484Arg) rs35759833 0.09968
NM_005751.5(AKAP9):c.9092A>G (p.Gln3031Arg) rs61757673 0.00583
NM_005751.5(AKAP9):c.2425A>G (p.Ile809Val) rs144615758 0.00298
NM_005751.5(AKAP9):c.10858A>G (p.Ile3620Val) rs142729919 0.00296
NM_005751.5(AKAP9):c.6134A>G (p.Asn2045Ser) rs139963188 0.00279
NM_005751.5(AKAP9):c.1372G>C (p.Ala458Pro) rs143894795 0.00241
NM_005751.5(AKAP9):c.11225G>C (p.Arg3742Pro) rs34101758 0.00217
NM_005751.5(AKAP9):c.5428A>G (p.Met1810Val) rs115624293 0.00167
NM_005751.5(AKAP9):c.11273G>A (p.Arg3758His) rs141856443 0.00158
NM_005751.5(AKAP9):c.6037G>A (p.Glu2013Lys) rs61757671 0.00142
NM_005751.5(AKAP9):c.288G>T (p.Glu96Asp) rs34953651 0.00112
NM_005751.5(AKAP9):c.10664A>T (p.Asp3555Val) rs139046510 0.00089
NM_005751.5(AKAP9):c.5369T>G (p.Val1790Gly) rs151021935 0.00082
NM_005751.5(AKAP9):c.1651A>G (p.Ile551Val) rs140664656 0.00081
NM_005751.5(AKAP9):c.9127G>A (p.Ala3043Thr) rs138390702 0.00080
NM_005751.5(AKAP9):c.6176A>G (p.Glu2059Gly) rs73226383 0.00070
NM_005751.5(AKAP9):c.10254G>C (p.Gln3418His) rs61757663 0.00065
NM_005751.5(AKAP9):c.10118C>A (p.Ser3373Tyr) rs140470576 0.00061
NM_005751.5(AKAP9):c.4127G>C (p.Ser1376Thr) rs144372406 0.00058
NM_005751.5(AKAP9):c.10459G>A (p.Glu3487Lys) rs61757664 0.00055
NM_005751.5(AKAP9):c.883A>G (p.Thr295Ala) rs149825027 0.00044
NM_005751.5(AKAP9):c.158A>G (p.His53Arg) rs142125596 0.00043
NM_005751.5(AKAP9):c.456C>A (p.Asp152Glu) rs138567837 0.00036
NM_005751.5(AKAP9):c.3580G>A (p.Ala1194Thr) rs139965373 0.00035
NM_005751.5(AKAP9):c.4917+3A>C rs200730225 0.00034
NM_005751.5(AKAP9):c.9214-6T>C rs377532409 0.00033
NM_005751.5(AKAP9):c.1099G>A (p.Val367Met) rs138161478 0.00031
NM_005751.5(AKAP9):c.4826G>A (p.Arg1609Lys) rs148146011 0.00026
NM_005751.5(AKAP9):c.8656A>G (p.Ile2886Val) rs143283097 0.00026
NM_005751.5(AKAP9):c.9763A>G (p.Arg3255Gly) rs201048693 0.00018
NM_005751.5(AKAP9):c.10741T>G (p.Cys3581Gly) rs149819328 0.00014
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.6177A>G (p.Glu2059=) rs752723636 0.00009
NM_005751.5(AKAP9):c.11519T>C (p.Ile3840Thr) rs145675748 0.00008
NM_005751.5(AKAP9):c.5284A>G (p.Lys1762Glu) rs568626378 0.00007
NM_005751.5(AKAP9):c.2477T>C (p.Ile826Thr) rs534185372 0.00006
NM_005751.5(AKAP9):c.3350G>A (p.Arg1117His) rs546600149 0.00006
NM_005751.5(AKAP9):c.5117A>G (p.Asp1706Gly) rs139468199 0.00006
NM_005751.5(AKAP9):c.289C>G (p.Gln97Glu) rs786205712 0.00005
NM_005751.5(AKAP9):c.1538A>G (p.Lys513Arg) rs786205713 0.00004
NM_005751.5(AKAP9):c.9032A>G (p.Asp3011Gly) rs745743634 0.00004
NM_005751.5(AKAP9):c.10495A>G (p.Ile3499Val) rs756721657 0.00003
NM_005751.5(AKAP9):c.5565A>G (p.Glu1855=) rs141094356 0.00003
NM_005751.5(AKAP9):c.7980A>C (p.Lys2660Asn) rs371461279 0.00003
NM_005751.5(AKAP9):c.6046C>T (p.Arg2016Cys) rs376950905 0.00002
NM_005751.5(AKAP9):c.10319T>C (p.Met3440Thr) rs751924200 0.00001
NM_005751.5(AKAP9):c.5870A>G (p.Asn1957Ser) rs767966419 0.00001
NM_005751.5(AKAP9):c.6996A>G (p.Glu2332=) rs1315064294 0.00001
NM_005751.5(AKAP9):c.7200G>A (p.Gln2400=) rs1813131577 0.00001
NM_005751.5(AKAP9):c.9881G>A (p.Arg3294Gln) rs752685614 0.00001
NM_005751.5(AKAP9):c.10526A>G (p.Asn3509Ser) rs786205711
NM_005751.5(AKAP9):c.11229G>A (p.Met3743Ile) rs143306820
NM_005751.5(AKAP9):c.11283C>G (p.Gly3761=) rs1817790066
NM_005751.5(AKAP9):c.1158A>T (p.Lys386Asn) rs142673316
NM_005751.5(AKAP9):c.1223A>G (p.Asn408Ser) rs761210281
NM_005751.5(AKAP9):c.235C>T (p.Pro79Ser) rs768026366
NM_005751.5(AKAP9):c.6974G>A (p.Arg2325Lys) rs786205708
NM_005751.5(AKAP9):c.8207T>G (p.Val2736Gly) rs769936861
NM_005751.5(AKAP9):c.8221G>T (p.Ala2741Ser) rs368001901
NM_005751.5(AKAP9):c.8850C>T (p.Val2950=) rs1814382203
NM_005751.5(AKAP9):c.8912A>G (p.His2971Arg) rs786205710

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