Ankrd26 Variant Search Result - Rat Genome Database

Advanced Search (OLGA)

Variants search result for Homo sapiens
(View Results for all Objects and Ontologies)

More than 1000 records found for search term Ankrd26 (Displaying 1000)
For a more accurate result, please refine your search term.

Refine Term:

Assembly:

Chr

Sort By:

Export

CSV

TAB

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

Gene Annotator (Functional Annotation) unavailable	Gene Annotator (Annotation Distribution) unavailable	Variant Visualizer (Genomic Variants) unavailble Variant Visualizer (Genomic Variants) unavailable
Gene Annotator (Functional Annotation)	Gene Annotator (Annotation Distribution)	Variant Visualizer (Genomic Variants)

InterViewer (Protein-Protein Interactions) unavailable	Gviewer (Genome Viewer) unavailable	Variant Visualizer (Damaging Variants) unavailble Variant Visualizer (Damaging Variants) unavailable
InterViewer (Protein-Protein Interactions)	GViewer (Genome Viewer)	Variant Visualizer (Damaging Variants)

Gene Annotator (Annotation Comparison) unavailable	OLGA (Gene List Generator) unavailable
Gene Annotator (Annotation Comparison)	OLGA (Gene List Generator)	Excel (Download)

MOET (Multi-Ontology Enrichement) unavailable	GOLF (Gene-Ortholog Location Finder) unavailable
MOET (Multi-Ontology Enrichement)	GOLF (Gene-Ortholog Location Finder)

Create Name:

Description:

Send us a Message