Bcl2l1 Variant Search Result - Rat Genome Database

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197 records found for search term Bcl2l1

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
407495482	CV3417674	single nucleotide variant	NM_138578.3(BCL2L1):c.65A>G (p.Tyr22Cys)	not specified [RCV004605838]	uncertain significance	20	31722154	31722154	Human		name
15116765	CV757414	single nucleotide variant	NM_138578.3(BCL2L1):c.345C>T (p.Thr115=)	not provided [RCV000917682]	likely benign	20	31721874	31721874	Human		name
15188988	CV773027	single nucleotide variant	NM_138578.3(BCL2L1):c.558C>T (p.Gly186=)	not provided [RCV000932107]	likely benign	20	31721661	31721661	Human		name
405707410	CV3297855	single nucleotide variant	NM_138578.3(BCL2L1):c.242T>A (p.Ile81Asn)	not specified [RCV004426283]	uncertain significance	20	31721977	31721977	Human		name
155978429	CV2266516	single nucleotide variant	NM_138578.3(BCL2L1):c.608G>A (p.Ser203Asn)	not specified [RCV004131077]	uncertain significance	20	31666043	31666043	Human		name
405707417	CV3297856	single nucleotide variant	NM_138578.3(BCL2L1):c.626G>A (p.Arg209His)	not specified [RCV004426284]	uncertain significance	20	31666025	31666025	Human		name
598276498	CV3938437	single nucleotide variant	NM_138578.3(BCL2L1):c.391T>C (p.Phe131Leu)	not specified [RCV005305632]	uncertain significance	20	31721828	31721828	Human		name
126908764	CV969969	single nucleotide variant	NM_138578.3(BCL2L1):c.674T>C (p.Leu225Pro)	Hereditary breast ovarian cancer syndrome [RCV001374576]	uncertain significance	20	31665977	31665977	Human	1	name
155956058	CV2303982	single nucleotide variant	NM_138639.2(BCL2L12):c.-35G>C	not specified [RCV004170038]	uncertain significance	19	49666041	49666041	Human		name
329389981	CV2457399	single nucleotide variant	NM_138639.2(BCL2L12):c.-24T>C	not specified [RCV004267227]	uncertain significance	19	49666052	49666052	Human		name
156207272	CV2298030	single nucleotide variant	NM_138639.2(BCL2L12):c.-135C>T	not specified [RCV004157927]	uncertain significance	19	49665941	49665941	Human		name
156389541	CV2380593	single nucleotide variant	NM_138639.2(BCL2L12):c.-123T>A	not specified [RCV004224914]	uncertain significance	19	49665953	49665953	Human		name
401863897	CV2770922	single nucleotide variant	NM_138639.2(BCL2L12):c.-126G>C	not specified [RCV004343593]	likely benign	19	49665950	49665950	Human		name
405707455	CV3297862	single nucleotide variant	NM_138639.2(BCL2L12):c.-128C>T	not specified [RCV004426290]	uncertain significance	19	49665948	49665948	Human		name
597736603	CV3639667	single nucleotide variant	NM_138639.2(BCL2L12):c.-104G>C	not specified [RCV004889721]	uncertain significance	19	49665972	49665972	Human		name
150451754	CV1232843	single nucleotide variant	NM_138621.5(BCL2L11):c.499-2716A>G	not provided [RCV001647918]	benign	2	111161417	111161417	Human		name
156368561	CV2193718	single nucleotide variant	NM_020396.4(BCL2L10):c.9C>A (p.Asp3Glu)	not specified [RCV004074482]	uncertain significance	15	52112718	52112718	Human		name
15195566	CV696964	single nucleotide variant	NM_138621.5(BCL2L11):c.39C>T (p.Asp13=)	not provided [RCV000955957]	benign	2	111123784	111123784	Human		name
8636938	CV92163	single nucleotide variant	NM_138639.1(BCL2L12):c.8G>A (p.Arg3Gln)	not specified [RCV004889720]	uncertain significance\|not provided	19	49665831	49665831	Human		name
408383525	CV3504096	single nucleotide variant	NM_138621.5(BCL2L11):c.575G>A (p.Arg192His)	BCL2L11-related condition [RCV004730688]	uncertain significance	2	111164209	111164209	Human		name , trait
597690993	CV3639668	single nucleotide variant	NM_138639.1(BCL2L12):c.13G>T (p.Ala5Ser)	not specified [RCV004889722]	uncertain significance	19	49665836	49665836	Human		name
598276506	CV3938448	single nucleotide variant	NM_020396.4(BCL2L10):c.17G>C (p.Arg6Pro)	not specified [RCV005305640]	uncertain significance	15	52112710	52112710	Human		name
598276568	CV3938557	single nucleotide variant	NM_138639.1(BCL2L12):c.22T>G (p.Phe8Val)	not specified [RCV005305702]	uncertain significance	19	49665845	49665845	Human		name
598276576	CV3938572	single nucleotide variant	NM_015367.4(BCL2L13):c.19G>A (p.Val7Met)	not specified [RCV005305710]	uncertain significance	22	17655730	17655730	Human		name
15193683	CV702168	single nucleotide variant	NM_138723.2(BCL2L14):c.207G>A (p.Glu69=)	not provided [RCV000955441]	benign	12	12079512	12079512	Human		name
150483384	CV1261777	single nucleotide variant	NM_020396.4(BCL2L10):c.62T>G (p.Leu21Arg)	not provided [RCV001686381]	benign	15	52112665	52112665	Human		name
155970635	CV2241508	single nucleotide variant	NM_138621.5(BCL2L11):c.85A>G (p.Arg29Gly)	not specified [RCV004104411]	uncertain significance	2	111123830	111123830	Human		name
156361787	CV2322859	single nucleotide variant	NM_138621.5(BCL2L11):c.40C>G (p.Arg14Gly)	not specified [RCV004185318]	uncertain significance	2	111123785	111123785	Human		name
155928751	CV2346821	single nucleotide variant	NM_020396.4(BCL2L10):c.38A>G (p.Asp13Gly)	not specified [RCV004199825]	uncertain significance	15	52112689	52112689	Human		name
156136139	CV2357125	single nucleotide variant	NM_138723.2(BCL2L14):c.44A>G (p.Asp15Gly)	not specified [RCV004206919]	uncertain significance	12	12079349	12079349	Human		name
156154726	CV2359642	single nucleotide variant	NM_138723.2(BCL2L14):c.82G>A (p.Ala28Thr)	not specified [RCV004210470]	uncertain significance	12	12079387	12079387	Human		name
156253294	CV2390142	single nucleotide variant	NM_138639.1(BCL2L12):c.95C>T (p.Ala32Val)	not specified [RCV004240530]	uncertain significance	19	49665918	49665918	Human		name
329371141	CV2431906	single nucleotide variant	NM_020396.4(BCL2L10):c.29C>T (p.Thr10Ile)	not specified [RCV004255039]	uncertain significance	15	52112698	52112698	Human		name
401884881	CV2766308	single nucleotide variant	NM_138621.5(BCL2L11):c.501A>G (p.Val167=)	not specified [RCV004342563]	likely benign	2	111164135	111164135	Human		name
405707473	CV3297865	single nucleotide variant	NM_138639.1(BCL2L12):c.40T>C (p.Phe14Leu)	not specified [RCV004426293]	uncertain significance	19	49665863	49665863	Human		name
597736562	CV3639657	single nucleotide variant	NM_138621.5(BCL2L11):c.94G>A (p.Ala32Thr)	not specified [RCV004889711]	uncertain significance	2	111123839	111123839	Human		name
597736589	CV3639664	single nucleotide variant	NM_138639.2(BCL2L12):c.83G>A (p.Gly28Glu)	not specified [RCV004889717]	uncertain significance	19	49666775	49666775	Human		name
597736598	CV3639666	single nucleotide variant	NM_138639.2(BCL2L12):c.82G>A (p.Gly28Arg)	not specified [RCV004889719]	uncertain significance	19	49666774	49666774	Human		name
597736651	CV3639679	single nucleotide variant	NM_015367.4(BCL2L13):c.49T>C (p.Tyr17His)	not specified [RCV004889732]	uncertain significance	22	17655760	17655760	Human		name
598201291	CV3938478	single nucleotide variant	NM_138621.5(BCL2L11):c.82C>G (p.Leu28Val)	not specified [RCV005314202]	uncertain significance	2	111123827	111123827	Human		name
598276562	CV3938546	single nucleotide variant	NM_138639.1(BCL2L12):c.40T>A (p.Phe14Ile)	not specified [RCV005305696]	uncertain significance	19	49665863	49665863	Human		name
8634548	CV89768	single nucleotide variant	NM_138723.1(BCL2L14):c.760C>T (p.Leu254=)	Malignant melanoma [RCV000069865]	not provided	12	12094745	12094745	Human		name
156400841	CV2217270	single nucleotide variant	NM_138639.2(BCL2L12):c.236A>G (p.Tyr79Cys)	not specified [RCV004087718]	uncertain significance	19	49667147	49667147	Human		name
156387783	CV2221614	single nucleotide variant	NM_138639.2(BCL2L12):c.122A>G (p.Glu41Gly)	not specified [RCV004096868]	uncertain significance	19	49667033	49667033	Human		name
156308821	CV2249564	single nucleotide variant	NM_020396.4(BCL2L10):c.182G>C (p.Arg61Pro)	not specified [RCV004120589]	uncertain significance	15	52112545	52112545	Human		name
156053757	CV2269530	single nucleotide variant	NM_138723.2(BCL2L14):c.124C>A (p.Leu42Ile)	not specified [RCV004124637]	uncertain significance	12	12079429	12079429	Human		name
156065621	CV2287390	single nucleotide variant	NM_020396.4(BCL2L10):c.220C>T (p.Arg74Cys)	not specified [RCV004146998]	uncertain significance	15	52112507	52112507	Human		name
156045098	CV2318982	single nucleotide variant	NM_138621.5(BCL2L11):c.127A>G (p.Asn43Asp)	not specified [RCV004178078]	uncertain significance	2	111123872	111123872	Human		name
156342352	CV2343865	single nucleotide variant	NM_138621.5(BCL2L11):c.209C>G (p.Pro70Arg)	not specified [RCV004193448]	uncertain significance	2	111123954	111123954	Human		name
156344674	CV2346165	single nucleotide variant	NM_015367.4(BCL2L13):c.257A>G (p.His86Arg)	not specified [RCV004201624]	uncertain significance	22	17689013	17689013	Human		name
156284799	CV2349046	single nucleotide variant	NM_138621.5(BCL2L11):c.148G>C (p.Gly50Arg)	not specified [RCV004205487]	uncertain significance	2	111123893	111123893	Human		name
155967004	CV2396135	single nucleotide variant	NM_138621.5(BCL2L11):c.140A>G (p.Asn47Ser)	not specified [RCV004237665]	uncertain significance	2	111123885	111123885	Human		name
329382706	CV2465334	single nucleotide variant	NM_020396.4(BCL2L10):c.176T>C (p.Ile59Thr)	not specified [RCV004281121]	uncertain significance	15	52112551	52112551	Human		name
329388630	CV2469432	single nucleotide variant	NM_138723.2(BCL2L14):c.167G>A (p.Arg56Lys)	not specified [RCV004282893]	likely benign	12	12079472	12079472	Human		name
401774969	CV2713717	single nucleotide variant	NM_020396.4(BCL2L10):c.268C>T (p.Pro90Ser)	not specified [RCV004321071]	uncertain significance	15	52112459	52112459	Human		name
401867166	CV2776727	single nucleotide variant	NM_015367.4(BCL2L13):c.165T>G (p.Ile55Met)	not specified [RCV004357884]	uncertain significance	22	17683257	17683257	Human		name
401895284	CV2786324	single nucleotide variant	NM_138723.2(BCL2L14):c.100C>T (p.His34Tyr)	not specified [RCV004361932]	uncertain significance	12	12079405	12079405	Human		name
405707436	CV3297859	single nucleotide variant	NM_138621.5(BCL2L11):c.103T>C (p.Ser35Pro)	not specified [RCV004426287]	uncertain significance	2	111123848	111123848	Human		name
405707442	CV3297860	single nucleotide variant	NM_138621.5(BCL2L11):c.293C>T (p.Ser98Phe)	not specified [RCV004426288]	uncertain significance	2	111124038	111124038	Human		name
405707461	CV3297863	single nucleotide variant	NM_138639.2(BCL2L12):c.113C>T (p.Pro38Leu)	not specified [RCV004426291]	uncertain significance	19	49667024	49667024	Human		name
405707469	CV3297864	single nucleotide variant	NM_138639.2(BCL2L12):c.152G>C (p.Arg51Pro)	not specified [RCV004426292]	uncertain significance	19	49667063	49667063	Human		name
405707501	CV3297869	single nucleotide variant	NM_015367.4(BCL2L13):c.102A>C (p.Gln34His)	not specified [RCV004426297]	uncertain significance	22	17655813	17655813	Human		name
405707580	CV3297880	single nucleotide variant	NM_138723.2(BCL2L14):c.214T>C (p.Trp72Arg)	not specified [RCV004426308]	uncertain significance	12	12079519	12079519	Human		name
405707591	CV3297881	single nucleotide variant	NM_138723.2(BCL2L14):c.270G>T (p.Lys90Asn)	not specified [RCV004426309]	uncertain significance	12	12079575	12079575	Human		name
407495487	CV3417675	single nucleotide variant	NM_020396.4(BCL2L10):c.109C>T (p.Pro37Ser)	not specified [RCV004605839]	uncertain significance	15	52112618	52112618	Human		name
407499885	CV3417680	single nucleotide variant	NM_138639.2(BCL2L12):c.215C>G (p.Ser72Cys)	not specified [RCV004607009]	uncertain significance	19	49667126	49667126	Human		name
407499889	CV3417682	single nucleotide variant	NM_015367.4(BCL2L13):c.292A>G (p.Ser98Gly)	not specified [RCV004607010]	uncertain significance	22	17689048	17689048	Human		name
596946976	CV3547036	single nucleotide variant	NM_138639.2(BCL2L12):c.202C>T (p.Pro68Ser)	not provided [RCV004810842]	likely benign	19	49667113	49667113	Human		name
597736581	CV3639662	single nucleotide variant	NM_138639.2(BCL2L12):c.179G>A (p.Arg60Gln)	not specified [RCV004889715]	uncertain significance	19	49667090	49667090	Human		name
597736656	CV3639680	single nucleotide variant	NM_138723.2(BCL2L14):c.152G>T (p.Arg51Ile)	not specified [RCV004889733]	uncertain significance	12	12079457	12079457	Human		name
597736668	CV3639684	single nucleotide variant	NM_138723.2(BCL2L14):c.193G>C (p.Glu65Gln)	not specified [RCV004889736]	uncertain significance	12	12079498	12079498	Human		name
598276516	CV3938467	single nucleotide variant	NM_020396.4(BCL2L10):c.119C>T (p.Ala40Val)	not specified [RCV005305650]	uncertain significance	15	52112608	52112608	Human		name
598201360	CV3938519	single nucleotide variant	NM_138639.2(BCL2L12):c.230C>T (p.Pro77Leu)	not specified [RCV005314214]	uncertain significance	19	49667141	49667141	Human		name
598276552	CV3938526	single nucleotide variant	NM_138639.2(BCL2L12):c.206G>A (p.Arg69Gln)	not specified [RCV005305686]	uncertain significance	19	49667117	49667117	Human		name
598201510	CV3938576	single nucleotide variant	NM_015367.4(BCL2L13):c.236C>T (p.Thr79Ile)	not specified [RCV005314242]	uncertain significance	22	17688992	17688992	Human		name
598201514	CV3938582	single nucleotide variant	NM_138723.2(BCL2L14):c.266A>T (p.Lys89Ile)	not specified [RCV005314243]	uncertain significance	12	12079571	12079571	Human		name
598201519	CV3938583	single nucleotide variant	NM_138723.2(BCL2L14):c.131C>T (p.Ser44Leu)	not specified [RCV005314244]	uncertain significance	12	12079436	12079436	Human		name
15167642	CV717287	single nucleotide variant	NM_015367.4(BCL2L13):c.137T>C (p.Ile46Thr)	not provided [RCV000971441]	benign	22	17683229	17683229	Human		name
8636939	CV92164	single nucleotide variant	NM_001040668.1(BCL2L12):c.51C>T (p.Phe17=)	Malignant melanoma [RCV000072262]	not provided	19	49665874	49665874	Human		name
156398902	CV2194854	single nucleotide variant	NM_138639.2(BCL2L12):c.326C>T (p.Pro109Leu)	not specified [RCV004075388]	uncertain significance	19	49668926	49668926	Human		name
156071569	CV2201270	single nucleotide variant	NM_138723.2(BCL2L14):c.976G>A (p.Val326Ile)	not specified [RCV004077404]	uncertain significance	12	12098980	12098980	Human		name
156379376	CV2214732	single nucleotide variant	NM_020396.4(BCL2L10):c.601A>G (p.Thr201Ala)	not specified [RCV004090544]	uncertain significance	15	52109862	52109862	Human		name
155991337	CV2256434	single nucleotide variant	NM_138621.5(BCL2L11):c.563G>A (p.Arg188His)	not specified [RCV004118652]	uncertain significance	2	111164197	111164197	Human		name
156367961	CV2266908	single nucleotide variant	NM_015367.4(BCL2L13):c.757C>T (p.Pro253Ser)	not specified [RCV004131570]	uncertain significance	22	17726833	17726833	Human		name
155990790	CV2281000	single nucleotide variant	NM_138639.2(BCL2L12):c.379C>T (p.Arg127Trp)	not specified [RCV004145498]	uncertain significance	19	49669065	49669065	Human		name
155909556	CV2303414	single nucleotide variant	NM_015367.4(BCL2L13):c.869A>G (p.Asp290Gly)	not specified [RCV004159754]	uncertain significance	22	17726945	17726945	Human		name
156266681	CV2305583	single nucleotide variant	NM_020396.4(BCL2L10):c.401T>G (p.Val134Gly)	not specified [RCV004165605]	uncertain significance	15	52112326	52112326	Human		name
156267982	CV2305712	single nucleotide variant	NM_138639.2(BCL2L12):c.596C>A (p.Ala199Asp)	not specified [RCV004167532]	uncertain significance	19	49670382	49670382	Human		name
156262292	CV2319776	single nucleotide variant	NM_138723.2(BCL2L14):c.956T>C (p.Leu319Pro)	not specified [RCV004187307]	uncertain significance	12	12098960	12098960	Human		name
156351944	CV2323864	single nucleotide variant	NM_138639.2(BCL2L12):c.518A>T (p.Asp173Val)	not specified [RCV004176396]	uncertain significance	19	49670304	49670304	Human		name
156174175	CV2326880	single nucleotide variant	NM_138639.2(BCL2L12):c.650G>A (p.Ser217Asn)	not specified [RCV004176703]	uncertain significance	19	49670436	49670436	Human		name
156174199	CV2326881	single nucleotide variant	NM_138639.2(BCL2L12):c.651C>A (p.Ser217Arg)	not specified [RCV004176704]	uncertain significance	19	49670437	49670437	Human		name
155967356	CV2329907	single nucleotide variant	NM_015367.4(BCL2L13):c.343C>G (p.Leu115Val)	not specified [RCV004183362]	uncertain significance	22	17689099	17689099	Human		name
155923809	CV2351881	single nucleotide variant	NM_015367.4(BCL2L13):c.320T>G (p.Leu107Arg)	not specified [RCV004198024]	uncertain significance	22	17689076	17689076	Human		name
155929549	CV2363549	single nucleotide variant	NM_138639.2(BCL2L12):c.553C>A (p.Pro185Thr)	not specified [RCV004216117]	uncertain significance	19	49670339	49670339	Human		name
155910497	CV2366460	single nucleotide variant	NM_138723.2(BCL2L14):c.581T>C (p.Val194Ala)	not specified [RCV004208440]	uncertain significance	12	12087360	12087360	Human		name
155933815	CV2372344	single nucleotide variant	NM_138639.2(BCL2L12):c.670T>C (p.Phe224Leu)	not specified [RCV004217112]	uncertain significance	19	49670456	49670456	Human		name
156207539	CV2382381	single nucleotide variant	NM_015367.4(BCL2L13):c.793G>C (p.Glu265Gln)	not specified [RCV004230720]	uncertain significance	22	17726869	17726869	Human		name
155907656	CV2389945	single nucleotide variant	NM_138723.2(BCL2L14):c.503A>C (p.Gln168Pro)	not specified [RCV004238198]	uncertain significance	12	12087282	12087282	Human		name
156245277	CV2396661	single nucleotide variant	NM_015367.4(BCL2L13):c.682C>A (p.Pro228Thr)	not specified [RCV004240479]	uncertain significance	22	17726758	17726758	Human		name
329385903	CV2428136	single nucleotide variant	NM_015367.4(BCL2L13):c.676A>G (p.Ile226Val)	not specified [RCV004251178]	uncertain significance	22	17726752	17726752	Human		name
329355601	CV2445464	single nucleotide variant	NM_138723.2(BCL2L14):c.977T>C (p.Val326Ala)	not specified [RCV004257524]	uncertain significance	12	12098981	12098981	Human		name
329352175	CV2452170	single nucleotide variant	NM_020396.4(BCL2L10):c.568T>C (p.Cys190Arg)	not specified [RCV004278882]	uncertain significance	15	52109895	52109895	Human		name
329361509	CV2459781	single nucleotide variant	NM_138639.2(BCL2L12):c.463G>T (p.Val155Phe)	not specified [RCV004277195]	uncertain significance	19	49670249	49670249	Human		name
401730370	CV2680284	single nucleotide variant	NM_015367.4(BCL2L13):c.403G>C (p.Ala135Pro)	not specified [RCV004286751]	uncertain significance	22	17696157	17696157	Human		name
401729343	CV2690161	single nucleotide variant	NM_138639.2(BCL2L12):c.301C>G (p.Leu101Val)	not specified [RCV004302176]	uncertain significance	19	49668901	49668901	Human		name
401776065	CV2692588	single nucleotide variant	NM_138723.2(BCL2L14):c.873C>G (p.Asn291Lys)	not specified [RCV004312325]	uncertain significance	12	12094858	12094858	Human		name
401759900	CV2698667	single nucleotide variant	NM_138621.5(BCL2L11):c.421G>A (p.Asp141Asn)	not specified [RCV004299135]	uncertain significance	2	111150070	111150070	Human		name
401889282	CV2759759	single nucleotide variant	NM_138639.2(BCL2L12):c.380G>A (p.Arg127Gln)	not specified [RCV004342804]	uncertain significance	19	49669066	49669066	Human		name
401870731	CV2766305	single nucleotide variant	NM_020396.4(BCL2L10):c.343A>T (p.Thr115Ser)	not specified [RCV004342561]	uncertain significance	15	52112384	52112384	Human		name
401885628	CV2778195	single nucleotide variant	NM_138723.2(BCL2L14):c.838G>A (p.Ala280Thr)	not specified [RCV004349918]	uncertain significance	12	12094823	12094823	Human		name
401880002	CV2783061	single nucleotide variant	NM_138723.2(BCL2L14):c.854T>C (p.Ile285Thr)	not specified [RCV004363427]	uncertain significance	12	12094839	12094839	Human		name
405707428	CV3297858	single nucleotide variant	NM_020396.4(BCL2L10):c.346G>C (p.Ala116Pro)	not specified [RCV004426286]	uncertain significance	15	52112381	52112381	Human		name
405707448	CV3297861	single nucleotide variant	NM_138621.5(BCL2L11):c.480C>A (p.Asn160Lys)	not specified [RCV004426289]	uncertain significance	2	111150129	111150129	Human		name
405707483	CV3297866	single nucleotide variant	NM_138639.2(BCL2L12):c.553C>T (p.Pro185Ser)	not specified [RCV004426294]	uncertain significance	19	49670339	49670339	Human		name
405707489	CV3297867	single nucleotide variant	NM_138639.2(BCL2L12):c.688G>T (p.Ala230Ser)	not specified [RCV004426295]	uncertain significance	19	49670474	49670474	Human		name
405707495	CV3297868	single nucleotide variant	NM_138639.2(BCL2L12):c.727G>A (p.Val243Met)	not specified [RCV004426296]	uncertain significance	19	49673722	49673722	Human		name
405707544	CV3297875	single nucleotide variant	NM_015367.4(BCL2L13):c.409C>G (p.Arg137Gly)	not specified [RCV004426303]	uncertain significance	22	17696163	17696163	Human		name
405707547	CV3297876	single nucleotide variant	NM_015367.4(BCL2L13):c.410G>A (p.Arg137Gln)	not specified [RCV004426304]	uncertain significance	22	17696164	17696164	Human		name
405707554	CV3297877	single nucleotide variant	NM_015367.4(BCL2L13):c.508C>T (p.Arg170Cys)	not specified [RCV004426305]	uncertain significance	22	17702294	17702294	Human		name
405707563	CV3297878	single nucleotide variant	NM_015367.4(BCL2L13):c.566A>G (p.Tyr189Cys)	not specified [RCV004426306]	uncertain significance	22	17702352	17702352	Human		name
405707571	CV3297879	single nucleotide variant	NM_015367.4(BCL2L13):c.832C>G (p.Gln278Glu)	not specified [RCV004426307]	uncertain significance	22	17726908	17726908	Human		name
405707601	CV3297882	single nucleotide variant	NM_138723.2(BCL2L14):c.332A>G (p.Lys111Arg)	not specified [RCV004426310]	uncertain significance	12	12079637	12079637	Human		name
405707608	CV3297883	single nucleotide variant	NM_138723.2(BCL2L14):c.513G>C (p.Gln171His)	not specified [RCV004426311]	uncertain significance	12	12087292	12087292	Human		name
405707618	CV3297884	single nucleotide variant	NM_138723.2(BCL2L14):c.638T>C (p.Val213Ala)	not specified [RCV004426312]	uncertain significance	12	12090809	12090809	Human		name
407495493	CV3417676	single nucleotide variant	NM_138621.5(BCL2L11):c.562C>T (p.Arg188Cys)	not specified [RCV004605840]	uncertain significance	2	111164196	111164196	Human		name
407495497	CV3417677	single nucleotide variant	NM_138621.5(BCL2L11):c.568A>G (p.Ile190Val)	not specified [RCV004605841]	uncertain significance	2	111164202	111164202	Human		name
407499880	CV3417678	single nucleotide variant	NM_138639.2(BCL2L12):c.732C>G (p.Asp244Glu)	not specified [RCV004607008]	uncertain significance	19	49673727	49673727	Human		name
407495515	CV3417685	single nucleotide variant	NM_015367.4(BCL2L13):c.461T>C (p.Leu154Ser)	not specified [RCV004605845]	uncertain significance	22	17702247	17702247	Human		name
407495519	CV3417686	single nucleotide variant	NM_138723.2(BCL2L14):c.613G>A (p.Glu205Lys)	not specified [RCV004605846]	uncertain significance	12	12090784	12090784	Human		name
407495524	CV3417687	single nucleotide variant	NM_138723.2(BCL2L14):c.850G>T (p.Ala284Ser)	not specified [RCV004605847]	uncertain significance	12	12094835	12094835	Human		name
597736552	CV3639655	single nucleotide variant	NM_020396.4(BCL2L10):c.600G>T (p.Trp200Cys)	not specified [RCV004889709]	uncertain significance	15	52109863	52109863	Human		name
597736556	CV3639656	single nucleotide variant	NM_020396.4(BCL2L10):c.463G>A (p.Ala155Thr)	not specified [RCV004889710]	uncertain significance	15	52112264	52112264	Human		name
597736567	CV3639658	single nucleotide variant	NM_138621.5(BCL2L11):c.481G>A (p.Ala161Thr)	not specified [RCV004889712]	uncertain significance	2	111150130	111150130	Human		name
597736572	CV3639659	single nucleotide variant	NM_138621.5(BCL2L11):c.367G>A (p.Ala123Thr)	not specified [RCV004889713]	uncertain significance	2	111124112	111124112	Human		name
597736577	CV3639660	single nucleotide variant	NM_138621.5(BCL2L11):c.438A>G (p.Ile146Met)	not specified [RCV004889714]	uncertain significance	2	111150087	111150087	Human		name
597736584	CV3639663	single nucleotide variant	NM_138639.2(BCL2L12):c.550G>A (p.Gly184Arg)	not specified [RCV004889716]	uncertain significance	19	49670336	49670336	Human		name
597736594	CV3639665	single nucleotide variant	NM_138639.2(BCL2L12):c.418A>T (p.Ile140Phe)	not specified [RCV004889718]	uncertain significance	19	49669104	49669104	Human		name
597736627	CV3639674	single nucleotide variant	NM_015367.4(BCL2L13):c.994C>T (p.Arg332Trp)	not specified [RCV004889727]	uncertain significance	22	17727070	17727070	Human		name
597736632	CV3639675	single nucleotide variant	NM_015367.4(BCL2L13):c.999G>T (p.Glu333Asp)	not specified [RCV004889728]	uncertain significance	22	17727075	17727075	Human		name
597736637	CV3639676	single nucleotide variant	NM_015367.4(BCL2L13):c.962A>G (p.Glu321Gly)	not specified [RCV004889729]	uncertain significance	22	17727038	17727038	Human		name
597736641	CV3639677	single nucleotide variant	NM_015367.4(BCL2L13):c.973G>C (p.Ala325Pro)	not specified [RCV004889730]	uncertain significance	22	17727049	17727049	Human		name
597736658	CV3639682	single nucleotide variant	NM_138723.2(BCL2L14):c.396G>T (p.Arg132Ser)	not specified [RCV004889734]	uncertain significance	12	12079701	12079701	Human		name
597736662	CV3639683	single nucleotide variant	NM_138723.2(BCL2L14):c.323C>T (p.Thr108Met)	not specified [RCV004889735]	uncertain significance	12	12079628	12079628	Human		name
598276512	CV3938457	single nucleotide variant	NM_020396.4(BCL2L10):c.349C>G (p.Arg117Gly)	not specified [RCV005305646]	uncertain significance	15	52112378	52112378	Human		name
598276526	CV3938489	single nucleotide variant	NM_138621.5(BCL2L11):c.461G>A (p.Arg154His)	not specified [RCV005305660]	uncertain significance	2	111150110	111150110	Human		name
598276542	CV3938508	single nucleotide variant	NM_138639.2(BCL2L12):c.334C>T (p.Pro112Ser)	not specified [RCV005305676]	uncertain significance	19	49668934	49668934	Human		name
598201406	CV3938535	single nucleotide variant	NM_138639.2(BCL2L12):c.300G>C (p.Gln100His)	not specified [RCV005314222]	uncertain significance	19	49668900	49668900	Human		name
598201499	CV3938573	single nucleotide variant	NM_015367.4(BCL2L13):c.496G>C (p.Glu166Gln)	not specified [RCV005314240]	uncertain significance	22	17702282	17702282	Human		name
598201505	CV3938574	single nucleotide variant	NM_015367.4(BCL2L13):c.887A>G (p.Glu296Gly)	not specified [RCV005314241]	uncertain significance	22	17726963	17726963	Human		name
598276579	CV3938578	single nucleotide variant	NM_015367.4(BCL2L13):c.506G>C (p.Arg169Thr)	not specified [RCV005305713]	uncertain significance	22	17702292	17702292	Human		name
598276580	CV3938579	single nucleotide variant	NM_138723.2(BCL2L14):c.979G>C (p.Asp327His)	not specified [RCV005305714]	uncertain significance	12	12098983	12098983	Human		name
598276581	CV3938580	single nucleotide variant	NM_138723.2(BCL2L14):c.747C>G (p.Ile249Met)	not specified [RCV005305715]	uncertain significance	12	12094732	12094732	Human		name
598276582	CV3938581	single nucleotide variant	NM_138723.2(BCL2L14):c.425A>G (p.Glu142Gly)	not specified [RCV005305716]	uncertain significance	12	12079730	12079730	Human		name
598276583	CV3938584	single nucleotide variant	NM_138723.2(BCL2L14):c.334G>C (p.Val112Leu)	not specified [RCV005305717]	uncertain significance	12	12079639	12079639	Human		name
15203014	CV705770	single nucleotide variant	NM_015367.4(BCL2L13):c.571G>T (p.Ala191Ser)	not provided [RCV000958169]	benign	22	17702357	17702357	Human		name
156247535	CV2202901	single nucleotide variant	NM_015367.4(BCL2L13):c.1300G>A (p.Val434Met)	not specified [RCV004069175]	uncertain significance	22	17727376	17727376	Human		name
156340044	CV2229394	single nucleotide variant	NM_015367.4(BCL2L13):c.1106A>G (p.Lys369Arg)	not specified [RCV004101173]	uncertain significance	22	17727182	17727182	Human		name
155986809	CV2275347	single nucleotide variant	NM_001010922.3(BCL2L15):c.37T>A (p.Cys13Ser)	not specified [RCV004135236]	uncertain significance	1	113887339	113887339	Human		name
156275273	CV2279950	single nucleotide variant	NM_015367.4(BCL2L13):c.1342G>A (p.Glu448Lys)	not specified [RCV004146324]	uncertain significance	22	17727418	17727418	Human		name
156346216	CV2300483	single nucleotide variant	NM_015367.4(BCL2L13):c.1022C>A (p.Ala341Asp)	not specified [RCV004153669]	uncertain significance	22	17727098	17727098	Human		name
156249359	CV2314144	single nucleotide variant	NM_015367.4(BCL2L13):c.1220C>T (p.Thr407Met)	not specified [RCV004166230]	likely benign	22	17727296	17727296	Human		name
156181300	CV2353070	single nucleotide variant	NM_015367.4(BCL2L13):c.1288G>A (p.Glu430Lys)	not specified [RCV004203554]	uncertain significance	22	17727364	17727364	Human		name
156336313	CV2360715	single nucleotide variant	NM_015367.4(BCL2L13):c.1380A>G (p.Ile460Met)	not specified [RCV004213504]	uncertain significance	22	17727456	17727456	Human		name
156252244	CV2369021	single nucleotide variant	NM_015367.4(BCL2L13):c.1358C>T (p.Pro453Leu)	not specified [RCV004207959]	uncertain significance	22	17727434	17727434	Human		name
329373126	CV2439291	single nucleotide variant	NM_015367.4(BCL2L13):c.1399G>A (p.Ala467Thr)	not specified [RCV004249603]	uncertain significance	22	17727475	17727475	Human		name
329392380	CV2468033	single nucleotide variant	NM_015367.4(BCL2L13):c.1040C>T (p.Pro347Leu)	not specified [RCV004273651]	uncertain significance	22	17727116	17727116	Human		name
401758254	CV2704251	single nucleotide variant	NM_015367.4(BCL2L13):c.1177A>G (p.Thr393Ala)	not specified [RCV004311249]	uncertain significance	22	17727253	17727253	Human		name
401761013	CV2706182	single nucleotide variant	NM_015367.4(BCL2L13):c.1015C>G (p.Pro339Ala)	not specified [RCV004314861]	uncertain significance	22	17727091	17727091	Human		name
401869333	CV2772362	single nucleotide variant	NM_015367.4(BCL2L13):c.1246G>C (p.Ala416Pro)	not specified [RCV004353373]	uncertain significance	22	17727322	17727322	Human		name
401880396	CV2783195	single nucleotide variant	NM_015367.4(BCL2L13):c.1120A>G (p.Thr374Ala)	not specified [RCV004363535]	uncertain significance	22	17727196	17727196	Human		name
405707510	CV3297870	single nucleotide variant	NM_015367.4(BCL2L13):c.1201G>A (p.Ala401Thr)	not specified [RCV004426298]	likely benign	22	17727277	17727277	Human		name
405707517	CV3297871	single nucleotide variant	NM_015367.4(BCL2L13):c.1307C>A (p.Pro436Gln)	not specified [RCV004426299]	uncertain significance	22	17727383	17727383	Human		name
405707522	CV3297872	single nucleotide variant	NM_015367.4(BCL2L13):c.1334C>G (p.Pro445Arg)	not specified [RCV004426300]	uncertain significance	22	17727410	17727410	Human		name
405707527	CV3297873	single nucleotide variant	NM_015367.4(BCL2L13):c.1354A>G (p.Met452Val)	not specified [RCV004426301]	uncertain significance	22	17727430	17727430	Human		name
405707636	CV3297887	single nucleotide variant	NM_001010922.3(BCL2L15):c.77C>T (p.Thr26Ile)	not specified [RCV004426315]	uncertain significance	1	113887299	113887299	Human		name
407495506	CV3417681	single nucleotide variant	NM_015367.4(BCL2L13):c.1226T>C (p.Leu409Pro)	not specified [RCV004605843]	uncertain significance	22	17727302	17727302	Human		name
407495511	CV3417683	single nucleotide variant	NM_015367.4(BCL2L13):c.1452G>T (p.Lys484Asn)	not specified [RCV004605844]	uncertain significance	22	17727528	17727528	Human		name
407499895	CV3417684	single nucleotide variant	NM_015367.4(BCL2L13):c.1291A>G (p.Lys431Glu)	not specified [RCV004607011]	uncertain significance	22	17727367	17727367	Human		name
597736608	CV3639669	single nucleotide variant	NM_015367.4(BCL2L13):c.1304C>T (p.Pro435Leu)	not specified [RCV004889723]	likely benign	22	17727380	17727380	Human		name
597736613	CV3639671	single nucleotide variant	NM_015367.4(BCL2L13):c.1426A>G (p.Ile476Val)	not specified [RCV004889724]	likely benign	22	17727502	17727502	Human		name
597736617	CV3639672	single nucleotide variant	NM_015367.4(BCL2L13):c.1370G>A (p.Gly457Asp)	not specified [RCV004889725]	uncertain significance	22	17727446	17727446	Human		name
597736622	CV3639673	single nucleotide variant	NM_015367.4(BCL2L13):c.1405G>T (p.Val469Phe)	not specified [RCV004889726]	uncertain significance	22	17727481	17727481	Human		name
597736646	CV3639678	single nucleotide variant	NM_015367.4(BCL2L13):c.1244A>T (p.Asn415Ile)	not specified [RCV004889731]	uncertain significance	22	17727320	17727320	Human		name
597736674	CV3639685	single nucleotide variant	NM_001010922.3(BCL2L15):c.58A>G (p.Met20Val)	not specified [RCV004889737]	uncertain significance	1	113887318	113887318	Human		name
598276574	CV3938567	single nucleotide variant	NM_015367.4(BCL2L13):c.1139T>C (p.Leu380Pro)	not specified [RCV005305708]	uncertain significance	22	17727215	17727215	Human		name
598276578	CV3938577	single nucleotide variant	NM_015367.4(BCL2L13):c.1192G>A (p.Val398Met)	not specified [RCV005305712]	uncertain significance	22	17727268	17727268	Human		name
401889407	CV2756491	single nucleotide variant	NM_001010922.3(BCL2L15):c.148G>A (p.Val50Met)	not specified [RCV004345024]	uncertain significance	1	113886638	113886638	Human		name
405707629	CV3297886	single nucleotide variant	NM_001010922.3(BCL2L15):c.214G>T (p.Ala72Ser)	not specified [RCV004426314]	uncertain significance	1	113886572	113886572	Human		name
407495528	CV3417688	single nucleotide variant	NM_001010922.3(BCL2L15):c.158T>C (p.Ile53Thr)	not specified [RCV004605848]	uncertain significance	1	113886628	113886628	Human		name
598276586	CV3938587	single nucleotide variant	NM_001010922.3(BCL2L15):c.236C>T (p.Thr79Ile)	not specified [RCV005305720]	uncertain significance	1	113886550	113886550	Human		name
598276587	CV3938588	single nucleotide variant	NM_001010922.3(BCL2L15):c.194A>G (p.Asn65Ser)	not specified [RCV005305721]	uncertain significance	1	113886592	113886592	Human		name
156389280	CV2226174	single nucleotide variant	NM_001010922.3(BCL2L15):c.307G>A (p.Asp103Asn)	not specified [RCV004105576]	uncertain significance	1	113881940	113881940	Human		name
407495532	CV3417689	single nucleotide variant	NM_001010922.3(BCL2L15):c.453C>A (p.Phe151Leu)	not specified [RCV004605849]	uncertain significance	1	113881794	113881794	Human		name
597736679	CV3639686	single nucleotide variant	NM_001010922.3(BCL2L15):c.470G>T (p.Gly157Val)	not specified [RCV004889738]	uncertain significance	1	113881777	113881777	Human		name
598276584	CV3938585	single nucleotide variant	NM_001010922.3(BCL2L15):c.446G>A (p.Arg149Gln)	not specified [RCV005305718]	uncertain significance	1	113881801	113881801	Human		name
598276588	CV3938589	single nucleotide variant	NM_001010922.3(BCL2L15):c.314G>T (p.Ser105Ile)	not specified [RCV005305722]	uncertain significance	1	113881933	113881933	Human		name

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