Ankrd26 Variant Search Result - Rat Genome Database

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
8568634	CV39812	single nucleotide variant	ANKRD26, -128G-A	Thrombocytopenia 2 [RCV000023840]	pathogenic				Human		name
151356344	CV1329108	single nucleotide variant	NM_014915.3(ANKRD26):c.*6A>G	not specified [RCV001822697]	uncertain significance	10	27005584	27005584	Human		name
156275180	CV2014909	single nucleotide variant	NM_014915.3(ANKRD26):c.-9G>T	not provided [RCV002715115]	uncertain significance	10	27100335	27100335	Human		name
401828615	CV2742956	single nucleotide variant	NM_014915.3(ANKRD26):c.-2C>G	not provided [RCV003325664]	uncertain significance	10	27100328	27100328	Human		name
11648903	CV310115	single nucleotide variant	NM_014915.3(ANKRD26):c.*8G>T	Thrombocytopenia 2 [RCV000284102]	uncertain significance	10	27005582	27005582	Human	1	name
11609676	CV321284	single nucleotide variant	NM_014915.3(ANKRD26):c.-4G>A	Thrombocytopenia 2 [RCV000371341]\|not provided [RCV002522154]	uncertain significance	10	27100330	27100330	Human	1	name
151355907	CV1327090	single nucleotide variant	NM_014915.3(ANKRD26):c.-53C>T	not specified [RCV001822260]	uncertain significance	10	27100379	27100379	Human		name
156221183	CV1960229	single nucleotide variant	NM_014915.3(ANKRD26):c.-88G>A	not provided [RCV002575534]	uncertain significance	10	27100414	27100414	Human		name
156227226	CV1991615	single nucleotide variant	NM_014915.3(ANKRD26):c.-16C>A	not provided [RCV002626663]	uncertain significance	10	27100342	27100342	Human		name
155945123	CV2032650	single nucleotide variant	NM_014915.3(ANKRD26):c.-77C>T	not provided [RCV002730357]	uncertain significance	10	27100403	27100403	Human		name
155903513	CV2037566	single nucleotide variant	NM_014915.3(ANKRD26):c.-86C>T	not provided [RCV002771120]	uncertain significance	10	27100412	27100412	Human		name
156135691	CV2097342	single nucleotide variant	NM_014915.3(ANKRD26):c.-80T>A	not provided [RCV002890114]	uncertain significance	10	27100406	27100406	Human		name
11550707	CV253740	single nucleotide variant	NM_014915.3(ANKRD26):c.-59G>A	Thrombocytopenia 2 [RCV000259816]\|not provided [RCV001683071]\|not specified [RCV000252103]	benign\|likely benign	10	27100385	27100385	Human	1	name
405128549	CV2957287	single nucleotide variant	NM_014915.3(ANKRD26):c.-73T>C	not provided [RCV003672197]	uncertain significance	10	27100399	27100399	Human		name
405134848	CV2957968	single nucleotide variant	NM_014915.3(ANKRD26):c.-88G>C	not provided [RCV003672724]	uncertain significance	10	27100414	27100414	Human		name
404981783	CV2986240	single nucleotide variant	NM_014915.3(ANKRD26):c.-84G>A	not provided [RCV003691329]	uncertain significance	10	27100410	27100410	Human		name
405207073	CV2994294	single nucleotide variant	NM_014915.3(ANKRD26):c.-83G>C	not provided [RCV003678812]	uncertain significance	10	27100409	27100409	Human		name
405225324	CV3042149	single nucleotide variant	NM_014915.3(ANKRD26):c.-51T>G	not provided [RCV003710597]	uncertain significance	10	27100377	27100377	Human		name
405113817	CV3115354	single nucleotide variant	NM_014915.3(ANKRD26):c.-83G>T	not provided [RCV003814036]	uncertain significance	10	27100409	27100409	Human		name
405134871	CV3160193	single nucleotide variant	NM_014915.3(ANKRD26):c.-88G>T	not provided [RCV003855008]	uncertain significance	10	27100414	27100414	Human		name
405246009	CV3162191	duplication	NM_014915.3(ANKRD26):c.-82dup	not provided [RCV003868710]	uncertain significance	10	27100407	27100408	Human		name
405214714	CV3164435	single nucleotide variant	NM_014915.3(ANKRD26):c.-72T>C	not provided [RCV003862670]	uncertain significance	10	27100398	27100398	Human		name
404982387	CV3179584	single nucleotide variant	NM_014915.3(ANKRD26):c.-70T>C	not provided [RCV003880565]	uncertain significance	10	27100396	27100396	Human		name
597940612	CV3757181	single nucleotide variant	NM_014915.3(ANKRD26):c.-14C>T	not provided [RCV005077366]	uncertain significance	10	27100340	27100340	Human		name
597936616	CV3759622	single nucleotide variant	NM_014915.3(ANKRD26):c.-42G>C	not provided [RCV005076742]	uncertain significance	10	27100368	27100368	Human		name
597891573	CV3785012	single nucleotide variant	NM_014915.3(ANKRD26):c.-47G>A	not provided [RCV005125791]	uncertain significance	10	27100373	27100373	Human		name
597968862	CV3791128	single nucleotide variant	NM_014915.3(ANKRD26):c.-71A>G	not provided [RCV005141160]	uncertain significance	10	27100397	27100397	Human		name
597867674	CV3857900	single nucleotide variant	NM_014915.3(ANKRD26):c.-14C>G	not provided [RCV005196848]	uncertain significance	10	27100340	27100340	Human		name
28907609	CV865768	single nucleotide variant	NM_014915.3(ANKRD26):c.*69T>C	Thrombocytopenia 2 [RCV001107324]	uncertain significance	10	27005521	27005521	Human	1	name
28909189	CV865798	single nucleotide variant	NM_014915.3(ANKRD26):c.-51T>A	Thrombocytopenia 2 [RCV001108235]\|not provided [RCV005056893]	likely benign\|uncertain significance	10	27100377	27100377	Human	1	name
28909192	CV865799	single nucleotide variant	NM_014915.3(ANKRD26):c.-77C>G	Thrombocytopenia 2 [RCV001108236]\|not provided [RCV002555055]\|not specified [RCV001819821]	benign\|conflicting interpretations of pathogenicity	10	27100403	27100403	Human	1	name
150334559	CV1165940	single nucleotide variant	NM_014915.3(ANKRD26):c.-127A>C	not provided [RCV001531052]	likely pathogenic	10	27100453	27100453	Human		name
151353619	CV1327171	single nucleotide variant	NM_014915.3(ANKRD26):c.-117G>A	ANKRD26-related disorder [RCV003892862]\|not provided [RCV002463041]\|not specified [RCV001817114]	likely benign\|uncertain significance	10	27100443	27100443	Human	1	name , alternate_id
151356031	CV1328795	single nucleotide variant	NM_014915.3(ANKRD26):c.-120A>G	not specified [RCV001822384]	uncertain significance	10	27100446	27100446	Human		name
152981104	CV1676376	single nucleotide variant	NM_014915.3(ANKRD26):c.-126T>G	Thrombocytopenia 2 [RCV002245453]	pathogenic	10	27100452	27100452	Human	1	name
155266086	CV1696193	single nucleotide variant	NM_014915.3(ANKRD26):c.-125T>G	Thrombocytopenia 2 [RCV002280967]\|not provided [RCV003560922]	pathogenic\|uncertain significance	10	27100451	27100451	Human	1	name
156118785	CV1972956	single nucleotide variant	NM_014915.3(ANKRD26):c.-137G>A	not provided [RCV002593048]	uncertain significance	10	27100463	27100463	Human		name
155947067	CV2150904	single nucleotide variant	NM_014915.3(ANKRD26):c.-126T>A	not provided [RCV003014630]	uncertain significance	10	27100452	27100452	Human		name
11547587	CV253741	single nucleotide variant	NM_014915.3(ANKRD26):c.-140C>G	Thrombocytopenia 2 [RCV000988338]\|not provided [RCV001660325]\|not specified [RCV000247955]	benign\|likely benign	10	27100466	27100466	Human	1	name
401722022	CV2737607	single nucleotide variant	NM_014915.3(ANKRD26):c.-149G>T	not provided [RCV003314779]	uncertain significance	10	27100475	27100475	Human		name
401830814	CV2748438	single nucleotide variant	NM_014915.3(ANKRD26):c.-107C>T	Thrombocytopenia 2 [RCV003330047]	likely pathogenic	10	27100433	27100433	Human	1	name
405012481	CV2933936	single nucleotide variant	NM_014915.3(ANKRD26):c.-120A>T	not provided [RCV003576856]	uncertain significance	10	27100446	27100446	Human		name
405086932	CV2943268	single nucleotide variant	NM_014915.3(ANKRD26):c.-115G>C	not provided [RCV003665014]	uncertain significance	10	27100441	27100441	Human		name
405135637	CV2959469	single nucleotide variant	NM_014915.3(ANKRD26):c.-106T>C	not provided [RCV003668651]	uncertain significance	10	27100432	27100432	Human		name
405188725	CV2974230	single nucleotide variant	NM_014915.3(ANKRD26):c.-138C>T	not provided [RCV003677000]	uncertain significance	10	27100464	27100464	Human		name
405254946	CV3000055	single nucleotide variant	NM_014915.3(ANKRD26):c.-164C>G	not provided [RCV003723240]	uncertain significance	10	27100490	27100490	Human		name
11647592	CV310113	single nucleotide variant	NM_014915.3(ANKRD26):c.*704C>G	Thrombocytopenia 2 [RCV000277079]	uncertain significance	10	27004886	27004886	Human	1	name
11609961	CV310162	single nucleotide variant	NM_014915.3(ANKRD26):c.-135A>C	Thrombocytopenia 2 [RCV000374820]\|not provided [RCV002522155]	uncertain significance	10	27100461	27100461	Human	1	name
405171296	CV3122475	single nucleotide variant	NM_014915.3(ANKRD26):c.-139C>T	not provided [RCV003819064]	uncertain significance	10	27100465	27100465	Human		name
405139864	CV3125769	single nucleotide variant	NM_014915.3(ANKRD26):c.-101G>A	not provided [RCV003816684]	uncertain significance	10	27100427	27100427	Human		name
405118676	CV3131096	single nucleotide variant	NM_014915.3(ANKRD26):c.-152C>T	not provided [RCV003837152]	uncertain significance	10	27100478	27100478	Human		name
405197476	CV3132052	single nucleotide variant	NM_014915.3(ANKRD26):c.-154C>T	not provided [RCV003821645]	uncertain significance	10	27100480	27100480	Human		name
11609542	CV315193	duplication	NM_014915.3(ANKRD26):c.*815dup	Thrombocytopenia [RCV000369449]	likely benign	10	27004774	27004775	Human	2	name
11661056	CV315197	single nucleotide variant	NM_014915.3(ANKRD26):c.*530C>G	Thrombocytopenia 2 [RCV000372829]	uncertain significance	10	27005060	27005060	Human	1	name
11654613	CV315198	single nucleotide variant	NM_014915.3(ANKRD26):c.*142G>A	Thrombocytopenia 2 [RCV000319073]	uncertain significance	10	27005448	27005448	Human	1	name
405235127	CV3155929	duplication	NM_014915.3(ANKRD26):c.-104dup	not provided [RCV003853662]	uncertain significance	10	27100429	27100430	Human		name
405268313	CV3189625	single nucleotide variant	NM_014915.3(ANKRD26):c.-135A>G	ANKRD26-related disorder [RCV003899017]\|not provided [RCV005101516]	likely benign\|uncertain significance	10	27100461	27100461	Human	1	name , alternate_id
405290527	CV3200922	single nucleotide variant	NM_014915.3(ANKRD26):c.-164C>T	ANKRD26-related disorder [RCV003984586]	likely benign	10	27100490	27100490	Human		name , trait , alternate_id
11654460	CV321292	single nucleotide variant	NM_014915.3(ANKRD26):c.-113A>C	ANKRD26-related disorder [RCV003920234]\|Thrombocytopenia [RCV000317917]\|not provided [RCV001571174]\|not specified [RCV001820874]	uncertain significance	10	27100439	27100439	Human	3	name , alternate_id
11604758	CV321782	single nucleotide variant	NM_014915.3(ANKRD26):c.*904C>A	Thrombocytopenia 2 [RCV000312396]	benign\|likely benign	10	27004686	27004686	Human	1	name
11605098	CV321788	single nucleotide variant	NM_014915.3(ANKRD26):c.*566G>T	Thrombocytopenia 2 [RCV000315772]	uncertain significance	10	27005024	27005024	Human	1	name
11598998	CV321795	single nucleotide variant	NM_014915.3(ANKRD26):c.*170G>A	Thrombocytopenia 2 [RCV000261843]	uncertain significance	10	27005420	27005420	Human	1	name
11645199	CV321904	single nucleotide variant	NM_014915.3(ANKRD26):c.-138C>G	Thrombocytopenia 2 [RCV000263784]\|not provided [RCV003765763]	uncertain significance	10	27100464	27100464	Human	1	name
408386711	CV3518504	single nucleotide variant	NM_014915.3(ANKRD26):c.-106T>G	not provided [RCV004760822]	uncertain significance	10	27100432	27100432	Human		name
597854814	CV3806193	single nucleotide variant	NM_014915.3(ANKRD26):c.-154C>A	not provided [RCV005145935]	uncertain significance	10	27100480	27100480	Human		name
597897471	CV3834731	single nucleotide variant	NM_014915.3(ANKRD26):c.-112G>A	not provided [RCV005180642]	uncertain significance	10	27100438	27100438	Human		name
8568632	CV39810	single nucleotide variant	NM_014915.3(ANKRD26):c.-134G>A	Thrombocytopenia 2 [RCV000023838]\|Thrombocytopenia [RCV000851622]\|not provided [RCV002262573]	pathogenic\|likely pathogenic	10	27100460	27100460	Human	3	name
13213363	CV429062	single nucleotide variant	NM_014915.3(ANKRD26):c.-119C>G	Thrombocytopenia 2 [RCV000499845]\|Thrombocytopenia [RCV001003520]\|not provided [RCV001755737]\|not specified [RCV003317243]	likely pathogenic\|conflicting interpretations of pathogenicity\|uncertain significance	10	27100445	27100445	Human	3	name
13214776	CV429063	single nucleotide variant	NM_014915.2(ANKRD26):c.-184G>T	Thrombocytopenia 2 [RCV002259967]\|not provided [RCV001536409]\|not specified [RCV000501684]	benign\|likely benign	10	27100510	27100510	Human	1	name
14975445	CV615432	single nucleotide variant	NM_014915.3(ANKRD26):c.-116C>T	ANKRD26-related disorder [RCV004723161]\|Thrombocytopenia 2 [RCV001580272]\|Thrombocytopenia [RCV000851616]\|not provided [RCV001531051]	pathogenic\|likely pathogenic\|drug response\|uncertain significance	10	27100442	27100442	Human	3	name , alternate_id
14975735	CV615433	single nucleotide variant	NM_014915.3(ANKRD26):c.-116C>G	Thrombocytopenia 2 [RCV002280889]\|Thrombocytopenia [RCV000851960]\|not provided [RCV003558572]	likely pathogenic\|uncertain significance	10	27100442	27100442	Human	3	name
14975993	CV615434	single nucleotide variant	NM_014915.3(ANKRD26):c.-118C>T	ANKRD26-related disorder [RCV004740446]\|Thrombocytopenia 2 [RCV002222632]\|Thrombocytopenia [RCV000852254]\|not provided [RCV002225724]	pathogenic\|likely pathogenic	10	27100444	27100444	Human	3	name , alternate_id
14975447	CV615435	single nucleotide variant	NM_014915.3(ANKRD26):c.-118C>G	Thrombocytopenia 2 [RCV002281127]\|Thrombocytopenia [RCV000851617]\|not provided [RCV003727820]\|not specified [RCV005240548]	likely pathogenic\|conflicting interpretations of pathogenicity\|uncertain significance	10	27100444	27100444	Human	3	name
14975449	CV615436	single nucleotide variant	NM_014915.3(ANKRD26):c.-126T>C	Inherited bleeding disorder, platelet-type [RCV000851618]\|Thrombocytopenia 2 [RCV000857238]\|Thrombocytopenia [RCV000851619]\|not provided [RCV001816826]	pathogenic\|likely pathogenic\|conflicting interpretations of pathogenicity	10	27100452	27100452	Human	4	name
14975452	CV615437	single nucleotide variant	NM_014915.3(ANKRD26):c.-127A>T	Thrombocytopenia 2 [RCV001615051]\|Thrombocytopenia [RCV000851621]\|not provided [RCV002533969]	pathogenic\|likely pathogenic	10	27100453	27100453	Human	3	name
14975450	CV615438	single nucleotide variant	NM_014915.3(ANKRD26):c.-127A>G	Thrombocytopenia 2 [RCV002245644]\|Thrombocytopenia [RCV000851620]\|not provided [RCV003558569]	pathogenic\|likely pathogenic\|uncertain significance	10	27100453	27100453	Human	3	name
14975401	CV615439	single nucleotide variant	NM_014915.3(ANKRD26):c.-128G>C	Thrombocytopenia 2 [RCV002245643]\|Thrombocytopenia [RCV000851578]	likely pathogenic	10	27100454	27100454	Human	3	name
21404596	CV801117	single nucleotide variant	NM_014915.3(ANKRD26):c.-118C>A	Thrombocytopenia [RCV001003519]	likely pathogenic	10	27100444	27100444	Human	2	name
21404599	CV801118	single nucleotide variant	NM_014915.3(ANKRD26):c.-128G>T	Thrombocytopenia [RCV001003522]\|not provided [RCV002549216]	pathogenic\|likely pathogenic	10	27100454	27100454	Human	2	name
21404597	CV801119	single nucleotide variant	NM_014915.3(ANKRD26):c.-128G>A	Thrombocytopenia 2 [RCV001594406]\|Thrombocytopenia [RCV001003521]\|not provided [RCV002225782]	pathogenic\|likely pathogenic	10	27100454	27100454	Human	3	name
28902209	CV865765	single nucleotide variant	NM_014915.3(ANKRD26):c.*595G>A	Thrombocytopenia 2 [RCV001104569]	uncertain significance	10	27004995	27004995	Human	1	name
28907604	CV865766	single nucleotide variant	NM_014915.3(ANKRD26):c.*566G>A	Thrombocytopenia 2 [RCV001107322]	uncertain significance	10	27005024	27005024	Human	1	name
28907606	CV865767	single nucleotide variant	NM_014915.3(ANKRD26):c.*482A>C	Thrombocytopenia 2 [RCV001107323]	uncertain significance	10	27005108	27005108	Human	1	name
28909193	CV865800	single nucleotide variant	NM_014915.3(ANKRD26):c.-138C>A	Thrombocytopenia 2 [RCV001108237]\|not provided [RCV005093504]	uncertain significance	10	27100464	27100464	Human	1	name
156081931	CV1909002	single nucleotide variant	NM_014915.3(ANKRD26):c.875-4G>A	not provided [RCV002591609]	likely benign	10	27077544	27077544	Human		name
155928188	CV1912316	single nucleotide variant	NM_014915.3(ANKRD26):c.741-4A>G	not provided [RCV002614865]	likely benign	10	27079165	27079165	Human		name
156077036	CV1912459	single nucleotide variant	NM_014915.3(ANKRD26):c.242+8G>A	not provided [RCV002591452]	likely benign	10	27100077	27100077	Human		name
156052555	CV2165336	single nucleotide variant	NM_014915.3(ANKRD26):c.358-3C>T	not provided [RCV003019446]	uncertain significance	10	27093525	27093525	Human		name
243049569	CV2416879	single nucleotide variant	NM_014915.3(ANKRD26):c.710-6T>C	not provided [RCV003548992]\|not specified [RCV003151551]	benign\|likely benign	10	27082839	27082839	Human		name
401908847	CV2796938	single nucleotide variant	NM_014915.3(ANKRD26):c.242+2T>C	ANKRD26-related disorder [RCV003397692]	uncertain significance	10	27100083	27100083	Human		name , trait , alternate_id
401912956	CV2830112	single nucleotide variant	NM_014915.3(ANKRD26):c.532-3C>G	not provided [RCV003441326]	uncertain significance	10	27092515	27092515	Human		name
405139492	CV3045440	single nucleotide variant	NM_014915.3(ANKRD26):c.741-9G>C	not provided [RCV003725524]	likely benign	10	27079170	27079170	Human		name
405140562	CV3045962	single nucleotide variant	NM_014915.3(ANKRD26):c.813+7T>G	not provided [RCV003725609]	likely benign	10	27079082	27079082	Human		name
405244214	CV3050525	single nucleotide variant	NM_014915.3(ANKRD26):c.709+8T>A	not provided [RCV003719926]	likely benign	10	27086531	27086531	Human		name
11664212	CV310109	single nucleotide variant	NM_014915.3(ANKRD26):c.*1174C>G	Thrombocytopenia 2 [RCV000403439]	uncertain significance	10	27004416	27004416	Human	1	name
11607574	CV315192	single nucleotide variant	NM_014915.3(ANKRD26):c.*1175C>T	Thrombocytopenia 2 [RCV000345364]\|not provided [RCV004718243]	benign\|likely benign	10	27004415	27004415	Human	1	name
11609798	CV315266	single nucleotide variant	NM_014915.3(ANKRD26):c.874+8G>T	ANKRD26-related disorder [RCV003940133]\|Thrombocytopenia 2 [RCV000372752]\|not provided [RCV002520583]	benign\|likely benign\|uncertain significance	10	27077625	27077625	Human	1	name , alternate_id
402474331	CV3182732	single nucleotide variant	NM_014915.3(ANKRD26):c.242+7G>C	not provided [RCV003874975]	likely benign	10	27100078	27100078	Human		name
11607103	CV321220	single nucleotide variant	NM_014915.3(ANKRD26):c.*1433A>G	Thrombocytopenia 2 [RCV000339488]	benign\|likely benign	10	27004157	27004157	Human	1	name
11653098	CV321230	single nucleotide variant	NM_014915.3(ANKRD26):c.*1170G>A	Thrombocytopenia 2 [RCV000309012]	uncertain significance	10	27004420	27004420	Human	1	name
11611158	CV321770	deletion	NM_014915.3(ANKRD26):c.*1235del	Thrombocytopenia [RCV000391005]	likely benign	10	27004355	27004355	Human	2	name
11603938	CV321777	single nucleotide variant	NM_014915.3(ANKRD26):c.*1212G>A	Thrombocytopenia 2 [RCV000304481]\|not provided [RCV004718242]	benign\|likely benign	10	27004378	27004378	Human	1	name
11609251	CV321778	single nucleotide variant	NM_014915.3(ANKRD26):c.*1120A>G	Thrombocytopenia 2 [RCV000365981]\|not provided [RCV004718244]	benign\|likely benign	10	27004470	27004470	Human	1	name
11600446	CV321780	single nucleotide variant	NM_014915.3(ANKRD26):c.*1012C>A	Thrombocytopenia 2 [RCV000273770]	benign\|uncertain significance	10	27004578	27004578	Human	1	name
596939000	CV3549944	single nucleotide variant	NM_014915.3(ANKRD26):c.709+5G>C	not provided [RCV004812985]	uncertain significance	10	27086534	27086534	Human		name
597926845	CV3836844	single nucleotide variant	NM_014915.3(ANKRD26):c.874+5G>A	not provided [RCV005185195]	uncertain significance	10	27077628	27077628	Human		name
597957036	CV3838381	single nucleotide variant	NM_014915.3(ANKRD26):c.710-9C>T	not provided [RCV005191756]	likely benign	10	27082842	27082842	Human		name
28897573	CV865761	single nucleotide variant	NM_014915.3(ANKRD26):c.*1351G>T	Thrombocytopenia 2 [RCV001102653]	uncertain significance	10	27004239	27004239	Human	1	name
28897576	CV865762	single nucleotide variant	NM_014915.3(ANKRD26):c.*1243A>G	Thrombocytopenia 2 [RCV001102654]	uncertain significance	10	27004347	27004347	Human	1	name
28902203	CV865763	single nucleotide variant	NM_014915.3(ANKRD26):c.*1169C>T	Thrombocytopenia 2 [RCV001104567]	uncertain significance	10	27004421	27004421	Human	1	name
28902206	CV865764	single nucleotide variant	NM_014915.3(ANKRD26):c.*1029G>A	Thrombocytopenia 2 [RCV001104568]	uncertain significance	10	27004561	27004561	Human	1	name
28898317	CV868469	single nucleotide variant	NM_014915.3(ANKRD26):c.531+9C>G	Thrombocytopenia 2 [RCV001102947]\|not provided [RCV002555002]\|not specified [RCV001819809]	benign	10	27093340	27093340	Human	1	name
150409964	CV1177292	single nucleotide variant	NM_014915.3(ANKRD26):c.531+41C>T	Thrombocytopenia 2 [RCV002260193]\|not provided [RCV001546430]	benign\|likely benign	10	27093308	27093308	Human	1	name
150432644	CV1200733	single nucleotide variant	NM_014915.3(ANKRD26):c.532-50C>T	not provided [RCV001581456]	likely benign	10	27092562	27092562	Human		name
150504449	CV1223952	single nucleotide variant	NM_014915.3(ANKRD26):c.531+73A>T	not provided [RCV001621601]	benign	10	27093276	27093276	Human		name
150456022	CV1236829	single nucleotide variant	NM_014915.3(ANKRD26):c.358-68G>A	Thrombocytopenia 2 [RCV002260253]\|not provided [RCV001648565]	benign	10	27093590	27093590	Human	1	name
150470966	CV1248118	single nucleotide variant	NM_014915.3(ANKRD26):c.357+28C>G	Thrombocytopenia 2 [RCV002260281]\|not provided [RCV001671154]	benign	10	27093657	27093657	Human	1	name
150494153	CV1256410	single nucleotide variant	NM_014915.3(ANKRD26):c.358-77C>T	Thrombocytopenia 2 [RCV002260297]\|not provided [RCV001675375]	benign	10	27093599	27093599	Human	1	name
150480647	CV1258765	single nucleotide variant	NM_014915.3(ANKRD26):c.709+91T>A	Thrombocytopenia 2 [RCV002260310]\|not provided [RCV001685895]	benign	10	27086448	27086448	Human	1	name
150487932	CV1262813	single nucleotide variant	NM_014915.3(ANKRD26):c.740+85A>G	Thrombocytopenia 2 [RCV002260328]\|not provided [RCV001687211]	benign	10	27082718	27082718	Human	1	name
150475576	CV1263522	single nucleotide variant	NM_014915.3(ANKRD26):c.740+82A>G	not provided [RCV001685045]	benign	10	27082721	27082721	Human		name
150441621	CV1265813	single nucleotide variant	NM_014915.3(ANKRD26):c.639-63A>T	not provided [RCV001690538]	benign	10	27086672	27086672	Human		name
150489653	CV1267480	single nucleotide variant	NM_014915.3(ANKRD26):c.709+57A>G	not provided [RCV001687503]	benign	10	27086482	27086482	Human		name
150499057	CV1270757	single nucleotide variant	NM_014915.3(ANKRD26):c.243-76G>A	not provided [RCV001689306]	benign	10	27093875	27093875	Human		name
150436386	CV1270952	single nucleotide variant	NM_014915.3(ANKRD26):c.531+38A>G	Thrombocytopenia 2 [RCV002260353]\|not provided [RCV001689502]	benign	10	27093311	27093311	Human	1	name
150476927	CV1271972	single nucleotide variant	NM_014915.3(ANKRD26):c.531+42G>A	Thrombocytopenia 2 [RCV002260350]\|not provided [RCV001696257]	benign	10	27093307	27093307	Human	1	name
150449908	CV1273696	single nucleotide variant	NM_014915.3(ANKRD26):c.639-21G>A	not provided [RCV001691796]	benign	10	27086630	27086630	Human		name
150478075	CV1281827	single nucleotide variant	NM_014915.3(ANKRD26):c.639-88T>C	not provided [RCV001714232]	benign	10	27086697	27086697	Human		name
150441722	CV1287613	single nucleotide variant	NM_014915.3(ANKRD26):c.741-36T>G	Thrombocytopenia 2 [RCV002260399]\|not provided [RCV001725333]	benign	10	27079197	27079197	Human	1	name
150534359	CV1299395	single nucleotide variant	NM_014915.3(ANKRD26):c.4724+5G>C	not provided [RCV001757088]	uncertain significance	10	27014489	27014489	Human		name
150536795	CV1302982	single nucleotide variant	NM_014915.3(ANKRD26):c.4216-2A>C	not provided [RCV001763727]	uncertain significance	10	27017794	27017794	Human		name
151354641	CV1327708	single nucleotide variant	NM_014915.3(ANKRD26):c.1208-3T>C	not provided [RCV002542546]\|not specified [RCV001819183]	likely benign	10	27066551	27066551	Human		name
151355664	CV1328731	single nucleotide variant	NM_014915.3(ANKRD26):c.2559+3A>G	ANKRD26-related disorder [RCV003948749]\|not provided [RCV002545161]\|not specified [RCV001820736]	benign\|likely benign	10	27037868	27037868	Human	1	name , alternate_id
151356474	CV1329238	single nucleotide variant	NM_014915.3(ANKRD26):c.4724+2T>A	not specified [RCV001822827]	uncertain significance	10	27014492	27014492	Human		name
151354313	CV1329446	single nucleotide variant	NM_014915.3(ANKRD26):c.4953+1G>T	not specified [RCV001817809]	uncertain significance	10	27012881	27012881	Human		name
151354322	CV1329455	single nucleotide variant	NM_014915.3(ANKRD26):c.1269+3A>G	not provided [RCV003728039]\|not specified [RCV001817818]	uncertain significance	10	27066484	27066484	Human		name
151354475	CV1329608	single nucleotide variant	NM_014915.3(ANKRD26):c.1363+1G>T	not specified [RCV001817972]	uncertain significance	10	27063987	27063987	Human		name
156170471	CV1867065	single nucleotide variant	NM_014915.3(ANKRD26):c.1462+1G>A	not provided [RCV002508617]	uncertain significance	10	27061143	27061143	Human		name
156020911	CV1882302	single nucleotide variant	NM_014915.3(ANKRD26):c.4086-4G>A	not provided [RCV003077615]	benign	10	27022691	27022691	Human		name
156221088	CV1899794	single nucleotide variant	NM_014915.3(ANKRD26):c.1463-4T>G	not provided [RCV003085000]	likely benign	10	27060544	27060544	Human		name
156318504	CV1900155	single nucleotide variant	NM_014915.3(ANKRD26):c.1077+5G>C	not provided [RCV003088858]	uncertain significance	10	27077333	27077333	Human		name
156359031	CV1904173	single nucleotide variant	NM_014915.3(ANKRD26):c.1815-3A>G	not provided [RCV002581597]	uncertain significance	10	27046526	27046526	Human		name
156101669	CV1907142	duplication	NM_014915.3(ANKRD26):c.1565-4dup	ANKRD26-related disorder [RCV003906507]\|not provided [RCV003080624]	benign\|likely benign\|conflicting interpretations of pathogenicity	10	27053393	27053394	Human	1	name , alternate_id
156025127	CV1922461	single nucleotide variant	NM_014915.3(ANKRD26):c.874+10T>A	not provided [RCV002636904]	uncertain significance	10	27077623	27077623	Human		name
156410405	CV1932328	single nucleotide variant	NM_014915.3(ANKRD26):c.3807+3A>G	not provided [RCV002607854]	uncertain significance	10	27033222	27033222	Human		name
156069058	CV1971710	single nucleotide variant	NM_014915.3(ANKRD26):c.741-14T>G	not provided [RCV002591217]	uncertain significance	10	27079175	27079175	Human		name
156258602	CV1977444	single nucleotide variant	NM_014915.3(ANKRD26):c.813+17T>A	not provided [RCV002597704]	likely benign	10	27079072	27079072	Human		name
156247756	CV2044810	single nucleotide variant	NM_014915.3(ANKRD26):c.358-16G>T	not provided [RCV002805902]	likely benign	10	27093538	27093538	Human		name
156288981	CV2047118	single nucleotide variant	NM_014915.3(ANKRD26):c.1636-9T>C	not provided [RCV002770684]	likely benign	10	27048988	27048988	Human		name
156215011	CV2047486	single nucleotide variant	NM_014915.3(ANKRD26):c.1269+7T>C	not provided [RCV002790398]	likely benign	10	27066480	27066480	Human		name
156217620	CV2047701	single nucleotide variant	NM_014915.3(ANKRD26):c.242+13G>T	not provided [RCV002790506]	benign	10	27100072	27100072	Human		name
156056856	CV2089897	single nucleotide variant	NM_014915.3(ANKRD26):c.2697+4T>C	not provided [RCV002867970]	uncertain significance	10	27037182	27037182	Human		name
11549600	CV253723	single nucleotide variant	NM_014915.3(ANKRD26):c.3972+3A>G	Thrombocytopenia 2 [RCV000315561]\|not provided [RCV001668536]\|not specified [RCV000250622]	benign\|likely benign	10	27028849	27028849	Human	1	name
11548251	CV253729	single nucleotide variant	NM_014915.3(ANKRD26):c.2376-4G>A	Thrombocytopenia 2 [RCV000385311]\|not provided [RCV000954133]\|not specified [RCV000248836]	benign\|likely benign	10	27038058	27038058	Human	1	name
11547852	CV253732	single nucleotide variant	NM_014915.3(ANKRD26):c.1564+6T>C	Thrombocytopenia 2 [RCV000405995]\|not provided [RCV001636796]\|not specified [RCV000248303]	benign\|likely benign	10	27060339	27060339	Human	1	name
401795846	CV2742798	deletion	NM_014915.3(ANKRD26):c.1636-8del	Thrombocytopenia 2 [RCV003325296]	uncertain significance	10	27048987	27048987	Human	1	name
401938202	CV2813066	deletion	NM_014915.3(ANKRD26):c.243-69del	not provided [RCV003417288]	benign	10	27093868	27093868	Human		name
405082364	CV2864933	single nucleotide variant	NM_014915.3(ANKRD26):c.2559+6T>A	not provided [RCV003549328]	uncertain significance	10	27037865	27037865	Human		name
405194785	CV2868583	single nucleotide variant	NM_014915.3(ANKRD26):c.1491+8G>A	not provided [RCV003550717]	likely benign	10	27060504	27060504	Human		name
405233038	CV2965413	single nucleotide variant	NM_014915.3(ANKRD26):c.3807+6T>G	not provided [RCV003682573]	uncertain significance	10	27033219	27033219	Human		name
404986990	CV3001635	single nucleotide variant	NM_014915.3(ANKRD26):c.4086-3C>A	not provided [RCV003691924]	uncertain significance	10	27022690	27022690	Human		name
405004807	CV3016467	single nucleotide variant	NM_014915.3(ANKRD26):c.242+20C>G	not provided [RCV003693450]	likely benign	10	27100065	27100065	Human		name
405044225	CV3017588	single nucleotide variant	NM_014915.3(ANKRD26):c.813+11C>G	not provided [RCV003696545]	likely benign	10	27079078	27079078	Human		name
405150845	CV3031357	single nucleotide variant	NM_014915.3(ANKRD26):c.357+19T>C	not provided [RCV003703284]	likely benign	10	27093666	27093666	Human		name
405125772	CV3043494	single nucleotide variant	NM_014915.3(ANKRD26):c.4953+7T>A	not provided [RCV003724282]	likely benign	10	27012875	27012875	Human		name
405140475	CV3045426	single nucleotide variant	NM_014915.3(ANKRD26):c.3655-3C>T	not provided [RCV003725514]	uncertain significance	10	27033380	27033380	Human		name
405123197	CV3046575	single nucleotide variant	NM_014915.3(ANKRD26):c.4507-5T>A	not provided [RCV003724117]	likely benign	10	27014716	27014716	Human		name
405217256	CV3048794	single nucleotide variant	NM_014915.3(ANKRD26):c.4085+6A>G	not provided [RCV003732813]	uncertain significance	10	27024441	27024441	Human		name
405240492	CV3060812	single nucleotide variant	NM_014915.3(ANKRD26):c.2020-2A>G	not provided [RCV003737160]	uncertain significance	10	27043569	27043569	Human		name
405240233	CV3064299	single nucleotide variant	NM_014915.3(ANKRD26):c.2161+5G>A	not provided [RCV003737085]	uncertain significance	10	27043421	27043421	Human		name
405155614	CV3064832	single nucleotide variant	NM_014915.3(ANKRD26):c.1269+1G>A	not provided [RCV003726725]	uncertain significance	10	27066486	27066486	Human		name
405153277	CV3068601	single nucleotide variant	NM_014915.3(ANKRD26):c.1565-6T>C	not provided [RCV003726571]	likely benign\|conflicting interpretations of pathogenicity	10	27053396	27053396	Human		name
405238393	CV3077837	single nucleotide variant	NM_014915.3(ANKRD26):c.5000-7A>G	not provided [RCV003736278]	likely benign	10	27005730	27005730	Human		name
11612341	CV310140	deletion	NM_014915.3(ANKRD26):c.1986-3del	Thrombocytopenia 2 [RCV002259795]\|Thrombocytopenia [RCV000407644]\|not provided [RCV001683209]	benign\|likely benign	10	27044193	27044193	Human	3	name
11607293	CV310145	single nucleotide variant	NM_014915.3(ANKRD26):c.531+10A>T	Thrombocytopenia 2 [RCV000341474]\|not provided [RCV000884457]\|not specified [RCV001820872]	benign\|uncertain significance	10	27093339	27093339	Human	1	name
405029559	CV3129912	single nucleotide variant	NM_014915.3(ANKRD26):c.740+20T>C	not provided [RCV003830510]	benign	10	27082783	27082783	Human		name
405120824	CV3131523	single nucleotide variant	NM_014915.3(ANKRD26):c.1078-7T>C	not provided [RCV003837387]	likely benign	10	27067293	27067293	Human		name
404994815	CV3132612	single nucleotide variant	NM_014915.3(ANKRD26):c.740+20T>A	not provided [RCV003827551]	likely benign	10	27082783	27082783	Human		name
405130793	CV3133400	single nucleotide variant	NM_014915.3(ANKRD26):c.741-17A>G	not provided [RCV003838370]	likely benign	10	27079178	27079178	Human		name
405109064	CV3136704	single nucleotide variant	NM_014915.3(ANKRD26):c.4086-8T>C	not provided [RCV003835858]	likely benign	10	27022695	27022695	Human		name
405020967	CV3139198	single nucleotide variant	NM_014915.3(ANKRD26):c.741-10T>C	not provided [RCV003829840]	likely benign	10	27079171	27079171	Human		name
11599372	CV315207	single nucleotide variant	NM_014915.3(ANKRD26):c.3655-4T>C	ANKRD26-related disorder [RCV003920233]\|Thrombocytopenia 2 [RCV000264921]\|not provided [RCV000900953]	benign\|likely benign	10	27033381	27033381	Human	1	name , alternate_id
11635486	CV315228	duplication	NM_014915.3(ANKRD26):c.1986-3dup	Thrombocytopenia 2 [RCV002259794]\|Thrombocytopenia [RCV000350757]\|not provided [RCV001642929]\|not specified [RCV001795919]	benign\|uncertain significance	10	27044192	27044193	Human	3	name
405204933	CV3165610	single nucleotide variant	NM_014915.3(ANKRD26):c.531+19T>C	not provided [RCV003861276]	likely benign	10	27093330	27093330	Human		name
405235585	CV3168672	single nucleotide variant	NM_014915.3(ANKRD26):c.1635+7T>C	not provided [RCV003866146]	likely benign	10	27053313	27053313	Human		name
402522642	CV3175752	single nucleotide variant	NM_014915.3(ANKRD26):c.242+16A>G	not provided [RCV003879852]	benign	10	27100069	27100069	Human		name
402512440	CV3178462	single nucleotide variant	NM_014915.3(ANKRD26):c.2698-3T>C	not provided [RCV003879079]	uncertain significance	10	27035755	27035755	Human		name
405259635	CV3189694	single nucleotide variant	NM_014915.3(ANKRD26):c.1364-5C>A	ANKRD26-related disorder [RCV003894287]\|Thrombocytopenia 2 [RCV005055229]	likely benign\|uncertain significance	10	27061247	27061247	Human	1	name , alternate_id
405264963	CV3190076	deletion	NM_014915.3(ANKRD26):c.2161+6del	ANKRD26-related disorder [RCV003897115]	likely benign	10	27043420	27043420	Human		name , trait , alternate_id
405288671	CV3193778	deletion	NM_014915.3(ANKRD26):c.1462+4del	ANKRD26-related disorder [RCV003982784]\|not provided [RCV004775540]	likely benign\|uncertain significance	10	27061140	27061140	Human	1	name , alternate_id
405295105	CV3211043	duplication	NM_014915.3(ANKRD26):c.4954-4dup	ANKRD26-related disorder [RCV003937044]	likely benign	10	27006965	27006966	Human		name , trait , alternate_id
11608658	CV321266	single nucleotide variant	NM_014915.3(ANKRD26):c.1565-4T>C	Thrombocytopenia 2 [RCV000357980]\|not provided [RCV001764267]	likely benign\|conflicting interpretations of pathogenicity\|uncertain significance	10	27053394	27053394	Human	1	name
11609291	CV321274	single nucleotide variant	NM_014915.3(ANKRD26):c.1269+7T>A	Thrombocytopenia 2 [RCV000366081]\|not provided [RCV000982766]	likely benign\|uncertain significance	10	27066480	27066480	Human	1	name
11612236	CV321832	single nucleotide variant	NM_014915.3(ANKRD26):c.1635+9T>C	Thrombocytopenia 2 [RCV000405616]\|not provided [RCV002520581]\|not specified [RCV001820870]	benign\|likely benign\|uncertain significance	10	27053311	27053311	Human	1	name
408382970	CV3506225	single nucleotide variant	NM_014915.3(ANKRD26):c.2698-6A>G	ANKRD26-related disorder [RCV004730288]	likely benign	10	27035758	27035758	Human		name , trait , alternate_id
408379223	CV3506786	single nucleotide variant	NM_014915.3(ANKRD26):c.4999+1G>A	ANKRD26-related disorder [RCV004728319]	uncertain significance	10	27006916	27006916	Human		name , trait , alternate_id
408385792	CV3520353	duplication	NM_014915.3(ANKRD26):c.2161+2dup	not provided [RCV004760174]	uncertain significance	10	27043423	27043424	Human		name
408391384	CV3521314	single nucleotide variant	NM_014915.3(ANKRD26):c.3654+1G>A	not provided [RCV004763136]	uncertain significance	10	27034795	27034795	Human		name
408391590	CV3523268	single nucleotide variant	NM_014915.3(ANKRD26):c.2698-2A>G	not provided [RCV004770641]	uncertain significance	10	27035754	27035754	Human		name
408387516	CV3524560	single nucleotide variant	NM_014915.3(ANKRD26):c.4999+5G>A	not provided [RCV004768434]	uncertain significance	10	27006912	27006912	Human		name
408392137	CV3526492	single nucleotide variant	NM_014915.3(ANKRD26):c.4954-1G>T	not provided [RCV004775741]	uncertain significance	10	27006963	27006963	Human		name
408385807	CV3528691	single nucleotide variant	NM_014915.3(ANKRD26):c.639-12T>C	not provided [RCV004772524]	uncertain significance	10	27086621	27086621	Human		name
597716839	CV3733297	single nucleotide variant	NM_014915.3(ANKRD26):c.2019+6G>A	not provided [RCV005052487]	uncertain significance	10	27044151	27044151	Human		name
597916319	CV3737397	single nucleotide variant	NM_014915.3(ANKRD26):c.357+17T>A	not provided [RCV005074186]	benign	10	27093668	27093668	Human		name
597904281	CV3738273	single nucleotide variant	NM_014915.3(ANKRD26):c.357+15G>C	not provided [RCV005072695]	likely benign	10	27093670	27093670	Human		name
597915294	CV3740709	single nucleotide variant	NM_014915.3(ANKRD26):c.709+13A>G	not provided [RCV005074046]	likely benign	10	27086526	27086526	Human		name
597884805	CV3745493	single nucleotide variant	NM_014915.3(ANKRD26):c.1492-5T>A	not provided [RCV005070329]	likely benign	10	27060422	27060422	Human		name
597959941	CV3746135	single nucleotide variant	NM_014915.3(ANKRD26):c.741-15A>G	not provided [RCV005081383]	likely benign	10	27079176	27079176	Human		name
597926588	CV3748921	single nucleotide variant	NM_014915.3(ANKRD26):c.2697+3A>G	not provided [RCV005075377]	uncertain significance	10	27037183	27037183	Human		name
597909667	CV3749451	single nucleotide variant	NM_014915.3(ANKRD26):c.358-19C>T	not provided [RCV005073299]	likely benign	10	27093541	27093541	Human		name
597958583	CV3751920	single nucleotide variant	NM_014915.3(ANKRD26):c.1492-7C>T	not provided [RCV005081050]	likely benign	10	27060424	27060424	Human		name
597967694	CV3760707	single nucleotide variant	NM_014915.3(ANKRD26):c.1269+4C>T	not provided [RCV005083274]	uncertain significance	10	27066483	27066483	Human		name
597878881	CV3783175	single nucleotide variant	NM_014915.3(ANKRD26):c.243-13G>A	not provided [RCV005123877]	likely benign	10	27093812	27093812	Human		name
597957573	CV3800440	single nucleotide variant	NM_014915.3(ANKRD26):c.243-18G>A	not provided [RCV005137532]	likely benign	10	27093817	27093817	Human		name
597908076	CV3806067	single nucleotide variant	NM_014915.3(ANKRD26):c.4725-7T>C	not provided [RCV005153825]	likely benign	10	27013117	27013117	Human		name
597846956	CV3828084	single nucleotide variant	NM_014915.3(ANKRD26):c.243-13G>T	not provided [RCV005173159]	likely benign	10	27093812	27093812	Human		name
597903288	CV3851531	single nucleotide variant	NM_014915.3(ANKRD26):c.4507-4T>A	not provided [RCV005202308]	likely benign	10	27014715	27014715	Human		name
597844988	CV3880346	single nucleotide variant	NM_014915.3(ANKRD26):c.1986-2A>T	not provided [RCV005227234]	uncertain significance	10	27044192	27044192	Human		name
15139620	CV759953	single nucleotide variant	NM_014915.3(ANKRD26):c.4953+3T>G	not provided [RCV000921539]\|not specified [RCV004800638]	likely benign\|uncertain significance	10	27012879	27012879	Human		name
28908857	CV868467	single nucleotide variant	NM_014915.3(ANKRD26):c.2697+9A>G	Thrombocytopenia 2 [RCV001108062]\|not provided [RCV002556115]\|not specified [RCV001819818]	benign\|likely benign	10	27037177	27037177	Human	1	name
28902705	CV868468	single nucleotide variant	NM_014915.3(ANKRD26):c.1492-6A>G	Thrombocytopenia 2 [RCV001104775]\|not provided [RCV003718323]	likely benign\|uncertain significance	10	27060423	27060423	Human	1	name
150339925	CV1168205	single nucleotide variant	NM_014915.3(ANKRD26):c.709+178A>G	not provided [RCV001534754]	benign	10	27086361	27086361	Human		name
150331130	CV1169392	single nucleotide variant	NM_014915.3(ANKRD26):c.243-124G>T	not provided [RCV001536347]	likely benign	10	27093923	27093923	Human		name
150406504	CV1177291	single nucleotide variant	NM_014915.3(ANKRD26):c.1077+73A>G	not provided [RCV001545273]	likely benign	10	27077265	27077265	Human		name
150423215	CV1184348	single nucleotide variant	NM_014915.3(ANKRD26):c.1985+25T>C	not provided [RCV001555023]	likely benign	10	27046328	27046328	Human		name
150425349	CV1184350	single nucleotide variant	NM_014915.3(ANKRD26):c.1463-94C>T	not provided [RCV001557883]	likely benign	10	27060634	27060634	Human		name
150423717	CV1184353	single nucleotide variant	NM_014915.3(ANKRD26):c.741-278T>C	not provided [RCV001555700]	likely benign	10	27079439	27079439	Human		name
150422319	CV1194327	duplication	NM_014915.3(ANKRD26):c.813+160dup	not provided [RCV001570986]	likely benign	10	27078910	27078911	Human		name
150439594	CV1201571	single nucleotide variant	NM_014915.3(ANKRD26):c.1635+24C>T	not provided [RCV001583383]	likely benign	10	27053296	27053296	Human		name
150476615	CV1203065	single nucleotide variant	NM_014915.3(ANKRD26):c.243-238G>T	not provided [RCV001589659]	likely benign	10	27094037	27094037	Human		name
150445614	CV1215524	single nucleotide variant	NM_014915.3(ANKRD26):c.531+304G>A	not provided [RCV001611117]	benign	10	27093045	27093045	Human		name
150455042	CV1220398	deletion	NM_014915.3(ANKRD26):c.813+178del	not provided [RCV001612491]	benign	10	27078911	27078911	Human		name
150484225	CV1222446	single nucleotide variant	NM_014915.3(ANKRD26):c.1364-30A>G	not provided [RCV001617449]	benign	10	27061272	27061272	Human		name
150501627	CV1224233	single nucleotide variant	NM_014915.3(ANKRD26):c.1077+75T>G	not provided [RCV001620874]	benign	10	27077263	27077263	Human		name
150500007	CV1224702	single nucleotide variant	NM_014915.3(ANKRD26):c.740+269G>A	not provided [RCV001620534]	benign	10	27082534	27082534	Human		name
150440388	CV1233379	single nucleotide variant	NM_014915.3(ANKRD26):c.709+100G>C	Thrombocytopenia 2 [RCV002260240]\|not provided [RCV001645067]	benign	10	27086439	27086439	Human	1	name
150475958	CV1239812	single nucleotide variant	NM_014915.3(ANKRD26):c.741-235C>T	not provided [RCV001651989]	benign	10	27079396	27079396	Human		name
150466032	CV1240340	single nucleotide variant	NM_014915.3(ANKRD26):c.3808-86C>T	not provided [RCV001650101]	benign	10	27029442	27029442	Human		name
150503662	CV1241850	single nucleotide variant	NM_014915.3(ANKRD26):c.1564+25T>C	not provided [RCV001657442]	benign	10	27060320	27060320	Human		name
150430614	CV1243395	single nucleotide variant	NM_014915.3(ANKRD26):c.639-255G>A	not provided [RCV001663012]	benign	10	27086864	27086864	Human		name
150502167	CV1255225	single nucleotide variant	NM_014915.3(ANKRD26):c.741-297C>G	not provided [RCV001677144]	benign	10	27079458	27079458	Human		name
150504387	CV1257986	single nucleotide variant	NM_014915.3(ANKRD26):c.1564+73A>G	not provided [RCV001677675]	benign	10	27060272	27060272	Human		name
150506965	CV1258099	single nucleotide variant	NM_014915.3(ANKRD26):c.2559+89G>T	not provided [RCV001678316]	benign	10	27037782	27037782	Human		name
150479298	CV1258231	single nucleotide variant	NM_014915.3(ANKRD26):c.1463-93G>A	Thrombocytopenia 2 [RCV002260308]\|not provided [RCV001685649]	benign	10	27060633	27060633	Human	1	name
150482548	CV1261639	single nucleotide variant	NM_014915.3(ANKRD26):c.3654+79A>G	not provided [RCV001686242]	benign	10	27034717	27034717	Human		name
150475431	CV1263501	deletion	NM_014915.3(ANKRD26):c.814-232del	not provided [RCV001685024]	benign	10	27077925	27077925	Human		name
150492197	CV1266606	single nucleotide variant	NM_014915.3(ANKRD26):c.2697+98G>A	not provided [RCV001687928]	benign	10	27037088	27037088	Human		name
150460013	CV1268428	single nucleotide variant	NM_014915.3(ANKRD26):c.2697+58A>G	Thrombocytopenia 2 [RCV002260346]\|not provided [RCV001693425]	benign	10	27037128	27037128	Human	1	name
150470712	CV1269905	duplication	NM_014915.3(ANKRD26):c.242+216dup	not provided [RCV001695192]	benign	10	27099866	27099867	Human		name
150446706	CV1271907	single nucleotide variant	NM_014915.3(ANKRD26):c.740+295T>C	not provided [RCV001691321]	benign	10	27082508	27082508	Human		name
150474487	CV1272343	single nucleotide variant	NM_014915.3(ANKRD26):c.4507-54A>G	not provided [RCV001695881]	benign	10	27014765	27014765	Human		name
150472991	CV1272580	deletion	NM_014915.3(ANKRD26):c.2559+34del	not provided [RCV001695636]	benign	10	27037837	27037837	Human		name
150449131	CV1275632	single nucleotide variant	NM_014915.3(ANKRD26):c.2162-60C>T	not provided [RCV001708087]	benign	10	27040238	27040238	Human		name
150452407	CV1276725	duplication	NM_014915.3(ANKRD26):c.4215+88dup	not provided [RCV001708515]	benign	10	27022459	27022460	Human		name
150489363	CV1278947	single nucleotide variant	NM_014915.3(ANKRD26):c.3655-85G>A	not provided [RCV001716276]	benign	10	27033462	27033462	Human		name
150490528	CV1279784	single nucleotide variant	NM_014915.3(ANKRD26):c.3808-85G>A	not provided [RCV001716489]	benign	10	27029441	27029441	Human		name
150510169	CV1286711	single nucleotide variant	NM_014915.3(ANKRD26):c.1492-21T>G	not provided [RCV001720946]	benign	10	27060438	27060438	Human		name
150441727	CV1287614	single nucleotide variant	NM_014915.3(ANKRD26):c.740+109C>T	not provided [RCV001725334]	benign	10	27082694	27082694	Human		name
151355148	CV1328215	single nucleotide variant	NM_014915.3(ANKRD26):c.2162-12T>C	not provided [RCV005057653]\|not specified [RCV001820220]	likely benign	10	27040190	27040190	Human		name
151355331	CV1328398	single nucleotide variant	NM_014915.3(ANKRD26):c.4724+11A>G	not specified [RCV001820403]	uncertain significance	10	27014483	27014483	Human		name
151356129	CV1328893	single nucleotide variant	NM_014915.3(ANKRD26):c.1269+10A>G	not provided [RCV005095271]\|not specified [RCV001822482]	likely benign\|uncertain significance	10	27066477	27066477	Human		name
156258050	CV1906356	single nucleotide variant	NM_014915.3(ANKRD26):c.4725-10A>G	Thrombocytopenia 2 [RCV003154270]\|not provided [RCV003086341]	uncertain significance	10	27013120	27013120	Human	1	name
156127932	CV1953067	single nucleotide variant	NM_014915.3(ANKRD26):c.3807+12A>G	not provided [RCV002572116]	benign	10	27033213	27033213	Human		name
156414904	CV1955184	deletion	NM_014915.3(ANKRD26):c.1462+14del	not provided [RCV002588870]	benign	10	27061130	27061130	Human		name
156175649	CV1956561	single nucleotide variant	NM_014915.3(ANKRD26):c.3878+15A>G	not provided [RCV002573952]	likely benign	10	27029271	27029271	Human		name
156102360	CV1960456	single nucleotide variant	NM_014915.3(ANKRD26):c.1492-18G>A	not provided [RCV002570895]\|not specified [RCV004587359]	likely benign	10	27060435	27060435	Human		name
156346177	CV1970540	single nucleotide variant	NM_014915.3(ANKRD26):c.1364-16A>G	not provided [RCV002601536]	likely benign	10	27061258	27061258	Human		name
156238507	CV1973104	single nucleotide variant	NM_014915.3(ANKRD26):c.1814+18T>A	not provided [RCV002597066]	likely benign	10	27048783	27048783	Human		name
156241977	CV1973247	single nucleotide variant	NM_014915.3(ANKRD26):c.2162-20T>C	not provided [RCV002597176]	likely benign	10	27040198	27040198	Human		name
156056132	CV1974576	single nucleotide variant	NM_014915.3(ANKRD26):c.2020-15T>C	not provided [RCV002590820]	likely benign	10	27043582	27043582	Human		name
156411175	CV1976134	single nucleotide variant	NM_014915.3(ANKRD26):c.1462+17C>T	not provided [RCV002587406]	likely benign	10	27061127	27061127	Human		name
156419616	CV1977696	single nucleotide variant	NM_014915.3(ANKRD26):c.1815-14T>A	not provided [RCV002612855]	uncertain significance	10	27046537	27046537	Human		name
156078127	CV1979447	single nucleotide variant	NM_014915.3(ANKRD26):c.2560-15T>A	not provided [RCV002621455]	likely benign	10	27037338	27037338	Human		name
156052542	CV2006843	single nucleotide variant	NM_014915.3(ANKRD26):c.1492-19T>C	not provided [RCV002659413]	likely benign	10	27060436	27060436	Human		name
156022603	CV2040762	single nucleotide variant	NM_014915.3(ANKRD26):c.1565-14T>C	not provided [RCV002795658]	benign	10	27053404	27053404	Human		name
155952701	CV2043810	single nucleotide variant	NM_014915.3(ANKRD26):c.2697+17T>C	not provided [RCV002775857]	benign	10	27037169	27037169	Human		name
156040280	CV2044006	duplication	NM_014915.3(ANKRD26):c.3808-15dup	Thrombocytopenia 2 [RCV005233018]\|not provided [RCV002781465]	benign	10	27029370	27029371	Human	1	name
156248445	CV2044833	single nucleotide variant	NM_014915.3(ANKRD26):c.3808-15T>A	Thrombocytopenia 2 [RCV005233019]\|not provided [RCV002805921]	likely benign	10	27029371	27029371	Human	1	name
156022705	CV2081648	single nucleotide variant	NM_014915.3(ANKRD26):c.4999+12A>G	not provided [RCV002866686]	likely benign	10	27006905	27006905	Human		name
156313415	CV2089374	single nucleotide variant	NM_014915.3(ANKRD26):c.1635+19A>G	not provided [RCV002898849]	likely benign	10	27053301	27053301	Human		name
156256909	CV2090084	single nucleotide variant	NM_014915.3(ANKRD26):c.4216-20A>C	not provided [RCV002877133]	likely benign	10	27017812	27017812	Human		name
156259115	CV2090182	single nucleotide variant	NM_014915.3(ANKRD26):c.1814+14A>G	not provided [RCV002877207]	likely benign	10	27048787	27048787	Human		name
156275540	CV2164371	single nucleotide variant	NM_014915.3(ANKRD26):c.1462+12A>G	not provided [RCV003027138]	uncertain significance	10	27061132	27061132	Human		name
156258735	CV2185446	single nucleotide variant	NM_014915.3(ANKRD26):c.1985+12G>A	not provided [RCV003044044]	likely benign	10	27046341	27046341	Human		name
156369109	CV2190591	single nucleotide variant	NM_014915.3(ANKRD26):c.2560-20A>T	not provided [RCV003066156]	likely benign	10	27037343	27037343	Human		name
11545253	CV253730	single nucleotide variant	NM_014915.3(ANKRD26):c.2376-16A>G	Thrombocytopenia 2 [RCV001801655]\|not provided [RCV001651202]\|not specified [RCV000244882]	benign	10	27038070	27038070	Human	1	name
11544276	CV253733	single nucleotide variant	NM_014915.3(ANKRD26):c.1462+17C>A	Thrombocytopenia 2 [RCV001801654]\|not provided [RCV001668534]\|not specified [RCV000243571]	benign	10	27061127	27061127	Human	1	name
11545115	CV253736	single nucleotide variant	NM_014915.3(ANKRD26):c.1207+15A>G	Thrombocytopenia 2 [RCV000273840]\|not provided [RCV001582867]\|not specified [RCV000244706]	benign\|likely benign	10	27067142	27067142	Human	1	name
401828717	CV2743052	single nucleotide variant	NM_014915.3(ANKRD26):c.1815-13G>A	not provided [RCV003325760]	uncertain significance	10	27046536	27046536	Human		name
405241796	CV2901550	single nucleotide variant	NM_014915.3(ANKRD26):c.1270-11A>G	not provided [RCV003557553]	likely benign	10	27064092	27064092	Human		name
405101686	CV2942068	single nucleotide variant	NM_014915.3(ANKRD26):c.1364-18T>C	not provided [RCV003666262]	likely benign	10	27061260	27061260	Human		name
405155081	CV2949465	single nucleotide variant	NM_014915.3(ANKRD26):c.1078-17G>T	not provided [RCV003674276]	likely benign	10	27067303	27067303	Human		name
405137020	CV2954366	single nucleotide variant	NM_014915.3(ANKRD26):c.2560-12A>G	not provided [RCV003672901]	uncertain significance	10	27037335	27037335	Human		name
405132020	CV2959168	single nucleotide variant	NM_014915.3(ANKRD26):c.4999+20G>C	not provided [RCV003668464]	likely benign	10	27006897	27006897	Human		name
402501827	CV3010660	single nucleotide variant	NM_014915.3(ANKRD26):c.1364-16A>T	not provided [RCV003688576]	likely benign	10	27061258	27061258	Human		name
405027404	CV3015490	single nucleotide variant	NM_014915.3(ANKRD26):c.4999+19T>C	not provided [RCV003695312]	likely benign	10	27006898	27006898	Human		name
405132894	CV3022012	single nucleotide variant	NM_014915.3(ANKRD26):c.2559+13T>A	not provided [RCV003701830]	likely benign	10	27037858	27037858	Human		name
405199311	CV3041059	duplication	NM_014915.3(ANKRD26):c.1462+14dup	not provided [RCV003707288]	benign	10	27061129	27061130	Human		name
405244587	CV3050696	single nucleotide variant	NM_014915.3(ANKRD26):c.2161+10T>C	not provided [RCV003720028]	likely benign	10	27043416	27043416	Human		name
11606213	CV310137	single nucleotide variant	NM_014915.3(ANKRD26):c.2559+10T>A	Thrombocytopenia 2 [RCV000328649]\|not provided [RCV002522150]\|not specified [RCV001820869]	benign\|likely benign\|uncertain significance	10	27037861	27037861	Human	1	name
405131266	CV3115086	single nucleotide variant	NM_014915.3(ANKRD26):c.3808-12T>G	not provided [RCV003815931]	likely benign	10	27029368	27029368	Human		name
405215895	CV3124584	single nucleotide variant	NM_014915.3(ANKRD26):c.1462+17C>G	not provided [RCV003823946]	likely benign	10	27061127	27061127	Human		name
405218585	CV3135650	single nucleotide variant	NM_014915.3(ANKRD26):c.2559+17T>A	not provided [RCV003824275]	likely benign	10	27037854	27037854	Human		name
405077133	CV3136927	single nucleotide variant	NM_014915.3(ANKRD26):c.1815-15A>G	not provided [RCV003833825]	likely benign	10	27046538	27046538	Human		name
405078238	CV3136948	single nucleotide variant	NM_014915.3(ANKRD26):c.2375+11C>T	not provided [RCV003833846]	likely benign	10	27039954	27039954	Human		name
405215076	CV3143208	single nucleotide variant	NM_014915.3(ANKRD26):c.1363+17A>G	not provided [RCV003846371]	likely benign	10	27063971	27063971	Human		name
405190815	CV3157031	single nucleotide variant	NM_014915.3(ANKRD26):c.1462+14A>G	not provided [RCV003859719]	uncertain significance	10	27061130	27061130	Human		name
405131314	CV3163704	single nucleotide variant	NM_014915.3(ANKRD26):c.3879-18T>G	not provided [RCV003854692]	likely benign	10	27028963	27028963	Human		name
405255488	CV3172469	single nucleotide variant	NM_014915.3(ANKRD26):c.3878+19C>T	not provided [RCV003872407]	likely benign	10	27029267	27029267	Human		name
11610057	CV321798	deletion	NM_014915.3(ANKRD26):c.68_69del	Thrombocytopenia 2 [RCV002259793]\|Thrombocytopenia [RCV000376096]\|not provided [RCV001642927]	benign\|likely benign	10	27005521	27005522	Human	3	name
408381498	CV3523892	single nucleotide variant	NM_014915.3(ANKRD26):c.3973-13T>G	not provided [RCV004766290]	uncertain significance	10	27024572	27024572	Human		name
408383794	CV3525844	single nucleotide variant	NM_014915.3(ANKRD26):c.2560-11T>C	not specified [RCV004766754]	likely benign	10	27037334	27037334	Human		name
597847020	CV3736684	single nucleotide variant	NM_014915.3(ANKRD26):c.1462+18G>A	not provided [RCV005065843]	likely benign	10	27061126	27061126	Human		name
597836192	CV3739820	single nucleotide variant	NM_014915.3(ANKRD26):c.1270-19T>C	not provided [RCV005064040]	likely benign	10	27064100	27064100	Human		name
597882580	CV3744985	single nucleotide variant	NM_014915.3(ANKRD26):c.4086-20C>T	not provided [RCV005070010]	likely benign	10	27022707	27022707	Human		name
597938151	CV3760045	single nucleotide variant	NM_014915.3(ANKRD26):c.1564+17A>G	not provided [RCV005076969]	likely benign	10	27060328	27060328	Human		name
597911090	CV3778210	single nucleotide variant	NM_014915.3(ANKRD26):c.2697+14C>T	not provided [RCV005128749]	likely benign	10	27037172	27037172	Human		name
597887654	CV3787510	single nucleotide variant	NM_014915.3(ANKRD26):c.1491+20T>A	not provided [RCV005125076]	likely benign	10	27060492	27060492	Human		name
597927453	CV3819854	single nucleotide variant	NM_014915.3(ANKRD26):c.3655-20G>A	not provided [RCV005156554]	likely benign	10	27033397	27033397	Human		name
597837299	CV3828755	single nucleotide variant	NM_014915.3(ANKRD26):c.1078-12T>C	not provided [RCV005171448]	likely benign	10	27067298	27067298	Human		name
597832249	CV3830947	single nucleotide variant	NM_014915.3(ANKRD26):c.4086-11C>T	not provided [RCV005170344]	likely benign	10	27022698	27022698	Human		name
597895700	CV3833716	single nucleotide variant	NM_014915.3(ANKRD26):c.1985+12G>T	not provided [RCV005180408]	likely benign	10	27046341	27046341	Human		name
598127364	CV3882621	single nucleotide variant	NM_014915.3(ANKRD26):c.1492-11A>G	Thrombocytopenia 2 [RCV005234151]	uncertain significance	10	27060428	27060428	Human	1	name
598127944	CV3882979	single nucleotide variant	NM_014915.3(ANKRD26):c.1985+19T>G	Thrombocytopenia 2 [RCV005234512]	likely benign	10	27046334	27046334	Human	1	name
28908705	CV868466	single nucleotide variant	NM_014915.3(ANKRD26):c.4725-15C>T	Thrombocytopenia 2 [RCV001107978]\|not provided [RCV003769108]	likely benign\|uncertain significance	10	27013125	27013125	Human	1	name
150340437	CV1168203	single nucleotide variant	NM_014915.3(ANKRD26):c.4215+195G>A	not provided [RCV001535369]	benign	10	27022363	27022363	Human		name
150332909	CV1169390	single nucleotide variant	NM_014915.3(ANKRD26):c.4215+188G>A	not provided [RCV001537069]	benign	10	27022370	27022370	Human		name
150331172	CV1169391	duplication	NM_014915.3(ANKRD26):c.3807+129dup	not provided [RCV001536374]	likely benign	10	27033082	27033083	Human		name
150332540	CV1172094	single nucleotide variant	NM_014915.3(ANKRD26):c.1985+157A>G	not provided [RCV001539088]	likely benign	10	27046196	27046196	Human		name
150410031	CV1177290	single nucleotide variant	NM_014915.3(ANKRD26):c.1985+269T>A	not provided [RCV001546454]	likely benign	10	27046084	27046084	Human		name
150421832	CV1180668	single nucleotide variant	NM_014915.3(ANKRD26):c.3973-326T>C	not provided [RCV001552195]	likely benign	10	27024885	27024885	Human		name
150423772	CV1184347	single nucleotide variant	NM_014915.3(ANKRD26):c.3973-311T>C	not provided [RCV001555773]	likely benign	10	27024870	27024870	Human		name
150423915	CV1184351	single nucleotide variant	NM_014915.3(ANKRD26):c.1463-104T>G	not provided [RCV001555963]	likely benign	10	27060644	27060644	Human		name
150425525	CV1184352	single nucleotide variant	NM_014915.3(ANKRD26):c.1078-129C>T	not provided [RCV001558109]	likely benign	10	27067415	27067415	Human		name
150429357	CV1187578	single nucleotide variant	NM_014915.3(ANKRD26):c.2697+225G>A	not provided [RCV001563492]	likely benign	10	27036961	27036961	Human		name
150427926	CV1187580	single nucleotide variant	NM_014915.3(ANKRD26):c.1815-221T>A	not provided [RCV001561580]	likely benign	10	27046744	27046744	Human		name
150420268	CV1194325	single nucleotide variant	NM_014915.3(ANKRD26):c.4999+282C>T	not provided [RCV001570044]	likely benign	10	27006635	27006635	Human		name
150418065	CV1194326	single nucleotide variant	NM_014915.3(ANKRD26):c.1463-281A>G	not provided [RCV001569048]	likely benign	10	27060821	27060821	Human		name
150415130	CV1198038	deletion	NM_014915.3(ANKRD26):c.2161+249del	not provided [RCV001575260]	likely benign	10	27043177	27043177	Human		name
150418118	CV1198039	single nucleotide variant	NM_014915.3(ANKRD26):c.2020-222A>T	not provided [RCV001576605]	likely benign	10	27043789	27043789	Human		name
150432371	CV1200623	single nucleotide variant	NM_014915.3(ANKRD26):c.3807+194G>A	not provided [RCV001581346]	likely benign	10	27033031	27033031	Human		name
150495697	CV1205071	duplication	NM_014915.3(ANKRD26):c.2161+200dup	not provided [RCV001593563]	likely benign	10	27043219	27043220	Human		name
150452813	CV1205575	duplication	NM_014915.3(ANKRD26):c.1269+231dup	not provided [RCV001585476]	likely benign	10	27066245	27066246	Human		name
150468640	CV1207441	deletion	NM_014915.3(ANKRD26):c.4216-308del	not provided [RCV001588130]	likely benign	10	27018100	27018100	Human		name
150478933	CV1207752	single nucleotide variant	NM_014915.3(ANKRD26):c.1270-281G>A	not provided [RCV001590028]	likely benign	10	27064362	27064362	Human		name
150489928	CV1208528	single nucleotide variant	NM_014915.3(ANKRD26):c.1462+226C>T	not provided [RCV001592389]	likely benign	10	27060918	27060918	Human		name
150514580	CV1212060	single nucleotide variant	NM_014915.3(ANKRD26):c.1077+273T>C	not provided [RCV001599129]	likely benign	10	27077065	27077065	Human		name
150513748	CV1213861	single nucleotide variant	NM_014915.3(ANKRD26):c.4085+132G>T	not provided [RCV001598597]	benign	10	27024315	27024315	Human		name
150446629	CV1215685	duplication	NM_014915.3(ANKRD26):c.2698-136dup	not provided [RCV001611278]	benign	10	27035877	27035878	Human		name
150443592	CV1216518	single nucleotide variant	NM_014915.3(ANKRD26):c.1463-231T>C	not provided [RCV001610817]	benign	10	27060771	27060771	Human		name
150477631	CV1218653	single nucleotide variant	NM_014915.3(ANKRD26):c.2375+226G>T	not provided [RCV001616280]	benign	10	27039739	27039739	Human		name
150456546	CV1219502	single nucleotide variant	NM_014915.3(ANKRD26):c.4507-197T>C	not provided [RCV001612717]	benign	10	27014908	27014908	Human		name
150499837	CV1224665	single nucleotide variant	NM_014915.3(ANKRD26):c.1208-263A>T	not provided [RCV001620497]	benign	10	27066811	27066811	Human		name
150517425	CV1226875	single nucleotide variant	NM_014915.3(ANKRD26):c.3807+136T>C	not provided [RCV001639970]	benign	10	27033089	27033089	Human		name
150516934	CV1227373	single nucleotide variant	NM_014915.3(ANKRD26):c.1364-120T>A	not provided [RCV001639474]	benign	10	27061362	27061362	Human		name
150514478	CV1228529	deletion	NM_014915.3(ANKRD26):c.3807+142del	not provided [RCV001638516]	benign	10	27033083	27033083	Human		name
150513416	CV1229002	single nucleotide variant	NM_014915.3(ANKRD26):c.3807+156G>A	not provided [RCV001637844]	benign	10	27033069	27033069	Human		name
150436454	CV1234065	single nucleotide variant	NM_014915.3(ANKRD26):c.1986-165A>G	not provided [RCV001644192]	benign	10	27044355	27044355	Human		name
150431728	CV1236504	single nucleotide variant	NM_014915.3(ANKRD26):c.3807+309G>T	not provided [RCV001641908]	benign	10	27032916	27032916	Human		name
150480467	CV1239585	single nucleotide variant	NM_014915.3(ANKRD26):c.2698-100C>G	not provided [RCV001652748]	benign	10	27035852	27035852	Human		name
150447373	CV1250818	single nucleotide variant	NM_014915.3(ANKRD26):c.1270-283G>A	not provided [RCV001667323]	benign	10	27064364	27064364	Human		name
150464541	CV1252709	single nucleotide variant	NM_014915.3(ANKRD26):c.1270-240T>C	not provided [RCV001670033]	benign	10	27064321	27064321	Human		name
150444503	CV1258528	single nucleotide variant	NM_014915.3(ANKRD26):c.2697+101G>A	not provided [RCV001679726]	benign	10	27037085	27037085	Human		name
150442170	CV1264389	single nucleotide variant	NM_014915.3(ANKRD26):c.3973-179G>A	not provided [RCV001679372]	benign	10	27024738	27024738	Human		name
150442992	CV1264526	single nucleotide variant	NM_014915.3(ANKRD26):c.2697+304C>T	not provided [RCV001679510]	benign	10	27036882	27036882	Human		name
150443442	CV1266396	single nucleotide variant	NM_014915.3(ANKRD26):c.2019+157G>T	not provided [RCV001690832]	benign	10	27044000	27044000	Human		name
150493495	CV1267157	single nucleotide variant	NM_014915.3(ANKRD26):c.2697+118A>G	not provided [RCV001688185]	benign	10	27037068	27037068	Human		name
150494066	CV1267277	single nucleotide variant	NM_014915.3(ANKRD26):c.4507-109C>A	not provided [RCV001688305]	benign	10	27014820	27014820	Human		name
150477791	CV1272100	single nucleotide variant	NM_014915.3(ANKRD26):c.1564+282T>C	not provided [RCV001696386]	benign	10	27060063	27060063	Human		name
150466296	CV1277381	single nucleotide variant	NM_014915.3(ANKRD26):c.1985+236G>A	not provided [RCV001710676]	benign	10	27046117	27046117	Human		name
150510165	CV1286709	single nucleotide variant	NM_014915.3(ANKRD26):c.1564+149G>A	not provided [RCV001720944]	benign	10	27060196	27060196	Human		name
150510177	CV1286715	single nucleotide variant	NM_014915.3(ANKRD26):c.1985+167A>G	not provided [RCV001720950]	benign	10	27046186	27046186	Human		name
150546841	CV1302876	microsatellite	NM_014915.2(ANKRD26):c.1816_1818del	ANKRD26-related disorder [RCV004741071]\|not provided [RCV001763621]\|not specified [RCV003151350]	likely benign\|conflicting interpretations of pathogenicity\|uncertain significance	10	27046520	27046522	Human		name , alternate_id
156416968	CV1970131	duplication	NM_014915.3(ANKRD26):c.-138_-135dup	not provided [RCV002589967]	uncertain significance	10	27100460	27100461	Human		name
401938200	CV2813064	single nucleotide variant	NM_014915.3(ANKRD26):c.3808-1249C>T	not provided [RCV003417286]	benign	10	27030605	27030605	Human		name
401739260	CV2738517	duplication	NM_014915.3(ANKRD26):c.875-19_896dup	not provided [RCV005102875]\|not specified [RCV003317909]	likely benign\|uncertain significance	10	27077518	27077519	Human		name
402515329	CV2855702	deletion	NM_014915.3(ANKRD26):c.-7_242+276del	not provided [RCV003547354]	uncertain significance	10	27099809	27100333	Human		name
402493304	CV2981993	indel	NM_014915.3(ANKRD26):c.-3_-2delinsCA	not provided [RCV003713988]	uncertain significance	10	27100328	27100329	Human		name
150536864	CV1303762	microsatellite	NM_014915.3(ANKRD26):c.243-6_243-5del	not provided [RCV001763865]	uncertain significance	10	27093804	27093805	Human		name
156192681	CV1974595	microsatellite	NM_014915.3(ANKRD26):c.1078-25GTTT[2]	not provided [RCV002625470]	likely benign	10	27067300	27067303	Human		name
598272707	CV3988192	single nucleotide variant	NM_014915.3(ANKRD26):c.6G>A (p.Lys2=)	Inborn genetic diseases [RCV005350550]	likely benign	10	27100321	27100321	Human	1	name
405243889	CV3053965	single nucleotide variant	NM_014915.3(ANKRD26):c.24G>A (p.Lys8=)	Inborn genetic diseases [RCV004950622]\|not provided [RCV003719843]	benign\|likely benign	10	27100303	27100303	Human	1	name
150340381	CV1168204	deletion	NM_014915.3(ANKRD26):c.874+34_874+35del	not provided [RCV001535305]	benign	10	27077598	27077599	Human		name
153304220	CV1690656	microsatellite	NM_014915.3(ANKRD26):c.3654+4_3654+7del	not provided [RCV002269700]	uncertain significance	10	27034789	27034792	Human		name
156414648	CV1908970	single nucleotide variant	NM_014915.3(ANKRD26):c.72G>A (p.Ala24=)	not provided [RCV002588729]	likely benign	10	27100255	27100255	Human		name
156065477	CV1927821	deletion	NM_014915.3(ANKRD26):c.1364-9_1364-6del	not provided [RCV002638426]	benign	10	27061248	27061251	Human		name
10406657	CV207739	deletion	NM_014915.3(ANKRD26):c.243-85_243-76del	not specified [RCV000193597]	uncertain significance	10	27093875	27093884	Human		name
402476025	CV2920642	microsatellite	NM_014915.3(ANKRD26):c.531+13_531+16del	not provided [RCV003571352]	likely benign	10	27093333	27093336	Human		name
405244561	CV3050521	single nucleotide variant	NM_014915.3(ANKRD26):c.93G>C (p.Gly31=)	not provided [RCV003719922]	likely benign	10	27100234	27100234	Human		name
405252203	CV3050893	microsatellite	NM_014915.3(ANKRD26):c.4724+3_4724+6del	not provided [RCV003722115]	uncertain significance	10	27014488	27014491	Human		name
11609386	CV310154	single nucleotide variant	NM_014915.3(ANKRD26):c.93G>A (p.Gly31=)	ANKRD26-related disorder [RCV003897680]\|Inborn genetic diseases [RCV004955404]\|Thrombocytopenia 2 [RCV000367704]	likely benign\|uncertain significance	10	27100234	27100234	Human	2	name , alternate_id
405150275	CV3142089	single nucleotide variant	NM_014915.3(ANKRD26):c.78C>A (p.Gly26=)	Inborn genetic diseases [RCV005363284]\|not provided [RCV003840011]	likely benign	10	27100249	27100249	Human	1	name
597683023	CV3557165	single nucleotide variant	NM_014915.3(ANKRD26):c.90G>T (p.Pro30=)	Inborn genetic diseases [RCV004952207]\|not provided [RCV005107525]	likely benign	10	27100237	27100237	Human	1	name
597908675	CV3739029	microsatellite	NM_014915.3(ANKRD26):c.2020-9_2020-6del	not provided [RCV005073264]	likely benign\|conflicting interpretations of pathogenicity	10	27043573	27043576	Human		name
597954432	CV3808938	deletion	NM_014915.3(ANKRD26):c.875-23_875-19del	not provided [RCV005161856]	likely benign	10	27077559	27077563	Human		name
597955977	CV3838107	deletion	NM_014915.3(ANKRD26):c.813+10_813+14del	not provided [RCV005191481]	likely benign	10	27079075	27079079	Human		name
598177519	CV3981751	single nucleotide variant	NM_014915.3(ANKRD26):c.90G>A (p.Pro30=)	Inborn genetic diseases [RCV005371610]	likely benign	10	27100237	27100237	Human	1	name
598198479	CV3985410	single nucleotide variant	NM_014915.3(ANKRD26):c.57G>A (p.Arg19=)	Inborn genetic diseases [RCV005375564]	likely benign	10	27100270	27100270	Human	1	name
598241334	CV3985725	single nucleotide variant	NM_014915.3(ANKRD26):c.33G>T (p.Ser11=)	Inborn genetic diseases [RCV005364794]	likely benign	10	27100294	27100294	Human	1	name
598250842	CV3988287	single nucleotide variant	NM_014915.3(ANKRD26):c.8A>G (p.Lys3Arg)	Inborn genetic diseases [RCV005366580]	uncertain significance	10	27100319	27100319	Human	1	name
598240189	CV3988904	single nucleotide variant	NM_014915.3(ANKRD26):c.48C>T (p.Phe16=)	Inborn genetic diseases [RCV005364570]	likely benign	10	27100279	27100279	Human	1	name
598230772	CV3991750	single nucleotide variant	NM_014915.3(ANKRD26):c.54G>T (p.Arg18=)	Inborn genetic diseases [RCV005362759]	likely benign	10	27100273	27100273	Human	1	name
598164953	CV3992374	single nucleotide variant	NM_014915.3(ANKRD26):c.30G>A (p.Glu10=)	Inborn genetic diseases [RCV005369088]	likely benign	10	27100297	27100297	Human	1	name
598165374	CV3992525	single nucleotide variant	NM_014915.3(ANKRD26):c.84C>T (p.Gly28=)	Inborn genetic diseases [RCV005369160]	likely benign	10	27100243	27100243	Human	1	name
598211689	CV3992925	single nucleotide variant	NM_014915.3(ANKRD26):c.90G>C (p.Pro30=)	Inborn genetic diseases [RCV005378060]	likely benign	10	27100237	27100237	Human	1	name
15176113	CV777866	deletion	NM_014915.3(ANKRD26):c.1269+7_1269+9del	Thrombocytopenia 2 [RCV005231990]\|not provided [RCV000950749]	benign	10	27066478	27066480	Human	1	name
28905369	CV865797	single nucleotide variant	NM_014915.3(ANKRD26):c.3G>A (p.Met1Ile)	Thrombocytopenia 2 [RCV001106019]\|not provided [RCV001655676]\|not specified [RCV001819815]	benign\|conflicting interpretations of pathogenicity\|uncertain significance	10	27100324	27100324	Human	1	name
150548593	CV1294404	single nucleotide variant	NM_014915.3(ANKRD26):c.26G>A (p.Gly9Asp)	not provided [RCV001751896]	uncertain significance	10	27100301	27100301	Human		name
151355431	CV1328498	single nucleotide variant	NM_014915.3(ANKRD26):c.267C>T (p.Ala89=)	not specified [RCV001820503]	uncertain significance	10	27093775	27093775	Human		name
151356396	CV1329160	single nucleotide variant	NM_014915.3(ANKRD26):c.20A>G (p.Lys7Arg)	not specified [RCV001822749]	uncertain significance	10	27100307	27100307	Human		name
156220061	CV1899719	single nucleotide variant	NM_014915.3(ANKRD26):c.216C>T (p.Gly72=)	Inborn genetic diseases [RCV004961039]\|not provided [RCV003084960]	likely benign	10	27100111	27100111	Human	1	name
156031716	CV1899738	single nucleotide variant	NM_014915.3(ANKRD26):c.240C>T (p.Asn80=)	ANKRD26-related disorder [RCV003963644]\|Inborn genetic diseases [RCV004961040]\|not provided [RCV003100679]	likely benign\|uncertain significance	10	27100087	27100087	Human	2	name , alternate_id
156379321	CV1903326	single nucleotide variant	NM_014915.3(ANKRD26):c.141C>T (p.Leu47=)	Inborn genetic diseases [RCV004948985]\|not provided [RCV003093149]	likely benign	10	27100186	27100186	Human	1	name
156005299	CV2126536	microsatellite	NM_014915.3(ANKRD26):c.1078-11_1078-6del	not provided [RCV002975376]	likely benign	10	27067292	27067297	Human		name
156033162	CV2142234	single nucleotide variant	NM_014915.3(ANKRD26):c.108G>C (p.Ser36=)	Inborn genetic diseases [RCV004948866]\|not provided [RCV002976692]	likely benign	10	27100219	27100219	Human	1	name
156100498	CV2386726	single nucleotide variant	NM_014915.3(ANKRD26):c.17G>T (p.Ser6Ile)	Inborn genetic diseases [RCV002739073]\|not provided [RCV005099154]	uncertain significance	10	27100310	27100310	Human	1	name
402478056	CV2854476	single nucleotide variant	NM_014915.3(ANKRD26):c.204C>G (p.Leu68=)	Inborn genetic diseases [RCV004950375]\|not provided [RCV003543699]	likely benign	10	27100123	27100123	Human	1	name
405199496	CV2877025	single nucleotide variant	NM_014915.3(ANKRD26):c.246G>A (p.Thr82=)	not provided [RCV003551244]	likely benign	10	27093796	27093796	Human		name
405203927	CV2986224	single nucleotide variant	NM_014915.3(ANKRD26):c.22A>C (p.Lys8Gln)	not provided [RCV003678490]	uncertain significance	10	27100305	27100305	Human		name
405120501	CV2994040	single nucleotide variant	NM_014915.3(ANKRD26):c.261C>A (p.Ala87=)	not provided [RCV003723838]	likely benign	10	27093781	27093781	Human		name
405217339	CV3048820	single nucleotide variant	NM_014915.3(ANKRD26):c.26G>T (p.Gly9Val)	Inborn genetic diseases [RCV005353260]\|not provided [RCV003732823]	uncertain significance	10	27100301	27100301	Human	1	name
405081592	CV3050337	single nucleotide variant	NM_014915.3(ANKRD26):c.114C>T (p.Pro38=)	Inborn genetic diseases [RCV004953432]\|not provided [RCV003717026]	likely benign	10	27100213	27100213	Human	1	name
405245085	CV3054754	single nucleotide variant	NM_014915.3(ANKRD26):c.114C>G (p.Pro38=)	Inborn genetic diseases [RCV004953447]\|not provided [RCV003720112]	likely benign	10	27100213	27100213	Human	1	name
405147145	CV3067314	single nucleotide variant	NM_014915.3(ANKRD26):c.102C>T (p.Ala34=)	Inborn genetic diseases [RCV004950641]\|not provided [RCV003726144]	likely benign	10	27100225	27100225	Human	1	name
11612052	CV310153	single nucleotide variant	NM_014915.3(ANKRD26):c.162C>T (p.Ala54=)	Thrombocytopenia 2 [RCV000402860]\|not provided [RCV003718164]	benign\|likely benign\|uncertain significance	10	27100165	27100165	Human	1	name
11606131	CV315253	deletion	NM_014915.3(ANKRD26):c.1269+8_1269+12del	Thrombocytopenia [RCV000327787]\|not provided [RCV002522152]	likely benign\|conflicting interpretations of pathogenicity\|uncertain significance	10	27066475	27066479	Human	2	name
402469681	CV3174740	single nucleotide variant	NM_014915.3(ANKRD26):c.295C>T (p.Leu99=)	not provided [RCV003873850]	likely benign	10	27093747	27093747	Human		name
408392081	CV3526466	single nucleotide variant	NM_014915.3(ANKRD26):c.21G>T (p.Lys7Asn)	Inborn genetic diseases [RCV004950842]\|Thrombocytopenia 2 [RCV005230789]\|not provided [RCV004775715]	uncertain significance	10	27100306	27100306	Human	2	name
596929406	CV3531050	single nucleotide variant	NM_014915.3(ANKRD26):c.17G>A (p.Ser6Asn)	not provided [RCV004779624]	uncertain significance	10	27100310	27100310	Human		name
597681932	CV3556588	single nucleotide variant	NM_014915.3(ANKRD26):c.123C>T (p.His41=)	Inborn genetic diseases [RCV004952047]\|not provided [RCV005107489]	likely benign	10	27100204	27100204	Human	1	name
597682954	CV3557013	single nucleotide variant	NM_014915.3(ANKRD26):c.25G>A (p.Gly9Ser)	Inborn genetic diseases [RCV004952198]	uncertain significance	10	27100302	27100302	Human	1	name
597903934	CV3793190	single nucleotide variant	NM_014915.3(ANKRD26):c.204C>T (p.Leu68=)	not provided [RCV005153158]	likely benign	10	27100123	27100123	Human		name
597941242	CV3837042	deletion	NM_014915.3(ANKRD26):c.94del (p.Glu32fs)	not provided [RCV005187873]	uncertain significance	10	27100233	27100233	Human		name
597954813	CV3844516	deletion	NM_014915.3(ANKRD26):c.4953+8_4953+12del	not provided [RCV005191190]	likely benign	10	27012870	27012874	Human		name
597905594	CV3856415	single nucleotide variant	NM_014915.3(ANKRD26):c.129A>G (p.Arg43=)	not provided [RCV005202643]	likely benign	10	27100198	27100198	Human		name
598224155	CV3981262	single nucleotide variant	NM_014915.3(ANKRD26):c.120C>T (p.Tyr40=)	Inborn genetic diseases [RCV005380164]	likely benign	10	27100207	27100207	Human	1	name
598163988	CV3981488	single nucleotide variant	NM_014915.3(ANKRD26):c.252A>G (p.Leu84=)	Inborn genetic diseases [RCV005368919]	likely benign	10	27093790	27093790	Human	1	name
598225458	CV3985732	single nucleotide variant	NM_014915.3(ANKRD26):c.159T>G (p.Ala53=)	Inborn genetic diseases [RCV005380403]	likely benign	10	27100168	27100168	Human	1	name
598197005	CV3988700	single nucleotide variant	NM_014915.3(ANKRD26):c.297G>C (p.Leu99=)	Inborn genetic diseases [RCV005375364]	likely benign	10	27093745	27093745	Human	1	name
598240119	CV3988867	single nucleotide variant	NM_014915.3(ANKRD26):c.20A>T (p.Lys7Met)	Inborn genetic diseases [RCV005364555]	uncertain significance	10	27100307	27100307	Human	1	name
598238481	CV3991723	single nucleotide variant	NM_014915.3(ANKRD26):c.111G>A (p.Gln37=)	Inborn genetic diseases [RCV005364256]	likely benign	10	27100216	27100216	Human	1	name
28902877	CV865796	single nucleotide variant	NM_014915.3(ANKRD26):c.141C>A (p.Leu47=)	Inborn genetic diseases [RCV004960453]\|Thrombocytopenia 2 [RCV001104856]\|not provided [RCV002555033]\|not specified [RCV001819813]	benign\|likely benign	10	27100186	27100186	Human	2	name
126912065	CV1037972	single nucleotide variant	NM_014915.3(ANKRD26):c.98G>T (p.Gly33Val)	Inborn genetic diseases [RCV005348465]\|not provided [RCV001356100]	uncertain significance	10	27100229	27100229	Human	1	name
150417828	CV1180669	duplication	NM_014915.3(ANKRD26):c.813+160_813+162dup	not provided [RCV001550319]	likely benign	10	27078910	27078911	Human		name
150414308	CV1198041	deletion	NM_014915.3(ANKRD26):c.1269+11_1269+12del	ANKRD26-related disorder [RCV003983981]\|Thrombocytopenia 2 [RCV005232631]\|not provided [RCV001574900]	benign\|likely benign	10	27066475	27066476	Human	1	name , alternate_id
150437134	CV1200930	deletion	NM_014915.3(ANKRD26):c.638+160_638+171del	not provided [RCV001583010]	likely benign	10	27092235	27092246	Human		name
150431259	CV1206289	single nucleotide variant	NM_014915.3(ANKRD26):c.936C>T (p.Ser312=)	Inborn genetic diseases [RCV004946723]\|not provided [RCV001580938]	likely benign	10	27077479	27077479	Human	1	name
150511250	CV1212683	deletion	NM_014915.3(ANKRD26):c.3655-68_3655-67del	not provided [RCV001597914]	benign	10	27033444	27033445	Human		name
150514005	CV1228008	duplication	NM_014915.3(ANKRD26):c.813+160_813+161dup	not provided [RCV001638286]	benign	10	27078910	27078911	Human		name
150450260	CV1260936	microsatellite	NM_014915.3(ANKRD26):c.2019+29_2019+31del	not provided [RCV001680605]	benign	10	27044126	27044128	Human		name
150510167	CV1286710	deletion	NM_014915.3(ANKRD26):c.243-127_243-100del	not provided [RCV001720945]	benign	10	27093899	27093926	Human		name
151354053	CV1327605	single nucleotide variant	NM_014915.3(ANKRD26):c.513T>C (p.Asn171=)	not provided [RCV002542540]\|not specified [RCV001817549]	likely benign\|uncertain significance	10	27093367	27093367	Human		name
151354994	CV1328061	single nucleotide variant	NM_014915.3(ANKRD26):c.83G>T (p.Gly28Val)	Inborn genetic diseases [RCV004946748]\|not provided [RCV004692746]\|not specified [RCV001819537]	uncertain significance	10	27100244	27100244	Human	1	name
151355998	CV1328762	single nucleotide variant	NM_014915.3(ANKRD26):c.945A>G (p.Gln315=)	ANKRD26-related disorder [RCV003923330]\|Inborn genetic diseases [RCV004953102]\|not provided [RCV002542646]\|not specified [RCV001822351]	benign\|likely benign	10	27077470	27077470	Human	2	name , alternate_id
156219104	CV1899639	single nucleotide variant	NM_014915.3(ANKRD26):c.648A>G (p.Gln216=)	ANKRD26-related disorder [RCV004741397]\|Inborn genetic diseases [RCV004961037]\|Thrombocytopenia 2 [RCV005233089]\|not provided [RCV003084920]	benign\|likely benign	10	27086600	27086600	Human	2	name , alternate_id
156362278	CV1900651	single nucleotide variant	NM_014915.3(ANKRD26):c.79G>T (p.Gly27Trp)	Inborn genetic diseases [RCV004948997]\|not provided [RCV002581807]	uncertain significance	10	27100248	27100248	Human	1	name
156107704	CV1903676	single nucleotide variant	NM_014915.3(ANKRD26):c.739A>C (p.Arg247=)	not provided [RCV003080845]	uncertain significance	10	27082804	27082804	Human		name
156366812	CV1906539	single nucleotide variant	NM_014915.3(ANKRD26):c.96G>C (p.Glu32Asp)	Inborn genetic diseases [RCV005363016]\|not provided [RCV003092117]	likely benign\|uncertain significance	10	27100231	27100231	Human	1	name
156446410	CV1937882	single nucleotide variant	NM_014915.3(ANKRD26):c.510A>G (p.Ala170=)	Inborn genetic diseases [RCV005353138]\|not provided [RCV003117914]	likely benign	10	27093370	27093370	Human	1	name
156282007	CV2161036	single nucleotide variant	NM_014915.3(ANKRD26):c.441C>T (p.Asn147=)	not provided [RCV003027350]	likely benign	10	27093439	27093439	Human		name
156434675	CV2403046	single nucleotide variant	NM_014915.3(ANKRD26):c.31T>A (p.Ser11Thr)	Inborn genetic diseases [RCV005377334]\|not provided [RCV003127002]	uncertain significance	10	27100296	27100296	Human	1	name
156434930	CV2403198	single nucleotide variant	NM_014915.3(ANKRD26):c.66C>A (p.Ser22Arg)	not provided [RCV003127154]	uncertain significance	10	27100261	27100261	Human		name
329350210	CV2477298	single nucleotide variant	NM_014915.3(ANKRD26):c.56G>T (p.Arg19Leu)	Inborn genetic diseases [RCV004285597]\|not provided [RCV003221623]	uncertain significance	10	27100271	27100271	Human	1	name
11547395	CV253737	single nucleotide variant	NM_014915.3(ANKRD26):c.624A>G (p.Val208=)	Thrombocytopenia 2 [RCV000284156]\|not provided [RCV001683072]\|not specified [RCV000247701]	benign\|likely benign	10	27092420	27092420	Human	1	name
11551211	CV253738	single nucleotide variant	NM_014915.3(ANKRD26):c.576G>A (p.Gln192=)	Thrombocytopenia 2 [RCV001102944]\|not provided [RCV001576558]\|not specified [RCV000252746]	benign\|likely benign	10	27092468	27092468	Human	1	name
11543765	CV253739	single nucleotide variant	NM_014915.3(ANKRD26):c.59A>G (p.Gln20Arg)	Thrombocytopenia 2 [RCV000275550]\|not provided [RCV001539381]\|not specified [RCV000242897]	benign\|likely benign	10	27100268	27100268	Human	1	name
402525432	CV2868538	single nucleotide variant	NM_014915.3(ANKRD26):c.333C>T (p.Asn111=)	ANKRD26-related disorder [RCV003908998]\|Inborn genetic diseases [RCV004950399]\|not provided [RCV003548072]	likely benign	10	27093709	27093709	Human	2	name , alternate_id
402492830	CV2877972	single nucleotide variant	NM_014915.3(ANKRD26):c.74G>C (p.Gly25Ala)	not provided [RCV003545113]	uncertain significance	10	27100253	27100253	Human		name
405240759	CV2889360	single nucleotide variant	NM_014915.3(ANKRD26):c.564T>C (p.Ser188=)	Inborn genetic diseases [RCV005377415]\|not provided [RCV003557360]	likely benign\|uncertain significance	10	27092480	27092480	Human	1	name
405183746	CV2920293	single nucleotide variant	NM_014915.3(ANKRD26):c.606A>G (p.Lys202=)	Inborn genetic diseases [RCV004950457]\|not provided [RCV003564248]\|not specified [RCV005240843]	likely benign	10	27092438	27092438	Human	1	name
405162478	CV2950401	deletion	NM_014915.3(ANKRD26):c.2020-19_2020-18del	not provided [RCV003674728]	likely benign	10	27043585	27043586	Human		name
405245986	CV2965638	duplication	NM_014915.3(ANKRD26):c.226dup (p.Arg76fs)	not provided [RCV003685312]	uncertain significance	10	27100100	27100101	Human		name
405229524	CV2977276	single nucleotide variant	NM_014915.3(ANKRD26):c.831C>T (p.Ser277=)	Inborn genetic diseases [RCV005377462]\|not provided [RCV003711277]	likely benign	10	27077676	27077676	Human	1	name
402513723	CV3039882	single nucleotide variant	NM_014915.3(ANKRD26):c.507T>C (p.Asp169=)	not provided [RCV003715894]	likely benign	10	27093373	27093373	Human		name
405124544	CV3043385	single nucleotide variant	NM_014915.3(ANKRD26):c.429T>C (p.Asp143=)	Inborn genetic diseases [RCV005363212]\|not provided [RCV003724241]	likely benign	10	27093451	27093451	Human	1	name
405094417	CV3045707	single nucleotide variant	NM_014915.3(ANKRD26):c.537C>T (p.Asp179=)	not provided [RCV003718054]	likely benign	10	27092507	27092507	Human		name
405122965	CV3046480	single nucleotide variant	NM_014915.3(ANKRD26):c.939T>C (p.Asp313=)	Inborn genetic diseases [RCV004950607]\|not provided [RCV003724094]	likely benign	10	27077476	27077476	Human	1	name
405122975	CV3046493	single nucleotide variant	NM_014915.3(ANKRD26):c.789C>T (p.Asp263=)	Inborn genetic diseases [RCV004950608]\|not provided [RCV003724095]	likely benign	10	27079113	27079113	Human	1	name
405083207	CV3046948	single nucleotide variant	NM_014915.3(ANKRD26):c.79G>C (p.Gly27Arg)	not provided [RCV003717291]	uncertain significance	10	27100248	27100248	Human		name
405134565	CV3047659	single nucleotide variant	NM_014915.3(ANKRD26):c.366A>G (p.Gln122=)	Inborn genetic diseases [RCV004950630]\|not provided [RCV003725045]	likely benign	10	27093514	27093514	Human	1	name
405079014	CV3050270	single nucleotide variant	NM_014915.3(ANKRD26):c.435T>C (p.His145=)	Inborn genetic diseases [RCV004950617]\|not provided [RCV003716988]	benign\|likely benign	10	27093445	27093445	Human	1	name
405246100	CV3051786	single nucleotide variant	NM_014915.3(ANKRD26):c.837A>G (p.Ala279=)	not provided [RCV003720461]	likely benign	10	27077670	27077670	Human		name
405127307	CV3053685	single nucleotide variant	NM_014915.3(ANKRD26):c.89C>A (p.Pro30Gln)	not provided [RCV003724496]	uncertain significance	10	27100238	27100238	Human		name
405253421	CV3054176	single nucleotide variant	NM_014915.3(ANKRD26):c.85G>A (p.Glu29Lys)	Inborn genetic diseases [RCV004950627]\|not provided [RCV003722518]	uncertain significance	10	27100242	27100242	Human	1	name
405092473	CV3054697	single nucleotide variant	NM_014915.3(ANKRD26):c.843A>C (p.Leu281=)	not provided [RCV003717916]	likely benign	10	27077664	27077664	Human		name
405040857	CV3063975	single nucleotide variant	NM_014915.3(ANKRD26):c.92G>A (p.Gly31Glu)	not provided [RCV003739909]	uncertain significance	10	27100235	27100235	Human		name
405228352	CV3065784	single nucleotide variant	NM_014915.3(ANKRD26):c.82G>C (p.Gly28Arg)	not provided [RCV003734453]	uncertain significance	10	27100245	27100245	Human		name
405203474	CV3116818	duplication	NM_014915.3(ANKRD26):c.1985+11_1985+12dup	not provided [RCV003822302]	likely benign	10	27046340	27046341	Human		name
405094547	CV3134728	single nucleotide variant	NM_014915.3(ANKRD26):c.396G>A (p.Leu132=)	not provided [RCV003835074]	likely benign	10	27093484	27093484	Human		name
11608938	CV321267	microsatellite	NM_014915.3(ANKRD26):c.1364-17_1364-15del	Thrombocytopenia [RCV000361502]\|not provided [RCV002522151]	benign\|uncertain significance	10	27061257	27061259	Human		name
11605090	CV321850	single nucleotide variant	NM_014915.3(ANKRD26):c.948T>C (p.Asp316=)	ANKRD26-related disorder [RCV003930263]\|Inborn genetic diseases [RCV004948256]\|Thrombocytopenia 2 [RCV000315965]\|not provided [RCV000900746]	benign\|likely benign\|uncertain significance	10	27077467	27077467	Human	2	name , alternate_id
11654008	CV321899	single nucleotide variant	NM_014915.3(ANKRD26):c.50C>T (p.Ala17Val)	ANKRD26-related disorder [RCV003401287]\|Inborn genetic diseases [RCV004948258]\|Thrombocytopenia 2 [RCV000314326]	uncertain significance	10	27100277	27100277	Human	2	name , alternate_id
408389402	CV3523078	single nucleotide variant	NM_014915.3(ANKRD26):c.867G>A (p.Arg289=)	Inborn genetic diseases [RCV005377660]\|not provided [RCV004769459]	likely benign\|uncertain significance	10	27077640	27077640	Human	1	name
408382004	CV3526671	single nucleotide variant	NM_014915.3(ANKRD26):c.79G>A (p.Gly27Arg)	Inborn genetic diseases [RCV004950844]\|not provided [RCV004771984]	uncertain significance	10	27100248	27100248	Human	1	name
597699765	CV3553707	single nucleotide variant	NM_014915.3(ANKRD26):c.888T>C (p.Tyr296=)	Inborn genetic diseases [RCV004956435]	likely benign	10	27077527	27077527	Human	1	name
597700809	CV3554205	single nucleotide variant	NM_014915.3(ANKRD26):c.438C>A (p.Gly146=)	Inborn genetic diseases [RCV004956576]	likely benign	10	27093442	27093442	Human	1	name
597682843	CV3556939	single nucleotide variant	NM_014915.3(ANKRD26):c.486A>C (p.Ala162=)	Inborn genetic diseases [RCV004952183]	likely benign	10	27093394	27093394	Human	1	name
597682871	CV3556966	single nucleotide variant	NM_014915.3(ANKRD26):c.318C>T (p.Leu106=)	Inborn genetic diseases [RCV004952187]	likely benign	10	27093724	27093724	Human	1	name
597682916	CV3556991	single nucleotide variant	NM_014915.3(ANKRD26):c.885A>G (p.Thr295=)	Inborn genetic diseases [RCV004952193]	likely benign	10	27077530	27077530	Human	1	name
597700286	CV3557109	single nucleotide variant	NM_014915.3(ANKRD26):c.504T>C (p.Tyr168=)	Inborn genetic diseases [RCV004956519]	likely benign	10	27093376	27093376	Human	1	name
597700063	CV3560476	single nucleotide variant	NM_014915.3(ANKRD26):c.832T>C (p.Leu278=)	Inborn genetic diseases [RCV004956485]\|not provided [RCV005107513]	likely benign	10	27077675	27077675	Human	1	name
597698846	CV3560510	single nucleotide variant	NM_014915.3(ANKRD26):c.76G>A (p.Gly26Ser)	Inborn genetic diseases [RCV004956491]\|not provided [RCV005052115]	uncertain significance	10	27100251	27100251	Human	1	name
597699810	CV3563417	single nucleotide variant	NM_014915.3(ANKRD26):c.585G>C (p.Val195=)	Inborn genetic diseases [RCV004956444]	likely benign	10	27092459	27092459	Human	1	name
597682450	CV3563639	single nucleotide variant	NM_014915.3(ANKRD26):c.750C>T (p.Gly250=)	Inborn genetic diseases [RCV004952126]	likely benign	10	27079152	27079152	Human	1	name
597682456	CV3563649	single nucleotide variant	NM_014915.3(ANKRD26):c.975A>G (p.Thr325=)	Inborn genetic diseases [RCV004952127]	likely benign	10	27077440	27077440	Human	1	name
597700832	CV3563789	single nucleotide variant	NM_014915.3(ANKRD26):c.91G>T (p.Gly31Trp)	Inborn genetic diseases [RCV004956580]	uncertain significance	10	27100236	27100236	Human	1	name
597700879	CV3563827	single nucleotide variant	NM_014915.3(ANKRD26):c.927T>C (p.Asp309=)	Inborn genetic diseases [RCV004956587]	likely benign	10	27077488	27077488	Human	1	name
597894672	CV3744106	single nucleotide variant	NM_014915.3(ANKRD26):c.44C>T (p.Ser15Phe)	not provided [RCV005071576]	uncertain significance	10	27100283	27100283	Human		name
597957672	CV3755135	single nucleotide variant	NM_014915.3(ANKRD26):c.56G>A (p.Arg19Gln)	not provided [RCV005080805]	uncertain significance	10	27100271	27100271	Human		name
597910851	CV3830220	single nucleotide variant	NM_014915.3(ANKRD26):c.32C>T (p.Ser11Leu)	not provided [RCV005182790]	uncertain significance	10	27100295	27100295	Human		name
597925066	CV3840499	single nucleotide variant	NM_014915.3(ANKRD26):c.89C>T (p.Pro30Leu)	not provided [RCV005184970]	uncertain significance	10	27100238	27100238	Human		name
597947982	CV3852396	single nucleotide variant	NM_014915.3(ANKRD26):c.88C>G (p.Pro30Ala)	not provided [RCV005189473]	uncertain significance	10	27100239	27100239	Human		name
598252575	CV3981238	single nucleotide variant	NM_014915.3(ANKRD26):c.447T>C (p.Ala149=)	Inborn genetic diseases [RCV005366825]	likely benign	10	27093433	27093433	Human	1	name
598164011	CV3981498	single nucleotide variant	NM_014915.3(ANKRD26):c.48C>A (p.Phe16Leu)	Inborn genetic diseases [RCV005368924]	uncertain significance	10	27100279	27100279	Human	1	name
598182950	CV3981510	single nucleotide variant	NM_014915.3(ANKRD26):c.55C>T (p.Arg19Trp)	Inborn genetic diseases [RCV005372834]	uncertain significance	10	27100272	27100272	Human	1	name
598210170	CV3981993	single nucleotide variant	NM_014915.3(ANKRD26):c.432C>A (p.Val144=)	Inborn genetic diseases [RCV005377821]	likely benign	10	27093448	27093448	Human	1	name
598185010	CV3988435	single nucleotide variant	NM_014915.3(ANKRD26):c.972T>G (p.Pro324=)	Inborn genetic diseases [RCV005373179]	likely benign	10	27077443	27077443	Human	1	name
598224864	CV3989170	single nucleotide variant	NM_014915.3(ANKRD26):c.543A>G (p.Thr181=)	Inborn genetic diseases [RCV005380290]	likely benign	10	27092501	27092501	Human	1	name
598230935	CV3991909	single nucleotide variant	NM_014915.3(ANKRD26):c.95A>C (p.Glu32Ala)	Inborn genetic diseases [RCV005362786]	uncertain significance	10	27100232	27100232	Human	1	name
598178203	CV3992536	single nucleotide variant	NM_014915.3(ANKRD26):c.654T>C (p.Ile218=)	Inborn genetic diseases [RCV005371738]	likely benign	10	27086594	27086594	Human	1	name
598211039	CV3992738	single nucleotide variant	NM_014915.3(ANKRD26):c.666A>G (p.Lys222=)	Inborn genetic diseases [RCV005377955]	likely benign	10	27086582	27086582	Human	1	name
13214528	CV429059	single nucleotide variant	NM_014915.3(ANKRD26):c.678A>T (p.Ile226=)	Inborn genetic diseases [RCV004948371]\|not provided [RCV002524150]\|not specified [RCV000501222]	benign\|likely benign	10	27086570	27086570	Human	1	name
13213162	CV429061	single nucleotide variant	NM_014915.3(ANKRD26):c.92G>C (p.Gly31Ala)	ANKRD26-related disorder [RCV003925444]\|Inborn genetic diseases [RCV002527194]\|Thrombocytopenia 2 [RCV001106017]\|not provided [RCV000883893]\|not specified [RCV000499626]	benign\|likely benign\|uncertain significance	10	27100235	27100235	Human	2	name , alternate_id
15175844	CV723900	single nucleotide variant	NM_014915.3(ANKRD26):c.40G>A (p.Gly14Ser)	Inborn genetic diseases [RCV002539327]\|Thrombocytopenia 2 [RCV001106018]\|not provided [RCV000884458]\|not specified [RCV001817089]	benign\|likely benign\|uncertain significance	10	27100287	27100287	Human	2	name
28909041	CV865791	single nucleotide variant	NM_014915.3(ANKRD26):c.756G>A (p.Pro252=)	Inborn genetic diseases [RCV004950293]\|Thrombocytopenia 2 [RCV001108155]\|not provided [RCV003542321]\|not specified [RCV001819820]	benign\|likely benign	10	27079146	27079146	Human	2	name
28902871	CV865794	single nucleotide variant	NM_014915.3(ANKRD26):c.426G>A (p.Ala142=)	Thrombocytopenia 2 [RCV001104854]	uncertain significance	10	27093454	27093454	Human	1	name
126726465	CV1017281	single nucleotide variant	NM_014915.3(ANKRD26):c.244A>G (p.Thr82Ala)	Thrombocytopenia 2 [RCV001331985]	uncertain significance	10	27093798	27093798	Human	1	name
150545969	CV1291291	single nucleotide variant	NM_014915.3(ANKRD26):c.1728T>C (p.Asp576=)	ANKRD26-related disorder [RCV003910989]\|Inborn genetic diseases [RCV004946728]\|not provided [RCV001732733]	benign\|likely benign	10	27048887	27048887	Human	2	name , alternate_id
150541950	CV1302432	single nucleotide variant	NM_014915.3(ANKRD26):c.121C>T (p.His41Tyr)	not provided [RCV001761122]	uncertain significance	10	27100206	27100206	Human		name
150546829	CV1302874	single nucleotide variant	NM_014915.3(ANKRD26):c.105C>G (p.Tyr35Ter)	ANKRD26-related disorder [RCV003407797]\|not provided [RCV001763619]	uncertain significance	10	27100222	27100222	Human	1	name , alternate_id
150555738	CV1304896	single nucleotide variant	NM_014915.3(ANKRD26):c.1998A>G (p.Lys666=)	ANKRD26-related disorder [RCV003976161]\|Inborn genetic diseases [RCV004946734]\|not provided [RCV001773144]	likely benign\|conflicting interpretations of pathogenicity\|uncertain significance	10	27044178	27044178	Human	2	name , alternate_id
151356017	CV1328781	single nucleotide variant	NM_014915.3(ANKRD26):c.110A>G (p.Gln37Arg)	ANKRD26-related disorder [RCV003956405]\|Inborn genetic diseases [RCV004946750]\|not provided [RCV002265034]\|not specified [RCV001822370]	likely benign\|uncertain significance	10	27100217	27100217	Human	2	name , alternate_id
155803924	CV1858492	single nucleotide variant	NM_014915.3(ANKRD26):c.218T>C (p.Leu73Ser)	Inborn genetic diseases [RCV004948705]\|not provided [RCV002462802]	uncertain significance	10	27100109	27100109	Human	1	name
155937482	CV1867640	single nucleotide variant	NM_014915.3(ANKRD26):c.167C>T (p.Ala56Val)	Inborn genetic diseases [RCV005350948]\|not provided [RCV002510112]	likely benign\|uncertain significance	10	27100160	27100160	Human	1	name
156400207	CV1892794	single nucleotide variant	NM_014915.3(ANKRD26):c.1530A>G (p.Ala510=)	Inborn genetic diseases [RCV004948961]\|not provided [RCV003069062]	benign\|likely benign	10	27060379	27060379	Human	1	name
156183620	CV1898286	single nucleotide variant	NM_014915.3(ANKRD26):c.2749T>C (p.Leu917=)	Inborn genetic diseases [RCV004949004]\|not provided [RCV002595143]	likely benign	10	27035701	27035701	Human	1	name
156276724	CV1900276	single nucleotide variant	NM_014915.3(ANKRD26):c.1086A>G (p.Pro362=)	ANKRD26-related disorder [RCV004741399]\|Inborn genetic diseases [RCV004948993]\|not provided [RCV003086974]	likely benign	10	27067278	27067278	Human	2	name , alternate_id
156362456	CV1900678	single nucleotide variant	NM_014915.3(ANKRD26):c.2133C>T (p.Leu711=)	Inborn genetic diseases [RCV004948998]\|not provided [RCV002581819]	likely benign	10	27043454	27043454	Human	1	name
156216218	CV1903359	single nucleotide variant	NM_014915.3(ANKRD26):c.245C>T (p.Thr82Met)	Thrombocytopenia 2 [RCV003389087]\|not provided [RCV003084808]	uncertain significance	10	27093797	27093797	Human	1	name
156160292	CV1906854	single nucleotide variant	NM_014915.3(ANKRD26):c.187C>G (p.Gln63Glu)	Inborn genetic diseases [RCV004961035]\|not provided [RCV003082866]	uncertain significance	10	27100140	27100140	Human	1	name
156162088	CV1906983	single nucleotide variant	NM_014915.3(ANKRD26):c.2403G>A (p.Lys801=)	ANKRD26-related disorder [RCV003898802]\|Inborn genetic diseases [RCV004948983]\|not provided [RCV003082934]	likely benign	10	27038027	27038027	Human	2	name , alternate_id
156314935	CV1910197	single nucleotide variant	NM_014915.3(ANKRD26):c.2382C>T (p.Ser794=)	Inborn genetic diseases [RCV005363037]\|not provided [RCV002599882]	likely benign	10	27038048	27038048	Human	1	name
156070255	CV1972112	single nucleotide variant	NM_014915.3(ANKRD26):c.2355A>G (p.Glu785=)	not provided [RCV002621222]	likely benign	10	27039985	27039985	Human		name
156411628	CV1973576	single nucleotide variant	NM_014915.3(ANKRD26):c.2601A>G (p.Arg867=)	Inborn genetic diseases [RCV005370247]\|not provided [RCV002608309]	likely benign	10	27037282	27037282	Human	1	name
10405494	CV207740	single nucleotide variant	NM_014915.3(ANKRD26):c.153C>G (p.His51Gln)	ANKRD26-related disorder [RCV003955136]\|Thrombocytopenia 2 [RCV000764891]\|not provided [RCV001563310]\|not specified [RCV000194457]	likely benign\|conflicting interpretations of pathogenicity\|uncertain significance	10	27100174	27100174	Human	1	name , alternate_id
156366071	CV2116466	single nucleotide variant	NM_014915.3(ANKRD26):c.2421G>A (p.Thr807=)	ANKRD26-related disorder [RCV003963447]\|Inborn genetic diseases [RCV004948841]\|Thrombocytopenia 2 [RCV005233038]\|not provided [RCV002941960]	likely benign	10	27038009	27038009	Human	2	name , alternate_id
156434858	CV2403158	single nucleotide variant	NM_014915.3(ANKRD26):c.228A>C (p.Arg76Ser)	Inborn genetic diseases [RCV004949039]\|not provided [RCV003127114]	conflicting interpretations of pathogenicity\|uncertain significance	10	27100099	27100099	Human	1	name
243063398	CV2411715	single nucleotide variant	NM_014915.3(ANKRD26):c.2325A>G (p.Ser775=)	Inborn genetic diseases [RCV004961222]\|not provided [RCV003141438]	likely benign\|conflicting interpretations of pathogenicity\|uncertain significance	10	27040015	27040015	Human	1	name
243049502	CV2416881	single nucleotide variant	NM_014915.3(ANKRD26):c.133C>T (p.Arg45Ter)	not specified [RCV003151553]	uncertain significance	10	27100194	27100194	Human		name
329349947	CV2477240	single nucleotide variant	NM_014915.3(ANKRD26):c.1323A>G (p.Ala441=)	Inborn genetic diseases [RCV005363083]\|not provided [RCV003221565]	likely benign\|uncertain significance	10	27064028	27064028	Human	1	name
329350886	CV2477716	single nucleotide variant	NM_014915.3(ANKRD26):c.250C>G (p.Leu84Val)	Inborn genetic diseases [RCV005377350]\|not provided [RCV003223828]	uncertain significance	10	27093792	27093792	Human	1	name
11551842	CV253728	single nucleotide variant	NM_014915.3(ANKRD26):c.2679A>G (p.Gln893=)	Inborn genetic diseases [RCV004948242]\|Thrombocytopenia 2 [RCV001108063]\|not provided [RCV000954273]\|not specified [RCV000253576]	benign\|likely benign	10	27037204	27037204	Human	2	name
329953756	CV2668560	single nucleotide variant	NM_014915.3(ANKRD26):c.136G>A (p.Asp46Asn)	ANKRD26-related disorder [RCV003396959]\|not provided [RCV003230213]	uncertain significance	10	27100191	27100191	Human	1	name , alternate_id
401798496	CV2739287	single nucleotide variant	NM_014915.3(ANKRD26):c.142G>A (p.Gly48Ser)	not provided [RCV003318935]	uncertain significance	10	27100185	27100185	Human		name
401828741	CV2743076	single nucleotide variant	NM_014915.3(ANKRD26):c.104A>T (p.Tyr35Phe)	not provided [RCV003325784]	uncertain significance	10	27100223	27100223	Human		name
401938203	CV2813067	single nucleotide variant	NM_014915.3(ANKRD26):c.196C>G (p.Leu66Val)	not provided [RCV003417289]	uncertain significance	10	27100131	27100131	Human		name
405171256	CV2854225	single nucleotide variant	NM_014915.3(ANKRD26):c.1326C>T (p.Asp442=)	Inborn genetic diseases [RCV004950370]\|not provided [RCV003542072]	benign\|likely benign	10	27064025	27064025	Human	1	name
405203390	CV2858314	single nucleotide variant	NM_014915.3(ANKRD26):c.2580C>T (p.Asp860=)	Inborn genetic diseases [RCV004953298]\|not provided [RCV003551635]	likely benign	10	27037303	27037303	Human	1	name
402495127	CV2883701	single nucleotide variant	NM_014915.3(ANKRD26):c.1779G>A (p.Gln593=)	Inborn genetic diseases [RCV004950434]\|not provided [RCV003573411]	likely benign	10	27048836	27048836	Human	1	name
405121290	CV2888096	single nucleotide variant	NM_014915.3(ANKRD26):c.1875G>A (p.Ser625=)	Inborn genetic diseases [RCV004953316]\|not provided [RCV003559120]	benign\|likely benign	10	27046463	27046463	Human	1	name
405222421	CV2891014	single nucleotide variant	NM_014915.3(ANKRD26):c.174T>G (p.Asn58Lys)	not provided [RCV003554130]	uncertain significance	10	27100153	27100153	Human		name
402471847	CV2912052	single nucleotide variant	NM_014915.3(ANKRD26):c.2121T>C (p.Asn707=)	not provided [RCV003570662]	likely benign	10	27043466	27043466	Human		name
405124836	CV3043440	single nucleotide variant	NM_014915.3(ANKRD26):c.223G>T (p.Asp75Tyr)	not provided [RCV003724268]	uncertain significance	10	27100104	27100104	Human		name
405124875	CV3043457	single nucleotide variant	NM_014915.3(ANKRD26):c.1548A>G (p.Val516=)	Inborn genetic diseases [RCV004950612]\|not provided [RCV003724272]	likely benign	10	27060361	27060361	Human	1	name
405089498	CV3044677	single nucleotide variant	NM_014915.3(ANKRD26):c.2175A>G (p.Leu725=)	Inborn genetic diseases [RCV004950632]\|not provided [RCV003717716]	likely benign	10	27040165	27040165	Human	1	name
405219736	CV3045794	single nucleotide variant	NM_014915.3(ANKRD26):c.2490A>G (p.Lys830=)	not provided [RCV003733030]	likely benign	10	27037940	27037940	Human		name
405133345	CV3047533	single nucleotide variant	NM_014915.3(ANKRD26):c.1053G>A (p.Ser351=)	Inborn genetic diseases [RCV005377520]\|not provided [RCV003725025]	likely benign	10	27077362	27077362	Human	1	name
405251147	CV3049684	single nucleotide variant	NM_014915.3(ANKRD26):c.1431A>C (p.Thr477=)	Inborn genetic diseases [RCV004950603]\|not provided [RCV003721820]	benign\|likely benign	10	27061175	27061175	Human	1	name
405079990	CV3050269	single nucleotide variant	NM_014915.3(ANKRD26):c.2988G>A (p.Lys996=)	Inborn genetic diseases [RCV004953431]\|not provided [RCV003716987]	benign\|likely benign	10	27035462	27035462	Human	1	name
405244190	CV3050519	single nucleotide variant	NM_014915.3(ANKRD26):c.227G>C (p.Arg76Thr)	not provided [RCV003719920]	uncertain significance	10	27100100	27100100	Human		name
405244193	CV3050520	single nucleotide variant	NM_014915.3(ANKRD26):c.210G>C (p.Lys70Asn)	not provided [RCV003719921]	uncertain significance	10	27100117	27100117	Human		name
405244671	CV3050735	single nucleotide variant	NM_014915.3(ANKRD26):c.151C>T (p.His51Tyr)	Inborn genetic diseases [RCV005363216]\|not provided [RCV003720055]	uncertain significance	10	27100176	27100176	Human	1	name
405244750	CV3050768	single nucleotide variant	NM_014915.3(ANKRD26):c.1269G>A (p.Glu423=)	not provided [RCV003720080]	uncertain significance	10	27066487	27066487	Human		name
405223394	CV3061286	single nucleotide variant	NM_014915.3(ANKRD26):c.1368G>C (p.Val456=)	Inborn genetic diseases [RCV005363239]\|not provided [RCV003733658]	likely benign	10	27061238	27061238	Human	1	name
405159302	CV3061720	single nucleotide variant	NM_014915.3(ANKRD26):c.1677A>G (p.Glu559=)	Inborn genetic diseases [RCV005363242]\|not provided [RCV003726981]	likely benign	10	27048938	27048938	Human	1	name
405208203	CV3064625	single nucleotide variant	NM_014915.3(ANKRD26):c.1908G>A (p.Lys636=)	Inborn genetic diseases [RCV004950646]\|not provided [RCV003731521]	likely benign	10	27046430	27046430	Human	1	name
405155866	CV3064881	single nucleotide variant	NM_014915.3(ANKRD26):c.146A>G (p.Lys49Arg)	not provided [RCV003726744]	uncertain significance	10	27100181	27100181	Human		name
405208817	CV3065523	single nucleotide variant	NM_014915.3(ANKRD26):c.109C>G (p.Gln37Glu)	Inborn genetic diseases [RCV005377546]\|not provided [RCV003731696]	uncertain significance	10	27100218	27100218	Human	1	name
405200884	CV3066830	single nucleotide variant	NM_014915.3(ANKRD26):c.1218C>T (p.Ser406=)	not provided [RCV003730761]	likely benign	10	27066538	27066538	Human		name
11609136	CV310150	single nucleotide variant	NM_014915.3(ANKRD26):c.269A>G (p.Asn90Ser)	Thrombocytopenia 2 [RCV000364191]\|not provided [RCV003718163]	likely benign\|uncertain significance	10	27093773	27093773	Human	1	name
405102803	CV3119533	single nucleotide variant	NM_014915.3(ANKRD26):c.1077G>A (p.Lys359=)	not provided [RCV003811795]	uncertain significance	10	27077338	27077338	Human		name
405006262	CV3120955	single nucleotide variant	NM_014915.3(ANKRD26):c.2301A>C (p.Leu767=)	Inborn genetic diseases [RCV005377576]\|not provided [RCV003828558]	likely benign	10	27040039	27040039	Human	1	name
405128025	CV3132949	single nucleotide variant	NM_014915.3(ANKRD26):c.1185A>G (p.Glu395=)	not provided [RCV003838112]	likely benign	10	27067179	27067179	Human		name
405168519	CV3149833	single nucleotide variant	NM_014915.3(ANKRD26):c.1848G>A (p.Lys616=)	not provided [RCV003841304]	likely benign	10	27046490	27046490	Human		name
11602319	CV315227	single nucleotide variant	NM_014915.3(ANKRD26):c.2787C>T (p.Asp929=)	Inborn genetic diseases [RCV005372280]\|Thrombocytopenia 2 [RCV000290010]	benign\|likely benign\|uncertain significance	10	27035663	27035663	Human	2	name
405169935	CV3155448	single nucleotide variant	NM_014915.3(ANKRD26):c.107C>A (p.Ser36Ter)	not provided [RCV003857670]	uncertain significance	10	27100220	27100220	Human		name
402474336	CV3182733	single nucleotide variant	NM_014915.3(ANKRD26):c.236T>G (p.Met79Arg)	Inborn genetic diseases [RCV004950758]\|not provided [RCV003874976]	uncertain significance	10	27100091	27100091	Human	1	name
405259376	CV3194788	single nucleotide variant	NM_014915.3(ANKRD26):c.2778A>G (p.Leu926=)	ANKRD26-related disorder [RCV003894177]\|Inborn genetic diseases [RCV004953645]	likely benign	10	27035672	27035672	Human	2	name , alternate_id
405268780	CV3201149	single nucleotide variant	NM_014915.3(ANKRD26):c.2562C>T (p.Val854=)	ANKRD26-related disorder [RCV003899256]\|not provided [RCV005101527]	likely benign	10	27037321	27037321	Human	1	name , alternate_id
405294429	CV3211395	single nucleotide variant	NM_014915.3(ANKRD26):c.1611A>G (p.Glu537=)	ANKRD26-related disorder [RCV003934368]	likely benign	10	27053344	27053344	Human		name , trait , alternate_id
11610480	CV321263	single nucleotide variant	NM_014915.3(ANKRD26):c.2974C>T (p.Leu992=)	Inborn genetic diseases [RCV004948255]\|Thrombocytopenia 2 [RCV000382004]\|not provided [RCV001642928]	benign\|likely benign	10	27035476	27035476	Human	2	name
11606411	CV321278	single nucleotide variant	NM_014915.3(ANKRD26):c.1176T>C (p.Tyr392=)	Inborn genetic diseases [RCV004955403]\|Thrombocytopenia 2 [RCV000331160]	likely benign\|uncertain significance	10	27067188	27067188	Human	2	name
11604573	CV321880	single nucleotide variant	NM_014915.3(ANKRD26):c.101C>T (p.Ala34Val)	Inborn genetic diseases [RCV002520585]\|Thrombocytopenia 2 [RCV000310711]\|not provided [RCV002520584]\|not specified [RCV001820873]	benign\|likely benign\|uncertain significance	10	27100226	27100226	Human	2	name
405267604	CV3219357	single nucleotide variant	NM_014915.3(ANKRD26):c.1116T>C (p.Asn372=)	ANKRD26-related disorder [RCV003969607]\|Inborn genetic diseases [RCV004953665]\|not provided [RCV005103037]	benign\|likely benign	10	27067248	27067248	Human	2	name , alternate_id
405669128	CV3288757	single nucleotide variant	NM_014915.3(ANKRD26):c.106T>G (p.Ser36Ala)	Inborn genetic diseases [RCV004419137]	uncertain significance	10	27100221	27100221	Human	1	name
405669482	CV3288826	single nucleotide variant	NM_014915.3(ANKRD26):c.263G>A (p.Cys88Tyr)	Inborn genetic diseases [RCV004419206]	uncertain significance	10	27093779	27093779	Human	1	name
407425026	CV3411045	single nucleotide variant	NM_014915.3(ANKRD26):c.205A>G (p.Arg69Gly)	not provided [RCV004588735]	uncertain significance	10	27100122	27100122	Human		name
407429084	CV3413471	deletion	NM_014915.3(ANKRD26):c.506del (p.Asp169fs)	Thrombocytopenia 2 [RCV004594879]	uncertain significance	10	27093374	27093374	Human	1	name
408365420	CV3499894	single nucleotide variant	NM_014915.3(ANKRD26):c.196C>T (p.Leu66Phe)	Inborn genetic diseases [RCV004953700]\|not provided [RCV004721936]	uncertain significance	10	27100131	27100131	Human	1	name
408368957	CV3502700	single nucleotide variant	NM_014915.3(ANKRD26):c.248C>T (p.Ala83Val)	Inborn genetic diseases [RCV004953707]\|not provided [RCV004723821]	uncertain significance	10	27093794	27093794	Human	1	name
408393058	CV3519689	single nucleotide variant	NM_014915.3(ANKRD26):c.185T>C (p.Val62Ala)	not provided [RCV004763985]	uncertain significance	10	27100142	27100142	Human		name
408388920	CV3522823	single nucleotide variant	NM_014915.3(ANKRD26):c.1296G>A (p.Lys432=)	not provided [RCV004769204]	uncertain significance	10	27064055	27064055	Human		name
408393080	CV3528355	single nucleotide variant	NM_014915.3(ANKRD26):c.173A>G (p.Asn58Ser)	Inborn genetic diseases [RCV005358148]\|not provided [RCV004776123]	uncertain significance	10	27100154	27100154	Human	1	name
597700533	CV3553983	single nucleotide variant	NM_014915.3(ANKRD26):c.165C>G (p.Ser55Arg)	Inborn genetic diseases [RCV004956556]	uncertain significance	10	27100162	27100162	Human	1	name
597683395	CV3553993	single nucleotide variant	NM_014915.3(ANKRD26):c.101C>G (p.Ala34Gly)	Inborn genetic diseases [RCV004952260]	uncertain significance	10	27100226	27100226	Human	1	name
597700546	CV3554014	single nucleotide variant	NM_014915.3(ANKRD26):c.185T>A (p.Val62Glu)	Inborn genetic diseases [RCV004956558]	uncertain significance	10	27100142	27100142	Human	1	name
597683421	CV3554068	single nucleotide variant	NM_014915.3(ANKRD26):c.1155A>C (p.Thr385=)	Inborn genetic diseases [RCV004952264]	likely benign	10	27067209	27067209	Human	1	name
597683454	CV3554138	single nucleotide variant	NM_014915.3(ANKRD26):c.111G>T (p.Gln37His)	Inborn genetic diseases [RCV004952269]	uncertain significance	10	27100216	27100216	Human	1	name
597682762	CV3556890	single nucleotide variant	NM_014915.3(ANKRD26):c.1821T>A (p.Gly607=)	Inborn genetic diseases [RCV004952172]	likely benign	10	27046517	27046517	Human	1	name
597700203	CV3556895	single nucleotide variant	NM_014915.3(ANKRD26):c.104A>G (p.Tyr35Cys)	Inborn genetic diseases [RCV004956506]	uncertain significance	10	27100223	27100223	Human	1	name
597682798	CV3556898	single nucleotide variant	NM_014915.3(ANKRD26):c.275A>C (p.His92Pro)	Inborn genetic diseases [RCV004952177]	uncertain significance	10	27093767	27093767	Human	1	name
597682821	CV3556901	single nucleotide variant	NM_014915.3(ANKRD26):c.116G>T (p.Gly39Val)	Inborn genetic diseases [RCV004952180]	uncertain significance	10	27100211	27100211	Human	1	name
597700240	CV3556914	single nucleotide variant	NM_014915.3(ANKRD26):c.1752A>G (p.Lys584=)	Inborn genetic diseases [RCV004956511]	likely benign	10	27048863	27048863	Human	1	name
597700265	CV3556973	single nucleotide variant	NM_014915.3(ANKRD26):c.2391A>G (p.Gln797=)	Inborn genetic diseases [RCV004956515]	likely benign	10	27038039	27038039	Human	1	name
597682925	CV3557001	single nucleotide variant	NM_014915.3(ANKRD26):c.2814A>G (p.Lys938=)	Inborn genetic diseases [RCV004952194]	likely benign	10	27035636	27035636	Human	1	name
597682961	CV3557019	single nucleotide variant	NM_014915.3(ANKRD26):c.1377A>C (p.Ile459=)	Inborn genetic diseases [RCV004952199]	likely benign	10	27061229	27061229	Human	1	name
597683008	CV3557099	single nucleotide variant	NM_014915.3(ANKRD26):c.2838T>A (p.Leu946=)	Inborn genetic diseases [RCV004952205]	likely benign	10	27035612	27035612	Human	1	name
597700302	CV3557146	single nucleotide variant	NM_014915.3(ANKRD26):c.2982T>C (p.Asn994=)	Inborn genetic diseases [RCV004956521]	likely benign	10	27035468	27035468	Human	1	name
597682524	CV3560425	single nucleotide variant	NM_014915.3(ANKRD26):c.109C>A (p.Gln37Lys)	Inborn genetic diseases [RCV004952137]\|not provided [RCV005107512]	uncertain significance	10	27100218	27100218	Human	1	name
597682530	CV3560465	single nucleotide variant	NM_014915.3(ANKRD26):c.1188G>A (p.Val396=)	Inborn genetic diseases [RCV004952138]	likely benign	10	27067176	27067176	Human	1	name
597682640	CV3560578	single nucleotide variant	NM_014915.3(ANKRD26):c.2454A>G (p.Arg818=)	Inborn genetic diseases [RCV004952153]	likely benign	10	27037976	27037976	Human	1	name
597682654	CV3560590	single nucleotide variant	NM_014915.3(ANKRD26):c.215G>T (p.Gly72Val)	Inborn genetic diseases [RCV004952155]	uncertain significance	10	27100112	27100112	Human	1	name
597682660	CV3560595	single nucleotide variant	NM_014915.3(ANKRD26):c.2487G>A (p.Val829=)	Inborn genetic diseases [RCV004952156]	likely benign	10	27037943	27037943	Human	1	name
597700132	CV3560678	single nucleotide variant	NM_014915.3(ANKRD26):c.2088G>A (p.Glu696=)	Inborn genetic diseases [RCV004956496]	likely benign	10	27043499	27043499	Human	1	name
597682706	CV3560732	single nucleotide variant	NM_014915.3(ANKRD26):c.283G>A (p.Val95Ile)	Inborn genetic diseases [RCV004952162]\|not provided [RCV005107519]	uncertain significance	10	27093759	27093759	Human	1	name
597699802	CV3563407	single nucleotide variant	NM_014915.3(ANKRD26):c.157G>T (p.Ala53Ser)	Inborn genetic diseases [RCV004956443]	uncertain significance	10	27100170	27100170	Human	1	name
597700024	CV3563567	single nucleotide variant	NM_014915.3(ANKRD26):c.2337T>C (p.His779=)	Inborn genetic diseases [RCV004956478]\|not provided [RCV005107511]	likely benign	10	27040003	27040003	Human	1	name
597683678	CV3563999	single nucleotide variant	NM_014915.3(ANKRD26):c.182A>C (p.Lys61Thr)	Inborn genetic diseases [RCV004952302]	uncertain significance	10	27100145	27100145	Human	1	name
597702288	CV3728905	microsatellite	NM_014915.3(ANKRD26):c.5AGA[1] (p.Lys3del)	Thrombocytopenia 2 [RCV005033639]	uncertain significance	10	27100317	27100319	Human		name
597966850	CV3751680	single nucleotide variant	NM_014915.3(ANKRD26):c.1101T>C (p.Ile367=)	not provided [RCV005083050]	likely benign	10	27067263	27067263	Human		name
597842340	CV3752970	single nucleotide variant	NM_014915.3(ANKRD26):c.2016C>T (p.Asn672=)	not provided [RCV005086699]	likely benign	10	27044160	27044160	Human		name
597957749	CV3755154	single nucleotide variant	NM_014915.3(ANKRD26):c.1920A>C (p.Leu640=)	not provided [RCV005080824]	likely benign	10	27046418	27046418	Human		name
597886444	CV3787413	single nucleotide variant	NM_014915.3(ANKRD26):c.260C>T (p.Ala87Val)	not provided [RCV005124979]	uncertain significance	10	27093782	27093782	Human		name
597972604	CV3790410	single nucleotide variant	NM_014915.3(ANKRD26):c.2958A>G (p.Ala986=)	not provided [RCV005142833]	likely benign	10	27035492	27035492	Human		name
597973875	CV3820734	single nucleotide variant	NM_014915.3(ANKRD26):c.2169T>C (p.Val723=)	not provided [RCV005168251]	likely benign	10	27040171	27040171	Human		name
597960760	CV3840315	single nucleotide variant	NM_014915.3(ANKRD26):c.1890T>C (p.Asn630=)	Inborn genetic diseases [RCV005353441]\|not provided [RCV005192799]	likely benign	10	27046448	27046448	Human	1	name
597925432	CV3840552	single nucleotide variant	NM_014915.3(ANKRD26):c.1683A>G (p.Ser561=)	Inborn genetic diseases [RCV005379814]\|not provided [RCV005185023]	likely benign	10	27048932	27048932	Human	1	name
597962952	CV3841356	single nucleotide variant	NM_014915.3(ANKRD26):c.172A>G (p.Asn58Asp)	not provided [RCV005193459]	uncertain significance	10	27100155	27100155	Human		name
597954705	CV3844486	single nucleotide variant	NM_014915.3(ANKRD26):c.142G>C (p.Gly48Arg)	Inborn genetic diseases [RCV005365488]\|not provided [RCV005191160]	uncertain significance	10	27100185	27100185	Human	1	name
597898299	CV3854545	single nucleotide variant	NM_014915.3(ANKRD26):c.231C>G (p.Asp77Glu)	Inborn genetic diseases [RCV005379836]\|not provided [RCV005201652]	uncertain significance	10	27100096	27100096	Human	1	name
597922236	CV3861885	single nucleotide variant	NM_014915.3(ANKRD26):c.190C>T (p.Gln64Ter)	not provided [RCV005205261]	uncertain significance	10	27100137	27100137	Human		name
598126949	CV3887936	single nucleotide variant	NM_014915.3(ANKRD26):c.103T>A (p.Tyr35Asn)	Inborn genetic diseases [RCV005379864]\|not provided [RCV005242622]	likely benign\|uncertain significance	10	27100224	27100224	Human	1	name
598223883	CV3981166	single nucleotide variant	NM_014915.3(ANKRD26):c.1782A>G (p.Gln594=)	Inborn genetic diseases [RCV005380118]	likely benign	10	27048833	27048833	Human	1	name
598252662	CV3981198	single nucleotide variant	NM_014915.3(ANKRD26):c.1146A>G (p.Leu382=)	Inborn genetic diseases [RCV005366803]	likely benign	10	27067218	27067218	Human	1	name
598182296	CV3981305	single nucleotide variant	NM_014915.3(ANKRD26):c.2091T>C (p.Asp697=)	Inborn genetic diseases [RCV005372717]	likely benign	10	27043496	27043496	Human	1	name
598182347	CV3981322	single nucleotide variant	NM_014915.3(ANKRD26):c.2082C>T (p.Ala694=)	Inborn genetic diseases [RCV005372726]	likely benign	10	27043505	27043505	Human	1	name
598182557	CV3981386	single nucleotide variant	NM_014915.3(ANKRD26):c.1023T>C (p.Pro341=)	Inborn genetic diseases [RCV005372764]	likely benign	10	27077392	27077392	Human	1	name
598182900	CV3981495	single nucleotide variant	NM_014915.3(ANKRD26):c.2640C>G (p.Thr880=)	Inborn genetic diseases [RCV005372825]	likely benign	10	27037243	27037243	Human	1	name
598183006	CV3981525	single nucleotide variant	NM_014915.3(ANKRD26):c.115G>A (p.Gly39Ser)	Inborn genetic diseases [RCV005372845]	uncertain significance	10	27100212	27100212	Human	1	name
598199343	CV3981694	single nucleotide variant	NM_014915.3(ANKRD26):c.1470T>A (p.Pro490=)	Inborn genetic diseases [RCV005375685]	likely benign	10	27060533	27060533	Human	1	name
598178063	CV3981974	single nucleotide variant	NM_014915.3(ANKRD26):c.1494T>C (p.Pro498=)	Inborn genetic diseases [RCV005371717]	likely benign	10	27060415	27060415	Human	1	name
598251266	CV3984806	single nucleotide variant	NM_014915.3(ANKRD26):c.179C>T (p.Ala60Val)	Inborn genetic diseases [RCV005366655]	uncertain significance	10	27100148	27100148	Human	1	name
598222905	CV3984837	single nucleotide variant	NM_014915.3(ANKRD26):c.2070A>G (p.Ser690=)	Inborn genetic diseases [RCV005379963]	likely benign	10	27043517	27043517	Human	1	name
598176081	CV3985157	single nucleotide variant	NM_014915.3(ANKRD26):c.229G>C (p.Asp77His)	Inborn genetic diseases [RCV005371357]	uncertain significance	10	27100098	27100098	Human	1	name
598197539	CV3985176	single nucleotide variant	NM_014915.3(ANKRD26):c.1575C>T (p.Asp525=)	Inborn genetic diseases [RCV005375435]	likely benign	10	27053380	27053380	Human	1	name
598176680	CV3985369	single nucleotide variant	NM_014915.3(ANKRD26):c.181A>G (p.Lys61Glu)	Inborn genetic diseases [RCV005371456]	uncertain significance	10	27100146	27100146	Human	1	name
598198454	CV3985402	single nucleotide variant	NM_014915.3(ANKRD26):c.2530T>C (p.Leu844=)	Inborn genetic diseases [RCV005375559]	likely benign	10	27037900	27037900	Human	1	name
598176861	CV3985469	single nucleotide variant	NM_014915.3(ANKRD26):c.2886G>A (p.Gln962=)	Inborn genetic diseases [RCV005371492]	likely benign	10	27035564	27035564	Human	1	name
598240962	CV3985609	single nucleotide variant	NM_014915.3(ANKRD26):c.2037G>A (p.Gln679=)	Inborn genetic diseases [RCV005364732]	likely benign	10	27043550	27043550	Human	1	name
598241158	CV3985672	single nucleotide variant	NM_014915.3(ANKRD26):c.1812T>C (p.Ala604=)	Inborn genetic diseases [RCV005364765]	likely benign	10	27048803	27048803	Human	1	name
598241184	CV3985681	single nucleotide variant	NM_014915.3(ANKRD26):c.2457A>G (p.Lys819=)	Inborn genetic diseases [RCV005364770]	likely benign	10	27037973	27037973	Human	1	name
598225668	CV3985806	single nucleotide variant	NM_014915.3(ANKRD26):c.259G>T (p.Ala87Ser)	Inborn genetic diseases [RCV005380442]	uncertain significance	10	27093783	27093783	Human	1	name
598249756	CV3987927	single nucleotide variant	NM_014915.3(ANKRD26):c.2503C>T (p.Leu835=)	Inborn genetic diseases [RCV005366415]	likely benign	10	27037927	27037927	Human	1	name
598262131	CV3987937	single nucleotide variant	NM_014915.3(ANKRD26):c.2139A>G (p.Glu713=)	Inborn genetic diseases [RCV005347986]	likely benign	10	27043448	27043448	Human	1	name
598250043	CV3988010	single nucleotide variant	NM_014915.3(ANKRD26):c.1533A>G (p.Gly511=)	Inborn genetic diseases [RCV005366455]	likely benign	10	27060376	27060376	Human	1	name
598184766	CV3988367	single nucleotide variant	NM_014915.3(ANKRD26):c.155A>G (p.Lys52Arg)	Inborn genetic diseases [RCV005373135]	uncertain significance	10	27100172	27100172	Human	1	name
598184904	CV3988402	single nucleotide variant	NM_014915.3(ANKRD26):c.2910A>G (p.Thr970=)	Inborn genetic diseases [RCV005373159]	likely benign	10	27035540	27035540	Human	1	name
598185125	CV3988464	single nucleotide variant	NM_014915.3(ANKRD26):c.2889T>C (p.Asn963=)	Inborn genetic diseases [RCV005373197]	likely benign	10	27035561	27035561	Human	1	name
598196896	CV3988671	single nucleotide variant	NM_014915.3(ANKRD26):c.1200T>C (p.Asn400=)	Inborn genetic diseases [RCV005375345]	likely benign	10	27067164	27067164	Human	1	name
598239944	CV3988790	single nucleotide variant	NM_014915.3(ANKRD26):c.1125T>C (p.Asp375=)	Inborn genetic diseases [RCV005364520]	likely benign	10	27067239	27067239	Human	1	name
598239992	CV3988801	single nucleotide variant	NM_014915.3(ANKRD26):c.207G>C (p.Arg69Ser)	Inborn genetic diseases [RCV005364528]	uncertain significance	10	27100120	27100120	Human	1	name
598240153	CV3988885	single nucleotide variant	NM_014915.3(ANKRD26):c.2052T>C (p.Val684=)	Inborn genetic diseases [RCV005364562]	likely benign	10	27043535	27043535	Human	1	name
598224881	CV3989178	single nucleotide variant	NM_014915.3(ANKRD26):c.1110A>G (p.Lys370=)	Inborn genetic diseases [RCV005380295]	likely benign	10	27067254	27067254	Human	1	name
598224906	CV3989189	single nucleotide variant	NM_014915.3(ANKRD26):c.2979G>A (p.Glu993=)	Inborn genetic diseases [RCV005380301]	likely benign	10	27035471	27035471	Human	1	name
598238892	CV3991900	single nucleotide variant	NM_014915.3(ANKRD26):c.1974G>A (p.Glu658=)	Inborn genetic diseases [RCV005364332]	likely benign	10	27046364	27046364	Human	1	name
598230963	CV3991936	single nucleotide variant	NM_014915.3(ANKRD26):c.1905G>C (p.Gly635=)	Inborn genetic diseases [RCV005362791]	likely benign	10	27046433	27046433	Human	1	name
598183398	CV3992167	single nucleotide variant	NM_014915.3(ANKRD26):c.2880A>C (p.Ile960=)	Inborn genetic diseases [RCV005372917]	likely benign	10	27035570	27035570	Human	1	name
598183439	CV3992177	single nucleotide variant	NM_014915.3(ANKRD26):c.2551T>C (p.Leu851=)	Inborn genetic diseases [RCV005372925]	likely benign	10	27037879	27037879	Human	1	name
598164520	CV3992230	single nucleotide variant	NM_014915.3(ANKRD26):c.2277G>A (p.Lys759=)	Inborn genetic diseases [RCV005369018]	likely benign	10	27040063	27040063	Human	1	name
598164552	CV3992239	single nucleotide variant	NM_014915.3(ANKRD26):c.2901A>G (p.Leu967=)	Inborn genetic diseases [RCV005369023]	likely benign	10	27035549	27035549	Human	1	name
598183647	CV3992248	single nucleotide variant	NM_014915.3(ANKRD26):c.1959A>G (p.Leu653=)	Inborn genetic diseases [RCV005372963]	likely benign	10	27046379	27046379	Human	1	name
598164990	CV3992391	single nucleotide variant	NM_014915.3(ANKRD26):c.2301A>G (p.Leu767=)	Inborn genetic diseases [RCV005369095]	likely benign	10	27040039	27040039	Human	1	name
598165022	CV3992401	single nucleotide variant	NM_014915.3(ANKRD26):c.2538T>G (p.Thr846=)	Inborn genetic diseases [RCV005369100]	likely benign	10	27037892	27037892	Human	1	name
598165090	CV3992429	single nucleotide variant	NM_014915.3(ANKRD26):c.1770T>A (p.Thr590=)	Inborn genetic diseases [RCV005369113]	likely benign	10	27048845	27048845	Human	1	name
598184406	CV3992469	single nucleotide variant	NM_014915.3(ANKRD26):c.2001A>G (p.Thr667=)	Inborn genetic diseases [RCV005373079]	likely benign	10	27044175	27044175	Human	1	name
598184574	CV3992514	single nucleotide variant	NM_014915.3(ANKRD26):c.163A>G (p.Ser55Gly)	Inborn genetic diseases [RCV005373103]	uncertain significance	10	27100164	27100164	Human	1	name
598210316	CV3992543	single nucleotide variant	NM_014915.3(ANKRD26):c.1341T>C (p.Asn447=)	Inborn genetic diseases [RCV005377843]	likely benign	10	27064010	27064010	Human	1	name
598210665	CV3992643	single nucleotide variant	NM_014915.3(ANKRD26):c.1428T>C (p.Asp476=)	Inborn genetic diseases [RCV005377899]	likely benign	10	27061178	27061178	Human	1	name
598178561	CV3992659	single nucleotide variant	NM_014915.3(ANKRD26):c.2637G>T (p.Leu879=)	Inborn genetic diseases [RCV005371790]	likely benign	10	27037246	27037246	Human	1	name
598210787	CV3992669	single nucleotide variant	NM_014915.3(ANKRD26):c.2635C>T (p.Leu879=)	Inborn genetic diseases [RCV005377916]	likely benign	10	27037248	27037248	Human	1	name
598239391	CV3992781	single nucleotide variant	NM_014915.3(ANKRD26):c.268A>C (p.Asn90His)	Inborn genetic diseases [RCV005364422]	uncertain significance	10	27093774	27093774	Human	1	name
598211276	CV3992814	single nucleotide variant	NM_014915.3(ANKRD26):c.127C>G (p.Arg43Gly)	Inborn genetic diseases [RCV005377993]	uncertain significance	10	27100200	27100200	Human	1	name
598211537	CV3992877	single nucleotide variant	NM_014915.3(ANKRD26):c.2877T>C (p.Thr959=)	Inborn genetic diseases [RCV005378036]	likely benign	10	27035573	27035573	Human	1	name
13488313	CV444598	single nucleotide variant	NM_014915.3(ANKRD26):c.112C>T (p.Pro38Ser)	ANKRD26-related disorder [RCV003392351]\|Inborn genetic diseases [RCV004955578]\|not provided [RCV000523525]\|not specified [RCV001821459]	uncertain significance	10	27100215	27100215	Human	2	name , alternate_id
15129804	CV737439	single nucleotide variant	NM_014915.3(ANKRD26):c.1806G>A (p.Glu602=)	Inborn genetic diseases [RCV004958244]\|Thrombocytopenia 2 [RCV002260102]\|not provided [RCV000897503]\|not specified [RCV001818727]	benign\|likely benign	10	27048809	27048809	Human	2	name
8633593	CV88808	single nucleotide variant	NM_014915.2(ANKRD26):c.1788C>A (p.Pro596=)	Malignant melanoma [RCV000068903]	not provided	10	27048827	27048827	Human		name
126741295	CV1020723	single nucleotide variant	NM_014915.3(ANKRD26):c.371A>T (p.Gln124Leu)	ANKRD26-related disorder [RCV003928847]\|Thrombocytopenia 2 [RCV001336218]\|not provided [RCV002546767]\|not specified [RCV001820032]	likely benign\|conflicting interpretations of pathogenicity\|uncertain significance	10	27093509	27093509	Human	1	name , alternate_id
150424023	CV1184354	single nucleotide variant	NM_014915.3(ANKRD26):c.371A>G (p.Gln124Arg)	not provided [RCV001556113]	uncertain significance	10	27093509	27093509	Human		name
150428182	CV1187579	deletion	NM_014915.3(ANKRD26):c.1985+283_1985+286del	not provided [RCV001561927]	likely benign	10	27046067	27046070	Human		name
150502810	CV1254626	deletion	NM_014915.3(ANKRD26):c.2020-125_2020-124del	not provided [RCV001677328]	benign	10	27043691	27043692	Human		name
150482385	CV1261612	microsatellite	NM_014915.3(ANKRD26):c.1269+141_1269+144del	not provided [RCV001686215]	benign	10	27066343	27066346	Human		name
150545999	CV1291547	single nucleotide variant	NM_014915.3(ANKRD26):c.3735G>A (p.Thr1245=)	ANKRD26-related disorder [RCV003913355]\|Inborn genetic diseases [RCV004953009]\|not provided [RCV001732801]\|not specified [RCV001821971]	benign\|likely benign	10	27033297	27033297	Human	2	name , alternate_id
150530696	CV1293457	single nucleotide variant	NM_014915.3(ANKRD26):c.473A>G (p.Asp158Gly)	not provided [RCV001756678]	uncertain significance	10	27093407	27093407	Human		name
150527905	CV1300911	single nucleotide variant	NM_014915.3(ANKRD26):c.951A>C (p.Glu317Asp)	Inborn genetic diseases [RCV004953032]\|not provided [RCV001754771]	uncertain significance	10	27077464	27077464	Human	1	name
150553486	CV1303490	single nucleotide variant	NM_014915.3(ANKRD26):c.682A>C (p.Lys228Gln)	Inborn genetic diseases [RCV005374799]\|not provided [RCV001769180]	uncertain significance	10	27086566	27086566	Human	1	name
150554650	CV1304367	single nucleotide variant	NM_014915.3(ANKRD26):c.501G>T (p.Leu167Phe)	ANKRD26-related disorder [RCV004741073]\|Inborn genetic diseases [RCV002540534]\|not provided [RCV001771337]	likely benign\|conflicting interpretations of pathogenicity\|uncertain significance	10	27093379	27093379	Human	2	name , alternate_id
150555662	CV1304817	single nucleotide variant	NM_014915.3(ANKRD26):c.434A>G (p.His145Arg)	Inborn genetic diseases [RCV004953058]\|not provided [RCV001773065]\|not specified [RCV004526146]	uncertain significance	10	27093446	27093446	Human	1	name
151353837	CV1327389	single nucleotide variant	NM_014915.3(ANKRD26):c.937G>T (p.Asp313Tyr)	ANKRD26-related disorder [RCV003911029]\|Inborn genetic diseases [RCV004946745]\|not provided [RCV002541988]\|not specified [RCV001817333]	benign\|likely benign\|uncertain significance	10	27077478	27077478	Human	2	name , alternate_id
151353879	CV1327431	single nucleotide variant	NM_014915.3(ANKRD26):c.4299G>A (p.Glu1433=)	Inborn genetic diseases [RCV004946746]\|not provided [RCV003718433]\|not specified [RCV001817375]	likely benign	10	27017709	27017709	Human	1	name
151354045	CV1327597	single nucleotide variant	NM_014915.3(ANKRD26):c.770C>T (p.Ser257Leu)	ANKRD26-related disorder [RCV004741088]\|Inborn genetic diseases [RCV004953083]\|not provided [RCV004783987]\|not specified [RCV001817541]	uncertain significance	10	27079132	27079132	Human	2	name , alternate_id
151354653	CV1327720	single nucleotide variant	NM_014915.3(ANKRD26):c.301G>A (p.Asp101Asn)	ANKRD26-related disorder [RCV003892866]\|not provided [RCV002542548]\|not specified [RCV001819195]	likely benign\|uncertain significance	10	27093741	27093741	Human	1	name , alternate_id
151355242	CV1328309	single nucleotide variant	NM_014915.3(ANKRD26):c.599A>G (p.Lys200Arg)	ANKRD26-related disorder [RCV003913406]\|Inborn genetic diseases [RCV004953092]\|not provided [RCV002285500]\|not specified [RCV001820314]	likely benign\|conflicting interpretations of pathogenicity\|uncertain significance	10	27092445	27092445	Human	2	name , alternate_id
151355443	CV1328510	single nucleotide variant	NM_014915.3(ANKRD26):c.710T>C (p.Val237Ala)	Inborn genetic diseases [RCV005374816]\|not provided [RCV003728026]\|not specified [RCV001820515]	uncertain significance	10	27082833	27082833	Human	1	name
151356143	CV1328907	single nucleotide variant	NM_014915.3(ANKRD26):c.697A>G (p.Asn233Asp)	not specified [RCV001822496]	uncertain significance	10	27086551	27086551	Human		name
151356316	CV1329080	single nucleotide variant	NM_014915.3(ANKRD26):c.826C>T (p.Pro276Ser)	Inborn genetic diseases [RCV004946755]\|Thrombocytopenia 2 [RCV005038346]\|not provided [RCV003324833]\|not specified [RCV001822669]	uncertain significance	10	27077681	27077681	Human	2	name
151356402	CV1329166	single nucleotide variant	NM_014915.3(ANKRD26):c.320A>G (p.Asn107Ser)	Inborn genetic diseases [RCV004946757]\|Thrombocytopenia 2 [RCV003154198]\|not provided [RCV003718444]\|not specified [RCV001822755]	uncertain significance	10	27093722	27093722	Human	2	name
151354343	CV1329476	single nucleotide variant	NM_014915.3(ANKRD26):c.349C>G (p.Leu117Val)	not specified [RCV001817839]	uncertain significance	10	27093693	27093693	Human		name
151354420	CV1329553	duplication	NM_014915.3(ANKRD26):c.1110dup (p.Glu371fs)	not provided [RCV004770218]\|not specified [RCV001817916]	uncertain significance	10	27067253	27067254	Human		name
152980254	CV1675890	single nucleotide variant	NM_014915.3(ANKRD26):c.334G>A (p.Glu112Lys)	not provided [RCV002244481]	uncertain significance	10	27093708	27093708	Human		name
153000961	CV1683992	single nucleotide variant	NM_014915.3(ANKRD26):c.425C>T (p.Ala142Val)	Inborn genetic diseases [RCV005375077]\|Thrombocytopenia 2 [RCV002254842]\|not provided [RCV003738168]	likely benign\|uncertain significance	10	27093455	27093455	Human	2	name
153304397	CV1686992	single nucleotide variant	NM_014915.3(ANKRD26):c.3406T>C (p.Leu1136=)	Inborn genetic diseases [RCV005370182]\|not provided [RCV002262279]	likely benign	10	27035044	27035044	Human	1	name
153348891	CV1692937	single nucleotide variant	NM_014915.3(ANKRD26):c.539T>G (p.Leu180Arg)	ANKRD26-related disorder [RCV004741278]\|Inborn genetic diseases [RCV004047503]\|not provided [RCV002274793]	uncertain significance	10	27092505	27092505	Human	2	name , alternate_id
155645783	CV1709137	single nucleotide variant	NM_014915.3(ANKRD26):c.358G>A (p.Ala120Thr)	not provided [RCV002292013]	uncertain significance	10	27093522	27093522	Human		name
155646002	CV1709366	single nucleotide variant	NM_014915.3(ANKRD26):c.821C>G (p.Pro274Arg)	Inborn genetic diseases [RCV005375086]\|Thrombocytopenia 2 [RCV002292242]	uncertain significance	10	27077686	27077686	Human	2	name
155750122	CV1779419	single nucleotide variant	NM_014915.3(ANKRD26):c.316C>T (p.Leu106Phe)	not provided [RCV002305375]	uncertain significance	10	27093726	27093726	Human		name
155797056	CV1859222	deletion	NM_014915.3(ANKRD26):c.2127del (p.Met709fs)	not provided [RCV002464850]	uncertain significance	10	27043460	27043460	Human		name
155795276	CV1861212	single nucleotide variant	NM_014915.3(ANKRD26):c.755C>T (p.Pro252Leu)	Inborn genetic diseases [RCV004067571]\|not provided [RCV002469492]	uncertain significance	10	27079147	27079147	Human	1	name
156373646	CV1874908	single nucleotide variant	NM_014915.3(ANKRD26):c.3528A>G (p.Gln1176=)	Inborn genetic diseases [RCV004948945]\|not provided [RCV003066512]	likely benign	10	27034922	27034922	Human	1	name
156413486	CV1900966	single nucleotide variant	NM_014915.3(ANKRD26):c.3423T>C (p.Ser1141=)	Inborn genetic diseases [RCV004961069]\|not provided [RCV002588180]	likely benign	10	27035027	27035027	Human	1	name
156029631	CV1903278	single nucleotide variant	NM_014915.3(ANKRD26):c.4204C>T (p.Leu1402=)	Inborn genetic diseases [RCV004948984]\|not provided [RCV003100590]	likely benign	10	27022569	27022569	Human	1	name
156030916	CV1903527	single nucleotide variant	NM_014915.3(ANKRD26):c.4644T>C (p.Asn1548=)	Inborn genetic diseases [RCV004961036]\|not provided [RCV003100646]	likely benign	10	27014574	27014574	Human	1	name
156107970	CV1903696	single nucleotide variant	NM_014915.3(ANKRD26):c.3462C>T (p.His1154=)	ANKRD26-related disorder [RCV004741398]\|Inborn genetic diseases [RCV004948992]\|not provided [RCV003080855]	likely benign	10	27034988	27034988	Human	2	name , alternate_id
156028666	CV1906981	single nucleotide variant	NM_014915.3(ANKRD26):c.4650C>T (p.Thr1550=)	Inborn genetic diseases [RCV004948982]\|not provided [RCV003100546]	likely benign	10	27014568	27014568	Human	1	name
156291659	CV1907923	single nucleotide variant	NM_014915.3(ANKRD26):c.3924A>G (p.Gln1308=)	not provided [RCV002598780]	likely benign	10	27028900	27028900	Human		name
156401227	CV1907948	single nucleotide variant	NM_014915.3(ANKRD26):c.475A>T (p.Ile159Leu)	Inborn genetic diseases [RCV004654138]\|Thrombocytopenia 2 [RCV003154272]\|not provided [RCV002584897]	uncertain significance	10	27093405	27093405	Human	2	name
156217954	CV1910764	single nucleotide variant	NM_014915.3(ANKRD26):c.3798C>A (p.Ile1266=)	not provided [RCV002596345]	likely benign	10	27033234	27033234	Human		name
156133187	CV1914301	single nucleotide variant	NM_014915.3(ANKRD26):c.4776G>A (p.Gln1592=)	not provided [RCV002623386]	likely benign	10	27013059	27013059	Human		name
156442418	CV1938648	single nucleotide variant	NM_014915.3(ANKRD26):c.3072G>A (p.Glu1024=)	Inborn genetic diseases [RCV005363071]\|not provided [RCV003112761]	likely benign	10	27035378	27035378	Human	1	name
156434064	CV1946782	single nucleotide variant	NM_014915.3(ANKRD26):c.736A>G (p.Ser246Gly)	not provided [RCV003104246]	uncertain significance	10	27082807	27082807	Human		name
155903030	CV1975788	single nucleotide variant	NM_014915.3(ANKRD26):c.487A>G (p.Thr163Ala)	not provided [RCV002613505]	uncertain significance	10	27093393	27093393	Human		name
156283725	CV2012627	single nucleotide variant	NM_014915.3(ANKRD26):c.998T>C (p.Phe333Ser)	Inborn genetic diseases [RCV005375143]\|not provided [RCV002715384]	uncertain significance	10	27077417	27077417	Human	1	name
156210509	CV2018845	single nucleotide variant	NM_014915.3(ANKRD26):c.881C>T (p.Ala294Val)	not provided [RCV002700608]	uncertain significance	10	27077534	27077534	Human		name
156021281	CV2040652	single nucleotide variant	NM_014915.3(ANKRD26):c.3954C>T (p.Asn1318=)	not provided [RCV002795599]	likely benign	10	27028870	27028870	Human		name
156110661	CV2068951	single nucleotide variant	NM_014915.3(ANKRD26):c.3826C>A (p.Arg1276=)	not provided [RCV002870882]	uncertain significance	10	27029338	27029338	Human		name
155973966	CV2079387	single nucleotide variant	NM_014915.3(ANKRD26):c.3093A>G (p.Glu1031=)	not provided [RCV002881616]	likely benign	10	27035357	27035357	Human		name
156091076	CV2106126	single nucleotide variant	NM_014915.3(ANKRD26):c.4293A>G (p.Gln1431=)	Inborn genetic diseases [RCV004948842]\|not provided [RCV002952361]	likely benign	10	27017715	27017715	Human	1	name
156089344	CV2132231	single nucleotide variant	NM_014915.3(ANKRD26):c.521C>G (p.Ala174Gly)	Inborn genetic diseases [RCV004960875]\|not provided [RCV002979544]	likely benign\|conflicting interpretations of pathogenicity\|uncertain significance	10	27093359	27093359	Human	1	name
156172527	CV2326783	single nucleotide variant	NM_014915.3(ANKRD26):c.343A>G (p.Thr115Ala)	Inborn genetic diseases [RCV002929917]	uncertain significance	10	27093699	27093699	Human	1	name
156100191	CV2386702	single nucleotide variant	NM_014915.3(ANKRD26):c.682A>G (p.Lys228Glu)	Inborn genetic diseases [RCV002739054]	uncertain significance	10	27086566	27086566	Human	1	name
155940127	CV2386741	single nucleotide variant	NM_014915.3(ANKRD26):c.757G>A (p.Gly253Ser)	Inborn genetic diseases [RCV002730055]\|not provided [RCV004725627]	uncertain significance	10	27079145	27079145	Human	1	name
243052183	CV2404328	single nucleotide variant	NM_014915.3(ANKRD26):c.811A>G (p.Lys271Glu)	not provided [RCV003129354]	uncertain significance	10	27079091	27079091	Human		name
243054067	CV2416496	single nucleotide variant	NM_014915.3(ANKRD26):c.524A>C (p.Lys175Thr)	Inborn genetic diseases [RCV005356368]\|not provided [RCV003149557]	uncertain significance	10	27093356	27093356	Human	1	name
243049585	CV2416895	single nucleotide variant	NM_014915.3(ANKRD26):c.329A>G (p.Asp110Gly)	not specified [RCV003151567]	uncertain significance	10	27093713	27093713	Human		name
329350832	CV2477666	single nucleotide variant	NM_014915.3(ANKRD26):c.584T>C (p.Val195Ala)	ANKRD26-related disorder [RCV003395727]\|Inborn genetic diseases [RCV004949048]\|not provided [RCV003223778]\|not specified [RCV005406647]	uncertain significance	10	27092460	27092460	Human	2	name , alternate_id
11549232	CV253726	single nucleotide variant	NM_014915.3(ANKRD26):c.3384G>A (p.Lys1128=)	Thrombocytopenia 2 [RCV000322406]\|not provided [RCV001357665]\|not specified [RCV000250144]	benign\|likely benign\|uncertain significance	10	27035066	27035066	Human	1	name
329848212	CV2667831	single nucleotide variant	NM_014915.3(ANKRD26):c.582G>C (p.Met194Ile)	not provided [RCV003229398]	uncertain significance	10	27092462	27092462	Human		name
329953900	CV2669239	deletion	NM_014915.3(ANKRD26):c.1101del (p.Ile367fs)	not provided [RCV003231744]	uncertain significance	10	27067263	27067263	Human		name
329954639	CV2670580	single nucleotide variant	NM_014915.3(ANKRD26):c.556G>A (p.Ala186Thr)	not provided [RCV003235847]	uncertain significance	10	27092488	27092488	Human		name
401724617	CV2672291	single nucleotide variant	NM_014915.3(ANKRD26):c.428A>T (p.Asp143Val)	not provided [RCV003239192]	uncertain significance	10	27093452	27093452	Human		name
401731773	CV2674477	single nucleotide variant	NM_014915.3(ANKRD26):c.436G>A (p.Gly146Ser)	Inborn genetic diseases [RCV003248702]	uncertain significance	10	27093444	27093444	Human	1	name
401796718	CV2739698	single nucleotide variant	NM_014915.3(ANKRD26):c.644A>G (p.His215Arg)	not provided [RCV003319659]	uncertain significance	10	27086604	27086604	Human		name
401856509	CV2752550	single nucleotide variant	NM_014915.3(ANKRD26):c.317T>G (p.Leu106Arg)	Thrombocytopenia 2 [RCV003340888]	uncertain significance	10	27093725	27093725	Human	1	name
401926171	CV2803441	single nucleotide variant	NM_014915.3(ANKRD26):c.922G>C (p.Glu308Gln)	ANKRD26-related disorder [RCV003405869]	uncertain significance	10	27077493	27077493	Human		name , trait , alternate_id
401938198	CV2813062	single nucleotide variant	NM_014915.3(ANKRD26):c.5106G>A (p.Gln1702=)	not provided [RCV003417284]	likely benign	10	27005617	27005617	Human		name
405190588	CV2871263	single nucleotide variant	NM_014915.3(ANKRD26):c.4866C>T (p.Asn1622=)	not provided [RCV003550339]	likely benign	10	27012969	27012969	Human		name
405071656	CV2876590	single nucleotide variant	NM_014915.3(ANKRD26):c.4077G>A (p.Glu1359=)	ANKRD26-related disorder [RCV003901139]\|Inborn genetic diseases [RCV004950408]\|not provided [RCV003548568]	likely benign	10	27024455	27024455	Human	2	name , alternate_id
405199358	CV2877004	single nucleotide variant	NM_014915.3(ANKRD26):c.4659A>G (p.Glu1553=)	not provided [RCV003551232]	likely benign	10	27014559	27014559	Human		name
405065850	CV2879155	single nucleotide variant	NM_014915.3(ANKRD26):c.974C>T (p.Thr325Ile)	not provided [RCV003548231]	uncertain significance	10	27077441	27077441	Human		name
405214696	CV2879671	single nucleotide variant	NM_014915.3(ANKRD26):c.911G>T (p.Arg304Ile)	Inborn genetic diseases [RCV004950405]\|not provided [RCV003553003]	uncertain significance	10	27077504	27077504	Human	1	name
405237419	CV2881171	single nucleotide variant	NM_014915.3(ANKRD26):c.340A>G (p.Arg114Gly)	Inborn genetic diseases [RCV004369152]\|not provided [RCV003556671]	uncertain significance	10	27093702	27093702	Human	1	name
402505720	CV2884468	single nucleotide variant	NM_014915.3(ANKRD26):c.803T>C (p.Phe268Ser)	Inborn genetic diseases [RCV004369126]\|not provided [RCV003546342]	uncertain significance	10	27079099	27079099	Human	1	name
402478499	CV2909940	single nucleotide variant	NM_014915.3(ANKRD26):c.4237C>T (p.Leu1413=)	not provided [RCV003571811]	likely benign	10	27017771	27017771	Human		name
405204071	CV2915398	single nucleotide variant	NM_014915.3(ANKRD26):c.476T>C (p.Ile159Thr)	not provided [RCV003566274]	uncertain significance	10	27093404	27093404	Human		name
405193223	CV2925506	single nucleotide variant	NM_014915.3(ANKRD26):c.496C>G (p.Leu166Val)	not provided [RCV003565104]	uncertain significance	10	27093384	27093384	Human		name
405083653	CV2946398	single nucleotide variant	NM_014915.3(ANKRD26):c.448C>G (p.Leu150Val)	not provided [RCV003664799]	uncertain significance	10	27093432	27093432	Human		name
405242645	CV2967389	single nucleotide variant	NM_014915.3(ANKRD26):c.902C>T (p.Thr301Ile)	not provided [RCV003684403]	uncertain significance	10	27077513	27077513	Human		name
402515410	CV2992072	single nucleotide variant	NM_014915.3(ANKRD26):c.4818C>T (p.Val1606=)	not provided [RCV003689891]	likely benign	10	27013017	27013017	Human		name
402520817	CV3000389	single nucleotide variant	NM_014915.3(ANKRD26):c.545C>T (p.Pro182Leu)	not provided [RCV003716415]	uncertain significance	10	27092499	27092499	Human		name
405129369	CV3010764	single nucleotide variant	NM_014915.3(ANKRD26):c.867G>C (p.Arg289Ser)	not provided [RCV003701533]	uncertain significance	10	27077640	27077640	Human		name
404978598	CV3012263	single nucleotide variant	NM_014915.3(ANKRD26):c.4836G>A (p.Val1612=)	Inborn genetic diseases [RCV004950568]\|not provided [RCV003690755]	likely benign	10	27012999	27012999	Human	1	name
405084092	CV3018258	single nucleotide variant	NM_014915.3(ANKRD26):c.3585G>A (p.Glu1195=)	not provided [RCV003699254]	likely benign	10	27034865	27034865	Human		name
405140515	CV3026180	single nucleotide variant	NM_014915.3(ANKRD26):c.3543G>A (p.Glu1181=)	not provided [RCV003702468]	likely benign	10	27034907	27034907	Human		name
405124074	CV3043245	single nucleotide variant	NM_014915.3(ANKRD26):c.460G>A (p.Val154Ile)	ANKRD26-related disorder [RCV004738846]\|Inborn genetic diseases [RCV005356502]\|not provided [RCV003724176]	uncertain significance	10	27093420	27093420	Human	2	name , alternate_id
405124909	CV3043473	single nucleotide variant	NM_014915.3(ANKRD26):c.3714A>G (p.Ser1238=)	Inborn genetic diseases [RCV004950613]\|not provided [RCV003724275]	likely benign	10	27033318	27033318	Human	1	name
405084569	CV3043709	single nucleotide variant	NM_014915.3(ANKRD26):c.407G>A (p.Gly136Asp)	not provided [RCV003717382]	likely benign	10	27093473	27093473	Human		name
405243327	CV3043999	single nucleotide variant	NM_014915.3(ANKRD26):c.722C>T (p.Ser241Phe)	Inborn genetic diseases [RCV005377517]\|not provided [RCV003719708]	uncertain significance	10	27082821	27082821	Human	1	name
405252907	CV3044100	single nucleotide variant	NM_014915.3(ANKRD26):c.484G>A (p.Ala162Thr)	not provided [RCV003722353]	uncertain significance	10	27093396	27093396	Human		name
405252922	CV3044112	single nucleotide variant	NM_014915.3(ANKRD26):c.5085A>G (p.Lys1695=)	Inborn genetic diseases [RCV004950625]\|not provided [RCV003722357]	likely benign	10	27005638	27005638	Human	1	name
405089134	CV3044638	single nucleotide variant	NM_014915.3(ANKRD26):c.3378T>C (p.Ile1126=)	Inborn genetic diseases [RCV004950631]\|not provided [RCV003717691]	likely benign	10	27035072	27035072	Human	1	name
405252106	CV3046393	single nucleotide variant	NM_014915.3(ANKRD26):c.4128A>G (p.Glu1376=)	ANKRD26-related disorder [RCV003981060]\|Inborn genetic diseases [RCV004950606]\|not provided [RCV003722073]	likely benign	10	27022645	27022645	Human	2	name , alternate_id
405081650	CV3046752	single nucleotide variant	NM_014915.3(ANKRD26):c.4707G>A (p.Leu1569=)	ANKRD26-related disorder [RCV003981063]\|Inborn genetic diseases [RCV005377514]\|not provided [RCV003717183]	likely benign	10	27014511	27014511	Human	2	name , alternate_id
405082167	CV3046816	single nucleotide variant	NM_014915.3(ANKRD26):c.790G>A (p.Glu264Lys)	Inborn genetic diseases [RCV004950619]\|not provided [RCV003717218]	uncertain significance	10	27079112	27079112	Human	1	name
405133408	CV3047585	single nucleotide variant	NM_014915.3(ANKRD26):c.3894T>C (p.Asn1298=)	Inborn genetic diseases [RCV005353256]\|not provided [RCV003725031]	likely benign	10	27028930	27028930	Human	1	name
405085523	CV3047712	single nucleotide variant	NM_014915.3(ANKRD26):c.4698A>G (p.Arg1566=)	Inborn genetic diseases [RCV004953443]\|not provided [RCV003717444]	likely benign	10	27014520	27014520	Human	1	name
405246483	CV3048120	single nucleotide variant	NM_014915.3(ANKRD26):c.3768A>G (p.Thr1256=)	not provided [RCV003720549]	likely benign	10	27033264	27033264	Human		name
405136944	CV3048388	single nucleotide variant	NM_014915.3(ANKRD26):c.560T>C (p.Val187Ala)	Inborn genetic diseases [RCV005356510]\|not provided [RCV003725276]	uncertain significance	10	27092484	27092484	Human	1	name
405217265	CV3048795	single nucleotide variant	NM_014915.3(ANKRD26):c.3564G>T (p.Leu1188=)	not provided [RCV003732814]	likely benign	10	27034886	27034886	Human		name
405127811	CV3050115	single nucleotide variant	NM_014915.3(ANKRD26):c.391A>C (p.Ile131Leu)	Inborn genetic diseases [RCV005377513]\|not provided [RCV003724541]	uncertain significance	10	27093489	27093489	Human	1	name
405080933	CV3050399	single nucleotide variant	NM_014915.3(ANKRD26):c.5011T>C (p.Leu1671=)	not provided [RCV003717063]	likely benign	10	27005712	27005712	Human		name
405244308	CV3050560	single nucleotide variant	NM_014915.3(ANKRD26):c.303C>G (p.Asp101Glu)	Inborn genetic diseases [RCV004953439]\|not provided [RCV003719950]	benign\|likely benign\|conflicting interpretations of pathogenicity	10	27093739	27093739	Human	1	name
405245239	CV3055010	single nucleotide variant	NM_014915.3(ANKRD26):c.880G>A (p.Ala294Thr)	Inborn genetic diseases [RCV004950633]\|not provided [RCV003720235]	uncertain significance	10	27077535	27077535	Human	1	name
405222715	CV3057136	duplication	NM_014915.3(ANKRD26):c.2266dup (p.Met756fs)	not provided [RCV003733556]	uncertain significance	10	27040073	27040074	Human		name
405183787	CV3057853	single nucleotide variant	NM_014915.3(ANKRD26):c.3120A>G (p.Glu1040=)	not provided [RCV003729059]	likely benign	10	27035330	27035330	Human		name
405220105	CV3059814	single nucleotide variant	NM_014915.3(ANKRD26):c.475A>C (p.Ile159Leu)	Inborn genetic diseases [RCV004953459]\|not provided [RCV003733177]	uncertain significance	10	27093405	27093405	Human	1	name
405209305	CV3065411	single nucleotide variant	NM_014915.3(ANKRD26):c.479C>T (p.Ser160Leu)	Inborn genetic diseases [RCV004953484]\|not provided [RCV003731642]	uncertain significance	10	27093401	27093401	Human	1	name
405146112	CV3067162	single nucleotide variant	NM_014915.3(ANKRD26):c.674G>A (p.Arg225Lys)	not provided [RCV003726072]	uncertain significance	10	27086574	27086574	Human		name
405214318	CV3078433	single nucleotide variant	NM_014915.3(ANKRD26):c.966C>A (p.Ser322Arg)	not provided [RCV003732433]	uncertain significance	10	27077449	27077449	Human		name
405162222	CV3125171	single nucleotide variant	NM_014915.3(ANKRD26):c.884C>T (p.Thr295Ile)	not provided [RCV003818443]	uncertain significance	10	27077531	27077531	Human		name
405059498	CV3148208	single nucleotide variant	NM_014915.3(ANKRD26):c.319A>T (p.Asn107Tyr)	Inborn genetic diseases [RCV004950735]\|not provided [RCV003850164]	uncertain significance	10	27093723	27093723	Human	1	name
11656714	CV315248	deletion	NM_014915.3(ANKRD26):c.1727del (p.Asp576fs)	not provided [RCV003727654]	uncertain significance	10	27048888	27048888	Human		name
11611216	CV315267	single nucleotide variant	NM_014915.3(ANKRD26):c.739A>T (p.Arg247Trp)	Thrombocytopenia 2 [RCV000391327]\|not provided [RCV004777645]	uncertain significance	10	27082804	27082804	Human	1	name
405144083	CV3155753	single nucleotide variant	NM_014915.3(ANKRD26):c.4317A>G (p.Thr1439=)	Inborn genetic diseases [RCV005377596]\|not provided [RCV003855795]	likely benign	10	27017691	27017691	Human	1	name
405216985	CV3160913	single nucleotide variant	NM_014915.3(ANKRD26):c.4341A>G (p.Leu1447=)	Inborn genetic diseases [RCV004950739]\|not provided [RCV003862975]	likely benign	10	27017667	27017667	Human	1	name
405213437	CV3169821	single nucleotide variant	NM_014915.3(ANKRD26):c.3111A>G (p.Ala1037=)	not provided [RCV003862420]	likely benign	10	27035339	27035339	Human		name
404995087	CV3172764	single nucleotide variant	NM_014915.3(ANKRD26):c.754C>G (p.Pro252Ala)	not provided [RCV003882046]	uncertain significance	10	27079148	27079148	Human		name
404981888	CV3179634	deletion	NM_014915.3(ANKRD26):c.1606del (p.Arg536fs)	not provided [RCV003880615]	uncertain significance	10	27053349	27053349	Human		name
402491803	CV3182533	duplication	NM_014915.3(ANKRD26):c.2798dup (p.Asn933fs)	not provided [RCV003877020]	uncertain significance	10	27035651	27035652	Human		name
405282867	CV3191203	single nucleotide variant	NM_014915.3(ANKRD26):c.5124T>C (p.Tyr1708=)	ANKRD26-related disorder [RCV003921610]\|Inborn genetic diseases [RCV004950764]\|not provided [RCV005101697]	likely benign	10	27005599	27005599	Human	2	name , alternate_id
405277691	CV3196057	single nucleotide variant	NM_014915.3(ANKRD26):c.3705A>G (p.Gln1235=)	ANKRD26-related disorder [RCV003904577]\|Inborn genetic diseases [RCV004953648]\|not provided [RCV005101687]	likely benign	10	27033327	27033327	Human	2	name , alternate_id
405256327	CV3203608	single nucleotide variant	NM_014915.3(ANKRD26):c.4098C>T (p.Leu1366=)	ANKRD26-related disorder [RCV003939844]	likely benign	10	27022675	27022675	Human		name , trait , alternate_id
11612304	CV321255	single nucleotide variant	NM_014915.3(ANKRD26):c.4497A>G (p.Leu1499=)	Inborn genetic diseases [RCV005365236]\|Thrombocytopenia 2 [RCV000406753]\|not provided [RCV002520578]	benign\|likely benign\|uncertain significance	10	27017511	27017511	Human	2	name
11608063	CV321261	single nucleotide variant	NM_014915.3(ANKRD26):c.4188T>C (p.Asp1396=)	ANKRD26-related disorder [RCV003967861]\|Inborn genetic diseases [RCV004948252]\|Thrombocytopenia 2 [RCV000350440]\|not provided [RCV002520579]\|not specified [RCV001820866]	benign\|likely benign\|uncertain significance	10	27022585	27022585	Human	2	name , alternate_id
11601244	CV321279	single nucleotide variant	NM_014915.3(ANKRD26):c.793G>A (p.Asp265Asn)	Thrombocytopenia 2 [RCV000280578]\|not provided [RCV000967164]	benign\|likely benign	10	27079109	27079109	Human	1	name
11604134	CV321283	single nucleotide variant	NM_014915.3(ANKRD26):c.332A>G (p.Asn111Ser)	Thrombocytopenia 2 [RCV000306427]\|not provided [RCV000971011]	benign\|likely benign	10	27093710	27093710	Human	1	name
11607011	CV321851	single nucleotide variant	NM_014915.3(ANKRD26):c.789C>G (p.Asp263Glu)	Inborn genetic diseases [RCV005365238]\|Thrombocytopenia 2 [RCV000337993]\|not provided [RCV005090438]	uncertain significance	10	27079113	27079113	Human	2	name
11611190	CV321869	single nucleotide variant	NM_014915.3(ANKRD26):c.452A>C (p.His151Pro)	Inborn genetic diseases [RCV004948257]\|Thrombocytopenia 2 [RCV000391316]	likely benign\|uncertain significance	10	27093428	27093428	Human	2	name
407427686	CV3411995	single nucleotide variant	NM_014915.3(ANKRD26):c.809C>T (p.Thr270Ile)	not provided [RCV004592166]	uncertain significance	10	27079093	27079093	Human		name
408382977	CV3506237	single nucleotide variant	NM_014915.3(ANKRD26):c.731C>G (p.Ser244Cys)	ANKRD26-related disorder [RCV004730295]	uncertain significance	10	27082812	27082812	Human		name , trait , alternate_id
408377954	CV3510797	single nucleotide variant	NM_014915.3(ANKRD26):c.643C>T (p.His215Tyr)	ANKRD26-related disorder [RCV004739833]\|not provided [RCV004767764]	uncertain significance	10	27086605	27086605	Human	1	name , alternate_id
408390002	CV3519084	single nucleotide variant	NM_014915.3(ANKRD26):c.320A>T (p.Asn107Ile)	Inborn genetic diseases [RCV005363355]\|not provided [RCV004762393]	uncertain significance	10	27093722	27093722	Human	1	name
408390063	CV3519181	single nucleotide variant	NM_014915.3(ANKRD26):c.538C>T (p.Leu180Phe)	Inborn genetic diseases [RCV004950836]\|not provided [RCV004762490]	uncertain significance	10	27092506	27092506	Human	1	name
408388958	CV3522836	single nucleotide variant	NM_014915.3(ANKRD26):c.410C>T (p.Ala137Val)	not provided [RCV004769217]	uncertain significance	10	27093470	27093470	Human		name
408386827	CV3524249	single nucleotide variant	NM_014915.3(ANKRD26):c.5010A>G (p.Glu1670=)	Inborn genetic diseases [RCV005358145]\|not provided [RCV004768123]	likely benign\|uncertain significance	10	27005713	27005713	Human	1	name
408392008	CV3526430	single nucleotide variant	NM_014915.3(ANKRD26):c.5100T>C (p.Tyr1700=)	Inborn genetic diseases [RCV005377664]\|not provided [RCV004775679]	likely benign\|uncertain significance	10	27005623	27005623	Human	1	name
408381883	CV3526632	deletion	NM_014915.3(ANKRD26):c.1498del (p.Ile500fs)	not provided [RCV004771945]	uncertain significance	10	27060411	27060411	Human		name
408385811	CV3528693	single nucleotide variant	NM_014915.3(ANKRD26):c.4953G>A (p.Lys1651=)	not provided [RCV004772526]	uncertain significance	10	27012882	27012882	Human		name
596929760	CV3531135	single nucleotide variant	NM_014915.3(ANKRD26):c.626A>G (p.Asp209Gly)	not provided [RCV004779709]	uncertain significance	10	27092418	27092418	Human		name
596922224	CV3536996	single nucleotide variant	NM_014915.3(ANKRD26):c.418A>G (p.Asn140Asp)	Thrombocytopenia 2 [RCV004785990]\|not provided [RCV005105073]	uncertain significance	10	27093462	27093462	Human	1	name
596932511	CV3539132	single nucleotide variant	NM_014915.3(ANKRD26):c.428A>G (p.Asp143Gly)	not provided [RCV004793258]	uncertain significance	10	27093452	27093452	Human		name
596945071	CV3543702	single nucleotide variant	NM_014915.3(ANKRD26):c.394C>G (p.Leu132Val)	not provided [RCV004801824]	uncertain significance	10	27093486	27093486	Human		name
597682079	CV3553678	single nucleotide variant	NM_014915.3(ANKRD26):c.4785A>G (p.Arg1595=)	Inborn genetic diseases [RCV004952068]	likely benign	10	27013050	27013050	Human	1	name
597683242	CV3553852	single nucleotide variant	NM_014915.3(ANKRD26):c.4518A>T (p.Ala1506=)	Inborn genetic diseases [RCV004952238]	likely benign	10	27014700	27014700	Human	1	name
597683264	CV3553870	single nucleotide variant	NM_014915.3(ANKRD26):c.917T>C (p.Leu306Ser)	Inborn genetic diseases [RCV004952241]	uncertain significance	10	27077498	27077498	Human	1	name
597683282	CV3553891	single nucleotide variant	NM_014915.3(ANKRD26):c.4353A>G (p.Lys1451=)	Inborn genetic diseases [RCV004952243]	likely benign	10	27017655	27017655	Human	1	name
597683316	CV3553938	single nucleotide variant	NM_014915.3(ANKRD26):c.517G>A (p.Glu173Lys)	Inborn genetic diseases [RCV004952248]	uncertain significance	10	27093363	27093363	Human	1	name
597683325	CV3553947	single nucleotide variant	NM_014915.3(ANKRD26):c.3240C>T (p.Phe1080=)	Inborn genetic diseases [RCV004952249]	likely benign	10	27035210	27035210	Human	1	name
597683402	CV3554003	single nucleotide variant	NM_014915.3(ANKRD26):c.716A>G (p.Glu239Gly)	Inborn genetic diseases [RCV004952261]	uncertain significance	10	27082827	27082827	Human	1	name
597683407	CV3554034	single nucleotide variant	NM_014915.3(ANKRD26):c.3621G>A (p.Gln1207=)	Inborn genetic diseases [RCV004952262]	likely benign	10	27034829	27034829	Human	1	name
597683414	CV3554064	single nucleotide variant	NM_014915.3(ANKRD26):c.3441A>G (p.Arg1147=)	Inborn genetic diseases [RCV004952263]	likely benign	10	27035009	27035009	Human	1	name
597700574	CV3554148	single nucleotide variant	NM_014915.3(ANKRD26):c.992A>G (p.Gln331Arg)	Inborn genetic diseases [RCV004956562]	uncertain significance	10	27077423	27077423	Human	1	name
597700580	CV3554156	single nucleotide variant	NM_014915.3(ANKRD26):c.3339A>G (p.Gln1113=)	Inborn genetic diseases [RCV004956563]	likely benign	10	27035111	27035111	Human	1	name
597683542	CV3554182	single nucleotide variant	NM_014915.3(ANKRD26):c.365A>G (p.Gln122Arg)	Inborn genetic diseases [RCV004952282]	uncertain significance	10	27093515	27093515	Human	1	name
597700654	CV3554184	single nucleotide variant	NM_014915.3(ANKRD26):c.947A>G (p.Asp316Gly)	Inborn genetic diseases [RCV004956575]	uncertain significance	10	27077468	27077468	Human	1	name
597700814	CV3554216	single nucleotide variant	NM_014915.3(ANKRD26):c.566G>A (p.Gly189Glu)	Inborn genetic diseases [RCV004956577]	likely benign	10	27092478	27092478	Human	1	name
597700821	CV3554242	single nucleotide variant	NM_014915.3(ANKRD26):c.4830T>C (p.Pro1610=)	Inborn genetic diseases [RCV004956578]	likely benign	10	27013005	27013005	Human	1	name
597683598	CV3554276	single nucleotide variant	NM_014915.3(ANKRD26):c.4536G>A (p.Glu1512=)	Inborn genetic diseases [RCV004952291]	likely benign	10	27014682	27014682	Human	1	name
597699834	CV3556659	single nucleotide variant	NM_014915.3(ANKRD26):c.4641T>C (p.Phe1547=)	Inborn genetic diseases [RCV004956422]\|not provided [RCV005107498]	likely benign	10	27014577	27014577	Human	1	name
597700184	CV3556876	single nucleotide variant	NM_014915.3(ANKRD26):c.3222T>C (p.Asn1074=)	Inborn genetic diseases [RCV004956503]	likely benign	10	27035228	27035228	Human	1	name
597700196	CV3556892	single nucleotide variant	NM_014915.3(ANKRD26):c.752A>C (p.Lys251Thr)	Inborn genetic diseases [RCV004956505]	uncertain significance	10	27079150	27079150	Human	1	name
597682776	CV3556893	single nucleotide variant	NM_014915.3(ANKRD26):c.751A>C (p.Lys251Gln)	Inborn genetic diseases [RCV004952174]	uncertain significance	10	27079151	27079151	Human	1	name
597682805	CV3556899	single nucleotide variant	NM_014915.3(ANKRD26):c.3156G>A (p.Val1052=)	Inborn genetic diseases [RCV004952178]	likely benign	10	27035294	27035294	Human	1	name
597700211	CV3556903	single nucleotide variant	NM_014915.3(ANKRD26):c.485C>T (p.Ala162Val)	Inborn genetic diseases [RCV004956507]	uncertain significance	10	27093395	27093395	Human	1	name
597682865	CV3556965	single nucleotide variant	NM_014915.3(ANKRD26):c.475A>G (p.Ile159Val)	Inborn genetic diseases [RCV004952186]	uncertain significance	10	27093405	27093405	Human	1	name
597682909	CV3556983	single nucleotide variant	NM_014915.3(ANKRD26):c.3297G>A (p.Lys1099=)	Inborn genetic diseases [RCV004952192]	likely benign	10	27035153	27035153	Human	1	name
597700270	CV3556986	single nucleotide variant	NM_014915.3(ANKRD26):c.602A>G (p.Lys201Arg)	Inborn genetic diseases [RCV004956516]	uncertain significance	10	27092442	27092442	Human	1	name
597682945	CV3557012	single nucleotide variant	NM_014915.3(ANKRD26):c.3294A>G (p.Gln1098=)	Inborn genetic diseases [RCV004952197]	likely benign	10	27035156	27035156	Human	1	name
597682969	CV3557047	single nucleotide variant	NM_014915.3(ANKRD26):c.398T>C (p.Leu133Pro)	Inborn genetic diseases [RCV004952200]	uncertain significance	10	27093482	27093482	Human	1	name
597682987	CV3557068	single nucleotide variant	NM_014915.3(ANKRD26):c.925G>T (p.Asp309Tyr)	Inborn genetic diseases [RCV004952202]	uncertain significance	10	27077490	27077490	Human	1	name
597700295	CV3557128	single nucleotide variant	NM_014915.3(ANKRD26):c.3291A>G (p.Val1097=)	Inborn genetic diseases [RCV004956520]	likely benign	10	27035159	27035159	Human	1	name
597683018	CV3557156	single nucleotide variant	NM_014915.3(ANKRD26):c.895G>A (p.Val299Met)	Inborn genetic diseases [RCV004952206]	uncertain significance	10	27077520	27077520	Human	1	name
597683107	CV3557240	single nucleotide variant	NM_014915.3(ANKRD26):c.753A>C (p.Lys251Asn)	Inborn genetic diseases [RCV004952218]	uncertain significance	10	27079149	27079149	Human	1	name
597700375	CV3557276	single nucleotide variant	NM_014915.3(ANKRD26):c.544C>T (p.Pro182Ser)	Inborn genetic diseases [RCV004956533]	uncertain significance	10	27092500	27092500	Human	1	name
597682615	CV3560529	single nucleotide variant	NM_014915.3(ANKRD26):c.3249G>A (p.Thr1083=)	Inborn genetic diseases [RCV004952150]\|not provided [RCV005107514]	likely benign	10	27035201	27035201	Human	1	name
597682624	CV3560539	single nucleotide variant	NM_014915.3(ANKRD26):c.926A>G (p.Asp309Gly)	Inborn genetic diseases [RCV004952151]	uncertain significance	10	27077489	27077489	Human	1	name
597700102	CV3560584	single nucleotide variant	NM_014915.3(ANKRD26):c.4848T>C (p.Asn1616=)	Inborn genetic diseases [RCV004956492]\|not provided [RCV005107516]	likely benign	10	27012987	27012987	Human	1	name
597700108	CV3560605	single nucleotide variant	NM_014915.3(ANKRD26):c.3123T>C (p.Cys1041=)	Inborn genetic diseases [RCV004956493]	likely benign	10	27035327	27035327	Human	1	name
597700149	CV3560714	single nucleotide variant	NM_014915.3(ANKRD26):c.4701A>G (p.Lys1567=)	Inborn genetic diseases [RCV004956498]\|not provided [RCV005107518]	likely benign	10	27014517	27014517	Human	1	name
597682168	CV3563427	single nucleotide variant	NM_014915.3(ANKRD26):c.4938G>A (p.Glu1646=)	Inborn genetic diseases [RCV004952084]	likely benign	10	27012897	27012897	Human	1	name
597700854	CV3563814	single nucleotide variant	NM_014915.3(ANKRD26):c.305G>C (p.Arg102Thr)	Inborn genetic diseases [RCV004956583]	uncertain significance	10	27093737	27093737	Human	1	name
597683660	CV3563848	single nucleotide variant	NM_014915.3(ANKRD26):c.382T>C (p.Cys128Arg)	Inborn genetic diseases [RCV004952299]	uncertain significance	10	27093498	27093498	Human	1	name
597700899	CV3564004	single nucleotide variant	NM_014915.3(ANKRD26):c.474C>A (p.Asp158Glu)	Inborn genetic diseases [RCV004956590]	uncertain significance	10	27093406	27093406	Human	1	name
12741149	CV359960	single nucleotide variant	NM_014915.3(ANKRD26):c.556G>T (p.Ala186Ser)	Inborn genetic diseases [RCV004649144]\|Thrombocytopenia 2 [RCV005055106]\|not provided [RCV002521438]\|not specified [RCV000414230]	uncertain significance	10	27092488	27092488	Human	2	name
597702203	CV3728888	single nucleotide variant	NM_014915.3(ANKRD26):c.862T>C (p.Ser288Pro)	Thrombocytopenia 2 [RCV005047855]	uncertain significance	10	27077645	27077645	Human	1	name
597669468	CV3732802	single nucleotide variant	NM_014915.3(ANKRD26):c.687T>G (p.His229Gln)	not provided [RCV005004634]	uncertain significance	10	27086561	27086561	Human		name
597831003	CV3743739	single nucleotide variant	NM_014915.3(ANKRD26):c.4605T>C (p.Ser1535=)	Inborn genetic diseases [RCV005377708]\|not provided [RCV005062556]	likely benign	10	27014613	27014613	Human	1	name
597947028	CV3755694	single nucleotide variant	NM_014915.3(ANKRD26):c.937G>C (p.Asp313His)	Inborn genetic diseases [RCV005365404]\|not provided [RCV005078704]	uncertain significance	10	27077478	27077478	Human	1	name
597836931	CV3761412	single nucleotide variant	NM_014915.3(ANKRD26):c.5038C>T (p.Leu1680=)	not provided [RCV005085783]	likely benign	10	27005685	27005685	Human		name
597867878	CV3764169	single nucleotide variant	NM_014915.3(ANKRD26):c.800A>G (p.Asn267Ser)	not provided [RCV005107166]	uncertain significance	10	27079102	27079102	Human		name
597885847	CV3777318	single nucleotide variant	NM_014915.3(ANKRD26):c.3651A>G (p.Arg1217=)	not provided [RCV005124917]	likely benign	10	27034799	27034799	Human		name
597913690	CV3778746	single nucleotide variant	NM_014915.3(ANKRD26):c.4218T>C (p.Ile1406=)	not provided [RCV005129091]	likely benign	10	27017790	27017790	Human		name
597902613	CV3804527	single nucleotide variant	NM_014915.3(ANKRD26):c.326G>A (p.Cys109Tyr)	Inborn genetic diseases [RCV005353416]\|not provided [RCV005152962]	uncertain significance	10	27093716	27093716	Human	1	name
597960589	CV3840260	single nucleotide variant	NM_014915.3(ANKRD26):c.3258C>T (p.Ala1086=)	Inborn genetic diseases [RCV005379813]\|not provided [RCV005192742]	likely benign	10	27035192	27035192	Human	1	name
597925013	CV3840492	duplication	NM_014915.3(ANKRD26):c.2231dup (p.Asn744fs)	not provided [RCV005184963]	uncertain significance	10	27040108	27040109	Human		name
597947336	CV3841908	single nucleotide variant	NM_014915.3(ANKRD26):c.982A>G (p.Ile328Val)	Inborn genetic diseases [RCV005365494]\|not provided [RCV005189342]	likely benign\|uncertain significance	10	27077433	27077433	Human	1	name
597955696	CV3841922	single nucleotide variant	NM_014915.3(ANKRD26):c.3990A>G (p.Glu1330=)	Inborn genetic diseases [RCV005353451]\|not provided [RCV005191419]	likely benign	10	27024542	27024542	Human	1	name
597952441	CV3843744	single nucleotide variant	NM_014915.3(ANKRD26):c.3477T>C (p.Asn1159=)	Inborn genetic diseases [RCV005365485]\|not provided [RCV005190606]	likely benign	10	27034973	27034973	Human	1	name
597934101	CV3844812	single nucleotide variant	NM_014915.3(ANKRD26):c.857A>G (p.Gln286Arg)	not provided [RCV005186318]	uncertain significance	10	27077650	27077650	Human		name
597944739	CV3847960	single nucleotide variant	NM_014915.3(ANKRD26):c.3966A>G (p.Ala1322=)	Inborn genetic diseases [RCV005379820]\|not provided [RCV005188690]	likely benign	10	27028858	27028858	Human	1	name
597964549	CV3848083	single nucleotide variant	NM_014915.3(ANKRD26):c.3447A>G (p.Gln1149=)	not provided [RCV005193962]	likely benign	10	27035003	27035003	Human		name
597959572	CV3848675	single nucleotide variant	NM_014915.3(ANKRD26):c.4425C>T (p.Val1475=)	not provided [RCV005192376]	likely benign	10	27017583	27017583	Human		name
597947991	CV3852398	single nucleotide variant	NM_014915.3(ANKRD26):c.670G>A (p.Glu224Lys)	not provided [RCV005189476]	uncertain significance	10	27086578	27086578	Human		name
597937591	CV3852638	single nucleotide variant	NM_014915.3(ANKRD26):c.4203G>A (p.Lys1401=)	not provided [RCV005187037]	likely benign	10	27022570	27022570	Human		name
597867489	CV3858174	single nucleotide variant	NM_014915.3(ANKRD26):c.4923A>G (p.Ser1641=)	not provided [RCV005196917]	likely benign	10	27012912	27012912	Human		name
597933360	CV3858609	single nucleotide variant	NM_014915.3(ANKRD26):c.331A>G (p.Asn111Asp)	not provided [RCV005207078]	uncertain significance	10	27093711	27093711	Human		name
598163784	CV3981406	single nucleotide variant	NM_014915.3(ANKRD26):c.5025A>G (p.Ser1675=)	Inborn genetic diseases [RCV005368884]	likely benign	10	27005698	27005698	Human	1	name
598182693	CV3981426	single nucleotide variant	NM_014915.3(ANKRD26):c.3415C>T (p.Leu1139=)	Inborn genetic diseases [RCV005372787]	likely benign	10	27035035	27035035	Human	1	name
598182721	CV3981434	single nucleotide variant	NM_014915.3(ANKRD26):c.4267C>T (p.Leu1423=)	Inborn genetic diseases [RCV005372792]	likely benign	10	27017741	27017741	Human	1	name
598163920	CV3981452	single nucleotide variant	NM_014915.3(ANKRD26):c.322G>A (p.Val108Ile)	Inborn genetic diseases [RCV005368906]	uncertain significance	10	27093720	27093720	Human	1	name
598163934	CV3981464	single nucleotide variant	NM_014915.3(ANKRD26):c.3567A>G (p.Leu1189=)	Inborn genetic diseases [RCV005368909]	likely benign	10	27034883	27034883	Human	1	name
598182872	CV3981486	single nucleotide variant	NM_014915.3(ANKRD26):c.815A>T (p.Asn272Ile)	Inborn genetic diseases [RCV005372820]	uncertain significance	10	27077692	27077692	Human	1	name
598163996	CV3981490	single nucleotide variant	NM_014915.3(ANKRD26):c.4518A>G (p.Ala1506=)	Inborn genetic diseases [RCV005368921]	likely benign	10	27014700	27014700	Human	1	name
598182925	CV3981501	single nucleotide variant	NM_014915.3(ANKRD26):c.4653A>G (p.Glu1551=)	Inborn genetic diseases [RCV005372829]	likely benign	10	27014565	27014565	Human	1	name
598177153	CV3981638	single nucleotide variant	NM_014915.3(ANKRD26):c.645C>G (p.His215Gln)	Inborn genetic diseases [RCV005371549]	uncertain significance	10	27086603	27086603	Human	1	name
598177507	CV3981747	single nucleotide variant	NM_014915.3(ANKRD26):c.556G>C (p.Ala186Pro)	Inborn genetic diseases [RCV005371608]	uncertain significance	10	27092488	27092488	Human	1	name
598177590	CV3981775	single nucleotide variant	NM_014915.3(ANKRD26):c.4968G>A (p.Leu1656=)	Inborn genetic diseases [RCV005371622]	likely benign	10	27006948	27006948	Human	1	name
598209711	CV3981861	single nucleotide variant	NM_014915.3(ANKRD26):c.4020G>A (p.Gln1340=)	Inborn genetic diseases [RCV005377747]	likely benign	10	27024512	27024512	Human	1	name
598209721	CV3981864	single nucleotide variant	NM_014915.3(ANKRD26):c.4275A>G (p.Thr1425=)	Inborn genetic diseases [RCV005377749]	likely benign	10	27017733	27017733	Human	1	name
598209736	CV3981867	single nucleotide variant	NM_014915.3(ANKRD26):c.4905C>T (p.Thr1635=)	Inborn genetic diseases [RCV005377752]	likely benign	10	27012930	27012930	Human	1	name
598177885	CV3981909	single nucleotide variant	NM_014915.3(ANKRD26):c.533A>T (p.Asp178Val)	Inborn genetic diseases [RCV005371688]	uncertain significance	10	27092511	27092511	Human	1	name
598209920	CV3981930	single nucleotide variant	NM_014915.3(ANKRD26):c.457G>T (p.Ala153Ser)	Inborn genetic diseases [RCV005377781]	uncertain significance	10	27093423	27093423	Human	1	name
598210135	CV3981985	single nucleotide variant	NM_014915.3(ANKRD26):c.3978A>G (p.Glu1326=)	Inborn genetic diseases [RCV005377815]	likely benign	10	27024554	27024554	Human	1	name
598175857	CV3985103	single nucleotide variant	NM_014915.3(ANKRD26):c.644A>C (p.His215Pro)	Inborn genetic diseases [RCV005371327]	uncertain significance	10	27086604	27086604	Human	1	name
598176220	CV3985198	single nucleotide variant	NM_014915.3(ANKRD26):c.848C>G (p.Thr283Ser)	Inborn genetic diseases [RCV005371376]	uncertain significance	10	27077659	27077659	Human	1	name
598197972	CV3985266	single nucleotide variant	NM_014915.3(ANKRD26):c.4668G>A (p.Lys1556=)	Inborn genetic diseases [RCV005375490]	likely benign	10	27014550	27014550	Human	1	name
598198222	CV3985330	single nucleotide variant	NM_014915.3(ANKRD26):c.4827A>G (p.Pro1609=)	Inborn genetic diseases [RCV005375522]	likely benign	10	27013008	27013008	Human	1	name
598198286	CV3985351	single nucleotide variant	NM_014915.3(ANKRD26):c.3489A>G (p.Thr1163=)	Inborn genetic diseases [RCV005375531]	likely benign	10	27034961	27034961	Human	1	name
598176707	CV3985388	single nucleotide variant	NM_014915.3(ANKRD26):c.796C>T (p.Leu266Phe)	Inborn genetic diseases [RCV005371463]	uncertain significance	10	27079106	27079106	Human	1	name
598176740	CV3985397	single nucleotide variant	NM_014915.3(ANKRD26):c.4635A>G (p.Glu1545=)	Inborn genetic diseases [RCV005371468]	likely benign	10	27014583	27014583	Human	1	name
598198561	CV3985428	single nucleotide variant	NM_014915.3(ANKRD26):c.808A>G (p.Thr270Ala)	Inborn genetic diseases [RCV005375576]	uncertain significance	10	27079094	27079094	Human	1	name
598198831	CV3985479	single nucleotide variant	NM_014915.3(ANKRD26):c.4705T>C (p.Leu1569=)	Inborn genetic diseases [RCV005375610]	likely benign	10	27014513	27014513	Human	1	name
598176911	CV3985491	single nucleotide variant	NM_014915.3(ANKRD26):c.815A>G (p.Asn272Ser)	Inborn genetic diseases [RCV005371502]	uncertain significance	10	27077692	27077692	Human	1	name
598177013	CV3985531	single nucleotide variant	NM_014915.3(ANKRD26):c.446C>T (p.Ala149Val)	Inborn genetic diseases [RCV005371521]	uncertain significance	10	27093434	27093434	Human	1	name
598165462	CV3988356	single nucleotide variant	NM_014915.3(ANKRD26):c.4809C>G (p.Thr1603=)	Inborn genetic diseases [RCV005369176]	likely benign	10	27013026	27013026	Human	1	name
598165697	CV3988457	single nucleotide variant	NM_014915.3(ANKRD26):c.4833T>C (p.Cys1611=)	Inborn genetic diseases [RCV005369216]	likely benign	10	27013002	27013002	Human	1	name
598196331	CV3988496	single nucleotide variant	NM_014915.3(ANKRD26):c.3957G>C (p.Leu1319=)	Inborn genetic diseases [RCV005375249]	likely benign	10	27028867	27028867	Human	1	name
598165876	CV3988525	single nucleotide variant	NM_014915.3(ANKRD26):c.3108A>G (p.Arg1036=)	Inborn genetic diseases [RCV005369243]	likely benign	10	27035342	27035342	Human	1	name
598165995	CV3988582	single nucleotide variant	NM_014915.3(ANKRD26):c.892A>G (p.Thr298Ala)	Inborn genetic diseases [RCV005369267]	uncertain significance	10	27077523	27077523	Human	1	name
598196761	CV3988620	single nucleotide variant	NM_014915.3(ANKRD26):c.779C>T (p.Thr260Ile)	Inborn genetic diseases [RCV005375319]	uncertain significance	10	27079123	27079123	Human	1	name
598196826	CV3988641	single nucleotide variant	NM_014915.3(ANKRD26):c.464A>G (p.Tyr155Cys)	Inborn genetic diseases [RCV005375329]	uncertain significance	10	27093416	27093416	Human	1	name
598196966	CV3988690	single nucleotide variant	NM_014915.3(ANKRD26):c.478T>C (p.Ser160Pro)	Inborn genetic diseases [RCV005375358]	likely benign	10	27093402	27093402	Human	1	name
598164199	CV3992109	single nucleotide variant	NM_014915.3(ANKRD26):c.559G>A (p.Val187Ile)	Inborn genetic diseases [RCV005368961]	uncertain significance	10	27092485	27092485	Human	1	name
598183305	CV3992135	single nucleotide variant	NM_014915.3(ANKRD26):c.333C>G (p.Asn111Lys)	Inborn genetic diseases [RCV005372902]	uncertain significance	10	27093709	27093709	Human	1	name
598183337	CV3992146	single nucleotide variant	NM_014915.3(ANKRD26):c.3189T>C (p.Ser1063=)	Inborn genetic diseases [RCV005372907]	likely benign	10	27035261	27035261	Human	1	name
598164405	CV3992185	single nucleotide variant	NM_014915.3(ANKRD26):c.3087A>G (p.Glu1029=)	Inborn genetic diseases [RCV005368996]	likely benign	10	27035363	27035363	Human	1	name
598164622	CV3992268	single nucleotide variant	NM_014915.3(ANKRD26):c.361G>A (p.Val121Ile)	Inborn genetic diseases [RCV005369035]	uncertain significance	10	27093519	27093519	Human	1	name
598164843	CV3992342	single nucleotide variant	NM_014915.3(ANKRD26):c.5076A>T (p.Leu1692=)	Inborn genetic diseases [RCV005369071]	likely benign	10	27005647	27005647	Human	1	name
598184470	CV3992491	single nucleotide variant	NM_014915.3(ANKRD26):c.3936T>A (p.Ile1312=)	Inborn genetic diseases [RCV005373088]	likely benign	10	27028888	27028888	Human	1	name
598210379	CV3992567	single nucleotide variant	NM_014915.3(ANKRD26):c.4830T>A (p.Pro1610=)	Inborn genetic diseases [RCV005377854]	likely benign	10	27013005	27013005	Human	1	name
598210872	CV3992697	single nucleotide variant	NM_014915.3(ANKRD26):c.3891T>C (p.Asp1297=)	Inborn genetic diseases [RCV005377930]	likely benign	10	27028933	27028933	Human	1	name
13215923	CV429060	single nucleotide variant	NM_014915.3(ANKRD26):c.542C>T (p.Thr181Ile)	ANKRD26-related disorder [RCV003902757]\|Thrombocytopenia 2 [RCV001102946]\|not provided [RCV000880419]\|not specified [RCV000503032]	benign\|likely benign	10	27092502	27092502	Human	1	name , alternate_id
13527113	CV503329	single nucleotide variant	NM_014915.3(ANKRD26):c.3627A>G (p.Gln1209=)	not provided [RCV003718263]\|not specified [RCV000605033]	likely benign	10	27034823	27034823	Human		name
26921531	CV836779	deletion	NM_014915.3(ANKRD26):c.1869del (p.Thr624fs)	not provided [RCV001050139]	uncertain significance	10	27046469	27046469	Human		name
28904996	CV865776	single nucleotide variant	NM_014915.3(ANKRD26):c.3216A>G (p.Lys1072=)	Thrombocytopenia 2 [RCV001105830]\|not provided [RCV005093496]	likely benign\|uncertain significance	10	27035234	27035234	Human	1	name
28909039	CV865790	single nucleotide variant	NM_014915.3(ANKRD26):c.937G>A (p.Asp313Asn)	Thrombocytopenia 2 [RCV001108154]\|not provided [RCV002555054]	benign\|likely benign	10	27077478	27077478	Human	1	name
28898307	CV865792	single nucleotide variant	NM_014915.3(ANKRD26):c.679C>T (p.Pro227Ser)	ANKRD26-related disorder [RCV003938447]\|Thrombocytopenia 2 [RCV001102943]\|not provided [RCV001356450]\|not specified [RCV001819808]	benign\|likely benign\|conflicting interpretations of pathogenicity\|uncertain significance	10	27086569	27086569	Human	1	name , alternate_id
28898312	CV865793	single nucleotide variant	NM_014915.3(ANKRD26):c.565G>A (p.Gly189Arg)	Thrombocytopenia 2 [RCV001102945]	uncertain significance	10	27092479	27092479	Human	1	name
28902874	CV865795	single nucleotide variant	NM_014915.3(ANKRD26):c.319A>G (p.Asn107Asp)	Inborn genetic diseases [RCV004960452]\|Thrombocytopenia 2 [RCV001104855]\|not provided [RCV002556073]	uncertain significance	10	27093723	27093723	Human	2	name
150423430	CV1184349	single nucleotide variant	NM_014915.3(ANKRD26):c.1790G>C (p.Arg597Thr)	ANKRD26-related disorder [RCV003405713]\|Inborn genetic diseases [RCV004946716]\|not provided [RCV001555311]\|not specified [RCV001821877]	uncertain significance	10	27048825	27048825	Human	2	alternate_id
151235030	CV1318289	single nucleotide variant	NM_014915.3(ANKRD26):c.2855A>C (p.Lys952Thr)	ANKRD26-related disorder [RCV003911014]\|not provided [RCV001794612]	likely benign\|conflicting interpretations of pathogenicity\|uncertain significance	10	27035595	27035595	Human	1	alternate_id
151356176	CV1328940	single nucleotide variant	NM_014915.3(ANKRD26):c.3761A>G (p.Asp1254Gly)	ANKRD26-related disorder [RCV003948752]\|Inborn genetic diseases [RCV004946753]\|Thrombocytopenia 2 [RCV003230286]\|not provided [RCV002285501]\|not specified [RCV001822529]	likely benign\|conflicting interpretations of pathogenicity\|uncertain significance	10	27033271	27033271	Human	2	alternate_id
151354155	CV1329288	single nucleotide variant	NM_014915.3(ANKRD26):c.2458G>C (p.Glu820Gln)	ANKRD26-related disorder [RCV003407828]\|not provided [RCV003154199]\|not specified [RCV001817651]	uncertain significance	10	27037972	27037972	Human	1	alternate_id
153302408	CV1688215	single nucleotide variant	NM_014915.3(ANKRD26):c.4762C>T (p.Leu1588Phe)	ANKRD26-related disorder [RCV004741272]\|Inborn genetic diseases [RCV005375079]\|not provided [RCV002265441]	uncertain significance	10	27013073	27013073	Human	2	alternate_id
156378583	CV1906963	single nucleotide variant	NM_014915.3(ANKRD26):c.4078A>G (p.Ile1360Val)	ANKRD26-related disorder [RCV003918899]\|Thrombocytopenia 2 [RCV005034692]\|not provided [RCV003093083]	uncertain significance	10	27024454	27024454	Human	1	alternate_id
10405504	CV207737	single nucleotide variant	NM_014915.3(ANKRD26):c.4259G>A (p.Cys1420Tyr)	ANKRD26-related disorder [RCV003917734]\|Thrombocytopenia 2 [RCV001102742]\|not provided [RCV000901427]\|not specified [RCV000194625]	benign\|likely benign	10	27017749	27017749	Human	1	alternate_id
156030343	CV2135437	single nucleotide variant	NM_014915.3(ANKRD26):c.1867C>T (p.Arg623Trp)	ANKRD26-related disorder [RCV003916698]\|Inborn genetic diseases [RCV004948867]\|not provided [RCV002999115]	benign\|likely benign	10	27046471	27046471	Human	2	alternate_id
243053711	CV2416380	single nucleotide variant	NM_014915.3(ANKRD26):c.4007T>A (p.Met1336Lys)	ANKRD26-related disorder [RCV004741459]\|Inborn genetic diseases [RCV005377344]\|not provided [RCV003149441]	uncertain significance	10	27024525	27024525	Human	2	alternate_id
243054401	CV2418608	single nucleotide variant	NM_014915.3(ANKRD26):c.2053G>A (p.Asp685Asn)	ANKRD26-related disorder [RCV003892217]\|Inborn genetic diseases [RCV004961229]\|Thrombocytopenia 2 [RCV003154588]\|not provided [RCV003699035]	likely benign\|uncertain significance	10	27043534	27043534	Human	2	alternate_id
401781669	CV2682090	single nucleotide variant	NM_014915.3(ANKRD26):c.4980A>G (p.Ile1660Met)	ANKRD26-related disorder [RCV003906681]\|Inborn genetic diseases [RCV003265318]\|not provided [RCV003443192]	uncertain significance	10	27006936	27006936	Human	2	alternate_id
401829208	CV2747282	single nucleotide variant	NM_014915.3(ANKRD26):c.4564A>G (p.Met1522Val)	ANKRD26-related disorder [RCV003973797]\|Inborn genetic diseases [RCV005353165]\|not provided [RCV003328747]	likely benign\|conflicting interpretations of pathogenicity\|uncertain significance	10	27014654	27014654	Human	2	alternate_id
401919445	CV2798235	single nucleotide variant	NM_014915.3(ANKRD26):c.4534G>A (p.Glu1512Lys)	ANKRD26-related disorder [RCV003402257]\|Inborn genetic diseases [RCV005377361]\|not provided [RCV004723298]	uncertain significance	10	27014684	27014684	Human	2	alternate_id
401913587	CV2798953	single nucleotide variant	NM_014915.3(ANKRD26):c.2536A>G (p.Thr846Ala)	ANKRD26-related disorder [RCV003400170]\|Inborn genetic diseases [RCV005377365]	uncertain significance	10	27037894	27037894	Human	2	alternate_id
401914873	CV2799347	single nucleotide variant	NM_014915.3(ANKRD26):c.2083T>C (p.Ser695Pro)	ANKRD26-related disorder [RCV003400463]	uncertain significance	10	27043504	27043504	Human		trait , alternate_id
401913734	CV2799659	single nucleotide variant	NM_014915.3(ANKRD26):c.1210A>G (p.Met404Val)	ANKRD26-related disorder [RCV003427958]\|Inborn genetic diseases [RCV005353174]\|Thrombocytopenia 2 [RCV005055220]\|not provided [RCV005099958]	uncertain significance	10	27066546	27066546	Human	2	alternate_id
401933760	CV2799769	microsatellite	NM_014915.3(ANKRD26):c.1028TTC[1] (p.Leu344del)	ANKRD26-related disorder [RCV003410636]\|not provided [RCV005099960]	uncertain significance	10	27077382	27077384	Human		alternate_id
401907130	CV2800108	single nucleotide variant	NM_014915.3(ANKRD26):c.1255C>T (p.Pro419Ser)	ANKRD26-related disorder [RCV003397244]	uncertain significance	10	27066501	27066501	Human		trait , alternate_id
401912518	CV2800597	indel	NM_014915.3(ANKRD26):c.4590_4591delinsAAT (p.Lys1531fs)	ANKRD26-related disorder [RCV003399872]	uncertain significance	10	27014627	27014628	Human		trait , alternate_id
401912718	CV2800774	single nucleotide variant	NM_014915.3(ANKRD26):c.2279T>G (p.Val760Gly)	ANKRD26-related disorder [RCV003399946]\|Inborn genetic diseases [RCV005363104]\|not provided [RCV003778210]	uncertain significance	10	27040061	27040061	Human	2	alternate_id
401933600	CV2801863	single nucleotide variant	NM_014915.3(ANKRD26):c.2830G>T (p.Glu944Ter)	ANKRD26-related disorder [RCV003410401]	uncertain significance	10	27035620	27035620	Human		trait , alternate_id
401933623	CV2802272	single nucleotide variant	NM_014915.3(ANKRD26):c.4325A>T (p.Lys1442Met)	ANKRD26-related disorder [RCV003410497]	uncertain significance	10	27017683	27017683	Human		trait , alternate_id
401913060	CV2802891	single nucleotide variant	NM_014915.3(ANKRD26):c.4828C>A (p.Pro1610Thr)	ANKRD26-related disorder [RCV003427767]	uncertain significance	10	27013007	27013007	Human		trait , alternate_id
401901813	CV2804756	single nucleotide variant	NM_014915.3(ANKRD26):c.4901C>A (p.Ser1634Tyr)	ANKRD26-related disorder [RCV003393248]\|not provided [RCV004780551]	uncertain significance	10	27012934	27012934	Human	1	alternate_id
405126763	CV2886552	deletion	NM_014915.3(ANKRD26):c.3609_3612del (p.Glu1205fs)	ANKRD26-related disorder [RCV004738800]\|not provided [RCV003559569]	uncertain significance	10	27034838	27034841	Human	1	alternate_id
405224939	CV3058305	single nucleotide variant	NM_014915.3(ANKRD26):c.1331A>G (p.Lys444Arg)	ANKRD26-related disorder [RCV004723448]\|Inborn genetic diseases [RCV004636837]\|not provided [RCV003733880]	likely benign\|uncertain significance	10	27064020	27064020	Human	2	alternate_id
405153254	CV3068599	single nucleotide variant	NM_014915.3(ANKRD26):c.4721C>A (p.Thr1574Asn)	ANKRD26-related disorder [RCV004723450]\|Inborn genetic diseases [RCV004953476]\|not provided [RCV003726569]	likely benign\|uncertain significance	10	27014497	27014497	Human	2	alternate_id
11610944	CV310144	single nucleotide variant	NM_014915.3(ANKRD26):c.1153A>G (p.Thr385Ala)	ANKRD26-related disorder [RCV004739672]\|Inborn genetic diseases [RCV002520582]\|Thrombocytopenia 2 [RCV000388034]\|not provided [RCV002522153]\|not specified [RCV001820871]	benign\|uncertain significance	10	27067211	27067211	Human	2	alternate_id
11599789	CV315226	single nucleotide variant	NM_014915.3(ANKRD26):c.3286C>T (p.Arg1096Trp)	ANKRD26-related disorder [RCV003940132]\|Inborn genetic diseases [RCV004948254]\|Thrombocytopenia 2 [RCV000268421]\|not provided [RCV000935162]\|not specified [RCV001820868]	benign\|likely benign\|uncertain significance	10	27035164	27035164	Human	2	alternate_id
11601010	CV315247	single nucleotide variant	NM_014915.3(ANKRD26):c.1868G>A (p.Arg623Gln)	ANKRD26-related disorder [RCV003983001]\|Thrombocytopenia 2 [RCV000278393]\|not provided [RCV000963501]	benign\|likely benign	10	27046470	27046470	Human	1	alternate_id
405282395	CV3190987	deletion	NM_014915.3(ANKRD26):c.4060del (p.Val1354fs)	ANKRD26-related disorder [RCV003921411]	uncertain significance	10	27024472	27024472	Human		trait , alternate_id
405288502	CV3193606	single nucleotide variant	NM_014915.3(ANKRD26):c.2674G>T (p.Ala892Ser)	ANKRD26-related disorder [RCV003982612]	uncertain significance	10	27037209	27037209	Human		trait , alternate_id
11602321	CV321249	single nucleotide variant	NM_014915.3(ANKRD26):c.4676A>G (p.Tyr1559Cys)	ANKRD26-related disorder [RCV004739671]\|Inborn genetic diseases [RCV004948251]\|Thrombocytopenia [RCV000289600]\|not provided [RCV001770238]	uncertain significance	10	27014542	27014542	Human	4	alternate_id
408378578	CV3505353	single nucleotide variant	NM_014915.3(ANKRD26):c.4685A>C (p.Glu1562Ala)	ANKRD26-related disorder [RCV004728033]	uncertain significance	10	27014533	27014533	Human		trait , alternate_id
408370175	CV3508097	single nucleotide variant	NM_014915.3(ANKRD26):c.4513G>A (p.Ala1505Thr)	ANKRD26-related disorder [RCV004739074]\|not provided [RCV005059809]	uncertain significance	10	27014705	27014705	Human	1	alternate_id
13211469	CV425871	single nucleotide variant	NM_014915.3(ANKRD26):c.4445T>C (p.Ile1482Thr)	ANKRD26-related disorder [RCV003915355]\|Thrombocytopenia 2 [RCV001102741]\|not provided [RCV000497483]	benign\|likely benign\|conflicting interpretations of pathogenicity\|uncertain significance	10	27017563	27017563	Human	1	alternate_id
15097737	CV701301	single nucleotide variant	NM_014915.3(ANKRD26):c.3007G>A (p.Glu1003Lys)	ANKRD26-related disorder [RCV003978323]\|Abnormal bleeding [RCV001270519]\|Thrombocytopenia 2 [RCV001105832]\|not provided [RCV000958382]\|not specified [RCV001819014]	benign\|likely benign\|conflicting interpretations of pathogenicity\|uncertain significance	10	27035443	27035443	Human	5	alternate_id
15197219	CV723897	single nucleotide variant	NM_014915.3(ANKRD26):c.2170A>C (p.Ser724Arg)	ANKRD26-related disorder [RCV003940657]\|Thrombocytopenia 2 [RCV001102848]\|not provided [RCV000889996]\|not specified [RCV001818659]	benign\|likely benign\|conflicting interpretations of pathogenicity	10	27040170	27040170	Human	1	alternate_id
28898083	CV865782	single nucleotide variant	NM_014915.3(ANKRD26):c.1970A>T (p.Asp657Val)	ANKRD26-related disorder [RCV003906195]\|Thrombocytopenia 2 [RCV001102850]\|not provided [RCV002558028]	benign\|likely benign\|conflicting interpretations of pathogenicity	10	27046368	27046368	Human	1	alternate_id
28905173	CV865786	single nucleotide variant	NM_014915.3(ANKRD26):c.1364A>G (p.Asp455Gly)	ANKRD26-related disorder [RCV003898099]\|Inborn genetic diseases [RCV004032114]\|Thrombocytopenia 2 [RCV001105905]\|not provided [RCV005093497]	likely benign\|uncertain significance	10	27061242	27061242	Human	2	alternate_id
150456798	CV1278547	insertion	NM_014915.3(ANKRD26):c.709+270_709+271insAAG	not provided [RCV001709162]	benign	10	27086268	27086269	Human		name
11548703	CV253735	indel	NM_014915.3(ANKRD26):c.1269+7_1269+12delinsA	Thrombocytopenia 2 [RCV005230205]\|not provided [RCV004791375]\|not specified [RCV000249437]	likely benign\|uncertain significance	10	27066475	27066480	Human		name
150421866	CV1198040	insertion	NM_014915.3(ANKRD26):c.1985+281_1985+282insCCCA	not provided [RCV001578211]	likely benign	10	27046071	27046072	Human		name

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