ClinVar Miner

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

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Total variants: 34
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HGVS dbSNP
NM_005751.4(AKAP9):c.10254G>C (p.Gln3418His) rs61757663
NM_005751.4(AKAP9):c.10319T>C (p.Met3440Thr) rs751924200
NM_005751.4(AKAP9):c.10495A>G (p.Ile3499Val) rs756721657
NM_005751.4(AKAP9):c.10526A>G (p.Asn3509Ser) rs786205711
NM_005751.4(AKAP9):c.10664A>T (p.Asp3555Val) rs139046510
NM_005751.4(AKAP9):c.1099G>A (p.Val367Met) rs138161478
NM_005751.4(AKAP9):c.11225G>C (p.Arg3742Pro) rs34101758
NM_005751.4(AKAP9):c.11519T>C (p.Ile3840Thr) rs145675748
NM_005751.4(AKAP9):c.1158A>T (p.Lys386Asn) rs142673316
NM_005751.4(AKAP9):c.119G>A (p.Arg40Lys) rs755408339
NM_005751.4(AKAP9):c.1223A>G (p.Asn408Ser) rs761210281
NM_005751.4(AKAP9):c.1538A>G (p.Lys513Arg) rs786205713
NM_005751.4(AKAP9):c.158A>G (p.His53Arg) rs142125596
NM_005751.4(AKAP9):c.1651A>G (p.Ile551Val) rs140664656
NM_005751.4(AKAP9):c.235C>T (p.Pro79Ser) rs768026366
NM_005751.4(AKAP9):c.2425A>G (p.Ile809Val) rs144615758
NM_005751.4(AKAP9):c.2477T>C (p.Ile826Thr) rs534185372
NM_005751.4(AKAP9):c.288G>T (p.Glu96Asp) rs34953651
NM_005751.4(AKAP9):c.289C>G (p.Gln97Glu) rs786205712
NM_005751.4(AKAP9):c.4127G>C (p.Ser1376Thr) rs144372406
NM_005751.4(AKAP9):c.4800A>G (p.Glu1600=) rs138765069
NM_005751.4(AKAP9):c.4814C>T (p.Thr1605Met) rs777627168
NM_005751.4(AKAP9):c.4872A>G (p.Glu1624=) rs570384292
NM_005751.4(AKAP9):c.4917+14del rs765796287
NM_005751.4(AKAP9):c.4917+3A>C rs200730225
NM_005751.4(AKAP9):c.4927A>C (p.Ile1643Leu) rs141990258
NM_005751.4(AKAP9):c.5117A>G (p.Asp1706Gly) rs139468199
NM_005751.4(AKAP9):c.5369T>G (p.Val1790Gly) rs151021935
NM_005751.4(AKAP9):c.6974G>A (p.Arg2325Lys) rs786205708
NM_005751.4(AKAP9):c.8207T>G (p.Val2736Gly) rs769936861
NM_005751.4(AKAP9):c.8221G>T (p.Ala2741Ser) rs368001901
NM_005751.4(AKAP9):c.8656A>G (p.Ile2886Val) rs143283097
NM_005751.4(AKAP9):c.8912A>G (p.His2971Arg) rs786205710
NM_005751.4(AKAP9):c.9214-6T>C rs377532409

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