Akap1 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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865 records found for search term Akap1

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
15098016	CV731168	single nucleotide variant	NM_003488.4(AKAP1):c.2432+7G>A	not provided [RCV000891638]	benign	17	57116268	57116268	Human		name
15169151	CV778518	single nucleotide variant	NM_003488.4(AKAP1):c.1976-6A>G	not provided [RCV000949402]	benign	17	57112485	57112485	Human		name
401906445	CV2811527	single nucleotide variant	NM_003488.4(AKAP1):c.177C>T (p.Pro59=)	not provided [RCV003421367]	likely benign	17	57105641	57105641	Human		name
598225151	CV3965941	single nucleotide variant	NM_003488.4(AKAP1):c.16C>T (p.Arg6Cys)	not specified [RCV005341401]	uncertain significance	17	57105480	57105480	Human		name
156178286	CV2201581	single nucleotide variant	NM_003488.4(AKAP1):c.98T>G (p.Val33Gly)	not specified [RCV004080070]	uncertain significance	17	57105562	57105562	Human		name
329357446	CV2453604	single nucleotide variant	NM_003488.4(AKAP1):c.28C>T (p.Pro10Ser)	not specified [RCV004269272]	uncertain significance	17	57105492	57105492	Human		name
405790013	CV3266357	single nucleotide variant	NM_003488.4(AKAP1):c.82C>A (p.Arg28Ser)	not specified [RCV004399367]	uncertain significance	17	57105546	57105546	Human		name
9686894	CV171606	single nucleotide variant	NM_003488.4(AKAP1):c.239A>G (p.Lys80Arg)	Prostate cancer [RCV000149112]	uncertain significance	17	57105703	57105703	Human	2	name
156259109	CV2216186	single nucleotide variant	NM_003488.4(AKAP1):c.164A>G (p.Lys55Arg)	not specified [RCV004097169]	uncertain significance	17	57105628	57105628	Human		name
156338579	CV2224959	single nucleotide variant	NM_003488.4(AKAP1):c.215C>G (p.Pro72Arg)	not specified [RCV004094809]	uncertain significance	17	57105679	57105679	Human		name
329394145	CV2450105	single nucleotide variant	NM_003488.4(AKAP1):c.269C>T (p.Ala90Val)	not specified [RCV004269147]	likely benign	17	57105733	57105733	Human		name
401914447	CV2808060	single nucleotide variant	NM_003488.4(AKAP1):c.2205G>A (p.Ala735=)	not provided [RCV003428345]	likely benign	17	57114560	57114560	Human		name
405789724	CV3266290	single nucleotide variant	NM_003488.4(AKAP1):c.220G>A (p.Val74Ile)	not specified [RCV004399300]	uncertain significance	17	57105684	57105684	Human		name
405789804	CV3266309	single nucleotide variant	NM_003488.4(AKAP1):c.285G>T (p.Leu95Phe)	not specified [RCV004399319]	uncertain significance	17	57105749	57105749	Human		name
407485193	CV3439402	single nucleotide variant	NM_003488.4(AKAP1):c.101G>A (p.Ser34Asn)	not specified [RCV004618871]	uncertain significance	17	57105565	57105565	Human		name
597698440	CV3669251	single nucleotide variant	NM_003488.4(AKAP1):c.127G>A (p.Ala43Thr)	not specified [RCV004916124]	uncertain significance	17	57105591	57105591	Human		name
15097943	CV704246	single nucleotide variant	NM_003488.4(AKAP1):c.1164C>T (p.Ser388=)	not provided [RCV000958434]	benign	17	57106628	57106628	Human		name
15097948	CV704247	single nucleotide variant	NM_003488.4(AKAP1):c.1425G>A (p.Pro475=)	not provided [RCV000958435]	benign	17	57106889	57106889	Human		name
15173067	CV715581	single nucleotide variant	NM_003488.4(AKAP1):c.178G>A (p.Val60Met)	not provided [RCV000972540]	benign	17	57105642	57105642	Human		name
15154495	CV715582	single nucleotide variant	NM_003488.4(AKAP1):c.2454G>A (p.Pro818=)	not provided [RCV000968747]	benign	17	57116881	57116881	Human		name
15181500	CV727307	single nucleotide variant	NM_003488.4(AKAP1):c.1749C>T (p.Ser583=)	not provided [RCV000885780]	benign	17	57110059	57110059	Human		name
15186862	CV727308	single nucleotide variant	NM_003488.4(AKAP1):c.2160C>T (p.Ala720=)	not provided [RCV000887093]	benign	17	57114515	57114515	Human		name
15151778	CV740898	single nucleotide variant	NM_003488.4(AKAP1):c.1644G>A (p.Leu548=)	not provided [RCV000901432]	likely benign	17	57107108	57107108	Human		name
15129818	CV740899	single nucleotide variant	NM_003488.4(AKAP1):c.2550G>A (p.Thr850=)	not provided [RCV000897505]	benign	17	57118430	57118430	Human		name
15105542	CV755981	single nucleotide variant	NM_003488.4(AKAP1):c.1305C>T (p.Tyr435=)	not provided [RCV000915569]\|not specified [RCV004917656]	likely benign	17	57106769	57106769	Human		name
156317798	CV2204067	single nucleotide variant	NM_003488.4(AKAP1):c.400G>T (p.Ala134Ser)	not specified [RCV004076534]	uncertain significance	17	57105864	57105864	Human		name
156259569	CV2204746	single nucleotide variant	NM_003488.4(AKAP1):c.851C>T (p.Ala284Val)	not specified [RCV004075006]	uncertain significance	17	57106315	57106315	Human		name
156247681	CV2221913	single nucleotide variant	NM_003488.4(AKAP1):c.308G>A (p.Arg103Gln)	not specified [RCV004102925]	uncertain significance	17	57105772	57105772	Human		name
156243395	CV2231510	single nucleotide variant	NM_003488.4(AKAP1):c.787G>T (p.Val263Leu)	not specified [RCV004096574]	uncertain significance	17	57106251	57106251	Human		name
155932639	CV2290783	single nucleotide variant	NM_003488.4(AKAP1):c.994G>T (p.Asp332Tyr)	not specified [RCV004149290]	uncertain significance	17	57106458	57106458	Human		name
156204956	CV2297834	single nucleotide variant	NM_003488.4(AKAP1):c.736G>A (p.Gly246Arg)	not specified [RCV004157778]	uncertain significance	17	57106200	57106200	Human		name
156044150	CV2307981	single nucleotide variant	NM_003488.4(AKAP1):c.407C>T (p.Thr136Ile)	not specified [RCV004170415]	uncertain significance	17	57105871	57105871	Human		name
155969970	CV2338014	single nucleotide variant	NM_003488.4(AKAP1):c.371G>T (p.Arg124Leu)	not specified [RCV004186055]	uncertain significance	17	57105835	57105835	Human		name
155922317	CV2340601	single nucleotide variant	NM_003488.4(AKAP1):c.798G>C (p.Lys266Asn)	not specified [RCV004197309]	uncertain significance	17	57106262	57106262	Human		name
156388605	CV2375929	single nucleotide variant	NM_003488.4(AKAP1):c.323C>T (p.Ser108Leu)	not specified [RCV004218139]	uncertain significance	17	57105787	57105787	Human		name
156192709	CV2388796	single nucleotide variant	NM_003488.4(AKAP1):c.810G>T (p.Arg270Ser)	not specified [RCV004239650]	likely benign	17	57106274	57106274	Human		name
329399849	CV2444287	single nucleotide variant	NM_003488.4(AKAP1):c.848A>G (p.Asp283Gly)	not specified [RCV004263053]	uncertain significance	17	57106312	57106312	Human		name
401743158	CV2684030	single nucleotide variant	NM_003488.4(AKAP1):c.344C>T (p.Thr115Ile)	not specified [RCV004295634]	likely benign	17	57105808	57105808	Human		name
401875802	CV2777535	single nucleotide variant	NM_003488.4(AKAP1):c.407C>A (p.Thr136Lys)	not specified [RCV004343394]	uncertain significance	17	57105871	57105871	Human		name
401897143	CV2789863	single nucleotide variant	NM_003488.4(AKAP1):c.620A>G (p.Asp207Gly)	not specified [RCV004362250]	uncertain significance	17	57106084	57106084	Human		name
405789853	CV3266320	single nucleotide variant	NM_003488.4(AKAP1):c.359G>A (p.Arg120Gln)	not specified [RCV004399330]	likely benign	17	57105823	57105823	Human		name
405789933	CV3266338	single nucleotide variant	NM_003488.4(AKAP1):c.790G>C (p.Ala264Pro)	not specified [RCV004399348]	uncertain significance	17	57106254	57106254	Human		name
405789991	CV3266352	single nucleotide variant	NM_003488.4(AKAP1):c.824C>A (p.Ala275Asp)	not specified [RCV004399362]	uncertain significance	17	57106288	57106288	Human		name
405790035	CV3266362	single nucleotide variant	NM_003488.4(AKAP1):c.859G>A (p.Ala287Thr)	not specified [RCV004399372]	uncertain significance	17	57106323	57106323	Human		name
407484940	CV3439358	single nucleotide variant	NM_003488.4(AKAP1):c.743G>A (p.Ser248Asn)	not specified [RCV004618827]	uncertain significance	17	57106207	57106207	Human		name
407485064	CV3439380	single nucleotide variant	NM_003488.4(AKAP1):c.871G>A (p.Ala291Thr)	not specified [RCV004618849]	likely benign	17	57106335	57106335	Human		name
597698750	CV3669214	single nucleotide variant	NM_003488.4(AKAP1):c.583A>T (p.Arg195Trp)	not specified [RCV004916088]	uncertain significance	17	57106047	57106047	Human		name
597698213	CV3669226	single nucleotide variant	NM_003488.4(AKAP1):c.524C>T (p.Pro175Leu)	not specified [RCV004916099]	uncertain significance	17	57105988	57105988	Human		name
597698265	CV3669232	single nucleotide variant	NM_003488.4(AKAP1):c.559G>A (p.Ala187Thr)	not specified [RCV004916105]	uncertain significance	17	57106023	57106023	Human		name
597698349	CV3669241	single nucleotide variant	NM_003488.4(AKAP1):c.927C>G (p.Ser309Arg)	not specified [RCV004916114]	uncertain significance	17	57106391	57106391	Human		name
597699600	CV3669268	single nucleotide variant	NM_003488.4(AKAP1):c.425C>T (p.Ser142Leu)	not specified [RCV004916139]	uncertain significance	17	57105889	57105889	Human		name
598224754	CV3965875	single nucleotide variant	NM_003488.4(AKAP1):c.559G>T (p.Ala187Ser)	not specified [RCV005341341]	uncertain significance	17	57106023	57106023	Human		name
598224826	CV3965885	single nucleotide variant	NM_003488.4(AKAP1):c.828C>A (p.His276Gln)	not specified [RCV005341351]	uncertain significance	17	57106292	57106292	Human		name
598194974	CV3965906	single nucleotide variant	NM_003488.4(AKAP1):c.362C>T (p.Pro121Leu)	not specified [RCV005335495]	uncertain significance	17	57105826	57105826	Human		name
598194981	CV3965926	single nucleotide variant	NM_003488.4(AKAP1):c.716T>C (p.Leu239Ser)	not specified [RCV005335496]	uncertain significance	17	57106180	57106180	Human		name
598225297	CV3965970	single nucleotide variant	NM_003488.4(AKAP1):c.905G>C (p.Gly302Ala)	not specified [RCV005341426]	uncertain significance	17	57106369	57106369	Human		name
15097937	CV704243	single nucleotide variant	NM_003488.4(AKAP1):c.652G>A (p.Ala218Thr)	not provided [RCV000958433]	benign	17	57106116	57106116	Human		name
15172319	CV704244	single nucleotide variant	NM_003488.4(AKAP1):c.967G>A (p.Gly323Ser)	not provided [RCV000950001]	benign	17	57106431	57106431	Human		name
15172323	CV704245	single nucleotide variant	NM_003488.4(AKAP1):c.988A>G (p.Ser330Gly)	not provided [RCV000950002]	benign	17	57106452	57106452	Human		name
15196516	CV727305	single nucleotide variant	NM_003488.4(AKAP1):c.722G>C (p.Gly241Ala)	not provided [RCV000889796]	benign\|likely benign	17	57106186	57106186	Human		name
8636255	CV91479	single nucleotide variant	NM_003488.3(AKAP1):c.548C>T (p.Pro183Leu)	Malignant melanoma [RCV000071577]	not provided	17	57106012	57106012	Human		name
155961904	CV2200809	single nucleotide variant	NM_003488.4(AKAP1):c.1759C>T (p.Leu587Phe)	not specified [RCV004081441]	uncertain significance	17	57110069	57110069	Human		name
156260160	CV2204795	single nucleotide variant	NM_003488.4(AKAP1):c.1669G>T (p.Ala557Ser)	not specified [RCV004075050]	uncertain significance	17	57107133	57107133	Human		name
156238291	CV2207106	single nucleotide variant	NM_003488.4(AKAP1):c.2453C>T (p.Pro818Leu)	not specified [RCV004085706]	uncertain significance	17	57116880	57116880	Human		name
156327700	CV2217334	single nucleotide variant	NM_003488.4(AKAP1):c.1462G>A (p.Val488Ile)	not specified [RCV004087772]	uncertain significance	17	57106926	57106926	Human		name
156387197	CV2221438	single nucleotide variant	NM_003488.4(AKAP1):c.1217C>A (p.Ala406Asp)	not specified [RCV004096728]	uncertain significance	17	57106681	57106681	Human		name
155975729	CV2231441	single nucleotide variant	NM_003488.4(AKAP1):c.1259C>T (p.Pro420Leu)	not specified [RCV004096520]	uncertain significance	17	57106723	57106723	Human		name
156116905	CV2231745	single nucleotide variant	NM_003488.4(AKAP1):c.1430G>A (p.Arg477Gln)	not specified [RCV004098563]	uncertain significance	17	57106894	57106894	Human		name
156269768	CV2293348	single nucleotide variant	NM_003488.4(AKAP1):c.1639G>C (p.Val547Leu)	not specified [RCV004150828]	uncertain significance	17	57107103	57107103	Human		name
156040293	CV2310789	single nucleotide variant	NM_003488.4(AKAP1):c.1921A>T (p.Ile641Phe)	not specified [RCV004157714]	uncertain significance	17	57111870	57111870	Human		name
156343683	CV2349202	single nucleotide variant	NM_003488.4(AKAP1):c.1060C>G (p.Gln354Glu)	not specified [RCV004199159]	uncertain significance	17	57106524	57106524	Human		name
329357443	CV2453603	single nucleotide variant	NM_003488.4(AKAP1):c.1243C>T (p.Pro415Ser)	not specified [RCV004269271]	likely benign	17	57106707	57106707	Human		name
329360466	CV2458765	single nucleotide variant	NM_003488.4(AKAP1):c.2531C>G (p.Ala844Gly)	not specified [RCV004270199]	uncertain significance	17	57118411	57118411	Human		name
401771000	CV2686134	single nucleotide variant	NM_003488.4(AKAP1):c.2056C>T (p.Pro686Ser)	not specified [RCV004297140]	uncertain significance	17	57112571	57112571	Human		name
401734859	CV2690697	single nucleotide variant	NM_003488.4(AKAP1):c.1424C>T (p.Pro475Leu)	not specified [RCV004298426]	likely benign	17	57106888	57106888	Human		name
401775393	CV2710550	single nucleotide variant	NM_003488.4(AKAP1):c.1479C>G (p.Asp493Glu)	not specified [RCV004319473]	uncertain significance	17	57106943	57106943	Human		name
401774833	CV2713660	single nucleotide variant	NM_003488.4(AKAP1):c.2380G>A (p.Val794Met)	not specified [RCV004321027]	uncertain significance	17	57116209	57116209	Human		name
401764088	CV2725431	single nucleotide variant	NM_003488.4(AKAP1):c.2018A>G (p.Lys673Arg)	not specified [RCV004320068]	uncertain significance	17	57112533	57112533	Human		name
401728505	CV2729612	single nucleotide variant	NM_003488.4(AKAP1):c.1484G>T (p.Ser495Ile)	not specified [RCV004331876]	uncertain significance	17	57106948	57106948	Human		name
401860566	CV2758527	single nucleotide variant	NM_003488.4(AKAP1):c.1120C>T (p.Arg374Cys)	not specified [RCV004337619]	likely benign	17	57106584	57106584	Human		name
405789473	CV3266230	single nucleotide variant	NM_003488.4(AKAP1):c.1097C>T (p.Thr366Ile)	not specified [RCV004399240]	uncertain significance	17	57106561	57106561	Human		name
405789559	CV3266251	single nucleotide variant	NM_003488.4(AKAP1):c.1291C>T (p.Pro431Ser)	not specified [RCV004399261]	uncertain significance	17	57106755	57106755	Human		name
405789572	CV3266254	single nucleotide variant	NM_003488.4(AKAP1):c.1370A>G (p.His457Arg)	not specified [RCV004399264]	uncertain significance	17	57106834	57106834	Human		name
405789774	CV3266302	single nucleotide variant	NM_003488.4(AKAP1):c.2549C>T (p.Thr850Met)	not specified [RCV004399312]	uncertain significance	17	57118429	57118429	Human		name
407485000	CV3439369	single nucleotide variant	NM_003488.4(AKAP1):c.2657C>T (p.Ser886Phe)	not specified [RCV004618838]	uncertain significance	17	57120269	57120269	Human		name
407485128	CV3439391	single nucleotide variant	NM_003488.4(AKAP1):c.2536A>G (p.Met846Val)	not specified [RCV004618860]	uncertain significance	17	57118416	57118416	Human		name
407485246	CV3439413	single nucleotide variant	NM_003488.4(AKAP1):c.2687T>C (p.Val896Ala)	not specified [RCV004618882]	uncertain significance	17	57120299	57120299	Human		name
407485306	CV3439424	single nucleotide variant	NM_003488.4(AKAP1):c.1674G>C (p.Glu558Asp)	not specified [RCV004618893]	uncertain significance	17	57107138	57107138	Human		name
597699143	CV3669188	single nucleotide variant	NM_003488.4(AKAP1):c.1715G>A (p.Gly572Asp)	not specified [RCV004916085]	uncertain significance	17	57110025	57110025	Human		name
597698944	CV3669198	single nucleotide variant	NM_003488.4(AKAP1):c.1403C>T (p.Thr468Ile)	not specified [RCV004916086]	uncertain significance	17	57106867	57106867	Human		name
597698935	CV3669207	single nucleotide variant	NM_003488.4(AKAP1):c.2252G>T (p.Gly751Val)	not specified [RCV004916087]	uncertain significance	17	57114607	57114607	Human		name
597698511	CV3669262	single nucleotide variant	NM_003488.4(AKAP1):c.2392G>A (p.Gly798Arg)	not specified [RCV004916133]	uncertain significance	17	57116221	57116221	Human		name
598225349	CV3962032	single nucleotide variant	NM_003488.4(AKAP1):c.2528A>G (p.Asp843Gly)	not specified [RCV005341435]	uncertain significance	17	57118408	57118408	Human		name
598224604	CV3965855	single nucleotide variant	NM_003488.4(AKAP1):c.2233C>T (p.Leu745Phe)	not specified [RCV005341322]	uncertain significance	17	57114588	57114588	Human		name
598224675	CV3965865	single nucleotide variant	NM_003488.4(AKAP1):c.1466C>T (p.Thr489Ile)	not specified [RCV005341331]	uncertain significance	17	57106930	57106930	Human		name
598194962	CV3965896	single nucleotide variant	NM_003488.4(AKAP1):c.1487A>G (p.Gln496Arg)	not specified [RCV005335493]	uncertain significance	17	57106951	57106951	Human		name
598225022	CV3965915	single nucleotide variant	NM_003488.4(AKAP1):c.2173G>A (p.Val725Met)	not specified [RCV005341378]	uncertain significance	17	57114528	57114528	Human		name
598225105	CV3965932	single nucleotide variant	NM_003488.4(AKAP1):c.2143G>T (p.Val715Phe)	not specified [RCV005341393]	uncertain significance	17	57114498	57114498	Human		name
598225204	CV3965951	single nucleotide variant	NM_003488.4(AKAP1):c.1079C>G (p.Thr360Ser)	not specified [RCV005341410]	uncertain significance	17	57106543	57106543	Human		name
598225252	CV3965962	single nucleotide variant	NM_003488.4(AKAP1):c.1721A>T (p.Asp574Val)	not specified [RCV005341418]	uncertain significance	17	57110031	57110031	Human		name
15184092	CV727306	single nucleotide variant	NM_003488.4(AKAP1):c.1562C>T (p.Thr521Ile)	not provided [RCV000886369]	likely benign	17	57107026	57107026	Human		name
11039547	CV223060	microsatellite	NM_003488.4(AKAP1):c.946GGCTTGGATAGAAATGAGGAG[1] (p.316GLDRNEE[1])	Breast ductal adenocarcinoma [RCV000207020]\|not provided [RCV004692828]	uncertain significance	17	57106390	57106410	Human		name
405291829	CV3206141	single nucleotide variant	NM_178813.6(AKAP14):c.442-7T>G	AKAP14-related disorder [RCV003964207]	benign	X	119919904	119919904	Human		name , trait , alternate_id
401855188	CV2752779	single nucleotide variant	NM_007202.4(AKAP10):c.1467+5C>A	Conduction disorder of the heart [RCV003337833]	uncertain significance	17	19936281	19936281	Human	1	name
405281852	CV3216183	single nucleotide variant	NM_007202.4(AKAP10):c.1323-4A>G	AKAP10-related disorder [RCV003956710]	likely benign	17	19936434	19936434	Human		name , trait , alternate_id
405278073	CV3221656	single nucleotide variant	NM_007202.4(AKAP10):c.1641+6G>A	AKAP10-related disorder [RCV003976270]	benign	17	19931799	19931799	Human		name , trait , alternate_id
405283263	CV3217001	duplication	NM_007200.5(AKAP13):c.4238-43dup	AKAP13-related disorder [RCV003979147]	likely benign	15	85645774	85645775	Human		name , trait , alternate_id
8582834	CV117390	single nucleotide variant	NM_016248.3(AKAP11):c.-100+614A>G	Lung cancer [RCV000097911]	uncertain significance	13	42272842	42272842	Human		name
401916474	CV2814440	single nucleotide variant	NM_007200.5(AKAP13):c.4162-19269A>G	not provided [RCV003401002]	likely benign	15	85620105	85620105	Human		name
8584607	CV119183	single nucleotide variant	NM_001270546.1(AKAP13):c.1463-1279G>C	Lung cancer [RCV000099703]	uncertain significance	15	85714509	85714509	Human		name
9831747	CV166891	deletion	NM_005100.4(AKAP12):c.163-8647_163-5271del	Preeclampsia [RCV000161457]	not provided	6	151297100	151300476	Human		name
8558671	CV20443	single nucleotide variant	NM_007202.4(AKAP10):c.1936A>G (p.Ile646Val)	AKAP10-related disorder [RCV003974800]\|Reclassified - variant of unknown significance [RCV004703181]	risk factor\|benign\|uncertain significance	17	19909228	19909228	Human	4	name , trait , alternate_id
8558671	CV20443	single nucleotide variant	NM_007202.4(AKAP10):c.1936A>G (p.Ile646Val)	AKAP10-related disorder [RCV003974800]\|Reclassified - variant of unknown significance [RCV004703181]	risk factor\|benign\|uncertain significance	17	19909228	19909229	Human	4	name , trait , alternate_id
405275927	CV3193149	single nucleotide variant	NM_007202.4(AKAP10):c.746G>A (p.Arg249His)	AKAP10-related disorder [RCV003974315]	benign	17	19958145	19958145	Human		name , trait , alternate_id
405277187	CV3195369	single nucleotide variant	NM_007202.4(AKAP10):c.1221A>G (p.Gln407=)	AKAP10-related disorder [RCV003904159]	likely benign	17	19939814	19939814	Human		name , trait , alternate_id
405290671	CV3207555	single nucleotide variant	NM_007202.4(AKAP10):c.1020C>T (p.Phe340=)	AKAP10-related disorder [RCV003927131]	likely benign	17	19941867	19941867	Human		name , trait , alternate_id
405274422	CV3208750	single nucleotide variant	NM_016248.4(AKAP11):c.2708G>A (p.Arg903His)	AKAP11-related disorder [RCV003951565]	likely benign	13	42301454	42301454	Human		name , trait , alternate_id
405274382	CV3211712	single nucleotide variant	NM_016248.4(AKAP11):c.3953T>G (p.Phe1318Cys)	AKAP11-related disorder [RCV003951515]	likely benign	13	42302699	42302699	Human		name , trait , alternate_id
405293768	CV3214485	single nucleotide variant	NM_007202.4(AKAP10):c.1568C>T (p.Ser523Leu)	AKAP10-related disorder [RCV003932166]	benign	17	19931878	19931878	Human		name , trait , alternate_id
405270162	CV3215390	single nucleotide variant	NM_007202.4(AKAP10):c.618A>G (p.Arg206=)	AKAP10-related disorder [RCV003949143]	likely benign	17	19958273	19958273	Human		name , trait , alternate_id
408385168	CV3505663	single nucleotide variant	NM_016248.4(AKAP11):c.3643G>C (p.Ala1215Pro)	AKAP11-related disorder [RCV004732390]	uncertain significance	13	42302389	42302389	Human		name , trait , alternate_id
408367855	CV3517756	single nucleotide variant	NM_016248.4(AKAP11):c.3525G>C (p.Glu1175Asp)	AKAP11-related disorder [RCV004759274]	uncertain significance	13	42302271	42302271	Human		name , trait , alternate_id
401920959	CV2820785	single nucleotide variant	NM_005100.4(AKAP12):c.99G>A (p.Ser33=)	not provided [RCV003432095]	likely benign	6	151240661	151240661	Human		name
156292806	CV2246736	single nucleotide variant	NM_007202.4(AKAP10):c.13G>A (p.Gly5Arg)	not specified [RCV004112278]	uncertain significance	17	19977667	19977667	Human		name
156049689	CV2271819	single nucleotide variant	NM_016248.4(AKAP11):c.13A>G (p.Arg5Gly)	not specified [RCV004130653]	uncertain significance	13	42286361	42286361	Human		name
156338630	CV2351453	single nucleotide variant	NM_005100.4(AKAP12):c.11G>A (p.Gly4Glu)	not specified [RCV004193139]	uncertain significance	6	151240573	151240573	Human		name
407503642	CV3436404	single nucleotide variant	NM_007200.5(AKAP13):c.240C>T (p.Pro80=)	not specified [RCV004623815]	likely benign	15	85533642	85533642	Human		name
156351528	CV2323776	single nucleotide variant	NM_007200.5(AKAP13):c.70G>C (p.Asp24His)	not specified [RCV004176324]	uncertain significance	15	85521464	85521464	Human		name
401781742	CV2722250	single nucleotide variant	NM_007202.4(AKAP10):c.47G>T (p.Arg16Leu)	not specified [RCV004328808]	uncertain significance	17	19977633	19977633	Human		name
405802526	CV3263152	single nucleotide variant	NM_005100.4(AKAP12):c.44C>G (p.Pro15Arg)	not specified [RCV004403962]	uncertain significance	6	151240606	151240606	Human		name
405802658	CV3273537	single nucleotide variant	NM_005100.4(AKAP12):c.85G>A (p.Gly29Ser)	not specified [RCV004404033]	uncertain significance	6	151240647	151240647	Human		name
407486532	CV3436162	single nucleotide variant	NM_005100.4(AKAP12):c.396C>T (p.His132=)	not specified [RCV004619135]	likely benign	6	151348787	151348787	Human		name
407462246	CV3436413	single nucleotide variant	NM_178813.6(AKAP14):c.74C>T (p.Pro25Leu)	not specified [RCV004634491]	uncertain significance	X	119903297	119903297	Human		name
407486754	CV3439614	single nucleotide variant	NM_005100.4(AKAP12):c.86G>C (p.Gly29Ala)	not specified [RCV004619083]	uncertain significance	6	151240648	151240648	Human		name
597719599	CV3665806	single nucleotide variant	NM_007202.4(AKAP10):c.74T>C (p.Phe25Ser)	not specified [RCV004918659]	uncertain significance	17	19977606	19977606	Human		name
598238659	CV3958566	single nucleotide variant	NM_005100.4(AKAP12):c.37G>C (p.Glu13Gln)	not specified [RCV005343842]	uncertain significance	6	151240599	151240599	Human		name
15100246	CV699378	single nucleotide variant	NM_005100.4(AKAP12):c.591G>A (p.Gln197=)	not provided [RCV000958886]	benign	6	151348982	151348982	Human		name
15191916	CV721800	single nucleotide variant	NM_005100.4(AKAP12):c.531G>A (p.Lys177=)	not provided [RCV000888514]	benign	6	151348922	151348922	Human		name
126910003	CV1038512	single nucleotide variant	NM_007202.4(AKAP10):c.113C>T (p.Thr38Ile)	not provided [RCV001354261]	uncertain significance	17	19968437	19968437	Human		name
156300528	CV2248828	single nucleotide variant	NM_007202.4(AKAP10):c.268A>G (p.Thr90Ala)	not specified [RCV004115842]	uncertain significance	17	19962891	19962891	Human		name
156081842	CV2368845	single nucleotide variant	NM_007200.5(AKAP13):c.218G>A (p.Cys73Tyr)	not specified [RCV004207806]	uncertain significance	15	85533620	85533620	Human		name
156153322	CV2394955	single nucleotide variant	NM_007202.4(AKAP10):c.205A>G (p.Ser69Gly)	not specified [RCV004234603]	uncertain significance	17	19962954	19962954	Human		name
156261057	CV2395595	single nucleotide variant	NM_007200.5(AKAP13):c.124C>T (p.Arg42Cys)	not specified [RCV004241444]	uncertain significance	15	85521518	85521518	Human		name
401728918	CV2693916	single nucleotide variant	NM_007202.4(AKAP10):c.217A>G (p.Ile73Val)	not specified [RCV004300214]	uncertain significance	17	19962942	19962942	Human		name
401764558	CV2721374	single nucleotide variant	NM_005100.4(AKAP12):c.226C>T (p.Leu76Phe)	not specified [RCV004322123]	uncertain significance	6	151305810	151305810	Human		name
401891147	CV2778669	single nucleotide variant	NM_005100.4(AKAP12):c.146C>T (p.Ser49Leu)	not specified [RCV004346308]	uncertain significance	6	151240708	151240708	Human		name
401916462	CV2814435	single nucleotide variant	NM_007200.5(AKAP13):c.1932C>T (p.Ser644=)	not provided [RCV003400997]	likely benign	15	85580000	85580000	Human		name
405797317	CV3263032	single nucleotide variant	NM_005100.4(AKAP12):c.257G>A (p.Gly86Glu)	not specified [RCV004401859]	uncertain significance	6	151305841	151305841	Human		name
405797334	CV3263038	single nucleotide variant	NM_005100.4(AKAP12):c.268G>C (p.Gly90Arg)	not specified [RCV004401865]	uncertain significance	6	151305852	151305852	Human		name
405790149	CV3266394	single nucleotide variant	NM_007202.4(AKAP10):c.181G>C (p.Ala61Pro)	not specified [RCV004399404]	uncertain significance	17	19962978	19962978	Human		name
405796053	CV3266457	single nucleotide variant	NM_016248.4(AKAP11):c.116G>T (p.Ser39Ile)	not specified [RCV004401449]	uncertain significance	13	42292449	42292449	Human		name
405802894	CV3273663	single nucleotide variant	NM_007200.5(AKAP13):c.221C>G (p.Ala74Gly)	not specified [RCV004404159]	uncertain significance	15	85533623	85533623	Human		name
407503298	CV3436246	single nucleotide variant	NM_007200.5(AKAP13):c.290A>G (p.Tyr97Cys)	not specified [RCV004623719]	uncertain significance	15	85533692	85533692	Human		name
407503482	CV3436297	single nucleotide variant	NM_007200.5(AKAP13):c.241G>A (p.Val81Met)	not specified [RCV004623770]	uncertain significance	15	85533643	85533643	Human		name
407462269	CV3436425	single nucleotide variant	NM_178813.6(AKAP14):c.211G>A (p.Gly71Ser)	not specified [RCV004634499]	uncertain significance	X	119903536	119903536	Human		name
597722004	CV3666046	single nucleotide variant	NM_016248.4(AKAP11):c.248A>G (p.Asp83Gly)	not specified [RCV004918887]	uncertain significance	13	42297079	42297079	Human		name
597723259	CV3666152	single nucleotide variant	NM_016248.4(AKAP11):c.208C>T (p.His70Tyr)	not specified [RCV004918992]	uncertain significance	13	42295734	42295734	Human		name
597724491	CV3675854	single nucleotide variant	NM_005100.4(AKAP12):c.148G>T (p.Asp50Tyr)	not specified [RCV004919102]	uncertain significance	6	151240710	151240710	Human		name
597739755	CV3676032	single nucleotide variant	NM_007200.5(AKAP13):c.274G>A (p.Val92Ile)	not specified [RCV004921327]	likely benign	15	85533676	85533676	Human		name
598238696	CV3958577	single nucleotide variant	NM_005100.4(AKAP12):c.134C>A (p.Ala45Asp)	not specified [RCV005343852]	uncertain significance	6	151240696	151240696	Human		name
598239213	CV3958674	single nucleotide variant	NM_005100.4(AKAP12):c.248G>T (p.Gly83Val)	not specified [RCV005343941]	uncertain significance	6	151305832	151305832	Human		name
598239409	CV3958723	single nucleotide variant	NM_007200.5(AKAP13):c.151A>G (p.Ser51Gly)	not specified [RCV005343986]	uncertain significance	15	85521545	85521545	Human		name
598239777	CV3958822	single nucleotide variant	NM_007200.5(AKAP13):c.116C>T (p.Ser39Phe)	not specified [RCV005344076]	uncertain significance	15	85521510	85521510	Human		name
598197249	CV3958842	single nucleotide variant	NM_007200.5(AKAP13):c.220G>T (p.Ala74Ser)	not specified [RCV005336103]	uncertain significance	15	85533622	85533622	Human		name
598197605	CV3958911	single nucleotide variant	NM_178813.6(AKAP14):c.199T>A (p.Trp67Arg)	not specified [RCV005336164]	uncertain significance	X	119903524	119903524	Human		name
598226058	CV3962162	single nucleotide variant	NM_016248.4(AKAP11):c.169G>C (p.Val57Leu)	not specified [RCV005341551]	uncertain significance	13	42295695	42295695	Human		name
598237225	CV3962247	single nucleotide variant	NM_016248.4(AKAP11):c.115A>G (p.Ser39Gly)	not specified [RCV005343608]	uncertain significance	13	42292448	42292448	Human		name
15171295	CV703387	single nucleotide variant	NM_007200.5(AKAP13):c.1230G>A (p.Lys410=)	not provided [RCV000949806]	benign	15	85579298	85579298	Human		name
15193881	CV703388	single nucleotide variant	NM_007200.5(AKAP13):c.1491G>A (p.Val497=)	not provided [RCV000955495]	benign	15	85579559	85579559	Human		name
15173598	CV703389	single nucleotide variant	NM_007200.5(AKAP13):c.1917A>G (p.Ser639=)	not provided [RCV000950244]	benign	15	85579985	85579985	Human		name
15169048	CV703391	single nucleotide variant	NM_007200.5(AKAP13):c.2745G>C (p.Leu915=)	not provided [RCV000949383]	benign	15	85580813	85580813	Human		name
15191088	CV721803	single nucleotide variant	NM_005100.4(AKAP12):c.2394C>T (p.Pro798=)	not provided [RCV000888282]	benign	6	151350785	151350785	Human		name
151232873	CV1317401	single nucleotide variant	NM_007202.4(AKAP10):c.850A>G (p.Lys284Glu)	SUDDEN INFANT DEATH SYNDROME [RCV001787413]	uncertain significance	17	19958041	19958041	Human	1	name
156236318	CV2193467	single nucleotide variant	NM_007202.4(AKAP10):c.878G>A (p.Ser293Asn)	not specified [RCV004072955]	uncertain significance	17	19947505	19947505	Human		name
156312665	CV2196404	single nucleotide variant	NM_005100.4(AKAP12):c.949A>G (p.Lys317Glu)	not specified [RCV004073708]	uncertain significance	6	151349340	151349340	Human		name
156328519	CV2213629	single nucleotide variant	NM_007200.5(AKAP13):c.914A>G (p.Gln305Arg)	not specified [RCV004089712]	uncertain significance	15	85578982	85578982	Human		name
156221763	CV2222626	single nucleotide variant	NM_005100.4(AKAP12):c.923G>A (p.Arg308His)	not specified [RCV004099451]	uncertain significance	6	151349314	151349314	Human		name
155974444	CV2235703	single nucleotide variant	NM_007200.5(AKAP13):c.515T>C (p.Val172Ala)	not specified [RCV004111842]	uncertain significance	15	85543808	85543808	Human		name
156077072	CV2251452	single nucleotide variant	NM_007200.5(AKAP13):c.643C>G (p.Leu215Val)	not specified [RCV004117431]	uncertain significance	15	85543936	85543936	Human		name
155971512	CV2262344	single nucleotide variant	NM_007200.5(AKAP13):c.458G>A (p.Gly153Glu)	not specified [RCV004128535]	uncertain significance	15	85533860	85533860	Human		name
156131760	CV2279994	single nucleotide variant	NM_005100.4(AKAP12):c.386C>T (p.Ala129Val)	not specified [RCV004146359]	uncertain significance	6	151348777	151348777	Human		name
156347382	CV2297950	single nucleotide variant	NM_007200.5(AKAP13):c.468G>C (p.Gln156His)	not specified [RCV004157872]	uncertain significance	15	85533870	85533870	Human		name
156096291	CV2310173	single nucleotide variant	NM_178813.6(AKAP14):c.508C>T (p.Arg170Cys)	not specified [RCV004163282]	likely benign	X	119920521	119920521	Human		name
156167664	CV2315326	single nucleotide variant	NM_007200.5(AKAP13):c.758A>C (p.Tyr253Ser)	not specified [RCV004167306]	uncertain significance	15	85575226	85575226	Human		name
156044610	CV2340120	single nucleotide variant	NM_005100.4(AKAP12):c.494C>A (p.Ser165Tyr)	not specified [RCV004192360]	uncertain significance	6	151348885	151348885	Human		name
155928258	CV2346571	single nucleotide variant	NM_016248.4(AKAP11):c.667G>T (p.Val223Phe)	not specified [RCV004206485]	uncertain significance	13	42299413	42299413	Human		name
156180848	CV2356116	single nucleotide variant	NM_007202.4(AKAP10):c.778G>A (p.Val260Ile)	not specified [RCV004203526]	uncertain significance	17	19958113	19958113	Human		name
155908469	CV2387337	single nucleotide variant	NM_007200.5(AKAP13):c.704A>G (p.Tyr235Cys)	not specified [RCV004238420]	uncertain significance	15	85575172	85575172	Human		name
156162560	CV2395715	single nucleotide variant	NM_016248.4(AKAP11):c.826T>C (p.Trp276Arg)	not specified [RCV004235254]	uncertain significance	13	42299572	42299572	Human		name
156225710	CV2400949	single nucleotide variant	NM_005100.4(AKAP12):c.755T>C (p.Ile252Thr)	not specified [RCV004244237]	uncertain significance	6	151349146	151349146	Human		name
329359586	CV2435412	single nucleotide variant	NM_007202.4(AKAP10):c.691A>C (p.Ser231Arg)	not specified [RCV004253065]	uncertain significance	17	19958200	19958200	Human		name
329354001	CV2436756	single nucleotide variant	NM_005100.4(AKAP12):c.748G>A (p.Ala250Thr)	not specified [RCV004258122]	likely benign	6	151349139	151349139	Human		name
329367622	CV2456954	single nucleotide variant	NM_007202.4(AKAP10):c.803C>T (p.Ser268Phe)	not specified [RCV004270896]	uncertain significance	17	19958088	19958088	Human		name
329389914	CV2457275	single nucleotide variant	NM_005100.4(AKAP12):c.499G>C (p.Ala167Pro)	not specified [RCV004267127]	uncertain significance	6	151348890	151348890	Human		name
329396291	CV2459489	single nucleotide variant	NM_007202.4(AKAP10):c.890A>T (p.Asp297Val)	not specified [RCV004276955]	uncertain significance	17	19947493	19947493	Human		name
329401317	CV2460756	single nucleotide variant	NM_005100.4(AKAP12):c.328A>G (p.Arg110Gly)	not specified [RCV004271084]	uncertain significance	6	151348719	151348719	Human		name
401759076	CV2712395	single nucleotide variant	NM_005100.4(AKAP12):c.361G>A (p.Asp121Asn)	not specified [RCV004313869]	uncertain significance	6	151348752	151348752	Human		name
401771955	CV2723003	single nucleotide variant	NM_016248.4(AKAP11):c.497T>C (p.Leu166Pro)	not specified [RCV004327175]	uncertain significance	13	42298678	42298678	Human		name
401768314	CV2735260	single nucleotide variant	NM_005100.4(AKAP12):c.967G>A (p.Ala323Thr)	not specified [RCV004333934]	uncertain significance	6	151349358	151349358	Human		name
401885375	CV2762935	single nucleotide variant	NM_005100.4(AKAP12):c.439G>A (p.Glu147Lys)	not specified [RCV004342685]	uncertain significance	6	151348830	151348830	Human		name
401883846	CV2764238	single nucleotide variant	NM_007200.5(AKAP13):c.588C>G (p.His196Gln)	not specified [RCV004336776]	uncertain significance	15	85543881	85543881	Human		name
401870227	CV2765727	single nucleotide variant	NM_007202.4(AKAP10):c.977C>G (p.Ala326Gly)	not specified [RCV004335732]	uncertain significance	17	19941910	19941910	Human		name
401887756	CV2772153	single nucleotide variant	NM_016248.4(AKAP11):c.406C>G (p.Leu136Val)	not specified [RCV004344802]	uncertain significance	13	42298587	42298587	Human		name
401881704	CV2784787	single nucleotide variant	NM_016248.4(AKAP11):c.773A>G (p.His258Arg)	not specified [RCV004352580]	uncertain significance	13	42299519	42299519	Human		name
401916468	CV2814438	single nucleotide variant	NM_007200.5(AKAP13):c.3162C>T (p.Ser1054=)	not provided [RCV003401000]	likely benign	15	85581230	85581230	Human		name
401916471	CV2814439	single nucleotide variant	NM_007200.5(AKAP13):c.3264G>A (p.Thr1088=)	not provided [RCV003401001]	likely benign	15	85581332	85581332	Human		name
401916476	CV2814441	single nucleotide variant	NM_007200.5(AKAP13):c.4917G>T (p.Arg1639=)	not provided [RCV003401003]	likely benign	15	85664680	85664680	Human		name
401934322	CV2814442	single nucleotide variant	NM_007200.5(AKAP13):c.6240G>A (p.Val2080=)	not provided [RCV003411211]	likely benign	15	85719314	85719314	Human		name
401916482	CV2814444	single nucleotide variant	NM_007200.5(AKAP13):c.7761G>A (p.Leu2587=)	not provided [RCV003401005]	likely benign	15	85741198	85741198	Human		name
405796967	CV3262904	single nucleotide variant	NM_016248.4(AKAP11):c.581T>C (p.Leu194Ser)	not specified [RCV004401731]	uncertain significance	13	42298762	42298762	Human		name
405796981	CV3262909	single nucleotide variant	NM_016248.4(AKAP11):c.589G>C (p.Glu197Gln)	not specified [RCV004401736]	uncertain significance	13	42298770	42298770	Human		name
405797201	CV3262911	single nucleotide variant	NM_016248.4(AKAP11):c.611A>T (p.Asn204Ile)	not specified [RCV004401738]	uncertain significance	13	42298792	42298792	Human		name
405797177	CV3262920	single nucleotide variant	NM_016248.4(AKAP11):c.836G>T (p.Arg279Met)	not specified [RCV004401747]	uncertain significance	13	42299582	42299582	Human		name
405797164	CV3262925	single nucleotide variant	NM_016248.4(AKAP11):c.938G>A (p.Ser313Asn)	not specified [RCV004401752]	uncertain significance	13	42299684	42299684	Human		name
405797436	CV3263073	single nucleotide variant	NM_005100.4(AKAP12):c.314C>T (p.Thr105Ile)	not specified [RCV004401900]	uncertain significance	6	151305898	151305898	Human		name
405802423	CV3263095	single nucleotide variant	NM_005100.4(AKAP12):c.344T>A (p.Val115Glu)	not specified [RCV004403905]	uncertain significance	6	151348735	151348735	Human		name
405790200	CV3266412	single nucleotide variant	NM_007202.4(AKAP10):c.500C>T (p.Ser167Leu)	not specified [RCV004399422]	uncertain significance	17	19958391	19958391	Human		name
405790212	CV3266416	single nucleotide variant	NM_007202.4(AKAP10):c.505A>G (p.Ile169Val)	not specified [RCV004399426]	uncertain significance	17	19958386	19958386	Human		name
405790226	CV3266421	single nucleotide variant	NM_007202.4(AKAP10):c.560C>T (p.Ser187Phe)	not specified [RCV004399431]	uncertain significance	17	19958331	19958331	Human		name
405795953	CV3266425	single nucleotide variant	NM_007202.4(AKAP10):c.668T>C (p.Ile223Thr)	not specified [RCV004401417]	uncertain significance	17	19958223	19958223	Human		name
405795962	CV3266428	single nucleotide variant	NM_007202.4(AKAP10):c.762A>C (p.Arg254Ser)	not specified [RCV004401420]	uncertain significance	17	19958129	19958129	Human		name
405796000	CV3266440	single nucleotide variant	NM_007202.4(AKAP10):c.821C>T (p.Ala274Val)	not specified [RCV004401432]	uncertain significance	17	19958070	19958070	Human		name
405796603	CV3266616	single nucleotide variant	NM_016248.4(AKAP11):c.331A>G (p.Ser111Gly)	not specified [RCV004401608]	uncertain significance	13	42297162	42297162	Human		name
405777367	CV3270025	single nucleotide variant	NM_007200.5(AKAP13):c.716A>C (p.Tyr239Ser)	not specified [RCV004396942]	uncertain significance	15	85575184	85575184	Human		name
405777061	CV3270056	single nucleotide variant	NM_007200.5(AKAP13):c.751G>A (p.Asp251Asn)	not specified [RCV004396973]	uncertain significance	15	85575219	85575219	Human		name
405777181	CV3270075	single nucleotide variant	NM_007200.5(AKAP13):c.770C>G (p.Ser257Cys)	not specified [RCV004396992]	uncertain significance	15	85575238	85575238	Human		name
405777543	CV3270111	single nucleotide variant	NM_007200.5(AKAP13):c.815G>A (p.Cys272Tyr)	not specified [RCV004397028]	uncertain significance	15	85575283	85575283	Human		name
405777571	CV3270116	single nucleotide variant	NM_007200.5(AKAP13):c.818C>G (p.Thr273Ser)	not specified [RCV004397033]	uncertain significance	15	85575286	85575286	Human		name
405778417	CV3270133	single nucleotide variant	NM_007200.5(AKAP13):c.851A>C (p.Gln284Pro)	not specified [RCV004397050]	uncertain significance	15	85575319	85575319	Human		name
405778382	CV3270139	single nucleotide variant	NM_178813.6(AKAP14):c.398C>T (p.Ala133Val)	not specified [RCV004397056]	uncertain significance	X	119914835	119914835	Human		name
405778356	CV3270144	single nucleotide variant	NM_178813.6(AKAP14):c.404C>A (p.Thr135Asn)	not specified [RCV004397061]	uncertain significance	X	119914841	119914841	Human		name
405778338	CV3270147	single nucleotide variant	NM_178813.6(AKAP14):c.445G>A (p.Ala149Thr)	not specified [RCV004397064]	uncertain significance	X	119919914	119919914	Human		name
405802654	CV3273535	single nucleotide variant	NM_005100.4(AKAP12):c.799G>A (p.Glu267Lys)	not specified [RCV004404031]	uncertain significance	6	151349190	151349190	Human		name
405803178	CV3273811	single nucleotide variant	NM_007200.5(AKAP13):c.491G>A (p.Arg164Gln)	not specified [RCV004404307]	uncertain significance	15	85543784	85543784	Human		name
405803253	CV3273851	single nucleotide variant	NM_007200.5(AKAP13):c.552G>T (p.Leu184Phe)	not specified [RCV004404347]	uncertain significance	15	85543845	85543845	Human		name
405803272	CV3273861	single nucleotide variant	NM_007200.5(AKAP13):c.560C>A (p.Pro187Gln)	not specified [RCV004404357]	uncertain significance	15	85543853	85543853	Human		name
407503242	CV3436231	single nucleotide variant	NM_007200.5(AKAP13):c.440C>A (p.Thr147Lys)	not specified [RCV004623704]	uncertain significance	15	85533842	85533842	Human		name
407503507	CV3436306	single nucleotide variant	NM_007200.5(AKAP13):c.904A>G (p.Met302Val)	not specified [RCV004623779]	likely benign	15	85578972	85578972	Human		name
407485417	CV3439444	single nucleotide variant	NM_007202.4(AKAP10):c.838G>A (p.Ala280Thr)	not specified [RCV004618913]	uncertain significance	17	19958053	19958053	Human		name
407485455	CV3439453	single nucleotide variant	NM_007202.4(AKAP10):c.998G>A (p.Gly333Glu)	not specified [RCV004618922]	uncertain significance	17	19941889	19941889	Human		name
407485511	CV3439464	single nucleotide variant	NM_007202.4(AKAP10):c.958A>G (p.Met320Val)	not specified [RCV004618933]	uncertain significance	17	19947425	19947425	Human		name
407485694	CV3439493	single nucleotide variant	NM_007202.4(AKAP10):c.523A>C (p.Asn175His)	not specified [RCV004618962]	uncertain significance	17	19958368	19958368	Human		name
407485767	CV3439505	single nucleotide variant	NM_007202.4(AKAP10):c.727G>A (p.Asp243Asn)	not specified [RCV004618974]	uncertain significance	17	19958164	19958164	Human		name
407486295	CV3439624	single nucleotide variant	NM_005100.4(AKAP12):c.888C>A (p.Phe296Leu)	not specified [RCV004619093]	uncertain significance	6	151349279	151349279	Human		name
407486364	CV3439634	single nucleotide variant	NM_005100.4(AKAP12):c.560A>G (p.Lys187Arg)	not specified [RCV004619103]	uncertain significance	6	151348951	151348951	Human		name
407486859	CV3439645	single nucleotide variant	NM_005100.4(AKAP12):c.916G>A (p.Gly306Ser)	not specified [RCV004619114]	uncertain significance	6	151349307	151349307	Human		name
597719794	CV3665826	single nucleotide variant	NM_007202.4(AKAP10):c.491C>T (p.Thr164Ile)	not specified [RCV004918679]	uncertain significance	17	19958400	19958400	Human		name
597719904	CV3665837	single nucleotide variant	NM_007202.4(AKAP10):c.667A>G (p.Ile223Val)	not specified [RCV004918690]	uncertain significance	17	19958224	19958224	Human		name
597719986	CV3665847	single nucleotide variant	NM_007202.4(AKAP10):c.647T>G (p.Phe216Cys)	not specified [RCV004918700]	uncertain significance	17	19958244	19958244	Human		name
597721629	CV3666014	single nucleotide variant	NM_016248.4(AKAP11):c.911C>T (p.Ala304Val)	not specified [RCV004918856]	uncertain significance	13	42299657	42299657	Human		name
597721747	CV3666025	single nucleotide variant	NM_016248.4(AKAP11):c.323T>C (p.Leu108Ser)	not specified [RCV004918866]	likely benign	13	42297154	42297154	Human		name
597721863	CV3666035	single nucleotide variant	NM_016248.4(AKAP11):c.625A>C (p.Ile209Leu)	not specified [RCV004918876]	uncertain significance	13	42299371	42299371	Human		name
597722132	CV3666056	single nucleotide variant	NM_016248.4(AKAP11):c.835A>G (p.Arg279Gly)	not specified [RCV004918897]	uncertain significance	13	42299581	42299581	Human		name
597723132	CV3666141	single nucleotide variant	NM_016248.4(AKAP11):c.320C>T (p.Pro107Leu)	not specified [RCV004918982]	uncertain significance	13	42297151	42297151	Human		name
597724007	CV3666226	single nucleotide variant	NM_005100.4(AKAP12):c.344T>G (p.Val115Gly)	not specified [RCV004919057]	uncertain significance	6	151348735	151348735	Human		name
597741199	CV3672453	single nucleotide variant	NM_007200.5(AKAP13):c.569G>A (p.Arg190His)	not specified [RCV004921620]	uncertain significance	15	85543862	85543862	Human		name
597751161	CV3672532	single nucleotide variant	NM_007200.5(AKAP13):c.517C>T (p.Arg173Trp)	not specified [RCV004923675]	uncertain significance	15	85543810	85543810	Human		name
597751652	CV3672658	single nucleotide variant	NM_178813.6(AKAP14):c.389G>A (p.Arg130Gln)	not specified [RCV004923769]	likely benign	X	119914826	119914826	Human		name
597751675	CV3672665	single nucleotide variant	NM_178813.6(AKAP14):c.586C>T (p.Arg196Cys)	not specified [RCV004923773]	likely benign	X	119920599	119920599	Human		name
597751730	CV3672675	single nucleotide variant	NM_178813.6(AKAP14):c.509G>A (p.Arg170His)	not specified [RCV004923783]	uncertain significance	X	119920522	119920522	Human		name
597724243	CV3675830	single nucleotide variant	NM_005100.4(AKAP12):c.430G>A (p.Glu144Lys)	not specified [RCV004919078]	uncertain significance	6	151348821	151348821	Human		name
597739390	CV3675954	single nucleotide variant	NM_005100.4(AKAP12):c.914C>A (p.Ala305Asp)	not specified [RCV004921250]	uncertain significance	6	151349305	151349305	Human		name
597739417	CV3675965	single nucleotide variant	NM_005100.4(AKAP12):c.668G>A (p.Gly223Glu)	not specified [RCV004921261]	uncertain significance	6	151349059	151349059	Human		name
598238748	CV3958587	single nucleotide variant	NM_005100.4(AKAP12):c.796A>G (p.Lys266Glu)	not specified [RCV005343862]	uncertain significance	6	151349187	151349187	Human		name
598238842	CV3958605	single nucleotide variant	NM_005100.4(AKAP12):c.652C>G (p.Pro218Ala)	not specified [RCV005343878]	uncertain significance	6	151349043	151349043	Human		name
598239192	CV3958667	single nucleotide variant	NM_005100.4(AKAP12):c.811G>A (p.Glu271Lys)	not specified [RCV005343936]	uncertain significance	6	151349202	151349202	Human		name
598197634	CV3958915	single nucleotide variant	NM_178813.6(AKAP14):c.353A>G (p.His118Arg)	not specified [RCV005336168]	likely benign	X	119914790	119914790	Human		name
598197663	CV3958921	single nucleotide variant	NM_178813.6(AKAP14):c.449C>T (p.Pro150Leu)	not specified [RCV005336173]	uncertain significance	X	119919918	119919918	Human		name
598197688	CV3958925	single nucleotide variant	NM_178813.6(AKAP14):c.586C>A (p.Arg196Ser)	not specified [RCV005336177]	uncertain significance	X	119920599	119920599	Human		name
598225442	CV3962051	single nucleotide variant	NM_007202.4(AKAP10):c.421C>G (p.Gln141Glu)	not specified [RCV005341452]	uncertain significance	17	19958470	19958470	Human		name
598195047	CV3962062	single nucleotide variant	NM_007202.4(AKAP10):c.649A>G (p.Met217Val)	not specified [RCV005335506]	uncertain significance	17	19958242	19958242	Human		name
598195198	CV3962327	single nucleotide variant	NM_016248.4(AKAP11):c.503C>A (p.Thr168Asn)	not specified [RCV005335530]	uncertain significance	13	42298684	42298684	Human		name
598238071	CV3962403	single nucleotide variant	NM_005100.4(AKAP12):c.749C>G (p.Ala250Gly)	not specified [RCV005343746]	uncertain significance	6	151349140	151349140	Human		name
15197312	CV699377	single nucleotide variant	NM_005100.4(AKAP12):c.509T>C (p.Ile170Thr)	not provided [RCV000956431]	likely benign	6	151348900	151348900	Human		name
15157927	CV699379	single nucleotide variant	NM_005100.4(AKAP12):c.761C>T (p.Pro254Leu)	not provided [RCV000946975]	benign	6	151349152	151349152	Human		name
15100261	CV699383	single nucleotide variant	NM_005100.4(AKAP12):c.3246A>G (p.Glu1082=)	not provided [RCV000958888]	benign	6	151351637	151351637	Human		name
15161263	CV703392	single nucleotide variant	NM_007200.5(AKAP13):c.3216T>C (p.Thr1072=)	not provided [RCV000947640]	benign	15	85581284	85581284	Human		name
15099065	CV703393	single nucleotide variant	NM_007200.5(AKAP13):c.3525G>A (p.Glu1175=)	not provided [RCV000958694]	benign\|likely benign	15	85581593	85581593	Human		name
15176336	CV703394	single nucleotide variant	NM_007200.5(AKAP13):c.3780C>T (p.Ile1260=)	not provided [RCV000950801]	benign	15	85581848	85581848	Human		name
15161269	CV703395	single nucleotide variant	NM_007200.5(AKAP13):c.4482C>T (p.Ser1494=)	not provided [RCV000947641]	benign	15	85655524	85655524	Human		name
15171327	CV714661	single nucleotide variant	NM_007200.5(AKAP13):c.6078G>A (p.Ala2026=)	not provided [RCV000972176]	benign\|likely benign	15	85719152	85719152	Human		name
15113127	CV721801	single nucleotide variant	NM_005100.4(AKAP12):c.812A>G (p.Glu271Gly)	not provided [RCV000894603]	benign	6	151349203	151349203	Human		name
15099076	CV721805	single nucleotide variant	NM_005100.4(AKAP12):c.4155G>A (p.Gly1385=)	not provided [RCV000891876]	benign	6	151352546	151352546	Human		name
15156565	CV725489	single nucleotide variant	NM_016248.4(AKAP11):c.314A>G (p.Asn105Ser)	not provided [RCV000880655]	benign	13	42297145	42297145	Human		name
15132700	CV735477	single nucleotide variant	NM_005100.4(AKAP12):c.4767C>T (p.Asp1589=)	not provided [RCV000898004]	benign	6	151353158	151353158	Human		name
15155293	CV739836	single nucleotide variant	NM_007200.5(AKAP13):c.6924A>G (p.Pro2308=)	not provided [RCV000902114]	benign	15	85727167	85727167	Human		name
15194311	CV754739	single nucleotide variant	NM_007200.5(AKAP13):c.7383G>A (p.Leu2461=)	not provided [RCV000911088]	benign	15	85735092	85735092	Human		name
34890641	CV904581	single nucleotide variant	NM_016248.4(AKAP11):c.3951G>A (p.Pro1317=)	not provided [RCV001171671]	likely benign	13	42302697	42302697	Human		name
8635612	CV90834	single nucleotide variant	NM_006738.5(AKAP13):c.3546A>G (p.Glu1182=)	Malignant melanoma [RCV000070932]	not provided	15	85581614	85581614	Human		name
150431057	CV1235320	single nucleotide variant	NM_007200.5(AKAP13):c.2534T>C (p.Val845Ala)	not provided [RCV001641690]	benign	15	85580602	85580602	Human		name
156256363	CV2194565	single nucleotide variant	NM_007200.5(AKAP13):c.2591G>A (p.Ser864Asn)	not specified [RCV004081626]	uncertain significance	15	85580659	85580659	Human		name
156133788	CV2195977	single nucleotide variant	NM_016248.4(AKAP11):c.2288A>G (p.Glu763Gly)	not specified [RCV004072229]	uncertain significance	13	42301034	42301034	Human		name
156142639	CV2200028	single nucleotide variant	NM_016248.4(AKAP11):c.1219G>T (p.Ala407Ser)	not specified [RCV004074187]	uncertain significance	13	42299965	42299965	Human		name
155962395	CV2200972	single nucleotide variant	NM_007202.4(AKAP10):c.1606T>A (p.Ser536Thr)	not specified [RCV004074741]	uncertain significance	17	19931840	19931840	Human		name
155926034	CV2208093	single nucleotide variant	NM_005100.4(AKAP12):c.1184A>C (p.Lys395Thr)	not specified [RCV004086779]	uncertain significance	6	151349575	151349575	Human		name
156118390	CV2209254	single nucleotide variant	NM_007200.5(AKAP13):c.1174G>C (p.Gly392Arg)	not specified [RCV004093440]	uncertain significance	15	85579242	85579242	Human		name
156331091	CV2220478	single nucleotide variant	NM_005100.4(AKAP12):c.2974G>A (p.Glu992Lys)	not specified [RCV004097708]	uncertain significance	6	151351365	151351365	Human		name
155928709	CV2224422	single nucleotide variant	NM_016248.4(AKAP11):c.1999T>C (p.Tyr667His)	not specified [RCV004098029]	uncertain significance	13	42300745	42300745	Human		name
156338881	CV2225004	single nucleotide variant	NM_007200.5(AKAP13):c.2190T>A (p.Asp730Glu)	not specified [RCV004094838]	uncertain significance	15	85580258	85580258	Human		name
156252316	CV2232393	single nucleotide variant	NM_005100.4(AKAP12):c.2011C>T (p.Arg671Cys)	not specified [RCV004099022]	uncertain significance	6	151350402	151350402	Human		name
156292958	CV2233500	single nucleotide variant	NM_016248.4(AKAP11):c.1186A>G (p.Met396Val)	not specified [RCV004099984]	uncertain significance	13	42299932	42299932	Human		name
156292970	CV2233501	single nucleotide variant	NM_016248.4(AKAP11):c.2360G>T (p.Ser787Ile)	not specified [RCV004099985]	uncertain significance	13	42301106	42301106	Human		name
156159162	CV2236191	single nucleotide variant	NM_016248.4(AKAP11):c.2494T>A (p.Cys832Ser)	not specified [RCV004107902]	uncertain significance	13	42301240	42301240	Human		name
156058841	CV2239268	single nucleotide variant	NM_007200.5(AKAP13):c.1013G>C (p.Ser338Thr)	not specified [RCV004112236]	uncertain significance	15	85579081	85579081	Human		name
155921421	CV2240523	single nucleotide variant	NM_016248.4(AKAP11):c.1446T>G (p.Asp482Glu)	not specified [RCV004119185]	uncertain significance	13	42300192	42300192	Human		name
156170644	CV2247395	single nucleotide variant	NM_016248.4(AKAP11):c.1403G>A (p.Cys468Tyr)	not specified [RCV004108730]	uncertain significance	13	42300149	42300149	Human		name
156273536	CV2247676	single nucleotide variant	NM_016248.4(AKAP11):c.2332A>G (p.Thr778Ala)	not specified [RCV004115091]	uncertain significance	13	42301078	42301078	Human		name
155925098	CV2248948	single nucleotide variant	NM_007200.5(AKAP13):c.1610C>T (p.Ala537Val)	not specified [RCV004115948]	likely benign	15	85579678	85579678	Human		name
156282296	CV2252395	single nucleotide variant	NM_016248.4(AKAP11):c.2486A>C (p.Lys829Thr)	not specified [RCV004116237]	uncertain significance	13	42301232	42301232	Human		name
156034759	CV2252885	single nucleotide variant	NM_007202.4(AKAP10):c.1691C>T (p.Ala564Val)	not specified [RCV004120718]	uncertain significance	17	19924468	19924468	Human		name
155979868	CV2263586	single nucleotide variant	NM_005100.4(AKAP12):c.2108G>T (p.Gly703Val)	not specified [RCV004135596]	uncertain significance	6	151350499	151350499	Human		name
156021276	CV2264442	single nucleotide variant	NM_005100.4(AKAP12):c.1723G>A (p.Glu575Lys)	not specified [RCV004138340]	uncertain significance	6	151350114	151350114	Human		name
155950459	CV2267858	single nucleotide variant	NM_005100.4(AKAP12):c.1498G>T (p.Val500Leu)	not specified [RCV004136157]	uncertain significance	6	151349889	151349889	Human		name
156054288	CV2269569	single nucleotide variant	NM_005100.4(AKAP12):c.1228G>C (p.Val410Leu)	not specified [RCV004124670]	uncertain significance	6	151349619	151349619	Human		name
156023515	CV2273773	single nucleotide variant	NM_005100.4(AKAP12):c.2423A>G (p.Lys808Arg)	not specified [RCV004132414]	uncertain significance	6	151350814	151350814	Human		name
155902025	CV2274614	single nucleotide variant	NM_016248.4(AKAP11):c.1529A>G (p.Asn510Ser)	not specified [RCV004139004]	uncertain significance	13	42300275	42300275	Human		name
156122254	CV2276080	single nucleotide variant	NM_016248.4(AKAP11):c.2477G>C (p.Arg826Thr)	not specified [RCV004141750]	uncertain significance	13	42301223	42301223	Human		name
156173364	CV2284079	single nucleotide variant	NM_016248.4(AKAP11):c.2186G>A (p.Ser729Asn)	not specified [RCV004144681]	uncertain significance	13	42300932	42300932	Human		name
156285872	CV2289110	single nucleotide variant	NM_005100.4(AKAP12):c.1375C>T (p.Pro459Ser)	not specified [RCV004150046]	uncertain significance	6	151349766	151349766	Human		name
155932149	CV2290474	single nucleotide variant	NM_016248.4(AKAP11):c.1807C>T (p.Arg603Cys)	not specified [RCV004155172]	likely benign	13	42300553	42300553	Human		name
156011510	CV2291150	single nucleotide variant	NM_016248.4(AKAP11):c.2852T>C (p.Ile951Thr)	not specified [RCV004153457]	uncertain significance	13	42301598	42301598	Human		name
156198892	CV2293735	single nucleotide variant	NM_007200.5(AKAP13):c.2335G>A (p.Val779Ile)	not specified [RCV004155021]	uncertain significance	15	85580403	85580403	Human		name
156047424	CV2304340	single nucleotide variant	NM_016248.4(AKAP11):c.2574A>C (p.Glu858Asp)	not specified [RCV004164456]	uncertain significance	13	42301320	42301320	Human		name
156044259	CV2305904	single nucleotide variant	NM_007200.5(AKAP13):c.2787T>A (p.Asp929Glu)	not specified [RCV004167691]	uncertain significance	15	85580855	85580855	Human		name
156054619	CV2308681	single nucleotide variant	NM_007200.5(AKAP13):c.1816C>A (p.Leu606Ile)	not specified [RCV004169016]	uncertain significance	15	85579884	85579884	Human		name
156194681	CV2309456	single nucleotide variant	NM_016248.4(AKAP11):c.1624A>G (p.Lys542Glu)	not specified [RCV004158865]	uncertain significance	13	42300370	42300370	Human		name
156042500	CV2310978	single nucleotide variant	NM_005100.4(AKAP12):c.2536G>A (p.Val846Met)	not specified [RCV004164009]	uncertain significance	6	151350927	151350927	Human		name
156168035	CV2320059	single nucleotide variant	NM_007200.5(AKAP13):c.1711T>C (p.Ser571Pro)	not specified [RCV004167916]	uncertain significance	15	85579779	85579779	Human		name
155975123	CV2327674	single nucleotide variant	NM_007200.5(AKAP13):c.1825G>T (p.Ala609Ser)	not specified [RCV004177251]	uncertain significance	15	85579893	85579893	Human		name
156289386	CV2333123	single nucleotide variant	NM_007200.5(AKAP13):c.2951C>T (p.Pro984Leu)	not specified [RCV004194416]	likely benign	15	85581019	85581019	Human		name
156335636	CV2333556	single nucleotide variant	NM_007200.5(AKAP13):c.1508G>A (p.Ser503Asn)	not specified [RCV004190242]	uncertain significance	15	85579576	85579576	Human		name
156080197	CV2337460	single nucleotide variant	NM_016248.4(AKAP11):c.2156G>A (p.Ser719Asn)	not specified [RCV004187897]	uncertain significance	13	42300902	42300902	Human		name
156280225	CV2348430	single nucleotide variant	NM_005100.4(AKAP12):c.1444C>G (p.Leu482Val)	not specified [RCV004193620]	uncertain significance	6	151349835	151349835	Human		name
156283246	CV2348921	single nucleotide variant	NM_005100.4(AKAP12):c.2345A>C (p.Asp782Ala)	not specified [RCV004203357]	uncertain significance	6	151350736	151350736	Human		name
156383154	CV2361434	single nucleotide variant	NM_007200.5(AKAP13):c.1588A>G (p.Lys530Glu)	not specified [RCV004221078]	uncertain significance	15	85579656	85579656	Human		name
155938098	CV2364965	single nucleotide variant	NM_016248.4(AKAP11):c.2707C>T (p.Arg903Cys)	not specified [RCV004222258]	uncertain significance	13	42301453	42301453	Human		name
156149239	CV2377393	single nucleotide variant	NM_007200.5(AKAP13):c.1148T>C (p.Val383Ala)	not specified [RCV004225570]	likely benign	15	85579216	85579216	Human		name
155936324	CV2379804	single nucleotide variant	NM_007200.5(AKAP13):c.1679C>T (p.Thr560Ile)	not specified [RCV004219918]	uncertain significance	15	85579747	85579747	Human		name
156390793	CV2383420	single nucleotide variant	NM_016248.4(AKAP11):c.2663T>C (p.Leu888Ser)	not specified [RCV004222442]	uncertain significance	13	42301409	42301409	Human		name
156391138	CV2385122	single nucleotide variant	NM_007202.4(AKAP10):c.1226G>T (p.Trp409Leu)	not specified [RCV004228382]	uncertain significance	17	19939809	19939809	Human		name
156204873	CV2385123	single nucleotide variant	NM_007202.4(AKAP10):c.1227G>C (p.Trp409Cys)	not specified [RCV004228383]	uncertain significance	17	19939808	19939808	Human		name
156051933	CV2386492	single nucleotide variant	NM_016248.4(AKAP11):c.2002C>T (p.Pro668Ser)	not specified [RCV004230854]	uncertain significance	13	42300748	42300748	Human		name
155968435	CV2391459	single nucleotide variant	NM_007200.5(AKAP13):c.1567G>A (p.Val523Ile)	not specified [RCV004239851]	uncertain significance	15	85579635	85579635	Human		name
156223271	CV2399982	single nucleotide variant	NM_016248.4(AKAP11):c.2165C>T (p.Thr722Met)	not specified [RCV004246910]	uncertain significance	13	42300911	42300911	Human		name
329372515	CV2424119	single nucleotide variant	NM_016248.4(AKAP11):c.2821C>T (p.Arg941Trp)	not specified [RCV004248018]	uncertain significance	13	42301567	42301567	Human		name
329370306	CV2435541	single nucleotide variant	NM_005100.4(AKAP12):c.1417G>A (p.Gly473Arg)	not specified [RCV004253179]	uncertain significance	6	151349808	151349808	Human		name
329361496	CV2437574	single nucleotide variant	NM_005100.4(AKAP12):c.2815A>G (p.Arg939Gly)	not specified [RCV004258857]	uncertain significance	6	151351206	151351206	Human		name
329399026	CV2439240	single nucleotide variant	NM_007200.5(AKAP13):c.2575G>A (p.Gly859Arg)	not specified [RCV004255525]	uncertain significance	15	85580643	85580643	Human		name
329373129	CV2439292	single nucleotide variant	NM_005100.4(AKAP12):c.2690C>T (p.Ala897Val)	not specified [RCV004249604]	likely benign	6	151351081	151351081	Human		name
329358354	CV2450286	single nucleotide variant	NM_007200.5(AKAP13):c.1382C>T (p.Ser461Phe)	not specified [RCV004271381]	uncertain significance	15	85579450	85579450	Human		name
329352026	CV2455634	single nucleotide variant	NM_016248.4(AKAP11):c.1585A>C (p.Lys529Gln)	not specified [RCV004276880]	uncertain significance	13	42300331	42300331	Human		name
329379543	CV2456306	single nucleotide variant	NM_016248.4(AKAP11):c.2648T>A (p.Ile883Lys)	not specified [RCV004275475]	uncertain significance	13	42301394	42301394	Human		name
329394725	CV2457609	single nucleotide variant	NM_007202.4(AKAP10):c.1693A>G (p.Ile565Val)	not specified [RCV004269468]	uncertain significance	17	19924466	19924466	Human		name
329382357	CV2465191	single nucleotide variant	NM_005100.4(AKAP12):c.1744G>A (p.Gly582Ser)	not specified [RCV004287230]	uncertain significance	6	151350135	151350135	Human		name
329376197	CV2465330	single nucleotide variant	NM_016248.4(AKAP11):c.2894C>T (p.Ala965Val)	not specified [RCV004281118]	likely benign	13	42301640	42301640	Human		name
329376341	CV2465551	single nucleotide variant	NM_016248.4(AKAP11):c.1106T>C (p.Leu369Ser)	not specified [RCV004283130]	uncertain significance	13	42299852	42299852	Human		name
329362204	CV2466173	single nucleotide variant	NM_016248.4(AKAP11):c.1727G>A (p.Cys576Tyr)	not specified [RCV004279822]	uncertain significance	13	42300473	42300473	Human		name
401766216	CV2679611	single nucleotide variant	NM_007200.5(AKAP13):c.1721G>T (p.Arg574Leu)	not specified [RCV004282090]	uncertain significance	15	85579789	85579789	Human		name
401768850	CV2686397	single nucleotide variant	NM_005100.4(AKAP12):c.1223T>C (p.Ile408Thr)	not specified [RCV004297467]	uncertain significance	6	151349614	151349614	Human		name
401744761	CV2688226	single nucleotide variant	NM_007200.5(AKAP13):c.1218T>A (p.Asp406Glu)	not specified [RCV004298913]	uncertain significance	15	85579286	85579286	Human		name
401747434	CV2696697	single nucleotide variant	NM_005100.4(AKAP12):c.2504G>A (p.Gly835Glu)	not specified [RCV004290676]	likely benign	6	151350895	151350895	Human		name
401721134	CV2702280	single nucleotide variant	NM_005100.4(AKAP12):c.2032T>C (p.Ser678Pro)	not specified [RCV004314611]	uncertain significance	6	151350423	151350423	Human		name
401776788	CV2703364	single nucleotide variant	NM_016248.4(AKAP11):c.1921A>C (p.Asn641His)	not specified [RCV004315712]	uncertain significance	13	42300667	42300667	Human		name
401783001	CV2703706	single nucleotide variant	NM_007200.5(AKAP13):c.1841C>T (p.Ala614Val)	not specified [RCV004306595]	uncertain significance	15	85579909	85579909	Human		name
401718578	CV2704674	single nucleotide variant	NM_005100.4(AKAP12):c.1989G>C (p.Glu663Asp)	not specified [RCV004307283]	uncertain significance	6	151350380	151350380	Human		name
401757841	CV2707991	single nucleotide variant	NM_016248.4(AKAP11):c.2389A>G (p.Thr797Ala)	not specified [RCV004309243]	uncertain significance	13	42301135	42301135	Human		name
401751267	CV2708539	single nucleotide variant	NM_016248.4(AKAP11):c.1300C>T (p.Pro434Ser)	not specified [RCV004307536]	uncertain significance	13	42300046	42300046	Human		name
401749463	CV2712363	single nucleotide variant	NM_007200.5(AKAP13):c.2786A>G (p.Asp929Gly)	not specified [RCV004313846]	uncertain significance	15	85580854	85580854	Human		name
401770058	CV2719016	single nucleotide variant	NM_005100.4(AKAP12):c.2959G>A (p.Ala987Thr)	not specified [RCV004322602]	uncertain significance	6	151351350	151351350	Human		name
401744008	CV2722347	single nucleotide variant	NM_005100.4(AKAP12):c.1105C>T (p.Arg369Trp)	not specified [RCV004322758]	uncertain significance	6	151349496	151349496	Human		name
401766432	CV2725539	single nucleotide variant	NM_005100.4(AKAP12):c.1735C>G (p.Leu579Val)	not specified [RCV004320153]	uncertain significance	6	151350126	151350126	Human		name
401725099	CV2725701	single nucleotide variant	NM_016248.4(AKAP11):c.1193C>T (p.Pro398Leu)	not specified [RCV004322398]	uncertain significance	13	42299939	42299939	Human		name
401751724	CV2727118	single nucleotide variant	NM_007200.5(AKAP13):c.1672G>A (p.Glu558Lys)	not specified [RCV004325481]	uncertain significance	15	85579740	85579740	Human		name
401781601	CV2731714	single nucleotide variant	NM_005100.4(AKAP12):c.2881C>T (p.Arg961Trp)	not specified [RCV004331816]	uncertain significance	6	151351272	151351272	Human		name
401856103	CV2764354	single nucleotide variant	NM_007202.4(AKAP10):c.1107G>C (p.Gln369His)	not specified [RCV004338927]	uncertain significance	17	19940965	19940965	Human		name
401884069	CV2765955	single nucleotide variant	NM_016248.4(AKAP11):c.1733A>G (p.Asn578Ser)	not specified [RCV004337979]	uncertain significance	13	42300479	42300479	Human		name
401864109	CV2767472	single nucleotide variant	NM_016248.4(AKAP11):c.2836A>G (p.Ile946Val)	not specified [RCV004343636]	uncertain significance	13	42301582	42301582	Human		name
401898118	CV2769975	single nucleotide variant	NM_016248.4(AKAP11):c.1274G>T (p.Gly425Val)	not specified [RCV004353809]	uncertain significance	13	42300020	42300020	Human		name
401863773	CV2770821	single nucleotide variant	NM_005100.4(AKAP12):c.1895A>G (p.Glu632Gly)	not specified [RCV004349854]	uncertain significance	6	151350286	151350286	Human		name
401870294	CV2772696	single nucleotide variant	NM_007200.5(AKAP13):c.1258A>G (p.Asn420Asp)	not specified [RCV004357216]	uncertain significance	15	85579326	85579326	Human		name
401863007	CV2775528	single nucleotide variant	NM_007200.5(AKAP13):c.1195A>G (p.Ser399Gly)	not specified [RCV004350702]	uncertain significance	15	85579263	85579263	Human		name
401873588	CV2776625	single nucleotide variant	NM_005100.4(AKAP12):c.1708C>G (p.Pro570Ala)	not specified [RCV004357497]	uncertain significance	6	151350099	151350099	Human		name
401878856	CV2777947	single nucleotide variant	NM_007202.4(AKAP10):c.1442G>A (p.Arg481His)	not specified [RCV004347911]	uncertain significance	17	19936311	19936311	Human		name
401891237	CV2779154	single nucleotide variant	NM_007202.4(AKAP10):c.1963C>A (p.Pro655Thr)	not specified [RCV004349068]	uncertain significance	17	19909201	19909201	Human		name
401861370	CV2779675	single nucleotide variant	NM_005100.4(AKAP12):c.1720G>A (p.Glu574Lys)	not specified [RCV004351369]	uncertain significance	6	151350111	151350111	Human		name
401884130	CV2782357	single nucleotide variant	NM_007200.5(AKAP13):c.1486A>T (p.Asn496Tyr)	not specified [RCV004365104]	uncertain significance	15	85579554	85579554	Human		name
401899222	CV2783750	single nucleotide variant	NM_016248.4(AKAP11):c.2788G>A (p.Glu930Lys)	not specified [RCV004360669]	uncertain significance	13	42301534	42301534	Human		name
401866154	CV2786253	single nucleotide variant	NM_007200.5(AKAP13):c.1684A>C (p.Thr562Pro)	not specified [RCV004361574]	uncertain significance	15	85579752	85579752	Human		name
401884942	CV2786626	single nucleotide variant	NM_005100.4(AKAP12):c.2396G>A (p.Gly799Asp)	not specified [RCV004363765]	uncertain significance	6	151350787	151350787	Human		name
401888024	CV2791894	single nucleotide variant	NM_005100.4(AKAP12):c.1363C>G (p.Gln455Glu)	not specified [RCV004359330]	uncertain significance	6	151349754	151349754	Human		name
401872530	CV2793111	single nucleotide variant	NM_005100.4(AKAP12):c.1222A>G (p.Ile408Val)	not specified [RCV004360426]	likely benign	6	151349613	151349613	Human		name
401916463	CV2814436	single nucleotide variant	NM_007200.5(AKAP13):c.2510C>T (p.Thr837Met)	not provided [RCV003400998]	likely benign	15	85580578	85580578	Human		name
401916465	CV2814437	single nucleotide variant	NM_007200.5(AKAP13):c.2534T>G (p.Val845Gly)	not provided [RCV003400999]	likely benign	15	85580602	85580602	Human		name
405797155	CV3262928	single nucleotide variant	NM_005100.4(AKAP12):c.1094C>T (p.Ala365Val)	not specified [RCV004401755]	likely benign	6	151349485	151349485	Human		name
405797031	CV3262950	single nucleotide variant	NM_005100.4(AKAP12):c.1253A>G (p.Glu418Gly)	not specified [RCV004401777]	uncertain significance	6	151349644	151349644	Human		name
405797047	CV3262956	single nucleotide variant	NM_005100.4(AKAP12):c.1285G>A (p.Glu429Lys)	not specified [RCV004401783]	uncertain significance	6	151349676	151349676	Human		name
405797093	CV3262974	single nucleotide variant	NM_005100.4(AKAP12):c.1642A>T (p.Thr548Ser)	not specified [RCV004401801]	uncertain significance	6	151350033	151350033	Human		name
405797101	CV3262977	single nucleotide variant	NM_005100.4(AKAP12):c.1687G>A (p.Gly563Ser)	not specified [RCV004401804]	uncertain significance	6	151350078	151350078	Human		name
405797214	CV3262995	single nucleotide variant	NM_005100.4(AKAP12):c.1934C>G (p.Ser645Cys)	not specified [RCV004401822]	uncertain significance	6	151350325	151350325	Human		name
405797241	CV3263005	single nucleotide variant	NM_005100.4(AKAP12):c.2168C>T (p.Thr723Met)	not specified [RCV004401832]	uncertain significance	6	151350559	151350559	Human		name
405797252	CV3263009	single nucleotide variant	NM_005100.4(AKAP12):c.2231C>T (p.Pro744Leu)	not specified [RCV004401836]	uncertain significance	6	151350622	151350622	Human		name
405797268	CV3263015	single nucleotide variant	NM_005100.4(AKAP12):c.2309A>T (p.Lys770Ile)	not specified [RCV004401842]	uncertain significance	6	151350700	151350700	Human		name
405797321	CV3263034	single nucleotide variant	NM_005100.4(AKAP12):c.2617G>A (p.Glu873Lys)	not specified [RCV004401861]	uncertain significance	6	151351008	151351008	Human		name
405797360	CV3263047	single nucleotide variant	NM_005100.4(AKAP12):c.2692G>A (p.Asp898Asn)	not specified [RCV004401874]	uncertain significance	6	151351083	151351083	Human		name
405797366	CV3263049	single nucleotide variant	NM_005100.4(AKAP12):c.2699C>T (p.Thr900Met)	not specified [RCV004401876]	uncertain significance	6	151351090	151351090	Human		name
405797381	CV3263054	single nucleotide variant	NM_005100.4(AKAP12):c.2905G>A (p.Ala969Thr)	not specified [RCV004401881]	uncertain significance	6	151351296	151351296	Human		name
405797387	CV3263056	single nucleotide variant	NM_005100.4(AKAP12):c.2915C>A (p.Thr972Asn)	not specified [RCV004401883]	uncertain significance	6	151351306	151351306	Human		name
405790068	CV3266370	single nucleotide variant	NM_007202.4(AKAP10):c.1021G>A (p.Val341Ile)	not specified [RCV004399380]	uncertain significance	17	19941866	19941866	Human		name
405790140	CV3266390	single nucleotide variant	NM_007202.4(AKAP10):c.1609C>T (p.His537Tyr)	not specified [RCV004399400]	uncertain significance	17	19931837	19931837	Human		name
405790145	CV3266392	single nucleotide variant	NM_007202.4(AKAP10):c.1630T>G (p.Ser544Ala)	not specified [RCV004399402]	uncertain significance	17	19931816	19931816	Human		name
405790160	CV3266398	single nucleotide variant	NM_007202.4(AKAP10):c.1946A>G (p.Gln649Arg)	not specified [RCV004399408]	uncertain significance	17	19909218	19909218	Human		name
405796041	CV3266453	single nucleotide variant	NM_016248.4(AKAP11):c.1115G>T (p.Cys372Phe)	not specified [RCV004401445]	uncertain significance	13	42299861	42299861	Human		name
405796070	CV3266463	single nucleotide variant	NM_016248.4(AKAP11):c.1213C>T (p.Arg405Cys)	not specified [RCV004401455]	uncertain significance	13	42299959	42299959	Human		name
405796092	CV3266471	single nucleotide variant	NM_016248.4(AKAP11):c.1267C>G (p.Pro423Ala)	not specified [RCV004401463]	uncertain significance	13	42300013	42300013	Human		name
405796150	CV3266492	single nucleotide variant	NM_016248.4(AKAP11):c.1481G>A (p.Ser494Asn)	not specified [RCV004401484]	likely benign	13	42300227	42300227	Human		name
405796170	CV3266499	single nucleotide variant	NM_016248.4(AKAP11):c.1490G>A (p.Cys497Tyr)	not specified [RCV004401491]	uncertain significance	13	42300236	42300236	Human		name
405796298	CV3266539	single nucleotide variant	NM_016248.4(AKAP11):c.2221A>G (p.Thr741Ala)	not specified [RCV004401531]	uncertain significance	13	42300967	42300967	Human		name
405796594	CV3266613	single nucleotide variant	NM_016248.4(AKAP11):c.2920T>G (p.Ser974Ala)	not specified [RCV004401605]	uncertain significance	13	42301666	42301666	Human		name
405802693	CV3273556	single nucleotide variant	NM_007200.5(AKAP13):c.1133G>A (p.Arg378Lys)	not specified [RCV004404052]	uncertain significance	15	85579201	85579201	Human		name
405802706	CV3273563	single nucleotide variant	NM_007200.5(AKAP13):c.1172C>G (p.Ser391Cys)	not specified [RCV004404059]	uncertain significance	15	85579240	85579240	Human		name
405802766	CV3273595	single nucleotide variant	NM_007200.5(AKAP13):c.1640A>C (p.Lys547Thr)	not specified [RCV004404091]	uncertain significance	15	85579708	85579708	Human		name
405802816	CV3273622	single nucleotide variant	NM_007200.5(AKAP13):c.1751A>G (p.Gln584Arg)	not specified [RCV004404118]	uncertain significance	15	85579819	85579819	Human		name
405802822	CV3273625	single nucleotide variant	NM_007200.5(AKAP13):c.1804G>A (p.Glu602Lys)	not specified [RCV004404121]	uncertain significance	15	85579872	85579872	Human		name
405802850	CV3273640	single nucleotide variant	NM_007200.5(AKAP13):c.1843A>G (p.Met615Val)	not specified [RCV004404136]	likely benign	15	85579911	85579911	Human		name
405802854	CV3273642	single nucleotide variant	NM_007200.5(AKAP13):c.1861G>A (p.Ala621Thr)	not specified [RCV004404138]	likely benign	15	85579929	85579929	Human		name
405802863	CV3273647	single nucleotide variant	NM_007200.5(AKAP13):c.2056A>C (p.Ile686Leu)	not specified [RCV004404143]	uncertain significance	15	85580124	85580124	Human		name
405802874	CV3273653	single nucleotide variant	NM_007200.5(AKAP13):c.2063G>A (p.Ser688Asn)	not specified [RCV004404149]	uncertain significance	15	85580131	85580131	Human		name
405802888	CV3273660	single nucleotide variant	NM_007200.5(AKAP13):c.2197C>A (p.Pro733Thr)	not specified [RCV004404156]	uncertain significance	15	85580265	85580265	Human		name
407486659	CV3436183	single nucleotide variant	NM_005100.4(AKAP12):c.1865G>A (p.Arg622His)	not specified [RCV004619156]	uncertain significance	6	151350256	151350256	Human		name
407503338	CV3436257	single nucleotide variant	NM_007200.5(AKAP13):c.2029G>A (p.Asp677Asn)	not specified [RCV004623730]	uncertain significance	15	85580097	85580097	Human		name
407503373	CV3436267	single nucleotide variant	NM_007200.5(AKAP13):c.2372C>T (p.Pro791Leu)	not specified [RCV004623740]	uncertain significance	15	85580440	85580440	Human		name
407503445	CV3436287	single nucleotide variant	NM_007200.5(AKAP13):c.1520G>C (p.Arg507Thr)	not specified [RCV004623760]	uncertain significance	15	85579588	85579588	Human		name
407503592	CV3436328	single nucleotide variant	NM_007200.5(AKAP13):c.1600C>T (p.Pro534Ser)	not specified [RCV004623801]	uncertain significance	15	85579668	85579668	Human		name
407462210	CV3436394	single nucleotide variant	NM_007200.5(AKAP13):c.1859T>C (p.Leu620Ser)	not specified [RCV004634476]	uncertain significance	15	85579927	85579927	Human		name
407485575	CV3439474	single nucleotide variant	NM_007202.4(AKAP10):c.1556G>A (p.Gly519Asp)	not specified [RCV004618943]	uncertain significance	17	19931890	19931890	Human		name
407485632	CV3439484	single nucleotide variant	NM_007202.4(AKAP10):c.1583G>T (p.Gly528Val)	not specified [RCV004618953]	uncertain significance	17	19931863	19931863	Human		name
407485814	CV3439513	single nucleotide variant	NM_007202.4(AKAP10):c.1013A>G (p.Asn338Ser)	not specified [RCV004618982]	uncertain significance	17	19941874	19941874	Human		name
407485838	CV3439517	single nucleotide variant	NM_007202.4(AKAP10):c.1750G>A (p.Gly584Arg)	not specified [RCV004618986]	uncertain significance	17	19924409	19924409	Human		name
407485871	CV3439525	single nucleotide variant	NM_016248.4(AKAP11):c.2025G>T (p.Gln675His)	not specified [RCV004618994]	uncertain significance	13	42300771	42300771	Human		name
407485935	CV3439536	single nucleotide variant	NM_016248.4(AKAP11):c.1803G>T (p.Arg601Ser)	not specified [RCV004619005]	uncertain significance	13	42300549	42300549	Human		name
407486205	CV3439585	single nucleotide variant	NM_016248.4(AKAP11):c.2182G>A (p.Val728Met)	not specified [RCV004619054]	uncertain significance	13	42300928	42300928	Human		name
407486251	CV3439593	single nucleotide variant	NM_005100.4(AKAP12):c.1853C>T (p.Thr618Met)	not specified [RCV004619062]	uncertain significance	6	151350244	151350244	Human		name
597719496	CV3665795	single nucleotide variant	NM_007202.4(AKAP10):c.1219C>A (p.Gln407Lys)	not specified [RCV004918648]	uncertain significance	17	19939816	19939816	Human		name
597719702	CV3665816	single nucleotide variant	NM_007202.4(AKAP10):c.1952A>G (p.Gln651Arg)	not specified [RCV004918669]	uncertain significance	17	19909212	19909212	Human		name
597720197	CV3665868	single nucleotide variant	NM_016248.4(AKAP11):c.2662T>G (p.Leu888Val)	not specified [RCV004918721]	uncertain significance	13	42301408	42301408	Human		name
597720283	CV3665878	single nucleotide variant	NM_016248.4(AKAP11):c.2326A>G (p.Ile776Val)	not specified [RCV004918731]	uncertain significance	13	42301072	42301072	Human		name
597720364	CV3665888	single nucleotide variant	NM_016248.4(AKAP11):c.1519C>T (p.His507Tyr)	not specified [RCV004918741]	uncertain significance	13	42300265	42300265	Human		name
597720710	CV3665936	single nucleotide variant	NM_016248.4(AKAP11):c.1213C>A (p.Arg405Ser)	not specified [RCV004918782]	uncertain significance	13	42299959	42299959	Human		name
597720844	CV3665953	single nucleotide variant	NM_016248.4(AKAP11):c.1685T>C (p.Phe562Ser)	not specified [RCV004918795]	uncertain significance	13	42300431	42300431	Human		name
597720945	CV3665962	single nucleotide variant	NM_016248.4(AKAP11):c.1314G>C (p.Lys438Asn)	not specified [RCV004918804]	uncertain significance	13	42300060	42300060	Human		name
597721083	CV3665973	single nucleotide variant	NM_016248.4(AKAP11):c.2972C>T (p.Ser991Phe)	not specified [RCV004918815]	uncertain significance	13	42301718	42301718	Human		name
597721224	CV3665984	single nucleotide variant	NM_016248.4(AKAP11):c.1740G>T (p.Leu580Phe)	not specified [RCV004918826]	uncertain significance	13	42300486	42300486	Human		name
597722319	CV3666074	single nucleotide variant	NM_016248.4(AKAP11):c.2785A>G (p.Ser929Gly)	not specified [RCV004918915]	uncertain significance	13	42301531	42301531	Human		name
597722658	CV3666101	single nucleotide variant	NM_016248.4(AKAP11):c.2536A>T (p.Asn846Tyr)	not specified [RCV004918942]	uncertain significance	13	42301282	42301282	Human		name
597723035	CV3666132	single nucleotide variant	NM_016248.4(AKAP11):c.1485T>G (p.Ile495Met)	not specified [RCV004918973]	uncertain significance	13	42300231	42300231	Human		name
597723297	CV3666160	single nucleotide variant	NM_016248.4(AKAP11):c.2189C>T (p.Ala730Val)	not specified [RCV004918995]	uncertain significance	13	42300935	42300935	Human		name
597723390	CV3666169	single nucleotide variant	NM_016248.4(AKAP11):c.2744C>G (p.Thr915Ser)	not specified [RCV004919003]	uncertain significance	13	42301490	42301490	Human		name
597723509	CV3666180	single nucleotide variant	NM_016248.4(AKAP11):c.1806G>C (p.Gln602His)	not specified [RCV004919014]	uncertain significance	13	42300552	42300552	Human		name
597723627	CV3666190	single nucleotide variant	NM_005100.4(AKAP12):c.2993A>G (p.Glu998Gly)	not specified [RCV004919024]	uncertain significance	6	151351384	151351384	Human		name
597719399	CV3669286	single nucleotide variant	NM_007202.4(AKAP10):c.1465A>G (p.Lys489Glu)	not specified [RCV004918637]	uncertain significance	17	19936288	19936288	Human		name
597741056	CV3672415	single nucleotide variant	NM_007200.5(AKAP13):c.1963A>G (p.Thr655Ala)	not specified [RCV004921589]	uncertain significance	15	85580031	85580031	Human		name
597741181	CV3672444	single nucleotide variant	NM_007200.5(AKAP13):c.1579C>T (p.Pro527Ser)	not specified [RCV004921616]	uncertain significance	15	85579647	85579647	Human		name
597741309	CV3672480	single nucleotide variant	NM_007200.5(AKAP13):c.2304A>C (p.Lys768Asn)	not specified [RCV004921644]	uncertain significance	15	85580372	85580372	Human		name
597751452	CV3672616	single nucleotide variant	NM_007200.5(AKAP13):c.1370C>A (p.Ala457Asp)	not specified [RCV004923731]	uncertain significance	15	85579438	85579438	Human		name
597751557	CV3672636	single nucleotide variant	NM_007200.5(AKAP13):c.1513A>G (p.Lys505Glu)	not specified [RCV004923751]	uncertain significance	15	85579581	85579581	Human		name
597751614	CV3672647	single nucleotide variant	NM_007200.5(AKAP13):c.1762G>A (p.Val588Met)	not specified [RCV004923762]	uncertain significance	15	85579830	85579830	Human		name
597724365	CV3675840	single nucleotide variant	NM_005100.4(AKAP12):c.2395G>A (p.Gly799Ser)	not specified [RCV004919088]	uncertain significance	6	151350786	151350786	Human		name
597739084	CV3675872	single nucleotide variant	NM_005100.4(AKAP12):c.2015A>G (p.Lys672Arg)	not specified [RCV004921169]	uncertain significance	6	151350406	151350406	Human		name
597739164	CV3675890	single nucleotide variant	NM_005100.4(AKAP12):c.1163C>T (p.Ser388Leu)	not specified [RCV004921187]	uncertain significance	6	151349554	151349554	Human		name
597739236	CV3675910	single nucleotide variant	NM_005100.4(AKAP12):c.1102C>A (p.Pro368Thr)	not specified [RCV004921207]	uncertain significance	6	151349493	151349493	Human		name
597739551	CV3675993	single nucleotide variant	NM_007200.5(AKAP13):c.1676A>G (p.Glu559Gly)	not specified [RCV004921289]	uncertain significance	15	85579744	85579744	Human		name
597739593	CV3676001	single nucleotide variant	NM_007200.5(AKAP13):c.1456C>G (p.Leu486Val)	not specified [RCV004921297]	uncertain significance	15	85579524	85579524	Human		name
597739811	CV3676042	single nucleotide variant	NM_007200.5(AKAP13):c.1885G>A (p.Val629Ile)	not specified [RCV004921337]	uncertain significance	15	85579953	85579953	Human		name
597740030	CV3676083	single nucleotide variant	NM_007200.5(AKAP13):c.2459C>T (p.Thr820Ile)	not specified [RCV004921378]	uncertain significance	15	85580527	85580527	Human		name
597740404	CV3676165	single nucleotide variant	NM_007200.5(AKAP13):c.2809A>C (p.Ile937Leu)	not specified [RCV004921459]	uncertain significance	15	85580877	85580877	Human		name
597740442	CV3676173	single nucleotide variant	NM_007200.5(AKAP13):c.1241G>A (p.Gly414Asp)	not specified [RCV004921467]	uncertain significance	15	85579309	85579309	Human		name
597740606	CV3676214	single nucleotide variant	NM_007200.5(AKAP13):c.1089G>C (p.Glu363Asp)	not specified [RCV004921502]	uncertain significance	15	85579157	85579157	Human		name
597740634	CV3676223	single nucleotide variant	NM_007200.5(AKAP13):c.2800T>G (p.Cys934Gly)	not specified [RCV004921508]	uncertain significance	15	85580868	85580868	Human		name
597740689	CV3676234	single nucleotide variant	NM_007200.5(AKAP13):c.2108C>T (p.Pro703Leu)	not specified [RCV004921519]	likely benign	15	85580176	85580176	Human		name
12842578	CV374891	single nucleotide variant	NM_007202.4(AKAP10):c.1972A>G (p.Lys658Glu)	not provided [RCV000434669]	uncertain significance	17	19909192	19909192	Human		name
598238576	CV3958547	single nucleotide variant	NM_005100.4(AKAP12):c.2429T>G (p.Phe810Cys)	not specified [RCV005343826]	uncertain significance	6	151350820	151350820	Human		name
598195320	CV3958555	single nucleotide variant	NM_005100.4(AKAP12):c.2266G>A (p.Val756Ile)	not specified [RCV005335551]	uncertain significance	6	151350657	151350657	Human		name
598238784	CV3958595	single nucleotide variant	NM_005100.4(AKAP12):c.1441G>A (p.Asp481Asn)	not specified [RCV005343868]	uncertain significance	6	151349832	151349832	Human		name
598238898	CV3958615	single nucleotide variant	NM_005100.4(AKAP12):c.2568A>T (p.Glu856Asp)	not specified [RCV005343888]	uncertain significance	6	151350959	151350959	Human		name
598238958	CV3958626	single nucleotide variant	NM_005100.4(AKAP12):c.2506G>A (p.Ala836Thr)	not specified [RCV005343898]	uncertain significance	6	151350897	151350897	Human		name
598195374	CV3958688	single nucleotide variant	NM_005100.4(AKAP12):c.2777A>C (p.Glu926Ala)	not specified [RCV005335563]	uncertain significance	6	151351168	151351168	Human		name
598239345	CV3958706	single nucleotide variant	NM_007200.5(AKAP13):c.1349T>C (p.Leu450Ser)	not specified [RCV005343971]	uncertain significance	15	85579417	85579417	Human		name
598239791	CV3958826	single nucleotide variant	NM_007200.5(AKAP13):c.1273A>C (p.Thr425Pro)	not specified [RCV005344080]	uncertain significance	15	85579341	85579341	Human		name
598239811	CV3958831	single nucleotide variant	NM_007200.5(AKAP13):c.1645G>A (p.Ala549Thr)	not specified [RCV005344085]	uncertain significance	15	85579713	85579713	Human		name
598197315	CV3958856	single nucleotide variant	NM_007200.5(AKAP13):c.1180G>A (p.Val394Ile)	not specified [RCV005336114]	uncertain significance	15	85579248	85579248	Human		name
598197461	CV3958882	single nucleotide variant	NM_007200.5(AKAP13):c.1632T>A (p.Asp544Glu)	not specified [RCV005336138]	uncertain significance	15	85579700	85579700	Human		name
598195456	CV3958887	single nucleotide variant	NM_007200.5(AKAP13):c.1772C>T (p.Ala591Val)	not specified [RCV005335580]	uncertain significance	15	85579840	85579840	Human		name
598225558	CV3962073	single nucleotide variant	NM_007202.4(AKAP10):c.1529A>G (p.His510Arg)	not specified [RCV005341472]	uncertain significance	17	19931917	19931917	Human		name
598225607	CV3962083	single nucleotide variant	NM_007202.4(AKAP10):c.1849C>A (p.Gln617Lys)	not specified [RCV005341480]	uncertain significance	17	19909964	19909964	Human		name
598226243	CV3962188	single nucleotide variant	NM_016248.4(AKAP11):c.1914A>G (p.Ile638Met)	not specified [RCV005341577]	uncertain significance	13	42300660	42300660	Human		name
598226296	CV3962197	single nucleotide variant	NM_016248.4(AKAP11):c.2828C>A (p.Ser943Tyr)	not specified [RCV005341585]	uncertain significance	13	42301574	42301574	Human		name
598237435	CV3962286	single nucleotide variant	NM_016248.4(AKAP11):c.1009A>G (p.Lys337Glu)	not specified [RCV005343643]	uncertain significance	13	42299755	42299755	Human		name
598237488	CV3962296	single nucleotide variant	NM_016248.4(AKAP11):c.1895A>G (p.Gln632Arg)	not specified [RCV005343653]	uncertain significance	13	42300641	42300641	Human		name
598237678	CV3962336	single nucleotide variant	NM_016248.4(AKAP11):c.1016C>T (p.Pro339Leu)	not specified [RCV005343685]	uncertain significance	13	42299762	42299762	Human		name
598237811	CV3962364	single nucleotide variant	NM_005100.4(AKAP12):c.1690G>A (p.Glu564Lys)	not specified [RCV005343709]	uncertain significance	6	151350081	151350081	Human		name
598237866	CV3962373	single nucleotide variant	NM_005100.4(AKAP12):c.1486G>A (p.Val496Ile)	not specified [RCV005343718]	likely benign	6	151349877	151349877	Human		name
598238002	CV3962393	single nucleotide variant	NM_005100.4(AKAP12):c.2839C>A (p.Pro947Thr)	not specified [RCV005343737]	likely benign	6	151351230	151351230	Human		name
598238144	CV3962414	single nucleotide variant	NM_005100.4(AKAP12):c.1117G>A (p.Glu373Lys)	not specified [RCV005343757]	uncertain significance	6	151349508	151349508	Human		name
598238410	CV3962464	single nucleotide variant	NM_005100.4(AKAP12):c.2920G>A (p.Glu974Lys)	not specified [RCV005343797]	uncertain significance	6	151351311	151351311	Human		name
15175992	CV699380	single nucleotide variant	NM_005100.4(AKAP12):c.1127A>C (p.Lys376Thr)	not provided [RCV000950720]	likely benign	6	151349518	151349518	Human		name
15100253	CV699381	single nucleotide variant	NM_005100.4(AKAP12):c.1839C>A (p.Phe613Leu)	not provided [RCV000958887]	likely benign	6	151350230	151350230	Human		name
15160634	CV702692	single nucleotide variant	NM_016248.4(AKAP11):c.1828C>T (p.Arg610Cys)	not provided [RCV000947523]	benign	13	42300574	42300574	Human		name
15171290	CV703386	single nucleotide variant	NM_007200.5(AKAP13):c.1000G>A (p.Glu334Lys)	not provided [RCV000949805]	benign	15	85579068	85579068	Human		name
15099060	CV703390	single nucleotide variant	NM_007200.5(AKAP13):c.2471A>T (p.Tyr824Phe)	not provided [RCV000958693]	likely benign	15	85580539	85580539	Human		name
15107387	CV713933	single nucleotide variant	NM_016248.4(AKAP11):c.2705A>G (p.Glu902Gly)	not provided [RCV000960280]	benign	13	42301451	42301451	Human		name
15102227	CV721802	single nucleotide variant	NM_005100.4(AKAP12):c.1130T>C (p.Val377Ala)	not provided [RCV000892438]	benign	6	151349521	151349521	Human		name
15156567	CV725490	single nucleotide variant	NM_016248.4(AKAP11):c.1808G>A (p.Arg603His)	not provided [RCV000880656]	benign	13	42300554	42300554	Human		name
15161379	CV726310	single nucleotide variant	NM_007200.5(AKAP13):c.1786A>G (p.Lys596Glu)	not provided [RCV000881561]	benign	15	85579854	85579854	Human		name
8627722	CV82866	single nucleotide variant	NM_006738.5(AKAP13):c.1103C>T (p.Ser368Phe)	Malignant melanoma [RCV000062946]	not provided	15	85579171	85579171	Human		name
8635048	CV90270	single nucleotide variant	NM_016248.3(AKAP11):c.1628C>T (p.Ser543Phe)	Malignant melanoma [RCV000070368]	not provided	13	42300374	42300374	Human		name
156231795	CV2199689	single nucleotide variant	NM_007200.5(AKAP13):c.3883G>A (p.Ala1295Thr)	not specified [RCV004072425]	uncertain significance	15	85581951	85581951	Human		name
155962027	CV2200843	single nucleotide variant	NM_007200.5(AKAP13):c.3459A>G (p.Ile1153Met)	not specified [RCV004081472]	uncertain significance	15	85581527	85581527	Human		name
156373736	CV2201361	single nucleotide variant	NM_007200.5(AKAP13):c.4162A>G (p.Ile1388Val)	not specified [RCV004077485]	uncertain significance	15	85639374	85639374	Human		name
155919566	CV2202661	single nucleotide variant	NM_016248.4(AKAP11):c.4917G>T (p.Gln1639His)	not specified [RCV004082911]	uncertain significance	13	42303663	42303663	Human		name
156248470	CV2203130	single nucleotide variant	NM_005100.4(AKAP12):c.3748G>A (p.Val1250Met)	not specified [RCV004069369]	uncertain significance	6	151352139	151352139	Human		name
156326023	CV2205530	single nucleotide variant	NM_016248.4(AKAP11):c.5159G>C (p.Ser1720Thr)	not specified [RCV004082461]	uncertain significance	13	42308495	42308495	Human		name
156090169	CV2206565	single nucleotide variant	NM_005100.4(AKAP12):c.3476C>T (p.Pro1159Leu)	not specified [RCV004080913]	uncertain significance	6	151351867	151351867	Human		name
156331078	CV2210766	single nucleotide variant	NM_016248.4(AKAP11):c.5252G>A (p.Ser1751Asn)	not specified [RCV004085861]	uncertain significance	13	42308588	42308588	Human		name
156033867	CV2211644	single nucleotide variant	NM_007200.5(AKAP13):c.7852C>T (p.Leu2618Phe)	not specified [RCV004084537]	uncertain significance	15	85741289	85741289	Human		name
156375112	CV2213499	single nucleotide variant	NM_005100.4(AKAP12):c.2998A>C (p.Thr1000Pro)	not specified [RCV004087465]	uncertain significance	6	151351389	151351389	Human		name
155977896	CV2214929	single nucleotide variant	NM_007200.5(AKAP13):c.5402G>A (p.Gly1801Asp)	not specified [RCV004084715]	uncertain significance	15	85693389	85693389	Human		name
156386900	CV2221349	single nucleotide variant	NM_005100.4(AKAP12):c.3170C>G (p.Pro1057Arg)	not specified [RCV004096657]	uncertain significance	6	151351561	151351561	Human		name
156342741	CV2222456	single nucleotide variant	NM_007200.5(AKAP13):c.5132A>G (p.Asn1711Ser)	not specified [RCV004099310]	uncertain significance	15	85682188	85682188	Human		name
156341198	CV2225782	single nucleotide variant	NM_007200.5(AKAP13):c.8314C>T (p.Arg2772Cys)	not specified [RCV004103191]	uncertain significance	15	85743747	85743747	Human		name
156386505	CV2228234	single nucleotide variant	NM_005100.4(AKAP12):c.4939G>C (p.Glu1647Gln)	not specified [RCV004097968]	uncertain significance	6	151353330	151353330	Human		name
156334312	CV2230907	single nucleotide variant	NM_005100.4(AKAP12):c.4813G>C (p.Ala1605Pro)	not specified [RCV004092379]	uncertain significance	6	151353204	151353204	Human		name
156334331	CV2230909	single nucleotide variant	NM_005100.4(AKAP12):c.4814C>T (p.Ala1605Val)	not specified [RCV004092381]	uncertain significance	6	151353205	151353205	Human		name
156062361	CV2231977	single nucleotide variant	NM_007200.5(AKAP13):c.6181A>G (p.Lys2061Glu)	not specified [RCV004093039]	likely benign	15	85719255	85719255	Human		name
155974675	CV2235752	single nucleotide variant	NM_007200.5(AKAP13):c.7342A>T (p.Ser2448Cys)	not specified [RCV004111886]	uncertain significance	15	85735051	85735051	Human		name
155976037	CV2235978	single nucleotide variant	NM_016248.4(AKAP11):c.4243A>G (p.Lys1415Glu)	not specified [RCV004113855]	uncertain significance	13	42302989	42302989	Human		name
156296328	CV2236509	single nucleotide variant	NM_016248.4(AKAP11):c.4424C>T (p.Ala1475Val)	not specified [RCV004110509]	uncertain significance	13	42303170	42303170	Human		name
156198349	CV2237421	single nucleotide variant	NM_016248.4(AKAP11):c.3494A>G (p.Lys1165Arg)	not specified [RCV004106389]	uncertain significance	13	42302240	42302240	Human		name
156044037	CV2237595	single nucleotide variant	NM_007200.5(AKAP13):c.7590G>C (p.Glu2530Asp)	not specified [RCV004106532]	uncertain significance	15	85740254	85740254	Human		name
155946353	CV2238108	single nucleotide variant	NM_007200.5(AKAP13):c.4196G>A (p.Cys1399Tyr)	not specified [RCV004111123]	uncertain significance	15	85639408	85639408	Human		name
155981328	CV2244064	single nucleotide variant	NM_016248.4(AKAP11):c.3861G>C (p.Lys1287Asn)	not specified [RCV004108543]	uncertain significance	13	42302607	42302607	Human		name
156234242	CV2245326	single nucleotide variant	NM_007200.5(AKAP13):c.3154G>T (p.Asp1052Tyr)	not specified [RCV004107078]	uncertain significance	15	85581222	85581222	Human		name
156079131	CV2248539	single nucleotide variant	NM_005100.4(AKAP12):c.5105A>G (p.Asp1702Gly)	not specified [RCV004119664]	uncertain significance	6	151353496	151353496	Human		name
156298929	CV2248570	single nucleotide variant	NM_007200.5(AKAP13):c.4020G>C (p.Gln1340His)	not specified [RCV004121765]	uncertain significance	15	85582088	85582088	Human		name
156206142	CV2249932	single nucleotide variant	NM_007200.5(AKAP13):c.7349C>G (p.Pro2450Arg)	not specified [RCV004122904]	uncertain significance	15	85735058	85735058	Human		name
156091893	CV2256624	single nucleotide variant	NM_016248.4(AKAP11):c.5251A>G (p.Ser1751Gly)	not specified [RCV004118809]	uncertain significance	13	42308587	42308587	Human		name
156235705	CV2268017	single nucleotide variant	NM_007200.5(AKAP13):c.6335A>G (p.Lys2112Arg)	not specified [RCV004136573]	uncertain significance	15	85722073	85722073	Human		name
156367201	CV2269838	single nucleotide variant	NM_007200.5(AKAP13):c.3648G>T (p.Met1216Ile)	not specified [RCV004127073]	uncertain significance	15	85581716	85581716	Human		name
155917593	CV2274945	single nucleotide variant	NM_016248.4(AKAP11):c.4666C>G (p.Leu1556Val)	not specified [RCV004134999]	uncertain significance	13	42303412	42303412	Human		name
156120256	CV2275910	single nucleotide variant	NM_007200.5(AKAP13):c.4928T>C (p.Leu1643Ser)	not specified [RCV004139567]	uncertain significance	15	85664691	85664691	Human		name
155918788	CV2279293	single nucleotide variant	NM_007200.5(AKAP13):c.8168C>T (p.Ser2723Leu)	not specified [RCV004139812]	uncertain significance	15	85743601	85743601	Human		name
155918257	CV2283512	single nucleotide variant	NM_005100.4(AKAP12):c.3242C>A (p.Ala1081Asp)	not specified [RCV004139727]	uncertain significance	6	151351633	151351633	Human		name
155965834	CV2284080	single nucleotide variant	NM_016248.4(AKAP11):c.4837G>C (p.Ala1613Pro)	not specified [RCV004144682]	uncertain significance	13	42303583	42303583	Human		name
156278348	CV2286773	single nucleotide variant	NM_007200.5(AKAP13):c.7168A>G (p.Ser2390Gly)	not specified [RCV004142583]	uncertain significance	15	85730593	85730593	Human		name
155965089	CV2286864	single nucleotide variant	NM_007200.5(AKAP13):c.7954G>C (p.Glu2652Gln)	not specified [RCV004142663]	uncertain significance	15	85741391	85741391	Human		name
156189162	CV2289158	single nucleotide variant	NM_005100.4(AKAP12):c.4687C>T (p.Arg1563Cys)	not specified [RCV004150378]	uncertain significance	6	151353078	151353078	Human		name
156015934	CV2299016	single nucleotide variant	NM_007200.5(AKAP13):c.4251C>G (p.Phe1417Leu)	not specified [RCV004158537]	uncertain significance	15	85645831	85645831	Human		name
156079673	CV2300940	single nucleotide variant	NM_005100.4(AKAP12):c.3740A>G (p.Asp1247Gly)	not specified [RCV004158126]	uncertain significance	6	151352131	151352131	Human		name
156191791	CV2301838	single nucleotide variant	NM_007200.5(AKAP13):c.4261G>C (p.Gly1421Arg)	not specified [RCV004156634]	uncertain significance	15	85645841	85645841	Human		name
156269647	CV2305905	single nucleotide variant	NM_007200.5(AKAP13):c.3031G>C (p.Gly1011Arg)	not specified [RCV004167692]	uncertain significance	15	85581099	85581099	Human		name
156209874	CV2309571	single nucleotide variant	NM_007200.5(AKAP13):c.4649T>G (p.Val1550Gly)	not specified [RCV004158951]	uncertain significance	15	85655691	85655691	Human		name
156210620	CV2309784	single nucleotide variant	NM_007200.5(AKAP13):c.4522C>G (p.Leu1508Val)	not specified [RCV004160905]	uncertain significance	15	85655564	85655564	Human		name
155967645	CV2312749	single nucleotide variant	NM_007200.5(AKAP13):c.7893G>C (p.Gln2631His)	not specified [RCV004169470]	uncertain significance	15	85741330	85741330	Human		name
156348409	CV2312781	single nucleotide variant	NM_007200.5(AKAP13):c.3056C>T (p.Pro1019Leu)	not specified [RCV004169495]	uncertain significance	15	85581124	85581124	Human		name
156102968	CV2313657	single nucleotide variant	NM_007200.5(AKAP13):c.4313G>A (p.Gly1438Glu)	not specified [RCV004157588]	uncertain significance	15	85645893	85645893	Human		name
156186978	CV2324766	single nucleotide variant	NM_005100.4(AKAP12):c.4768G>T (p.Ala1590Ser)	not specified [RCV004173001]	uncertain significance	6	151353159	151353159	Human		name
156286430	CV2327236	single nucleotide variant	NM_007200.5(AKAP13):c.8087G>C (p.Arg2696Thr)	not specified [RCV004174693]	uncertain significance	15	85743520	85743520	Human		name
156288001	CV2327373	single nucleotide variant	NM_007200.5(AKAP13):c.4900T>C (p.Phe1634Leu)	not specified [RCV004174802]	uncertain significance	15	85664663	85664663	Human		name
156155625	CV2328798	single nucleotide variant	NM_007200.5(AKAP13):c.6703G>C (p.Asp2235His)	not specified [RCV004178023]	uncertain significance	15	85723278	85723278	Human		name
156053666	CV2329108	single nucleotide variant	NM_007200.5(AKAP13):c.7085A>C (p.Lys2362Thr)	not specified [RCV004173872]	uncertain significance	15	85727461	85727461	Human		name
156329006	CV2332338	single nucleotide variant	NM_005100.4(AKAP12):c.4383T>G (p.Asn1461Lys)	not specified [RCV004182504]	uncertain significance	6	151352774	151352774	Human		name
156332259	CV2339754	single nucleotide variant	NM_007200.5(AKAP13):c.7375G>A (p.Val2459Ile)	not specified [RCV004196453]	uncertain significance	15	85735084	85735084	Human		name
156041718	CV2342167	single nucleotide variant	NM_007200.5(AKAP13):c.4219G>A (p.Ala1407Thr)	not specified [RCV004191755]	uncertain significance	15	85639431	85639431	Human		name
156057489	CV2343550	single nucleotide variant	NM_007200.5(AKAP13):c.3827G>A (p.Cys1276Tyr)	not specified [RCV004190584]	uncertain significance	15	85581895	85581895	Human		name
156066640	CV2346843	single nucleotide variant	NM_005100.4(AKAP12):c.4637G>C (p.Ser1546Thr)	not specified [RCV004199842]	uncertain significance	6	151353028	151353028	Human		name
156281287	CV2348533	single nucleotide variant	NM_016248.4(AKAP11):c.3784G>T (p.Asp1262Tyr)	not specified [RCV004193716]	uncertain significance	13	42302530	42302530	Human		name
155987932	CV2354990	single nucleotide variant	NM_007200.5(AKAP13):c.7393G>A (p.Ala2465Thr)	not specified [RCV004198391]	uncertain significance	15	85735102	85735102	Human		name
156173361	CV2355168	single nucleotide variant	NM_007200.5(AKAP13):c.6557G>C (p.Gly2186Ala)	not specified [RCV004198554]	uncertain significance	15	85723132	85723132	Human		name
156224544	CV2355667	single nucleotide variant	NM_007200.5(AKAP13):c.4723G>A (p.Asp1575Asn)	not specified [RCV004198623]	uncertain significance	15	85655765	85655765	Human		name
156147986	CV2358052	single nucleotide variant	NM_005100.4(AKAP12):c.5005G>A (p.Gly1669Arg)	not specified [RCV004209819]	uncertain significance	6	151353396	151353396	Human		name
155924678	CV2358191	single nucleotide variant	NM_016248.4(AKAP11):c.3582G>T (p.Lys1194Asn)	not specified [RCV004211991]	uncertain significance	13	42302328	42302328	Human		name
156142744	CV2358519	single nucleotide variant	NM_016248.4(AKAP11):c.5462C>T (p.Thr1821Met)	not specified [RCV004207403]	uncertain significance	13	42317585	42317585	Human		name
156150452	CV2359612	single nucleotide variant	NM_007200.5(AKAP13):c.6520C>G (p.Leu2174Val)	not specified [RCV004214908]	uncertain significance	15	85723095	85723095	Human		name
156285128	CV2360752	single nucleotide variant	NM_005100.4(AKAP12):c.3269C>T (p.Thr1090Met)	not specified [RCV004213535]	likely benign	6	151351660	151351660	Human		name
155930651	CV2361207	single nucleotide variant	NM_016248.4(AKAP11):c.4535A>G (p.Gln1512Arg)	not specified [RCV004216386]	uncertain significance	13	42303281	42303281	Human		name
156197883	CV2362739	single nucleotide variant	NM_007200.5(AKAP13):c.6359G>A (p.Arg2120His)	not specified [RCV004208857]	uncertain significance	15	85722097	85722097	Human		name
155928395	CV2363275	single nucleotide variant	NM_007200.5(AKAP13):c.4279A>G (p.Thr1427Ala)	not specified [RCV004213830]	likely benign	15	85645859	85645859	Human		name
155986991	CV2363746	single nucleotide variant	NM_005100.4(AKAP12):c.4160A>T (p.Lys1387Met)	not specified [RCV004218733]	uncertain significance	6	151352551	151352551	Human		name
156198984	CV2365221	single nucleotide variant	NM_007200.5(AKAP13):c.7422T>G (p.His2474Gln)	not specified [RCV004209327]	uncertain significance	15	85735131	85735131	Human		name
156268311	CV2372001	single nucleotide variant	NM_007200.5(AKAP13):c.6685C>T (p.Arg2229Trp)	not specified [RCV004221676]	uncertain significance	15	85723260	85723260	Human		name
156387136	CV2372650	single nucleotide variant	NM_016248.4(AKAP11):c.3998A>G (p.Tyr1333Cys)	not specified [RCV004221852]	uncertain significance	13	42302744	42302744	Human		name
156184646	CV2377753	single nucleotide variant	NM_007200.5(AKAP13):c.4325A>T (p.Asp1442Val)	not specified [RCV004230336]	uncertain significance	15	85645905	85645905	Human		name
155992470	CV2381497	single nucleotide variant	NM_016248.4(AKAP11):c.4713C>A (p.Asp1571Glu)	not specified [RCV004229975]	uncertain significance	13	42303459	42303459	Human		name
156143552	CV2383865	single nucleotide variant	NM_007200.5(AKAP13):c.5623C>T (p.Arg1875Trp)	not specified [RCV004231726]	uncertain significance	15	85715811	85715811	Human		name
156206644	CV2385348	single nucleotide variant	NM_016248.4(AKAP11):c.3916A>G (p.Ile1306Val)	not specified [RCV004230621]	likely benign	13	42302662	42302662	Human		name
155902514	CV2386244	single nucleotide variant	NM_007200.5(AKAP13):c.3040G>T (p.Ala1014Ser)	not specified [RCV004228598]	uncertain significance	15	85581108	85581108	Human		name
156252781	CV2390081	single nucleotide variant	NM_007200.5(AKAP13):c.8143A>G (p.Ile2715Val)	not specified [RCV004238683]	likely benign	15	85743576	85743576	Human		name
156199276	CV2392242	single nucleotide variant	NM_016248.4(AKAP11):c.5032G>A (p.Gly1678Arg)	not specified [RCV004243853]	uncertain significance	13	42303778	42303778	Human		name
155905856	CV2393808	single nucleotide variant	NM_007200.5(AKAP13):c.6701G>A (p.Arg2234His)	not specified [RCV004233639]	uncertain significance	15	85723276	85723276	Human		name
156004755	CV2396983	single nucleotide variant	NM_007200.5(AKAP13):c.3956C>T (p.Thr1319Met)	not specified [RCV004234091]	uncertain significance	15	85582024	85582024	Human		name
155933345	CV2399305	single nucleotide variant	NM_016248.4(AKAP11):c.3632C>G (p.Thr1211Ser)	not specified [RCV004242597]	uncertain significance	13	42302378	42302378	Human		name
156006594	CV2401214	single nucleotide variant	NM_016248.4(AKAP11):c.3307T>A (p.Ser1103Thr)	not specified [RCV004245768]	uncertain significance	13	42302053	42302053	Human		name
329367267	CV2427327	single nucleotide variant	NM_005100.4(AKAP12):c.3388A>G (p.Ile1130Val)	not specified [RCV004248187]	likely benign	6	151351779	151351779	Human		name
329357048	CV2431231	single nucleotide variant	NM_007200.5(AKAP13):c.3466G>A (p.Asp1156Asn)	not specified [RCV004250570]	uncertain significance	15	85581534	85581534	Human		name
329371581	CV2432019	single nucleotide variant	NM_016248.4(AKAP11):c.4185G>A (p.Met1395Ile)	not specified [RCV004249171]	uncertain significance	13	42302931	42302931	Human		name
329385467	CV2432157	single nucleotide variant	NM_007200.5(AKAP13):c.3686C>G (p.Ser1229Cys)	not specified [RCV004249303]	uncertain significance	15	85581754	85581754	Human		name
329374058	CV2434683	single nucleotide variant	NM_016248.4(AKAP11):c.3323C>T (p.Pro1108Leu)	not specified [RCV004248400]	uncertain significance	13	42302069	42302069	Human		name
329359386	CV2436136	single nucleotide variant	NM_016248.4(AKAP11):c.5020G>A (p.Asp1674Asn)	not specified [RCV004249379]	uncertain significance	13	42303766	42303766	Human		name
329361630	CV2437713	single nucleotide variant	NM_007200.5(AKAP13):c.8019G>C (p.Glu2673Asp)	not specified [RCV004261024]	uncertain significance	15	85741456	85741456	Human		name
329365782	CV2441059	single nucleotide variant	NM_007200.5(AKAP13):c.4192C>T (p.Pro1398Ser)	not specified [RCV004261426]	uncertain significance	15	85639404	85639404	Human		name
329389122	CV2448738	single nucleotide variant	NM_007200.5(AKAP13):c.3533A>G (p.Gln1178Arg)	not specified [RCV004259392]	uncertain significance	15	85581601	85581601	Human		name
329359204	CV2450920	single nucleotide variant	NM_005100.4(AKAP12):c.4403C>G (p.Pro1468Arg)	not specified [RCV004267818]	uncertain significance	6	151352794	151352794	Human		name
329402707	CV2451257	single nucleotide variant	NM_016248.4(AKAP11):c.4090A>G (p.Met1364Val)	not specified [RCV004270168]	uncertain significance	13	42302836	42302836	Human		name
329384729	CV2458449	single nucleotide variant	NM_007200.5(AKAP13):c.7001C>T (p.Thr2334Ile)	not specified [RCV004266075]	uncertain significance	15	85727244	85727244	Human		name
329360468	CV2458766	single nucleotide variant	NM_007200.5(AKAP13):c.4639A>G (p.Asn1547Asp)	not specified [RCV004270200]	uncertain significance	15	85655681	85655681	Human		name
329378861	CV2460003	single nucleotide variant	NM_007200.5(AKAP13):c.4471G>A (p.Val1491Met)	not specified [RCV004279478]	uncertain significance	15	85655513	85655513	Human		name
329374177	CV2463417	single nucleotide variant	NM_016248.4(AKAP11):c.4175A>G (p.Asn1392Ser)	not specified [RCV004277252]	likely benign	13	42302921	42302921	Human		name
329398065	CV2464745	single nucleotide variant	NM_016248.4(AKAP11):c.4922A>T (p.His1641Leu)	not specified [RCV004284710]	uncertain significance	13	42303668	42303668	Human		name
329397494	CV2466253	single nucleotide variant	NM_007200.5(AKAP13):c.6950C>A (p.Ser2317Tyr)	not specified [RCV004279879]	uncertain significance	15	85727193	85727193	Human		name
329352880	CV2470595	single nucleotide variant	NM_005100.4(AKAP12):c.3277G>A (p.Val1093Met)	not specified [RCV004273593]	uncertain significance	6	151351668	151351668	Human		name
401726388	CV2674123	single nucleotide variant	NM_007200.5(AKAP13):c.5080A>G (p.Ile1694Val)	not specified [RCV004295529]	uncertain significance	15	85669809	85669809	Human		name
401732627	CV2675142	single nucleotide variant	NM_007200.5(AKAP13):c.4562G>A (p.Arg1521Gln)	not specified [RCV004289921]	uncertain significance	15	85655604	85655604	Human		name
401755932	CV2675600	single nucleotide variant	NM_007200.5(AKAP13):c.8296T>G (p.Ser2766Ala)	not specified [RCV004297260]	uncertain significance	15	85743729	85743729	Human		name
401781553	CV2682037	single nucleotide variant	NM_007200.5(AKAP13):c.8204C>T (p.Ser2735Phe)	not specified [RCV004290104]	uncertain significance	15	85743637	85743637	Human		name
401752169	CV2682727	single nucleotide variant	NM_016248.4(AKAP11):c.4432G>A (p.Val1478Ile)	not specified [RCV004281706]	uncertain significance	13	42303178	42303178	Human		name
401782543	CV2686915	single nucleotide variant	NM_007200.5(AKAP13):c.4514G>A (p.Arg1505Gln)	not specified [RCV004302086]	likely benign	15	85655556	85655556	Human		name
401744076	CV2688091	single nucleotide variant	NM_005100.4(AKAP12):c.3605C>G (p.Ser1202Cys)	not specified [RCV004305151]	uncertain significance	6	151351996	151351996	Human		name
401750518	CV2689438	single nucleotide variant	NM_007200.5(AKAP13):c.8085G>A (p.Met2695Ile)	not specified [RCV004306243]	uncertain significance	15	85743518	85743518	Human		name
401733217	CV2691237	single nucleotide variant	NM_016248.4(AKAP11):c.4525A>C (p.Lys1509Gln)	not specified [RCV004303004]	uncertain significance	13	42303271	42303271	Human		name
401764161	CV2700510	single nucleotide variant	NM_007200.5(AKAP13):c.5024A>G (p.Asn1675Ser)	not specified [RCV004311136]	uncertain significance	15	85669753	85669753	Human		name
401719557	CV2701174	single nucleotide variant	NM_007200.5(AKAP13):c.5767T>C (p.Trp1923Arg)	not specified [RCV004309754]	uncertain significance	15	85717321	85717321	Human		name
401735080	CV2706656	single nucleotide variant	NM_016248.4(AKAP11):c.5363G>C (p.Gly1788Ala)	not specified [RCV004319233]	uncertain significance	13	42313899	42313899	Human		name
401772733	CV2712880	single nucleotide variant	NM_007200.5(AKAP13):c.5579C>A (p.Thr1860Lys)	not specified [RCV004314289]	uncertain significance	15	85710625	85710625	Human		name
401762485	CV2714159	single nucleotide variant	NM_016248.4(AKAP11):c.4951G>T (p.Ala1651Ser)	not specified [RCV004317408]	uncertain significance	13	42303697	42303697	Human		name
401762488	CV2714161	single nucleotide variant	NM_016248.4(AKAP11):c.4952C>G (p.Ala1651Gly)	not specified [RCV004317409]	uncertain significance	13	42303698	42303698	Human		name
401770227	CV2715088	single nucleotide variant	NM_007200.5(AKAP13):c.7073C>G (p.Ala2358Gly)	not specified [RCV004322673]	uncertain significance	15	85727449	85727449	Human		name
401782888	CV2716028	single nucleotide variant	NM_007200.5(AKAP13):c.6598C>T (p.Arg2200Cys)	not specified [RCV004323283]	uncertain significance	15	85723173	85723173	Human		name
401737320	CV2718070	single nucleotide variant	NM_005100.4(AKAP12):c.4633A>C (p.Lys1545Gln)	not specified [RCV004315791]	uncertain significance	6	151353024	151353024	Human		name
401770999	CV2726328	single nucleotide variant	NM_016248.4(AKAP11):c.3499A>T (p.Met1167Leu)	not specified [RCV004326768]	uncertain significance	13	42302245	42302245	Human		name
401767631	CV2727226	single nucleotide variant	NM_016248.4(AKAP11):c.4007C>T (p.Pro1336Leu)	not specified [RCV004327354]	uncertain significance	13	42302753	42302753	Human		name
401769025	CV2729454	single nucleotide variant	NM_007200.5(AKAP13):c.7672C>T (p.Leu2558Phe)	not specified [RCV004332753]	uncertain significance	15	85741109	85741109	Human		name
401756710	CV2732052	single nucleotide variant	NM_016248.4(AKAP11):c.4604A>G (p.Asn1535Ser)	not specified [RCV004330670]	uncertain significance	13	42303350	42303350	Human		name
401768711	CV2735401	single nucleotide variant	NM_007200.5(AKAP13):c.3275C>T (p.Thr1092Ile)	not specified [RCV004334053]	uncertain significance	15	85581343	85581343	Human		name
401861721	CV2756449	single nucleotide variant	NM_005100.4(AKAP12):c.3011C>T (p.Ser1004Leu)	not specified [RCV004342984]	uncertain significance	6	151351402	151351402	Human		name
401860818	CV2758645	single nucleotide variant	NM_007200.5(AKAP13):c.7388G>A (p.Arg2463Gln)	not specified [RCV004337719]	uncertain significance	15	85735097	85735097	Human		name
401873195	CV2761390	single nucleotide variant	NM_007200.5(AKAP13):c.6988G>C (p.Asp2330His)	not specified [RCV004334569]	uncertain significance	15	85727231	85727231	Human		name
401877011	CV2767795	single nucleotide variant	NM_016248.4(AKAP11):c.5311G>A (p.Glu1771Lys)	not specified [RCV004345917]	uncertain significance	13	42313084	42313084	Human		name
401862575	CV2768456	single nucleotide variant	NM_016248.4(AKAP11):c.5213A>G (p.Asn1738Ser)	not specified [RCV004344344]	uncertain significance	13	42308549	42308549	Human		name
401859015	CV2775048	single nucleotide variant	NM_007200.5(AKAP13):c.3053T>A (p.Val1018Glu)	not specified [RCV004346427]	uncertain significance	15	85581121	85581121	Human		name
401879083	CV2778142	single nucleotide variant	NM_007200.5(AKAP13):c.4022G>A (p.Gly1341Glu)	not specified [RCV004348080]	uncertain significance	15	85582090	85582090	Human		name
401861457	CV2779758	single nucleotide variant	NM_016248.4(AKAP11):c.5371G>T (p.Asp1791Tyr)	not specified [RCV004353395]	uncertain significance	13	42313907	42313907	Human		name
401892563	CV2782210	single nucleotide variant	NM_007200.5(AKAP13):c.5884G>A (p.Gly1962Arg)	not specified [RCV004359184]	uncertain significance	15	85718042	85718042	Human		name
401880369	CV2783186	single nucleotide variant	NM_005100.4(AKAP12):c.3869C>T (p.Thr1290Ile)	not specified [RCV004363528]	uncertain significance	6	151352260	151352260	Human		name
401898571	CV2784666	single nucleotide variant	NM_007200.5(AKAP13):c.4465A>G (p.Ser1489Gly)	not specified [RCV004352486]	uncertain significance	15	85655507	85655507	Human		name
401881410	CV2784683	single nucleotide variant	NM_007200.5(AKAP13):c.4549G>A (p.Gly1517Arg)	not specified [RCV004352499]	uncertain significance	15	85655591	85655591	Human		name
401865440	CV2788056	single nucleotide variant	NM_005100.4(AKAP12):c.4307A>C (p.Asn1436Thr)	not specified [RCV004359002]	uncertain significance	6	151352698	151352698	Human		name
401882751	CV2788575	single nucleotide variant	NM_007200.5(AKAP13):c.5563A>G (p.Thr1855Ala)	not specified [RCV004361073]	uncertain significance	15	85710609	85710609	Human		name
401870669	CV2792468	single nucleotide variant	NM_007200.5(AKAP13):c.3761G>C (p.Arg1254Pro)	not specified [RCV004363210]	uncertain significance	15	85581829	85581829	Human		name
401916479	CV2814443	single nucleotide variant	NM_007200.5(AKAP13):c.7588G>A (p.Glu2530Lys)	not provided [RCV003401004]	likely benign	15	85740252	85740252	Human		name
401920960	CV2820786	single nucleotide variant	NM_005100.4(AKAP12):c.3887G>T (p.Arg1296Leu)	not provided [RCV003432096]	likely benign	6	151352278	151352278	Human		name
405796622	CV3262788	single nucleotide variant	NM_016248.4(AKAP11):c.3442A>G (p.Ser1148Gly)	not specified [RCV004401615]	uncertain significance	13	42302188	42302188	Human		name
405796668	CV3262804	single nucleotide variant	NM_016248.4(AKAP11):c.3841A>G (p.Met1281Val)	not specified [RCV004401631]	likely benign	13	42302587	42302587	Human		name
405796675	CV3262806	single nucleotide variant	NM_016248.4(AKAP11):c.3851A>T (p.Lys1284Met)	not specified [RCV004401633]	uncertain significance	13	42302597	42302597	Human		name
405796748	CV3262831	single nucleotide variant	NM_016248.4(AKAP11):c.4190C>T (p.Pro1397Leu)	not specified [RCV004401658]	uncertain significance	13	42302936	42302936	Human		name
405796816	CV3262852	single nucleotide variant	NM_016248.4(AKAP11):c.4638A>T (p.Lys1546Asn)	not specified [RCV004401679]	uncertain significance	13	42303384	42303384	Human		name
405796933	CV3262892	single nucleotide variant	NM_016248.4(AKAP11):c.5293T>C (p.Trp1765Arg)	not specified [RCV004401719]	uncertain significance	13	42313066	42313066	Human		name
405802438	CV3263103	single nucleotide variant	NM_005100.4(AKAP12):c.3622G>A (p.Gly1208Ser)	not specified [RCV004403913]	uncertain significance	6	151352013	151352013	Human		name
405802444	CV3263106	single nucleotide variant	NM_005100.4(AKAP12):c.3659G>A (p.Arg1220Lys)	not specified [RCV004403916]	uncertain significance	6	151352050	151352050	Human		name
405802459	CV3263114	single nucleotide variant	NM_005100.4(AKAP12):c.3763G>A (p.Val1255Ile)	not specified [RCV004403924]	uncertain significance	6	151352154	151352154	Human		name
405802464	CV3263117	single nucleotide variant	NM_005100.4(AKAP12):c.3818A>C (p.Glu1273Ala)	not specified [RCV004403927]	uncertain significance	6	151352209	151352209	Human		name
405802472	CV3263121	single nucleotide variant	NM_005100.4(AKAP12):c.3865G>A (p.Asp1289Asn)	not specified [RCV004403931]	uncertain significance	6	151352256	151352256	Human		name
405802484	CV3263128	single nucleotide variant	NM_005100.4(AKAP12):c.3880G>C (p.Val1294Leu)	not specified [RCV004403938]	uncertain significance	6	151352271	151352271	Human		name
405802487	CV3263130	single nucleotide variant	NM_005100.4(AKAP12):c.4051A>G (p.Thr1351Ala)	not specified [RCV004403940]	uncertain significance	6	151352442	151352442	Human		name
405802523	CV3263150	single nucleotide variant	NM_005100.4(AKAP12):c.4459A>G (p.Ile1487Val)	not specified [RCV004403960]	uncertain significance	6	151352850	151352850	Human		name
405802554	CV3263167	single nucleotide variant	NM_005100.4(AKAP12):c.4731G>C (p.Gln1577His)	not specified [RCV004403977]	uncertain significance	6	151353122	151353122	Human		name
405802576	CV3263179	single nucleotide variant	NM_005100.4(AKAP12):c.4829C>T (p.Pro1610Leu)	not specified [RCV004403989]	uncertain significance	6	151353220	151353220	Human		name
405802617	CV3263201	single nucleotide variant	NM_005100.4(AKAP12):c.5023G>A (p.Val1675Met)	not specified [RCV004404011]	uncertain significance	6	151353414	151353414	Human		name
405802639	CV3263213	single nucleotide variant	NM_005100.4(AKAP12):c.5275A>T (p.Ile1759Phe)	not specified [RCV004404023]	uncertain significance	6	151353666	151353666	Human		name
405777351	CV3270028	single nucleotide variant	NM_007200.5(AKAP13):c.7190G>C (p.Cys2397Ser)	not specified [RCV004396945]	uncertain significance	15	85730615	85730615	Human		name
405777271	CV3270040	single nucleotide variant	NM_007200.5(AKAP13):c.7379C>T (p.Ser2460Phe)	not specified [RCV004396957]	uncertain significance	15	85735088	85735088	Human		name
405777085	CV3270060	single nucleotide variant	NM_007200.5(AKAP13):c.7573G>A (p.Val2525Ile)	not specified [RCV004396977]	likely benign	15	85740237	85740237	Human		name
405777155	CV3270071	single nucleotide variant	NM_007200.5(AKAP13):c.7696A>G (p.Ser2566Gly)	not specified [RCV004396988]	uncertain significance	15	85741133	85741133	Human		name
405777192	CV3270077	single nucleotide variant	NM_007200.5(AKAP13):c.7844G>T (p.Arg2615Leu)	not specified [RCV004396994]	uncertain significance	15	85741281	85741281	Human		name
405777401	CV3270087	single nucleotide variant	NM_007200.5(AKAP13):c.8009G>A (p.Arg2670Gln)	not specified [RCV004397004]	uncertain significance	15	85741446	85741446	Human		name
405777472	CV3270099	single nucleotide variant	NM_007200.5(AKAP13):c.8137C>A (p.Pro2713Thr)	not specified [RCV004397016]	uncertain significance	15	85743570	85743570	Human		name
405777484	CV3270101	single nucleotide variant	NM_007200.5(AKAP13):c.8138C>G (p.Pro2713Arg)	not specified [RCV004397018]	uncertain significance	15	85743571	85743571	Human		name
405777527	CV3270108	single nucleotide variant	NM_007200.5(AKAP13):c.8144T>C (p.Ile2715Thr)	not specified [RCV004397025]	uncertain significance	15	85743577	85743577	Human		name
405777644	CV3270128	single nucleotide variant	NM_007200.5(AKAP13):c.8372C>T (p.Thr2791Ile)	not specified [RCV004397045]	uncertain significance	15	85743805	85743805	Human		name
405802934	CV3273683	single nucleotide variant	NM_007200.5(AKAP13):c.3048C>A (p.Ser1016Arg)	not specified [RCV004404179]	uncertain significance	15	85581116	85581116	Human		name
405802960	CV3273697	single nucleotide variant	NM_007200.5(AKAP13):c.3505T>C (p.Cys1169Arg)	not specified [RCV004404193]	uncertain significance	15	85581573	85581573	Human		name
405802969	CV3273702	single nucleotide variant	NM_007200.5(AKAP13):c.3542A>G (p.Asp1181Gly)	not specified [RCV004404198]	uncertain significance	15	85581610	85581610	Human		name
405802981	CV3273708	single nucleotide variant	NM_007200.5(AKAP13):c.3656C>T (p.Pro1219Leu)	not specified [RCV004404204]	likely benign	15	85581724	85581724	Human		name
405802991	CV3273713	single nucleotide variant	NM_007200.5(AKAP13):c.3823G>A (p.Ala1275Thr)	not specified [RCV004404209]	uncertain significance	15	85581891	85581891	Human		name
405802997	CV3273716	single nucleotide variant	NM_007200.5(AKAP13):c.3881G>A (p.Ser1294Asn)	not specified [RCV004404212]	likely benign	15	85581949	85581949	Human		name
405803017	CV3273726	single nucleotide variant	NM_007200.5(AKAP13):c.3905C>T (p.Thr1302Ile)	not specified [RCV004404222]	uncertain significance	15	85581973	85581973	Human		name
405803032	CV3273734	single nucleotide variant	NM_007200.5(AKAP13):c.4160C>T (p.Ala1387Val)	not specified [RCV004404230]	uncertain significance	15	85585822	85585822	Human		name
405803076	CV3273756	single nucleotide variant	NM_007200.5(AKAP13):c.4340C>G (p.Pro1447Arg)	not specified [RCV004404252]	uncertain significance	15	85645920	85645920	Human		name
405803102	CV3273770	single nucleotide variant	NM_007200.5(AKAP13):c.4485G>C (p.Gln1495His)	not specified [RCV004404266]	uncertain significance	15	85655527	85655527	Human		name
405803113	CV3273776	single nucleotide variant	NM_007200.5(AKAP13):c.4519A>T (p.Ser1507Cys)	not specified [RCV004404272]	likely benign	15	85655561	85655561	Human		name
405803156	CV3273799	single nucleotide variant	NM_007200.5(AKAP13):c.4750A>T (p.Met1584Leu)	not specified [RCV004404295]	uncertain significance	15	85658541	85658541	Human		name
405803163	CV3273803	single nucleotide variant	NM_007200.5(AKAP13):c.4763G>A (p.Gly1588Glu)	not specified [RCV004404299]	uncertain significance	15	85658554	85658554	Human		name
405803171	CV3273807	single nucleotide variant	NM_007200.5(AKAP13):c.4766A>T (p.Asp1589Val)	not specified [RCV004404303]	uncertain significance	15	85658557	85658557	Human		name
405803201	CV3273823	single nucleotide variant	NM_007200.5(AKAP13):c.4956G>T (p.Glu1652Asp)	not specified [RCV004404319]	uncertain significance	15	85664719	85664719	Human		name
405803231	CV3273839	single nucleotide variant	NM_007200.5(AKAP13):c.5189A>G (p.His1730Arg)	not specified [RCV004404335]	uncertain significance	15	85684773	85684773	Human		name
405803240	CV3273844	single nucleotide variant	NM_007200.5(AKAP13):c.5219A>G (p.Lys1740Arg)	not specified [RCV004404340]	uncertain significance	15	85684803	85684803	Human		name
405803252	CV3273850	single nucleotide variant	NM_007200.5(AKAP13):c.5411G>C (p.Ser1804Thr)	not specified [RCV004404346]	uncertain significance	15	85693398	85693398	Human		name
405803282	CV3273866	single nucleotide variant	NM_007200.5(AKAP13):c.5705C>G (p.Ser1902Cys)	not specified [RCV004404362]	uncertain significance	15	85715893	85715893	Human		name
405803304	CV3273877	single nucleotide variant	NM_007200.5(AKAP13):c.5983C>T (p.Arg1995Trp)	not specified [RCV004404373]	uncertain significance	15	85718141	85718141	Human		name
405803308	CV3273879	single nucleotide variant	NM_007200.5(AKAP13):c.6127G>A (p.Asp2043Asn)	not specified [RCV004404375]	uncertain significance	15	85719201	85719201	Human		name
405803327	CV3273889	single nucleotide variant	NM_007200.5(AKAP13):c.6227G>A (p.Arg2076Lys)	not specified [RCV004404385]	uncertain significance	15	85719301	85719301	Human		name
405776771	CV3273927	single nucleotide variant	NM_007200.5(AKAP13):c.6536G>A (p.Ser2179Asn)	not specified [RCV004396902]	uncertain significance	15	85723111	85723111	Human		name
405776820	CV3273935	single nucleotide variant	NM_007200.5(AKAP13):c.6595G>A (p.Val2199Met)	not specified [RCV004396910]	uncertain significance	15	85723170	85723170	Human		name
407486600	CV3436173	single nucleotide variant	NM_005100.4(AKAP12):c.5078T>C (p.Val1693Ala)	not specified [RCV004619146]	uncertain significance	6	151353469	151353469	Human		name
407486699	CV3436191	single nucleotide variant	NM_005100.4(AKAP12):c.4966C>G (p.Leu1656Val)	not specified [RCV004619164]	uncertain significance	6	151353357	151353357	Human		name
407486882	CV3436199	single nucleotide variant	NM_005100.4(AKAP12):c.3475C>T (p.Pro1159Ser)	not specified [RCV004619172]	uncertain significance	6	151351866	151351866	Human		name
407486950	CV3436210	single nucleotide variant	NM_007200.5(AKAP13):c.8117A>G (p.Glu2706Gly)	not specified [RCV004619183]	uncertain significance	15	85743550	85743550	Human		name
407503188	CV3436216	single nucleotide variant	NM_007200.5(AKAP13):c.7874A>T (p.Glu2625Val)	not specified [RCV004623689]	uncertain significance	15	85741311	85741311	Human		name
407503192	CV3436217	single nucleotide variant	NM_007200.5(AKAP13):c.7652T>C (p.Leu2551Pro)	not specified [RCV004623690]	uncertain significance	15	85741089	85741089	Human		name
407503195	CV3436218	single nucleotide variant	NM_007200.5(AKAP13):c.3385G>A (p.Val1129Ile)	not specified [RCV004623691]	likely benign	15	85581453	85581453	Human		name
407503203	CV3436220	single nucleotide variant	NM_007200.5(AKAP13):c.7834C>A (p.Leu2612Met)	not specified [RCV004623693]	uncertain significance	15	85741271	85741271	Human		name
407503215	CV3436223	single nucleotide variant	NM_007200.5(AKAP13):c.4594G>A (p.Asp1532Asn)	not specified [RCV004623696]	uncertain significance	15	85655636	85655636	Human		name
407503226	CV3436226	single nucleotide variant	NM_007200.5(AKAP13):c.5932C>T (p.Arg1978Trp)	not specified [RCV004623699]	uncertain significance	15	85718090	85718090	Human		name
407503257	CV3436235	single nucleotide variant	NM_007200.5(AKAP13):c.3998A>G (p.Glu1333Gly)	not specified [RCV004623708]	uncertain significance	15	85582066	85582066	Human		name
407503405	CV3436276	single nucleotide variant	NM_007200.5(AKAP13):c.5107C>T (p.Arg1703Trp)	not specified [RCV004623749]	uncertain significance	15	85682163	85682163	Human		name
407503552	CV3436317	single nucleotide variant	NM_007200.5(AKAP13):c.6262G>A (p.Glu2088Lys)	not specified [RCV004623790]	uncertain significance	15	85722000	85722000	Human		name
407462747	CV3436338	single nucleotide variant	NM_007200.5(AKAP13):c.3407T>C (p.Leu1136Pro)	not specified [RCV004634425]	uncertain significance	15	85581475	85581475	Human		name
407503621	CV3436349	single nucleotide variant	NM_007200.5(AKAP13):c.6217C>G (p.Leu2073Val)	not specified [RCV004623809]	uncertain significance	15	85719291	85719291	Human		name
407462598	CV3436356	single nucleotide variant	NM_007200.5(AKAP13):c.8280G>C (p.Gln2760His)	not specified [RCV004634441]	uncertain significance	15	85743713	85743713	Human		name
407462171	CV3436362	single nucleotide variant	NM_007200.5(AKAP13):c.3473A>G (p.Glu1158Gly)	not specified [RCV004634447]	uncertain significance	15	85581541	85581541	Human		name
407462144	CV3436372	single nucleotide variant	NM_007200.5(AKAP13):c.4085G>C (p.Ser1362Thr)	not specified [RCV004634454]	uncertain significance	15	85585747	85585747	Human		name
407462174	CV3436383	single nucleotide variant	NM_007200.5(AKAP13):c.4235C>T (p.Pro1412Leu)	not specified [RCV004634465]	uncertain significance	15	85639447	85639447	Human		name
407485855	CV3439521	single nucleotide variant	NM_016248.4(AKAP11):c.5141A>T (p.Gln1714Leu)	not specified [RCV004618990]	uncertain significance	13	42308477	42308477	Human		name
407486002	CV3439547	single nucleotide variant	NM_016248.4(AKAP11):c.3925G>A (p.Val1309Ile)	not specified [RCV004619016]	uncertain significance	13	42302671	42302671	Human		name
407486069	CV3439558	single nucleotide variant	NM_016248.4(AKAP11):c.5047A>G (p.Ser1683Gly)	not specified [RCV004619027]	uncertain significance	13	42303793	42303793	Human		name
407486126	CV3439569	single nucleotide variant	NM_016248.4(AKAP11):c.4242C>G (p.Asn1414Lys)	not specified [RCV004619038]	uncertain significance	13	42302988	42302988	Human		name
407486177	CV3439579	single nucleotide variant	NM_016248.4(AKAP11):c.5086G>C (p.Ala1696Pro)	not specified [RCV004619048]	uncertain significance	13	42303832	42303832	Human		name
407486815	CV3439603	single nucleotide variant	NM_005100.4(AKAP12):c.4789G>A (p.Glu1597Lys)	not specified [RCV004619072]	uncertain significance	6	151353180	151353180	Human		name
407486464	CV3439655	single nucleotide variant	NM_005100.4(AKAP12):c.4448C>T (p.Ser1483Leu)	not specified [RCV004619124]	uncertain significance	6	151352839	151352839	Human		name
597720092	CV3665858	single nucleotide variant	NM_016248.4(AKAP11):c.4252C>T (p.His1418Tyr)	not specified [RCV004918711]	uncertain significance	13	42302998	42302998	Human		name
597720561	CV3665916	single nucleotide variant	NM_016248.4(AKAP11):c.4303T>C (p.Cys1435Arg)	not specified [RCV004918762]	uncertain significance	13	42303049	42303049	Human		name
597720660	CV3665927	single nucleotide variant	NM_016248.4(AKAP11):c.3802A>G (p.Ile1268Val)	not specified [RCV004918773]	uncertain significance	13	42302548	42302548	Human		name
597720785	CV3665944	single nucleotide variant	NM_016248.4(AKAP11):c.5699A>C (p.Asn1900Thr)	not specified [RCV004918789]	uncertain significance	13	42319221	42319221	Human		name
597721343	CV3665993	single nucleotide variant	NM_016248.4(AKAP11):c.4753C>G (p.Gln1585Glu)	not specified [RCV004918835]	uncertain significance	13	42303499	42303499	Human		name
597721494	CV3666004	single nucleotide variant	NM_016248.4(AKAP11):c.4359A>T (p.Gln1453His)	not specified [RCV004918846]	uncertain significance	13	42303105	42303105	Human		name
597722251	CV3666067	single nucleotide variant	NM_016248.4(AKAP11):c.5200G>C (p.Gly1734Arg)	not specified [RCV004918908]	uncertain significance	13	42308536	42308536	Human		name
597722411	CV3666081	single nucleotide variant	NM_016248.4(AKAP11):c.3599A>T (p.Glu1200Val)	not specified [RCV004918922]	uncertain significance	13	42302345	42302345	Human		name
597722539	CV3666091	single nucleotide variant	NM_016248.4(AKAP11):c.3550G>A (p.Glu1184Lys)	not specified [RCV004918932]	uncertain significance	13	42302296	42302296	Human		name
597722774	CV3666111	single nucleotide variant	NM_016248.4(AKAP11):c.4760G>C (p.Cys1587Ser)	not specified [RCV004918952]	uncertain significance	13	42303506	42303506	Human		name
597722921	CV3666122	single nucleotide variant	NM_016248.4(AKAP11):c.5543C>T (p.Ser1848Phe)	not specified [RCV004918963]	uncertain significance	13	42317666	42317666	Human		name
597723712	CV3666197	single nucleotide variant	NM_005100.4(AKAP12):c.3119A>T (p.Gln1040Leu)	not specified [RCV004919031]	uncertain significance	6	151351510	151351510	Human		name
597723816	CV3666206	single nucleotide variant	NM_005100.4(AKAP12):c.4861A>G (p.Thr1621Ala)	not specified [RCV004919040]	uncertain significance	6	151353252	151353252	Human		name
597723883	CV3666215	single nucleotide variant	NM_005100.4(AKAP12):c.4642A>G (p.Lys1548Glu)	not specified [RCV004919046]	uncertain significance	6	151353033	151353033	Human		name
597740801	CV3672365	single nucleotide variant	NM_007200.5(AKAP13):c.6478A>C (p.Ile2160Leu)	not specified [RCV004921540]	uncertain significance	15	85722329	85722329	Human		name
597740860	CV3672376	single nucleotide variant	NM_007200.5(AKAP13):c.3833T>G (p.Met1278Arg)	not specified [RCV004921551]	uncertain significance	15	85581901	85581901	Human		name
597740915	CV3672387	single nucleotide variant	NM_007200.5(AKAP13):c.8126C>T (p.Ser2709Leu)	not specified [RCV004921562]	likely benign	15	85743559	85743559	Human		name
597740974	CV3672398	single nucleotide variant	NM_007200.5(AKAP13):c.7837C>G (p.Arg2613Gly)	not specified [RCV004921573]	uncertain significance	15	85741274	85741274	Human		name
597741015	CV3672406	single nucleotide variant	NM_007200.5(AKAP13):c.5602T>A (p.Ser1868Thr)	not specified [RCV004921581]	uncertain significance	15	85715790	85715790	Human		name
597741107	CV3672426	single nucleotide variant	NM_007200.5(AKAP13):c.3134G>C (p.Cys1045Ser)	not specified [RCV004921600]	uncertain significance	15	85581202	85581202	Human		name
597741157	CV3672437	single nucleotide variant	NM_007200.5(AKAP13):c.7684T>A (p.Leu2562Met)	not specified [RCV004921611]	uncertain significance	15	85741121	85741121	Human		name
597741221	CV3672459	single nucleotide variant	NM_007200.5(AKAP13):c.3901A>T (p.Ser1301Cys)	not specified [RCV004921625]	uncertain significance	15	85581969	85581969	Human		name
597741258	CV3672469	single nucleotide variant	NM_007200.5(AKAP13):c.5554G>A (p.Ala1852Thr)	not specified [RCV004921633]	uncertain significance	15	85710600	85710600	Human		name
597741359	CV3672491	single nucleotide variant	NM_007200.5(AKAP13):c.5603C>T (p.Ser1868Leu)	not specified [RCV004921655]	uncertain significance	15	85715791	85715791	Human		name
597741394	CV3672499	single nucleotide variant	NM_007200.5(AKAP13):c.7795C>T (p.Arg2599Cys)	not specified [RCV004921663]	uncertain significance	15	85741232	85741232	Human		name
597751049	CV3672511	single nucleotide variant	NM_007200.5(AKAP13):c.5126T>G (p.Phe1709Cys)	not specified [RCV004923654]	uncertain significance	15	85682182	85682182	Human		name
597751108	CV3672522	single nucleotide variant	NM_007200.5(AKAP13):c.4123G>C (p.Ala1375Pro)	not specified [RCV004923665]	uncertain significance	15	85585785	85585785	Human		name
597751199	CV3672541	single nucleotide variant	NM_007200.5(AKAP13):c.5015A>C (p.Gln1672Pro)	not specified [RCV004923682]	uncertain significance	15	85669744	85669744	Human		name
597751204	CV3672552	single nucleotide variant	NM_007200.5(AKAP13):c.3816G>C (p.Glu1272Asp)	not specified [RCV004923683]	uncertain significance	15	85581884	85581884	Human		name
597751209	CV3672560	single nucleotide variant	NM_007200.5(AKAP13):c.4024C>T (p.Pro1342Ser)	not specified [RCV004923684]	uncertain significance	15	85582092	85582092	Human		name
597751236	CV3672569	single nucleotide variant	NM_007200.5(AKAP13):c.5675A>C (p.Asn1892Thr)	not specified [RCV004923689]	uncertain significance	15	85715863	85715863	Human		name
597751288	CV3672579	single nucleotide variant	NM_007200.5(AKAP13):c.6755C>G (p.Ala2252Gly)	not specified [RCV004923699]	uncertain significance	15	85726419	85726419	Human		name
597751347	CV3672590	single nucleotide variant	NM_007200.5(AKAP13):c.3229A>C (p.Lys1077Gln)	not specified [RCV004923710]	uncertain significance	15	85581297	85581297	Human		name
597751364	CV3672597	single nucleotide variant	NM_007200.5(AKAP13):c.4477C>G (p.Leu1493Val)	not specified [RCV004923713]	uncertain significance	15	85655519	85655519	Human		name
597751398	CV3672606	single nucleotide variant	NM_007200.5(AKAP13):c.6464T>C (p.Val2155Ala)	not specified [RCV004923720]	uncertain significance	15	85722315	85722315	Human		name
597751509	CV3672627	single nucleotide variant	NM_007200.5(AKAP13):c.4042A>G (p.Met1348Val)	not specified [RCV004923742]	uncertain significance	15	85585704	85585704	Human		name
597724119	CV3675819	single nucleotide variant	NM_005100.4(AKAP12):c.3925A>G (p.Thr1309Ala)	not specified [RCV004919067]	uncertain significance	6	151352316	151352316	Human		name
597724426	CV3675848	single nucleotide variant	NM_005100.4(AKAP12):c.5193T>G (p.Asn1731Lys)	not specified [RCV004919096]	uncertain significance	6	151353584	151353584	Human		name
597739126	CV3675881	single nucleotide variant	NM_005100.4(AKAP12):c.5249A>G (p.Lys1750Arg)	not specified [RCV004921178]	uncertain significance	6	151353640	151353640	Human		name
597739198	CV3675899	single nucleotide variant	NM_005100.4(AKAP12):c.3065T>C (p.Val1022Ala)	not specified [RCV004921196]	uncertain significance	6	151351456	151351456	Human		name
597739285	CV3675922	single nucleotide variant	NM_005100.4(AKAP12):c.3976G>A (p.Ala1326Thr)	not specified [RCV004921218]	uncertain significance	6	151352367	151352367	Human		name
597739319	CV3675933	single nucleotide variant	NM_005100.4(AKAP12):c.4108G>C (p.Val1370Leu)	not specified [RCV004921229]	likely benign	6	151352499	151352499	Human		name
597739350	CV3675943	single nucleotide variant	NM_005100.4(AKAP12):c.4190C>T (p.Pro1397Leu)	not specified [RCV004921239]	uncertain significance	6	151352581	151352581	Human		name
597739458	CV3675974	single nucleotide variant	NM_005100.4(AKAP12):c.4018C>A (p.Gln1340Lys)	not specified [RCV004921270]	uncertain significance	6	151352409	151352409	Human		name
597739649	CV3676013	single nucleotide variant	NM_007200.5(AKAP13):c.4177T>A (p.Trp1393Arg)	not specified [RCV004921308]	uncertain significance	15	85639389	85639389	Human		name
597739706	CV3676023	single nucleotide variant	NM_007200.5(AKAP13):c.5126T>A (p.Phe1709Tyr)	not specified [RCV004921318]	uncertain significance	15	85682182	85682182	Human		name
597739874	CV3676053	single nucleotide variant	NM_007200.5(AKAP13):c.8191A>G (p.Arg2731Gly)	not specified [RCV004921348]	uncertain significance	15	85743624	85743624	Human		name
597739929	CV3676063	single nucleotide variant	NM_007200.5(AKAP13):c.3562C>A (p.Leu1188Met)	not specified [RCV004921358]	uncertain significance	15	85581630	85581630	Human		name
597740164	CV3676113	single nucleotide variant	NM_007200.5(AKAP13):c.5675A>G (p.Asn1892Ser)	not specified [RCV004921407]	likely benign	15	85715863	85715863	Human		name
597740205	CV3676122	single nucleotide variant	NM_007200.5(AKAP13):c.5694T>A (p.Ser1898Arg)	not specified [RCV004921416]	uncertain significance	15	85715882	85715882	Human		name
597740251	CV3676132	single nucleotide variant	NM_007200.5(AKAP13):c.5539A>G (p.Lys1847Glu)	not specified [RCV004921426]	uncertain significance	15	85710585	85710585	Human		name
597740302	CV3676143	single nucleotide variant	NM_007200.5(AKAP13):c.4814G>C (p.Gly1605Ala)	not specified [RCV004921437]	uncertain significance	15	85664577	85664577	Human		name
597740351	CV3676154	single nucleotide variant	NM_007200.5(AKAP13):c.7352T>C (p.Ile2451Thr)	not specified [RCV004921448]	uncertain significance	15	85735061	85735061	Human		name
597740493	CV3676184	single nucleotide variant	NM_007200.5(AKAP13):c.8033G>A (p.Arg2678Gln)	not specified [RCV004921478]	uncertain significance	15	85741470	85741470	Human		name
597740534	CV3676193	single nucleotide variant	NM_007200.5(AKAP13):c.7736A>G (p.Lys2579Arg)	not specified [RCV004921487]	uncertain significance	15	85741173	85741173	Human		name
597740588	CV3676205	single nucleotide variant	NM_007200.5(AKAP13):c.8018A>T (p.Glu2673Val)	not specified [RCV004921498]	uncertain significance	15	85741455	85741455	Human		name
597740747	CV3676245	single nucleotide variant	NM_007200.5(AKAP13):c.4618A>G (p.Ser1540Gly)	not specified [RCV004921530]	uncertain significance	15	85655660	85655660	Human		name
598238473	CV3958527	single nucleotide variant	NM_005100.4(AKAP12):c.5339C>A (p.Thr1780Lys)	not specified [RCV005343808]	uncertain significance	6	151353730	151353730	Human		name
598238527	CV3958537	single nucleotide variant	NM_005100.4(AKAP12):c.5066A>C (p.Glu1689Ala)	not specified [RCV005343817]	uncertain significance	6	151353457	151353457	Human		name
598239033	CV3958637	single nucleotide variant	NM_005100.4(AKAP12):c.3068A>G (p.Gln1023Arg)	not specified [RCV005343909]	uncertain significance	6	151351459	151351459	Human		name
598239106	CV3958648	single nucleotide variant	NM_005100.4(AKAP12):c.3384G>C (p.Glu1128Asp)	not specified [RCV005343920]	uncertain significance	6	151351775	151351775	Human		name
598239165	CV3958659	single nucleotide variant	NM_005100.4(AKAP12):c.3421G>A (p.Ala1141Thr)	not specified [RCV005343930]	uncertain significance	6	151351812	151351812	Human		name
598239229	CV3958679	single nucleotide variant	NM_005100.4(AKAP12):c.4982T>G (p.Leu1661Arg)	not specified [RCV005343945]	uncertain significance	6	151353373	151353373	Human		name
598239253	CV3958684	single nucleotide variant	NM_005100.4(AKAP12):c.3304A>G (p.Lys1102Glu)	not specified [RCV005343950]	uncertain significance	6	151351695	151351695	Human		name
598239281	CV3958691	single nucleotide variant	NM_007200.5(AKAP13):c.4721G>T (p.Ser1574Ile)	not specified [RCV005343956]	uncertain significance	15	85655763	85655763	Human		name
598239326	CV3958702	single nucleotide variant	NM_007200.5(AKAP13):c.5588T>A (p.Met1863Lys)	not specified [RCV005343967]	uncertain significance	15	85710634	85710634	Human		name
598239367	CV3958711	single nucleotide variant	NM_007200.5(AKAP13):c.8260A>G (p.Asn2754Asp)	not specified [RCV005343976]	uncertain significance	15	85743693	85743693	Human		name
598239389	CV3958717	single nucleotide variant	NM_007200.5(AKAP13):c.4667G>A (p.Arg1556His)	not specified [RCV005343981]	uncertain significance	15	85655709	85655709	Human		name
598239424	CV3958726	single nucleotide variant	NM_007200.5(AKAP13):c.6142A>G (p.Ile2048Val)	not specified [RCV005343989]	uncertain significance	15	85719216	85719216	Human		name
598239444	CV3958731	single nucleotide variant	NM_007200.5(AKAP13):c.3541G>A (p.Asp1181Asn)	not specified [RCV005343994]	uncertain significance	15	85581609	85581609	Human		name
598239500	CV3958746	single nucleotide variant	NM_007200.5(AKAP13):c.7909C>T (p.Arg2637Trp)	not specified [RCV005344008]	uncertain significance	15	85741346	85741346	Human		name
598239513	CV3958750	single nucleotide variant	NM_007200.5(AKAP13):c.3239C>A (p.Ala1080Asp)	not specified [RCV005344011]	uncertain significance	15	85581307	85581307	Human		name
598239529	CV3958754	single nucleotide variant	NM_007200.5(AKAP13):c.4850C>G (p.Ser1617Cys)	not specified [RCV005344015]	uncertain significance	15	85664613	85664613	Human		name
598195401	CV3958772	single nucleotide variant	NM_007200.5(AKAP13):c.3007C>T (p.Pro1003Ser)	not specified [RCV005335569]	uncertain significance	15	85581075	85581075	Human		name
598239612	CV3958777	single nucleotide variant	NM_007200.5(AKAP13):c.4207G>A (p.Ala1403Thr)	not specified [RCV005344036]	uncertain significance	15	85639419	85639419	Human		name
598239628	CV3958782	single nucleotide variant	NM_007200.5(AKAP13):c.6724A>C (p.Asn2242His)	not specified [RCV005344040]	uncertain significance	15	85723299	85723299	Human		name
598239652	CV3958787	single nucleotide variant	NM_007200.5(AKAP13):c.7706T>C (p.Ile2569Thr)	not specified [RCV005344045]	uncertain significance	15	85741143	85741143	Human		name
598239670	CV3958791	single nucleotide variant	NM_007200.5(AKAP13):c.7028T>C (p.Ile2343Thr)	not specified [RCV005344049]	uncertain significance	15	85727404	85727404	Human		name
598239684	CV3958795	single nucleotide variant	NM_007200.5(AKAP13):c.4826G>C (p.Gly1609Ala)	not specified [RCV005344052]	uncertain significance	15	85664589	85664589	Human		name
598195415	CV3958801	single nucleotide variant	NM_007200.5(AKAP13):c.8378G>A (p.Arg2793His)	not specified [RCV005335572]	uncertain significance	15	85743811	85743811	Human		name
598195421	CV3958805	single nucleotide variant	NM_007200.5(AKAP13):c.8132C>A (p.Ser2711Tyr)	not specified [RCV005335573]	uncertain significance	15	85743565	85743565	Human		name
598239738	CV3958811	single nucleotide variant	NM_007200.5(AKAP13):c.5606A>G (p.Gln1869Arg)	not specified [RCV005344066]	uncertain significance	15	85715794	85715794	Human		name
598239757	CV3958816	single nucleotide variant	NM_007200.5(AKAP13):c.3417A>T (p.Lys1139Asn)	not specified [RCV005344071]	uncertain significance	15	85581485	85581485	Human		name
598197207	CV3958837	single nucleotide variant	NM_007200.5(AKAP13):c.3087G>T (p.Arg1029Ser)	not specified [RCV005336098]	likely benign	15	85581155	85581155	Human		name
598197279	CV3958849	single nucleotide variant	NM_007200.5(AKAP13):c.5087A>G (p.His1696Arg)	not specified [RCV005336108]	uncertain significance	15	85669816	85669816	Human		name
598195445	CV3958863	single nucleotide variant	NM_007200.5(AKAP13):c.4360A>G (p.Ile1454Val)	not specified [RCV005335578]	uncertain significance	15	85645940	85645940	Human		name
598197377	CV3958868	single nucleotide variant	NM_007200.5(AKAP13):c.4069G>A (p.Val1357Met)	not specified [RCV005336125]	uncertain significance	15	85585731	85585731	Human		name
598197401	CV3958872	single nucleotide variant	NM_007200.5(AKAP13):c.5333A>T (p.Asp1778Val)	not specified [RCV005336129]	uncertain significance	15	85693320	85693320	Human		name
598197417	CV3958874	single nucleotide variant	NM_007200.5(AKAP13):c.6937G>T (p.Val2313Phe)	not specified [RCV005336131]	uncertain significance	15	85727180	85727180	Human		name
598197501	CV3958891	single nucleotide variant	NM_007200.5(AKAP13):c.7732G>C (p.Glu2578Gln)	not specified [RCV005336145]	uncertain significance	15	85741169	85741169	Human		name
598197538	CV3958899	single nucleotide variant	NM_007200.5(AKAP13):c.7127T>C (p.Leu2376Ser)	not specified [RCV005336152]	uncertain significance	15	85730552	85730552	Human		name
598197572	CV3958905	single nucleotide variant	NM_007200.5(AKAP13):c.4990C>G (p.Gln1664Glu)	not specified [RCV005336158]	uncertain significance	15	85664753	85664753	Human		name
598225641	CV3962091	single nucleotide variant	NM_016248.4(AKAP11):c.3767T>C (p.Leu1256Ser)	not specified [RCV005341486]	uncertain significance	13	42302513	42302513	Human		name
598225822	CV3962123	single nucleotide variant	NM_016248.4(AKAP11):c.4454C>T (p.Thr1485Ile)	not specified [RCV005341515]	uncertain significance	13	42303200	42303200	Human		name
598225863	CV3962129	single nucleotide variant	NM_016248.4(AKAP11):c.3080C>T (p.Pro1027Leu)	not specified [RCV005341521]	uncertain significance	13	42301826	42301826	Human		name
598225928	CV3962140	single nucleotide variant	NM_016248.4(AKAP11):c.5428C>G (p.Leu1810Val)	not specified [RCV005341531]	uncertain significance	13	42317551	42317551	Human		name
598225995	CV3962151	single nucleotide variant	NM_016248.4(AKAP11):c.5395G>A (p.Glu1799Lys)	not specified [RCV005341541]	uncertain significance	13	42313931	42313931	Human		name
598226137	CV3962173	single nucleotide variant	NM_016248.4(AKAP11):c.3805A>G (p.Thr1269Ala)	not specified [RCV005341562]	uncertain significance	13	42302551	42302551	Human		name
598226211	CV3962183	single nucleotide variant	NM_016248.4(AKAP11):c.5126A>G (p.Glu1709Gly)	not specified [RCV005341572]	uncertain significance	13	42308462	42308462	Human		name
598226355	CV3962206	single nucleotide variant	NM_016248.4(AKAP11):c.4036G>T (p.Ala1346Ser)	not specified [RCV005341594]	uncertain significance	13	42302782	42302782	Human		name
598226423	CV3962217	single nucleotide variant	NM_016248.4(AKAP11):c.4249C>T (p.His1417Tyr)	not specified [RCV005341604]	uncertain significance	13	42302995	42302995	Human		name
598226482	CV3962225	single nucleotide variant	NM_016248.4(AKAP11):c.4840A>G (p.Ser1614Gly)	not specified [RCV005341612]	uncertain significance	13	42303586	42303586	Human		name
598237169	CV3962236	single nucleotide variant	NM_016248.4(AKAP11):c.4976T>C (p.Ile1659Thr)	not specified [RCV005343598]	uncertain significance	13	42303722	42303722	Human		name
598237280	CV3962257	single nucleotide variant	NM_016248.4(AKAP11):c.4613A>G (p.Gln1538Arg)	not specified [RCV005343617]	uncertain significance	13	42303359	42303359	Human		name
598237338	CV3962266	single nucleotide variant	NM_016248.4(AKAP11):c.3419C>T (p.Thr1140Ile)	not specified [RCV005343626]	uncertain significance	13	42302165	42302165	Human		name
598237389	CV3962275	single nucleotide variant	NM_016248.4(AKAP11):c.4264G>A (p.Asp1422Asn)	not specified [RCV005343635]	uncertain significance	13	42303010	42303010	Human		name
598237552	CV3962307	single nucleotide variant	NM_016248.4(AKAP11):c.3506C>T (p.Ser1169Phe)	not specified [RCV005343663]	uncertain significance	13	42302252	42302252	Human		name
598237602	CV3962318	single nucleotide variant	NM_016248.4(AKAP11):c.5188G>T (p.Asp1730Tyr)	not specified [RCV005343672]	uncertain significance	13	42308524	42308524	Human		name
598237714	CV3962345	single nucleotide variant	NM_016248.4(AKAP11):c.4837G>A (p.Ala1613Thr)	not specified [RCV005343692]	uncertain significance	13	42303583	42303583	Human		name
598195228	CV3962356	single nucleotide variant	NM_016248.4(AKAP11):c.3530G>A (p.Ser1177Asn)	not specified [RCV005335535]	uncertain significance	13	42302276	42302276	Human		name
598238214	CV3962424	single nucleotide variant	NM_005100.4(AKAP12):c.4672G>A (p.Val1558Ile)	not specified [RCV005343767]	uncertain significance	6	151353063	151353063	Human		name
598195267	CV3962433	single nucleotide variant	NM_005100.4(AKAP12):c.3085G>A (p.Val1029Ile)	not specified [RCV005335542]	uncertain significance	6	151351476	151351476	Human		name
598238295	CV3962444	single nucleotide variant	NM_005100.4(AKAP12):c.4108G>A (p.Val1370Ile)	not specified [RCV005343779]	uncertain significance	6	151352499	151352499	Human		name
598238359	CV3962454	single nucleotide variant	NM_005100.4(AKAP12):c.4551G>T (p.Glu1517Asp)	not specified [RCV005343788]	uncertain significance	6	151352942	151352942	Human		name
15191956	CV699382	single nucleotide variant	NM_005100.4(AKAP12):c.3047C>T (p.Thr1016Ile)	not provided [RCV000954927]	likely benign	6	151351438	151351438	Human		name
15197316	CV699384	single nucleotide variant	NM_005100.4(AKAP12):c.4345G>A (p.Ala1449Thr)	not provided [RCV000956432]	benign	6	151352736	151352736	Human		name
15193821	CV702693	single nucleotide variant	NM_016248.4(AKAP11):c.3209A>G (p.His1070Arg)	not provided [RCV000955479]	benign	13	42301955	42301955	Human		name
15160640	CV702694	single nucleotide variant	NM_016248.4(AKAP11):c.4876C>T (p.Arg1626Cys)	not provided [RCV000947524]	benign	13	42303622	42303622	Human		name
15129881	CV713934	single nucleotide variant	NM_016248.4(AKAP11):c.3221C>T (p.Ser1074Phe)	not provided [RCV000964335]	benign	13	42301967	42301967	Human		name
15177770	CV713935	single nucleotide variant	NM_016248.4(AKAP11):c.5344C>G (p.Pro1782Ala)	not provided [RCV000973507]	benign	13	42313117	42313117	Human		name
15175215	CV714662	single nucleotide variant	NM_007200.5(AKAP13):c.8032C>T (p.Arg2678Trp)	not provided [RCV000972892]	benign	15	85741469	85741469	Human		name
15110938	CV721804	single nucleotide variant	NM_005100.4(AKAP12):c.3653A>T (p.Lys1218Ile)	not provided [RCV000894170]	benign	6	151352044	151352044	Human		name
15155385	CV721806	single nucleotide variant	NM_005100.4(AKAP12):c.4670C>G (p.Ala1557Gly)	not provided [RCV000880407]	likely benign	6	151353061	151353061	Human		name
15156573	CV725491	single nucleotide variant	NM_016248.4(AKAP11):c.4375A>G (p.Thr1459Ala)	not provided [RCV000880657]	benign	13	42303121	42303121	Human		name
15161473	CV726311	single nucleotide variant	NM_007200.5(AKAP13):c.4573A>G (p.Ser1525Gly)	not provided [RCV000881578]	benign	15	85655615	85655615	Human		name
8635613	CV90835	single nucleotide variant	NM_006738.5(AKAP13):c.7397C>T (p.Pro2466Leu)	Malignant melanoma [RCV000070933]	not provided	15	85735094	85735094	Human		name
15183964	CV735478	microsatellite	NM_005100.4(AKAP12):c.4787AAG[1] (p.Glu1597del)	not provided [RCV000908173]	benign	6	151353178	151353180	Human		name
401901883	CV2813878	deletion	NM_016248.4(AKAP11):c.3767_3769del (p.Leu1256del)	not provided [RCV003393297]	likely benign	13	42302511	42302513	Human		name

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