Wnt2 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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201 records found for search term Wnt2

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
8590234	CV124924	single nucleotide variant	NM_003391.2(WNT2):c.853+2448G>A	Lung cancer [RCV000105443]	uncertain significance	7	117295164	117295164	Human		name
405812124	CV3352925	single nucleotide variant	NM_003391.3(WNT2):c.88A>G (p.Met30Val)	not specified [RCV004483125]	uncertain significance	7	117320789	117320789	Human		name
15190302	CV699772	single nucleotide variant	NM_003391.3(WNT2):c.792G>A (p.Thr264=)	not provided [RCV000954435]	benign	7	117297673	117297673	Human		name
156296506	CV2297581	single nucleotide variant	NM_003391.3(WNT2):c.203G>C (p.Gly68Ala)	not specified [RCV004155284]	uncertain significance	7	117320674	117320674	Human		name
401741570	CV2697578	single nucleotide variant	NM_003391.3(WNT2):c.187C>T (p.Arg63Cys)	not specified [RCV004298332]	uncertain significance	7	117320690	117320690	Human		name
407524813	CV3487976	single nucleotide variant	NM_003391.3(WNT2):c.200A>G (p.Gln67Arg)	not specified [RCV004678567]	uncertain significance	7	117320677	117320677	Human		name
407524816	CV3487977	single nucleotide variant	NM_003391.3(WNT2):c.209C>T (p.Ala70Val)	not specified [RCV004678568]	uncertain significance	7	117320668	117320668	Human		name
407524821	CV3487980	single nucleotide variant	NM_003391.3(WNT2):c.161T>C (p.Leu54Pro)	not specified [RCV004678570]	uncertain significance	7	117320716	117320716	Human		name
598275514	CV3937170	single nucleotide variant	NM_003391.3(WNT2):c.1059C>T (p.Asn353=)	not specified [RCV005304648]	likely benign	7	117278179	117278179	Human		name
156139545	CV2202914	single nucleotide variant	NM_003391.3(WNT2):c.317G>A (p.Arg106Gln)	not specified [RCV004069187]	uncertain significance	7	117315342	117315342	Human		name
155918260	CV2236777	single nucleotide variant	NM_003391.3(WNT2):c.506G>A (p.Arg169His)	not specified [RCV004112546]	uncertain significance	7	117315153	117315153	Human		name
156086069	CV2244666	single nucleotide variant	NM_003391.3(WNT2):c.418A>G (p.Lys140Glu)	not specified [RCV004102375]	uncertain significance	7	117315241	117315241	Human		name
156302686	CV2311962	single nucleotide variant	NM_003391.3(WNT2):c.731T>C (p.Val244Ala)	not specified [RCV004170779]	uncertain significance	7	117297734	117297734	Human		name
156224090	CV2399327	single nucleotide variant	NM_003391.3(WNT2):c.913G>A (p.Glu305Lys)	not specified [RCV004242617]	uncertain significance	7	117278325	117278325	Human		name
405812120	CV3352923	single nucleotide variant	NM_003391.3(WNT2):c.517G>T (p.Asp173Tyr)	not specified [RCV004483123]	uncertain significance	7	117315142	117315142	Human		name
405812122	CV3352924	single nucleotide variant	NM_003391.3(WNT2):c.689C>T (p.Thr230Met)	not specified [RCV004483124]	uncertain significance	7	117297776	117297776	Human		name
405812126	CV3352926	single nucleotide variant	NM_003391.3(WNT2):c.955A>G (p.Thr319Ala)	not specified [RCV004483126]	uncertain significance	7	117278283	117278283	Human		name
405812128	CV3352927	single nucleotide variant	NM_003391.3(WNT2):c.959G>A (p.Arg320Gln)	not specified [RCV004483127]	uncertain significance	7	117278279	117278279	Human		name
405812130	CV3352928	single nucleotide variant	NM_003391.3(WNT2):c.997G>A (p.Ala333Thr)	not specified [RCV004483128]	uncertain significance	7	117278241	117278241	Human		name
407524819	CV3487978	single nucleotide variant	NM_003391.3(WNT2):c.937T>C (p.Tyr313His)	not specified [RCV004678569]	uncertain significance	7	117278301	117278301	Human		name
407465497	CV3487979	single nucleotide variant	NM_003391.3(WNT2):c.603C>A (p.Phe201Leu)	not specified [RCV004688784]	uncertain significance	7	117297862	117297862	Human		name
597799999	CV3624214	single nucleotide variant	NM_003391.3(WNT2):c.534A>T (p.Lys178Asn)	not specified [RCV004879974]	uncertain significance	7	117315125	117315125	Human		name
597800000	CV3624215	single nucleotide variant	NM_003391.3(WNT2):c.599G>A (p.Arg200Gln)	not specified [RCV004879975]	uncertain significance	7	117297866	117297866	Human		name
597800002	CV3624216	single nucleotide variant	NM_003391.3(WNT2):c.746A>G (p.Asp249Gly)	not specified [RCV004879976]	uncertain significance	7	117297719	117297719	Human		name
597741004	CV3624217	single nucleotide variant	NM_003391.3(WNT2):c.482T>C (p.Ile161Thr)	not specified [RCV004890665]	uncertain significance	7	117315177	117315177	Human		name
598192242	CV3937169	single nucleotide variant	NM_003391.3(WNT2):c.940G>A (p.Asp314Asn)	not specified [RCV005288488]	uncertain significance	7	117278298	117278298	Human		name
598192246	CV3937171	single nucleotide variant	NM_003391.3(WNT2):c.443G>T (p.Ser148Ile)	not specified [RCV005288489]	uncertain significance	7	117315216	117315216	Human		name
598192252	CV3937172	single nucleotide variant	NM_003391.3(WNT2):c.801C>G (p.Asp267Glu)	not specified [RCV005288490]	uncertain significance	7	117297664	117297664	Human		name
8626317	CV81461	single nucleotide variant	NM_003391.2(WNT2):c.505C>T (p.Arg169Cys)	Malignant melanoma [RCV000061539]	not provided	7	117315154	117315154	Human		name
15104208	CV722263	single nucleotide variant	NM_003391.3(WNT2):c.1057A>G (p.Asn353Asp)	not provided [RCV000892838]	benign	7	117278181	117278181	Human		name
156135938	CV2032719	single nucleotide variant	NM_024494.3(WNT2B):c.947-4C>T	not provided [RCV002740729]	likely benign	1	112520276	112520276	Human		name
155974237	CV2079405	single nucleotide variant	NM_024494.3(WNT2B):c.404-6C>A	not provided [RCV002881628]	likely benign	1	112516134	112516134	Human		name
156018552	CV2173961	deletion	NM_024494.3(WNT2B):c.182+8del	not provided [RCV003035611]	likely benign	1	112509452	112509452	Human		name
597880570	CV3826404	single nucleotide variant	NM_024494.3(WNT2B):c.946+9G>A	not provided [RCV005178101]	likely benign	1	112517394	112517394	Human		name
598204995	CV3896767	deletion	NM_004185.4(WNT2B):c.125+1del	Diarrhea 9 [RCV005356948]	uncertain significance	1	112491081	112491081	Human	1	name
156172726	CV2026356	single nucleotide variant	NM_024494.3(WNT2B):c.183-13C>T	not provided [RCV002765368]	likely benign	1	112514861	112514861	Human		name
155919161	CV2027253	single nucleotide variant	NM_024494.3(WNT2B):c.403+15C>T	not provided [RCV002750623]	likely benign	1	112515109	112515109	Human		name
156251082	CV2029611	single nucleotide variant	NM_024494.3(WNT2B):c.946+11A>C	not provided [RCV002745990]	likely benign	1	112517396	112517396	Human		name
156152521	CV2101420	single nucleotide variant	NM_024494.3(WNT2B):c.947-16C>G	not provided [RCV002890701]	likely benign	1	112520264	112520264	Human		name
405187139	CV2917629	single nucleotide variant	NM_024494.3(WNT2B):c.946+17G>C	not provided [RCV003564540]	likely benign	1	112517402	112517402	Human		name
405123152	CV2954249	single nucleotide variant	NM_024494.3(WNT2B):c.947-18C>T	not provided [RCV003667661]	likely benign	1	112520262	112520262	Human		name
405240257	CV2993552	single nucleotide variant	NM_024494.3(WNT2B):c.946+17G>A	not provided [RCV003718986]	likely benign	1	112517402	112517402	Human		name
405180954	CV3027865	single nucleotide variant	NM_024494.3(WNT2B):c.182+15C>A	not provided [RCV003705523]	likely benign	1	112509459	112509459	Human		name
597931843	CV3786083	single nucleotide variant	NM_024494.3(WNT2B):c.183-16C>A	not provided [RCV005131791]	likely benign	1	112514858	112514858	Human		name
597972394	CV3790252	single nucleotide variant	NM_024494.3(WNT2B):c.947-14C>A	not provided [RCV005142675]	likely benign	1	112520266	112520266	Human		name
597957262	CV3814306	single nucleotide variant	NM_024494.3(WNT2B):c.404-16A>G	not provided [RCV005162637]	likely benign	1	112516124	112516124	Human		name
597861376	CV3822504	single nucleotide variant	NM_024494.3(WNT2B):c.182+12T>C	not provided [RCV005175034]	likely benign	1	112509456	112509456	Human		name
156318542	CV2137890	microsatellite	NM_024494.3(WNT2B):c.404-11TC[3]	not provided [RCV002963047]	likely benign	1	112516129	112516130	Human		name
156289491	CV1897310	single nucleotide variant	NM_024494.3(WNT2B):c.456C>T (p.His152=)	WNT2B-related disorder [RCV003898812]\|not provided [RCV002598693]	likely benign	1	112516192	112516192	Human	1	name , trait , alternate_id
156327321	CV1956343	single nucleotide variant	NM_024494.3(WNT2B):c.225C>T (p.Ile75=)	WNT2B-related disorder [RCV003896221]\|not provided [RCV002579798]	likely benign	1	112514916	112514916	Human	1	name , trait , alternate_id
156360353	CV2126403	single nucleotide variant	NM_024494.3(WNT2B):c.723C>T (p.Gly241=)	WNT2B-related disorder [RCV003906400]\|not provided [RCV002966941]	likely benign	1	112517162	112517162	Human	1	name , trait , alternate_id
15112434	CV706576	single nucleotide variant	NM_024494.3(WNT2B):c.732T>C (p.Gly244=)	WNT2B-related disorder [RCV003970830]\|not provided [RCV000961298]	benign	1	112517171	112517171	Human	1	name , trait , alternate_id
15112440	CV706577	single nucleotide variant	NM_024494.3(WNT2B):c.1140A>G (p.Lys380=)	WNT2B-related disorder [RCV003978372]\|not provided [RCV000961299]	benign	1	112520473	112520473	Human	1	name , trait , alternate_id
15099863	CV718099	single nucleotide variant	NM_024494.3(WNT2B):c.302G>A (p.Arg101Gln)	WNT2B-related disorder [RCV003957963]\|not provided [RCV000892012]	benign	1	112514993	112514993	Human	1	name , trait , alternate_id
402479357	CV3033156	single nucleotide variant	NM_024494.3(WNT2B):c.9A>G (p.Arg3=)	not provided [RCV003712668]	likely benign	1	112509271	112509271	Human		name
402515345	CV2936303	single nucleotide variant	NM_024494.3(WNT2B):c.12G>C (p.Pro4=)	not provided [RCV003662902]	likely benign	1	112509274	112509274	Human		name
405191926	CV2984899	single nucleotide variant	NM_024494.3(WNT2B):c.12G>A (p.Pro4=)	not provided [RCV003706543]	likely benign	1	112509274	112509274	Human		name
155936577	CV2044839	single nucleotide variant	NM_024494.3(WNT2B):c.78G>A (p.Ser26=)	not provided [RCV002774912]	likely benign	1	112509340	112509340	Human		name
402517697	CV2936548	single nucleotide variant	NM_024494.3(WNT2B):c.69T>C (p.Pro23=)	not provided [RCV003663076]	likely benign	1	112509331	112509331	Human		name
405125011	CV2958277	single nucleotide variant	NM_024494.3(WNT2B):c.90C>T (p.Pro30=)	not provided [RCV003667837]	likely benign	1	112509352	112509352	Human		name
405218208	CV2968663	single nucleotide variant	NM_024494.3(WNT2B):c.54C>G (p.Ala18=)	not provided [RCV003680303]	likely benign	1	112509316	112509316	Human		name
597858565	CV3769644	single nucleotide variant	NM_024494.3(WNT2B):c.81C>A (p.Pro27=)	not provided [RCV005105686]	likely benign	1	112509343	112509343	Human		name
597910875	CV3769846	single nucleotide variant	NM_024494.3(WNT2B):c.87C>T (p.Ala29=)	not provided [RCV005113349]	likely benign	1	112509349	112509349	Human		name
597936789	CV3807716	single nucleotide variant	NM_024494.3(WNT2B):c.63G>T (p.Pro21=)	not provided [RCV005158095]	likely benign	1	112509325	112509325	Human		name
156105971	CV1917213	single nucleotide variant	NM_024494.3(WNT2B):c.201G>A (p.Gly67=)	not provided [RCV002592449]	likely benign	1	112514892	112514892	Human		name
156078200	CV2025803	single nucleotide variant	NM_024494.3(WNT2B):c.25G>A (p.Glu9Lys)	not provided [RCV002760538]	benign	1	112509287	112509287	Human		name
155951083	CV2026224	single nucleotide variant	NM_024494.3(WNT2B):c.13G>C (p.Gly5Arg)	not provided [RCV002730684]\|not specified [RCV004067813]	uncertain significance	1	112509275	112509275	Human		name
155918071	CV2030060	single nucleotide variant	NM_024494.3(WNT2B):c.222T>C (p.Asn74=)	not provided [RCV002750567]	likely benign	1	112514913	112514913	Human		name
156102403	CV2084227	single nucleotide variant	NM_024494.3(WNT2B):c.228T>C (p.Pro76=)	not provided [RCV002848131]	likely benign	1	112514919	112514919	Human		name
155941371	CV2158112	single nucleotide variant	NM_024494.3(WNT2B):c.23A>C (p.Glu8Ala)	not provided [RCV003014290]\|not specified [RCV005288878]	uncertain significance	1	112509285	112509285	Human		name
155960378	CV2183416	single nucleotide variant	NM_024494.3(WNT2B):c.11C>T (p.Pro4Leu)	not provided [RCV003032908]	uncertain significance	1	112509273	112509273	Human		name
405219793	CV2904072	single nucleotide variant	NM_024494.3(WNT2B):c.126C>G (p.Ala42=)	not provided [RCV003568258]	likely benign	1	112509388	112509388	Human		name
405170953	CV3025811	single nucleotide variant	NM_024494.3(WNT2B):c.153G>T (p.Thr51=)	not provided [RCV003704678]	likely benign	1	112509415	112509415	Human		name
405145177	CV3027434	single nucleotide variant	NM_024494.3(WNT2B):c.102G>A (p.Arg34=)	not provided [RCV003702859]	likely benign	1	112509364	112509364	Human		name
405224049	CV3035889	single nucleotide variant	NM_024494.3(WNT2B):c.150G>A (p.Leu50=)	not provided [RCV003710393]	likely benign	1	112509412	112509412	Human		name
405117936	CV3116029	single nucleotide variant	NM_024494.3(WNT2B):c.291C>T (p.Gly97=)	not provided [RCV003814519]	likely benign	1	112514982	112514982	Human		name
597928985	CV3816212	single nucleotide variant	NM_024494.3(WNT2B):c.174G>A (p.Thr58=)	not provided [RCV005156793]	likely benign	1	112509436	112509436	Human		name
597846672	CV3828039	single nucleotide variant	NM_024494.3(WNT2B):c.126C>T (p.Ala42=)	not provided [RCV005173114]	likely benign	1	112509388	112509388	Human		name
597837025	CV3828503	single nucleotide variant	NM_024494.3(WNT2B):c.240C>T (p.Ser80=)	not provided [RCV005171396]	likely benign	1	112514931	112514931	Human		name
597895247	CV3833652	single nucleotide variant	NM_024494.3(WNT2B):c.108G>A (p.Ser36=)	not provided [RCV005180344]	likely benign	1	112509370	112509370	Human		name
156360930	CV1900481	single nucleotide variant	NM_024494.3(WNT2B):c.888G>A (p.Arg296=)	not provided [RCV002581719]	likely benign	1	112517327	112517327	Human		name
156133623	CV2022843	single nucleotide variant	NM_024494.3(WNT2B):c.49C>T (p.Arg17Cys)	not provided [RCV002740653]	uncertain significance	1	112509311	112509311	Human		name
156028029	CV2025823	single nucleotide variant	NM_024494.3(WNT2B):c.82G>A (p.Ala28Thr)	not provided [RCV002735684]\|not specified [RCV005288803]	likely benign\|uncertain significance	1	112509344	112509344	Human		name
156051821	CV2027381	single nucleotide variant	NM_024494.3(WNT2B):c.67C>T (p.Pro23Ser)	not provided [RCV002736537]\|not specified [RCV004067883]	uncertain significance	1	112509329	112509329	Human		name
155917591	CV2029980	single nucleotide variant	NM_024494.3(WNT2B):c.35A>G (p.Gln12Arg)	not provided [RCV002750544]	uncertain significance	1	112509297	112509297	Human		name
156037669	CV2030097	single nucleotide variant	NM_024494.3(WNT2B):c.52G>A (p.Ala18Thr)	not provided [RCV002736060]\|not specified [RCV004067831]	uncertain significance	1	112509314	112509314	Human		name
155983985	CV2030296	single nucleotide variant	NM_024494.3(WNT2B):c.366C>T (p.Asp122=)	not provided [RCV002755454]	likely benign	1	112515057	112515057	Human		name
155952674	CV2033202	single nucleotide variant	NM_024494.3(WNT2B):c.62C>G (p.Pro21Arg)	not provided [RCV002730766]	uncertain significance	1	112509324	112509324	Human		name
155936790	CV2044894	single nucleotide variant	NM_024494.3(WNT2B):c.73C>A (p.Pro25Thr)	not provided [RCV002774927]	uncertain significance	1	112509335	112509335	Human		name
156176076	CV2052053	single nucleotide variant	NM_024494.3(WNT2B):c.351C>T (p.Asn117=)	not provided [RCV002828148]	likely benign	1	112515042	112515042	Human		name
155941656	CV2055022	single nucleotide variant	NM_024494.3(WNT2B):c.387C>T (p.Gly129=)	not provided [RCV002815734]	likely benign	1	112515078	112515078	Human		name
155944490	CV2072495	single nucleotide variant	NM_024494.3(WNT2B):c.321T>C (p.Cys107=)	not provided [RCV002861985]	likely benign	1	112515012	112515012	Human		name
156038502	CV2089515	single nucleotide variant	NM_024494.3(WNT2B):c.426A>G (p.Val142=)	not provided [RCV002867344]	likely benign	1	112516162	112516162	Human		name
156024856	CV2106033	single nucleotide variant	NM_024494.3(WNT2B):c.468C>T (p.Arg156=)	not provided [RCV002923241]	likely benign	1	112516204	112516204	Human		name
156131473	CV2112886	single nucleotide variant	NM_024494.3(WNT2B):c.642G>A (p.Arg214=)	not provided [RCV002914569]	likely benign	1	112516378	112516378	Human		name
156119379	CV2115878	single nucleotide variant	NM_024494.3(WNT2B):c.603C>T (p.Ala201=)	not provided [RCV002927752]	likely benign	1	112516339	112516339	Human		name
156169520	CV2133509	single nucleotide variant	NM_024494.3(WNT2B):c.582C>T (p.Tyr194=)	not provided [RCV003005343]	likely benign	1	112516318	112516318	Human		name
156115637	CV2136420	single nucleotide variant	NM_024494.3(WNT2B):c.816T>C (p.Ala272=)	not provided [RCV003002772]	likely benign	1	112517255	112517255	Human		name
155962953	CV2140782	single nucleotide variant	NM_024494.3(WNT2B):c.47G>C (p.Arg16Pro)	not provided [RCV003015561]	uncertain significance	1	112509309	112509309	Human		name
156074154	CV2294734	single nucleotide variant	NM_024494.3(WNT2B):c.65T>C (p.Val22Ala)	not specified [RCV004161974]	uncertain significance	1	112509327	112509327	Human		name
401723476	CV2674965	single nucleotide variant	NM_024494.3(WNT2B):c.79C>T (p.Pro27Ser)	not specified [RCV004296273]	uncertain significance	1	112509341	112509341	Human		name
402492738	CV2863290	single nucleotide variant	NM_024494.3(WNT2B):c.324G>A (p.Gln108=)	not provided [RCV003573179]	likely benign	1	112515015	112515015	Human		name
402490344	CV2866543	single nucleotide variant	NM_024494.3(WNT2B):c.855C>T (p.Thr285=)	not provided [RCV003572870]	likely benign	1	112517294	112517294	Human		name
405239734	CV2882571	single nucleotide variant	NM_024494.3(WNT2B):c.816T>A (p.Ala272=)	not provided [RCV003557139]	likely benign	1	112517255	112517255	Human		name
405125614	CV2886489	single nucleotide variant	NM_024494.3(WNT2B):c.819G>A (p.Val273=)	not provided [RCV003559540]	likely benign	1	112517258	112517258	Human		name
405048134	CV2886691	single nucleotide variant	NM_024494.3(WNT2B):c.969T>C (p.Arg323=)	not provided [RCV003579597]	likely benign	1	112520302	112520302	Human		name
402523417	CV2900294	single nucleotide variant	NM_024494.3(WNT2B):c.468C>G (p.Arg156=)	not provided [RCV003576031]	likely benign	1	112516204	112516204	Human		name
405112473	CV2900485	single nucleotide variant	NM_024494.3(WNT2B):c.645C>T (p.Ala215=)	not provided [RCV003558072]	likely benign	1	112516381	112516381	Human		name
405121307	CV2952460	single nucleotide variant	NM_024494.3(WNT2B):c.861C>A (p.Ala287=)	not provided [RCV003671502]	likely benign	1	112517300	112517300	Human		name
404979152	CV3009488	single nucleotide variant	NM_024494.3(WNT2B):c.504T>C (p.Cys168=)	not provided [RCV003690930]	likely benign	1	112516240	112516240	Human		name
402485320	CV3036848	single nucleotide variant	NM_024494.3(WNT2B):c.885C>T (p.Thr295=)	not provided [RCV003713170]	likely benign	1	112517324	112517324	Human		name
405221374	CV3060186	single nucleotide variant	NM_024494.3(WNT2B):c.822G>A (p.Gln274=)	not provided [RCV003733364]	likely benign	1	112517261	112517261	Human		name
405192502	CV3066138	single nucleotide variant	NM_024494.3(WNT2B):c.948T>C (p.Gly316=)	not provided [RCV003729859]	likely benign	1	112520281	112520281	Human		name
405812139	CV3352933	single nucleotide variant	NM_024494.3(WNT2B):c.94G>C (p.Gly32Arg)	not specified [RCV004483133]	uncertain significance	1	112509356	112509356	Human		name
407524824	CV3487981	single nucleotide variant	NM_024494.3(WNT2B):c.37C>T (p.Leu13Phe)	not specified [RCV004678571]	uncertain significance	1	112509299	112509299	Human		name
597863889	CV3814099	single nucleotide variant	NM_024494.3(WNT2B):c.714G>A (p.Lys238=)	not provided [RCV005147168]	likely benign	1	112517153	112517153	Human		name
597831655	CV3830699	single nucleotide variant	NM_024494.3(WNT2B):c.612T>C (p.Asp204=)	not provided [RCV005170097]	likely benign	1	112516348	112516348	Human		name
597953609	CV3844030	single nucleotide variant	NM_024494.3(WNT2B):c.924C>T (p.Tyr308=)	not provided [RCV005190892]	likely benign	1	112517363	112517363	Human		name
597903832	CV3846040	single nucleotide variant	NM_024494.3(WNT2B):c.513C>T (p.Tyr171=)	not provided [RCV005181662]	likely benign	1	112516249	112516249	Human		name
597873019	CV3859189	single nucleotide variant	NM_024494.3(WNT2B):c.621G>A (p.Glu207=)	not provided [RCV005197778]	likely benign	1	112516357	112516357	Human		name
597922181	CV3861879	single nucleotide variant	NM_024494.3(WNT2B):c.495G>A (p.Val165=)	not provided [RCV005205255]	likely benign	1	112516231	112516231	Human		name
598192272	CV3937175	single nucleotide variant	NM_024494.3(WNT2B):c.58G>T (p.Ala20Ser)	not specified [RCV005288493]	uncertain significance	1	112509320	112509320	Human		name
15135084	CV745578	single nucleotide variant	NM_024494.3(WNT2B):c.909C>T (p.Asp303=)	not provided [RCV000920791]	likely benign	1	112517348	112517348	Human		name
152065366	CV1539745	single nucleotide variant	NM_024494.3(WNT2B):c.1170A>G (p.Gln390=)	not provided [RCV002147343]	benign	1	112520503	112520503	Human		name
156257595	CV1905519	single nucleotide variant	NM_024494.3(WNT2B):c.289G>A (p.Gly97Ser)	not provided [RCV003086327]\|not specified [RCV004877779]	uncertain significance	1	112514980	112514980	Human		name
156146292	CV2026625	single nucleotide variant	NM_024494.3(WNT2B):c.242G>A (p.Arg81Gln)	not provided [RCV002741077]\|not specified [RCV004877749]	uncertain significance	1	112514933	112514933	Human		name
156147765	CV2026681	single nucleotide variant	NM_024494.3(WNT2B):c.160G>A (p.Ala54Thr)	not provided [RCV002741126]	uncertain significance	1	112509422	112509422	Human		name
156175737	CV2052020	single nucleotide variant	NM_024494.3(WNT2B):c.194C>T (p.Ala65Val)	not provided [RCV002828137]	uncertain significance	1	112514885	112514885	Human		name
156256337	CV2102400	single nucleotide variant	NM_024494.3(WNT2B):c.1059C>G (p.Thr353=)	not provided [RCV002895427]	benign	1	112520392	112520392	Human		name
156246582	CV2105673	single nucleotide variant	NM_024494.3(WNT2B):c.151A>G (p.Thr51Ala)	not provided [RCV002933394]\|not specified [RCV004877762]	uncertain significance	1	112509413	112509413	Human		name
156214137	CV2127899	single nucleotide variant	NM_024494.3(WNT2B):c.176C>G (p.Ser59Cys)	not provided [RCV002957873]\|not specified [RCV004067294]	uncertain significance	1	112509438	112509438	Human		name
155981623	CV2163126	single nucleotide variant	NM_024494.3(WNT2B):c.252G>C (p.Gln84His)	not provided [RCV003033908]	uncertain significance	1	112514943	112514943	Human		name
156273518	CV2164237	single nucleotide variant	NM_024494.3(WNT2B):c.199G>T (p.Gly67Trp)	not provided [RCV003027075]	uncertain significance	1	112514890	112514890	Human		name
156120209	CV2174854	single nucleotide variant	NM_024494.3(WNT2B):c.158C>G (p.Pro53Arg)	not provided [RCV003055436]	uncertain significance	1	112509420	112509420	Human		name
156045783	CV2186435	single nucleotide variant	NM_024494.3(WNT2B):c.250C>T (p.Gln84Ter)	not provided [RCV003036735]	pathogenic	1	112514941	112514941	Human		name
405191263	CV2871386	single nucleotide variant	NM_024494.3(WNT2B):c.1158G>A (p.Glu386=)	not provided [RCV003550396]	likely benign	1	112520491	112520491	Human		name
402498656	CV2871894	single nucleotide variant	NM_024494.3(WNT2B):c.1096C>A (p.Arg366=)	not provided [RCV003545676]	likely benign	1	112520429	112520429	Human		name
405114613	CV2896585	single nucleotide variant	NM_024494.3(WNT2B):c.1143C>T (p.Ala381=)	not provided [RCV003558257]	likely benign	1	112520476	112520476	Human		name
405248906	CV3003853	single nucleotide variant	NM_024494.3(WNT2B):c.1062G>A (p.Gln354=)	not provided [RCV003721226]	likely benign	1	112520395	112520395	Human		name
405128732	CV3054415	single nucleotide variant	NM_024494.3(WNT2B):c.1173C>G (p.Thr391=)	not provided [RCV003724627]	likely benign	1	112520506	112520506	Human		name
405208931	CV3065549	single nucleotide variant	NM_024494.3(WNT2B):c.1032C>T (p.Tyr344=)	not provided [RCV003731710]	likely benign	1	112520365	112520365	Human		name
405193044	CV3066234	single nucleotide variant	NM_024494.3(WNT2B):c.1017C>T (p.Cys339=)	not provided [RCV003729909]	likely benign	1	112520350	112520350	Human		name
597924859	CV3808702	single nucleotide variant	NM_024494.3(WNT2B):c.1092T>C (p.Ala364=)	not provided [RCV005156216]	likely benign	1	112520425	112520425	Human		name
597858946	CV3817092	single nucleotide variant	NM_024494.3(WNT2B):c.1005T>C (p.Cys335=)	not provided [RCV005146473]	likely benign	1	112520338	112520338	Human		name
597832669	CV3831333	single nucleotide variant	NM_024494.3(WNT2B):c.163C>A (p.Arg55Ser)	not provided [RCV005170536]	uncertain significance	1	112509425	112509425	Human		name
13674008	CV535693	single nucleotide variant	NM_024494.3(WNT2B):c.205C>T (p.Arg69Ter)	Diarrhea 9 [RCV000714963]\|Failure to thrive [RCV000656393]	pathogenic	1	112514896	112514896	Human	7	name
40886479	CV972507	deletion	NM_024494.3(WNT2B):c.423del (p.Phe141fs)	Diarrhea 9 [RCV004998782]\|not provided [RCV001264389]	pathogenic\|uncertain significance	1	112516156	112516156	Human	1	name
156403884	CV1871941	single nucleotide variant	NM_024494.3(WNT2B):c.377C>G (p.Thr126Ser)	not provided [RCV003052707]	uncertain significance	1	112515068	112515068	Human		name
156403557	CV1885829	single nucleotide variant	NM_024494.3(WNT2B):c.539G>A (p.Arg180His)	not provided [RCV003069500]	uncertain significance	1	112516275	112516275	Human		name
156193944	CV1912176	single nucleotide variant	NM_024494.3(WNT2B):c.334C>T (p.Arg112Cys)	not provided [RCV002595467]	uncertain significance	1	112515025	112515025	Human		name
156418984	CV1915183	single nucleotide variant	NM_024494.3(WNT2B):c.368G>A (p.Arg123Gln)	not provided [RCV002612196]	uncertain significance	1	112515059	112515059	Human		name
156089517	CV1919675	single nucleotide variant	NM_024494.3(WNT2B):c.802C>T (p.Arg268Cys)	not provided [RCV002591861]	uncertain significance	1	112517241	112517241	Human		name
156209870	CV1932424	single nucleotide variant	NM_024494.3(WNT2B):c.621G>T (p.Glu207Asp)	not provided [RCV002643953]\|not specified [RCV004877790]	uncertain significance	1	112516357	112516357	Human		name
156414516	CV1986700	single nucleotide variant	NM_024494.3(WNT2B):c.641G>A (p.Arg214Gln)	not provided [RCV002609238]	uncertain significance	1	112516377	112516377	Human		name
156323712	CV2022396	single nucleotide variant	NM_024494.3(WNT2B):c.856G>A (p.Ala286Thr)	not provided [RCV002717264]	uncertain significance	1	112517295	112517295	Human		name
156084439	CV2023759	single nucleotide variant	NM_024494.3(WNT2B):c.692G>A (p.Arg231Gln)	not provided [RCV002760733]	uncertain significance	1	112517131	112517131	Human		name
156011395	CV2041893	single nucleotide variant	NM_024494.3(WNT2B):c.650T>C (p.Met217Thr)	not provided [RCV002780162]	uncertain significance	1	112516386	112516386	Human		name
155937447	CV2045960	single nucleotide variant	NM_024494.3(WNT2B):c.518G>A (p.Arg173His)	not provided [RCV002751558]\|not specified [RCV004067978]	uncertain significance	1	112516254	112516254	Human		name
156239268	CV2053015	single nucleotide variant	NM_024494.3(WNT2B):c.433A>T (p.Ile145Phe)	not provided [RCV002791290]	uncertain significance	1	112516169	112516169	Human		name
156189604	CV2086694	single nucleotide variant	NM_024494.3(WNT2B):c.719A>G (p.His240Arg)	not provided [RCV002852094]	uncertain significance	1	112517158	112517158	Human		name
156001898	CV2103382	single nucleotide variant	NM_024494.3(WNT2B):c.457G>A (p.Ala153Thr)	Diarrhea 9 [RCV005399007]\|not provided [RCV002908673]	uncertain significance	1	112516193	112516193	Human	1	name
155994371	CV2122483	single nucleotide variant	NM_024494.3(WNT2B):c.601G>T (p.Ala201Ser)	not provided [RCV002974880]	uncertain significance	1	112516337	112516337	Human		name
156245624	CV2126432	single nucleotide variant	NM_024494.3(WNT2B):c.779G>A (p.Arg260His)	not provided [RCV002959027]\|not specified [RCV004877768]	uncertain significance	1	112517218	112517218	Human		name
156009874	CV2126806	single nucleotide variant	NM_024494.3(WNT2B):c.877C>T (p.Arg293Cys)	not provided [RCV002975590]	uncertain significance	1	112517316	112517316	Human		name
156111969	CV2171736	single nucleotide variant	NM_024494.3(WNT2B):c.760G>A (p.Ala254Thr)	not provided [RCV003038982]	uncertain significance	1	112517199	112517199	Human		name
156105367	CV2180926	single nucleotide variant	NM_024494.3(WNT2B):c.929T>A (p.Val310Asp)	not provided [RCV003054878]	uncertain significance	1	112517368	112517368	Human		name
156186132	CV2232615	single nucleotide variant	NM_024494.3(WNT2B):c.602C>T (p.Ala201Val)	not specified [RCV004101290]	uncertain significance	1	112516338	112516338	Human		name
155900929	CV2298087	single nucleotide variant	NM_024494.3(WNT2B):c.551A>C (p.Asp184Ala)	not specified [RCV004157975]	uncertain significance	1	112516287	112516287	Human		name
156348592	CV2312878	single nucleotide variant	NM_024494.3(WNT2B):c.692G>C (p.Arg231Pro)	not specified [RCV004171369]	uncertain significance	1	112517131	112517131	Human		name
329398058	CV2464737	single nucleotide variant	NM_024494.3(WNT2B):c.994A>G (p.Thr332Ala)	not specified [RCV004284702]	uncertain significance	1	112520327	112520327	Human		name
11525772	CV246859	single nucleotide variant	NM_024494.3(WNT2B):c.313C>T (p.Arg105Ter)	Diarrhea 9 [RCV000714964]\|not specified [RCV000238850]	pathogenic\|uncertain significance	1	112515004	112515004	Human	1	name
402475528	CV2863842	single nucleotide variant	NM_024494.3(WNT2B):c.914C>T (p.Ser305Phe)	not provided [RCV003543306]	uncertain significance	1	112517353	112517353	Human		name
405127594	CV2958533	single nucleotide variant	NM_024494.3(WNT2B):c.799C>T (p.Arg267Ter)	not provided [RCV003668006]	pathogenic	1	112517238	112517238	Human		name
405148558	CV2962832	single nucleotide variant	NM_024494.3(WNT2B):c.745C>T (p.Arg249Cys)	not provided [RCV003673761]	uncertain significance	1	112517184	112517184	Human		name
405812136	CV3352931	single nucleotide variant	NM_024494.3(WNT2B):c.314G>A (p.Arg105Gln)	not specified [RCV004483131]	uncertain significance	1	112515005	112515005	Human		name
405812138	CV3352932	single nucleotide variant	NM_024494.3(WNT2B):c.668G>A (p.Arg223His)	not specified [RCV004483132]	uncertain significance	1	112516404	112516404	Human		name
405812141	CV3352934	single nucleotide variant	NM_024494.3(WNT2B):c.967C>T (p.Arg323Cys)	not specified [RCV004483134]	uncertain significance	1	112520300	112520300	Human		name
405812143	CV3352935	single nucleotide variant	NM_024494.3(WNT2B):c.983C>T (p.Thr328Ile)	not specified [RCV004483135]	uncertain significance	1	112520316	112520316	Human		name
407465501	CV3487982	single nucleotide variant	NM_024494.3(WNT2B):c.491G>T (p.Ser164Ile)	not specified [RCV004688785]	uncertain significance	1	112516227	112516227	Human		name
407524826	CV3487983	single nucleotide variant	NM_024494.3(WNT2B):c.962C>T (p.Ala321Val)	not specified [RCV004678572]	uncertain significance	1	112520295	112520295	Human		name
597800005	CV3624219	single nucleotide variant	NM_024494.3(WNT2B):c.668G>T (p.Arg223Leu)	not specified [RCV004879977]	uncertain significance	1	112516404	112516404	Human		name
597800006	CV3624220	single nucleotide variant	NM_024494.3(WNT2B):c.638C>T (p.Ala213Val)	not specified [RCV004879978]	uncertain significance	1	112516374	112516374	Human		name
597741009	CV3624221	single nucleotide variant	NM_024494.3(WNT2B):c.803G>A (p.Arg268His)	not specified [RCV004890666]	uncertain significance	1	112517242	112517242	Human		name
597942142	CV3785952	single nucleotide variant	NM_024494.3(WNT2B):c.544G>A (p.Asp182Asn)	not provided [RCV005133845]	uncertain significance	1	112516280	112516280	Human		name
597939201	CV3818587	single nucleotide variant	NM_024494.3(WNT2B):c.769G>T (p.Asp257Tyr)	not provided [RCV005158593]	uncertain significance	1	112517208	112517208	Human		name
598192258	CV3937173	single nucleotide variant	NM_024494.3(WNT2B):c.379G>A (p.Val127Ile)	not specified [RCV005288491]	uncertain significance	1	112515070	112515070	Human		name
598192266	CV3937174	single nucleotide variant	NM_024494.3(WNT2B):c.758G>A (p.Arg253His)	not specified [RCV005288492]	uncertain significance	1	112517197	112517197	Human		name
598275515	CV3937177	single nucleotide variant	NM_024494.3(WNT2B):c.568G>A (p.Asp190Asn)	not specified [RCV005304649]	uncertain significance	1	112516304	112516304	Human		name
8624647	CV79760	single nucleotide variant	NM_024494.2(WNT2B):c.619G>A (p.Glu207Lys)	Malignant melanoma [RCV000059836]	not provided	1	112516355	112516355	Human		name
40886480	CV972508	single nucleotide variant	NM_024494.3(WNT2B):c.722G>A (p.Gly241Asp)	Diarrhea 9 [RCV004998783]\|not provided [RCV001264390]	likely pathogenic\|uncertain significance	1	112517161	112517161	Human	1	name
156315583	CV1907358	single nucleotide variant	NM_024494.3(WNT2B):c.1000G>A (p.Gly334Ser)	not provided [RCV003088701]	uncertain significance	1	112520333	112520333	Human		name
156189227	CV2030191	single nucleotide variant	NM_024494.3(WNT2B):c.1052G>A (p.Arg351His)	not provided [RCV002765857]	uncertain significance	1	112520385	112520385	Human		name
156081538	CV2098696	single nucleotide variant	NM_024494.3(WNT2B):c.1126G>A (p.Val376Ile)	not provided [RCV002912720]	uncertain significance	1	112520459	112520459	Human		name
156224197	CV2121726	single nucleotide variant	NM_024494.3(WNT2B):c.1142C>T (p.Ala381Val)	not provided [RCV002958264]	uncertain significance	1	112520475	112520475	Human		name
156002087	CV2179150	single nucleotide variant	NM_024494.3(WNT2B):c.1172C>A (p.Thr391Asn)	not provided [RCV003034826]	uncertain significance	1	112520505	112520505	Human		name
156205621	CV2311427	single nucleotide variant	NM_024494.3(WNT2B):c.1159T>C (p.Trp387Arg)	not specified [RCV004168274]	uncertain significance	1	112520492	112520492	Human		name
401718193	CV2700216	single nucleotide variant	NM_024494.3(WNT2B):c.1033G>A (p.Asp345Asn)	not specified [RCV004310890]	uncertain significance	1	112520366	112520366	Human		name
405812134	CV3352930	single nucleotide variant	NM_024494.3(WNT2B):c.1097G>A (p.Arg366Gln)	not specified [RCV004483130]	uncertain significance	1	112520430	112520430	Human		name
597863722	CV3814071	single nucleotide variant	NM_024494.3(WNT2B):c.1088G>A (p.Cys363Tyr)	not provided [RCV005147140]	uncertain significance	1	112520421	112520421	Human		name
597875926	CV3829759	single nucleotide variant	NM_024494.3(WNT2B):c.1058C>A (p.Thr353Asn)	not provided [RCV005177467]	uncertain significance	1	112520391	112520391	Human		name
156323404	CV2067775	microsatellite	NM_024494.3(WNT2B):c.139CTG[5] (p.Leu50_Thr51insLeu)	not provided [RCV002834855]	uncertain significance	1	112509400	112509401	Human		name

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