Ahnak2 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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1003 records found for search term Ahnak2

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
15201147	CV725587	single nucleotide variant	NM_138420.4(AHNAK2):c.66T>A (p.Arg22=)	AHNAK2-related disorder [RCV003930793]\|not provided [RCV000891112]	benign	14	104957662	104957662	Human		name , alternate_id
15200503	CV753945	single nucleotide variant	NM_138420.4(AHNAK2):c.99G>A (p.Thr33=)	not provided [RCV000912865]	likely benign	14	104957629	104957629	Human		name
401910425	CV2807614	single nucleotide variant	NM_138420.4(AHNAK2):c.288G>C (p.Arg96=)	not provided [RCV003425057]	likely benign	14	104956615	104956615	Human		name
401911281	CV2807615	single nucleotide variant	NM_138420.4(AHNAK2):c.273T>C (p.Asp91=)	not provided [RCV003426406]	likely benign	14	104956630	104956630	Human		name
15158686	CV725585	single nucleotide variant	NM_138420.4(AHNAK2):c.156G>A (p.Pro52=)	AHNAK2-related disorder [RCV003955825]\|not provided [RCV000881055]	likely benign	14	104957467	104957467	Human		name , alternate_id
15201143	CV725586	single nucleotide variant	NM_138420.4(AHNAK2):c.132G>A (p.Ala44=)	AHNAK2-related disorder [RCV003930792]\|not provided [RCV000891111]	benign	14	104957491	104957491	Human		name , alternate_id
15200043	CV769702	single nucleotide variant	NM_138420.4(AHNAK2):c.168A>T (p.Ser56=)	not provided [RCV000935274]	likely benign	14	104957455	104957455	Human		name
401910421	CV2807610	single nucleotide variant	NM_138420.4(AHNAK2):c.855C>T (p.Tyr285=)	not provided [RCV003425053]	likely benign	14	104954596	104954596	Human		name
401910422	CV2807611	single nucleotide variant	NM_138420.4(AHNAK2):c.819G>A (p.Pro273=)	not provided [RCV003425054]	likely benign	14	104954632	104954632	Human		name
401910423	CV2807612	single nucleotide variant	NM_138420.4(AHNAK2):c.615C>T (p.Ser205=)	not provided [RCV003425055]	likely benign	14	104954993	104954993	Human		name
405270181	CV3215451	single nucleotide variant	NM_138420.4(AHNAK2):c.627C>T (p.His209=)	AHNAK2-related disorder [RCV003949193]	likely benign	14	104954981	104954981	Human		name , trait , alternate_id
598180143	CV3961726	single nucleotide variant	NM_138420.4(AHNAK2):c.61G>A (p.Gly21Ser)	not specified [RCV005332656]	uncertain significance	14	104957667	104957667	Human		name
156242770	CV2283216	single nucleotide variant	NM_138420.4(AHNAK2):c.292T>C (p.Phe98Leu)	not specified [RCV004145893]	uncertain significance	14	104956611	104956611	Human		name
401740083	CV2683254	single nucleotide variant	NM_138420.4(AHNAK2):c.185C>T (p.Thr62Met)	not specified [RCV004288039]	uncertain significance	14	104957438	104957438	Human		name
401765586	CV2683354	single nucleotide variant	NM_138420.4(AHNAK2):c.286C>T (p.Arg96Trp)	not specified [RCV004288128]	uncertain significance	14	104956617	104956617	Human		name
401910399	CV2807588	single nucleotide variant	NM_138420.4(AHNAK2):c.2970C>T (p.Asp990=)	not provided [RCV003425031]	likely benign	14	104952481	104952481	Human		name
401910400	CV2807589	single nucleotide variant	NM_138420.4(AHNAK2):c.2946G>A (p.Gly982=)	not provided [RCV003425032]	likely benign	14	104952505	104952505	Human		name
401910402	CV2807591	single nucleotide variant	NM_138420.4(AHNAK2):c.2799C>G (p.Gly933=)	not provided [RCV003425034]	benign	14	104952652	104952652	Human		name
401910404	CV2807593	single nucleotide variant	NM_138420.4(AHNAK2):c.2703T>C (p.Leu901=)	not provided [RCV003425036]	likely benign	14	104952748	104952748	Human		name
401910409	CV2807598	single nucleotide variant	NM_138420.4(AHNAK2):c.2428C>T (p.Leu810=)	not provided [RCV003425041]	likely benign	14	104953023	104953023	Human		name
401910410	CV2807599	single nucleotide variant	NM_138420.4(AHNAK2):c.2418G>A (p.Pro806=)	not provided [RCV003425042]	likely benign	14	104953033	104953033	Human		name
401910411	CV2807600	single nucleotide variant	NM_138420.4(AHNAK2):c.2241C>T (p.Pro747=)	not provided [RCV003425043]	likely benign	14	104953210	104953210	Human		name
401910413	CV2807602	single nucleotide variant	NM_138420.4(AHNAK2):c.2124C>T (p.Asp708=)	not provided [RCV003425045]	likely benign	14	104953327	104953327	Human		name
401910414	CV2807603	single nucleotide variant	NM_138420.4(AHNAK2):c.2109G>A (p.Pro703=)	not provided [RCV003425046]	likely benign	14	104953342	104953342	Human		name
401910415	CV2807604	single nucleotide variant	NM_138420.4(AHNAK2):c.2091G>A (p.Ser697=)	not provided [RCV003425047]	benign	14	104953360	104953360	Human		name
401910416	CV2807605	single nucleotide variant	NM_138420.4(AHNAK2):c.2064A>G (p.Ser688=)	not provided [RCV003425048]	benign	14	104953387	104953387	Human		name
405278845	CV3220428	single nucleotide variant	NM_138420.4(AHNAK2):c.151C>T (p.Arg51Trp)	AHNAK2-related disorder [RCV003976631]	benign	14	104957472	104957472	Human		name , trait , alternate_id
405769413	CV3262269	single nucleotide variant	NM_138420.4(AHNAK2):c.226G>A (p.Gly76Ser)	not specified [RCV004395659]	uncertain significance	14	104956677	104956677	Human		name
405769666	CV3262311	single nucleotide variant	NM_138420.4(AHNAK2):c.248G>T (p.Arg83Ile)	not specified [RCV004395701]	uncertain significance	14	104956655	104956655	Human		name
596945392	CV3547889	single nucleotide variant	NM_138420.4(AHNAK2):c.2901T>C (p.Asp967=)	not provided [RCV004809220]	likely benign	14	104952550	104952550	Human		name
596945393	CV3547890	single nucleotide variant	NM_138420.4(AHNAK2):c.2754A>G (p.Lys918=)	not provided [RCV004809221]	likely benign	14	104952697	104952697	Human		name
598270020	CV3954372	single nucleotide variant	NM_138420.4(AHNAK2):c.280G>A (p.Asp94Asn)	not specified [RCV005327447]	uncertain significance	14	104956623	104956623	Human		name
617153144	CV4021117	single nucleotide variant	NM_138420.4(AHNAK2):c.2956C>T (p.Leu986=)	not provided [RCV005428870]	likely benign	14	104952495	104952495	Human		name
150461354	CV1215794	single nucleotide variant	NM_138420.4(AHNAK2):c.8463G>A (p.Pro2821=)	not provided [RCV001613497]	benign	14	104946988	104946988	Human		name
150510265	CV1286760	single nucleotide variant	NM_138420.4(AHNAK2):c.8565T>C (p.Asp2855=)	not provided [RCV001720995]	benign	14	104946886	104946886	Human	1	name
150510265	CV1286760	single nucleotide variant	NM_138420.4(AHNAK2):c.8565T>C (p.Asp2855=)	not provided [RCV001720995]	benign	14	104946886	104946887	Human	1	name
156253098	CV2311431	single nucleotide variant	NM_138420.4(AHNAK2):c.721A>G (p.Arg241Gly)	not specified [RCV004168277]	uncertain significance	14	104954730	104954730	Human		name
156158399	CV2322649	single nucleotide variant	NM_138420.4(AHNAK2):c.956G>A (p.Arg319Lys)	not specified [RCV004182781]	uncertain significance	14	104954495	104954495	Human		name
156305992	CV2359801	single nucleotide variant	NM_138420.4(AHNAK2):c.490G>C (p.Val164Leu)	not specified [RCV004212661]	uncertain significance	14	104955118	104955118	Human		name
329390066	CV2441305	single nucleotide variant	NM_138420.4(AHNAK2):c.739A>G (p.Arg247Gly)	not specified [RCV004257121]	uncertain significance	14	104954712	104954712	Human		name
329360509	CV2443586	single nucleotide variant	NM_138420.4(AHNAK2):c.796T>C (p.Ser266Pro)	not specified [RCV004262410]	uncertain significance	14	104954655	104954655	Human		name
401740274	CV2683310	single nucleotide variant	NM_138420.4(AHNAK2):c.370A>G (p.Ser124Gly)	not specified [RCV004288088]	uncertain significance	14	104955579	104955579	Human		name
401877548	CV2769502	single nucleotide variant	NM_138420.4(AHNAK2):c.601G>A (p.Glu201Lys)	not specified [RCV004351165]	uncertain significance	14	104955007	104955007	Human		name
401915727	CV2807400	single nucleotide variant	NM_138420.4(AHNAK2):c.9789G>C (p.Thr3263=)	not provided [RCV003400714]	likely benign	14	104945662	104945662	Human		name
401934196	CV2807402	single nucleotide variant	NM_138420.4(AHNAK2):c.9651C>T (p.Leu3217=)	not provided [RCV003411083]	likely benign	14	104945800	104945800	Human		name
401934198	CV2807404	single nucleotide variant	NM_138420.4(AHNAK2):c.9624C>T (p.Asp3208=)	not provided [RCV003411085]	likely benign	14	104945827	104945827	Human		name
401934199	CV2807405	single nucleotide variant	NM_138420.4(AHNAK2):c.9453G>A (p.Pro3151=)	not provided [RCV003411086]	likely benign	14	104945998	104945998	Human		name
401915731	CV2807406	single nucleotide variant	NM_138420.4(AHNAK2):c.9336T>C (p.Asp3112=)	not provided [RCV003400716]	likely benign	14	104946115	104946115	Human		name
401934200	CV2807409	single nucleotide variant	NM_138420.4(AHNAK2):c.9057G>C (p.Gly3019=)	not provided [RCV003411087]	likely benign	14	104946394	104946394	Human		name
401915740	CV2807411	single nucleotide variant	NM_138420.4(AHNAK2):c.8655C>T (p.His2885=)	not provided [RCV003400720]	likely benign	14	104946796	104946796	Human		name
401915743	CV2807412	single nucleotide variant	NM_138420.4(AHNAK2):c.8604C>T (p.Ala2868=)	not provided [RCV003400721]	benign	14	104946847	104946847	Human		name
401915745	CV2807413	single nucleotide variant	NM_138420.4(AHNAK2):c.8601C>T (p.Ser2867=)	not provided [RCV003400722]	likely benign	14	104946850	104946850	Human		name
401934201	CV2807414	single nucleotide variant	NM_138420.4(AHNAK2):c.8598C>T (p.Pro2866=)	not provided [RCV003411088]	benign	14	104946853	104946853	Human		name
401915747	CV2807415	single nucleotide variant	NM_138420.4(AHNAK2):c.8538C>T (p.Asp2846=)	not provided [RCV003400723]	benign	14	104946913	104946913	Human		name
401915750	CV2807416	single nucleotide variant	NM_138420.4(AHNAK2):c.8502C>G (p.Ala2834=)	not provided [RCV003400724]	likely benign	14	104946949	104946949	Human		name
401915754	CV2807418	single nucleotide variant	NM_138420.4(AHNAK2):c.8496C>T (p.Ile2832=)	not provided [RCV003400726]	likely benign	14	104946955	104946955	Human		name
401915757	CV2807419	single nucleotide variant	NM_138420.4(AHNAK2):c.8493C>T (p.Ser2831=)	not provided [RCV003400727]	likely benign	14	104946958	104946958	Human		name
401915759	CV2807420	single nucleotide variant	NM_138420.4(AHNAK2):c.8430C>T (p.Asp2810=)	not provided [RCV003400728]	benign	14	104947021	104947021	Human		name
401915764	CV2807422	single nucleotide variant	NM_138420.4(AHNAK2):c.8391G>T (p.Gly2797=)	not provided [RCV003400730]	likely benign	14	104947060	104947060	Human		name
401934202	CV2807423	single nucleotide variant	NM_138420.4(AHNAK2):c.8310C>G (p.Pro2770=)	not provided [RCV003411089]	likely benign	14	104947141	104947141	Human		name
401915766	CV2807424	single nucleotide variant	NM_138420.4(AHNAK2):c.8196C>A (p.Pro2732=)	not provided [RCV003400731]	likely benign	14	104947255	104947255	Human		name
401934203	CV2807425	single nucleotide variant	NM_138420.4(AHNAK2):c.8157C>T (p.Gly2719=)	not provided [RCV003411090]	benign	14	104947294	104947294	Human		name
401934204	CV2807427	single nucleotide variant	NM_138420.4(AHNAK2):c.8037A>G (p.Glu2679=)	not provided [RCV003411091]	likely benign	14	104947414	104947414	Human		name
401915775	CV2807429	single nucleotide variant	NM_138420.4(AHNAK2):c.8007G>C (p.Ala2669=)	not provided [RCV003400734]	benign	14	104947444	104947444	Human		name
401934205	CV2807430	single nucleotide variant	NM_138420.4(AHNAK2):c.8007G>A (p.Ala2669=)	not provided [RCV003411092]	benign	14	104947444	104947444	Human		name
401915778	CV2807431	single nucleotide variant	NM_138420.4(AHNAK2):c.7992C>T (p.Gly2664=)	not provided [RCV003400735]	likely benign	14	104947459	104947459	Human		name
401915780	CV2807432	single nucleotide variant	NM_138420.4(AHNAK2):c.7863G>A (p.Pro2621=)	not provided [RCV003400736]	likely benign	14	104947588	104947588	Human		name
401915792	CV2807437	single nucleotide variant	NM_138420.4(AHNAK2):c.7638A>G (p.Gln2546=)	not provided [RCV003400741]	likely benign	14	104947813	104947813	Human		name
401915795	CV2807438	single nucleotide variant	NM_138420.4(AHNAK2):c.7599T>A (p.Ile2533=)	not provided [RCV003400742]	likely benign	14	104947852	104947852	Human		name
401915797	CV2807439	single nucleotide variant	NM_138420.4(AHNAK2):c.7593C>G (p.Leu2531=)	not provided [RCV003400743]	likely benign	14	104947858	104947858	Human		name
401934206	CV2807441	single nucleotide variant	NM_138420.4(AHNAK2):c.7476A>C (p.Ser2492=)	not provided [RCV003411093]	likely benign	14	104947975	104947975	Human		name
401915800	CV2807442	single nucleotide variant	NM_138420.4(AHNAK2):c.7473G>C (p.Pro2491=)	not provided [RCV003400745]	likely benign	14	104947978	104947978	Human		name
401934207	CV2807443	single nucleotide variant	NM_138420.4(AHNAK2):c.7473G>A (p.Pro2491=)	not provided [RCV003411094]	likely benign	14	104947978	104947978	Human		name
401934208	CV2807444	single nucleotide variant	NM_138420.4(AHNAK2):c.7380G>A (p.Leu2460=)	not provided [RCV003411095]	likely benign	14	104948071	104948071	Human		name
401915802	CV2807445	single nucleotide variant	NM_138420.4(AHNAK2):c.7323C>T (p.Asp2441=)	not provided [RCV003400746]	likely benign	14	104948128	104948128	Human		name
401915804	CV2807446	single nucleotide variant	NM_138420.4(AHNAK2):c.7176G>A (p.Pro2392=)	not provided [RCV003400747]	benign	14	104948275	104948275	Human		name
401915807	CV2807447	single nucleotide variant	NM_138420.4(AHNAK2):c.7020A>G (p.Ser2340=)	not provided [RCV003400748]	likely benign	14	104948431	104948431	Human		name
401915808	CV2807448	single nucleotide variant	NM_138420.4(AHNAK2):c.6999T>A (p.Leu2333=)	not provided [RCV003400749]	benign	14	104948452	104948452	Human		name
401915810	CV2807449	single nucleotide variant	NM_138420.4(AHNAK2):c.6762C>T (p.Pro2254=)	not provided [RCV003400750]	likely benign	14	104948689	104948689	Human		name
401915817	CV2807452	single nucleotide variant	NM_138420.4(AHNAK2):c.6648G>A (p.Gln2216=)	not provided [RCV003400753]	likely benign	14	104948803	104948803	Human		name
401934209	CV2807454	single nucleotide variant	NM_138420.4(AHNAK2):c.6597T>G (p.Thr2199=)	not provided [RCV003411096]	likely benign	14	104948854	104948854	Human		name
401934210	CV2807455	single nucleotide variant	NM_138420.4(AHNAK2):c.6504A>T (p.Pro2168=)	not provided [RCV003411097]	likely benign	14	104948947	104948947	Human		name
401915822	CV2807456	single nucleotide variant	NM_138420.4(AHNAK2):c.6435C>T (p.Asp2145=)	not provided [RCV003400755]	likely benign	14	104949016	104949016	Human		name
401934211	CV2807457	single nucleotide variant	NM_138420.4(AHNAK2):c.6421C>T (p.Leu2141=)	not provided [RCV003411098]	likely benign	14	104949030	104949030	Human		name
401915824	CV2807458	single nucleotide variant	NM_138420.4(AHNAK2):c.6403C>T (p.Leu2135=)	not provided [RCV003400756]	likely benign	14	104949048	104949048	Human		name
401915828	CV2807460	single nucleotide variant	NM_138420.4(AHNAK2):c.6399G>A (p.Ala2133=)	not provided [RCV003400758]	likely benign	14	104949052	104949052	Human		name
401915830	CV2807461	single nucleotide variant	NM_138420.4(AHNAK2):c.6393T>C (p.Asp2131=)	not provided [RCV003400759]	benign\|likely benign	14	104949058	104949058	Human		name
401915837	CV2807464	single nucleotide variant	NM_138420.4(AHNAK2):c.6183G>T (p.Val2061=)	not provided [RCV003400762]	likely benign	14	104949268	104949268	Human		name
401915839	CV2807465	single nucleotide variant	NM_138420.4(AHNAK2):c.6180C>T (p.His2060=)	not provided [RCV003400763]	likely benign	14	104949271	104949271	Human		name
401934212	CV2807467	single nucleotide variant	NM_138420.4(AHNAK2):c.6165G>A (p.Lys2055=)	not provided [RCV003411099]	likely benign	14	104949286	104949286	Human		name
401915843	CV2807468	single nucleotide variant	NM_138420.4(AHNAK2):c.6153G>A (p.Gln2051=)	not provided [RCV003400765]	benign	14	104949298	104949298	Human		name
401934213	CV2807469	single nucleotide variant	NM_138420.4(AHNAK2):c.6138G>A (p.Lys2046=)	not provided [RCV003411100]	likely benign	14	104949313	104949313	Human		name
401934214	CV2807473	single nucleotide variant	NM_138420.4(AHNAK2):c.6093G>C (p.Leu2031=)	not provided [RCV003411101]	likely benign	14	104949358	104949358	Human		name
401915863	CV2807477	single nucleotide variant	NM_138420.4(AHNAK2):c.6048C>G (p.Pro2016=)	not provided [RCV003400771]	benign	14	104949403	104949403	Human		name
401934216	CV2807478	single nucleotide variant	NM_138420.4(AHNAK2):c.6045A>G (p.Ala2015=)	not provided [RCV003411103]	benign	14	104949406	104949406	Human		name
401915870	CV2807484	single nucleotide variant	NM_138420.4(AHNAK2):c.6000A>G (p.Val2000=)	not provided [RCV003400774]	likely benign	14	104949451	104949451	Human		name
401915880	CV2807488	single nucleotide variant	NM_138420.4(AHNAK2):c.5931C>T (p.Ala1977=)	not provided [RCV003400778]	likely benign	14	104949520	104949520	Human		name
401915882	CV2807489	single nucleotide variant	NM_138420.4(AHNAK2):c.5916A>G (p.Gly1972=)	not provided [RCV003400779]	benign\|likely benign	14	104949535	104949535	Human		name
401915884	CV2807490	single nucleotide variant	NM_138420.4(AHNAK2):c.5904G>A (p.Ala1968=)	not provided [RCV003400780]	likely benign	14	104949547	104949547	Human		name
401915889	CV2807492	single nucleotide variant	NM_138420.4(AHNAK2):c.5820G>A (p.Ala1940=)	not provided [RCV003400782]	likely benign	14	104949631	104949631	Human		name
401915892	CV2807494	single nucleotide variant	NM_138420.4(AHNAK2):c.5778A>C (p.Thr1926=)	not provided [RCV003400784]	likely benign	14	104949673	104949673	Human		name
401915904	CV2807499	single nucleotide variant	NM_138420.4(AHNAK2):c.5676G>A (p.Pro1892=)	not provided [RCV003400788]	likely benign	14	104949775	104949775	Human		name
401915906	CV2807500	single nucleotide variant	NM_138420.4(AHNAK2):c.5670G>A (p.Lys1890=)	not provided [RCV003400789]	likely benign	14	104949781	104949781	Human		name
401915912	CV2807504	single nucleotide variant	NM_138420.4(AHNAK2):c.5574C>T (p.Ser1858=)	not provided [RCV003400792]	likely benign	14	104949877	104949877	Human		name
401915915	CV2807506	single nucleotide variant	NM_138420.4(AHNAK2):c.5538G>C (p.Val1846=)	not provided [RCV003400793]	likely benign	14	104949913	104949913	Human		name
401934248	CV2807508	single nucleotide variant	NM_138420.4(AHNAK2):c.5505G>A (p.Val1835=)	not provided [RCV003411111]	benign\|likely benign	14	104949946	104949946	Human		name
401915918	CV2807510	single nucleotide variant	NM_138420.4(AHNAK2):c.5496G>C (p.Ser1832=)	not provided [RCV003400794]	likely benign	14	104949955	104949955	Human		name
401934251	CV2807515	single nucleotide variant	NM_138420.4(AHNAK2):c.5403C>T (p.Asp1801=)	not provided [RCV003411114]	benign	14	104950048	104950048	Human		name
401915928	CV2807519	single nucleotide variant	NM_138420.4(AHNAK2):c.5193T>G (p.Leu1731=)	not provided [RCV003400798]	likely benign	14	104950258	104950258	Human		name
401934255	CV2807522	single nucleotide variant	NM_138420.4(AHNAK2):c.5112T>G (p.Thr1704=)	not provided [RCV003411118]	benign	14	104950339	104950339	Human		name
401915936	CV2807526	single nucleotide variant	NM_138420.4(AHNAK2):c.5040G>A (p.Ser1680=)	not provided [RCV003400802]	likely benign	14	104950411	104950411	Human		name
401915941	CV2807531	single nucleotide variant	NM_138420.4(AHNAK2):c.4950G>C (p.Ala1650=)	not provided [RCV003400804]	likely benign	14	104950501	104950501	Human		name
401915945	CV2807533	single nucleotide variant	NM_138420.4(AHNAK2):c.4881C>T (p.Asp1627=)	not provided [RCV003400806]	likely benign	14	104950570	104950570	Human		name
401915951	CV2807535	single nucleotide variant	NM_138420.4(AHNAK2):c.4779G>C (p.Gly1593=)	not provided [RCV003400808]	likely benign	14	104950672	104950672	Human		name
401915953	CV2807536	single nucleotide variant	NM_138420.4(AHNAK2):c.4770C>T (p.Asp1590=)	not provided [RCV003400809]	likely benign	14	104950681	104950681	Human		name
401915956	CV2807537	single nucleotide variant	NM_138420.4(AHNAK2):c.4701C>G (p.Ser1567=)	not provided [RCV003400810]	likely benign	14	104950750	104950750	Human		name
401915958	CV2807539	single nucleotide variant	NM_138420.4(AHNAK2):c.4668A>G (p.Gln1556=)	not provided [RCV003400811]	likely benign	14	104950783	104950783	Human		name
401915961	CV2807540	single nucleotide variant	NM_138420.4(AHNAK2):c.4590C>T (p.Pro1530=)	not provided [RCV003400812]	likely benign	14	104950861	104950861	Human		name
401934263	CV2807544	single nucleotide variant	NM_138420.4(AHNAK2):c.4527C>G (p.Gly1509=)	not provided [RCV003411126]	likely benign	14	104950924	104950924	Human		name
401915968	CV2807545	single nucleotide variant	NM_138420.4(AHNAK2):c.4506G>C (p.Ser1502=)	not provided [RCV003400815]	benign	14	104950945	104950945	Human		name
401915970	CV2807546	single nucleotide variant	NM_138420.4(AHNAK2):c.4503G>C (p.Pro1501=)	not provided [RCV003400816]	likely benign	14	104950948	104950948	Human		name
401934264	CV2807548	single nucleotide variant	NM_138420.4(AHNAK2):c.4320A>G (p.Leu1440=)	not provided [RCV003411127]	likely benign	14	104951131	104951131	Human		name
401915975	CV2807549	single nucleotide variant	NM_138420.4(AHNAK2):c.4290A>G (p.Glu1430=)	not provided [RCV003400818]	likely benign	14	104951161	104951161	Human		name
401934265	CV2807551	single nucleotide variant	NM_138420.4(AHNAK2):c.4203G>T (p.Val1401=)	not provided [RCV003411128]	likely benign	14	104951248	104951248	Human		name
401915982	CV2807552	single nucleotide variant	NM_138420.4(AHNAK2):c.4068C>G (p.Pro1356=)	not provided [RCV003400820]	likely benign	14	104951383	104951383	Human		name
401915984	CV2807553	single nucleotide variant	NM_138420.4(AHNAK2):c.4065A>G (p.Ala1355=)	not provided [RCV003400821]	likely benign	14	104951386	104951386	Human		name
401915991	CV2807555	single nucleotide variant	NM_138420.4(AHNAK2):c.4032C>G (p.Gly1344=)	not provided [RCV003400823]	likely benign	14	104951419	104951419	Human		name
401915993	CV2807557	single nucleotide variant	NM_138420.4(AHNAK2):c.3708G>T (p.Val1236=)	not provided [RCV003400824]	likely benign	14	104951743	104951743	Human		name
401915995	CV2807558	single nucleotide variant	NM_138420.4(AHNAK2):c.3705C>T (p.His1235=)	not provided [RCV003400825]	likely benign	14	104951746	104951746	Human		name
401915997	CV2807560	single nucleotide variant	NM_138420.4(AHNAK2):c.3600C>T (p.Pro1200=)	not provided [RCV003400826]	likely benign	14	104951851	104951851	Human		name
401916004	CV2807564	single nucleotide variant	NM_138420.4(AHNAK2):c.3555G>A (p.Ser1185=)	not provided [RCV003400829]	likely benign	14	104951896	104951896	Human		name
401916005	CV2807565	single nucleotide variant	NM_138420.4(AHNAK2):c.3534A>T (p.Pro1178=)	not provided [RCV003400830]	likely benign	14	104951917	104951917	Human		name
401934269	CV2807567	single nucleotide variant	NM_138420.4(AHNAK2):c.3525G>A (p.Ala1175=)	not provided [RCV003411132]	likely benign	14	104951926	104951926	Human		name
401934270	CV2807569	single nucleotide variant	NM_138420.4(AHNAK2):c.3408G>A (p.Pro1136=)	not provided [RCV003411133]	likely benign	14	104952043	104952043	Human		name
401916017	CV2807572	single nucleotide variant	NM_138420.4(AHNAK2):c.3372G>T (p.Val1124=)	not provided [RCV003400835]	benign	14	104952079	104952079	Human		name
401910385	CV2807574	single nucleotide variant	NM_138420.4(AHNAK2):c.3321G>A (p.Lys1107=)	not provided [RCV003425017]	likely benign	14	104952130	104952130	Human		name
401910386	CV2807575	single nucleotide variant	NM_138420.4(AHNAK2):c.3270G>A (p.Lys1090=)	not provided [RCV003425018]	likely benign	14	104952181	104952181	Human		name
401910387	CV2807576	single nucleotide variant	NM_138420.4(AHNAK2):c.3255G>A (p.Glu1085=)	not provided [RCV003425019]	likely benign	14	104952196	104952196	Human		name
401910388	CV2807577	single nucleotide variant	NM_138420.4(AHNAK2):c.3249G>A (p.Lys1083=)	not provided [RCV003425020]	likely benign	14	104952202	104952202	Human		name
401910389	CV2807578	single nucleotide variant	NM_138420.4(AHNAK2):c.3210C>T (p.His1070=)	not provided [RCV003425021]	likely benign	14	104952241	104952241	Human		name
401910390	CV2807579	single nucleotide variant	NM_138420.4(AHNAK2):c.3123G>C (p.Leu1041=)	not provided [RCV003425022]	likely benign	14	104952328	104952328	Human		name
401910391	CV2807580	single nucleotide variant	NM_138420.4(AHNAK2):c.3099T>C (p.Ser1033=)	not provided [RCV003425023]	likely benign	14	104952352	104952352	Human		name
401910393	CV2807582	single nucleotide variant	NM_138420.4(AHNAK2):c.3081G>A (p.Lys1027=)	not provided [RCV003425025]	likely benign	14	104952370	104952370	Human		name
401910394	CV2807583	single nucleotide variant	NM_138420.4(AHNAK2):c.3069G>A (p.Val1023=)	not provided [RCV003425026]	likely benign	14	104952382	104952382	Human		name
401910395	CV2807584	single nucleotide variant	NM_138420.4(AHNAK2):c.3042G>C (p.Gly1014=)	not provided [RCV003425027]	likely benign	14	104952409	104952409	Human		name
401910396	CV2807585	single nucleotide variant	NM_138420.4(AHNAK2):c.3033G>A (p.Ser1011=)	not provided [RCV003425028]	likely benign	14	104952418	104952418	Human		name
401910397	CV2807586	single nucleotide variant	NM_138420.4(AHNAK2):c.3030A>G (p.Val1010=)	not provided [RCV003425029]	likely benign	14	104952421	104952421	Human		name
401910424	CV2807613	single nucleotide variant	NM_138420.4(AHNAK2):c.442G>A (p.Ala148Thr)	not provided [RCV003425056]	benign	14	104955507	104955507	Human		name
401943571	CV2840094	single nucleotide variant	NM_138420.4(AHNAK2):c.5421T>G (p.Gly1807=)	not provided [RCV003456881]	benign	14	104950030	104950030	Human		name
405264357	CV3185306	single nucleotide variant	NM_138420.4(AHNAK2):c.4710C>T (p.Ala1570=)	not provided [RCV003885870]	likely benign	14	104950741	104950741	Human		name
405264631	CV3185350	single nucleotide variant	NM_138420.4(AHNAK2):c.3627T>G (p.Thr1209=)	not provided [RCV003885914]	likely benign	14	104951824	104951824	Human		name
405265510	CV3185729	single nucleotide variant	NM_138420.4(AHNAK2):c.4020G>A (p.Val1340=)	not provided [RCV003886293]	likely benign	14	104951431	104951431	Human		name
405260621	CV3185839	single nucleotide variant	NM_138420.4(AHNAK2):c.8346C>T (p.Asp2782=)	not provided [RCV003884915]	likely benign	14	104947105	104947105	Human		name
405755631	CV3252255	single nucleotide variant	NM_138420.4(AHNAK2):c.962G>A (p.Arg321Gln)	not specified [RCV004393411]	uncertain significance	14	104954489	104954489	Human		name
405716691	CV3255065	single nucleotide variant	NM_138420.4(AHNAK2):c.600A>C (p.Glu200Asp)	not specified [RCV004388213]	uncertain significance	14	104955008	104955008	Human		name
405770085	CV3258439	single nucleotide variant	NM_138420.4(AHNAK2):c.322C>A (p.Gln108Lys)	not specified [RCV004395771]	uncertain significance	14	104955627	104955627	Human		name
405787336	CV3258615	single nucleotide variant	NM_138420.4(AHNAK2):c.425T>C (p.Leu142Pro)	not specified [RCV004387928]	uncertain significance	14	104955524	104955524	Human		name
405787417	CV3258631	single nucleotide variant	NM_138420.4(AHNAK2):c.451T>C (p.Phe151Leu)	not specified [RCV004387944]	uncertain significance	14	104955498	104955498	Human		name
405787940	CV3258645	single nucleotide variant	NM_138420.4(AHNAK2):c.4578C>T (p.Asp1526=)	not specified [RCV004387958]	likely benign	14	104950873	104950873	Human		name
405852907	CV3393335	single nucleotide variant	NM_138420.4(AHNAK2):c.4608C>G (p.Leu1536=)	not provided [RCV004546065]	likely benign	14	104950843	104950843	Human		name
405852989	CV3393419	single nucleotide variant	NM_138420.4(AHNAK2):c.9030C>T (p.Ala3010=)	not provided [RCV004546149]	likely benign	14	104946421	104946421	Human		name
405853102	CV3393533	single nucleotide variant	NM_138420.4(AHNAK2):c.3030A>T (p.Val1010=)	not provided [RCV004546263]	likely benign	14	104952421	104952421	Human		name
405871662	CV3398004	single nucleotide variant	NM_138420.4(AHNAK2):c.9936A>G (p.Lys3312=)	not provided [RCV004575004]	likely benign	14	104945515	104945515	Human		name
405871939	CV3398150	single nucleotide variant	NM_138420.4(AHNAK2):c.8778A>G (p.Lys2926=)	not provided [RCV004575151]	likely benign	14	104946673	104946673	Human		name
405871976	CV3398168	single nucleotide variant	NM_138420.4(AHNAK2):c.5716T>C (p.Leu1906=)	not provided [RCV004575169]	likely benign	14	104949735	104949735	Human		name
407483866	CV3439000	single nucleotide variant	NM_138420.4(AHNAK2):c.937G>A (p.Ala313Thr)	not specified [RCV004618641]	uncertain significance	14	104954514	104954514	Human		name
408377793	CV3500831	single nucleotide variant	NM_138420.4(AHNAK2):c.6525G>A (p.Ser2175=)	not provided [RCV004722481]	likely benign	14	104948926	104948926	Human		name
408377859	CV3500854	single nucleotide variant	NM_138420.4(AHNAK2):c.6555C>T (p.Ala2185=)	not provided [RCV004722504]	likely benign	14	104948896	104948896	Human		name
596946985	CV3547045	single nucleotide variant	NM_138420.4(AHNAK2):c.3453G>A (p.Leu1151=)	not provided [RCV004810851]	likely benign	14	104951998	104951998	Human		name
596947676	CV3547256	single nucleotide variant	NM_138420.4(AHNAK2):c.4191A>G (p.Pro1397=)	not provided [RCV004811560]	likely benign	14	104951260	104951260	Human		name
596947677	CV3547257	single nucleotide variant	NM_138420.4(AHNAK2):c.4188C>T (p.Leu1396=)	not provided [RCV004811561]	likely benign	14	104951263	104951263	Human		name
596947864	CV3547450	single nucleotide variant	NM_138420.4(AHNAK2):c.6051G>A (p.Lys2017=)	not provided [RCV004811754]	likely benign	14	104949400	104949400	Human		name
596947933	CV3547523	single nucleotide variant	NM_138420.4(AHNAK2):c.4179C>T (p.Asp1393=)	not provided [RCV004811827]	likely benign	14	104951272	104951272	Human		name
596947998	CV3547590	single nucleotide variant	NM_138420.4(AHNAK2):c.6195T>C (p.Ala2065=)	not provided [RCV004811895]	likely benign	14	104949256	104949256	Human		name
596948091	CV3547686	single nucleotide variant	NM_138420.4(AHNAK2):c.6219G>A (p.Lys2073=)	not provided [RCV004811991]	likely benign	14	104949232	104949232	Human		name
596948092	CV3547687	single nucleotide variant	NM_138420.4(AHNAK2):c.3441G>T (p.Gly1147=)	not provided [RCV004811992]	likely benign	14	104952010	104952010	Human		name
596945381	CV3547882	single nucleotide variant	NM_138420.4(AHNAK2):c.7119T>C (p.Ala2373=)	not provided [RCV004809213]	likely benign	14	104948332	104948332	Human		name
596945823	CV3548081	single nucleotide variant	NM_138420.4(AHNAK2):c.6300A>G (p.Leu2100=)	not provided [RCV004809412]	likely benign	14	104949151	104949151	Human		name
596947246	CV3548796	single nucleotide variant	NM_138420.4(AHNAK2):c.4530G>A (p.Lys1510=)	not provided [RCV004811120]	likely benign	14	104950921	104950921	Human		name
597692307	CV3665276	single nucleotide variant	NM_138420.4(AHNAK2):c.403G>T (p.Gly135Trp)	not specified [RCV004915494]	uncertain significance	14	104955546	104955546	Human		name
597737467	CV3668557	single nucleotide variant	NM_138420.4(AHNAK2):c.510A>C (p.Lys170Asn)	not specified [RCV004920841]	uncertain significance	14	104955098	104955098	Human		name
597737934	CV3668657	single nucleotide variant	NM_138420.4(AHNAK2):c.818C>T (p.Pro273Leu)	not specified [RCV004920938]	uncertain significance	14	104954633	104954633	Human		name
597717456	CV3671631	single nucleotide variant	NM_138420.4(AHNAK2):c.7920T>C (p.Gly2640=)	not specified [RCV004918423]	likely benign	14	104947531	104947531	Human		name
597717679	CV3671661	single nucleotide variant	NM_138420.4(AHNAK2):c.7083C>G (p.Leu2361=)	not specified [RCV004918444]	likely benign	14	104948368	104948368	Human		name
597717915	CV3671717	single nucleotide variant	NM_138420.4(AHNAK2):c.7920T>G (p.Gly2640=)	not specified [RCV004918469]	likely benign	14	104947531	104947531	Human		name
597718301	CV3671757	single nucleotide variant	NM_138420.4(AHNAK2):c.3471T>G (p.Thr1157=)	not specified [RCV004918509]	likely benign	14	104951980	104951980	Human		name
597716236	CV3675252	single nucleotide variant	NM_138420.4(AHNAK2):c.689C>T (p.Thr230Met)	not specified [RCV004918301]	uncertain significance	14	104954762	104954762	Human		name
598129512	CV3886927	single nucleotide variant	NM_138420.4(AHNAK2):c.4419A>G (p.Gly1473=)	not provided [RCV005244987]	benign	14	104951032	104951032	Human		name
598129513	CV3886928	single nucleotide variant	NM_138420.4(AHNAK2):c.4404C>A (p.Ala1468=)	not provided [RCV005244988]	likely benign	14	104951047	104951047	Human		name
598129514	CV3886929	single nucleotide variant	NM_138420.4(AHNAK2):c.4386T>C (p.Asp1462=)	not provided [RCV005244989]	benign	14	104951065	104951065	Human		name
598127138	CV3888035	single nucleotide variant	NM_138420.4(AHNAK2):c.9270G>T (p.Leu3090=)	not provided [RCV005242721]	likely benign	14	104946181	104946181	Human		name
598192410	CV3957976	single nucleotide variant	NM_138420.4(AHNAK2):c.634C>A (p.Gln212Lys)	not specified [RCV005334995]	likely benign	14	104954974	104954974	Human		name
598168711	CV3965283	single nucleotide variant	NM_138420.4(AHNAK2):c.403G>C (p.Gly135Arg)	not specified [RCV005330290]	uncertain significance	14	104955546	104955546	Human		name
598169435	CV3965423	single nucleotide variant	NM_138420.4(AHNAK2):c.619G>T (p.Ala207Ser)	not specified [RCV005330431]	uncertain significance	14	104954989	104954989	Human		name
616939545	CV4014040	single nucleotide variant	NM_138420.4(AHNAK2):c.5223C>G (p.Leu1741=)	not provided [RCV005413532]	likely benign	14	104950228	104950228	Human		name
616939585	CV4014080	single nucleotide variant	NM_138420.4(AHNAK2):c.5229G>A (p.Lys1743=)	not provided [RCV005413572]	likely benign	14	104950222	104950222	Human		name
617152626	CV4020840	single nucleotide variant	NM_138420.4(AHNAK2):c.5124T>C (p.Ile1708=)	not provided [RCV005428593]	likely benign	14	104950327	104950327	Human		name
617153299	CV4021192	single nucleotide variant	NM_138420.4(AHNAK2):c.3033G>T (p.Ser1011=)	not provided [RCV005428945]	likely benign	14	104952418	104952418	Human		name
617149793	CV4021248	single nucleotide variant	NM_138420.4(AHNAK2):c.6495G>T (p.Val2165=)	not provided [RCV005425217]	likely benign	14	104948956	104948956	Human		name
13519240	CV486117	deletion	NM_138420.4(AHNAK2):c.1849del (p.Ala617fs)	not provided [RCV000585496]	uncertain significance	14	104953602	104953602	Human		name
15171253	CV702782	single nucleotide variant	NM_138420.4(AHNAK2):c.386C>G (p.Thr129Arg)	not provided [RCV000949798]	likely benign	14	104955563	104955563	Human	1	name
15171253	CV702782	single nucleotide variant	NM_138420.4(AHNAK2):c.386C>G (p.Thr129Arg)	not provided [RCV000949798]	likely benign	14	104955563	104955564	Human	1	name
15103493	CV725584	single nucleotide variant	NM_138420.4(AHNAK2):c.628G>A (p.Gly210Ser)	AHNAK2-related disorder [RCV003940721]\|not provided [RCV000892688]	benign	14	104954980	104954980	Human		name , alternate_id
8635121	CV90343	single nucleotide variant	NM_138420.2(AHNAK2):c.860C>T (p.Pro287Leu)	Malignant melanoma [RCV000070441]	not provided	14	104954591	104954591	Human		name
8635122	CV90344	single nucleotide variant	NM_138420.2(AHNAK2):c.463G>A (p.Glu155Lys)	Malignant melanoma [RCV000070442]	not provided	14	104955486	104955486	Human		name
34891492	CV904587	single nucleotide variant	NM_138420.4(AHNAK2):c.5634A>G (p.Ala1878=)	not provided [RCV001172081]	likely benign	14	104949817	104949817	Human		name
41405828	CV981850	single nucleotide variant	NM_138420.4(AHNAK2):c.299G>A (p.Arg100Lys)	not provided [RCV001810592]	uncertain significance	14	104956604	104956604	Human		name
127286751	CV1151284	single nucleotide variant	NM_138420.4(AHNAK2):c.1198G>A (p.Gly400Ser)	Dysmetria [RCV001507307]\|not provided [RCV003426165]	benign\|likely benign\|conflicting interpretations of pathogenicity\|uncertain significance	14	104954253	104954253	Human	2	name
150488469	CV1251673	single nucleotide variant	NM_138420.4(AHNAK2):c.13473A>G (p.Pro4491=)	not provided [RCV001674345]	benign	14	104941978	104941978	Human		name
10411834	CV205476	single nucleotide variant	NM_138420.4(AHNAK2):c.2695G>T (p.Val899Leu)	Abnormality of neuronal migration [RCV000201398]\|not provided [RCV004714536]	pathogenic\|benign	14	104952756	104952756	Human	1	name
156028298	CV2195743	single nucleotide variant	NM_138420.4(AHNAK2):c.2395A>G (p.Met799Val)	not specified [RCV004076099]	likely benign	14	104953056	104953056	Human		name
156400337	CV2199118	single nucleotide variant	NM_138420.4(AHNAK2):c.2684G>T (p.Gly895Val)	not specified [RCV004080514]	likely benign	14	104952767	104952767	Human		name
156178531	CV2201599	single nucleotide variant	NM_138420.4(AHNAK2):c.2158A>G (p.Thr720Ala)	not specified [RCV004080088]	uncertain significance	14	104953293	104953293	Human		name
156380789	CV2208404	single nucleotide variant	NM_138420.4(AHNAK2):c.2985C>G (p.Asp995Glu)	not specified [RCV004088832]	uncertain significance	14	104952466	104952466	Human		name
156252300	CV2212429	single nucleotide variant	NM_138420.4(AHNAK2):c.2582C>G (p.Pro861Arg)	not specified [RCV004091345]	uncertain significance	14	104952869	104952869	Human		name
156259021	CV2216176	single nucleotide variant	NM_138420.4(AHNAK2):c.1540G>A (p.Gly514Arg)	not specified [RCV004095628]	uncertain significance	14	104953911	104953911	Human		name
156330406	CV2227002	single nucleotide variant	NM_138420.4(AHNAK2):c.2530G>T (p.Gly844Trp)	not specified [RCV004097389]	uncertain significance	14	104952921	104952921	Human		name
155975485	CV2235883	single nucleotide variant	NM_138420.4(AHNAK2):c.2562C>A (p.Asp854Glu)	not specified [RCV004111993]	uncertain significance	14	104952889	104952889	Human		name
156184591	CV2239227	single nucleotide variant	NM_138420.4(AHNAK2):c.2066C>T (p.Ala689Val)	not specified [RCV004112202]	uncertain significance	14	104953385	104953385	Human		name
156103732	CV2260526	single nucleotide variant	NM_138420.4(AHNAK2):c.2644A>T (p.Ser882Cys)	not specified [RCV004123308]	uncertain significance	14	104952807	104952807	Human		name
156067231	CV2270824	single nucleotide variant	NM_138420.4(AHNAK2):c.2221G>C (p.Val741Leu)	not specified [RCV004131874]	uncertain significance	14	104953230	104953230	Human		name
155919158	CV2279365	single nucleotide variant	NM_138420.4(AHNAK2):c.2315A>G (p.Asp772Gly)	not specified [RCV004141919]	uncertain significance	14	104953136	104953136	Human		name
156280280	CV2281740	single nucleotide variant	NM_138420.4(AHNAK2):c.2053T>G (p.Phe685Val)	not specified [RCV004147884]	uncertain significance	14	104953398	104953398	Human		name
156179990	CV2288054	single nucleotide variant	NM_138420.4(AHNAK2):c.1888G>C (p.Glu630Gln)	not specified [RCV004147809]	uncertain significance	14	104953563	104953563	Human		name
156002190	CV2296489	single nucleotide variant	NM_138420.4(AHNAK2):c.2173G>A (p.Val725Ile)	not specified [RCV004148224]	likely benign	14	104953278	104953278	Human		name
156208999	CV2298169	single nucleotide variant	NM_138420.4(AHNAK2):c.2401G>A (p.Val801Met)	not specified [RCV004159827]	uncertain significance	14	104953050	104953050	Human		name
156273407	CV2323646	single nucleotide variant	NM_138420.4(AHNAK2):c.2471A>G (p.Lys824Arg)	not specified [RCV004165833]	uncertain significance	14	104952980	104952980	Human		name
156053642	CV2329107	single nucleotide variant	NM_138420.4(AHNAK2):c.1181C>T (p.Pro394Leu)	not specified [RCV004173871]	uncertain significance	14	104954270	104954270	Human		name
156076951	CV2331845	single nucleotide variant	NM_138420.4(AHNAK2):c.2458T>C (p.Ser820Pro)	not specified [RCV004184458]	uncertain significance	14	104952993	104952993	Human		name
156272797	CV2333959	single nucleotide variant	NM_138420.4(AHNAK2):c.2475G>T (p.Glu825Asp)	not specified [RCV004183491]	likely benign	14	104952976	104952976	Human		name
156044022	CV2342361	single nucleotide variant	NM_138420.4(AHNAK2):c.2005G>A (p.Ala669Thr)	not specified [RCV004191927]	uncertain significance	14	104953446	104953446	Human		name
156282959	CV2348899	single nucleotide variant	NM_138420.4(AHNAK2):c.2806A>C (p.Ile936Leu)	not specified [RCV004203334]	uncertain significance	14	104952645	104952645	Human		name
156133526	CV2350349	single nucleotide variant	NM_138420.4(AHNAK2):c.2962G>A (p.Asp988Asn)	not specified [RCV004202295]	uncertain significance	14	104952489	104952489	Human		name
156306180	CV2359873	single nucleotide variant	NM_138420.4(AHNAK2):c.1746G>A (p.Met582Ile)	not specified [RCV004212724]	uncertain significance	14	104953705	104953705	Human		name
156386974	CV2364905	single nucleotide variant	NM_138420.4(AHNAK2):c.2821C>G (p.Pro941Ala)	not specified [RCV004221805]	uncertain significance	14	104952630	104952630	Human		name
156151669	CV2369192	single nucleotide variant	NM_138420.4(AHNAK2):c.2705C>T (p.Pro902Leu)	not provided [RCV003427662]\|not specified [RCV004208113]	likely benign\|uncertain significance	14	104952746	104952746	Human		name
155999241	CV2373395	single nucleotide variant	NM_138420.4(AHNAK2):c.1801G>A (p.Gly601Ser)	not specified [RCV004220097]	uncertain significance	14	104953650	104953650	Human		name
155995607	CV2375045	single nucleotide variant	NM_138420.4(AHNAK2):c.1714G>A (p.Gly572Ser)	not specified [RCV004230096]	uncertain significance	14	104953737	104953737	Human		name
155935973	CV2379741	single nucleotide variant	NM_138420.4(AHNAK2):c.2956C>A (p.Leu986Met)	not specified [RCV004219861]	uncertain significance	14	104952495	104952495	Human		name
156344204	CV2384725	single nucleotide variant	NM_138420.4(AHNAK2):c.2092G>C (p.Val698Leu)	not specified [RCV004232493]	uncertain significance	14	104953359	104953359	Human		name
156112218	CV2387895	single nucleotide variant	NM_138420.4(AHNAK2):c.2134C>T (p.Leu712Phe)	not specified [RCV004236446]	uncertain significance	14	104953317	104953317	Human		name
155967978	CV2391405	single nucleotide variant	NM_138420.4(AHNAK2):c.1831C>G (p.Gln611Glu)	not specified [RCV004239808]	uncertain significance	14	104953620	104953620	Human		name
156000453	CV2391750	single nucleotide variant	NM_138420.4(AHNAK2):c.1184T>C (p.Leu395Ser)	not specified [RCV004242286]	uncertain significance	14	104954267	104954267	Human		name
155997990	CV2396169	single nucleotide variant	NM_138420.4(AHNAK2):c.1013C>T (p.Ser338Leu)	not specified [RCV004240132]	uncertain significance	14	104954438	104954438	Human		name
329391348	CV2447821	single nucleotide variant	NM_138420.4(AHNAK2):c.2782A>G (p.Lys928Glu)	not specified [RCV004258595]	uncertain significance	14	104952669	104952669	Human		name
329382507	CV2465190	single nucleotide variant	NM_138420.4(AHNAK2):c.2095G>A (p.Asp699Asn)	not specified [RCV004287229]	uncertain significance	14	104953356	104953356	Human		name
401736284	CV2682659	single nucleotide variant	NM_138420.4(AHNAK2):c.2566G>C (p.Val856Leu)	not specified [RCV004281642]	uncertain significance	14	104952885	104952885	Human		name
401721614	CV2683587	single nucleotide variant	NM_138420.4(AHNAK2):c.2872G>A (p.Glu958Lys)	not specified [RCV004282514]	uncertain significance	14	104952579	104952579	Human		name
401729288	CV2683631	single nucleotide variant	NM_138420.4(AHNAK2):c.1699G>A (p.Glu567Lys)	not specified [RCV004282550]	likely benign	14	104953752	104953752	Human		name
401740520	CV2684377	single nucleotide variant	NM_138420.4(AHNAK2):c.1616C>G (p.Pro539Arg)	not specified [RCV004289022]	uncertain significance	14	104953835	104953835	Human		name
401733801	CV2687837	single nucleotide variant	NM_138420.4(AHNAK2):c.2111A>C (p.Lys704Thr)	not specified [RCV004303146]	uncertain significance	14	104953340	104953340	Human		name
401726968	CV2691919	single nucleotide variant	NM_138420.4(AHNAK2):c.1327A>G (p.Thr443Ala)	not specified [RCV004299655]	likely benign	14	104954124	104954124	Human		name
401732204	CV2698248	single nucleotide variant	NM_138420.4(AHNAK2):c.2767A>T (p.Ser923Cys)	not specified [RCV004304807]	uncertain significance	14	104952684	104952684	Human		name
401740045	CV2709783	single nucleotide variant	NM_138420.4(AHNAK2):c.2039T>A (p.Phe680Tyr)	not specified [RCV004320765]	uncertain significance	14	104953412	104953412	Human		name
401783253	CV2716209	single nucleotide variant	NM_138420.4(AHNAK2):c.1060G>C (p.Gly354Arg)	not specified [RCV004323435]	uncertain significance	14	104954391	104954391	Human		name
401764318	CV2725538	single nucleotide variant	NM_138420.4(AHNAK2):c.2599G>A (p.Val867Met)	not specified [RCV004320152]	uncertain significance	14	104952852	104952852	Human		name
401729239	CV2735509	single nucleotide variant	NM_138420.4(AHNAK2):c.1820A>G (p.Glu607Gly)	not specified [RCV004331066]	uncertain significance	14	104953631	104953631	Human		name
401856062	CV2764311	single nucleotide variant	NM_138420.4(AHNAK2):c.1981C>A (p.Gln661Lys)	not specified [RCV004336841]	uncertain significance	14	104953470	104953470	Human		name
401890519	CV2768000	single nucleotide variant	NM_138420.4(AHNAK2):c.2416C>A (p.Pro806Thr)	not specified [RCV004348245]	uncertain significance	14	104953035	104953035	Human		name
401859765	CV2768326	single nucleotide variant	NM_138420.4(AHNAK2):c.2275C>A (p.Pro759Thr)	not specified [RCV004350592]	uncertain significance	14	104953176	104953176	Human		name
401879680	CV2769685	single nucleotide variant	NM_138420.4(AHNAK2):c.2941G>A (p.Glu981Lys)	not specified [RCV004351607]	uncertain significance	14	104952510	104952510	Human		name
401874360	CV2773917	single nucleotide variant	NM_138420.4(AHNAK2):c.2759A>C (p.Glu920Ala)	not specified [RCV004358346]	uncertain significance	14	104952692	104952692	Human		name
401891227	CV2778547	single nucleotide variant	NM_138420.4(AHNAK2):c.2455C>A (p.Leu819Met)	not specified [RCV004344202]	uncertain significance	14	104952996	104952996	Human		name
401900046	CV2780252	single nucleotide variant	NM_138420.4(AHNAK2):c.1907A>T (p.Lys636Ile)	not specified [RCV004355885]	uncertain significance	14	104953544	104953544	Human		name
401876553	CV2782960	single nucleotide variant	NM_138420.4(AHNAK2):c.1168G>C (p.Ala390Pro)	not specified [RCV004361755]	uncertain significance	14	104954283	104954283	Human		name
401898384	CV2787842	single nucleotide variant	NM_138420.4(AHNAK2):c.1967G>A (p.Arg656His)	not specified [RCV004358524]	uncertain significance	14	104953484	104953484	Human		name
401915629	CV2807345	single nucleotide variant	NM_138420.4(AHNAK2):c.16812A>G (p.Ser5604=)	not provided [RCV003400671]	likely benign	14	104938639	104938639	Human		name
401915631	CV2807346	single nucleotide variant	NM_138420.4(AHNAK2):c.16746T>C (p.Asn5582=)	not provided [RCV003400672]	likely benign	14	104938705	104938705	Human		name
401915635	CV2807347	single nucleotide variant	NM_138420.4(AHNAK2):c.16545G>A (p.Ser5515=)	not provided [RCV003400673]	likely benign	14	104938906	104938906	Human		name
401915639	CV2807349	single nucleotide variant	NM_138420.4(AHNAK2):c.15996G>A (p.Lys5332=)	not provided [RCV003400675]	likely benign	14	104939455	104939455	Human		name
401915643	CV2807351	single nucleotide variant	NM_138420.4(AHNAK2):c.15132C>T (p.Asp5044=)	not provided [RCV003400677]	likely benign	14	104940319	104940319	Human		name
401915647	CV2807353	single nucleotide variant	NM_138420.4(AHNAK2):c.14286G>A (p.Val4762=)	not provided [RCV003400679]	likely benign	14	104941165	104941165	Human		name
401915650	CV2807354	single nucleotide variant	NM_138420.4(AHNAK2):c.14091G>A (p.Ser4697=)	not provided [RCV003400680]	likely benign	14	104941360	104941360	Human		name
401915655	CV2807357	single nucleotide variant	NM_138420.4(AHNAK2):c.12858A>G (p.Leu4286=)	not provided [RCV003400682]	benign	14	104942593	104942593	Human		name
401915658	CV2807358	single nucleotide variant	NM_138420.4(AHNAK2):c.12711T>C (p.Asp4237=)	not provided [RCV003400683]	likely benign	14	104942740	104942740	Human		name
401915662	CV2807360	single nucleotide variant	NM_138420.4(AHNAK2):c.12381T>A (p.Thr4127=)	not provided [RCV003400684]	benign	14	104943070	104943070	Human		name
401915671	CV2807365	single nucleotide variant	NM_138420.4(AHNAK2):c.12114G>A (p.Glu4038=)	not provided [RCV003400688]	likely benign	14	104943337	104943337	Human		name
401915673	CV2807366	single nucleotide variant	NM_138420.4(AHNAK2):c.11871C>T (p.Ala3957=)	not provided [RCV003400689]	likely benign	14	104943580	104943580	Human		name
401915674	CV2807367	single nucleotide variant	NM_138420.4(AHNAK2):c.11787T>G (p.Val3929=)	not provided [RCV003400690]	likely benign	14	104943664	104943664	Human		name
401915677	CV2807369	single nucleotide variant	NM_138420.4(AHNAK2):c.11187G>A (p.Leu3729=)	not provided [RCV003400691]	likely benign	14	104944264	104944264	Human		name
401915680	CV2807371	single nucleotide variant	NM_138420.4(AHNAK2):c.11019T>C (p.Ser3673=)	not provided [RCV003400693]	likely benign	14	104944432	104944432	Human		name
401934188	CV2807372	single nucleotide variant	NM_138420.4(AHNAK2):c.11004G>A (p.Val3668=)	not provided [RCV003411075]	benign	14	104944447	104944447	Human		name
401915681	CV2807373	single nucleotide variant	NM_138420.4(AHNAK2):c.10950A>G (p.Val3650=)	not provided [RCV003400694]	likely benign	14	104944501	104944501	Human		name
401934189	CV2807374	single nucleotide variant	NM_138420.4(AHNAK2):c.10941A>C (p.Ser3647=)	not provided [RCV003411076]	likely benign	14	104944510	104944510	Human		name
401915684	CV2807375	single nucleotide variant	NM_138420.4(AHNAK2):c.10926A>G (p.Lys3642=)	not provided [RCV003400695]	likely benign	14	104944525	104944525	Human		name
401934246	CV2807377	single nucleotide variant	NM_138420.4(AHNAK2):c.10842G>A (p.Lys3614=)	not provided [RCV003411077]	likely benign	14	104944609	104944609	Human		name
401915687	CV2807379	single nucleotide variant	NM_138420.4(AHNAK2):c.10698G>A (p.Thr3566=)	not provided [RCV003400697]	likely benign	14	104944753	104944753	Human		name
401915689	CV2807380	single nucleotide variant	NM_138420.4(AHNAK2):c.10686C>T (p.Pro3562=)	not provided [RCV003400698]	likely benign	14	104944765	104944765	Human		name
401915692	CV2807381	single nucleotide variant	NM_138420.4(AHNAK2):c.10608A>G (p.Gln3536=)	not provided [RCV003400699]	likely benign	14	104944843	104944843	Human		name
401915694	CV2807382	single nucleotide variant	NM_138420.4(AHNAK2):c.10569T>A (p.Ile3523=)	not provided [RCV003400700]	likely benign	14	104944882	104944882	Human		name
401915696	CV2807383	single nucleotide variant	NM_138420.4(AHNAK2):c.10515C>T (p.Ala3505=)	not provided [RCV003400701]	likely benign	14	104944936	104944936	Human		name
401915699	CV2807384	single nucleotide variant	NM_138420.4(AHNAK2):c.10500G>A (p.Ala3500=)	not provided [RCV003400702]	likely benign	14	104944951	104944951	Human		name
401915702	CV2807386	single nucleotide variant	NM_138420.4(AHNAK2):c.10443C>G (p.Pro3481=)	not provided [RCV003400704]	likely benign	14	104945008	104945008	Human		name
401934192	CV2807387	single nucleotide variant	NM_138420.4(AHNAK2):c.10443C>A (p.Pro3481=)	not provided [RCV003411079]	likely benign	14	104945008	104945008	Human		name
401915705	CV2807388	single nucleotide variant	NM_138420.4(AHNAK2):c.10395T>C (p.Asp3465=)	not provided [RCV003400705]	likely benign	14	104945056	104945056	Human		name
401915707	CV2807389	single nucleotide variant	NM_138420.4(AHNAK2):c.10381C>T (p.Leu3461=)	not provided [RCV003400706]	likely benign	14	104945070	104945070	Human		name
401915709	CV2807390	single nucleotide variant	NM_138420.4(AHNAK2):c.10363C>T (p.Leu3455=)	not provided [RCV003400707]	likely benign	14	104945088	104945088	Human		name
401934193	CV2807391	single nucleotide variant	NM_138420.4(AHNAK2):c.10335C>T (p.Ala3445=)	not provided [RCV003411080]	likely benign	14	104945116	104945116	Human		name
401915711	CV2807392	single nucleotide variant	NM_138420.4(AHNAK2):c.10326C>T (p.Asp3442=)	not provided [RCV003400708]	benign	14	104945125	104945125	Human		name
401915713	CV2807393	single nucleotide variant	NM_138420.4(AHNAK2):c.10317G>C (p.Val3439=)	not provided [RCV003400709]	likely benign	14	104945134	104945134	Human		name
401934194	CV2807396	single nucleotide variant	NM_138420.4(AHNAK2):c.10140C>T (p.His3380=)	not provided [RCV003411081]	likely benign	14	104945311	104945311	Human		name
401915722	CV2807397	single nucleotide variant	NM_138420.4(AHNAK2):c.10023C>T (p.Asp3341=)	not provided [RCV003400712]	likely benign	14	104945428	104945428	Human		name
401910398	CV2807587	single nucleotide variant	NM_138420.4(AHNAK2):c.2990A>G (p.Lys997Arg)	not provided [RCV003425030]	benign	14	104952461	104952461	Human		name
401910401	CV2807590	single nucleotide variant	NM_138420.4(AHNAK2):c.2870G>T (p.Gly957Val)	not provided [RCV003425033]	likely benign	14	104952581	104952581	Human		name
401910403	CV2807592	single nucleotide variant	NM_138420.4(AHNAK2):c.2767A>C (p.Ser923Arg)	not provided [RCV003425035]\|not specified [RCV005333601]	likely benign\|uncertain significance	14	104952684	104952684	Human		name
401910405	CV2807594	single nucleotide variant	NM_138420.4(AHNAK2):c.2698A>G (p.Lys900Glu)	not provided [RCV003425037]	likely benign	14	104952753	104952753	Human		name
401910406	CV2807595	single nucleotide variant	NM_138420.4(AHNAK2):c.2608T>C (p.Ser870Pro)	not provided [RCV003425038]	benign	14	104952843	104952843	Human		name
401910407	CV2807596	single nucleotide variant	NM_138420.4(AHNAK2):c.2556G>C (p.Met852Ile)	not provided [RCV003425039]	likely benign	14	104952895	104952895	Human		name
401910408	CV2807597	single nucleotide variant	NM_138420.4(AHNAK2):c.2441G>A (p.Arg814Gln)	not provided [RCV003425040]	likely benign	14	104953010	104953010	Human		name
401910412	CV2807601	single nucleotide variant	NM_138420.4(AHNAK2):c.2207A>C (p.Asp736Ala)	not provided [RCV003425044]	benign\|likely benign	14	104953244	104953244	Human		name
401910417	CV2807606	single nucleotide variant	NM_138420.4(AHNAK2):c.1654G>A (p.Asp552Asn)	not provided [RCV003425049]	benign	14	104953797	104953797	Human		name
401910418	CV2807607	single nucleotide variant	NM_138420.4(AHNAK2):c.1616C>T (p.Pro539Leu)	not provided [RCV003425050]	likely benign	14	104953835	104953835	Human		name
401910419	CV2807608	single nucleotide variant	NM_138420.4(AHNAK2):c.1254G>T (p.Arg418Ser)	not provided [RCV003425051]	benign\|likely benign	14	104954197	104954197	Human		name
401910420	CV2807609	single nucleotide variant	NM_138420.4(AHNAK2):c.1208G>A (p.Arg403Lys)	not provided [RCV003425052]\|not specified [RCV004917844]	benign\|uncertain significance	14	104954243	104954243	Human		name
401943579	CV2840097	single nucleotide variant	NM_138420.4(AHNAK2):c.2242C>G (p.Leu748Val)	not provided [RCV003456884]	likely benign	14	104953209	104953209	Human		name
405263381	CV3185123	single nucleotide variant	NM_138420.4(AHNAK2):c.10296G>T (p.Val3432=)	not provided [RCV003885687]	likely benign	14	104945155	104945155	Human		name
405263769	CV3185229	single nucleotide variant	NM_138420.4(AHNAK2):c.10446C>A (p.Ser3482=)	not provided [RCV003885793]	likely benign	14	104945005	104945005	Human		name
405259535	CV3186311	single nucleotide variant	NM_138420.4(AHNAK2):c.2090C>T (p.Ser697Leu)	not provided [RCV003884070]	likely benign	14	104953361	104953361	Human		name
405753489	CV3251751	single nucleotide variant	NM_138420.4(AHNAK2):c.1172A>G (p.Gln391Arg)	not specified [RCV004393098]	uncertain significance	14	104954279	104954279	Human		name
405754101	CV3251839	single nucleotide variant	NM_138420.4(AHNAK2):c.1247C>A (p.Ala416Glu)	not specified [RCV004393186]	uncertain significance	14	104954204	104954204	Human		name
405754501	CV3251897	single nucleotide variant	NM_138420.4(AHNAK2):c.1292C>T (p.Thr431Ile)	not specified [RCV004393244]	uncertain significance	14	104954159	104954159	Human		name
405737484	CV3255004	single nucleotide variant	NM_138420.4(AHNAK2):c.1019G>A (p.Gly340Glu)	not specified [RCV004390822]	uncertain significance	14	104954432	104954432	Human		name
405767849	CV3262007	single nucleotide variant	NM_138420.4(AHNAK2):c.1408A>G (p.Thr470Ala)	not specified [RCV004395396]	uncertain significance	14	104954043	104954043	Human		name
405768241	CV3262075	single nucleotide variant	NM_138420.4(AHNAK2):c.1555G>C (p.Ala519Pro)	not specified [RCV004395465]	uncertain significance	14	104953896	104953896	Human		name
405768948	CV3262189	single nucleotide variant	NM_138420.4(AHNAK2):c.1708G>A (p.Asp570Asn)	not specified [RCV004395579]	uncertain significance	14	104953743	104953743	Human		name
405769125	CV3262219	single nucleotide variant	NM_138420.4(AHNAK2):c.1883G>C (p.Arg628Pro)	not specified [RCV004395609]	uncertain significance	14	104953568	104953568	Human		name
405769342	CV3262257	single nucleotide variant	NM_138420.4(AHNAK2):c.2166C>G (p.Asp722Glu)	not specified [RCV004395647]	uncertain significance	14	104953285	104953285	Human		name
405769356	CV3262259	single nucleotide variant	NM_138420.4(AHNAK2):c.2179A>C (p.Thr727Pro)	not specified [RCV004395649]	likely benign	14	104953272	104953272	Human		name
405769384	CV3262264	single nucleotide variant	NM_138420.4(AHNAK2):c.2248G>C (p.Glu750Gln)	not specified [RCV004395654]	uncertain significance	14	104953203	104953203	Human		name
405769472	CV3262279	single nucleotide variant	NM_138420.4(AHNAK2):c.2371G>A (p.Asp791Asn)	not specified [RCV004395669]	uncertain significance	14	104953080	104953080	Human		name
405769621	CV3262303	single nucleotide variant	NM_138420.4(AHNAK2):c.2473G>A (p.Glu825Lys)	not specified [RCV004395693]	uncertain significance	14	104952978	104952978	Human		name
405769789	CV3262332	single nucleotide variant	NM_138420.4(AHNAK2):c.2732G>A (p.Gly911Asp)	not specified [RCV004395722]	uncertain significance	14	104952719	104952719	Human		name
405852865	CV3393291	single nucleotide variant	NM_138420.4(AHNAK2):c.12429C>T (p.Phe4143=)	not provided [RCV004546021]	likely benign	14	104943022	104943022	Human		name
407456147	CV3415810	single nucleotide variant	NM_138420.4(AHNAK2):c.12328C>T (p.Leu4110=)	not provided [RCV004598687]	likely benign	14	104943123	104943123	Human		name
407492894	CV3432215	single nucleotide variant	NM_138420.4(AHNAK2):c.2354C>T (p.Ala785Val)	not specified [RCV004620913]	likely benign	14	104953097	104953097	Human		name
407483082	CV3438863	single nucleotide variant	NM_138420.4(AHNAK2):c.2681C>A (p.Ala894Asp)	not specified [RCV004618506]	uncertain significance	14	104952770	104952770	Human		name
407501324	CV3439091	single nucleotide variant	NM_138420.4(AHNAK2):c.1954C>T (p.His652Tyr)	not specified [RCV004623233]	uncertain significance	14	104953497	104953497	Human		name
407501851	CV3439204	single nucleotide variant	NM_138420.4(AHNAK2):c.1877A>T (p.Gln626Leu)	not specified [RCV004623346]	uncertain significance	14	104953574	104953574	Human		name
407493662	CV3442438	single nucleotide variant	NM_138420.4(AHNAK2):c.2012A>G (p.Lys671Arg)	not specified [RCV004621109]	uncertain significance	14	104953439	104953439	Human		name
408377834	CV3500845	single nucleotide variant	NM_138420.4(AHNAK2):c.2653C>T (p.Pro885Ser)	not provided [RCV004722495]	benign	14	104952798	104952798	Human		name
596948039	CV3547631	single nucleotide variant	NM_138420.4(AHNAK2):c.12465C>G (p.Ser4155=)	not provided [RCV004811936]	likely benign	14	104942986	104942986	Human		name
596948040	CV3547632	single nucleotide variant	NM_138420.4(AHNAK2):c.12462G>C (p.Ala4154=)	not provided [RCV004811937]	likely benign	14	104942989	104942989	Human		name
597691370	CV3665129	single nucleotide variant	NM_138420.4(AHNAK2):c.1045G>C (p.Gly349Arg)	not specified [RCV004915370]	uncertain significance	14	104954406	104954406	Human		name
597692292	CV3665267	single nucleotide variant	NM_138420.4(AHNAK2):c.2735C>T (p.Pro912Leu)	not specified [RCV004915492]	likely benign	14	104952716	104952716	Human		name
597739076	CV3665381	single nucleotide variant	NM_138420.4(AHNAK2):c.2195T>A (p.Leu732Gln)	not specified [RCV004921167]	uncertain significance	14	104953256	104953256	Human		name
597748759	CV3665423	single nucleotide variant	NM_138420.4(AHNAK2):c.1738A>C (p.Ile580Leu)	not specified [RCV004923193]	uncertain significance	14	104953713	104953713	Human		name
597738575	CV3668779	single nucleotide variant	NM_138420.4(AHNAK2):c.2492G>C (p.Ser831Thr)	not specified [RCV004921060]	uncertain significance	14	104952959	104952959	Human		name
597738786	CV3668821	single nucleotide variant	NM_138420.4(AHNAK2):c.2113G>C (p.Val705Leu)	not specified [RCV004921102]	uncertain significance	14	104953338	104953338	Human		name
597717227	CV3671584	single nucleotide variant	NM_138420.4(AHNAK2):c.11265G>A (p.Ala3755=)	not specified [RCV004918401]	likely benign	14	104944186	104944186	Human		name
597736659	CV3671900	single nucleotide variant	NM_138420.4(AHNAK2):c.1903G>A (p.Asp635Asn)	not specified [RCV004920680]	uncertain significance	14	104953548	104953548	Human		name
597716740	CV3675373	single nucleotide variant	NM_138420.4(AHNAK2):c.2045T>A (p.Met682Lys)	not specified [RCV004918356]	uncertain significance	14	104953406	104953406	Human		name
598269094	CV3954170	single nucleotide variant	NM_138420.4(AHNAK2):c.1176C>A (p.Ser392Arg)	not specified [RCV005327245]	uncertain significance	14	104954275	104954275	Human		name
598191712	CV3957863	single nucleotide variant	NM_138420.4(AHNAK2):c.2384C>T (p.Ser795Phe)	not specified [RCV005334882]	uncertain significance	14	104953067	104953067	Human		name
598192606	CV3958009	single nucleotide variant	NM_138420.4(AHNAK2):c.1763C>T (p.Pro588Leu)	not specified [RCV005335028]	uncertain significance	14	104953688	104953688	Human		name
598192718	CV3958030	single nucleotide variant	NM_138420.4(AHNAK2):c.2970C>G (p.Asp990Glu)	not specified [RCV005335049]	uncertain significance	14	104952481	104952481	Human		name
598169841	CV3961594	single nucleotide variant	NM_138420.4(AHNAK2):c.1186C>T (p.Pro396Ser)	not specified [RCV005330550]	uncertain significance	14	104954265	104954265	Human		name
598170177	CV3961709	single nucleotide variant	NM_138420.4(AHNAK2):c.2393G>T (p.Ser798Ile)	not specified [RCV005330665]	uncertain significance	14	104953058	104953058	Human		name
598180323	CV3961764	single nucleotide variant	NM_138420.4(AHNAK2):c.1913A>G (p.Asp638Gly)	not specified [RCV005332694]	uncertain significance	14	104953538	104953538	Human		name
598180450	CV3961791	single nucleotide variant	NM_138420.4(AHNAK2):c.2531G>A (p.Gly844Glu)	not specified [RCV005332721]	uncertain significance	14	104952920	104952920	Human		name
598168238	CV3965200	single nucleotide variant	NM_138420.4(AHNAK2):c.2250G>T (p.Glu750Asp)	not specified [RCV005330207]	uncertain significance	14	104953201	104953201	Human		name
598168269	CV3965207	single nucleotide variant	NM_138420.4(AHNAK2):c.11931G>A (p.Ser3977=)	not specified [RCV005330214]	likely benign	14	104943520	104943520	Human		name
598168369	CV3965226	single nucleotide variant	NM_138420.4(AHNAK2):c.10359G>A (p.Ala3453=)	not specified [RCV005330233]	likely benign	14	104945092	104945092	Human		name
598168893	CV3965312	single nucleotide variant	NM_138420.4(AHNAK2):c.2218G>A (p.Asp740Asn)	not specified [RCV005330319]	uncertain significance	14	104953233	104953233	Human		name
598169380	CV3965412	single nucleotide variant	NM_138420.4(AHNAK2):c.2210G>C (p.Gly737Ala)	not specified [RCV005330420]	uncertain significance	14	104953241	104953241	Human		name
598169540	CV3965450	single nucleotide variant	NM_138420.4(AHNAK2):c.2281G>A (p.Val761Met)	not specified [RCV005330458]	uncertain significance	14	104953170	104953170	Human		name
617152355	CV4020725	single nucleotide variant	NM_138420.4(AHNAK2):c.1311G>T (p.Lys437Asn)	not provided [RCV005427982]	benign	14	104954140	104954140	Human		name
150411826	CV1196113	single nucleotide variant	NM_138420.4(AHNAK2):c.5855C>T (p.Pro1952Leu)	not provided [RCV001573850]\|not specified [RCV001727898]	benign\|likely benign	14	104949596	104949596	Human		name
150485536	CV1250246	single nucleotide variant	NM_138420.4(AHNAK2):c.8470G>A (p.Gly2824Arg)	not provided [RCV001673859]	benign	14	104946981	104946981	Human		name
150451497	CV1260267	single nucleotide variant	NM_138420.4(AHNAK2):c.8584C>A (p.Arg2862Ser)	not provided [RCV001680757]	benign	14	104946867	104946867	Human		name
150442727	CV1266279	single nucleotide variant	NM_138420.4(AHNAK2):c.7411G>C (p.Val2471Leu)	not provided [RCV001690715]	benign	14	104948040	104948040	Human		name
10411800	CV205475	single nucleotide variant	NM_138420.4(AHNAK2):c.5025G>C (p.Lys1675Asn)	Abnormality of neuronal migration [RCV000201358]\|not provided [RCV005411366]	benign\|likely benign	14	104950426	104950426	Human	1	name
156315848	CV2192958	single nucleotide variant	NM_138420.4(AHNAK2):c.3644C>T (p.Pro1215Leu)	not specified [RCV004069516]	likely benign	14	104951807	104951807	Human		name
156365501	CV2193215	single nucleotide variant	NM_138420.4(AHNAK2):c.4490A>C (p.Lys1497Thr)	not specified [RCV004071205]	uncertain significance	14	104950961	104950961	Human		name
156234624	CV2193321	single nucleotide variant	NM_138420.4(AHNAK2):c.3943T>A (p.Ser1315Thr)	not specified [RCV004072827]	uncertain significance	14	104951508	104951508	Human		name
156234636	CV2193322	single nucleotide variant	NM_138420.4(AHNAK2):c.3952G>A (p.Asp1318Asn)	not specified [RCV004072828]	uncertain significance	14	104951499	104951499	Human		name
156136146	CV2196145	single nucleotide variant	NM_138420.4(AHNAK2):c.5380G>A (p.Glu1794Lys)	not specified [RCV004073505]	uncertain significance	14	104950071	104950071	Human		name
156076119	CV2198148	single nucleotide variant	NM_138420.4(AHNAK2):c.7123C>G (p.Leu2375Val)	not specified [RCV004079737]	uncertain significance	14	104948328	104948328	Human		name
156266773	CV2198774	single nucleotide variant	NM_138420.4(AHNAK2):c.5831C>A (p.Ala1944Asp)	not specified [RCV004077821]	uncertain significance	14	104949620	104949620	Human		name
156266792	CV2198775	single nucleotide variant	NM_138420.4(AHNAK2):c.7955A>C (p.Lys2652Thr)	not specified [RCV004077822]	uncertain significance	14	104947496	104947496	Human		name
156324767	CV2198868	single nucleotide variant	NM_138420.4(AHNAK2):c.9752C>T (p.Pro3251Leu)	not specified [RCV004077903]	uncertain significance	14	104945699	104945699	Human		name
156229489	CV2199491	single nucleotide variant	NM_138420.4(AHNAK2):c.9298C>G (p.Pro3100Ala)	not specified [RCV004071047]	uncertain significance	14	104946153	104946153	Human		name
156063667	CV2199954	single nucleotide variant	NM_138420.4(AHNAK2):c.5342A>T (p.Asp1781Val)	not specified [RCV004074126]	uncertain significance	14	104950109	104950109	Human		name
156144594	CV2200173	single nucleotide variant	NM_138420.4(AHNAK2):c.7676G>T (p.Gly2559Val)	not specified [RCV004069740]	uncertain significance	14	104947775	104947775	Human		name
156263425	CV2201167	single nucleotide variant	NM_138420.4(AHNAK2):c.4039A>G (p.Ile1347Val)	not specified [RCV004077318]	uncertain significance	14	104951412	104951412	Human		name
156257567	CV2204590	single nucleotide variant	NM_138420.4(AHNAK2):c.8578G>C (p.Asp2860His)	not specified [RCV004081698]	uncertain significance	14	104946873	104946873	Human		name
155965764	CV2206577	single nucleotide variant	NM_138420.4(AHNAK2):c.4706G>C (p.Gly1569Ala)	not specified [RCV004080922]	uncertain significance	14	104950745	104950745	Human		name
155922251	CV2207444	single nucleotide variant	NM_138420.4(AHNAK2):c.3935G>A (p.Gly1312Glu)	not specified [RCV004089929]	uncertain significance	14	104951516	104951516	Human		name
155922257	CV2207445	single nucleotide variant	NM_138420.4(AHNAK2):c.5392G>A (p.Ala1798Thr)	not specified [RCV004089930]	uncertain significance	14	104950059	104950059	Human		name
155926074	CV2208103	single nucleotide variant	NM_138420.4(AHNAK2):c.9604G>C (p.Val3202Leu)	not specified [RCV004086788]	uncertain significance	14	104945847	104945847	Human		name
155973558	CV2211052	single nucleotide variant	NM_138420.4(AHNAK2):c.5328G>T (p.Glu1776Asp)	not specified [RCV004088233]	uncertain significance	14	104950123	104950123	Human		name
155920916	CV2212010	single nucleotide variant	NM_138420.4(AHNAK2):c.3059T>C (p.Leu1020Ser)	not specified [RCV004088923]	likely benign	14	104952392	104952392	Human		name
156194314	CV2214272	single nucleotide variant	NM_138420.4(AHNAK2):c.5692G>A (p.Glu1898Lys)	not specified [RCV004086264]	uncertain significance	14	104949759	104949759	Human		name
156194443	CV2214304	single nucleotide variant	NM_138420.4(AHNAK2):c.7436A>G (p.Lys2479Arg)	not provided [RCV004695375]\|not specified [RCV004086294]	uncertain significance	14	104948015	104948015	Human		name
156400738	CV2217090	single nucleotide variant	NM_138420.4(AHNAK2):c.7624G>C (p.Val2542Leu)	not specified [RCV004085767]	uncertain significance	14	104947827	104947827	Human		name
156246018	CV2219036	single nucleotide variant	NM_138420.4(AHNAK2):c.7484T>C (p.Val2495Ala)	not specified [RCV004087206]	uncertain significance	14	104947967	104947967	Human		name
156387438	CV2221507	single nucleotide variant	NM_138420.4(AHNAK2):c.3053A>G (p.Lys1018Arg)	not specified [RCV004096780]	uncertain significance	14	104952398	104952398	Human		name
156247661	CV2221912	single nucleotide variant	NM_138420.4(AHNAK2):c.7607C>A (p.Pro2536His)	not specified [RCV004102924]	uncertain significance	14	104947844	104947844	Human		name
156341939	CV2225966	single nucleotide variant	NM_138420.4(AHNAK2):c.3748C>G (p.Gln1250Glu)	not specified [RCV004105132]	uncertain significance	14	104951703	104951703	Human		name
156336950	CV2228617	single nucleotide variant	NM_138420.4(AHNAK2):c.7219C>A (p.Pro2407Thr)	not specified [RCV004092845]	uncertain significance	14	104948232	104948232	Human		name
156119751	CV2229033	single nucleotide variant	NM_138420.4(AHNAK2):c.9067A>G (p.Thr3023Ala)	not specified [RCV004098816]	uncertain significance	14	104946384	104946384	Human		name
156178294	CV2229307	single nucleotide variant	NM_138420.4(AHNAK2):c.5627C>T (p.Pro1876Leu)	not specified [RCV004101106]	uncertain significance	14	104949824	104949824	Human		name
156077840	CV2230317	single nucleotide variant	NM_138420.4(AHNAK2):c.9461G>C (p.Gly3154Ala)	not specified [RCV004099926]	uncertain significance	14	104945990	104945990	Human		name
155925421	CV2230431	single nucleotide variant	NM_138420.4(AHNAK2):c.5964C>G (p.Phe1988Leu)	not specified [RCV004095883]	uncertain significance	14	104949487	104949487	Human		name
155925427	CV2230432	single nucleotide variant	NM_138420.4(AHNAK2):c.7478T>C (p.Phe2493Ser)	not specified [RCV004095884]	uncertain significance	14	104947973	104947973	Human		name
156284475	CV2231230	single nucleotide variant	NM_138420.4(AHNAK2):c.3590T>G (p.Val1197Gly)	not specified [RCV004094429]	uncertain significance	14	104951861	104951861	Human		name
156343640	CV2232831	single nucleotide variant	NM_138420.4(AHNAK2):c.4142C>A (p.Pro1381His)	not specified [RCV004101451]	uncertain significance	14	104951309	104951309	Human		name
155987980	CV2234163	single nucleotide variant	NM_138420.4(AHNAK2):c.4585C>A (p.Leu1529Ile)	not specified [RCV004106251]	uncertain significance	14	104950866	104950866	Human		name
156271108	CV2237108	single nucleotide variant	NM_138420.4(AHNAK2):c.9704A>G (p.Lys3235Arg)	not specified [RCV004114864]	uncertain significance	14	104945747	104945747	Human		name
155984414	CV2241116	single nucleotide variant	NM_138420.4(AHNAK2):c.3064G>C (p.Asp1022His)	not specified [RCV004104149]	uncertain significance	14	104952387	104952387	Human		name
156052992	CV2246372	single nucleotide variant	NM_138420.4(AHNAK2):c.5715C>G (p.His1905Gln)	not specified [RCV004107810]	uncertain significance	14	104949736	104949736	Human		name
156173293	CV2247589	single nucleotide variant	NM_138420.4(AHNAK2):c.3599C>T (p.Pro1200Leu)	not specified [RCV004108889]	uncertain significance	14	104951852	104951852	Human		name
156077656	CV2248130	single nucleotide variant	NM_138420.4(AHNAK2):c.4529A>G (p.Lys1510Arg)	not specified [RCV004117534]	uncertain significance	14	104950922	104950922	Human		name
156300514	CV2248827	single nucleotide variant	NM_138420.4(AHNAK2):c.9008T>G (p.Val3003Gly)	not specified [RCV004115841]	uncertain significance	14	104946443	104946443	Human		name
155994993	CV2250297	single nucleotide variant	NM_138420.4(AHNAK2):c.3436G>C (p.Glu1146Gln)	not specified [RCV004127195]	uncertain significance	14	104952015	104952015	Human		name
155995542	CV2250356	single nucleotide variant	NM_138420.4(AHNAK2):c.7126G>A (p.Glu2376Lys)	not specified [RCV004127245]	uncertain significance	14	104948325	104948325	Human		name
156098726	CV2250615	single nucleotide variant	NM_138420.4(AHNAK2):c.9833T>A (p.Val3278Asp)	not specified [RCV004129253]	uncertain significance	14	104945618	104945618	Human		name
156317881	CV2251108	single nucleotide variant	NM_138420.4(AHNAK2):c.4562C>T (p.Pro1521Leu)	not specified [RCV004123649]	uncertain significance	14	104950889	104950889	Human		name
156185081	CV2251641	single nucleotide variant	NM_138420.4(AHNAK2):c.9346C>T (p.Pro3116Ser)	not specified [RCV004117873]	uncertain significance	14	104946105	104946105	Human		name
156185106	CV2251642	single nucleotide variant	NM_138420.4(AHNAK2):c.9841C>T (p.Pro3281Ser)	not specified [RCV004117874]	uncertain significance	14	104945610	104945610	Human		name
156080482	CV2255914	single nucleotide variant	NM_138420.4(AHNAK2):c.5068G>A (p.Ala1690Thr)	not specified [RCV004122373]	uncertain significance	14	104950383	104950383	Human		name
156199183	CV2255971	single nucleotide variant	NM_138420.4(AHNAK2):c.7081C>A (p.Leu2361Ile)	not specified [RCV004122419]	uncertain significance	14	104948370	104948370	Human		name
156179469	CV2258323	single nucleotide variant	NM_138420.4(AHNAK2):c.7440C>G (p.Asp2480Glu)	not specified [RCV004121676]	uncertain significance	14	104948011	104948011	Human		name
156060316	CV2263045	single nucleotide variant	NM_138420.4(AHNAK2):c.6688G>T (p.Val2230Phe)	not specified [RCV004131302]	uncertain significance	14	104948763	104948763	Human		name
156370114	CV2263477	single nucleotide variant	NM_138420.4(AHNAK2):c.5318C>G (p.Pro1773Arg)	not specified [RCV004133719]	uncertain significance	14	104950133	104950133	Human		name
156155661	CV2266158	single nucleotide variant	NM_138420.4(AHNAK2):c.5896G>C (p.Asp1966His)	not specified [RCV004128741]	uncertain significance	14	104949555	104949555	Human		name
156016434	CV2266364	single nucleotide variant	NM_138420.4(AHNAK2):c.9913G>C (p.Asp3305His)	not specified [RCV004129176]	uncertain significance	14	104945538	104945538	Human		name
156070865	CV2267193	single nucleotide variant	NM_138420.4(AHNAK2):c.8293G>A (p.Ala2765Thr)	not specified [RCV004133879]	uncertain significance	14	104947158	104947158	Human		name
156144018	CV2268835	single nucleotide variant	NM_138420.4(AHNAK2):c.8031G>T (p.Lys2677Asn)	not specified [RCV004124212]	uncertain significance	14	104947420	104947420	Human		name
155973189	CV2271617	single nucleotide variant	NM_138420.4(AHNAK2):c.3358C>T (p.Pro1120Ser)	not specified [RCV004130483]	uncertain significance	14	104952093	104952093	Human		name
155944358	CV2271717	single nucleotide variant	NM_138420.4(AHNAK2):c.8894C>A (p.Ser2965Tyr)	not specified [RCV004130564]	uncertain significance	14	104946557	104946557	Human		name
156365018	CV2272037	single nucleotide variant	NM_138420.4(AHNAK2):c.3145C>G (p.Gln1049Glu)	not specified [RCV004124838]	uncertain significance	14	104952306	104952306	Human		name
156169641	CV2273330	single nucleotide variant	NM_138420.4(AHNAK2):c.8528T>C (p.Val2843Ala)	not specified [RCV004132113]	uncertain significance	14	104946923	104946923	Human		name
156169652	CV2273331	single nucleotide variant	NM_138420.4(AHNAK2):c.8530G>A (p.Glu2844Lys)	not specified [RCV004132114]	uncertain significance	14	104946921	104946921	Human		name
155921518	CV2276319	single nucleotide variant	NM_138420.4(AHNAK2):c.5477C>T (p.Pro1826Leu)	not specified [RCV004144066]	uncertain significance	14	104949974	104949974	Human		name
156028877	CV2278569	single nucleotide variant	NM_138420.4(AHNAK2):c.9088C>T (p.Pro3030Ser)	not specified [RCV004133001]	uncertain significance	14	104946363	104946363	Human		name
156061151	CV2280350	single nucleotide variant	NM_138420.4(AHNAK2):c.7466A>G (p.Lys2489Arg)	not specified [RCV004140541]	uncertain significance	14	104947985	104947985	Human		name
155993635	CV2281345	single nucleotide variant	NM_138420.4(AHNAK2):c.6057G>C (p.Glu2019Asp)	not specified [RCV004147567]	uncertain significance	14	104949394	104949394	Human		name
155928999	CV2281347	single nucleotide variant	NM_138420.4(AHNAK2):c.6552G>C (p.Glu2184Asp)	not specified [RCV004147569]	uncertain significance	14	104948899	104948899	Human		name
155957722	CV2282102	single nucleotide variant	NM_138420.4(AHNAK2):c.9389C>G (p.Ser3130Cys)	not specified [RCV004138846]	uncertain significance	14	104946062	104946062	Human		name
155998931	CV2287211	single nucleotide variant	NM_138420.4(AHNAK2):c.8830G>A (p.Val2944Met)	not specified [RCV004146861]	likely benign	14	104946621	104946621	Human		name
156283716	CV2288925	single nucleotide variant	NM_138420.4(AHNAK2):c.8993A>G (p.Glu2998Gly)	not specified [RCV004149894]	uncertain significance	14	104946458	104946458	Human		name
156271813	CV2290411	single nucleotide variant	NM_138420.4(AHNAK2):c.6103G>C (p.Asp2035His)	not specified [RCV004154830]	uncertain significance	14	104949348	104949348	Human		name
156102060	CV2291447	single nucleotide variant	NM_138420.4(AHNAK2):c.7314G>T (p.Met2438Ile)	not specified [RCV004155773]	uncertain significance	14	104948137	104948137	Human		name
156097794	CV2294493	single nucleotide variant	NM_138420.4(AHNAK2):c.3236G>A (p.Gly1079Glu)	not specified [RCV004159986]	uncertain significance	14	104952215	104952215	Human		name
156084947	CV2295225	single nucleotide variant	NM_138420.4(AHNAK2):c.7797G>C (p.Lys2599Asn)	not specified [RCV004158608]	uncertain significance	14	104947654	104947654	Human		name
156296594	CV2297591	single nucleotide variant	NM_138420.4(AHNAK2):c.5239C>T (p.Pro1747Ser)	not specified [RCV004155293]	uncertain significance	14	104950212	104950212	Human		name
156206063	CV2297930	single nucleotide variant	NM_138420.4(AHNAK2):c.9554A>C (p.Asp3185Ala)	not specified [RCV004157857]	uncertain significance	14	104945897	104945897	Human		name
156084512	CV2299073	single nucleotide variant	NM_138420.4(AHNAK2):c.5494T>C (p.Ser1832Pro)	not specified [RCV004158586]	uncertain significance	14	104949957	104949957	Human		name
156202290	CV2300623	single nucleotide variant	NM_138420.4(AHNAK2):c.7811C>T (p.Ala2604Val)	not specified [RCV004155578]	uncertain significance	14	104947640	104947640	Human		name
155955095	CV2302371	single nucleotide variant	NM_138420.4(AHNAK2):c.9040C>A (p.Leu3014Ile)	not specified [RCV004161123]	uncertain significance	14	104946411	104946411	Human		name
156304244	CV2304728	single nucleotide variant	NM_138420.4(AHNAK2):c.8585G>C (p.Arg2862Pro)	not specified [RCV004166883]	uncertain significance	14	104946866	104946866	Human		name
155912599	CV2308916	single nucleotide variant	NM_138420.4(AHNAK2):c.8829C>A (p.Ser2943Arg)	not specified [RCV004169206]	uncertain significance	14	104946622	104946622	Human		name
155911548	CV2313345	single nucleotide variant	NM_138420.4(AHNAK2):c.8557C>G (p.Gln2853Glu)	not specified [RCV004163674]	uncertain significance	14	104946894	104946894	Human		name
156064836	CV2317721	single nucleotide variant	NM_138420.4(AHNAK2):c.7697T>G (p.Leu2566Arg)	not specified [RCV004174983]	uncertain significance	14	104947754	104947754	Human		name
156355295	CV2324457	single nucleotide variant	NM_138420.4(AHNAK2):c.5062G>A (p.Val1688Met)	not specified [RCV004178943]	uncertain significance	14	104950389	104950389	Human		name
156175642	CV2327039	single nucleotide variant	NM_138420.4(AHNAK2):c.9073G>C (p.Asp3025His)	not specified [RCV004178627]	uncertain significance	14	104946378	104946378	Human		name
156285707	CV2327163	single nucleotide variant	NM_138420.4(AHNAK2):c.7344C>A (p.Ser2448Arg)	not specified [RCV004172589]	uncertain significance	14	104948107	104948107	Human		name
156289202	CV2327480	single nucleotide variant	NM_138420.4(AHNAK2):c.3548A>C (p.Glu1183Ala)	not provided [RCV003396826]\|not specified [RCV004176794]	likely benign\|uncertain significance	14	104951903	104951903	Human		name
156277779	CV2328339	single nucleotide variant	NM_138420.4(AHNAK2):c.5941A>C (p.Met1981Leu)	not specified [RCV004175455]	uncertain significance	14	104949510	104949510	Human		name
155966978	CV2329862	single nucleotide variant	NM_138420.4(AHNAK2):c.8635G>A (p.Val2879Met)	not specified [RCV004183320]	uncertain significance	14	104946816	104946816	Human		name
156167291	CV2330184	single nucleotide variant	NM_138420.4(AHNAK2):c.4523C>T (p.Pro1508Leu)	not specified [RCV004185669]	uncertain significance	14	104950928	104950928	Human		name
156085179	CV2331051	single nucleotide variant	NM_138420.4(AHNAK2):c.3521G>T (p.Gly1174Val)	not specified [RCV004188089]	uncertain significance	14	104951930	104951930	Human		name
156072542	CV2331518	single nucleotide variant	NM_138420.4(AHNAK2):c.4561C>T (p.Pro1521Ser)	not specified [RCV004182122]	uncertain significance	14	104950890	104950890	Human		name
156303362	CV2331846	single nucleotide variant	NM_138420.4(AHNAK2):c.7205C>G (p.Pro2402Arg)	not specified [RCV004184459]	uncertain significance	14	104948246	104948246	Human		name
156076972	CV2331847	single nucleotide variant	NM_138420.4(AHNAK2):c.7388C>T (p.Ala2463Val)	not specified [RCV004186505]	uncertain significance	14	104948063	104948063	Human		name
156326866	CV2332016	single nucleotide variant	NM_138420.4(AHNAK2):c.3535G>A (p.Gly1179Ser)	not specified [RCV004189072]	likely benign	14	104951916	104951916	Human		name
156307587	CV2332048	single nucleotide variant	NM_138420.4(AHNAK2):c.3301G>A (p.Val1101Met)	not specified [RCV004189099]	uncertain significance	14	104952150	104952150	Human		name
156185841	CV2332433	single nucleotide variant	NM_138420.4(AHNAK2):c.9150C>G (p.His3050Gln)	not specified [RCV004196164]	uncertain significance	14	104946301	104946301	Human		name
156037316	CV2332528	single nucleotide variant	NM_138420.4(AHNAK2):c.6905G>A (p.Gly2302Glu)	not provided [RCV003410202]\|not specified [RCV004196246]	likely benign\|uncertain significance	14	104948546	104948546	Human		name
156037690	CV2332562	single nucleotide variant	NM_138420.4(AHNAK2):c.5245T>A (p.Leu1749Met)	not specified [RCV004196277]	uncertain significance	14	104950206	104950206	Human		name
156040310	CV2332798	single nucleotide variant	NM_138420.4(AHNAK2):c.7840A>G (p.Met2614Val)	not specified [RCV004189466]	likely benign	14	104947611	104947611	Human		name
156081950	CV2333425	single nucleotide variant	NM_138420.4(AHNAK2):c.9839C>A (p.Ala3280Asp)	not specified [RCV004190131]	uncertain significance	14	104945612	104945612	Human		name
156334751	CV2333432	single nucleotide variant	NM_138420.4(AHNAK2):c.8504C>T (p.Ser2835Leu)	not provided [RCV003396846]\|not specified [RCV004190136]	benign\|uncertain significance	14	104946947	104946947	Human		name
156335765	CV2333575	single nucleotide variant	NM_138420.4(AHNAK2):c.9284C>T (p.Thr3095Met)	not specified [RCV004190260]	uncertain significance	14	104946167	104946167	Human		name
156173667	CV2333736	single nucleotide variant	NM_138420.4(AHNAK2):c.6408G>C (p.Gln2136His)	not specified [RCV004181248]	uncertain significance	14	104949043	104949043	Human		name
156271647	CV2333860	single nucleotide variant	NM_138420.4(AHNAK2):c.5344G>A (p.Val1782Met)	not specified [RCV004181357]	uncertain significance	14	104950107	104950107	Human		name
156273779	CV2334052	single nucleotide variant	NM_138420.4(AHNAK2):c.9433A>T (p.Met3145Leu)	not specified [RCV004183570]	uncertain significance	14	104946018	104946018	Human		name
155971554	CV2334229	single nucleotide variant	NM_138420.4(AHNAK2):c.3673G>A (p.Gly1225Ser)	not provided [RCV003396833]\|not specified [RCV004186213]	likely benign\|uncertain significance	14	104951778	104951778	Human		name
156198110	CV2334477	single nucleotide variant	NM_138420.4(AHNAK2):c.3472G>A (p.Ala1158Thr)	not specified [RCV004188446]	likely benign	14	104951979	104951979	Human		name
155969465	CV2335469	single nucleotide variant	NM_138420.4(AHNAK2):c.4051G>A (p.Val1351Met)	not provided [RCV004695586]\|not specified [RCV004191640]	uncertain significance	14	104951400	104951400	Human		name
156072114	CV2337802	single nucleotide variant	NM_138420.4(AHNAK2):c.6814G>A (p.Val2272Met)	not specified [RCV004183817]	uncertain significance	14	104948637	104948637	Human		name
156087782	CV2337803	single nucleotide variant	NM_138420.4(AHNAK2):c.6818C>G (p.Thr2273Arg)	not specified [RCV004183818]	uncertain significance	14	104948633	104948633	Human		name
156072122	CV2337804	single nucleotide variant	NM_138420.4(AHNAK2):c.6821C>T (p.Ala2274Val)	not specified [RCV004183819]	uncertain significance	14	104948630	104948630	Human		name
155970365	CV2338057	single nucleotide variant	NM_138420.4(AHNAK2):c.4735G>C (p.Val1579Leu)	not specified [RCV004186097]	uncertain significance	14	104950716	104950716	Human		name
156181460	CV2338124	single nucleotide variant	NM_138420.4(AHNAK2):c.5063T>C (p.Val1688Ala)	not provided [RCV004809936]\|not specified [RCV004184156]	likely benign	14	104950388	104950388	Human		name
156181474	CV2338125	single nucleotide variant	NM_138420.4(AHNAK2):c.5065G>A (p.Glu1689Lys)	not provided [RCV004809937]\|not specified [RCV004184157]	likely benign\|uncertain significance	14	104950386	104950386	Human		name
156305290	CV2338736	single nucleotide variant	NM_138420.4(AHNAK2):c.4769A>C (p.Asp1590Ala)	not specified [RCV004182306]	uncertain significance	14	104950682	104950682	Human		name
156035061	CV2338855	single nucleotide variant	NM_138420.4(AHNAK2):c.3428C>T (p.Ala1143Val)	not specified [RCV004182408]	uncertain significance	14	104952023	104952023	Human		name
155914885	CV2339016	single nucleotide variant	NM_138420.4(AHNAK2):c.7390T>C (p.Trp2464Arg)	not specified [RCV004187070]	likely benign	14	104948061	104948061	Human		name
155914891	CV2339017	single nucleotide variant	NM_138420.4(AHNAK2):c.7405C>A (p.Leu2469Met)	not specified [RCV004187071]	uncertain significance	14	104948046	104948046	Human		name
155979215	CV2340027	single nucleotide variant	NM_138420.4(AHNAK2):c.5993T>A (p.Phe1998Tyr)	not specified [RCV004192275]	uncertain significance	14	104949458	104949458	Human		name
155979228	CV2340028	single nucleotide variant	NM_138420.4(AHNAK2):c.5995G>A (p.Gly1999Arg)	not specified [RCV004192276]	uncertain significance	14	104949456	104949456	Human		name
155979240	CV2340029	single nucleotide variant	NM_138420.4(AHNAK2):c.5999T>C (p.Val2000Ala)	not specified [RCV004192277]	uncertain significance	14	104949452	104949452	Human		name
155979255	CV2340030	single nucleotide variant	NM_138420.4(AHNAK2):c.6488T>A (p.Phe2163Tyr)	not provided [RCV003396843]\|not specified [RCV004192278]	benign\|likely benign\|uncertain significance	14	104948963	104948963	Human		name
156292222	CV2340032	single nucleotide variant	NM_138420.4(AHNAK2):c.6490G>A (p.Gly2164Arg)	not provided [RCV003410208]\|not specified [RCV004192280]	benign\|likely benign\|uncertain significance	14	104948961	104948961	Human		name
156292529	CV2340186	single nucleotide variant	NM_138420.4(AHNAK2):c.7011C>G (p.Ile2337Met)	not specified [RCV004192420]	uncertain significance	14	104948440	104948440	Human		name
156046633	CV2340261	single nucleotide variant	NM_138420.4(AHNAK2):c.9645C>G (p.His3215Gln)	not provided [RCV003396844]\|not specified [RCV004194533]	likely benign\|uncertain significance	14	104945806	104945806	Human		name
155921495	CV2340463	single nucleotide variant	NM_138420.4(AHNAK2):c.8176G>A (p.Gly2726Ser)	not provided [RCV003410210]\|not specified [RCV004197190]	likely benign	14	104947275	104947275	Human		name
155921916	CV2340536	single nucleotide variant	NM_138420.4(AHNAK2):c.9278C>T (p.Pro3093Leu)	not provided [RCV004809944]\|not specified [RCV004197252]	likely benign\|uncertain significance	14	104946173	104946173	Human		name
155921923	CV2340537	single nucleotide variant	NM_138420.4(AHNAK2):c.9773C>T (p.Pro3258Leu)	not specified [RCV004197253]	uncertain significance	14	104945678	104945678	Human		name
156066178	CV2340883	single nucleotide variant	NM_138420.4(AHNAK2):c.6119C>T (p.Pro2040Leu)	not specified [RCV004188239]	likely benign	14	104949332	104949332	Human		name
156066207	CV2340884	single nucleotide variant	NM_138420.4(AHNAK2):c.6128C>T (p.Ala2043Val)	not specified [RCV004188240]	uncertain significance	14	104949323	104949323	Human		name
156068314	CV2341035	single nucleotide variant	NM_138420.4(AHNAK2):c.8746A>G (p.Ile2916Val)	not specified [RCV004181524]	likely benign	14	104946705	104946705	Human		name
156068343	CV2341036	single nucleotide variant	NM_138420.4(AHNAK2):c.8748A>G (p.Ile2916Met)	not specified [RCV004181525]	uncertain significance	14	104946703	104946703	Human		name
155975626	CV2341576	single nucleotide variant	NM_138420.4(AHNAK2):c.3634A>T (p.Ser1212Cys)	not provided [RCV003883918]\|not specified [RCV004188963]	likely benign\|uncertain significance	14	104951817	104951817	Human		name
156308730	CV2341675	single nucleotide variant	NM_138420.4(AHNAK2):c.7252G>C (p.Gly2418Arg)	not specified [RCV004182597]	uncertain significance	14	104948199	104948199	Human		name
156364329	CV2341948	single nucleotide variant	NM_138420.4(AHNAK2):c.4957G>A (p.Ala1653Thr)	not specified [RCV004184892]	uncertain significance	14	104950494	104950494	Human		name
156336893	CV2342971	single nucleotide variant	NM_138420.4(AHNAK2):c.7732G>A (p.Glu2578Lys)	not specified [RCV004192576]	likely benign	14	104947719	104947719	Human		name
156083555	CV2343047	single nucleotide variant	NM_138420.4(AHNAK2):c.9371G>A (p.Arg3124Gln)	not specified [RCV004192645]	likely benign	14	104946080	104946080	Human		name
156057998	CV2343592	single nucleotide variant	NM_138420.4(AHNAK2):c.8519A>C (p.Glu2840Ala)	not specified [RCV004190624]	likely benign	14	104946932	104946932	Human		name
156274368	CV2344227	single nucleotide variant	NM_138420.4(AHNAK2):c.6516C>G (p.Ile2172Met)	not specified [RCV004197864]	uncertain significance	14	104948935	104948935	Human		name
156054620	CV2344647	single nucleotide variant	NM_138420.4(AHNAK2):c.5335G>A (p.Ala1779Thr)	not specified [RCV004197415]	uncertain significance	14	104950116	104950116	Human		name
156219549	CV2344906	single nucleotide variant	NM_138420.4(AHNAK2):c.7327G>C (p.Glu2443Gln)	not specified [RCV004191041]	uncertain significance	14	104948124	104948124	Human		name
156165997	CV2345130	single nucleotide variant	NM_138420.4(AHNAK2):c.7324G>A (p.Val2442Met)	not specified [RCV004195872]	uncertain significance	14	104948127	104948127	Human		name
156185909	CV2346554	single nucleotide variant	NM_138420.4(AHNAK2):c.5608G>C (p.Asp1870His)	not specified [RCV004206469]	uncertain significance	14	104949843	104949843	Human		name
155928230	CV2346555	single nucleotide variant	NM_138420.4(AHNAK2):c.7886G>A (p.Arg2629Gln)	not specified [RCV004206470]	uncertain significance	14	104947565	104947565	Human		name
156243523	CV2347083	single nucleotide variant	NM_138420.4(AHNAK2):c.4820G>T (p.Gly1607Val)	not specified [RCV004204566]	uncertain significance	14	104950631	104950631	Human		name
156064951	CV2348692	single nucleotide variant	NM_138420.4(AHNAK2):c.7424A>C (p.Asp2475Ala)	not specified [RCV004201106]	uncertain significance	14	104948027	104948027	Human		name
156230587	CV2348693	single nucleotide variant	NM_138420.4(AHNAK2):c.7425T>G (p.Asp2475Glu)	not specified [RCV004201107]	uncertain significance	14	104948026	104948026	Human		name
156284782	CV2349045	single nucleotide variant	NM_138420.4(AHNAK2):c.5165T>A (p.Val1722Glu)	not specified [RCV004205486]	uncertain significance	14	104950286	104950286	Human		name
156116546	CV2349391	single nucleotide variant	NM_138420.4(AHNAK2):c.4186C>G (p.Leu1396Val)	not specified [RCV004199321]	uncertain significance	14	104951265	104951265	Human		name
156125525	CV2350204	single nucleotide variant	NM_138420.4(AHNAK2):c.3094C>G (p.Leu1032Val)	not provided [RCV003427654]\|not specified [RCV004200116]	benign\|likely benign	14	104952357	104952357	Human		name
156240556	CV2350350	single nucleotide variant	NM_138420.4(AHNAK2):c.7171G>A (p.Val2391Met)	not specified [RCV004202296]	likely benign	14	104948280	104948280	Human		name
156127835	CV2351274	single nucleotide variant	NM_138420.4(AHNAK2):c.5587C>A (p.Gln1863Lys)	not provided [RCV003396863]\|not specified [RCV004214120]	likely benign\|uncertain significance	14	104949864	104949864	Human		name
155982289	CV2351557	single nucleotide variant	NM_138420.4(AHNAK2):c.4546G>C (p.Val1516Leu)	not specified [RCV004195280]	uncertain significance	14	104950905	104950905	Human		name
156339249	CV2351558	single nucleotide variant	NM_138420.4(AHNAK2):c.5579C>T (p.Pro1860Leu)	not specified [RCV004195281]	uncertain significance	14	104949872	104949872	Human		name
156100937	CV2351680	single nucleotide variant	NM_138420.4(AHNAK2):c.8465C>T (p.Ser2822Leu)	not specified [RCV004195389]	uncertain significance	14	104946986	104946986	Human		name
155987473	CV2354920	single nucleotide variant	NM_138420.4(AHNAK2):c.7260G>T (p.Gln2420His)	not specified [RCV004191415]	uncertain significance	14	104948191	104948191	Human		name
155987628	CV2354949	single nucleotide variant	NM_138420.4(AHNAK2):c.7624G>A (p.Val2542Ile)	not specified [RCV004198350]	uncertain significance	14	104947827	104947827	Human		name
156239901	CV2356387	single nucleotide variant	NM_138420.4(AHNAK2):c.8654A>C (p.His2885Pro)	not specified [RCV004206190]	uncertain significance	14	104946797	104946797	Human		name
155905862	CV2357198	single nucleotide variant	NM_138420.4(AHNAK2):c.7699C>A (p.Pro2567Thr)	not specified [RCV004206982]	uncertain significance	14	104947752	104947752	Human		name
156196788	CV2357484	single nucleotide variant	NM_138420.4(AHNAK2):c.5686G>T (p.Val1896Leu)	not provided [RCV003396860]\|not specified [RCV004202770]	likely benign	14	104949765	104949765	Human		name
156004987	CV2357616	single nucleotide variant	NM_138420.4(AHNAK2):c.5024A>G (p.Lys1675Arg)	not specified [RCV004202878]	uncertain significance	14	104950427	104950427	Human		name
155925287	CV2358301	single nucleotide variant	NM_138420.4(AHNAK2):c.8105C>T (p.Ser2702Phe)	not specified [RCV004212084]	uncertain significance	14	104947346	104947346	Human		name
156011787	CV2358784	single nucleotide variant	NM_138420.4(AHNAK2):c.7388C>G (p.Ala2463Gly)	not specified [RCV004212137]	uncertain significance	14	104948063	104948063	Human		name
156386033	CV2364635	single nucleotide variant	NM_138420.4(AHNAK2):c.7598T>G (p.Ile2533Ser)	not specified [RCV004219526]	uncertain significance	14	104947853	104947853	Human		name
156098995	CV2367334	single nucleotide variant	NM_138420.4(AHNAK2):c.5987C>T (p.Pro1996Leu)	not specified [RCV004209242]	uncertain significance	14	104949464	104949464	Human		name
156050220	CV2367461	single nucleotide variant	NM_138420.4(AHNAK2):c.4510G>A (p.Gly1504Arg)	not provided [RCV003396871]\|not specified [RCV004211402]	likely benign\|uncertain significance	14	104950941	104950941	Human		name
155984007	CV2367851	single nucleotide variant	NM_138420.4(AHNAK2):c.7919G>A (p.Gly2640Asp)	not specified [RCV004222959]	likely benign	14	104947532	104947532	Human		name
156154326	CV2369495	single nucleotide variant	NM_138420.4(AHNAK2):c.7261A>C (p.Ile2421Leu)	not specified [RCV004210432]	uncertain significance	14	104948190	104948190	Human		name
156308395	CV2369917	single nucleotide variant	NM_138420.4(AHNAK2):c.3551C>A (p.Ala1184Asp)	not specified [RCV004208385]	uncertain significance	14	104951900	104951900	Human		name
156049221	CV2370761	single nucleotide variant	NM_138420.4(AHNAK2):c.5281A>C (p.Met1761Leu)	not specified [RCV004209159]	uncertain significance	14	104950170	104950170	Human		name
155999256	CV2373396	single nucleotide variant	NM_138420.4(AHNAK2):c.6779G>T (p.Gly2260Val)	not specified [RCV004220098]	uncertain significance	14	104948672	104948672	Human		name
156153432	CV2374846	single nucleotide variant	NM_138420.4(AHNAK2):c.5549C>T (p.Ala1850Val)	not specified [RCV004227878]	likely benign	14	104949902	104949902	Human		name
156033065	CV2376556	single nucleotide variant	NM_138420.4(AHNAK2):c.8518G>A (p.Glu2840Lys)	not specified [RCV004220720]	uncertain significance	14	104946933	104946933	Human		name
155999895	CV2378640	single nucleotide variant	NM_138420.4(AHNAK2):c.3040G>A (p.Gly1014Arg)	not specified [RCV004231113]	uncertain significance	14	104952411	104952411	Human		name
156001701	CV2378844	single nucleotide variant	NM_138420.4(AHNAK2):c.3326A>C (p.Asp1109Ala)	not specified [RCV004231286]	uncertain significance	14	104952125	104952125	Human		name
155992194	CV2379287	single nucleotide variant	NM_138420.4(AHNAK2):c.3556G>C (p.Val1186Leu)	not specified [RCV004223756]	uncertain significance	14	104951895	104951895	Human		name
156070651	CV2381329	single nucleotide variant	NM_138420.4(AHNAK2):c.7623G>T (p.Glu2541Asp)	not specified [RCV004227388]	uncertain significance	14	104947828	104947828	Human		name
156347987	CV2383023	single nucleotide variant	NM_138420.4(AHNAK2):c.6011G>A (p.Gly2004Glu)	not specified [RCV004217606]	uncertain significance	14	104949440	104949440	Human		name
155903821	CV2386625	single nucleotide variant	NM_138420.4(AHNAK2):c.3940C>G (p.Leu1314Val)	not specified [RCV004230967]	uncertain significance	14	104951511	104951511	Human		name
156392714	CV2386626	single nucleotide variant	NM_138420.4(AHNAK2):c.8636T>G (p.Val2879Gly)	not specified [RCV004230968]	uncertain significance	14	104946815	104946815	Human		name
156227148	CV2388163	single nucleotide variant	NM_138420.4(AHNAK2):c.6184C>T (p.Pro2062Ser)	not specified [RCV004234626]	uncertain significance	14	104949267	104949267	Human		name
156162901	CV2389508	single nucleotide variant	NM_138420.4(AHNAK2):c.8230G>A (p.Val2744Met)	not specified [RCV004243586]	uncertain significance	14	104947221	104947221	Human		name
156225685	CV2390658	single nucleotide variant	NM_138420.4(AHNAK2):c.8501C>A (p.Ala2834Asp)	not specified [RCV004239177]	uncertain significance	14	104946950	104946950	Human		name
156220940	CV2392342	single nucleotide variant	NM_138420.4(AHNAK2):c.7055T>G (p.Val2352Gly)	not specified [RCV004243939]	uncertain significance	14	104948396	104948396	Human		name
155998341	CV2393416	single nucleotide variant	NM_138420.4(AHNAK2):c.9230A>G (p.Lys3077Arg)	not specified [RCV004228914]	uncertain significance	14	104946221	104946221	Human		name
156006829	CV2394253	single nucleotide variant	NM_138420.4(AHNAK2):c.5527G>A (p.Glu1843Lys)	not specified [RCV004238487]	uncertain significance	14	104949924	104949924	Human		name
156153660	CV2395001	single nucleotide variant	NM_138420.4(AHNAK2):c.8496C>G (p.Ile2832Met)	not specified [RCV004236694]	uncertain significance	14	104946955	104946955	Human		name
156186527	CV2397689	single nucleotide variant	NM_138420.4(AHNAK2):c.7799C>T (p.Ala2600Val)	not specified [RCV004237132]	uncertain significance	14	104947652	104947652	Human		name
156006157	CV2401168	single nucleotide variant	NM_138420.4(AHNAK2):c.5633C>T (p.Ala1878Val)	not specified [RCV004245726]	uncertain significance	14	104949818	104949818	Human		name
329382688	CV2424523	single nucleotide variant	NM_138420.4(AHNAK2):c.5376C>A (p.Asp1792Glu)	not specified [RCV004252407]	uncertain significance	14	104950075	104950075	Human		name
329358740	CV2425355	single nucleotide variant	NM_138420.4(AHNAK2):c.3464A>C (p.Asp1155Ala)	not specified [RCV004251016]	uncertain significance	14	104951987	104951987	Human	2	name
329358740	CV2425355	single nucleotide variant	NM_138420.4(AHNAK2):c.3464A>C (p.Asp1155Ala)	not specified [RCV004251016]	uncertain significance	14	104951987	104951988	Human	2	name
329358742	CV2425356	single nucleotide variant	NM_138420.4(AHNAK2):c.4894A>G (p.Arg1632Gly)	not specified [RCV004251017]	likely benign	14	104950557	104950557	Human		name
329358744	CV2425357	single nucleotide variant	NM_138420.4(AHNAK2):c.4909G>A (p.Gly1637Ser)	not specified [RCV004251018]	uncertain significance	14	104950542	104950542	Human		name
329368490	CV2428038	single nucleotide variant	NM_138420.4(AHNAK2):c.3465T>G (p.Asp1155Glu)	not specified [RCV004254416]	likely benign	14	104951986	104951986	Human		name
329375248	CV2431432	single nucleotide variant	NM_138420.4(AHNAK2):c.3166A>G (p.Lys1056Glu)	not specified [RCV004254597]	likely benign	14	104952285	104952285	Human		name
329373706	CV2434194	single nucleotide variant	NM_138420.4(AHNAK2):c.5842G>C (p.Glu1948Gln)	not specified [RCV004250084]	uncertain significance	14	104949609	104949609	Human		name
329383863	CV2434898	single nucleotide variant	NM_138420.4(AHNAK2):c.4762A>G (p.Lys1588Glu)	not specified [RCV004250772]	uncertain significance	14	104950689	104950689	Human		name
329384532	CV2435100	single nucleotide variant	NM_138420.4(AHNAK2):c.7834T>C (p.Ser2612Pro)	not specified [RCV004252745]	likely benign	14	104947617	104947617	Human		name
329359208	CV2435343	single nucleotide variant	NM_138420.4(AHNAK2):c.8695G>C (p.Val2899Leu)	not provided [RCV003396941]\|not specified [RCV004253002]	likely benign\|uncertain significance	14	104946756	104946756	Human		name
329399242	CV2436461	single nucleotide variant	NM_138420.4(AHNAK2):c.6175G>T (p.Gly2059Cys)	not specified [RCV004251841]	uncertain significance	14	104949276	104949276	Human		name
329390639	CV2437153	single nucleotide variant	NM_138420.4(AHNAK2):c.6002C>T (p.Ser2001Leu)	not specified [RCV004262958]	uncertain significance	14	104949449	104949449	Human		name
329388476	CV2437447	single nucleotide variant	NM_138420.4(AHNAK2):c.8120T>G (p.Val2707Gly)	not specified [RCV004256312]	uncertain significance	14	104947331	104947331	Human		name
329392364	CV2438899	single nucleotide variant	NM_138420.4(AHNAK2):c.6755A>G (p.Lys2252Arg)	not specified [RCV004264428]	uncertain significance	14	104948696	104948696	Human		name
329372206	CV2443057	single nucleotide variant	NM_138420.4(AHNAK2):c.4544C>T (p.Ser1515Leu)	not provided [RCV003396943]\|not specified [RCV004253645]	likely benign\|uncertain significance	14	104950907	104950907	Human		name
329360551	CV2443617	single nucleotide variant	NM_138420.4(AHNAK2):c.9865C>T (p.Arg3289Trp)	not specified [RCV004262438]	uncertain significance	14	104945586	104945586	Human		name
329375061	CV2444854	single nucleotide variant	NM_138420.4(AHNAK2):c.9526G>A (p.Asp3176Asn)	not specified [RCV004259092]	uncertain significance	14	104945925	104945925	Human		name
329389372	CV2444994	single nucleotide variant	NM_138420.4(AHNAK2):c.3583G>A (p.Ala1195Thr)	not specified [RCV004261612]	uncertain significance	14	104951868	104951868	Human		name
329378679	CV2447078	single nucleotide variant	NM_138420.4(AHNAK2):c.4642G>T (p.Ala1548Ser)	not specified [RCV004259953]	uncertain significance	14	104950809	104950809	Human		name
329354372	CV2448061	single nucleotide variant	NM_138420.4(AHNAK2):c.4892C>T (p.Pro1631Leu)	not specified [RCV004263287]	uncertain significance	14	104950559	104950559	Human		name
329400844	CV2449757	single nucleotide variant	NM_138420.4(AHNAK2):c.7034C>T (p.Ala2345Val)	not specified [RCV004270436]	likely benign	14	104948417	104948417	Human		name
329368730	CV2450363	single nucleotide variant	NM_138420.4(AHNAK2):c.6488T>G (p.Phe2163Cys)	not specified [RCV004271437]	uncertain significance	14	104948963	104948963	Human		name
329385225	CV2451103	single nucleotide variant	NM_138420.4(AHNAK2):c.5294G>A (p.Gly1765Asp)	not specified [RCV004270043]	uncertain significance	14	104950157	104950157	Human		name
329386550	CV2456086	single nucleotide variant	NM_138420.4(AHNAK2):c.3434T>G (p.Leu1145Arg)	not specified [RCV004272980]	uncertain significance	14	104952017	104952017	Human		name
329367356	CV2456768	single nucleotide variant	NM_138420.4(AHNAK2):c.5315G>T (p.Gly1772Val)	not specified [RCV004270744]	uncertain significance	14	104950136	104950136	Human		name
329401653	CV2457274	single nucleotide variant	NM_138420.4(AHNAK2):c.3169G>C (p.Val1057Leu)	not specified [RCV004267126]	uncertain significance	14	104952282	104952282	Human		name
329362107	CV2466010	single nucleotide variant	NM_138420.4(AHNAK2):c.8576C>T (p.Thr2859Ile)	not specified [RCV004277910]	uncertain significance	14	104946875	104946875	Human		name
329380229	CV2466491	single nucleotide variant	NM_138420.4(AHNAK2):c.7717A>C (p.Ser2573Arg)	not specified [RCV004274039]	uncertain significance	14	104947734	104947734	Human		name
329387907	CV2468466	single nucleotide variant	NM_138420.4(AHNAK2):c.9877G>T (p.Asp3293Tyr)	not specified [RCV004278050]	uncertain significance	14	104945574	104945574	Human		name
329399273	CV2470020	single nucleotide variant	NM_138420.4(AHNAK2):c.4339G>T (p.Val1447Leu)	not specified [RCV004287295]	uncertain significance	14	104951112	104951112	Human		name
329392050	CV2470326	single nucleotide variant	NM_138420.4(AHNAK2):c.6910A>G (p.Met2304Val)	not specified [RCV004279718]	uncertain significance	14	104948541	104948541	Human		name
401720375	CV2673301	single nucleotide variant	NM_138420.4(AHNAK2):c.7603C>T (p.Pro2535Ser)	not specified [RCV004288289]	uncertain significance	14	104947848	104947848	Human		name
401780207	CV2673918	single nucleotide variant	NM_138420.4(AHNAK2):c.9955A>G (p.Arg3319Gly)	not specified [RCV004293292]	likely benign	14	104945496	104945496	Human		name
401780242	CV2673933	single nucleotide variant	NM_138420.4(AHNAK2):c.6965A>G (p.Lys2322Arg)	not specified [RCV004293307]	uncertain significance	14	104948486	104948486	Human		name
401720044	CV2675757	single nucleotide variant	NM_138420.4(AHNAK2):c.7667T>A (p.Val2556Glu)	not specified [RCV004288001]	uncertain significance	14	104947784	104947784	Human		name
401728209	CV2676010	single nucleotide variant	NM_138420.4(AHNAK2):c.8656G>A (p.Val2886Ile)	not specified [RCV004282000]	uncertain significance	14	104946795	104946795	Human		name
401719114	CV2679420	single nucleotide variant	NM_138420.4(AHNAK2):c.3259C>G (p.Pro1087Ala)	not provided [RCV003427712]\|not specified [RCV004285947]	likely benign\|uncertain significance	14	104952192	104952192	Human		name
401766133	CV2679579	single nucleotide variant	NM_138420.4(AHNAK2):c.7109C>T (p.Pro2370Leu)	not specified [RCV004282063]	likely benign	14	104948342	104948342	Human		name
401721953	CV2680754	single nucleotide variant	NM_138420.4(AHNAK2):c.8002G>C (p.Glu2668Gln)	not specified [RCV004293407]	uncertain significance	14	104947449	104947449	Human		name
401781550	CV2682036	single nucleotide variant	NM_138420.4(AHNAK2):c.4390G>C (p.Glu1464Gln)	not specified [RCV004290103]	likely benign	14	104951061	104951061	Human		name
401754205	CV2685195	single nucleotide variant	NM_138420.4(AHNAK2):c.4646A>G (p.Asp1549Gly)	not specified [RCV004289754]	uncertain significance	14	104950805	104950805	Human		name
401770876	CV2686058	single nucleotide variant	NM_138420.4(AHNAK2):c.7993G>A (p.Glu2665Lys)	not specified [RCV004297071]	likely benign	14	104947458	104947458	Human		name
401727037	CV2692130	single nucleotide variant	NM_138420.4(AHNAK2):c.7577T>A (p.Leu2526His)	not specified [RCV004301834]	uncertain significance	14	104947874	104947874	Human		name
401769189	CV2693496	single nucleotide variant	NM_138420.4(AHNAK2):c.9777G>T (p.Lys3259Asn)	not specified [RCV004295438]	uncertain significance	14	104945674	104945674	Human		name
401759349	CV2701506	single nucleotide variant	NM_138420.4(AHNAK2):c.9866G>C (p.Arg3289Pro)	not specified [RCV004313957]	uncertain significance	14	104945585	104945585	Human		name
401717766	CV2704008	single nucleotide variant	NM_138420.4(AHNAK2):c.6016T>A (p.Ser2006Thr)	not specified [RCV004308900]	uncertain significance	14	104949435	104949435	Human		name
401722281	CV2706451	single nucleotide variant	NM_138420.4(AHNAK2):c.7921G>A (p.Val2641Met)	not specified [RCV004317271]	uncertain significance	14	104947530	104947530	Human		name
401757838	CV2707989	single nucleotide variant	NM_138420.4(AHNAK2):c.5593G>T (p.Asp1865Tyr)	not specified [RCV004309241]	uncertain significance	14	104949858	104949858	Human		name
401738897	CV2708207	single nucleotide variant	NM_138420.4(AHNAK2):c.9943A>G (p.Met3315Val)	not specified [RCV004311564]	uncertain significance	14	104945508	104945508	Human		name
401732680	CV2708935	single nucleotide variant	NM_138420.4(AHNAK2):c.6877G>A (p.Ala2293Thr)	not specified [RCV004309903]	uncertain significance	14	104948574	104948574	Human		name
401762842	CV2710341	single nucleotide variant	NM_138420.4(AHNAK2):c.5842G>A (p.Glu1948Lys)	not specified [RCV004317512]	uncertain significance	14	104949609	104949609	Human		name
401749611	CV2710839	single nucleotide variant	NM_138420.4(AHNAK2):c.5008G>C (p.Val1670Leu)	not specified [RCV004308760]	uncertain significance	14	104950443	104950443	Human		name
401775113	CV2713781	single nucleotide variant	NM_138420.4(AHNAK2):c.4042G>A (p.Glu1348Lys)	not provided [RCV003396981]\|not specified [RCV004321125]	likely benign\|uncertain significance	14	104951409	104951409	Human		name
401761742	CV2713872	single nucleotide variant	NM_138420.4(AHNAK2):c.3256A>T (p.Met1086Leu)	not specified [RCV004315311]	uncertain significance	14	104952195	104952195	Human		name
401752040	CV2713916	single nucleotide variant	NM_138420.4(AHNAK2):c.6205G>T (p.Gly2069Trp)	not specified [RCV004315345]	uncertain significance	14	104949246	104949246	Human		name
401742798	CV2715321	single nucleotide variant	NM_138420.4(AHNAK2):c.3134A>G (p.Asp1045Gly)	not specified [RCV004324657]	uncertain significance	14	104952317	104952317	Human		name
401783254	CV2716210	single nucleotide variant	NM_138420.4(AHNAK2):c.5735C>G (p.Pro1912Arg)	not specified [RCV004323436]	uncertain significance	14	104949716	104949716	Human		name
401780549	CV2716830	single nucleotide variant	NM_138420.4(AHNAK2):c.6908A>T (p.Asp2303Val)	not specified [RCV004329643]	uncertain significance	14	104948543	104948543	Human		name
401784337	CV2721283	single nucleotide variant	NM_138420.4(AHNAK2):c.8957C>T (p.Pro2986Leu)	not specified [RCV004330188]	uncertain significance	14	104946494	104946494	Human		name
401769589	CV2731441	single nucleotide variant	NM_138420.4(AHNAK2):c.5276C>T (p.Pro1759Leu)	not specified [RCV004330799]	uncertain significance	14	104950175	104950175	Human		name
401729678	CV2733237	single nucleotide variant	NM_138420.4(AHNAK2):c.7975A>G (p.Arg2659Gly)	not provided [RCV003396987]\|not specified [RCV004332153]	likely benign	14	104947476	104947476	Human		name
401768439	CV2735306	single nucleotide variant	NM_138420.4(AHNAK2):c.8482C>G (p.Pro2828Ala)	not specified [RCV004333972]	uncertain significance	14	104946969	104946969	Human		name
401878652	CV2754763	single nucleotide variant	NM_138420.4(AHNAK2):c.3344C>T (p.Ala1115Val)	not provided [RCV003427743]\|not specified [RCV004341247]	benign\|likely benign	14	104952107	104952107	Human		name
401879722	CV2755244	single nucleotide variant	NM_138420.4(AHNAK2):c.4201G>C (p.Val1401Leu)	not specified [RCV004337427]	likely benign	14	104951250	104951250	Human		name
401861278	CV2755517	single nucleotide variant	NM_138420.4(AHNAK2):c.5599A>C (p.Lys1867Gln)	not specified [RCV004340101]	uncertain significance	14	104949852	104949852	Human		name
401857703	CV2756302	single nucleotide variant	NM_138420.4(AHNAK2):c.4257C>G (p.Phe1419Leu)	not specified [RCV004340437]	likely benign	14	104951194	104951194	Human		name
401870896	CV2756503	single nucleotide variant	NM_138420.4(AHNAK2):c.5545T>C (p.Ser1849Pro)	not specified [RCV004345036]	uncertain significance	14	104949906	104949906	Human		name
401855327	CV2757237	single nucleotide variant	NM_138420.4(AHNAK2):c.4882G>A (p.Val1628Ile)	not specified [RCV004338831]	likely benign	14	104950569	104950569	Human		name
401865175	CV2757598	single nucleotide variant	NM_138420.4(AHNAK2):c.6482C>T (p.Pro2161Leu)	not specified [RCV004340965]	uncertain significance	14	104948969	104948969	Human		name
401888589	CV2757805	single nucleotide variant	NM_138420.4(AHNAK2):c.3210C>G (p.His1070Gln)	not specified [RCV004336952]	uncertain significance	14	104952241	104952241	Human		name
401889750	CV2758432	single nucleotide variant	NM_138420.4(AHNAK2):c.9304G>A (p.Val3102Met)	not specified [RCV004335086]	uncertain significance	14	104946147	104946147	Human		name
401864203	CV2760809	single nucleotide variant	NM_138420.4(AHNAK2):c.3865G>A (p.Val1289Met)	not provided [RCV003883981]\|not specified [RCV004336449]	likely benign\|uncertain significance	14	104951586	104951586	Human		name
401890007	CV2762102	single nucleotide variant	NM_138420.4(AHNAK2):c.3628G>C (p.Asp1210His)	not specified [RCV004341918]	uncertain significance	14	104951823	104951823	Human		name
401856126	CV2764383	single nucleotide variant	NM_138420.4(AHNAK2):c.4579G>C (p.Val1527Leu)	not specified [RCV004338955]	uncertain significance	14	104950872	104950872	Human		name
401893612	CV2765371	single nucleotide variant	NM_138420.4(AHNAK2):c.3466G>A (p.Val1156Met)	not specified [RCV004339874]	likely benign	14	104951985	104951985	Human		name
401863217	CV2765597	single nucleotide variant	NM_138420.4(AHNAK2):c.5606C>T (p.Thr1869Met)	not specified [RCV004335611]	uncertain significance	14	104949845	104949845	Human		name
401863380	CV2765679	single nucleotide variant	NM_138420.4(AHNAK2):c.5377G>A (p.Val1793Ile)	not specified [RCV004335688]	likely benign	14	104950074	104950074	Human		name
401870402	CV2765944	single nucleotide variant	NM_138420.4(AHNAK2):c.5122A>G (p.Ile1708Val)	not specified [RCV004337969]	uncertain significance	14	104950329	104950329	Human		name
401884999	CV2766398	single nucleotide variant	NM_138420.4(AHNAK2):c.7597A>G (p.Ile2533Val)	not specified [RCV004342640]	uncertain significance	14	104947854	104947854	Human		name
401862037	CV2766563	single nucleotide variant	NM_138420.4(AHNAK2):c.6440C>G (p.Thr2147Ser)	not specified [RCV004347181]	uncertain significance	14	104949011	104949011	Human		name
401862110	CV2766604	single nucleotide variant	NM_138420.4(AHNAK2):c.8065G>A (p.Gly2689Arg)	not specified [RCV004347219]	uncertain significance	14	104947386	104947386	Human		name
401868664	CV2767303	single nucleotide variant	NM_138420.4(AHNAK2):c.6586C>T (p.Leu2196Phe)	not specified [RCV004349471]	uncertain significance	14	104948865	104948865	Human		name
401863634	CV2770767	single nucleotide variant	NM_138420.4(AHNAK2):c.4169G>A (p.Gly1390Asp)	not specified [RCV004349806]	uncertain significance	14	104951282	104951282	Human		name
401863635	CV2770768	single nucleotide variant	NM_138420.4(AHNAK2):c.4243C>G (p.Gln1415Glu)	not specified [RCV004349807]	uncertain significance	14	104951208	104951208	Human		name
401863669	CV2770788	single nucleotide variant	NM_138420.4(AHNAK2):c.7506C>G (p.Ile2502Met)	not specified [RCV004349824]	uncertain significance	14	104947945	104947945	Human		name
401863856	CV2770869	single nucleotide variant	NM_138420.4(AHNAK2):c.6640G>A (p.Ala2214Thr)	not specified [RCV004343545]	uncertain significance	14	104948811	104948811	Human		name
401863201	CV2776822	single nucleotide variant	NM_138420.4(AHNAK2):c.6748G>T (p.Asp2250Tyr)	not specified [RCV004357965]	uncertain significance	14	104948703	104948703	Human		name
401879474	CV2785136	single nucleotide variant	NM_138420.4(AHNAK2):c.9242T>C (p.Ile3081Thr)	not specified [RCV004355139]	uncertain significance	14	104946209	104946209	Human		name
401877943	CV2786874	single nucleotide variant	NM_138420.4(AHNAK2):c.4375G>A (p.Val1459Met)	not specified [RCV004366026]	likely benign	14	104951076	104951076	Human		name
401875519	CV2789075	single nucleotide variant	NM_138420.4(AHNAK2):c.9047C>T (p.Ser3016Phe)	not specified [RCV004363368]	uncertain significance	14	104946404	104946404	Human		name
401875931	CV2789213	single nucleotide variant	NM_138420.4(AHNAK2):c.8978C>T (p.Pro2993Leu)	not specified [RCV004365251]	uncertain significance	14	104946473	104946473	Human		name
401898189	CV2790930	single nucleotide variant	NM_138420.4(AHNAK2):c.7925C>G (p.Thr2642Arg)	not specified [RCV004354566]	uncertain significance	14	104947526	104947526	Human		name
401870401	CV2792363	single nucleotide variant	NM_138420.4(AHNAK2):c.6601C>A (p.Leu2201Ile)	not specified [RCV004361531]	uncertain significance	14	104948850	104948850	Human		name
401872525	CV2793110	single nucleotide variant	NM_138420.4(AHNAK2):c.6304G>C (p.Asp2102His)	not specified [RCV004360425]	uncertain significance	14	104949147	104949147	Human		name
401934195	CV2807398	single nucleotide variant	NM_138420.4(AHNAK2):c.9925A>G (p.Lys3309Glu)	not provided [RCV003411082]	benign	14	104945526	104945526	Human		name
401915724	CV2807399	single nucleotide variant	NM_138420.4(AHNAK2):c.9799G>A (p.Val3267Met)	not provided [RCV003400713]	likely benign	14	104945652	104945652	Human		name
401915729	CV2807401	single nucleotide variant	NM_138420.4(AHNAK2):c.9742A>G (p.Ile3248Val)	not provided [RCV003400715]\|not specified [RCV004917843]	likely benign	14	104945709	104945709	Human		name
401934197	CV2807403	single nucleotide variant	NM_138420.4(AHNAK2):c.9649C>A (p.Leu3217Ile)	not provided [RCV003411084]	likely benign	14	104945802	104945802	Human		name
401915733	CV2807407	single nucleotide variant	NM_138420.4(AHNAK2):c.9322G>A (p.Gly3108Ser)	not provided [RCV003400717]\|not specified [RCV004364519]	benign\|likely benign	14	104946129	104946129	Human		name
401915735	CV2807408	single nucleotide variant	NM_138420.4(AHNAK2):c.9151G>A (p.Val3051Ile)	not provided [RCV003400718]	likely benign	14	104946300	104946300	Human		name
401915739	CV2807410	single nucleotide variant	NM_138420.4(AHNAK2):c.8999C>T (p.Ser3000Leu)	not provided [RCV003400719]	benign\|likely benign	14	104946452	104946452	Human		name
401915751	CV2807417	single nucleotide variant	NM_138420.4(AHNAK2):c.8501C>T (p.Ala2834Val)	not provided [RCV003400725]	benign	14	104946950	104946950	Human		name
401915762	CV2807421	single nucleotide variant	NM_138420.4(AHNAK2):c.8416A>G (p.Met2806Val)	not provided [RCV003400729]	likely benign	14	104947035	104947035	Human		name
401915771	CV2807426	single nucleotide variant	NM_138420.4(AHNAK2):c.8129G>A (p.Gly2710Asp)	not provided [RCV003400732]	likely benign	14	104947322	104947322	Human		name
401915772	CV2807428	single nucleotide variant	NM_138420.4(AHNAK2):c.8009T>C (p.Leu2670Ser)	not provided [RCV003400733]	benign	14	104947442	104947442	Human		name
401915782	CV2807433	single nucleotide variant	NM_138420.4(AHNAK2):c.7803A>C (p.Glu2601Asp)	not provided [RCV003400737]	likely benign	14	104947648	104947648	Human		name
401915784	CV2807434	single nucleotide variant	NM_138420.4(AHNAK2):c.7798G>A (p.Ala2600Thr)	not provided [RCV003400738]	likely benign	14	104947653	104947653	Human		name
401915787	CV2807435	single nucleotide variant	NM_138420.4(AHNAK2):c.7756C>A (p.Leu2586Ile)	not provided [RCV003400739]	benign\|likely benign	14	104947695	104947695	Human		name
401915790	CV2807436	single nucleotide variant	NM_138420.4(AHNAK2):c.7735A>G (p.Met2579Val)	not provided [RCV003400740]	benign\|likely benign	14	104947716	104947716	Human		name
401915799	CV2807440	single nucleotide variant	NM_138420.4(AHNAK2):c.7582G>A (p.Ala2528Thr)	not provided [RCV003400744]	likely benign	14	104947869	104947869	Human		name
401915813	CV2807450	single nucleotide variant	NM_138420.4(AHNAK2):c.6757G>C (p.Gly2253Arg)	not provided [RCV003400751]	likely benign	14	104948694	104948694	Human		name
401915814	CV2807451	single nucleotide variant	NM_138420.4(AHNAK2):c.6674C>A (p.Pro2225His)	not provided [RCV003400752]	benign	14	104948777	104948777	Human		name
401915819	CV2807453	single nucleotide variant	NM_138420.4(AHNAK2):c.6628G>A (p.Val2210Met)	not provided [RCV003400754]	benign	14	104948823	104948823	Human		name
401915825	CV2807459	single nucleotide variant	NM_138420.4(AHNAK2):c.6402T>G (p.His2134Gln)	not provided [RCV003400757]	likely benign	14	104949049	104949049	Human		name
401915833	CV2807462	single nucleotide variant	NM_138420.4(AHNAK2):c.6379A>G (p.Arg2127Gly)	not provided [RCV003400760]	benign	14	104949072	104949072	Human		name
401915841	CV2807466	single nucleotide variant	NM_138420.4(AHNAK2):c.6179A>C (p.His2060Pro)	not provided [RCV003400764]	likely benign	14	104949272	104949272	Human		name
401915848	CV2807470	single nucleotide variant	NM_138420.4(AHNAK2):c.6136A>G (p.Lys2046Glu)	not provided [RCV003400766]	benign	14	104949315	104949315	Human		name
401915851	CV2807471	single nucleotide variant	NM_138420.4(AHNAK2):c.6127G>A (p.Ala2043Thr)	not provided [RCV003400767]	likely benign	14	104949324	104949324	Human		name
401915853	CV2807472	single nucleotide variant	NM_138420.4(AHNAK2):c.6121C>G (p.Pro2041Ala)	not provided [RCV003400768]	likely benign	14	104949330	104949330	Human		name
401915856	CV2807474	single nucleotide variant	NM_138420.4(AHNAK2):c.6064G>C (p.Val2022Leu)	not provided [RCV003400769]	likely benign	14	104949387	104949387	Human		name
401934215	CV2807475	single nucleotide variant	NM_138420.4(AHNAK2):c.6064G>A (p.Val2022Met)	not provided [RCV003411102]	benign	14	104949387	104949387	Human		name
401915859	CV2807476	single nucleotide variant	NM_138420.4(AHNAK2):c.6061G>A (p.Asp2021Asn)	not provided [RCV003400770]	likely benign	14	104949390	104949390	Human		name
401934217	CV2807479	single nucleotide variant	NM_138420.4(AHNAK2):c.6044C>A (p.Ala2015Glu)	not provided [RCV003411104]	benign	14	104949407	104949407	Human		name
401934218	CV2807480	single nucleotide variant	NM_138420.4(AHNAK2):c.6036T>A (p.Asp2012Glu)	not provided [RCV003411105]	likely benign	14	104949415	104949415	Human		name
401934219	CV2807481	single nucleotide variant	NM_138420.4(AHNAK2):c.6029C>T (p.Ser2010Leu)	not provided [RCV003411106]	benign	14	104949422	104949422	Human		name
401915865	CV2807482	single nucleotide variant	NM_138420.4(AHNAK2):c.6022G>A (p.Glu2008Lys)	not provided [RCV003400772]	benign	14	104949429	104949429	Human		name
401915867	CV2807483	single nucleotide variant	NM_138420.4(AHNAK2):c.6014G>A (p.Arg2005Lys)	not provided [RCV003400773]	benign	14	104949437	104949437	Human		name
401915873	CV2807485	single nucleotide variant	NM_138420.4(AHNAK2):c.5940C>G (p.Asp1980Glu)	not provided [RCV003400775]\|not specified [RCV004621787]	benign\|uncertain significance	14	104949511	104949511	Human		name
401915875	CV2807486	single nucleotide variant	NM_138420.4(AHNAK2):c.5939A>C (p.Asp1980Ala)	not provided [RCV003400776]\|not specified [RCV004621788]	benign\|uncertain significance	14	104949512	104949512	Human		name
401915878	CV2807487	single nucleotide variant	NM_138420.4(AHNAK2):c.5932G>A (p.Asp1978Asn)	not provided [RCV003400777]\|not specified [RCV004364520]	likely benign\|uncertain significance	14	104949519	104949519	Human		name
401915886	CV2807491	single nucleotide variant	NM_138420.4(AHNAK2):c.5884A>G (p.Lys1962Glu)	not provided [RCV003400781]	likely benign	14	104949567	104949567	Human		name
401915891	CV2807493	single nucleotide variant	NM_138420.4(AHNAK2):c.5816A>G (p.Lys1939Arg)	not provided [RCV003400783]	likely benign	14	104949635	104949635	Human		name
401934220	CV2807495	single nucleotide variant	NM_138420.4(AHNAK2):c.5730T>G (p.Asp1910Glu)	not provided [RCV003411107]	likely benign	14	104949721	104949721	Human		name
401915894	CV2807496	single nucleotide variant	NM_138420.4(AHNAK2):c.5689C>T (p.Pro1897Ser)	not provided [RCV003400785]	likely benign	14	104949762	104949762	Human		name
401915898	CV2807497	single nucleotide variant	NM_138420.4(AHNAK2):c.5685G>T (p.Gln1895His)	not provided [RCV003400786]	likely benign	14	104949766	104949766	Human		name
401915902	CV2807498	single nucleotide variant	NM_138420.4(AHNAK2):c.5684A>C (p.Gln1895Pro)	not provided [RCV003400787]	likely benign	14	104949767	104949767	Human		name
401915909	CV2807501	single nucleotide variant	NM_138420.4(AHNAK2):c.5665A>G (p.Met1889Val)	not provided [RCV003400790]	likely benign	14	104949786	104949786	Human		name
401915911	CV2807502	single nucleotide variant	NM_138420.4(AHNAK2):c.5614T>A (p.Cys1872Ser)	not provided [RCV003400791]	benign	14	104949837	104949837	Human		name
401934221	CV2807503	single nucleotide variant	NM_138420.4(AHNAK2):c.5611C>A (p.Leu1871Ile)	not provided [RCV003411108]	likely benign	14	104949840	104949840	Human		name
401934222	CV2807505	single nucleotide variant	NM_138420.4(AHNAK2):c.5569G>C (p.Val1857Leu)	not provided [RCV003411109]	likely benign	14	104949882	104949882	Human		name
401934247	CV2807507	single nucleotide variant	NM_138420.4(AHNAK2):c.5527G>C (p.Glu1843Gln)	not provided [RCV003411110]	benign	14	104949924	104949924	Human		name
401934249	CV2807509	single nucleotide variant	NM_138420.4(AHNAK2):c.5499C>A (p.Phe1833Leu)	not provided [RCV003411112]\|not specified [RCV004364521]	likely benign\|uncertain significance	14	104949952	104949952	Human		name
401934250	CV2807511	single nucleotide variant	NM_138420.4(AHNAK2):c.5492C>T (p.Pro1831Leu)	not provided [RCV003411113]	likely benign	14	104949959	104949959	Human		name
401915921	CV2807512	single nucleotide variant	NM_138420.4(AHNAK2):c.5452G>A (p.Ala1818Thr)	not provided [RCV003400795]	benign	14	104949999	104949999	Human		name
401915923	CV2807513	single nucleotide variant	NM_138420.4(AHNAK2):c.5445T>G (p.Asp1815Glu)	not provided [RCV003400796]	benign	14	104950006	104950006	Human		name
401915926	CV2807514	single nucleotide variant	NM_138420.4(AHNAK2):c.5444A>C (p.Asp1815Ala)	not provided [RCV003400797]	benign	14	104950007	104950007	Human		name
401934252	CV2807516	single nucleotide variant	NM_138420.4(AHNAK2):c.5365G>A (p.Val1789Met)	not provided [RCV003411115]	likely benign	14	104950086	104950086	Human		name
401934253	CV2807517	single nucleotide variant	NM_138420.4(AHNAK2):c.5209T>C (p.Phe1737Leu)	not provided [RCV003411116]	likely benign	14	104950242	104950242	Human		name
401934254	CV2807518	single nucleotide variant	NM_138420.4(AHNAK2):c.5197G>A (p.Glu1733Lys)	not provided [RCV003411117]	likely benign	14	104950254	104950254	Human		name
401915929	CV2807520	single nucleotide variant	NM_138420.4(AHNAK2):c.5170G>A (p.Val1724Met)	not provided [RCV003400799]	likely benign	14	104950281	104950281	Human		name
401915932	CV2807521	single nucleotide variant	NM_138420.4(AHNAK2):c.5154G>C (p.Gln1718His)	not provided [RCV003400800]\|not specified [RCV005333600]	likely benign\|uncertain significance	14	104950297	104950297	Human		name
401915934	CV2807523	single nucleotide variant	NM_138420.4(AHNAK2):c.5080C>T (p.Leu1694Phe)	not provided [RCV003400801]	likely benign	14	104950371	104950371	Human		name
401934256	CV2807524	single nucleotide variant	NM_138420.4(AHNAK2):c.5075T>G (p.Val1692Gly)	not provided [RCV003411119]	likely benign	14	104950376	104950376	Human		name
401934257	CV2807525	single nucleotide variant	NM_138420.4(AHNAK2):c.5057C>T (p.Pro1686Leu)	not provided [RCV003411120]	likely benign	14	104950394	104950394	Human		name
401934258	CV2807527	single nucleotide variant	NM_138420.4(AHNAK2):c.5036C>A (p.Ala1679Asp)	not provided [RCV003411121]	likely benign	14	104950415	104950415	Human		name
401934259	CV2807528	single nucleotide variant	NM_138420.4(AHNAK2):c.5009T>C (p.Val1670Ala)	not provided [RCV003411122]	benign	14	104950442	104950442	Human		name
401934260	CV2807529	single nucleotide variant	NM_138420.4(AHNAK2):c.4970A>G (p.Lys1657Arg)	not provided [RCV003411123]\|not specified [RCV004621789]	likely benign\|uncertain significance	14	104950481	104950481	Human		name
401915939	CV2807530	single nucleotide variant	NM_138420.4(AHNAK2):c.4951G>A (p.Val1651Met)	not provided [RCV003400803]	benign	14	104950500	104950500	Human		name
401915943	CV2807532	single nucleotide variant	NM_138420.4(AHNAK2):c.4892C>G (p.Pro1631Arg)	not provided [RCV003400805]\|not specified [RCV004621790]	likely benign\|uncertain significance	14	104950559	104950559	Human		name
401915947	CV2807534	single nucleotide variant	NM_138420.4(AHNAK2):c.4786A>C (p.Ile1596Leu)	not provided [RCV003400807]	likely benign	14	104950665	104950665	Human		name
401934261	CV2807538	single nucleotide variant	NM_138420.4(AHNAK2):c.4699T>C (p.Ser1567Pro)	not provided [RCV003411124]\|not specified [RCV004364522]	likely benign	14	104950752	104950752	Human		name
401915963	CV2807541	single nucleotide variant	NM_138420.4(AHNAK2):c.4589C>T (p.Pro1530Leu)	not provided [RCV003400813]	benign	14	104950862	104950862	Human		name
401934262	CV2807542	single nucleotide variant	NM_138420.4(AHNAK2):c.4547T>C (p.Val1516Ala)	not provided [RCV003411125]	likely benign	14	104950904	104950904	Human		name
401915966	CV2807543	single nucleotide variant	NM_138420.4(AHNAK2):c.4537G>A (p.Glu1513Lys)	not provided [RCV003400814]	likely benign	14	104950914	104950914	Human		name
401915973	CV2807547	single nucleotide variant	NM_138420.4(AHNAK2):c.4485G>T (p.Met1495Ile)	not provided [RCV003400817]	likely benign	14	104950966	104950966	Human		name
401915979	CV2807550	single nucleotide variant	NM_138420.4(AHNAK2):c.4282G>C (p.Gly1428Arg)	not provided [RCV003400819]	likely benign	14	104951169	104951169	Human		name
401915988	CV2807554	single nucleotide variant	NM_138420.4(AHNAK2):c.4049C>T (p.Ser1350Phe)	not provided [RCV003400822]	likely benign	14	104951402	104951402	Human		name
401934267	CV2807559	single nucleotide variant	NM_138420.4(AHNAK2):c.3704A>C (p.His1235Pro)	not provided [RCV003411130]	benign\|likely benign	14	104951747	104951747	Human		name
401934268	CV2807561	single nucleotide variant	NM_138420.4(AHNAK2):c.3598C>T (p.Pro1200Ser)	not provided [RCV003411131]	likely benign	14	104951853	104951853	Human		name
401915999	CV2807562	single nucleotide variant	NM_138420.4(AHNAK2):c.3589G>C (p.Val1197Leu)	not provided [RCV003400827]	likely benign	14	104951862	104951862	Human		name
401916001	CV2807563	single nucleotide variant	NM_138420.4(AHNAK2):c.3557T>C (p.Val1186Ala)	not provided [RCV003400828]	benign\|likely benign	14	104951894	104951894	Human		name
401916007	CV2807566	single nucleotide variant	NM_138420.4(AHNAK2):c.3526T>A (p.Ser1176Thr)	not provided [RCV003400831]	benign	14	104951925	104951925	Human		name
401916011	CV2807568	single nucleotide variant	NM_138420.4(AHNAK2):c.3428C>G (p.Ala1143Gly)	not provided [RCV003400832]\|not specified [RCV004364523]	benign\|uncertain significance	14	104952023	104952023	Human		name
401916013	CV2807570	single nucleotide variant	NM_138420.4(AHNAK2):c.3407C>T (p.Pro1136Leu)	not provided [RCV003400833]	benign	14	104952044	104952044	Human		name
401916016	CV2807571	single nucleotide variant	NM_138420.4(AHNAK2):c.3400G>C (p.Glu1134Gln)	not provided [RCV003400834]	benign	14	104952051	104952051	Human		name
401910384	CV2807573	single nucleotide variant	NM_138420.4(AHNAK2):c.3343G>A (p.Ala1115Thr)	not provided [RCV003425016]	likely benign	14	104952108	104952108	Human		name
401910392	CV2807581	single nucleotide variant	NM_138420.4(AHNAK2):c.3094C>A (p.Leu1032Met)	not provided [RCV003425024]	benign	14	104952357	104952357	Human		name
401943566	CV2840092	single nucleotide variant	NM_138420.4(AHNAK2):c.7471C>A (p.Pro2491Thr)	not provided [RCV003456879]	likely benign	14	104947980	104947980	Human		name
401943568	CV2840093	single nucleotide variant	NM_138420.4(AHNAK2):c.6559A>C (p.Met2187Leu)	not provided [RCV003456880]	likely benign	14	104948892	104948892	Human		name
401943573	CV2840095	single nucleotide variant	NM_138420.4(AHNAK2):c.5305G>T (p.Asp1769Tyr)	not provided [RCV003456882]	likely benign	14	104950146	104950146	Human		name
401943576	CV2840096	single nucleotide variant	NM_138420.4(AHNAK2):c.5209T>A (p.Phe1737Ile)	not provided [RCV003456883]	uncertain significance	14	104950242	104950242	Human		name
405265481	CV3185696	single nucleotide variant	NM_138420.4(AHNAK2):c.6535T>C (p.Ser2179Pro)	not provided [RCV003886260]	benign	14	104948916	104948916	Human		name
405265509	CV3185728	single nucleotide variant	NM_138420.4(AHNAK2):c.7415C>T (p.Ala2472Val)	not provided [RCV003886292]	benign\|likely benign	14	104948036	104948036	Human		name
405260518	CV3185789	single nucleotide variant	NM_138420.4(AHNAK2):c.3920G>A (p.Gly1307Asp)	not provided [RCV003884865]	likely benign	14	104951531	104951531	Human		name
405261061	CV3186039	single nucleotide variant	NM_138420.4(AHNAK2):c.7012G>A (p.Glu2338Lys)	not provided [RCV003885115]	likely benign	14	104948439	104948439	Human		name
405739158	CV3251982	single nucleotide variant	NM_138420.4(AHNAK2):c.8230G>C (p.Val2744Leu)	not specified [RCV004391066]	uncertain significance	14	104947221	104947221	Human		name
405739211	CV3251990	single nucleotide variant	NM_138420.4(AHNAK2):c.8341G>A (p.Val2781Met)	not specified [RCV004391074]	uncertain significance	14	104947110	104947110	Human		name
405739242	CV3251995	single nucleotide variant	NM_138420.4(AHNAK2):c.8380C>T (p.Arg2794Trp)	not specified [RCV004391079]	uncertain significance	14	104947071	104947071	Human		name
405739258	CV3251998	single nucleotide variant	NM_138420.4(AHNAK2):c.8392G>A (p.Asp2798Asn)	not specified [RCV004391082]	uncertain significance	14	104947059	104947059	Human		name
405739535	CV3252039	single nucleotide variant	NM_138420.4(AHNAK2):c.8620G>A (p.Ala2874Thr)	not specified [RCV004391123]	uncertain significance	14	104946831	104946831	Human		name
405739632	CV3252054	single nucleotide variant	NM_138420.4(AHNAK2):c.8655C>G (p.His2885Gln)	not specified [RCV004391138]	uncertain significance	14	104946796	104946796	Human		name
405739679	CV3252061	single nucleotide variant	NM_138420.4(AHNAK2):c.8729A>C (p.Asp2910Ala)	not specified [RCV004391145]	uncertain significance	14	104946722	104946722	Human		name
405739745	CV3252070	single nucleotide variant	NM_138420.4(AHNAK2):c.8788G>A (p.Ala2930Thr)	not specified [RCV004391154]	uncertain significance	14	104946663	104946663	Human		name
405739760	CV3252072	single nucleotide variant	NM_138420.4(AHNAK2):c.8789C>T (p.Ala2930Val)	not specified [RCV004391156]	uncertain significance	14	104946662	104946662	Human		name
405739786	CV3252076	single nucleotide variant	NM_138420.4(AHNAK2):c.8793G>C (p.Glu2931Asp)	not specified [RCV004391160]	uncertain significance	14	104946658	104946658	Human		name
405739830	CV3252083	single nucleotide variant	NM_138420.4(AHNAK2):c.8798C>T (p.Thr2933Met)	not specified [RCV004391167]	uncertain significance	14	104946653	104946653	Human		name
405739932	CV3252098	single nucleotide variant	NM_138420.4(AHNAK2):c.8845G>C (p.Glu2949Gln)	not specified [RCV004391182]	likely benign	14	104946606	104946606	Human		name
405739958	CV3252102	single nucleotide variant	NM_138420.4(AHNAK2):c.8876G>C (p.Arg2959Pro)	not specified [RCV004391186]	uncertain significance	14	104946575	104946575	Human		name
405740011	CV3252109	single nucleotide variant	NM_138420.4(AHNAK2):c.8905A>G (p.Lys2969Glu)	not specified [RCV004391193]	uncertain significance	14	104946546	104946546	Human		name
405740025	CV3252111	single nucleotide variant	NM_138420.4(AHNAK2):c.8942C>T (p.Pro2981Leu)	not specified [RCV004391195]	uncertain significance	14	104946509	104946509	Human		name
405740146	CV3252129	single nucleotide variant	NM_138420.4(AHNAK2):c.9014C>T (p.Ala3005Val)	not specified [RCV004391213]	uncertain significance	14	104946437	104946437	Human		name
405740187	CV3252135	single nucleotide variant	NM_138420.4(AHNAK2):c.9040C>T (p.Leu3014Phe)	not specified [RCV004391219]	uncertain significance	14	104946411	104946411	Human		name
405740212	CV3252139	single nucleotide variant	NM_138420.4(AHNAK2):c.9071C>T (p.Thr3024Ile)	not specified [RCV004391223]	uncertain significance	14	104946380	104946380	Human		name
405740253	CV3252144	single nucleotide variant	NM_138420.4(AHNAK2):c.9076A>C (p.Ile3026Leu)	not specified [RCV004391228]	likely benign	14	104946375	104946375	Human		name
405740317	CV3252153	single nucleotide variant	NM_138420.4(AHNAK2):c.9161G>A (p.Gly3054Glu)	not specified [RCV004391237]	uncertain significance	14	104946290	104946290	Human		name
405740364	CV3252160	single nucleotide variant	NM_138420.4(AHNAK2):c.9182T>G (p.Leu3061Arg)	not specified [RCV004391244]	uncertain significance	14	104946269	104946269	Human		name
405740492	CV3252178	single nucleotide variant	NM_138420.4(AHNAK2):c.9289G>T (p.Val3097Leu)	not specified [RCV004391262]	uncertain significance	14	104946162	104946162	Human		name
405740632	CV3252197	single nucleotide variant	NM_138420.4(AHNAK2):c.9326T>G (p.Met3109Arg)	not specified [RCV004391281]	uncertain significance	14	104946125	104946125	Human		name
405740733	CV3252211	single nucleotide variant	NM_138420.4(AHNAK2):c.9388T>C (p.Ser3130Pro)	not specified [RCV004391295]	uncertain significance	14	104946063	104946063	Human		name
405740808	CV3252222	single nucleotide variant	NM_138420.4(AHNAK2):c.9455C>T (p.Ser3152Leu)	not specified [RCV004391306]	uncertain significance	14	104945996	104945996	Human		name
405740895	CV3252235	single nucleotide variant	NM_138420.4(AHNAK2):c.9530T>G (p.Leu3177Arg)	not specified [RCV004391319]	uncertain significance	14	104945921	104945921	Human		name
405755582	CV3252248	single nucleotide variant	NM_138420.4(AHNAK2):c.9575G>A (p.Ser3192Asn)	not specified [RCV004393404]	uncertain significance	14	104945876	104945876	Human		name
405755677	CV3252262	single nucleotide variant	NM_138420.4(AHNAK2):c.9682A>G (p.Lys3228Glu)	not specified [RCV004393418]	uncertain significance	14	104945769	104945769	Human		name
405755800	CV3252280	single nucleotide variant	NM_138420.4(AHNAK2):c.9850A>C (p.Lys3284Gln)	not specified [RCV004393436]	uncertain significance	14	104945601	104945601	Human		name
405755841	CV3252286	single nucleotide variant	NM_138420.4(AHNAK2):c.9866G>A (p.Arg3289Gln)	not specified [RCV004393442]	uncertain significance	14	104945585	104945585	Human		name
405755896	CV3252294	single nucleotide variant	NM_138420.4(AHNAK2):c.9874G>A (p.Gly3292Arg)	not provided [RCV004810673]\|not specified [RCV004393450]	likely benign\|uncertain significance	14	104945577	104945577	Human		name
405755970	CV3252305	single nucleotide variant	NM_138420.4(AHNAK2):c.9967C>T (p.Pro3323Ser)	not specified [RCV004393461]	uncertain significance	14	104945484	104945484	Human		name
405788511	CV3255013	single nucleotide variant	NM_138420.4(AHNAK2):c.5759A>C (p.Asp1920Ala)	not specified [RCV004388161]	uncertain significance	14	104949692	104949692	Human		name
405788527	CV3255016	single nucleotide variant	NM_138420.4(AHNAK2):c.5761C>T (p.Leu1921Phe)	not specified [RCV004388164]	uncertain significance	14	104949690	104949690	Human		name
405788531	CV3255017	single nucleotide variant	NM_138420.4(AHNAK2):c.5770C>T (p.Pro1924Ser)	not specified [RCV004388165]	uncertain significance	14	104949681	104949681	Human		name
405788590	CV3255030	single nucleotide variant	NM_138420.4(AHNAK2):c.5882A>C (p.Gln1961Pro)	not specified [RCV004388178]	likely benign	14	104949569	104949569	Human		name
405788606	CV3255033	single nucleotide variant	NM_138420.4(AHNAK2):c.5920C>G (p.Leu1974Val)	not specified [RCV004388181]	uncertain significance	14	104949531	104949531	Human		name
405788654	CV3255042	single nucleotide variant	NM_138420.4(AHNAK2):c.5947G>A (p.Ala1983Thr)	not specified [RCV004388190]	uncertain significance	14	104949504	104949504	Human		name
405717594	CV3255050	single nucleotide variant	NM_138420.4(AHNAK2):c.5984T>A (p.Met1995Lys)	not specified [RCV004388198]	uncertain significance	14	104949467	104949467	Human		name
405717501	CV3255060	single nucleotide variant	NM_138420.4(AHNAK2):c.6002C>G (p.Ser2001Trp)	not specified [RCV004388208]	uncertain significance	14	104949449	104949449	Human		name
405788706	CV3255075	single nucleotide variant	NM_138420.4(AHNAK2):c.6020T>C (p.Ile2007Thr)	not specified [RCV004388223]	uncertain significance	14	104949431	104949431	Human		name
405788728	CV3255079	single nucleotide variant	NM_138420.4(AHNAK2):c.6023A>C (p.Glu2008Ala)	not specified [RCV004388227]	uncertain significance	14	104949428	104949428	Human		name
405716338	CV3255090	single nucleotide variant	NM_138420.4(AHNAK2):c.6149G>A (p.Gly2050Asp)	not specified [RCV004388238]	uncertain significance	14	104949302	104949302	Human		name
405716444	CV3255103	single nucleotide variant	NM_138420.4(AHNAK2):c.6187G>A (p.Glu2063Lys)	not specified [RCV004388251]	uncertain significance	14	104949264	104949264	Human		name
405716646	CV3255129	single nucleotide variant	NM_138420.4(AHNAK2):c.6514A>G (p.Ile2172Val)	not specified [RCV004388277]	uncertain significance	14	104948937	104948937	Human		name
405716697	CV3255136	single nucleotide variant	NM_138420.4(AHNAK2):c.6539C>T (p.Pro2180Leu)	not specified [RCV004388284]	uncertain significance	14	104948912	104948912	Human		name
405716825	CV3255153	single nucleotide variant	NM_138420.4(AHNAK2):c.6665T>C (p.Leu2222Pro)	not specified [RCV004388301]	likely benign	14	104948786	104948786	Human		name
405716915	CV3255164	single nucleotide variant	NM_138420.4(AHNAK2):c.6850G>A (p.Val2284Met)	not specified [RCV004388312]	uncertain significance	14	104948601	104948601	Human		name
405717009	CV3255177	single nucleotide variant	NM_138420.4(AHNAK2):c.6937G>A (p.Ala2313Thr)	not specified [RCV004388325]	likely benign	14	104948514	104948514	Human		name
405717129	CV3255192	single nucleotide variant	NM_138420.4(AHNAK2):c.7037T>C (p.Leu2346Ser)	not specified [RCV004388340]	uncertain significance	14	104948414	104948414	Human		name
405717209	CV3255201	single nucleotide variant	NM_138420.4(AHNAK2):c.7069A>G (p.Met2357Val)	not specified [RCV004388349]	likely benign	14	104948382	104948382	Human		name
405737638	CV3255217	single nucleotide variant	NM_138420.4(AHNAK2):c.7124T>G (p.Leu2375Arg)	not specified [RCV004390844]	uncertain significance	14	104948327	104948327	Human		name
405737664	CV3255221	single nucleotide variant	NM_138420.4(AHNAK2):c.7175C>T (p.Pro2392Leu)	not specified [RCV004390848]	uncertain significance	14	104948276	104948276	Human		name
405737706	CV3255227	single nucleotide variant	NM_138420.4(AHNAK2):c.7190T>A (p.Leu2397His)	not specified [RCV004390854]	uncertain significance	14	104948261	104948261	Human		name
405737894	CV3255254	single nucleotide variant	NM_138420.4(AHNAK2):c.7351G>A (p.Val2451Met)	not specified [RCV004390881]	uncertain significance	14	104948100	104948100	Human		name
405737911	CV3255257	single nucleotide variant	NM_138420.4(AHNAK2):c.7360G>A (p.Glu2454Lys)	not specified [RCV004390884]	uncertain significance	14	104948091	104948091	Human		name
405737929	CV3255260	single nucleotide variant	NM_138420.4(AHNAK2):c.7381G>A (p.Asp2461Asn)	not specified [RCV004390887]	uncertain significance	14	104948070	104948070	Human		name
405738011	CV3255272	single nucleotide variant	NM_138420.4(AHNAK2):c.7399G>T (p.Gly2467Trp)	not specified [RCV004390899]	uncertain significance	14	104948052	104948052	Human		name
405738130	CV3255289	single nucleotide variant	NM_138420.4(AHNAK2):c.7433C>A (p.Thr2478Asn)	not specified [RCV004390916]	uncertain significance	14	104948018	104948018	Human		name
405738274	CV3255311	single nucleotide variant	NM_138420.4(AHNAK2):c.7493C>T (p.Pro2498Leu)	not specified [RCV004390938]	uncertain significance	14	104947958	104947958	Human		name
405738321	CV3255318	single nucleotide variant	NM_138420.4(AHNAK2):c.7514C>T (p.Ser2505Leu)	not specified [RCV004390945]	uncertain significance	14	104947937	104947937	Human		name
405738344	CV3255321	single nucleotide variant	NM_138420.4(AHNAK2):c.7538T>C (p.Val2513Ala)	not specified [RCV004390948]	uncertain significance	14	104947913	104947913	Human		name
405738364	CV3255324	single nucleotide variant	NM_138420.4(AHNAK2):c.7566G>C (p.Met2522Ile)	not specified [RCV004390951]	uncertain significance	14	104947885	104947885	Human		name
405738433	CV3255335	single nucleotide variant	NM_138420.4(AHNAK2):c.7639G>A (p.Val2547Met)	not specified [RCV004390962]	uncertain significance	14	104947812	104947812	Human		name
405738475	CV3255341	single nucleotide variant	NM_138420.4(AHNAK2):c.7793C>A (p.Pro2598His)	not specified [RCV004390968]	uncertain significance	14	104947658	104947658	Human		name
405738550	CV3255352	single nucleotide variant	NM_138420.4(AHNAK2):c.7819G>A (p.Val2607Met)	not specified [RCV004390979]	uncertain significance	14	104947632	104947632	Human		name
405738608	CV3255361	single nucleotide variant	NM_138420.4(AHNAK2):c.7852G>A (p.Val2618Ile)	not specified [RCV004390988]	uncertain significance	14	104947599	104947599	Human		name
405738635	CV3255365	single nucleotide variant	NM_138420.4(AHNAK2):c.7862C>G (p.Pro2621Arg)	not specified [RCV004390992]	uncertain significance	14	104947589	104947589	Human		name
405738710	CV3255376	single nucleotide variant	NM_138420.4(AHNAK2):c.7913A>G (p.Asp2638Gly)	not specified [RCV004391003]	uncertain significance	14	104947538	104947538	Human		name
405738930	CV3255408	single nucleotide variant	NM_138420.4(AHNAK2):c.8043C>A (p.Asp2681Glu)	not specified [RCV004391035]	uncertain significance	14	104947408	104947408	Human		name
405739001	CV3255417	single nucleotide variant	NM_138420.4(AHNAK2):c.8113C>G (p.Leu2705Val)	not specified [RCV004391044]	uncertain significance	14	104947338	104947338	Human		name
405739052	CV3255424	single nucleotide variant	NM_138420.4(AHNAK2):c.8161G>A (p.Val2721Ile)	not specified [RCV004391051]	uncertain significance	14	104947290	104947290	Human		name
405739071	CV3255427	single nucleotide variant	NM_138420.4(AHNAK2):c.8168A>T (p.Glu2723Val)	not specified [RCV004391054]	uncertain significance	14	104947283	104947283	Human		name
405770184	CV3258457	single nucleotide variant	NM_138420.4(AHNAK2):c.3368A>G (p.Glu1123Gly)	not specified [RCV004395789]	uncertain significance	14	104952083	104952083	Human		name
405770417	CV3258495	single nucleotide variant	NM_138420.4(AHNAK2):c.3547G>A (p.Glu1183Lys)	not provided [RCV004546852]\|not specified [RCV004395827]	likely benign\|uncertain significance	14	104951904	104951904	Human		name
405770895	CV3258520	single nucleotide variant	NM_138420.4(AHNAK2):c.3586G>A (p.Asp1196Asn)	not specified [RCV004395852]	uncertain significance	14	104951865	104951865	Human		name
405770603	CV3258538	single nucleotide variant	NM_138420.4(AHNAK2):c.3706G>C (p.Val1236Leu)	not specified [RCV004395870]	likely benign	14	104951745	104951745	Human		name
405786893	CV3258547	single nucleotide variant	NM_138420.4(AHNAK2):c.3754C>A (p.Pro1252Thr)	not specified [RCV004387860]	uncertain significance	14	104951697	104951697	Human		name
405786920	CV3258553	single nucleotide variant	NM_138420.4(AHNAK2):c.3766A>G (p.Met1256Val)	not specified [RCV004387866]	uncertain significance	14	104951685	104951685	Human		name
405786933	CV3258556	single nucleotide variant	NM_138420.4(AHNAK2):c.3779A>C (p.Asp1260Ala)	not specified [RCV004387869]	uncertain significance	14	104951672	104951672	Human		name
405786945	CV3258559	single nucleotide variant	NM_138420.4(AHNAK2):c.3796G>A (p.Val1266Met)	not specified [RCV004387872]	uncertain significance	14	104951655	104951655	Human		name
405786965	CV3258563	single nucleotide variant	NM_138420.4(AHNAK2):c.3829G>A (p.Gly1277Ser)	not specified [RCV004387876]	uncertain significance	14	104951622	104951622	Human		name
405786975	CV3258565	single nucleotide variant	NM_138420.4(AHNAK2):c.3934G>A (p.Gly1312Arg)	not specified [RCV004387878]	uncertain significance	14	104951517	104951517	Human		name
405787158	CV3258577	single nucleotide variant	NM_138420.4(AHNAK2):c.4016G>A (p.Gly1339Glu)	not specified [RCV004387890]	uncertain significance	14	104951435	104951435	Human		name
405787257	CV3258598	single nucleotide variant	NM_138420.4(AHNAK2):c.4194G>C (p.Glu1398Asp)	not specified [RCV004387911]	uncertain significance	14	104951257	104951257	Human		name
405787288	CV3258605	single nucleotide variant	NM_138420.4(AHNAK2):c.4219C>T (p.Leu1407Phe)	not specified [RCV004387918]	uncertain significance	14	104951232	104951232	Human		name
405787351	CV3258618	single nucleotide variant	NM_138420.4(AHNAK2):c.4297A>G (p.Ile1433Val)	not specified [RCV004387931]	likely benign	14	104951154	104951154	Human		name
405787412	CV3258630	single nucleotide variant	NM_138420.4(AHNAK2):c.4510G>C (p.Gly1504Arg)	not specified [RCV004387943]	uncertain significance	14	104950941	104950941	Human		name
405787990	CV3258635	single nucleotide variant	NM_138420.4(AHNAK2):c.4541C>A (p.Ala1514Asp)	not specified [RCV004387948]	uncertain significance	14	104950910	104950910	Human		name
405787951	CV3258643	single nucleotide variant	NM_138420.4(AHNAK2):c.4567G>A (p.Val1523Met)	not specified [RCV004387956]	uncertain significance	14	104950884	104950884	Human		name
405787903	CV3258653	single nucleotide variant	NM_138420.4(AHNAK2):c.4621C>A (p.Leu1541Met)	not specified [RCV004387966]	uncertain significance	14	104950830	104950830	Human		name
405787506	CV3258656	single nucleotide variant	NM_138420.4(AHNAK2):c.4628T>A (p.Ile1543Lys)	not specified [RCV004387969]	uncertain significance	14	104950823	104950823	Human		name
405787491	CV3258670	single nucleotide variant	NM_138420.4(AHNAK2):c.4664G>T (p.Gly1555Val)	not specified [RCV004387983]	uncertain significance	14	104950787	104950787	Human		name
405787581	CV3258689	single nucleotide variant	NM_138420.4(AHNAK2):c.4765G>A (p.Val1589Met)	not specified [RCV004388002]	uncertain significance	14	104950686	104950686	Human		name
405787617	CV3258696	single nucleotide variant	NM_138420.4(AHNAK2):c.4841C>T (p.Ala1614Val)	not specified [RCV004388009]	uncertain significance	14	104950610	104950610	Human		name
405787626	CV3258698	single nucleotide variant	NM_138420.4(AHNAK2):c.4859C>G (p.Ser1620Cys)	not specified [RCV004388011]	uncertain significance	14	104950592	104950592	Human		name
405787694	CV3258713	single nucleotide variant	NM_138420.4(AHNAK2):c.5006G>A (p.Gly1669Glu)	not specified [RCV004388026]	uncertain significance	14	104950445	104950445	Human		name
405787729	CV3258720	single nucleotide variant	NM_138420.4(AHNAK2):c.5032G>C (p.Glu1678Gln)	not specified [RCV004388033]	uncertain significance	14	104950419	104950419	Human		name
405787822	CV3258738	single nucleotide variant	NM_138420.4(AHNAK2):c.5180C>T (p.Pro1727Leu)	not specified [RCV004388051]	likely benign	14	104950271	104950271	Human		name
405787868	CV3258747	single nucleotide variant	NM_138420.4(AHNAK2):c.5247G>T (p.Leu1749Phe)	not specified [RCV004388060]	likely benign	14	104950204	104950204	Human		name
405788093	CV3258770	single nucleotide variant	NM_138420.4(AHNAK2):c.5341G>A (p.Asp1781Asn)	not specified [RCV004388083]	uncertain significance	14	104950110	104950110	Human		name
405788149	CV3258782	single nucleotide variant	NM_138420.4(AHNAK2):c.5344G>C (p.Val1782Leu)	not specified [RCV004388095]	uncertain significance	14	104950107	104950107	Human		name
405788170	CV3258786	single nucleotide variant	NM_138420.4(AHNAK2):c.5357T>A (p.Leu1786Gln)	not specified [RCV004388099]	uncertain significance	14	104950094	104950094	Human		name
405788181	CV3258788	single nucleotide variant	NM_138420.4(AHNAK2):c.5362A>G (p.Ser1788Gly)	not specified [RCV004388101]	uncertain significance	14	104950089	104950089	Human		name
405788248	CV3258800	single nucleotide variant	NM_138420.4(AHNAK2):c.5428T>A (p.Ser1810Thr)	not specified [RCV004388113]	uncertain significance	14	104950023	104950023	Human		name
405788280	CV3258806	single nucleotide variant	NM_138420.4(AHNAK2):c.5503G>T (p.Val1835Leu)	not specified [RCV004388119]	uncertain significance	14	104949948	104949948	Human		name
405852906	CV3393334	single nucleotide variant	NM_138420.4(AHNAK2):c.4618G>C (p.Asp1540His)	not provided [RCV004546064]\|not specified [RCV004917906]	likely benign\|uncertain significance	14	104950833	104950833	Human		name
405871701	CV3398024	single nucleotide variant	NM_138420.4(AHNAK2):c.5107A>G (p.Thr1703Ala)	not provided [RCV004575024]	likely benign	14	104950344	104950344	Human		name
405871790	CV3398071	single nucleotide variant	NM_138420.4(AHNAK2):c.5247G>C (p.Leu1749Phe)	not provided [RCV004575072]	likely benign	14	104950204	104950204	Human		name
405871870	CV3398113	single nucleotide variant	NM_138420.4(AHNAK2):c.5233C>G (p.Gln1745Glu)	not provided [RCV004575114]	likely benign	14	104950218	104950218	Human		name
407425142	CV3409374	single nucleotide variant	NM_138420.4(AHNAK2):c.8602G>A (p.Ala2868Thr)	not provided [RCV004585305]	likely benign	14	104946849	104946849	Human		name
407455689	CV3415722	single nucleotide variant	NM_138420.4(AHNAK2):c.4276C>A (p.Leu1426Ile)	not provided [RCV004598598]	benign	14	104951175	104951175	Human		name
407492777	CV3432181	single nucleotide variant	NM_138420.4(AHNAK2):c.9274G>T (p.Gly3092Cys)	not specified [RCV004620879]	uncertain significance	14	104946177	104946177	Human		name
407492805	CV3432188	single nucleotide variant	NM_138420.4(AHNAK2):c.4138C>T (p.Pro1380Ser)	not specified [RCV004620887]	uncertain significance	14	104951313	104951313	Human		name
407492857	CV3432205	single nucleotide variant	NM_138420.4(AHNAK2):c.6715C>G (p.Leu2239Val)	not specified [RCV004620904]	likely benign	14	104948736	104948736	Human		name
407482691	CV3438786	single nucleotide variant	NM_138420.4(AHNAK2):c.5513C>T (p.Pro1838Leu)	not specified [RCV004618430]	uncertain significance	14	104949938	104949938	Human		name
407482747	CV3438797	single nucleotide variant	NM_138420.4(AHNAK2):c.6580G>C (p.Gly2194Arg)	not specified [RCV004618441]	uncertain significance	14	104948871	104948871	Human		name
407482791	CV3438808	single nucleotide variant	NM_138420.4(AHNAK2):c.4706G>A (p.Gly1569Glu)	not specified [RCV004618452]	uncertain significance	14	104950745	104950745	Human		name
407482961	CV3438842	single nucleotide variant	NM_138420.4(AHNAK2):c.3362A>G (p.Asp1121Gly)	not specified [RCV004618485]	uncertain significance	14	104952089	104952089	Human		name
407483025	CV3438853	single nucleotide variant	NM_138420.4(AHNAK2):c.7727T>C (p.Met2576Thr)	not specified [RCV004618496]	uncertain significance	14	104947724	104947724	Human		name
407483145	CV3438874	single nucleotide variant	NM_138420.4(AHNAK2):c.8102C>G (p.Pro2701Arg)	not specified [RCV004618517]	uncertain significance	14	104947349	104947349	Human		name
407483270	CV3438895	single nucleotide variant	NM_138420.4(AHNAK2):c.4613C>A (p.Ala1538Asp)	not specified [RCV004618538]	uncertain significance	14	104950838	104950838	Human		name
407483408	CV3438917	single nucleotide variant	NM_138420.4(AHNAK2):c.7187G>A (p.Gly2396Asp)	not specified [RCV004618560]	uncertain significance	14	104948264	104948264	Human		name
407483435	CV3438921	single nucleotide variant	NM_138420.4(AHNAK2):c.9941A>G (p.Lys3314Arg)	not specified [RCV004618564]	uncertain significance	14	104945510	104945510	Human		name
407483478	CV3438929	single nucleotide variant	NM_138420.4(AHNAK2):c.5279A>G (p.Gln1760Arg)	not specified [RCV004618572]	uncertain significance	14	104950172	104950172	Human		name
407483561	CV3438950	single nucleotide variant	NM_138420.4(AHNAK2):c.9182T>C (p.Leu3061Pro)	not specified [RCV004618593]	uncertain significance	14	104946269	104946269	Human		name
407483952	CV3439012	single nucleotide variant	NM_138420.4(AHNAK2):c.7178A>C (p.Glu2393Ala)	not specified [RCV004618653]	uncertain significance	14	104948273	104948273	Human		name
407484017	CV3439022	single nucleotide variant	NM_138420.4(AHNAK2):c.7397A>T (p.Glu2466Val)	not specified [RCV004618663]	uncertain significance	14	104948054	104948054	Human		name
407501142	CV3439052	single nucleotide variant	NM_138420.4(AHNAK2):c.6019A>G (p.Ile2007Val)	not specified [RCV004623194]	uncertain significance	14	104949432	104949432	Human		name
407501232	CV3439072	single nucleotide variant	NM_138420.4(AHNAK2):c.8105C>G (p.Ser2702Cys)	not specified [RCV004623214]	uncertain significance	14	104947346	104947346	Human		name
407501522	CV3439132	single nucleotide variant	NM_138420.4(AHNAK2):c.4492T>G (p.Phe1498Val)	not specified [RCV004623274]	uncertain significance	14	104950959	104950959	Human		name
407501588	CV3439151	single nucleotide variant	NM_138420.4(AHNAK2):c.5557G>A (p.Val1853Met)	not specified [RCV004623293]	uncertain significance	14	104949894	104949894	Human		name
407501638	CV3439161	single nucleotide variant	NM_138420.4(AHNAK2):c.6926A>G (p.Lys2309Arg)	not specified [RCV004623303]	uncertain significance	14	104948525	104948525	Human		name
407501682	CV3439170	single nucleotide variant	NM_138420.4(AHNAK2):c.6553G>A (p.Ala2185Thr)	not specified [RCV004623312]	uncertain significance	14	104948898	104948898	Human		name
407501785	CV3439190	single nucleotide variant	NM_138420.4(AHNAK2):c.6977T>A (p.Leu2326Gln)	not specified [RCV004623332]	uncertain significance	14	104948474	104948474	Human		name
407501835	CV3439201	single nucleotide variant	NM_138420.4(AHNAK2):c.3232A>G (p.Lys1078Glu)	not specified [RCV004623343]	uncertain significance	14	104952219	104952219	Human		name
407501889	CV3439211	single nucleotide variant	NM_138420.4(AHNAK2):c.5305G>C (p.Asp1769His)	not specified [RCV004623353]	uncertain significance	14	104950146	104950146	Human		name
407501894	CV3439212	single nucleotide variant	NM_138420.4(AHNAK2):c.8227G>A (p.Glu2743Lys)	not specified [RCV004623354]	likely benign	14	104947224	104947224	Human		name
407501902	CV3439214	single nucleotide variant	NM_138420.4(AHNAK2):c.6532G>T (p.Val2178Leu)	not specified [RCV004623356]	uncertain significance	14	104948919	104948919	Human		name
407493182	CV3442300	single nucleotide variant	NM_138420.4(AHNAK2):c.8471G>T (p.Gly2824Val)	not specified [RCV004620972]	uncertain significance	14	104946980	104946980	Human		name
407493202	CV3442306	single nucleotide variant	NM_138420.4(AHNAK2):c.5334G>A (p.Met1778Ile)	not specified [RCV004620978]	uncertain significance	14	104950117	104950117	Human		name
407493229	CV3442314	single nucleotide variant	NM_138420.4(AHNAK2):c.7825A>G (p.Met2609Val)	not specified [RCV004620986]	likely benign	14	104947626	104947626	Human		name
407493250	CV3442320	single nucleotide variant	NM_138420.4(AHNAK2):c.5560G>A (p.Glu1854Lys)	not specified [RCV004620992]	uncertain significance	14	104949891	104949891	Human		name
407493277	CV3442328	single nucleotide variant	NM_138420.4(AHNAK2):c.5548G>C (p.Ala1850Pro)	not specified [RCV004621000]	uncertain significance	14	104949903	104949903	Human		name
407493297	CV3442334	single nucleotide variant	NM_138420.4(AHNAK2):c.9989C>T (p.Ser3330Leu)	not specified [RCV004621006]	uncertain significance	14	104945462	104945462	Human		name
407493340	CV3442345	single nucleotide variant	NM_138420.4(AHNAK2):c.7033G>C (p.Ala2345Pro)	not specified [RCV004621016]	uncertain significance	14	104948418	104948418	Human		name
407493382	CV3442355	single nucleotide variant	NM_138420.4(AHNAK2):c.7276C>T (p.Pro2426Ser)	not specified [RCV004621026]	uncertain significance	14	104948175	104948175	Human		name
407493421	CV3442364	single nucleotide variant	NM_138420.4(AHNAK2):c.9835G>A (p.Glu3279Lys)	not specified [RCV004621035]	uncertain significance	14	104945616	104945616	Human		name
407493461	CV3442374	single nucleotide variant	NM_138420.4(AHNAK2):c.4633C>T (p.Pro1545Ser)	not specified [RCV004621045]	uncertain significance	14	104950818	104950818	Human		name
407493469	CV3442376	single nucleotide variant	NM_138420.4(AHNAK2):c.7210C>G (p.Leu2404Val)	not specified [RCV004621047]	likely benign	14	104948241	104948241	Human		name
407493475	CV3442378	single nucleotide variant	NM_138420.4(AHNAK2):c.3518T>A (p.Phe1173Tyr)	not specified [RCV004621049]	uncertain significance	14	104951933	104951933	Human		name
407493483	CV3442381	single nucleotide variant	NM_138420.4(AHNAK2):c.3606G>A (p.Met1202Ile)	not specified [RCV004621052]	uncertain significance	14	104951845	104951845	Human		name
407493533	CV3442398	single nucleotide variant	NM_138420.4(AHNAK2):c.6896G>A (p.Arg2299Gln)	not specified [RCV004621069]	likely benign	14	104948555	104948555	Human		name
407493543	CV3442402	single nucleotide variant	NM_138420.4(AHNAK2):c.7808C>T (p.Thr2603Ile)	not specified [RCV004621073]	uncertain significance	14	104947643	104947643	Human		name
407493558	CV3442408	single nucleotide variant	NM_138420.4(AHNAK2):c.6314T>C (p.Val2105Ala)	not specified [RCV004621079]	likely benign	14	104949137	104949137	Human		name
407493575	CV3442415	single nucleotide variant	NM_138420.4(AHNAK2):c.6321G>C (p.Met2107Ile)	not specified [RCV004621086]	uncertain significance	14	104949130	104949130	Human		name
407493625	CV3442429	single nucleotide variant	NM_138420.4(AHNAK2):c.6305A>G (p.Asp2102Gly)	not specified [RCV004621100]	likely benign	14	104949146	104949146	Human		name
407493705	CV3442449	single nucleotide variant	NM_138420.4(AHNAK2):c.7169C>T (p.Pro2390Leu)	not specified [RCV004621120]	uncertain significance	14	104948282	104948282	Human		name
407493788	CV3442469	single nucleotide variant	NM_138420.4(AHNAK2):c.8200C>G (p.Leu2734Val)	not specified [RCV004621140]	likely benign	14	104947251	104947251	Human		name
407493834	CV3442479	single nucleotide variant	NM_138420.4(AHNAK2):c.5681G>A (p.Gly1894Asp)	not specified [RCV004621150]	uncertain significance	14	104949770	104949770	Human		name
407493878	CV3442490	single nucleotide variant	NM_138420.4(AHNAK2):c.6910A>C (p.Met2304Leu)	not specified [RCV004621161]	likely benign	14	104948541	104948541	Human		name
407481422	CV3442500	single nucleotide variant	NM_138420.4(AHNAK2):c.6515T>C (p.Ile2172Thr)	not specified [RCV004618201]	uncertain significance	14	104948936	104948936	Human		name
407481769	CV3442561	single nucleotide variant	NM_138420.4(AHNAK2):c.5685G>C (p.Gln1895His)	not specified [RCV004618262]	likely benign	14	104949766	104949766	Human		name
407481946	CV3442592	single nucleotide variant	NM_138420.4(AHNAK2):c.8407G>A (p.Asp2803Asn)	not specified [RCV004618293]	uncertain significance	14	104947044	104947044	Human		name
407481996	CV3442602	single nucleotide variant	NM_138420.4(AHNAK2):c.5333T>G (p.Met1778Arg)	not specified [RCV004618303]	uncertain significance	14	104950118	104950118	Human		name
407482047	CV3442611	single nucleotide variant	NM_138420.4(AHNAK2):c.5336C>T (p.Ala1779Val)	not specified [RCV004618312]	uncertain significance	14	104950115	104950115	Human		name
407482114	CV3442622	single nucleotide variant	NM_138420.4(AHNAK2):c.7330G>A (p.Val2444Met)	not specified [RCV004618323]	uncertain significance	14	104948121	104948121	Human		name
407482235	CV3442644	single nucleotide variant	NM_138420.4(AHNAK2):c.7216A>G (p.Met2406Val)	not specified [RCV004618345]	uncertain significance	14	104948235	104948235	Human		name
407482294	CV3442653	single nucleotide variant	NM_138420.4(AHNAK2):c.8414G>A (p.Gly2805Asp)	not specified [RCV004618354]	likely benign	14	104947037	104947037	Human		name
407482353	CV3442664	single nucleotide variant	NM_138420.4(AHNAK2):c.3032C>T (p.Ser1011Leu)	not specified [RCV004618364]	uncertain significance	14	104952419	104952419	Human		name
407482415	CV3442674	single nucleotide variant	NM_138420.4(AHNAK2):c.5084C>T (p.Pro1695Leu)	not specified [RCV004618374]	uncertain significance	14	104950367	104950367	Human		name
407482477	CV3442684	single nucleotide variant	NM_138420.4(AHNAK2):c.5108C>A (p.Thr1703Asn)	not specified [RCV004618384]	uncertain significance	14	104950343	104950343	Human		name
407482526	CV3442694	single nucleotide variant	NM_138420.4(AHNAK2):c.4694C>A (p.Pro1565His)	not specified [RCV004618394]	likely benign	14	104950757	104950757	Human		name
407482635	CV3442713	single nucleotide variant	NM_138420.4(AHNAK2):c.8712C>G (p.Phe2904Leu)	not specified [RCV004618413]	uncertain significance	14	104946739	104946739	Human		name
408377995	CV3500902	single nucleotide variant	NM_138420.4(AHNAK2):c.3052A>G (p.Lys1018Glu)	not provided [RCV004722552]	likely benign	14	104952399	104952399	Human		name
408378436	CV3500939	single nucleotide variant	NM_138420.4(AHNAK2):c.3127A>G (p.Thr1043Ala)	not provided [RCV004722589]	likely benign	14	104952324	104952324	Human		name
408379451	CV3501033	single nucleotide variant	NM_138420.4(AHNAK2):c.3058T>A (p.Leu1020Met)	not provided [RCV004722683]	likely benign	14	104952393	104952393	Human		name
596947683	CV3547264	single nucleotide variant	NM_138420.4(AHNAK2):c.4147A>G (p.Thr1383Ala)	not provided [RCV004811568]	likely benign	14	104951304	104951304	Human		name
596947917	CV3547506	single nucleotide variant	NM_138420.4(AHNAK2):c.4159C>G (p.Leu1387Val)	not provided [RCV004811810]	likely benign	14	104951292	104951292	Human		name
596947934	CV3547524	single nucleotide variant	NM_138420.4(AHNAK2):c.4174T>G (p.Leu1392Val)	not provided [RCV004811828]	likely benign	14	104951277	104951277	Human		name
596947994	CV3547586	single nucleotide variant	NM_138420.4(AHNAK2):c.5791G>C (p.Ala1931Pro)	not provided [RCV004811890]	likely benign	14	104949660	104949660	Human		name
596948090	CV3547685	single nucleotide variant	NM_138420.4(AHNAK2):c.6223G>C (p.Glu2075Gln)	not provided [RCV004811990]	likely benign	14	104949228	104949228	Human		name
596945369	CV3547853	single nucleotide variant	NM_138420.4(AHNAK2):c.5777C>T (p.Thr1926Ile)	not provided [RCV004809184]	benign	14	104949674	104949674	Human		name
596948389	CV3549471	single nucleotide variant	NM_138420.4(AHNAK2):c.8473G>A (p.Val2825Met)	not provided [RCV004812292]	likely benign	14	104946978	104946978	Human		name
597689040	CV3664915	single nucleotide variant	NM_138420.4(AHNAK2):c.8845G>A (p.Glu2949Lys)	not specified [RCV004915173]	uncertain significance	14	104946606	104946606	Human		name
597689140	CV3664925	single nucleotide variant	NM_138420.4(AHNAK2):c.6160G>A (p.Val2054Met)	not specified [RCV004915183]	likely benign	14	104949291	104949291	Human		name
597689494	CV3664936	single nucleotide variant	NM_138420.4(AHNAK2):c.9439A>G (p.Lys3147Glu)	not specified [RCV004915194]	uncertain significance	14	104946012	104946012	Human		name
597689570	CV3664943	single nucleotide variant	NM_138420.4(AHNAK2):c.8078C>A (p.Thr2693Asn)	not specified [RCV004915201]	uncertain significance	14	104947373	104947373	Human		name
597689724	CV3664958	single nucleotide variant	NM_138420.4(AHNAK2):c.8095C>G (p.Gln2699Glu)	not specified [RCV004915216]	uncertain significance	14	104947356	104947356	Human		name
597690020	CV3665013	single nucleotide variant	NM_138420.4(AHNAK2):c.8490G>C (p.Lys2830Asn)	not specified [RCV004915268]	uncertain significance	14	104946961	104946961	Human		name
597691169	CV3665111	single nucleotide variant	NM_138420.4(AHNAK2):c.4454A>C (p.Asp1485Ala)	not specified [RCV004915352]	uncertain significance	14	104950997	104950997	Human		name
597691272	CV3665120	single nucleotide variant	NM_138420.4(AHNAK2):c.4925G>A (p.Gly1642Glu)	not specified [RCV004915361]	uncertain significance	14	104950526	104950526	Human		name
597691820	CV3665175	single nucleotide variant	NM_138420.4(AHNAK2):c.9364G>A (p.Gly3122Ser)	not specified [RCV004915416]	uncertain significance	14	104946087	104946087	Human		name
597691931	CV3665185	single nucleotide variant	NM_138420.4(AHNAK2):c.9685T>G (p.Leu3229Val)	not specified [RCV004915426]	likely benign	14	104945766	104945766	Human		name
597692138	CV3665213	single nucleotide variant	NM_138420.4(AHNAK2):c.5569G>A (p.Val1857Met)	not specified [RCV004915446]	uncertain significance	14	104949882	104949882	Human		name
597693137	CV3665223	single nucleotide variant	NM_138420.4(AHNAK2):c.4885C>G (p.Gln1629Glu)	not specified [RCV004915456]	uncertain significance	14	104950566	104950566	Human		name
597692252	CV3665255	single nucleotide variant	NM_138420.4(AHNAK2):c.3559G>C (p.Asp1187His)	not specified [RCV004915488]	uncertain significance	14	104951892	104951892	Human		name
597693194	CV3665262	single nucleotide variant	NM_138420.4(AHNAK2):c.4756A>G (p.Met1586Val)	not specified [RCV004915490]	uncertain significance	14	104950695	104950695	Human		name
597692325	CV3665288	single nucleotide variant	NM_138420.4(AHNAK2):c.8002G>A (p.Glu2668Lys)	not specified [RCV004915496]	uncertain significance	14	104947449	104947449	Human		name
597692440	CV3665318	single nucleotide variant	NM_138420.4(AHNAK2):c.6809T>C (p.Val2270Ala)	not specified [RCV004915508]	likely benign	14	104948642	104948642	Human		name
597692453	CV3665322	single nucleotide variant	NM_138420.4(AHNAK2):c.6691G>A (p.Gly2231Ser)	not specified [RCV004915509]	uncertain significance	14	104948760	104948760	Human		name
597692476	CV3665333	single nucleotide variant	NM_138420.4(AHNAK2):c.6527T>C (p.Val2176Ala)	not specified [RCV004915511]	uncertain significance	14	104948924	104948924	Human		name
597692487	CV3665346	single nucleotide variant	NM_138420.4(AHNAK2):c.6679C>T (p.Pro2227Ser)	not specified [RCV004915512]	uncertain significance	14	104948772	104948772	Human		name
597716936	CV3671510	single nucleotide variant	NM_138420.4(AHNAK2):c.6197G>T (p.Gly2066Val)	not specified [RCV004918375]	uncertain significance	14	104949254	104949254	Human		name
597716949	CV3671521	single nucleotide variant	NM_138420.4(AHNAK2):c.6847A>T (p.Ser2283Cys)	not specified [RCV004918376]	uncertain significance	14	104948604	104948604	Human		name
597716997	CV3671532	single nucleotide variant	NM_138420.4(AHNAK2):c.4054G>C (p.Asp1352His)	not specified [RCV004918380]	uncertain significance	14	104951397	104951397	Human		name
597717064	CV3671556	single nucleotide variant	NM_138420.4(AHNAK2):c.9812A>T (p.Gln3271Leu)	not specified [RCV004918386]	likely benign	14	104945639	104945639	Human		name
597717165	CV3671566	single nucleotide variant	NM_138420.4(AHNAK2):c.9820A>G (p.Met3274Val)	not specified [RCV004918395]	likely benign	14	104945631	104945631	Human		name
597717188	CV3671576	single nucleotide variant	NM_138420.4(AHNAK2):c.3919G>A (p.Gly1307Ser)	not specified [RCV004918397]	likely benign	14	104951532	104951532	Human		name
597717237	CV3671592	single nucleotide variant	NM_138420.4(AHNAK2):c.7478T>A (p.Phe2493Tyr)	not specified [RCV004918402]	uncertain significance	14	104947973	104947973	Human		name
597717251	CV3671602	single nucleotide variant	NM_138420.4(AHNAK2):c.5078G>A (p.Ser1693Asn)	not specified [RCV004918403]	uncertain significance	14	104950373	104950373	Human		name
597717262	CV3671611	single nucleotide variant	NM_138420.4(AHNAK2):c.6053T>C (p.Val2018Ala)	not specified [RCV004918404]	uncertain significance	14	104949398	104949398	Human		name
597717545	CV3671640	single nucleotide variant	NM_138420.4(AHNAK2):c.5690C>A (p.Pro1897His)	not specified [RCV004918432]	uncertain significance	14	104949761	104949761	Human		name
597717688	CV3671672	single nucleotide variant	NM_138420.4(AHNAK2):c.8480C>A (p.Ala2827Asp)	not specified [RCV004918445]	uncertain significance	14	104946971	104946971	Human		name
597717700	CV3671682	single nucleotide variant	NM_138420.4(AHNAK2):c.6578A>T (p.Gln2193Leu)	not specified [RCV004918446]	uncertain significance	14	104948873	104948873	Human		name
597717741	CV3671698	single nucleotide variant	NM_138420.4(AHNAK2):c.9241A>C (p.Ile3081Leu)	not specified [RCV004918450]	uncertain significance	14	104946210	104946210	Human		name
597717830	CV3671707	single nucleotide variant	NM_138420.4(AHNAK2):c.3353C>T (p.Thr1118Ile)	not specified [RCV004918459]	uncertain significance	14	104952098	104952098	Human		name
597718101	CV3671737	single nucleotide variant	NM_138420.4(AHNAK2):c.6025G>A (p.Ala2009Thr)	not specified [RCV004918489]	uncertain significance	14	104949426	104949426	Human		name
597718190	CV3671746	single nucleotide variant	NM_138420.4(AHNAK2):c.8025G>C (p.Glu2675Asp)	not specified [RCV004918498]	uncertain significance	14	104947426	104947426	Human		name
597718466	CV3671775	single nucleotide variant	NM_138420.4(AHNAK2):c.7689A>T (p.Lys2563Asn)	not specified [RCV004918526]	uncertain significance	14	104947762	104947762	Human		name
597718568	CV3671786	single nucleotide variant	NM_138420.4(AHNAK2):c.5575C>A (p.Leu1859Ile)	not specified [RCV004918537]	uncertain significance	14	104949876	104949876	Human		name
597718656	CV3671796	single nucleotide variant	NM_138420.4(AHNAK2):c.6892G>A (p.Ala2298Thr)	not specified [RCV004918547]	uncertain significance	14	104948559	104948559	Human		name
597718680	CV3671804	single nucleotide variant	NM_138420.4(AHNAK2):c.5435C>T (p.Ala1812Val)	not specified [RCV004918550]	uncertain significance	14	104950016	104950016	Human		name
597718749	CV3671812	single nucleotide variant	NM_138420.4(AHNAK2):c.7823A>G (p.Glu2608Gly)	not specified [RCV004918558]	uncertain significance	14	104947628	104947628	Human		name
597718913	CV3671832	single nucleotide variant	NM_138420.4(AHNAK2):c.7507G>C (p.Glu2503Gln)	not specified [RCV004918578]	uncertain significance	14	104947944	104947944	Human		name
597692575	CV3674939	single nucleotide variant	NM_138420.4(AHNAK2):c.4651G>A (p.Glu1551Lys)	not specified [RCV004915519]	uncertain significance	14	104950800	104950800	Human		name
597692681	CV3674948	single nucleotide variant	NM_138420.4(AHNAK2):c.5536G>T (p.Val1846Leu)	not specified [RCV004915528]	uncertain significance	14	104949915	104949915	Human		name
597693241	CV3674978	single nucleotide variant	NM_138420.4(AHNAK2):c.3367G>A (p.Glu1123Lys)	not specified [RCV004915558]	uncertain significance	14	104952084	104952084	Human		name
597693567	CV3675009	single nucleotide variant	NM_138420.4(AHNAK2):c.6613C>T (p.Pro2205Ser)	not specified [RCV004915589]	uncertain significance	14	104948838	104948838	Human		name
597693664	CV3675018	single nucleotide variant	NM_138420.4(AHNAK2):c.8401C>G (p.Leu2801Val)	not specified [RCV004915598]	uncertain significance	14	104947050	104947050	Human		name
597693776	CV3675029	single nucleotide variant	NM_138420.4(AHNAK2):c.9859G>A (p.Gly3287Ser)	not specified [RCV004915609]	uncertain significance	14	104945592	104945592	Human		name
597693892	CV3675040	single nucleotide variant	NM_138420.4(AHNAK2):c.4633C>A (p.Pro1545Thr)	not specified [RCV004915620]	uncertain significance	14	104950818	104950818	Human		name
597694074	CV3675057	single nucleotide variant	NM_138420.4(AHNAK2):c.4660G>A (p.Ala1554Thr)	not specified [RCV004915637]	uncertain significance	14	104950791	104950791	Human		name
597714454	CV3675068	single nucleotide variant	NM_138420.4(AHNAK2):c.6340G>C (p.Val2114Leu)	not specified [RCV004918128]	uncertain significance	14	104949111	104949111	Human		name
597714659	CV3675089	single nucleotide variant	NM_138420.4(AHNAK2):c.5746A>G (p.Met1916Val)	not specified [RCV004918149]	uncertain significance	14	104949705	104949705	Human		name
597715018	CV3675123	single nucleotide variant	NM_138420.4(AHNAK2):c.9688C>G (p.Gln3230Glu)	not specified [RCV004918183]	likely benign	14	104945763	104945763	Human		name
597715111	CV3675132	single nucleotide variant	NM_138420.4(AHNAK2):c.5617A>G (p.Ile1873Val)	not specified [RCV004918192]	uncertain significance	14	104949834	104949834	Human		name
597715488	CV3675168	single nucleotide variant	NM_138420.4(AHNAK2):c.6643G>A (p.Gly2215Ser)	not specified [RCV004918228]	uncertain significance	14	104948808	104948808	Human		name
597715689	CV3675188	single nucleotide variant	NM_138420.4(AHNAK2):c.4668A>C (p.Gln1556His)	not specified [RCV004918248]	uncertain significance	14	104950783	104950783	Human		name
597715811	CV3675200	single nucleotide variant	NM_138420.4(AHNAK2):c.5660T>A (p.Val1887Glu)	not specified [RCV004918260]	uncertain significance	14	104949791	104949791	Human		name
597715903	CV3675209	single nucleotide variant	NM_138420.4(AHNAK2):c.8471G>A (p.Gly2824Glu)	not specified [RCV004918269]	uncertain significance	14	104946980	104946980	Human		name
597716042	CV3675224	single nucleotide variant	NM_138420.4(AHNAK2):c.6521C>T (p.Ala2174Val)	not specified [RCV004918282]	uncertain significance	14	104948930	104948930	Human		name
597716062	CV3675235	single nucleotide variant	NM_138420.4(AHNAK2):c.6538C>T (p.Pro2180Ser)	not specified [RCV004918284]	uncertain significance	14	104948913	104948913	Human		name
597716332	CV3675262	single nucleotide variant	NM_138420.4(AHNAK2):c.3157A>G (p.Thr1053Ala)	not specified [RCV004918311]	likely benign	14	104952294	104952294	Human		name
597716397	CV3675278	single nucleotide variant	NM_138420.4(AHNAK2):c.6631A>G (p.Lys2211Glu)	not specified [RCV004918318]	likely benign	14	104948820	104948820	Human		name
597716538	CV3675324	single nucleotide variant	NM_138420.4(AHNAK2):c.4930C>A (p.Leu1644Met)	not specified [RCV004918334]	uncertain significance	14	104950521	104950521	Human		name
597716546	CV3675335	single nucleotide variant	NM_138420.4(AHNAK2):c.9986C>T (p.Ala3329Val)	not specified [RCV004918335]	uncertain significance	14	104945465	104945465	Human		name
597716555	CV3675346	single nucleotide variant	NM_138420.4(AHNAK2):c.6649G>T (p.Val2217Leu)	not specified [RCV004918336]	uncertain significance	14	104948802	104948802	Human		name
597716571	CV3675350	single nucleotide variant	NM_138420.4(AHNAK2):c.6026C>T (p.Ala2009Val)	not specified [RCV004918338]	uncertain significance	14	104949425	104949425	Human		name
12896296	CV390040	single nucleotide variant	NM_138420.4(AHNAK2):c.6509A>G (p.Lys2170Arg)	not provided [RCV004716463]\|not specified [RCV000455163]	benign	14	104948942	104948942	Human		name
12895782	CV390106	single nucleotide variant	NM_138420.4(AHNAK2):c.9779T>C (p.Met3260Thr)	not provided [RCV004715172]\|not specified [RCV000454445]	benign	14	104945672	104945672	Human		name
12896262	CV390164	single nucleotide variant	NM_138420.4(AHNAK2):c.9650T>C (p.Leu3217Pro)	not provided [RCV001683471]\|not specified [RCV000455111]	benign	14	104945801	104945801	Human		name
12896600	CV390167	single nucleotide variant	NM_138420.4(AHNAK2):c.9085G>C (p.Glu3029Gln)	not provided [RCV004715173]\|not specified [RCV000455570]	benign	14	104946366	104946366	Human		name
12895820	CV390168	single nucleotide variant	NM_138420.4(AHNAK2):c.6559A>G (p.Met2187Val)	not provided [RCV004715174]\|not specified [RCV000454497]	benign	14	104948892	104948892	Human		name
13794656	CV553387	single nucleotide variant	NM_138420.4(AHNAK2):c.5900G>A (p.Gly1967Asp)	not provided [RCV000681627]	uncertain significance	14	104949551	104949551	Human		name
13794654	CV553388	single nucleotide variant	NM_138420.4(AHNAK2):c.4274A>G (p.Asp1425Gly)	not provided [RCV000681628]	uncertain significance	14	104951177	104951177	Human		name

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