ClinVar Miner

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

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Total variants: 47
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HGVS dbSNP
NM_005751.4(AKAP9):c.10523G>A (p.Cys3508Tyr) rs750007670
NM_005751.4(AKAP9):c.10767G>A (p.Leu3589=) rs56198613
NM_005751.4(AKAP9):c.109A>G (p.Lys37Glu) rs752156538
NM_005751.4(AKAP9):c.11525C>T (p.Ser3842Phe) rs936516286
NM_005751.4(AKAP9):c.11714T>C (p.Met3905Thr) rs77447750
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.1859C>A (p.Ala620Asp) rs774013935
NM_005751.4(AKAP9):c.2370G>A (p.Met790Ile) rs1298504605
NM_005751.4(AKAP9):c.3580G>A (p.Ala1194Thr) rs139965373
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.3994G>C (p.Glu1332Gln) rs774110970
NM_005751.4(AKAP9):c.4156G>T (p.Val1386Phe) rs762293635
NM_005751.4(AKAP9):c.4360G>A (p.Ala1454Thr) rs760328706
NM_005751.4(AKAP9):c.460C>A (p.Pro154Thr) rs746612786
NM_005751.4(AKAP9):c.4709C>T (p.Ser1570Leu) rs121908566
NM_005751.4(AKAP9):c.4765G>A (p.Asp1589Asn) rs371957004
NM_005751.4(AKAP9):c.4814C>T (p.Thr1605Met) rs777627168
NM_005751.4(AKAP9):c.4840C>T (p.Arg1614Trp) rs772669837
NM_005751.4(AKAP9):c.5048C>T (p.Thr1683Met) rs146305558
NM_005751.4(AKAP9):c.510G>C (p.Glu170Asp) rs144888041
NM_005751.4(AKAP9):c.5233G>C (p.Val1745Leu) rs1060503578
NM_005751.4(AKAP9):c.5234T>C (p.Val1745Ala) rs201632145
NM_005751.4(AKAP9):c.5251C>T (p.Arg1751Cys) rs144269839
NM_005751.4(AKAP9):c.5505A>G (p.Ile1835Met) rs1057521238
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.6046C>T (p.Arg2016Cys) rs376950905
NM_005751.4(AKAP9):c.6188A>G (p.Glu2063Gly) rs778681643
NM_005751.4(AKAP9):c.6896A>G (p.Glu2299Gly) rs147841245
NM_005751.4(AKAP9):c.7488T>G (p.Asn2496Lys) rs201977551
NM_005751.4(AKAP9):c.7555T>C (p.Tyr2519His) rs752977579
NM_005751.4(AKAP9):c.7773A>C (p.Gln2591His) rs553800160
NM_005751.4(AKAP9):c.7921_7923AAG[1] (p.Lys2642del) rs786205262
NM_005751.4(AKAP9):c.8286A>C (p.Lys2762Asn) rs144875383
NM_005751.4(AKAP9):c.8585A>G (p.Gln2862Arg) rs752618658
NM_005751.4(AKAP9):c.8631T>G (p.Cys2877Trp) rs1563113459
NM_005751.4(AKAP9):c.8677G>C (p.Asp2893His) rs142573103
NM_005751.4(AKAP9):c.8894A>G (p.Tyr2965Cys) rs201958512
NM_005751.4(AKAP9):c.9244C>T (p.Leu3082Phe)
NM_005751.4(AKAP9):c.9577A>G (p.Arg3193Gly) rs199762211
NM_005751.4(AKAP9):c.9830T>C (p.Ile3277Thr) rs144021475
NM_005751.4(AKAP9):c.9881G>A (p.Arg3294Gln) rs752685614

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