Tex2 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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210 records found for search term Tex2

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
329374516	CV2430925	single nucleotide variant	NM_001288732.2(TEX2):c.46C>T (p.Pro16Ser)	not specified [RCV004248526]	uncertain significance	17	64214172	64214172	Human		name
401720087	CV2675770	single nucleotide variant	NM_001288732.2(TEX2):c.43A>G (p.Met15Val)	not specified [RCV004288012]	uncertain significance	17	64214175	64214175	Human		name
616940103	CV4014593	single nucleotide variant	NM_001288732.2(TEX2):c.531C>T (p.Ala177=)	not provided [RCV005414087]	likely benign	17	64213687	64213687	Human		name
156271753	CV2286468	single nucleotide variant	NM_001288732.2(TEX2):c.256G>A (p.Ala86Thr)	not specified [RCV004139976]	likely benign	17	64213962	64213962	Human		name
329397735	CV2456528	single nucleotide variant	NM_001288732.2(TEX2):c.296C>T (p.Ser99Phe)	not specified [RCV004275668]	uncertain significance	17	64213922	64213922	Human		name
401740824	CV2679812	single nucleotide variant	NM_001288732.2(TEX2):c.127G>A (p.Glu43Lys)	not specified [RCV004282273]	uncertain significance	17	64214091	64214091	Human		name
405782717	CV3342569	single nucleotide variant	NM_001288732.2(TEX2):c.272C>T (p.Ser91Leu)	not specified [RCV004472245]	uncertain significance	17	64213946	64213946	Human		name
156335652	CV2228422	single nucleotide variant	NM_001288732.2(TEX2):c.337A>C (p.Thr113Pro)	not specified [RCV004098397]	uncertain significance	17	64213881	64213881	Human		name
156268702	CV2239992	single nucleotide variant	NM_001288732.2(TEX2):c.940G>A (p.Gly314Ser)	not specified [RCV004110782]	uncertain significance	17	64213278	64213278	Human		name
156295268	CV2297454	single nucleotide variant	NM_001288732.2(TEX2):c.889G>A (p.Val297Ile)	not specified [RCV004153389]	uncertain significance	17	64213329	64213329	Human		name
156019996	CV2302049	single nucleotide variant	NM_001288732.2(TEX2):c.394T>A (p.Leu132Met)	not specified [RCV004158812]	uncertain significance	17	64213824	64213824	Human		name
156061667	CV2320223	single nucleotide variant	NM_001288732.2(TEX2):c.622G>A (p.Ala208Thr)	not specified [RCV004169843]	uncertain significance	17	64213596	64213596	Human		name
329398717	CV2471303	single nucleotide variant	NM_001288732.2(TEX2):c.634C>T (p.His212Tyr)	not specified [RCV004280320]	uncertain significance	17	64213584	64213584	Human		name
401719284	CV2679481	single nucleotide variant	NM_001288732.2(TEX2):c.846A>C (p.Glu282Asp)	not specified [RCV004287786]	uncertain significance	17	64213372	64213372	Human		name
401767438	CV2681663	single nucleotide variant	NM_001288732.2(TEX2):c.415T>A (p.Ser139Thr)	not specified [RCV004294218]	uncertain significance	17	64213803	64213803	Human		name
401777621	CV2704201	single nucleotide variant	NM_001288732.2(TEX2):c.757C>G (p.Pro253Ala)	not specified [RCV004311205]	uncertain significance	17	64213461	64213461	Human		name
401778796	CV2705679	single nucleotide variant	NM_001288732.2(TEX2):c.497C>G (p.Ser166Cys)	not specified [RCV004318532]	uncertain significance	17	64213721	64213721	Human		name
401895002	CV2792669	single nucleotide variant	NM_001288732.2(TEX2):c.514A>G (p.Ile172Val)	not specified [RCV004365452]	likely benign	17	64213704	64213704	Human		name
405782740	CV3342573	single nucleotide variant	NM_001288732.2(TEX2):c.364C>G (p.Pro122Ala)	not specified [RCV004472249]	uncertain significance	17	64213854	64213854	Human		name
407519914	CV3482521	single nucleotide variant	NM_001288732.2(TEX2):c.440C>T (p.Ser147Phe)	not specified [RCV004676753]	uncertain significance	17	64213778	64213778	Human		name
597751098	CV3619760	single nucleotide variant	NM_001288732.2(TEX2):c.824G>T (p.Arg275Leu)	not specified [RCV004866851]	uncertain significance	17	64213394	64213394	Human		name
598182889	CV3916967	single nucleotide variant	NM_001288732.2(TEX2):c.938G>A (p.Ser313Asn)	not specified [RCV005287016]	uncertain significance	17	64213280	64213280	Human		name
598182895	CV3916968	single nucleotide variant	NM_001288732.2(TEX2):c.679C>T (p.Arg227Trp)	not specified [RCV005287017]	uncertain significance	17	64213539	64213539	Human		name
598182913	CV3916974	single nucleotide variant	NM_001288732.2(TEX2):c.536C>T (p.Thr179Ile)	not specified [RCV005287020]	uncertain significance	17	64213682	64213682	Human		name
598182926	CV3916976	single nucleotide variant	NM_001288732.2(TEX2):c.341T>G (p.Val114Gly)	not specified [RCV005287022]	uncertain significance	17	64213877	64213877	Human		name
156225275	CV2226144	single nucleotide variant	NM_001288732.2(TEX2):c.1438A>G (p.Ile480Val)	not specified [RCV004105550]	uncertain significance	17	64212780	64212780	Human		name
156020442	CV2230360	single nucleotide variant	NM_001288732.2(TEX2):c.1471C>G (p.Leu491Val)	not specified [RCV004099957]	uncertain significance	17	64212747	64212747	Human		name
156027121	CV2242417	single nucleotide variant	NM_001288732.2(TEX2):c.2486G>C (p.Gly829Ala)	not specified [RCV004111417]	uncertain significance	17	64177410	64177410	Human		name
156194648	CV2251756	single nucleotide variant	NM_001288732.2(TEX2):c.1789C>T (p.Pro597Ser)	not specified [RCV004119752]	uncertain significance	17	64194951	64194951	Human		name
155925645	CV2258588	single nucleotide variant	NM_001288732.2(TEX2):c.1034G>C (p.Ser345Thr)	not specified [RCV004116064]	uncertain significance	17	64213184	64213184	Human		name
156018130	CV2263116	single nucleotide variant	NM_001288732.2(TEX2):c.2732A>G (p.Lys911Arg)	not specified [RCV004131358]	uncertain significance	17	64160873	64160873	Human		name
156282980	CV2288864	single nucleotide variant	NM_001288732.2(TEX2):c.1396G>A (p.Val466Met)	not specified [RCV004148060]	uncertain significance	17	64212822	64212822	Human		name
156150125	CV2289604	single nucleotide variant	NM_001288732.2(TEX2):c.1874G>A (p.Arg625Gln)	not specified [RCV004148529]	uncertain significance	17	64193861	64193861	Human		name
155909935	CV2303490	single nucleotide variant	NM_001288732.2(TEX2):c.1595G>A (p.Arg532Gln)	not specified [RCV004161596]	likely benign	17	64212623	64212623	Human		name
156294400	CV2306409	single nucleotide variant	NM_001288732.2(TEX2):c.1984G>A (p.Ala662Thr)	not specified [RCV004156756]	uncertain significance	17	64193751	64193751	Human		name
156101973	CV2313525	single nucleotide variant	NM_001288732.2(TEX2):c.1348G>A (p.Ala450Thr)	not specified [RCV004163825]	uncertain significance	17	64212870	64212870	Human		name
156201154	CV2338371	single nucleotide variant	NM_001288732.2(TEX2):c.1139T>C (p.Ile380Thr)	not specified [RCV004186420]	uncertain significance	17	64213079	64213079	Human		name
329374944	CV2440148	single nucleotide variant	NM_001288732.2(TEX2):c.1256G>T (p.Cys419Phe)	not specified [RCV004260606]	uncertain significance	17	64212962	64212962	Human		name
329401602	CV2457201	single nucleotide variant	NM_001288732.2(TEX2):c.1330C>G (p.Leu444Val)	not specified [RCV004265281]	uncertain significance	17	64212888	64212888	Human		name
401751949	CV2672630	single nucleotide variant	NM_001288732.2(TEX2):c.2135C>T (p.Ser712Leu)	not specified [RCV004287656]	uncertain significance	17	64193600	64193600	Human		name
401753467	CV2684950	single nucleotide variant	NM_001288732.2(TEX2):c.2325C>G (p.Asp775Glu)	not specified [RCV004296450]	uncertain significance	17	64188267	64188267	Human		name
401772236	CV2687458	single nucleotide variant	NM_001288732.2(TEX2):c.1488T>G (p.Ser496Arg)	not specified [RCV004300701]	uncertain significance	17	64212730	64212730	Human		name
401773198	CV2698129	single nucleotide variant	NM_001288732.2(TEX2):c.2923G>C (p.Ala975Pro)	not specified [RCV004302913]	uncertain significance	17	64154849	64154849	Human		name
401758146	CV2704200	single nucleotide variant	NM_001288732.2(TEX2):c.1092C>G (p.Ile364Met)	not specified [RCV004311204]	uncertain significance	17	64213126	64213126	Human		name
401887218	CV2773241	single nucleotide variant	NM_001288732.2(TEX2):c.1078A>G (p.Ser360Gly)	not specified [RCV004353917]	uncertain significance	17	64213140	64213140	Human		name
401888027	CV2781853	single nucleotide variant	NM_001288732.2(TEX2):c.1907G>T (p.Cys636Phe)	not specified [RCV004356800]	uncertain significance	17	64193828	64193828	Human		name
405782623	CV3342554	single nucleotide variant	NM_001288732.2(TEX2):c.1279G>T (p.Asp427Tyr)	not specified [RCV004472230]	uncertain significance	17	64212939	64212939	Human		name
405782629	CV3342555	single nucleotide variant	NM_001288732.2(TEX2):c.1289C>T (p.Thr430Met)	not specified [RCV004472231]	likely benign	17	64212929	64212929	Human		name
405782634	CV3342556	single nucleotide variant	NM_001288732.2(TEX2):c.1302T>A (p.Ser434Arg)	not specified [RCV004472232]	uncertain significance	17	64212916	64212916	Human		name
405782640	CV3342557	single nucleotide variant	NM_001288732.2(TEX2):c.1823T>C (p.Ile608Thr)	not specified [RCV004472233]	uncertain significance	17	64194917	64194917	Human		name
405782647	CV3342558	single nucleotide variant	NM_001288732.2(TEX2):c.2018G>A (p.Arg673His)	not specified [RCV004472234]	likely benign	17	64193717	64193717	Human		name
405782655	CV3342559	single nucleotide variant	NM_001288732.2(TEX2):c.2035A>G (p.Arg679Gly)	not specified [RCV004472235]	uncertain significance	17	64193700	64193700	Human		name
405782660	CV3342560	single nucleotide variant	NM_001288732.2(TEX2):c.2120C>A (p.Ala707Glu)	not specified [RCV004472236]	uncertain significance	17	64193615	64193615	Human		name
405782667	CV3342561	single nucleotide variant	NM_001288732.2(TEX2):c.2210C>T (p.Pro737Leu)	not specified [RCV004472237]	uncertain significance	17	64188382	64188382	Human		name
405782675	CV3342562	single nucleotide variant	NM_001288732.2(TEX2):c.2215G>A (p.Gly739Arg)	not specified [RCV004472238]	uncertain significance	17	64188377	64188377	Human		name
405782681	CV3342563	single nucleotide variant	NM_001288732.2(TEX2):c.2225C>T (p.Thr742Ile)	not specified [RCV004472239]	uncertain significance	17	64188367	64188367	Human		name
405782686	CV3342564	single nucleotide variant	NM_001288732.2(TEX2):c.2332G>A (p.Val778Met)	not specified [RCV004472240]	uncertain significance	17	64188260	64188260	Human		name
405782693	CV3342565	single nucleotide variant	NM_001288732.2(TEX2):c.2407C>T (p.Pro803Ser)	not specified [RCV004472241]	uncertain significance	17	64188185	64188185	Human		name
405782706	CV3342567	single nucleotide variant	NM_001288732.2(TEX2):c.2608C>A (p.Leu870Ile)	not specified [RCV004472243]	uncertain significance	17	64171163	64171163	Human		name
405782713	CV3342568	single nucleotide variant	NM_001288732.2(TEX2):c.2683G>A (p.Asp895Asn)	not specified [RCV004472244]	uncertain significance	17	64160922	64160922	Human		name
407519905	CV3482512	single nucleotide variant	NM_001288732.2(TEX2):c.2233C>T (p.Arg745Cys)	not specified [RCV004676749]	uncertain significance	17	64188359	64188359	Human		name
407518563	CV3482513	single nucleotide variant	NM_001288732.2(TEX2):c.2596A>G (p.Thr866Ala)	not specified [RCV004676036]	uncertain significance	17	64171175	64171175	Human		name
407518571	CV3482516	single nucleotide variant	NM_001288732.2(TEX2):c.1417G>A (p.Val473Met)	not specified [RCV004676039]	uncertain significance	17	64212801	64212801	Human		name
407518575	CV3482517	single nucleotide variant	NM_001288732.2(TEX2):c.2791A>G (p.Ile931Val)	not specified [RCV004676040]	uncertain significance	17	64160814	64160814	Human		name
407519908	CV3482518	single nucleotide variant	NM_001288732.2(TEX2):c.1770G>C (p.Arg590Ser)	not specified [RCV004676750]	uncertain significance	17	64194970	64194970	Human		name
407519910	CV3482519	single nucleotide variant	NM_001288732.2(TEX2):c.1109C>T (p.Pro370Leu)	not specified [RCV004676751]	uncertain significance	17	64213109	64213109	Human		name
407519912	CV3482520	single nucleotide variant	NM_001288732.2(TEX2):c.1278C>A (p.Phe426Leu)	not specified [RCV004676752]	uncertain significance	17	64212940	64212940	Human		name
597751053	CV3619750	single nucleotide variant	NM_001288732.2(TEX2):c.1252T>C (p.Phe418Leu)	not specified [RCV004866841]	uncertain significance	17	64212966	64212966	Human		name
597751062	CV3619752	single nucleotide variant	NM_001288732.2(TEX2):c.2935G>A (p.Val979Ile)	not specified [RCV004866843]	uncertain significance	17	64153150	64153150	Human		name
597751066	CV3619753	single nucleotide variant	NM_001288732.2(TEX2):c.1028A>G (p.Asn343Ser)	not specified [RCV004866844]	uncertain significance	17	64213190	64213190	Human		name
597751071	CV3619754	single nucleotide variant	NM_001288732.2(TEX2):c.1477C>G (p.His493Asp)	not specified [RCV004866845]	likely benign	17	64212741	64212741	Human		name
597751075	CV3619755	single nucleotide variant	NM_001288732.2(TEX2):c.1534G>A (p.Val512Met)	not specified [RCV004866846]	likely benign	17	64212684	64212684	Human		name
597751080	CV3619756	single nucleotide variant	NM_001288732.2(TEX2):c.2301C>A (p.Ser767Arg)	not specified [RCV004866847]	uncertain significance	17	64188291	64188291	Human		name
597751084	CV3619757	single nucleotide variant	NM_001288732.2(TEX2):c.2345G>C (p.Arg782Thr)	not specified [RCV004866848]	uncertain significance	17	64188247	64188247	Human		name
597751089	CV3619758	single nucleotide variant	NM_001288732.2(TEX2):c.2351T>C (p.Val784Ala)	not specified [RCV004866849]	uncertain significance	17	64188241	64188241	Human		name
597751093	CV3619759	single nucleotide variant	NM_001288732.2(TEX2):c.2902G>A (p.Asp968Asn)	not specified [RCV004866850]	uncertain significance	17	64154870	64154870	Human		name
598182901	CV3916969	single nucleotide variant	NM_001288732.2(TEX2):c.1157A>G (p.Gln386Arg)	not specified [RCV005287018]	uncertain significance	17	64213061	64213061	Human		name
598165573	CV3916972	single nucleotide variant	NM_001288732.2(TEX2):c.2659G>A (p.Val887Ile)	not specified [RCV005283474]	uncertain significance	17	64171112	64171112	Human		name
598182907	CV3916973	single nucleotide variant	NM_001288732.2(TEX2):c.2032A>G (p.Thr678Ala)	not specified [RCV005287019]	uncertain significance	17	64193703	64193703	Human		name
598182919	CV3916975	single nucleotide variant	NM_001288732.2(TEX2):c.1979C>A (p.Pro660Gln)	not specified [RCV005287021]	uncertain significance	17	64193756	64193756	Human		name
598165580	CV3916978	single nucleotide variant	NM_001288732.2(TEX2):c.1826A>G (p.Tyr609Cys)	not specified [RCV005283475]	uncertain significance	17	64194914	64194914	Human		name
156374652	CV2194707	single nucleotide variant	NM_001288732.2(TEX2):c.3352G>T (p.Asp1118Tyr)	not specified [RCV004075264]	uncertain significance	17	64149001	64149001	Human		name
401880789	CV2789381	single nucleotide variant	NM_001288732.2(TEX2):c.3271G>A (p.Val1091Ile)	not specified [RCV004365693]	uncertain significance	17	64149082	64149082	Human		name
405782723	CV3342570	single nucleotide variant	NM_001288732.2(TEX2):c.3118C>T (p.Pro1040Ser)	not specified [RCV004472246]	uncertain significance	17	64152967	64152967	Human		name
405782729	CV3342571	single nucleotide variant	NM_001288732.2(TEX2):c.3218A>C (p.His1073Pro)	not specified [RCV004472247]	uncertain significance	17	64150884	64150884	Human		name
407518565	CV3482514	single nucleotide variant	NM_001288732.2(TEX2):c.3218A>T (p.His1073Leu)	not specified [RCV004676037]	uncertain significance	17	64150884	64150884	Human		name
407518568	CV3482515	single nucleotide variant	NM_001288732.2(TEX2):c.3329G>A (p.Arg1110His)	not specified [RCV004676038]	uncertain significance	17	64149024	64149024	Human		name
598182883	CV3916966	single nucleotide variant	NM_001288732.2(TEX2):c.3152G>A (p.Arg1051Gln)	not specified [RCV005287015]	uncertain significance	17	64150950	64150950	Human		name
598165562	CV3916970	single nucleotide variant	NM_001288732.2(TEX2):c.3103G>A (p.Ala1035Thr)	not specified [RCV005283472]	uncertain significance	17	64152982	64152982	Human		name
598182931	CV3916977	single nucleotide variant	NM_001288732.2(TEX2):c.3164A>T (p.His1055Leu)	not specified [RCV005287023]	uncertain significance	17	64150938	64150938	Human		name
401929708	CV2813799	single nucleotide variant	NM_152325.3(TEX26):c.39C>T (p.Leu13=)	not provided [RCV003390350]	likely benign	13	30932754	30932754	Human		name
155966955	CV2261109	single nucleotide variant	NM_152325.3(TEX26):c.16C>A (p.Pro6Thr)	not specified [RCV004128010]	uncertain significance	13	30932731	30932731	Human		name
156096825	CV2375471	single nucleotide variant	NM_015926.6(TEX264):c.5C>G (p.Ser2Trp)	not specified [RCV004225982]	uncertain significance	3	51674309	51674309	Human		name
156291062	CV2226272	single nucleotide variant	NM_152325.3(TEX26):c.69C>A (p.Asp23Glu)	not specified [RCV004099515]	uncertain significance	13	30939701	30939701	Human		name
329380390	CV2466595	single nucleotide variant	NM_152325.3(TEX26):c.94A>G (p.Thr32Ala)	not specified [RCV004274123]	uncertain significance	13	30939726	30939726	Human		name
405782888	CV3342597	single nucleotide variant	NM_152324.3(TEX29):c.37C>A (p.His13Asn)	not specified [RCV004472273]	uncertain significance	13	111320927	111320927	Human		name
156166082	CV2200876	single nucleotide variant	NM_152324.3(TEX29):c.110G>A (p.Arg37Gln)	not specified [RCV004081499]	uncertain significance	13	111328234	111328234	Human		name
156382324	CV2227302	single nucleotide variant	NM_152324.3(TEX29):c.181G>C (p.Val61Leu)	not specified [RCV004091855]	uncertain significance	13	111339874	111339874	Human		name
156240676	CV2231296	single nucleotide variant	NM_152325.3(TEX26):c.226T>A (p.Tyr76Asn)	not specified [RCV004096404]	uncertain significance	13	30952739	30952739	Human		name
155990079	CV2285204	single nucleotide variant	NM_152325.3(TEX26):c.281G>A (p.Gly94Glu)	not specified [RCV004145411]	uncertain significance	13	30952794	30952794	Human		name
156176989	CV2327147	single nucleotide variant	NM_152325.3(TEX26):c.154G>A (p.Gly52Ser)	not specified [RCV004178711]	likely benign	13	30952667	30952667	Human		name
156081766	CV2333855	single nucleotide variant	NM_015926.6(TEX264):c.29T>C (p.Ile10Thr)	not specified [RCV004181353]	uncertain significance	3	51674333	51674333	Human		name
156053729	CV2361092	single nucleotide variant	NM_152324.3(TEX29):c.161C>T (p.Ala54Val)	not specified [RCV004216286]	uncertain significance	13	111328285	111328285	Human		name
156158927	CV2361402	single nucleotide variant	NM_152324.3(TEX29):c.145G>A (p.Val49Ile)	not specified [RCV004221051]	uncertain significance	13	111328269	111328269	Human		name
156149246	CV2394560	single nucleotide variant	NM_152324.3(TEX29):c.139G>A (p.Glu47Lys)	not specified [RCV004240913]	likely benign	13	111328263	111328263	Human		name
401745263	CV2693218	single nucleotide variant	NM_152324.3(TEX29):c.208G>A (p.Ala70Thr)	not specified [RCV004295193]	uncertain significance	13	111339901	111339901	Human		name
401762361	CV2723412	single nucleotide variant	NM_152325.3(TEX26):c.209C>G (p.Thr70Arg)	not specified [RCV004329617]	uncertain significance	13	30952722	30952722	Human		name
405782763	CV3342577	single nucleotide variant	NM_152325.3(TEX26):c.149A>G (p.Gln50Arg)	not specified [RCV004472253]	uncertain significance	13	30952662	30952662	Human		name
405782822	CV3342587	single nucleotide variant	NM_144582.3(TEX261):c.29T>C (p.Leu10Pro)	not specified [RCV004472263]	uncertain significance	2	70994729	70994729	Human		name
405782828	CV3342588	single nucleotide variant	NM_144582.3(TEX261):c.64G>A (p.Ala22Thr)	not specified [RCV004472264]	uncertain significance	2	70994694	70994694	Human		name
405782868	CV3342594	single nucleotide variant	NM_152324.3(TEX29):c.209C>G (p.Ala70Gly)	not specified [RCV004472270]	uncertain significance	13	111339902	111339902	Human		name
405782875	CV3342595	single nucleotide variant	NM_152324.3(TEX29):c.245T>C (p.Ile82Thr)	not specified [RCV004472271]	uncertain significance	13	111342761	111342761	Human		name
407518597	CV3482532	single nucleotide variant	NM_152324.3(TEX29):c.287C>T (p.Ala96Val)	not specified [RCV004676048]	uncertain significance	13	111342803	111342803	Human		name
597751144	CV3619770	single nucleotide variant	NM_152325.3(TEX26):c.134C>T (p.Pro45Leu)	not specified [RCV004866861]	uncertain significance	13	30939766	30939766	Human		name
597751162	CV3619774	single nucleotide variant	NM_144582.3(TEX261):c.34C>G (p.Leu12Val)	not specified [RCV004866865]	uncertain significance	2	70994724	70994724	Human		name
597751210	CV3619784	single nucleotide variant	NM_152324.3(TEX29):c.116A>G (p.Gln39Arg)	not specified [RCV004866875]	uncertain significance	13	111328240	111328240	Human		name
597795062	CV3619786	single nucleotide variant	NM_152324.3(TEX29):c.289C>A (p.Leu97Met)	not specified [RCV004878062]	uncertain significance	13	111342805	111342805	Human		name
597751219	CV3619787	single nucleotide variant	NM_152324.3(TEX29):c.179A>T (p.His60Leu)	not specified [RCV004866877]	uncertain significance	13	111339872	111339872	Human		name
598182973	CV3916985	single nucleotide variant	NM_015926.6(TEX264):c.59C>T (p.Thr20Met)	not specified [RCV005287029]	uncertain significance	3	51674363	51674363	Human		name
598182980	CV3916986	single nucleotide variant	NM_015926.6(TEX264):c.43C>T (p.Leu15Phe)	not specified [RCV005287030]	uncertain significance	3	51674347	51674347	Human		name
598165592	CV3916987	single nucleotide variant	NM_152324.3(TEX29):c.103A>G (p.Arg35Gly)	not specified [RCV005283477]	uncertain significance	13	111328227	111328227	Human		name
598182993	CV3916989	single nucleotide variant	NM_152324.3(TEX29):c.191C>G (p.Ala64Gly)	not specified [RCV005287032]	uncertain significance	13	111339884	111339884	Human		name
156373780	CV2201423	single nucleotide variant	NM_015926.6(TEX264):c.161T>C (p.Met54Thr)	not specified [RCV004079584]	uncertain significance	3	51674465	51674465	Human		name
156076003	CV2251216	single nucleotide variant	NM_144582.3(TEX261):c.207G>A (p.Met69Ile)	not specified [RCV004115441]	uncertain significance	2	70991927	70991927	Human		name
156064082	CV2272407	single nucleotide variant	NM_144582.3(TEX261):c.160G>T (p.Ala54Ser)	not specified [RCV004133330]	uncertain significance	2	70991974	70991974	Human		name
156041062	CV2279168	single nucleotide variant	NM_144582.3(TEX261):c.119C>T (p.Ala40Val)	not specified [RCV004139404]	uncertain significance	2	70993727	70993727	Human		name
156202905	CV2300682	single nucleotide variant	NM_152325.3(TEX26):c.755A>G (p.Asn252Ser)	not specified [RCV004155624]	uncertain significance	13	30968993	30968993	Human		name
156189397	CV2302950	single nucleotide variant	NM_152325.3(TEX26):c.389C>T (p.Ala130Val)	not specified [RCV004162828]	uncertain significance	13	30956949	30956949	Human		name
156303019	CV2308167	single nucleotide variant	NM_152325.3(TEX26):c.394A>G (p.Met132Val)	not specified [RCV004164674]	uncertain significance	13	30956954	30956954	Human		name
156395290	CV2325398	single nucleotide variant	NM_015926.6(TEX264):c.166C>A (p.Leu56Ile)	not specified [RCV004177764]	uncertain significance	3	51674470	51674470	Human		name
156135541	CV2347297	single nucleotide variant	NM_015926.6(TEX264):c.134A>G (p.Asn45Ser)	not specified [RCV004206776]	uncertain significance	3	51674438	51674438	Human		name
155935390	CV2371790	single nucleotide variant	NM_144582.3(TEX261):c.170T>C (p.Ile57Thr)	not specified [RCV004219451]	uncertain significance	2	70991964	70991964	Human		name
329382076	CV2438420	single nucleotide variant	NM_015926.6(TEX264):c.121C>T (p.Pro41Ser)	not specified [RCV004259575]	uncertain significance	3	51674425	51674425	Human		name
329373701	CV2452616	single nucleotide variant	NM_152325.3(TEX26):c.452T>C (p.Phe151Ser)	not specified [RCV004275190]	uncertain significance	13	30957012	30957012	Human		name
401737466	CV2679888	single nucleotide variant	NM_015926.6(TEX264):c.283G>T (p.Ala95Ser)	not specified [RCV004284176]	uncertain significance	3	51684437	51684437	Human		name
401773539	CV2716605	single nucleotide variant	NM_152325.3(TEX26):c.697C>G (p.Gln233Glu)	not specified [RCV004327676]	uncertain significance	13	30968935	30968935	Human		name
401767603	CV2727217	single nucleotide variant	NM_152325.3(TEX26):c.421A>T (p.Asn141Tyr)	not specified [RCV004327347]	uncertain significance	13	30956981	30956981	Human		name
401892973	CV2758316	single nucleotide variant	NM_152325.3(TEX26):c.434C>T (p.Ser145Phe)	not specified [RCV004341669]	uncertain significance	13	30956994	30956994	Human		name
405782769	CV3342578	single nucleotide variant	NM_152325.3(TEX26):c.403G>A (p.Val135Ile)	not specified [RCV004472254]	uncertain significance	13	30956963	30956963	Human		name
405782775	CV3342579	single nucleotide variant	NM_152325.3(TEX26):c.499T>A (p.Ser167Thr)	not specified [RCV004472255]	uncertain significance	13	30966251	30966251	Human		name
405782780	CV3342580	single nucleotide variant	NM_152325.3(TEX26):c.505G>C (p.Glu169Gln)	not specified [RCV004472256]	uncertain significance	13	30966257	30966257	Human		name
405782786	CV3342581	single nucleotide variant	NM_152325.3(TEX26):c.548G>A (p.Arg183Gln)	not specified [RCV004472257]	uncertain significance	13	30966300	30966300	Human		name
405782792	CV3342582	single nucleotide variant	NM_152325.3(TEX26):c.707A>T (p.Tyr236Phe)	not specified [RCV004472258]	uncertain significance	13	30968945	30968945	Human		name
405782798	CV3342583	single nucleotide variant	NM_152325.3(TEX26):c.721G>A (p.Asp241Asn)	not specified [RCV004472259]	uncertain significance	13	30968959	30968959	Human		name
405782805	CV3342584	single nucleotide variant	NM_152325.3(TEX26):c.767C>A (p.Ser256Tyr)	not specified [RCV004472260]	uncertain significance	13	30969005	30969005	Human		name
405782811	CV3342585	single nucleotide variant	NM_144582.3(TEX261):c.235G>A (p.Val79Ile)	not specified [RCV004472261]	uncertain significance	2	70991899	70991899	Human		name
405782835	CV3342589	single nucleotide variant	NM_015926.6(TEX264):c.232G>A (p.Ala78Thr)	not specified [RCV004472265]	uncertain significance	3	51674536	51674536	Human		name
405782881	CV3342596	single nucleotide variant	NM_152324.3(TEX29):c.308A>G (p.Glu103Gly)	not specified [RCV004472272]	uncertain significance	13	111342824	111342824	Human		name
405782895	CV3342598	single nucleotide variant	NM_152324.3(TEX29):c.439G>A (p.Glu147Lys)	not specified [RCV004472274]	uncertain significance	13	111344106	111344106	Human		name
407519916	CV3482524	single nucleotide variant	NM_001195082.2(TEX22):c.20C>G (p.Ser7Cys)	not specified [RCV004676754]	uncertain significance	14	105399360	105399360	Human		name
407518588	CV3482527	single nucleotide variant	NM_152325.3(TEX26):c.427T>C (p.Phe143Leu)	not specified [RCV004676044]	uncertain significance	13	30956987	30956987	Human		name
407518594	CV3482531	single nucleotide variant	NM_015926.6(TEX264):c.103G>A (p.Glu35Lys)	not specified [RCV004676047]	uncertain significance	3	51674407	51674407	Human		name
597751135	CV3619768	single nucleotide variant	NM_152325.3(TEX26):c.520C>A (p.Leu174Ile)	not specified [RCV004866859]	uncertain significance	13	30966272	30966272	Human		name
597751139	CV3619769	single nucleotide variant	NM_152325.3(TEX26):c.546C>G (p.Phe182Leu)	not specified [RCV004866860]	uncertain significance	13	30966298	30966298	Human		name
597751149	CV3619771	single nucleotide variant	NM_152325.3(TEX26):c.431T>C (p.Ile144Thr)	not specified [RCV004866862]	uncertain significance	13	30956991	30956991	Human		name
597751153	CV3619772	single nucleotide variant	NM_152325.3(TEX26):c.590A>T (p.Asp197Val)	not specified [RCV004866863]	uncertain significance	13	30966342	30966342	Human		name
597751167	CV3619775	single nucleotide variant	NM_144582.3(TEX261):c.251T>A (p.Leu84His)	not specified [RCV004866866]	uncertain significance	2	70991883	70991883	Human		name
597751171	CV3619776	single nucleotide variant	NM_144582.3(TEX261):c.158C>T (p.Thr53Ile)	not specified [RCV004866867]	uncertain significance	2	70991976	70991976	Human		name
597751180	CV3619778	single nucleotide variant	NM_015926.6(TEX264):c.200G>A (p.Ser67Asn)	not specified [RCV004866869]	uncertain significance	3	51674504	51674504	Human		name
597751200	CV3619782	single nucleotide variant	NM_015926.6(TEX264):c.136G>A (p.Val46Ile)	not specified [RCV004866873]	likely benign	3	51674440	51674440	Human		name
597751215	CV3619785	single nucleotide variant	NM_152324.3(TEX29):c.334A>C (p.Ser112Arg)	not specified [RCV004866876]	uncertain significance	13	111342850	111342850	Human		name
598182938	CV3916979	single nucleotide variant	NM_001195082.2(TEX22):c.20C>A (p.Ser7Tyr)	not specified [RCV005287024]	uncertain significance	14	105399360	105399360	Human		name
598165586	CV3916983	single nucleotide variant	NM_152325.3(TEX26):c.346C>G (p.Gln116Glu)	not specified [RCV005283476]	uncertain significance	13	30956906	30956906	Human		name
598182965	CV3916984	single nucleotide variant	NM_152325.3(TEX26):c.602A>T (p.Lys201Ile)	not specified [RCV005287028]	uncertain significance	13	30966354	30966354	Human		name
598182986	CV3916988	single nucleotide variant	NM_152324.3(TEX29):c.314C>T (p.Ala105Val)	not specified [RCV005287031]	uncertain significance	13	111342830	111342830	Human		name
13836558	CV587833	single nucleotide variant	NM_001195082.2(TEX22):c.17T>C (p.Leu6Pro)	not provided [RCV000732710]	uncertain significance	14	105399357	105399357	Human		name
15165666	CV725448	single nucleotide variant	NM_152325.3(TEX26):c.693G>T (p.Lys231Asn)	not provided [RCV000882463]	benign\|likely benign	13	30968931	30968931	Human		name
8627437	CV82581	single nucleotide variant	NM_152325.3(TEX26):c.436C>T (p.Leu146Phe)	not specified [RCV004086842]	uncertain significance\|not provided	13	30956996	30956996	Human		name
156087092	CV2258957	single nucleotide variant	NM_015926.6(TEX264):c.704G>A (p.Ser235Asn)	not specified [RCV004120234]	uncertain significance	3	51703778	51703778	Human		name
155970308	CV2262215	single nucleotide variant	NM_015926.6(TEX264):c.391G>A (p.Val131Met)	not specified [RCV004126641]	uncertain significance	3	51684545	51684545	Human		name
156292227	CV2306188	single nucleotide variant	NM_015926.6(TEX264):c.379G>T (p.Ala127Ser)	not provided [RCV004695525]\|not specified [RCV004162934]	uncertain significance	3	51684533	51684533	Human		name
156072446	CV2328787	single nucleotide variant	NM_144582.3(TEX261):c.584T>C (p.Ile195Thr)	not specified [RCV004178012]	uncertain significance	2	70988607	70988607	Human		name
156056291	CV2343462	single nucleotide variant	NM_015926.6(TEX264):c.455A>G (p.His152Arg)	not specified [RCV004197533]	uncertain significance	3	51684609	51684609	Human		name
156185313	CV2346507	single nucleotide variant	NM_144582.3(TEX261):c.434C>T (p.Ser145Leu)	not specified [RCV004206428]	uncertain significance	2	70988956	70988956	Human		name
156096862	CV2375483	single nucleotide variant	NM_015926.6(TEX264):c.382C>T (p.Pro128Ser)	not specified [RCV004225994]	uncertain significance	3	51684536	51684536	Human		name
329390709	CV2437173	single nucleotide variant	NM_015926.6(TEX264):c.808G>A (p.Gly270Ser)	not specified [RCV004262976]	uncertain significance	3	51703882	51703882	Human		name
401732408	CV2678095	single nucleotide variant	NM_015926.6(TEX264):c.922C>T (p.Pro308Ser)	not specified [RCV004296610]	uncertain significance	3	51703996	51703996	Human		name
401752786	CV2720518	single nucleotide variant	NM_015926.6(TEX264):c.671C>T (p.Thr224Met)	not specified [RCV004327922]	uncertain significance	3	51703745	51703745	Human		name
401865395	CV2778740	single nucleotide variant	NM_015926.6(TEX264):c.776G>C (p.Ser259Thr)	not specified [RCV004346649]	uncertain significance	3	51703850	51703850	Human		name
405782841	CV3342590	single nucleotide variant	NM_015926.6(TEX264):c.299T>C (p.Leu100Pro)	not specified [RCV004472266]	uncertain significance	3	51684453	51684453	Human		name
405782847	CV3342591	single nucleotide variant	NM_015926.6(TEX264):c.470C>T (p.Thr157Ile)	not specified [RCV004472267]	uncertain significance	3	51684624	51684624	Human		name
405782854	CV3342592	single nucleotide variant	NM_015926.6(TEX264):c.622G>A (p.Ala208Thr)	not specified [RCV004472268]	uncertain significance	3	51699547	51699547	Human		name
405782861	CV3342593	single nucleotide variant	NM_015926.6(TEX264):c.841G>A (p.Glu281Lys)	not specified [RCV004472269]	uncertain significance	3	51703915	51703915	Human		name
407518591	CV3482528	single nucleotide variant	NM_015926.6(TEX264):c.485G>A (p.Arg162Gln)	not specified [RCV004676045]	uncertain significance	3	51699410	51699410	Human		name
407519921	CV3482530	single nucleotide variant	NM_015926.6(TEX264):c.371C>T (p.Ser124Phe)	not specified [RCV004676756]	uncertain significance	3	51684525	51684525	Human		name
597751120	CV3619765	single nucleotide variant	NM_001195082.2(TEX22):c.32A>G (p.Lys11Arg)	not specified [RCV004866856]	uncertain significance	14	105399372	105399372	Human		name
597751130	CV3619767	single nucleotide variant	NM_001195082.2(TEX22):c.61C>A (p.His21Asn)	not specified [RCV004866858]	uncertain significance	14	105399401	105399401	Human		name
597751175	CV3619777	single nucleotide variant	NM_015926.6(TEX264):c.896C>G (p.Thr299Ser)	not specified [RCV004866868]	uncertain significance	3	51703970	51703970	Human		name
597751185	CV3619779	single nucleotide variant	NM_015926.6(TEX264):c.695G>C (p.Ser232Thr)	not specified [RCV004866870]	uncertain significance	3	51703769	51703769	Human		name
597751190	CV3619780	single nucleotide variant	NM_015926.6(TEX264):c.572A>G (p.Tyr191Cys)	not specified [RCV004866871]	uncertain significance	3	51699497	51699497	Human		name
597751195	CV3619781	single nucleotide variant	NM_015926.6(TEX264):c.773G>A (p.Arg258His)	not specified [RCV004866872]	uncertain significance	3	51703847	51703847	Human		name
597751205	CV3619783	single nucleotide variant	NM_015926.6(TEX264):c.745A>G (p.Ser249Gly)	not specified [RCV004866874]	uncertain significance	3	51703819	51703819	Human		name
155979927	CV2339266	single nucleotide variant	NM_001195082.2(TEX22):c.160C>G (p.Pro54Ala)	not specified [RCV004191506]	uncertain significance	14	105411377	105411377	Human		name
156194097	CV2350692	single nucleotide variant	NM_001195082.2(TEX22):c.272A>C (p.His91Pro)	not specified [RCV004207041]	uncertain significance	14	105411489	105411489	Human		name
156088838	CV2359288	single nucleotide variant	NM_001195082.2(TEX22):c.250G>A (p.Gly84Ser)	not specified [RCV004212576]	uncertain significance	14	105411467	105411467	Human		name
329372236	CV2443069	single nucleotide variant	NM_001195082.2(TEX22):c.169C>T (p.Arg57Cys)	not specified [RCV004253656]	uncertain significance	14	105411386	105411386	Human		name
329377513	CV2453441	single nucleotide variant	NM_001195082.2(TEX22):c.265C>G (p.Gln89Glu)	not specified [RCV004267046]	uncertain significance	14	105411482	105411482	Human		name
405782746	CV3342574	single nucleotide variant	NM_001195082.2(TEX22):c.218G>A (p.Arg73Gln)	not specified [RCV004472250]	uncertain significance	14	105411435	105411435	Human		name
407518578	CV3482522	single nucleotide variant	NM_001195082.2(TEX22):c.116G>T (p.Ser39Ile)	not specified [RCV004676041]	uncertain significance	14	105399456	105399456	Human		name
407518582	CV3482523	single nucleotide variant	NM_001195082.2(TEX22):c.125A>G (p.Gln42Arg)	not specified [RCV004676042]	uncertain significance	14	105399465	105399465	Human		name
407519918	CV3482525	single nucleotide variant	NM_001195082.2(TEX22):c.164C>T (p.Pro55Leu)	not specified [RCV004676755]	uncertain significance	14	105411381	105411381	Human		name
407518585	CV3482526	single nucleotide variant	NM_001195082.2(TEX22):c.107G>A (p.Ser36Asn)	not specified [RCV004676043]	uncertain significance	14	105399447	105399447	Human		name
597751103	CV3619761	single nucleotide variant	NM_001195082.2(TEX22):c.274T>A (p.Cys92Ser)	not specified [RCV004866852]	uncertain significance	14	105411491	105411491	Human		name
597751111	CV3619763	single nucleotide variant	NM_001195082.2(TEX22):c.182G>T (p.Gly61Val)	not specified [RCV004866854]	uncertain significance	14	105411399	105411399	Human		name
597751125	CV3619766	single nucleotide variant	NM_001195082.2(TEX22):c.169C>G (p.Arg57Gly)	not specified [RCV004866857]	uncertain significance	14	105411386	105411386	Human		name
598182958	CV3916982	single nucleotide variant	NM_001195082.2(TEX22):c.179C>T (p.Pro60Leu)	not specified [RCV005287027]	uncertain significance	14	105411396	105411396	Human		name
155995979	CV2375878	single nucleotide variant	NM_001195082.2(TEX22):c.419C>T (p.Ala140Val)	not specified [RCV004217722]	likely benign	14	105411799	105411799	Human		name
405782757	CV3342576	single nucleotide variant	NM_001195082.2(TEX22):c.340C>T (p.Pro114Ser)	not specified [RCV004472252]	uncertain significance	14	105411720	105411720	Human		name
597751116	CV3619764	single nucleotide variant	NM_001195082.2(TEX22):c.428A>G (p.Glu143Gly)	not specified [RCV004866855]	likely benign	14	105411808	105411808	Human		name
598182945	CV3916980	single nucleotide variant	NM_001195082.2(TEX22):c.298G>C (p.Ala100Pro)	not specified [RCV005287025]	uncertain significance	14	105411678	105411678	Human		name

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