ClinVar Miner

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

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Total variants: 57
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HGVS dbSNP
NM_005751.4(AKAP9):c.10118C>A (p.Ser3373Tyr) rs140470576
NM_005751.4(AKAP9):c.10249C>T (p.Arg3417Cys) rs146495719
NM_005751.4(AKAP9):c.10254G>C (p.Gln3418His) rs61757663
NM_005751.4(AKAP9):c.10331A>G (p.Gln3444Arg) rs34956633
NM_005751.4(AKAP9):c.10459G>A (p.Glu3487Lys) rs61757664
NM_005751.4(AKAP9):c.10607+109T>C
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.11135G>A (p.Arg3712Gln) rs186148498
NM_005751.4(AKAP9):c.11229G>A (p.Met3743Ile) rs143306820
NM_005751.4(AKAP9):c.11230G>T (p.Gly3744Trp) rs200327385
NM_005751.4(AKAP9):c.11273G>A (p.Arg3758His) rs141856443
NM_005751.4(AKAP9):c.11330+268T>A
NM_005751.4(AKAP9):c.11362G>C (p.Val3788Leu) rs199527737
NM_005751.4(AKAP9):c.11417-311C>T
NM_005751.4(AKAP9):c.1158A>T (p.Lys386Asn) rs142673316
NM_005751.4(AKAP9):c.1203C>T (p.Val401=) rs748951815
NM_005751.4(AKAP9):c.2230G>A (p.Glu744Lys) rs202091548
NM_005751.4(AKAP9):c.2425A>G (p.Ile809Val) rs144615758
NM_005751.4(AKAP9):c.2581T>C (p.Tyr861His) rs61757557
NM_005751.4(AKAP9):c.28C>T (p.Leu10=) rs778519429
NM_005751.4(AKAP9):c.306+63T>G
NM_005751.4(AKAP9):c.3319-214A>C
NM_005751.4(AKAP9):c.3533-141C>G
NM_005751.4(AKAP9):c.3580G>A (p.Ala1194Thr) rs139965373
NM_005751.4(AKAP9):c.3751+312T>C
NM_005751.4(AKAP9):c.3752-128A>G
NM_005751.4(AKAP9):c.3952+107C>T
NM_005751.4(AKAP9):c.4149-261A>G
NM_005751.4(AKAP9):c.4190A>G (p.Gln1397Arg) rs139612565
NM_005751.4(AKAP9):c.4339-156C>T
NM_005751.4(AKAP9):c.4342A>G (p.Ile1448Val) rs150379637
NM_005751.4(AKAP9):c.4826G>A (p.Arg1609Lys)
NM_005751.4(AKAP9):c.510G>C (p.Glu170Asp) rs144888041
NM_005751.4(AKAP9):c.5163-92A>G
NM_005751.4(AKAP9):c.5246T>C (p.Ile1749Thr) rs150016098
NM_005751.4(AKAP9):c.5369T>G (p.Val1790Gly) rs151021935
NM_005751.4(AKAP9):c.5601+24T>C
NM_005751.4(AKAP9):c.6037G>A (p.Glu2013Lys) rs61757671
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.6556T>C (p.Ser2186Pro) rs76177450
NM_005751.4(AKAP9):c.6996A>G (p.Glu2332=) rs1315064294
NM_005751.4(AKAP9):c.7488T>G (p.Asn2496Lys) rs201977551
NM_005751.4(AKAP9):c.8019+43A>G
NM_005751.4(AKAP9):c.80C>T (p.Ser27Leu) rs142401936
NM_005751.4(AKAP9):c.8286A>C (p.Lys2762Asn) rs144875383
NM_005751.4(AKAP9):c.8485G>A (p.Glu2829Lys) rs149946443
NM_005751.4(AKAP9):c.8647-80G>A
NM_005751.4(AKAP9):c.8935C>T (p.Pro2979Ser) rs1063242
NM_005751.4(AKAP9):c.9024+133C>T
NM_005751.4(AKAP9):c.9214-67T>A
NM_005751.4(AKAP9):c.9214-68T>A
NM_005751.4(AKAP9):c.971T>C (p.Ile324Thr) rs367857951
NM_005751.4(AKAP9):c.9763A>G (p.Arg3255Gly) rs201048693
NM_005751.4(AKAP9):c.9929G>A (p.Arg3310Gln) rs78351282

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