Bcl9l Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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191 records found for search term Bcl9l

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
156036388	CV2208405	single nucleotide variant	NM_001378213.1(BCL9L):c.16A>T (p.Asn6Tyr)	not specified [RCV004088833]	uncertain significance	11	118909924	118909924	Human		name
329373849	CV2434635	single nucleotide variant	NM_001378213.1(BCL9L):c.94C>A (p.Pro32Thr)	not specified [RCV004248359]	uncertain significance	11	118908588	118908588	Human		name
405667791	CV3297968	single nucleotide variant	NM_001378213.1(BCL9L):c.65C>T (p.Pro22Leu)	not specified [RCV004418875]	uncertain significance	11	118908617	118908617	Human		name
598276620	CV3938650	single nucleotide variant	NM_001378213.1(BCL9L):c.927G>A (p.Pro309=)	not specified [RCV005305754]	likely benign	11	118902816	118902816	Human		name
15183812	CV724232	single nucleotide variant	NM_001378213.1(BCL9L):c.768G>A (p.Leu256=)	not provided [RCV000886306]	benign	11	118903056	118903056	Human		name
156100832	CV2351664	single nucleotide variant	NM_001378213.1(BCL9L):c.200C>T (p.Thr67Ile)	not specified [RCV004195375]	uncertain significance	11	118908482	118908482	Human		name
329371203	CV2461975	single nucleotide variant	NM_001378213.1(BCL9L):c.247A>G (p.Lys83Glu)	not specified [RCV004271869]	uncertain significance	11	118908435	118908435	Human		name
401910160	CV2809927	single nucleotide variant	NM_001378213.1(BCL9L):c.1365C>T (p.Pro455=)	not provided [RCV003424833]	likely benign	11	118902378	118902378	Human		name
405707952	CV3297933	single nucleotide variant	NM_001378213.1(BCL9L):c.104C>G (p.Ala35Gly)	not specified [RCV004426361]	uncertain significance	11	118908578	118908578	Human		name
405707972	CV3297936	single nucleotide variant	NM_001378213.1(BCL9L):c.163G>A (p.Ala55Thr)	not specified [RCV004426364]	uncertain significance	11	118908519	118908519	Human		name
405667664	CV3297942	single nucleotide variant	NM_001378213.1(BCL9L):c.214T>C (p.Ser72Pro)	not specified [RCV004418849]	uncertain significance	11	118908468	118908468	Human		name
405667669	CV3297943	single nucleotide variant	NM_001378213.1(BCL9L):c.245C>T (p.Ala82Val)	not specified [RCV004418850]	uncertain significance	11	118908437	118908437	Human		name
405667689	CV3297947	single nucleotide variant	NM_001378213.1(BCL9L):c.272A>T (p.Asn91Ile)	not specified [RCV004418854]	uncertain significance	11	118908410	118908410	Human		name
407495658	CV3417723	single nucleotide variant	NM_001378213.1(BCL9L):c.101C>T (p.Pro34Leu)	not specified [RCV004605878]	uncertain significance	11	118908581	118908581	Human		name
597736804	CV3639741	single nucleotide variant	NM_001378213.1(BCL9L):c.160G>A (p.Gly54Arg)	not specified [RCV004889789]	uncertain significance	11	118908522	118908522	Human		name
597736838	CV3639750	single nucleotide variant	NM_001378213.1(BCL9L):c.223G>T (p.Val75Leu)	not specified [RCV004889796]	uncertain significance	11	118908459	118908459	Human		name
12896711	CV389900	single nucleotide variant	NM_001378213.1(BCL9L):c.2292C>T (p.Pro764=)	not provided [RCV004707264]\|not specified [RCV000455716]	benign	11	118901451	118901451	Human		name
12896983	CV389904	single nucleotide variant	NM_001378213.1(BCL9L):c.1272C>T (p.Ser424=)	not provided [RCV004707267]\|not specified [RCV000456081]	benign	11	118902471	118902471	Human		name
15107004	CV712635	single nucleotide variant	NM_001378213.1(BCL9L):c.2370G>A (p.Pro790=)	not provided [RCV000960197]	benign	11	118901373	118901373	Human		name
15199970	CV752470	single nucleotide variant	NM_001378213.1(BCL9L):c.1311A>T (p.Gly437=)	not provided [RCV000912707]	benign	11	118902432	118902432	Human		name
156073922	CV2230031	single nucleotide variant	NM_001378213.1(BCL9L):c.872T>G (p.Leu291Arg)	not specified [RCV004105830]	uncertain significance	11	118902871	118902871	Human		name
156341111	CV2268220	single nucleotide variant	NM_001378213.1(BCL9L):c.560C>T (p.Ala187Val)	not specified [RCV004138525]	uncertain significance	11	118903425	118903425	Human		name
156056756	CV2326693	single nucleotide variant	NM_001378213.1(BCL9L):c.338G>A (p.Arg113Lys)	not specified [RCV004185271]	uncertain significance	11	118908344	118908344	Human		name
155970166	CV2335552	single nucleotide variant	NM_001378213.1(BCL9L):c.673G>A (p.Gly225Arg)	not specified [RCV004193764]	uncertain significance	11	118903312	118903312	Human		name
156079527	CV2341259	single nucleotide variant	NM_001378213.1(BCL9L):c.717C>G (p.Phe239Leu)	not specified [RCV004186672]	uncertain significance	11	118903268	118903268	Human		name
156072054	CV2353316	single nucleotide variant	NM_001378213.1(BCL9L):c.613A>G (p.Ser205Gly)	not specified [RCV004205785]	uncertain significance	11	118903372	118903372	Human		name
156267815	CV2371887	single nucleotide variant	NM_001378213.1(BCL9L):c.935C>T (p.Pro312Leu)	not specified [RCV004221576]	uncertain significance	11	118902808	118902808	Human		name
401734693	CV2688593	single nucleotide variant	NM_001378213.1(BCL9L):c.659A>T (p.Asp220Val)	not specified [RCV004301549]	uncertain significance	11	118903326	118903326	Human		name
401782414	CV2719804	single nucleotide variant	NM_001378213.1(BCL9L):c.896C>T (p.Pro299Leu)	not specified [RCV004329226]	uncertain significance	11	118902847	118902847	Human		name
405667786	CV3297967	single nucleotide variant	NM_001378213.1(BCL9L):c.507C>G (p.Asp169Glu)	not specified [RCV004418874]	uncertain significance	11	118907508	118907508	Human		name
405667794	CV3297969	single nucleotide variant	NM_001378213.1(BCL9L):c.853A>C (p.Thr285Pro)	not specified [RCV004418876]	uncertain significance	11	118902890	118902890	Human		name
405667799	CV3297970	single nucleotide variant	NM_001378213.1(BCL9L):c.932C>T (p.Pro311Leu)	not specified [RCV004418877]	uncertain significance	11	118902811	118902811	Human		name
407495645	CV3417720	single nucleotide variant	NM_001378213.1(BCL9L):c.419C>T (p.Ala140Val)	not specified [RCV004605875]	uncertain significance	11	118907596	118907596	Human		name
407495654	CV3417722	single nucleotide variant	NM_001378213.1(BCL9L):c.629C>T (p.Pro210Leu)	not specified [RCV004605877]	uncertain significance	11	118903356	118903356	Human		name
407499920	CV3417724	single nucleotide variant	NM_001378213.1(BCL9L):c.580G>A (p.Gly194Ser)	not specified [RCV004607017]	uncertain significance	11	118903405	118903405	Human		name
407495663	CV3417725	single nucleotide variant	NM_001378213.1(BCL9L):c.301G>A (p.Val101Met)	not specified [RCV004605879]	uncertain significance	11	118908381	118908381	Human		name
407495666	CV3417726	single nucleotide variant	NM_001378213.1(BCL9L):c.946A>T (p.Ser316Cys)	not specified [RCV004605880]	uncertain significance	11	118902797	118902797	Human		name
407495684	CV3417730	single nucleotide variant	NM_001378213.1(BCL9L):c.634G>A (p.Gly212Ser)	not specified [RCV004605884]	uncertain significance	11	118903351	118903351	Human		name
407495697	CV3417733	single nucleotide variant	NM_001378213.1(BCL9L):c.422C>T (p.Pro141Leu)	not specified [RCV004605887]	uncertain significance	11	118907593	118907593	Human		name
407499924	CV3417734	single nucleotide variant	NM_001378213.1(BCL9L):c.391T>C (p.Ser131Pro)	not specified [RCV004607018]	uncertain significance	11	118908291	118908291	Human		name
407495705	CV3417736	single nucleotide variant	NM_001378213.1(BCL9L):c.355G>A (p.Val119Met)	not specified [RCV004605889]	uncertain significance	11	118908327	118908327	Human		name
597736824	CV3639746	single nucleotide variant	NM_001378213.1(BCL9L):c.718G>A (p.Val240Ile)	not specified [RCV004889793]	uncertain significance	11	118903267	118903267	Human		name
597736847	CV3639752	single nucleotide variant	NM_001378213.1(BCL9L):c.679G>A (p.Gly227Arg)	not specified [RCV004889798]	uncertain significance	11	118903306	118903306	Human		name
597736852	CV3639753	single nucleotide variant	NM_001378213.1(BCL9L):c.616G>A (p.Val206Met)	not specified [RCV004889799]	uncertain significance	11	118903369	118903369	Human		name
12896043	CV389899	single nucleotide variant	NM_001378213.1(BCL9L):c.4020G>A (p.Gln1340=)	not provided [RCV004708880]\|not specified [RCV000454808]	benign	11	118898895	118898895	Human		name
12896696	CV389959	single nucleotide variant	NM_001378213.1(BCL9L):c.4182T>C (p.Pro1394=)	not provided [RCV004707262]\|not specified [RCV000455696]	benign	11	118898733	118898733	Human		name
598201607	CV3938634	single nucleotide variant	NM_001378213.1(BCL9L):c.832C>G (p.Gln278Glu)	not specified [RCV005314264]	uncertain significance	11	118902992	118902992	Human		name
598201617	CV3938637	single nucleotide variant	NM_001378213.1(BCL9L):c.881C>T (p.Pro294Leu)	not specified [RCV005314267]	uncertain significance	11	118902862	118902862	Human		name
598276615	CV3938640	single nucleotide variant	NM_001378213.1(BCL9L):c.635G>C (p.Gly212Ala)	not specified [RCV005305749]	uncertain significance	11	118903350	118903350	Human		name
598201629	CV3938642	single nucleotide variant	NM_001378213.1(BCL9L):c.374G>A (p.Arg125Gln)	not specified [RCV005314270]	uncertain significance	11	118908308	118908308	Human		name
598276616	CV3938645	single nucleotide variant	NM_001378213.1(BCL9L):c.310T>C (p.Phe104Leu)	not specified [RCV005305750]	uncertain significance	11	118908372	118908372	Human		name
598276619	CV3938649	single nucleotide variant	NM_001378213.1(BCL9L):c.776G>A (p.Arg259Gln)	not specified [RCV005305753]	uncertain significance	11	118903048	118903048	Human		name
15107000	CV712633	single nucleotide variant	NM_001378213.1(BCL9L):c.4365G>A (p.Pro1455=)	not provided [RCV000960196]	benign	11	118898550	118898550	Human		name
15177959	CV737790	single nucleotide variant	NM_001378213.1(BCL9L):c.4035C>T (p.Ser1345=)	not provided [RCV000906766]	benign	11	118898880	118898880	Human		name
15118501	CV752469	single nucleotide variant	NM_001378213.1(BCL9L):c.3378C>A (p.Pro1126=)	not provided [RCV000917986]	likely benign	11	118899945	118899945	Human		name
156368810	CV2193794	single nucleotide variant	NM_001378213.1(BCL9L):c.2587A>G (p.Met863Val)	not specified [RCV004074549]	uncertain significance	11	118901156	118901156	Human		name
155980959	CV2212101	single nucleotide variant	NM_001378213.1(BCL9L):c.2824T>A (p.Ser942Thr)	not specified [RCV004089009]	uncertain significance	11	118900919	118900919	Human		name
155968430	CV2213147	single nucleotide variant	NM_001378213.1(BCL9L):c.2744C>T (p.Ser915Leu)	not specified [RCV004085380]	uncertain significance	11	118900999	118900999	Human		name
156356761	CV2257536	single nucleotide variant	NM_001378213.1(BCL9L):c.1838G>T (p.Gly613Val)	not specified [RCV004125590]	uncertain significance	11	118901905	118901905	Human		name
156048959	CV2271762	single nucleotide variant	NM_001378213.1(BCL9L):c.2053G>C (p.Glu685Gln)	not specified [RCV004130604]	uncertain significance	11	118901690	118901690	Human		name
156175750	CV2278235	single nucleotide variant	NM_001378213.1(BCL9L):c.1894C>A (p.Pro632Thr)	not specified [RCV004143464]	uncertain significance	11	118901849	118901849	Human		name
155926045	CV2287810	single nucleotide variant	NM_001378213.1(BCL9L):c.2458G>T (p.Val820Phe)	not specified [RCV004143254]	uncertain significance	11	118901285	118901285	Human		name
156290878	CV2296564	single nucleotide variant	NM_001378213.1(BCL9L):c.2257A>G (p.Met753Val)	not specified [RCV004154634]	uncertain significance	11	118901486	118901486	Human		name
156006515	CV2299573	single nucleotide variant	NM_001378213.1(BCL9L):c.1702C>T (p.Pro568Ser)	not specified [RCV004154903]	uncertain significance	11	118902041	118902041	Human		name
155954636	CV2302188	single nucleotide variant	NM_001378213.1(BCL9L):c.1829G>A (p.Arg610Gln)	not specified [RCV004159190]	uncertain significance	11	118901914	118901914	Human		name
156048891	CV2319273	single nucleotide variant	NM_001378213.1(BCL9L):c.2189G>A (p.Gly730Asp)	not specified [RCV004178314]	uncertain significance	11	118901554	118901554	Human		name
156333439	CV2335987	single nucleotide variant	NM_001378213.1(BCL9L):c.1403C>T (p.Pro468Leu)	not specified [RCV004189596]	uncertain significance	11	118902340	118902340	Human		name
155922373	CV2340610	single nucleotide variant	NM_001378213.1(BCL9L):c.2032C>A (p.Leu678Met)	not specified [RCV004197318]	uncertain significance	11	118901711	118901711	Human		name
156218459	CV2344749	single nucleotide variant	NM_001378213.1(BCL9L):c.1078A>G (p.Thr360Ala)	not specified [RCV004190903]	uncertain significance	11	118902665	118902665	Human		name
156277350	CV2352033	single nucleotide variant	NM_001378213.1(BCL9L):c.1342C>T (p.Pro448Ser)	not specified [RCV004191129]	uncertain significance	11	118902401	118902401	Human		name
156228359	CV2352901	single nucleotide variant	NM_001378213.1(BCL9L):c.2254C>T (p.Pro752Ser)	not specified [RCV004200948]	uncertain significance	11	118901489	118901489	Human		name
156171412	CV2354977	single nucleotide variant	NM_001378213.1(BCL9L):c.1402C>T (p.Pro468Ser)	not specified [RCV004198378]	uncertain significance	11	118902341	118902341	Human		name
156175441	CV2355686	single nucleotide variant	NM_001378213.1(BCL9L):c.2878C>A (p.Gln960Lys)	not specified [RCV004199048]	uncertain significance	11	118900865	118900865	Human		name
156006927	CV2357832	single nucleotide variant	NM_001378213.1(BCL9L):c.2290C>T (p.Pro764Ser)	not specified [RCV004205118]	uncertain significance	11	118901453	118901453	Human		name
156390479	CV2373433	single nucleotide variant	NM_001378213.1(BCL9L):c.1285C>G (p.Pro429Ala)	not specified [RCV004220133]	uncertain significance	11	118902458	118902458	Human		name
156140809	CV2383642	single nucleotide variant	NM_001378213.1(BCL9L):c.1864A>G (p.Met622Val)	not specified [RCV004229532]	uncertain significance	11	118901879	118901879	Human		name
156100468	CV2392948	single nucleotide variant	NM_001378213.1(BCL9L):c.2650A>G (p.Thr884Ala)	not specified [RCV004242803]	uncertain significance	11	118901093	118901093	Human		name
329374856	CV2440093	single nucleotide variant	NM_001378213.1(BCL9L):c.2237G>A (p.Arg746Gln)	not specified [RCV004260559]	uncertain significance	11	118901506	118901506	Human		name
329382380	CV2465202	single nucleotide variant	NM_001378213.1(BCL9L):c.1013C>T (p.Ser338Leu)	not specified [RCV004287238]	uncertain significance	11	118902730	118902730	Human		name
329381709	CV2471251	single nucleotide variant	NM_001378213.1(BCL9L):c.1778G>A (p.Arg593Gln)	not specified [RCV004280279]	uncertain significance	11	118901965	118901965	Human		name
401728263	CV2676037	single nucleotide variant	NM_001378213.1(BCL9L):c.2956C>T (p.Arg986Cys)	not specified [RCV004282021]	uncertain significance	11	118900787	118900787	Human		name
401748756	CV2694495	single nucleotide variant	NM_001378213.1(BCL9L):c.2149C>G (p.Gln717Glu)	not specified [RCV004298635]	uncertain significance	11	118901594	118901594	Human		name
401737623	CV2699864	single nucleotide variant	NM_001378213.1(BCL9L):c.1097C>T (p.Pro366Leu)	not specified [RCV004308505]	uncertain significance	11	118902646	118902646	Human		name
401743155	CV2715410	single nucleotide variant	NM_001378213.1(BCL9L):c.2711C>T (p.Ser904Leu)	not specified [RCV004324729]	uncertain significance	11	118901032	118901032	Human		name
401754506	CV2717412	single nucleotide variant	NM_001378213.1(BCL9L):c.2561G>A (p.Gly854Glu)	not specified [RCV004330243]	uncertain significance	11	118901182	118901182	Human		name
401881486	CV2759432	single nucleotide variant	NM_001378213.1(BCL9L):c.2906C>T (p.Pro969Leu)	not specified [RCV004338430]	uncertain significance	11	118900837	118900837	Human		name
401876589	CV2761119	single nucleotide variant	NM_001378213.1(BCL9L):c.2285A>G (p.Asp762Gly)	not specified [RCV004338775]	uncertain significance	11	118901458	118901458	Human		name
401898311	CV2791034	single nucleotide variant	NM_001378213.1(BCL9L):c.2558A>G (p.Gln853Arg)	not specified [RCV004354643]	uncertain significance	11	118901185	118901185	Human		name
405707959	CV3297934	single nucleotide variant	NM_001378213.1(BCL9L):c.1367C>T (p.Thr456Met)	not specified [RCV004426362]	uncertain significance	11	118902376	118902376	Human		name
405707989	CV3297938	single nucleotide variant	NM_001378213.1(BCL9L):c.2060G>A (p.Arg687Gln)	not specified [RCV004426366]	uncertain significance	11	118901683	118901683	Human		name
405707994	CV3297939	single nucleotide variant	NM_001378213.1(BCL9L):c.2119G>A (p.Glu707Lys)	not specified [RCV004426367]	uncertain significance	11	118901624	118901624	Human		name
405708001	CV3297940	single nucleotide variant	NM_001378213.1(BCL9L):c.2124G>A (p.Met708Ile)	not specified [RCV004426368]	uncertain significance	11	118901619	118901619	Human		name
405708005	CV3297941	single nucleotide variant	NM_001378213.1(BCL9L):c.2141C>T (p.Ala714Val)	not specified [RCV004426369]	uncertain significance	11	118901602	118901602	Human		name
405667673	CV3297944	single nucleotide variant	NM_001378213.1(BCL9L):c.2462G>A (p.Arg821Gln)	not specified [RCV004418851]	uncertain significance	11	118901281	118901281	Human		name
405667683	CV3297946	single nucleotide variant	NM_001378213.1(BCL9L):c.2631G>A (p.Met877Ile)	not specified [RCV004418853]	uncertain significance	11	118901112	118901112	Human		name
405667694	CV3297948	single nucleotide variant	NM_001378213.1(BCL9L):c.2780C>T (p.Pro927Leu)	not specified [RCV004418855]	uncertain significance	11	118900963	118900963	Human		name
407495676	CV3417728	single nucleotide variant	NM_001378213.1(BCL9L):c.1163A>G (p.Asn388Ser)	not specified [RCV004605882]	uncertain significance	11	118902580	118902580	Human		name
407495680	CV3417729	single nucleotide variant	NM_001378213.1(BCL9L):c.1364C>T (p.Pro455Leu)	not specified [RCV004605883]	uncertain significance	11	118902379	118902379	Human		name
407495688	CV3417731	single nucleotide variant	NM_001378213.1(BCL9L):c.2977A>G (p.Ser993Gly)	not specified [RCV004605885]	uncertain significance	11	118900766	118900766	Human		name
407495701	CV3417735	single nucleotide variant	NM_001378213.1(BCL9L):c.1583A>G (p.Tyr528Cys)	not specified [RCV004605888]	uncertain significance	11	118902160	118902160	Human		name
597736842	CV3639751	single nucleotide variant	NM_001378213.1(BCL9L):c.1049G>T (p.Gly350Val)	not specified [RCV004889797]	uncertain significance	11	118902694	118902694	Human		name
597736858	CV3639754	single nucleotide variant	NM_001378213.1(BCL9L):c.1411T>C (p.Ser471Pro)	not specified [RCV004889800]	uncertain significance	11	118902332	118902332	Human		name
597736862	CV3639755	single nucleotide variant	NM_001378213.1(BCL9L):c.1358A>C (p.Gln453Pro)	not specified [RCV004889801]	uncertain significance	11	118902385	118902385	Human		name
597736872	CV3639758	single nucleotide variant	NM_001378213.1(BCL9L):c.1880A>T (p.Asn627Ile)	not specified [RCV004889803]	uncertain significance	11	118901863	118901863	Human		name
597736877	CV3639759	single nucleotide variant	NM_001378213.1(BCL9L):c.1907G>T (p.Gly636Val)	not specified [RCV004889804]	uncertain significance	11	118901836	118901836	Human		name
597736887	CV3639761	single nucleotide variant	NM_001378213.1(BCL9L):c.1507A>G (p.Met503Val)	not specified [RCV004889806]	uncertain significance	11	118902236	118902236	Human		name
597736891	CV3639762	single nucleotide variant	NM_001378213.1(BCL9L):c.2644G>T (p.Val882Leu)	not specified [RCV004889807]	uncertain significance	11	118901099	118901099	Human		name
597736901	CV3639764	single nucleotide variant	NM_001378213.1(BCL9L):c.2992C>T (p.Pro998Ser)	not specified [RCV004889809]	uncertain significance	11	118900751	118900751	Human		name
597736906	CV3639765	single nucleotide variant	NM_001378213.1(BCL9L):c.1348C>A (p.Pro450Thr)	not specified [RCV004889810]	uncertain significance	11	118902395	118902395	Human		name
597736911	CV3639766	single nucleotide variant	NM_001378213.1(BCL9L):c.2137C>G (p.Gln713Glu)	not specified [RCV004889811]	uncertain significance	11	118901606	118901606	Human		name
597736915	CV3639767	single nucleotide variant	NM_001378213.1(BCL9L):c.2176C>G (p.Gln726Glu)	not specified [RCV004889812]	uncertain significance	11	118901567	118901567	Human		name
597736934	CV3639772	single nucleotide variant	NM_001378213.1(BCL9L):c.2858A>G (p.Lys953Arg)	not specified [RCV004889816]	uncertain significance	11	118900885	118900885	Human		name
597736939	CV3639773	single nucleotide variant	NM_001378213.1(BCL9L):c.1777C>T (p.Arg593Trp)	not specified [RCV004889817]	uncertain significance	11	118901966	118901966	Human		name
597736953	CV3639776	single nucleotide variant	NM_001378213.1(BCL9L):c.1328C>T (p.Pro443Leu)	not specified [RCV004889820]	uncertain significance	11	118902415	118902415	Human		name
597736959	CV3639777	single nucleotide variant	NM_001378213.1(BCL9L):c.1661G>A (p.Gly554Asp)	not specified [RCV004889821]	uncertain significance	11	118902082	118902082	Human		name
12896476	CV389902	single nucleotide variant	NM_001378213.1(BCL9L):c.1627A>G (p.Ser543Gly)	not provided [RCV004707266]\|not specified [RCV000455393]	benign	11	118902116	118902116	Human		name
12895989	CV389962	single nucleotide variant	NM_001378213.1(BCL9L):c.1936A>G (p.Met646Val)	not provided [RCV004707265]\|not specified [RCV000454728]	benign	11	118901807	118901807	Human		name
12896323	CV389964	single nucleotide variant	NM_001378213.1(BCL9L):c.2705T>C (p.Val902Ala)	not provided [RCV004707263]\|not specified [RCV000455196]	benign	11	118901038	118901038	Human		name
598201621	CV3938639	single nucleotide variant	NM_001378213.1(BCL9L):c.2803C>T (p.Pro935Ser)	not specified [RCV005314268]	uncertain significance	11	118900940	118900940	Human		name
598276617	CV3938646	single nucleotide variant	NM_001378213.1(BCL9L):c.1819C>A (p.Gln607Lys)	not specified [RCV005305751]	uncertain significance	11	118901924	118901924	Human		name
598201642	CV3938647	single nucleotide variant	NM_001378213.1(BCL9L):c.2620C>G (p.Gln874Glu)	not specified [RCV005314273]	uncertain significance	11	118901123	118901123	Human		name
598276618	CV3938648	single nucleotide variant	NM_001378213.1(BCL9L):c.2737C>T (p.Arg913Trp)	not specified [RCV005305752]	uncertain significance	11	118901006	118901006	Human		name
598276621	CV3938652	single nucleotide variant	NM_001378213.1(BCL9L):c.2670G>T (p.Met890Ile)	not specified [RCV005305755]	uncertain significance	11	118901073	118901073	Human		name
598276622	CV3938653	single nucleotide variant	NM_001378213.1(BCL9L):c.2722C>T (p.Arg908Trp)	not specified [RCV005305756]	uncertain significance	11	118901021	118901021	Human		name
598276623	CV3938654	single nucleotide variant	NM_001378213.1(BCL9L):c.1630C>T (p.Arg544Cys)	not specified [RCV005305757]	uncertain significance	11	118902113	118902113	Human		name
598201650	CV3938656	single nucleotide variant	NM_001378213.1(BCL9L):c.2181G>T (p.Met727Ile)	not specified [RCV005314275]	uncertain significance	11	118901562	118901562	Human		name
15142595	CV737791	single nucleotide variant	NM_001378213.1(BCL9L):c.2434C>T (p.Leu812Phe)	not provided [RCV000899699]	benign	11	118901309	118901309	Human		name
156377254	CV2207008	single nucleotide variant	NM_001378213.1(BCL9L):c.4423C>T (p.Arg1475Trp)	not specified [RCV004085626]	uncertain significance	11	118898492	118898492	Human		name
156109922	CV2211367	single nucleotide variant	NM_001378213.1(BCL9L):c.3736G>C (p.Gly1246Arg)	not specified [RCV004090286]	uncertain significance	11	118899179	118899179	Human		name
155979824	CV2222930	single nucleotide variant	NM_001378213.1(BCL9L):c.3038C>T (p.Thr1013Met)	not specified [RCV004101740]	uncertain significance	11	118900705	118900705	Human		name
155921491	CV2240531	single nucleotide variant	NM_001378213.1(BCL9L):c.3412A>G (p.Ser1138Gly)	not specified [RCV004119190]	uncertain significance	11	118899503	118899503	Human		name
155995054	CV2250304	single nucleotide variant	NM_001378213.1(BCL9L):c.3854T>C (p.Met1285Thr)	not specified [RCV004127202]	uncertain significance	11	118899061	118899061	Human		name
156139906	CV2250622	single nucleotide variant	NM_001378213.1(BCL9L):c.4405A>C (p.Met1469Leu)	not specified [RCV004129259]	uncertain significance	11	118898510	118898510	Human		name
156144133	CV2268843	single nucleotide variant	NM_001378213.1(BCL9L):c.4019A>G (p.Gln1340Arg)	not specified [RCV004124218]	uncertain significance	11	118898896	118898896	Human		name
155902992	CV2274803	single nucleotide variant	NM_001378213.1(BCL9L):c.3893T>C (p.Leu1298Pro)	not specified [RCV004139144]	uncertain significance	11	118899022	118899022	Human		name
156033630	CV2275142	single nucleotide variant	NM_001378213.1(BCL9L):c.3914T>C (p.Leu1305Pro)	not specified [RCV004136941]	uncertain significance	11	118899001	118899001	Human		name
155918948	CV2279322	single nucleotide variant	NM_001378213.1(BCL9L):c.4357C>T (p.Leu1453Phe)	not specified [RCV004139838]	uncertain significance	11	118898558	118898558	Human		name
155993364	CV2286294	single nucleotide variant	NM_001378213.1(BCL9L):c.3025G>T (p.Ala1009Ser)	not specified [RCV004146246]	uncertain significance	11	118900718	118900718	Human		name
155998644	CV2296104	single nucleotide variant	NM_001378213.1(BCL9L):c.3767C>T (p.Pro1256Leu)	not specified [RCV004154038]	uncertain significance	11	118899148	118899148	Human		name
156058024	CV2343594	single nucleotide variant	NM_001378213.1(BCL9L):c.3822G>T (p.Met1274Ile)	not specified [RCV004190626]	uncertain significance	11	118899093	118899093	Human		name
156168960	CV2345495	single nucleotide variant	NM_001378213.1(BCL9L):c.3481C>T (p.Pro1161Ser)	not provided [RCV003491294]\|not specified [RCV004198260]	uncertain significance	11	118899434	118899434	Human		name
156091784	CV2384779	single nucleotide variant	NM_001378213.1(BCL9L):c.4346C>T (p.Pro1449Leu)	not specified [RCV004232542]	uncertain significance	11	118898569	118898569	Human		name
156100019	CV2392912	single nucleotide variant	NM_001378213.1(BCL9L):c.4477G>A (p.Gly1493Ser)	not specified [RCV004247261]	likely benign	11	118898438	118898438	Human		name
329360450	CV2442806	single nucleotide variant	NM_001378213.1(BCL9L):c.4297T>A (p.Phe1433Ile)	not specified [RCV004251632]	uncertain significance	11	118898618	118898618	Human		name
329360317	CV2446672	single nucleotide variant	NM_001378213.1(BCL9L):c.3380C>A (p.Pro1127Gln)	not specified [RCV004251558]	uncertain significance	11	118899943	118899943	Human		name
329393681	CV2449791	single nucleotide variant	NM_001378213.1(BCL9L):c.3805C>A (p.Gln1269Lys)	not specified [RCV004267109]	uncertain significance	11	118899110	118899110	Human		name
329395969	CV2451824	single nucleotide variant	NM_001378213.1(BCL9L):c.3472A>G (p.Met1158Val)	not specified [RCV004276506]	uncertain significance	11	118899443	118899443	Human		name
329389299	CV2467252	single nucleotide variant	NM_001378213.1(BCL9L):c.3374C>A (p.Pro1125His)	not specified [RCV004285061]	uncertain significance	11	118899949	118899949	Human		name
329392555	CV2471320	single nucleotide variant	NM_001378213.1(BCL9L):c.4255G>A (p.Gly1419Arg)	not specified [RCV004280333]	uncertain significance	11	118898660	118898660	Human		name
401757484	CV2707805	single nucleotide variant	NM_001378213.1(BCL9L):c.3172G>A (p.Ala1058Thr)	not specified [RCV004309094]	uncertain significance	11	118900151	118900151	Human		name
401754099	CV2715549	single nucleotide variant	NM_001378213.1(BCL9L):c.4171A>G (p.Met1391Val)	not specified [RCV004326949]	uncertain significance	11	118898744	118898744	Human		name
401857084	CV2759958	single nucleotide variant	NM_001378213.1(BCL9L):c.4216C>T (p.Pro1406Ser)	not specified [RCV004345380]	uncertain significance	11	118898699	118898699	Human		name
401887362	CV2773399	single nucleotide variant	NM_001378213.1(BCL9L):c.4227G>C (p.Gln1409His)	not specified [RCV004354043]	uncertain significance	11	118898688	118898688	Human		name
401867074	CV2780103	single nucleotide variant	NM_001378213.1(BCL9L):c.3955A>G (p.Thr1319Ala)	not specified [RCV004355761]	uncertain significance	11	118898960	118898960	Human		name
401880680	CV2792933	single nucleotide variant	NM_001378213.1(BCL9L):c.3832C>G (p.Gln1278Glu)	not specified [RCV004365662]	uncertain significance	11	118899083	118899083	Human		name
401910158	CV2809926	single nucleotide variant	NM_001378213.1(BCL9L):c.4157G>A (p.Gly1386Glu)	not provided [RCV003424832]	uncertain significance	11	118898758	118898758	Human		name
405667703	CV3297950	single nucleotide variant	NM_001378213.1(BCL9L):c.3010T>A (p.Ser1004Thr)	not specified [RCV004418857]	uncertain significance	11	118900733	118900733	Human		name
405667708	CV3297951	single nucleotide variant	NM_001378213.1(BCL9L):c.3086A>C (p.Asn1029Thr)	not specified [RCV004418858]	uncertain significance	11	118900657	118900657	Human		name
405667713	CV3297952	single nucleotide variant	NM_001378213.1(BCL9L):c.3112A>T (p.Asn1038Tyr)	not specified [RCV004418859]	uncertain significance	11	118900631	118900631	Human		name
405667718	CV3297953	single nucleotide variant	NM_001378213.1(BCL9L):c.3161C>T (p.Ser1054Leu)	not specified [RCV004418860]	uncertain significance	11	118900162	118900162	Human		name
405667722	CV3297954	single nucleotide variant	NM_001378213.1(BCL9L):c.3166C>T (p.Pro1056Ser)	not specified [RCV004418861]	uncertain significance	11	118900157	118900157	Human		name
405667727	CV3297955	single nucleotide variant	NM_001378213.1(BCL9L):c.3400G>A (p.Gly1134Arg)	not specified [RCV004418862]	uncertain significance	11	118899923	118899923	Human		name
405667733	CV3297956	single nucleotide variant	NM_001378213.1(BCL9L):c.3451G>A (p.Ala1151Thr)	not specified [RCV004418863]	uncertain significance	11	118899464	118899464	Human		name
405667737	CV3297957	single nucleotide variant	NM_001378213.1(BCL9L):c.3545G>T (p.Gly1182Val)	not specified [RCV004418864]	uncertain significance	11	118899370	118899370	Human		name
405667742	CV3297958	single nucleotide variant	NM_001378213.1(BCL9L):c.3617C>T (p.Pro1206Leu)	not specified [RCV004418865]	uncertain significance	11	118899298	118899298	Human		name
405667746	CV3297959	single nucleotide variant	NM_001378213.1(BCL9L):c.3746C>T (p.Pro1249Leu)	not specified [RCV004418866]	uncertain significance	11	118899169	118899169	Human		name
405667756	CV3297961	single nucleotide variant	NM_001378213.1(BCL9L):c.3804C>A (p.Asn1268Lys)	not specified [RCV004418868]	uncertain significance	11	118899111	118899111	Human		name
405667763	CV3297962	single nucleotide variant	NM_001378213.1(BCL9L):c.3874G>A (p.Ala1292Thr)	not specified [RCV004418869]	likely benign	11	118899041	118899041	Human		name
405667768	CV3297963	single nucleotide variant	NM_001378213.1(BCL9L):c.3919G>A (p.Asp1307Asn)	not specified [RCV004418870]	uncertain significance	11	118898996	118898996	Human		name
405667771	CV3297964	single nucleotide variant	NM_001378213.1(BCL9L):c.3925G>A (p.Glu1309Lys)	not specified [RCV004418871]	uncertain significance	11	118898990	118898990	Human		name
405667778	CV3297965	single nucleotide variant	NM_001378213.1(BCL9L):c.3976T>A (p.Leu1326Met)	not specified [RCV004418872]	uncertain significance	11	118898939	118898939	Human		name
405667781	CV3297966	single nucleotide variant	NM_001378213.1(BCL9L):c.4048C>T (p.Pro1350Ser)	not specified [RCV004418873]	uncertain significance	11	118898867	118898867	Human		name
407495639	CV3417719	single nucleotide variant	NM_001378213.1(BCL9L):c.4279C>A (p.Leu1427Ile)	not specified [RCV004605874]	uncertain significance	11	118898636	118898636	Human		name
407495671	CV3417727	single nucleotide variant	NM_001378213.1(BCL9L):c.4183G>A (p.Gly1395Arg)	not specified [RCV004605881]	uncertain significance	11	118898732	118898732	Human		name
597736809	CV3639743	single nucleotide variant	NM_001378213.1(BCL9L):c.3376C>G (p.Pro1126Ala)	not specified [RCV004889790]	uncertain significance	11	118899947	118899947	Human		name
597736814	CV3639744	single nucleotide variant	NM_001378213.1(BCL9L):c.3973G>A (p.Asp1325Asn)	not specified [RCV004889791]	uncertain significance	11	118898942	118898942	Human		name
597736819	CV3639745	single nucleotide variant	NM_001378213.1(BCL9L):c.3466A>G (p.Met1156Val)	not specified [RCV004889792]	uncertain significance	11	118899449	118899449	Human		name
597736832	CV3639749	single nucleotide variant	NM_001378213.1(BCL9L):c.3692G>A (p.Arg1231Gln)	not specified [RCV004889795]	uncertain significance	11	118899223	118899223	Human		name
597736867	CV3639756	single nucleotide variant	NM_001378213.1(BCL9L):c.4395G>C (p.Gln1465His)	not specified [RCV004889802]	uncertain significance	11	118898520	118898520	Human		name
597736882	CV3639760	single nucleotide variant	NM_001378213.1(BCL9L):c.4118G>A (p.Arg1373Gln)	not specified [RCV004889805]	uncertain significance	11	118898797	118898797	Human		name
597737280	CV3639763	single nucleotide variant	NM_001378213.1(BCL9L):c.3474G>A (p.Met1158Ile)	not specified [RCV004889808]	uncertain significance	11	118899441	118899441	Human		name
597736919	CV3639769	single nucleotide variant	NM_001378213.1(BCL9L):c.4151A>G (p.Gln1384Arg)	not specified [RCV004889813]	uncertain significance	11	118898764	118898764	Human		name
597736924	CV3639770	single nucleotide variant	NM_001378213.1(BCL9L):c.3837C>G (p.His1279Gln)	not specified [RCV004889814]	uncertain significance	11	118899078	118899078	Human		name
597736930	CV3639771	single nucleotide variant	NM_001378213.1(BCL9L):c.3656T>C (p.Val1219Ala)	not specified [RCV004889815]	uncertain significance	11	118899259	118899259	Human		name
597736944	CV3639774	single nucleotide variant	NM_001378213.1(BCL9L):c.3571G>A (p.Ala1191Thr)	not specified [RCV004889818]	uncertain significance	11	118899344	118899344	Human		name
597736950	CV3639775	single nucleotide variant	NM_001378213.1(BCL9L):c.4145G>T (p.Gly1382Val)	not specified [RCV004889819]	uncertain significance	11	118898770	118898770	Human		name
598201611	CV3938635	single nucleotide variant	NM_001378213.1(BCL9L):c.3077C>T (p.Pro1026Leu)	not specified [RCV005314265]	uncertain significance	11	118900666	118900666	Human		name
598276614	CV3938638	single nucleotide variant	NM_001378213.1(BCL9L):c.3605T>C (p.Met1202Thr)	not specified [RCV005305748]	uncertain significance	11	118899310	118899310	Human		name
598201625	CV3938641	single nucleotide variant	NM_001378213.1(BCL9L):c.4433G>A (p.Ser1478Asn)	not specified [RCV005314269]	uncertain significance	11	118898482	118898482	Human		name
598201646	CV3938651	single nucleotide variant	NM_001378213.1(BCL9L):c.3581C>T (p.Thr1194Ile)	not specified [RCV005314274]	uncertain significance	11	118899334	118899334	Human		name
15117559	CV712634	single nucleotide variant	NM_001378213.1(BCL9L):c.4321G>A (p.Val1441Met)	not provided [RCV000962226]	benign	11	118898594	118898594	Human		name

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