Sipa1l1 Variant Search Result - Rat Genome Database

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156 records found for search term Sipa1l1

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
405751094	CV3332048	single nucleotide variant	NM_001386936.1(SIPA1L1):c.3647-465T>C	not specified [RCV004453796]	uncertain significance	14	71704757	71704757	Human		name
598257738	CV3910740	single nucleotide variant	NM_001386936.1(SIPA1L1):c.3647-484C>T	not specified [RCV005279266]	uncertain significance	14	71704738	71704738	Human		name
598257819	CV3910754	single nucleotide variant	NM_001386936.1(SIPA1L1):c.3647-488A>C	not specified [RCV005279280]	uncertain significance	14	71704734	71704734	Human		name
8583936	CV118505	single nucleotide variant	NM_001284245.1(SIPA1L1):c.-302-9566G>C	Lung cancer [RCV000099025]	uncertain significance	14	71578005	71578005	Human		name
156112012	CV2387874	single nucleotide variant	NM_001386936.1(SIPA1L1):c.17G>A (p.Arg6Gln)	not specified [RCV004236428]	uncertain significance	14	71587889	71587889	Human		name
150529743	CV1293135	single nucleotide variant	NM_001386936.1(SIPA1L1):c.879A>C (p.Ser293=)	not provided [RCV001756353]	benign	14	71588751	71588751	Human		name
401915406	CV2810537	single nucleotide variant	NM_001386936.1(SIPA1L1):c.435G>A (p.Pro145=)	not provided [RCV003400613]	likely benign	14	71588307	71588307	Human		name
15116455	CV743561	single nucleotide variant	NM_001386936.1(SIPA1L1):c.489C>G (p.Pro163=)	not provided [RCV000895204]	benign	14	71588361	71588361	Human		name
156299063	CV2244691	single nucleotide variant	NM_001386936.1(SIPA1L1):c.195A>G (p.Ile65Met)	not specified [RCV004102693]	uncertain significance	14	71588067	71588067	Human		name
156169513	CV2276761	single nucleotide variant	NM_001386936.1(SIPA1L1):c.113G>A (p.Arg38His)	not specified [RCV004146545]	uncertain significance	14	71587985	71587985	Human		name
155972550	CV2309420	single nucleotide variant	NM_001386936.1(SIPA1L1):c.197C>A (p.Thr66Asn)	not specified [RCV004165563]	uncertain significance	14	71588069	71588069	Human		name
156089109	CV2344350	single nucleotide variant	NM_001386936.1(SIPA1L1):c.281G>A (p.Ser94Asn)	not specified [RCV004195107]	uncertain significance	14	71588153	71588153	Human		name
405751026	CV3311673	single nucleotide variant	NM_001386936.1(SIPA1L1):c.109C>T (p.Arg37Trp)	not specified [RCV004453786]	uncertain significance	14	71587981	71587981	Human		name
405751032	CV3311674	single nucleotide variant	NM_001386936.1(SIPA1L1):c.118C>T (p.Arg40Trp)	not specified [RCV004453787]	uncertain significance	14	71587990	71587990	Human		name
405751040	CV3311675	single nucleotide variant	NM_001386936.1(SIPA1L1):c.128A>T (p.Asn43Ile)	not specified [RCV004453788]	uncertain significance	14	71588000	71588000	Human		name
597738422	CV3595905	single nucleotide variant	NM_001386936.1(SIPA1L1):c.151A>T (p.Met51Leu)	not specified [RCV004864248]	uncertain significance	14	71588023	71588023	Human		name
597738436	CV3595908	single nucleotide variant	NM_001386936.1(SIPA1L1):c.173G>A (p.Arg58Gln)	not specified [RCV004864251]	uncertain significance	14	71588045	71588045	Human		name
15201634	CV706434	single nucleotide variant	NM_001386936.1(SIPA1L1):c.1665C>T (p.Ala555=)	not provided [RCV000957679]	likely benign	14	71624083	71624083	Human		name
15187266	CV706435	single nucleotide variant	NM_001386936.1(SIPA1L1):c.166C>A (p.Pro56Thr)	not provided [RCV000953536]	benign	14	71588038	71588038	Human		name
15201630	CV706436	single nucleotide variant	NM_001386936.1(SIPA1L1):c.170C>A (p.Pro57His)	not provided [RCV000957678]	likely benign	14	71588042	71588042	Human		name
15130976	CV717969	single nucleotide variant	NM_001386936.1(SIPA1L1):c.119G>A (p.Arg40Gln)	not provided [RCV000964526]	benign	14	71587991	71587991	Human		name
15193740	CV729821	single nucleotide variant	NM_001386936.1(SIPA1L1):c.1674G>A (p.Ser558=)	not provided [RCV000889030]	benign	14	71624092	71624092	Human		name
15191746	CV729822	single nucleotide variant	NM_001386936.1(SIPA1L1):c.1689G>A (p.Ser563=)	not provided [RCV000888466]	likely benign	14	71624107	71624107	Human		name
15104682	CV729823	single nucleotide variant	NM_001386936.1(SIPA1L1):c.2202C>T (p.His734=)	not provided [RCV000892933]	benign	14	71661414	71661414	Human		name
8635277	CV90499	single nucleotide variant	NM_015556.2(SIPA1L1):c.3150G>A (p.Met1050Ile)	Malignant melanoma [RCV000070597]	not provided	14	71685407	71685407	Human		name
8635278	CV90500	single nucleotide variant	NM_015556.2(SIPA1L1):c.4478C>T (p.Thr1493Ile)	Malignant melanoma [RCV000070598]	not provided	14	71723853	71723853	Human		name
156399763	CV2202202	single nucleotide variant	NM_001386936.1(SIPA1L1):c.391A>G (p.Met131Val)	not specified [RCV004078149]	uncertain significance	14	71588263	71588263	Human		name
156300160	CV2244858	single nucleotide variant	NM_001386936.1(SIPA1L1):c.428C>T (p.Thr143Ile)	not specified [RCV004104618]	uncertain significance	14	71588300	71588300	Human		name
156301356	CV2248963	single nucleotide variant	NM_001386936.1(SIPA1L1):c.817A>G (p.Arg273Gly)	not specified [RCV004115961]	uncertain significance	14	71588689	71588689	Human		name
155998081	CV2287106	single nucleotide variant	NM_001386936.1(SIPA1L1):c.401G>T (p.Ser134Ile)	not specified [RCV004144977]	uncertain significance	14	71588273	71588273	Human		name
156162631	CV2323546	single nucleotide variant	NM_001386936.1(SIPA1L1):c.859A>G (p.Lys287Glu)	not specified [RCV004165745]	uncertain significance	14	71588731	71588731	Human		name
156330788	CV2339534	single nucleotide variant	NM_001386936.1(SIPA1L1):c.428C>G (p.Thr143Arg)	not specified [RCV004194200]	uncertain significance	14	71588300	71588300	Human		name
156124838	CV2350138	single nucleotide variant	NM_001386936.1(SIPA1L1):c.746C>T (p.Thr249Ile)	not specified [RCV004200058]	uncertain significance	14	71588618	71588618	Human		name
156052453	CV2388463	single nucleotide variant	NM_001386936.1(SIPA1L1):c.632C>T (p.Ser211Leu)	not specified [RCV004237322]	uncertain significance	14	71588504	71588504	Human		name
329370108	CV2461615	single nucleotide variant	NM_001386936.1(SIPA1L1):c.805A>G (p.Arg269Gly)	not specified [RCV004269791]	uncertain significance	14	71588677	71588677	Human		name
401891816	CV2779474	single nucleotide variant	NM_001386936.1(SIPA1L1):c.452C>T (p.Ser151Phe)	not specified [RCV004351107]	uncertain significance	14	71588324	71588324	Human		name
401934157	CV2810538	single nucleotide variant	NM_001386936.1(SIPA1L1):c.3576A>G (p.Ser1192=)	not provided [RCV003411042]	likely benign	14	71702435	71702435	Human		name
401915409	CV2810539	single nucleotide variant	NM_001386936.1(SIPA1L1):c.5298G>C (p.Ser1766=)	not provided [RCV003400614]	likely benign	14	71739107	71739107	Human		name
405751177	CV3332061	single nucleotide variant	NM_001386936.1(SIPA1L1):c.497C>G (p.Ala166Gly)	not specified [RCV004453809]	uncertain significance	14	71588369	71588369	Human		name
405751184	CV3332062	single nucleotide variant	NM_001386936.1(SIPA1L1):c.532A>G (p.Ile178Val)	not specified [RCV004453810]	uncertain significance	14	71588404	71588404	Human		name
405751190	CV3332063	single nucleotide variant	NM_001386936.1(SIPA1L1):c.596G>T (p.Gly199Val)	not specified [RCV004453811]	uncertain significance	14	71588468	71588468	Human		name
405751197	CV3332064	single nucleotide variant	NM_001386936.1(SIPA1L1):c.673T>G (p.Leu225Val)	not specified [RCV004453812]	uncertain significance	14	71588545	71588545	Human		name
405751206	CV3332065	single nucleotide variant	NM_001386936.1(SIPA1L1):c.928T>G (p.Ser310Ala)	not specified [RCV004453813]	uncertain significance	14	71588800	71588800	Human		name
405751213	CV3332066	single nucleotide variant	NM_001386936.1(SIPA1L1):c.969G>T (p.Arg323Ser)	not specified [RCV004453814]	uncertain significance	14	71588841	71588841	Human		name
407502017	CV3480797	single nucleotide variant	NM_001386936.1(SIPA1L1):c.724A>C (p.Lys242Gln)	not specified [RCV004669879]	uncertain significance	14	71588596	71588596	Human		name
597738396	CV3595899	single nucleotide variant	NM_001386936.1(SIPA1L1):c.437C>T (p.Ser146Leu)	not specified [RCV004864243]	uncertain significance	14	71588309	71588309	Human		name
597738402	CV3595900	single nucleotide variant	NM_001386936.1(SIPA1L1):c.902A>G (p.Asn301Ser)	not specified [RCV004864244]	uncertain significance	14	71588774	71588774	Human		name
597738407	CV3595901	single nucleotide variant	NM_001386936.1(SIPA1L1):c.732T>A (p.Ser244Arg)	not specified [RCV004864245]	uncertain significance	14	71588604	71588604	Human		name
597738427	CV3595906	single nucleotide variant	NM_001386936.1(SIPA1L1):c.571T>C (p.Cys191Arg)	not specified [RCV004864249]	uncertain significance	14	71588443	71588443	Human		name
598257724	CV3910737	single nucleotide variant	NM_001386936.1(SIPA1L1):c.796A>G (p.Ile266Val)	not specified [RCV005279263]	uncertain significance	14	71588668	71588668	Human		name
598257764	CV3910745	single nucleotide variant	NM_001386936.1(SIPA1L1):c.312T>G (p.Ser104Arg)	not specified [RCV005279271]	uncertain significance	14	71588184	71588184	Human		name
598257795	CV3910750	single nucleotide variant	NM_001386936.1(SIPA1L1):c.502C>T (p.Arg168Cys)	not specified [RCV005279276]	uncertain significance	14	71588374	71588374	Human		name
598257814	CV3910753	single nucleotide variant	NM_001386936.1(SIPA1L1):c.901A>G (p.Asn301Asp)	not specified [RCV005279279]	uncertain significance	14	71588773	71588773	Human		name
15164957	CV758718	single nucleotide variant	NM_001386936.1(SIPA1L1):c.3324C>T (p.Ala1108=)	not provided [RCV000926508]	likely benign	14	71685581	71685581	Human		name
15151018	CV758719	single nucleotide variant	NM_001386936.1(SIPA1L1):c.5097T>C (p.Ala1699=)	not provided [RCV000923587]	likely benign	14	71735365	71735365	Human		name
156145964	CV2196844	single nucleotide variant	NM_001386936.1(SIPA1L1):c.1772A>G (p.Asn591Ser)	not specified [RCV004069853]	uncertain significance	14	71624190	71624190	Human		name
156245496	CV2231685	single nucleotide variant	NM_001386936.1(SIPA1L1):c.2935C>T (p.Pro979Ser)	not specified [RCV004098247]	uncertain significance	14	71672453	71672453	Human		name
155968852	CV2244373	single nucleotide variant	NM_001386936.1(SIPA1L1):c.2746A>G (p.Ile916Val)	not specified [RCV004100350]	uncertain significance	14	71671609	71671609	Human		name
156276534	CV2255809	single nucleotide variant	NM_001386936.1(SIPA1L1):c.2629C>G (p.Leu877Val)	not specified [RCV004121973]	uncertain significance	14	71671492	71671492	Human		name
155987429	CV2259468	single nucleotide variant	NM_001386936.1(SIPA1L1):c.2081C>T (p.Pro694Leu)	not specified [RCV004122671]	uncertain significance	14	71658420	71658420	Human		name
156260118	CV2277888	single nucleotide variant	NM_001386936.1(SIPA1L1):c.1523A>T (p.Asp508Val)	not specified [RCV004147298]	uncertain significance	14	71618781	71618781	Human		name
155903766	CV2282293	single nucleotide variant	NM_001386936.1(SIPA1L1):c.1015A>G (p.Ile339Val)	not specified [RCV004133127]	uncertain significance	14	71588887	71588887	Human		name
156298994	CV2310681	single nucleotide variant	NM_001386936.1(SIPA1L1):c.2713A>G (p.Ile905Val)	not specified [RCV004157338]	uncertain significance	14	71671576	71671576	Human		name
155961792	CV2311949	single nucleotide variant	NM_001386936.1(SIPA1L1):c.2603A>G (p.Tyr868Cys)	not specified [RCV004170769]	uncertain significance	14	71671466	71671466	Human		name
156295296	CV2321491	single nucleotide variant	NM_001386936.1(SIPA1L1):c.2249G>A (p.Cys750Tyr)	not specified [RCV004177462]	uncertain significance	14	71661461	71661461	Human		name
156270576	CV2333778	single nucleotide variant	NM_001386936.1(SIPA1L1):c.1943G>A (p.Arg648Gln)	not specified [RCV004181283]	uncertain significance	14	71650459	71650459	Human		name
156078372	CV2351109	single nucleotide variant	NM_001386936.1(SIPA1L1):c.2776G>T (p.Val926Leu)	not specified [RCV004213971]	uncertain significance	14	71671639	71671639	Human		name
156193711	CV2351817	single nucleotide variant	NM_001386936.1(SIPA1L1):c.1159G>A (p.Gly387Ser)	not specified [RCV004197965]	uncertain significance	14	71589031	71589031	Human		name
156194851	CV2399206	single nucleotide variant	NM_001386936.1(SIPA1L1):c.2241C>A (p.Asp747Glu)	not specified [RCV004246634]	uncertain significance	14	71661453	71661453	Human		name
329354088	CV2436930	single nucleotide variant	NM_001386936.1(SIPA1L1):c.1156A>T (p.Met386Leu)	not specified [RCV004260311]	uncertain significance	14	71589028	71589028	Human		name
329355373	CV2445396	single nucleotide variant	NM_001386936.1(SIPA1L1):c.2357C>T (p.Ala786Val)	not specified [RCV004257470]	uncertain significance	14	71671220	71671220	Human		name
401731960	CV2684637	single nucleotide variant	NM_001386936.1(SIPA1L1):c.1771A>G (p.Asn591Asp)	not specified [RCV004293735]	uncertain significance	14	71624189	71624189	Human		name
401782269	CV2686635	single nucleotide variant	NM_001386936.1(SIPA1L1):c.2575A>G (p.Ile859Val)	not specified [RCV004300050]	uncertain significance	14	71671438	71671438	Human		name
401736194	CV2688726	single nucleotide variant	NM_001386936.1(SIPA1L1):c.2426G>A (p.Arg809His)	not specified [RCV004303761]	uncertain significance	14	71671289	71671289	Human		name
401757209	CV2692865	single nucleotide variant	NM_001386936.1(SIPA1L1):c.2683G>A (p.Val895Met)	not specified [RCV004306398]	uncertain significance	14	71671546	71671546	Human		name
401749575	CV2719329	single nucleotide variant	NM_001386936.1(SIPA1L1):c.2566A>G (p.Met856Val)	not specified [RCV004324964]	uncertain significance	14	71671429	71671429	Human		name
405751016	CV3311672	single nucleotide variant	NM_001386936.1(SIPA1L1):c.1052A>G (p.His351Arg)	not specified [RCV004453785]	uncertain significance	14	71588924	71588924	Human		name
405751045	CV3311676	single nucleotide variant	NM_001386936.1(SIPA1L1):c.1754G>C (p.Cys585Ser)	not specified [RCV004453789]	uncertain significance	14	71624172	71624172	Human		name
405751051	CV3311677	single nucleotide variant	NM_001386936.1(SIPA1L1):c.2111G>A (p.Arg704Gln)	not specified [RCV004453790]	uncertain significance	14	71661323	71661323	Human		name
405751059	CV3311678	single nucleotide variant	NM_001386936.1(SIPA1L1):c.2233T>C (p.Cys745Arg)	not specified [RCV004453791]	uncertain significance	14	71661445	71661445	Human		name
405751071	CV3311679	single nucleotide variant	NM_001386936.1(SIPA1L1):c.2279A>G (p.Asp760Gly)	not specified [RCV004453792]	uncertain significance	14	71671142	71671142	Human		name
405751077	CV3311680	single nucleotide variant	NM_001386936.1(SIPA1L1):c.2476A>G (p.Ile826Val)	not specified [RCV004453793]	uncertain significance	14	71671339	71671339	Human		name
405751081	CV3332046	single nucleotide variant	NM_001386936.1(SIPA1L1):c.2740C>G (p.Leu914Val)	not specified [RCV004453794]	uncertain significance	14	71671603	71671603	Human		name
407519308	CV3480793	single nucleotide variant	NM_001386936.1(SIPA1L1):c.2819A>G (p.Lys940Arg)	not specified [RCV004676442]	uncertain significance	14	71671682	71671682	Human		name
407519315	CV3480799	single nucleotide variant	NM_001386936.1(SIPA1L1):c.2131G>A (p.Val711Ile)	not specified [RCV004676445]	uncertain significance	14	71661343	71661343	Human		name
407502047	CV3480801	single nucleotide variant	NM_001386936.1(SIPA1L1):c.2623G>C (p.Asp875His)	not specified [RCV004669882]	uncertain significance	14	71671486	71671486	Human		name
597738386	CV3595897	single nucleotide variant	NM_001386936.1(SIPA1L1):c.1197C>G (p.Ser399Arg)	not specified [RCV004864241]	uncertain significance	14	71589069	71589069	Human		name
597738412	CV3595902	single nucleotide variant	NM_001386936.1(SIPA1L1):c.2654T>C (p.Ile885Thr)	not specified [RCV004864246]	uncertain significance	14	71671517	71671517	Human		name
597738457	CV3595914	single nucleotide variant	NM_001386936.1(SIPA1L1):c.2638A>G (p.Ile880Val)	not specified [RCV004864256]	likely benign	14	71671501	71671501	Human		name
598257719	CV3910736	single nucleotide variant	NM_001386936.1(SIPA1L1):c.2036A>G (p.Asp679Gly)	not specified [RCV005279262]	uncertain significance	14	71658375	71658375	Human		name
598257744	CV3910741	single nucleotide variant	NM_001386936.1(SIPA1L1):c.1196G>A (p.Ser399Asn)	not specified [RCV005279267]	uncertain significance	14	71589068	71589068	Human		name
598257754	CV3910743	single nucleotide variant	NM_001386936.1(SIPA1L1):c.2554G>A (p.Glu852Lys)	not specified [RCV005279269]	uncertain significance	14	71671417	71671417	Human		name
598257809	CV3910752	single nucleotide variant	NM_001386936.1(SIPA1L1):c.2620C>G (p.Leu874Val)	not specified [RCV005279278]	uncertain significance	14	71671483	71671483	Human		name
156150680	CV2213096	single nucleotide variant	NM_001386936.1(SIPA1L1):c.4513C>T (p.Arg1505Trp)	not specified [RCV004091651]	uncertain significance	14	71724734	71724734	Human		name
156247673	CV2215357	single nucleotide variant	NM_001386936.1(SIPA1L1):c.4223G>A (p.Arg1408Gln)	not specified [RCV004089169]	uncertain significance	14	71723661	71723661	Human		name
156234953	CV2224001	single nucleotide variant	NM_001386936.1(SIPA1L1):c.5132A>G (p.Asp1711Gly)	not specified [RCV004094250]	uncertain significance	14	71738249	71738249	Human		name
156137844	CV2236529	single nucleotide variant	NM_001386936.1(SIPA1L1):c.3703C>T (p.Pro1235Ser)	not specified [RCV004110526]	uncertain significance	14	71705278	71705278	Human		name
156181052	CV2246140	single nucleotide variant	NM_001386936.1(SIPA1L1):c.5095G>A (p.Ala1699Thr)	not specified [RCV004114040]	uncertain significance	14	71735363	71735363	Human		name
155996319	CV2250444	single nucleotide variant	NM_001386936.1(SIPA1L1):c.4622C>T (p.Ala1541Val)	not specified [RCV004127314]	uncertain significance	14	71730062	71730062	Human		name
156087437	CV2258986	single nucleotide variant	NM_001386936.1(SIPA1L1):c.4667G>T (p.Arg1556Leu)	not specified [RCV004120259]	uncertain significance	14	71730107	71730107	Human		name
156318684	CV2260728	single nucleotide variant	NM_001386936.1(SIPA1L1):c.4622C>G (p.Ala1541Gly)	not specified [RCV004125655]	uncertain significance	14	71730062	71730062	Human		name
156113321	CV2261343	single nucleotide variant	NM_001386936.1(SIPA1L1):c.3124C>T (p.Arg1042Cys)	not specified [RCV004129990]	uncertain significance	14	71685381	71685381	Human		name
156261040	CV2287464	single nucleotide variant	NM_001386936.1(SIPA1L1):c.4085G>T (p.Gly1362Val)	not specified [RCV004140934]	uncertain significance	14	71709541	71709541	Human		name
156305117	CV2305025	single nucleotide variant	NM_001386936.1(SIPA1L1):c.3119C>G (p.Thr1040Ser)	not specified [RCV004168913]	uncertain significance	14	71685376	71685376	Human		name
156271420	CV2312402	single nucleotide variant	NM_001386936.1(SIPA1L1):c.3267G>T (p.Met1089Ile)	not specified [RCV004167093]	uncertain significance	14	71685524	71685524	Human		name
156345091	CV2346367	single nucleotide variant	NM_001386936.1(SIPA1L1):c.4607G>A (p.Ser1536Asn)	not specified [RCV004203848]	likely benign	14	71724828	71724828	Human		name
156248546	CV2357149	single nucleotide variant	NM_001386936.1(SIPA1L1):c.4667G>A (p.Arg1556Gln)	not specified [RCV004206940]	uncertain significance	14	71730107	71730107	Human		name
156006782	CV2394241	single nucleotide variant	NM_001386936.1(SIPA1L1):c.3751A>T (p.Asn1251Tyr)	not specified [RCV004238476]	uncertain significance	14	71705326	71705326	Human		name
155964557	CV2395856	single nucleotide variant	NM_001386936.1(SIPA1L1):c.5278G>A (p.Glu1760Lys)	not specified [RCV004235372]	uncertain significance	14	71739087	71739087	Human		name
329372384	CV2424073	single nucleotide variant	NM_001386936.1(SIPA1L1):c.4910G>A (p.Arg1637His)	not specified [RCV004247980]	uncertain significance	14	71733714	71733714	Human		name
329385577	CV2432185	single nucleotide variant	NM_001386936.1(SIPA1L1):c.3962C>T (p.Ser1321Leu)	not specified [RCV004249327]	uncertain significance	14	71709418	71709418	Human		name
329360443	CV2442802	single nucleotide variant	NM_001386936.1(SIPA1L1):c.4259G>A (p.Arg1420Gln)	not specified [RCV004251628]	uncertain significance	14	71723697	71723697	Human		name
329388747	CV2447826	single nucleotide variant	NM_001386936.1(SIPA1L1):c.4492C>T (p.Arg1498Cys)	not specified [RCV004258600]	uncertain significance	14	71724713	71724713	Human		name
329370390	CV2461701	single nucleotide variant	NM_001386936.1(SIPA1L1):c.4243G>T (p.Val1415Phe)	not specified [RCV004269856]	uncertain significance	14	71723681	71723681	Human		name
401720430	CV2673322	single nucleotide variant	NM_001386936.1(SIPA1L1):c.3439C>T (p.Arg1147Trp)	not specified [RCV004288308]	uncertain significance	14	71699045	71699045	Human		name
401739533	CV2683095	single nucleotide variant	NM_001386936.1(SIPA1L1):c.3125G>T (p.Arg1042Leu)	not specified [RCV004286102]	uncertain significance	14	71685382	71685382	Human		name
401762671	CV2714230	single nucleotide variant	NM_001386936.1(SIPA1L1):c.3157G>A (p.Gly1053Ser)	not specified [RCV004317458]	uncertain significance	14	71685414	71685414	Human		name
401725596	CV2721846	single nucleotide variant	NM_001386936.1(SIPA1L1):c.3396C>G (p.Ile1132Met)	not specified [RCV004326359]	uncertain significance	14	71699002	71699002	Human		name
401857122	CV2758526	single nucleotide variant	NM_001386936.1(SIPA1L1):c.4442C>T (p.Thr1481Met)	not specified [RCV004337618]	uncertain significance	14	71723880	71723880	Human		name
401890692	CV2775738	single nucleotide variant	NM_001386936.1(SIPA1L1):c.4471G>A (p.Glu1491Lys)	not specified [RCV004350861]	uncertain significance	14	71724692	71724692	Human		name
401895947	CV2779643	single nucleotide variant	NM_001386936.1(SIPA1L1):c.4588A>G (p.Thr1530Ala)	not specified [RCV004351346]	uncertain significance	14	71724809	71724809	Human		name
401875250	CV2787620	single nucleotide variant	NM_001386936.1(SIPA1L1):c.4060C>T (p.Arg1354Trp)	not specified [RCV004356555]	uncertain significance	14	71709516	71709516	Human		name
405751087	CV3332047	single nucleotide variant	NM_001386936.1(SIPA1L1):c.3533G>A (p.Ser1178Asn)	not specified [RCV004453795]	uncertain significance	14	71702392	71702392	Human		name
405751101	CV3332049	single nucleotide variant	NM_001386936.1(SIPA1L1):c.3761G>A (p.Gly1254Glu)	not specified [RCV004453797]	uncertain significance	14	71705336	71705336	Human		name
405751116	CV3332051	single nucleotide variant	NM_001386936.1(SIPA1L1):c.4063A>T (p.Thr1355Ser)	not specified [RCV004453799]	uncertain significance	14	71709519	71709519	Human		name
405751123	CV3332052	single nucleotide variant	NM_001386936.1(SIPA1L1):c.4142C>G (p.Ala1381Gly)	not specified [RCV004453800]	uncertain significance	14	71709598	71709598	Human		name
405751131	CV3332053	single nucleotide variant	NM_001386936.1(SIPA1L1):c.4154C>T (p.Pro1385Leu)	not specified [RCV004453801]	uncertain significance	14	71709610	71709610	Human		name
405751138	CV3332054	single nucleotide variant	NM_001386936.1(SIPA1L1):c.4226A>G (p.His1409Arg)	not specified [RCV004453802]	uncertain significance	14	71723664	71723664	Human		name
405751150	CV3332056	single nucleotide variant	NM_001386936.1(SIPA1L1):c.4250C>T (p.Thr1417Ile)	not specified [RCV004453804]	uncertain significance	14	71723688	71723688	Human		name
405751156	CV3332057	single nucleotide variant	NM_001386936.1(SIPA1L1):c.4270A>G (p.Lys1424Glu)	not specified [RCV004453805]	uncertain significance	14	71723708	71723708	Human		name
405751162	CV3332058	single nucleotide variant	NM_001386936.1(SIPA1L1):c.4426G>A (p.Val1476Met)	not specified [RCV004453806]	uncertain significance	14	71723864	71723864	Human		name
405751169	CV3332059	single nucleotide variant	NM_001386936.1(SIPA1L1):c.4589C>T (p.Thr1530Ile)	not specified [RCV004453807]	uncertain significance	14	71724810	71724810	Human		name
405751175	CV3332060	single nucleotide variant	NM_001386936.1(SIPA1L1):c.4670G>A (p.Arg1557Gln)	not specified [RCV004453808]	uncertain significance	14	71730110	71730110	Human		name
407502009	CV3480794	single nucleotide variant	NM_001386936.1(SIPA1L1):c.3218G>T (p.Ser1073Ile)	not specified [RCV004669878]	uncertain significance	14	71685475	71685475	Human		name
407519310	CV3480795	single nucleotide variant	NM_001386936.1(SIPA1L1):c.3274C>T (p.Arg1092Trp)	not specified [RCV004676443]	uncertain significance	14	71685531	71685531	Human		name
407519313	CV3480796	single nucleotide variant	NM_001386936.1(SIPA1L1):c.3850G>A (p.Asp1284Asn)	not specified [RCV004676444]	uncertain significance	14	71709306	71709306	Human		name
407502029	CV3480798	single nucleotide variant	NM_001386936.1(SIPA1L1):c.4516G>A (p.Ala1506Thr)	not specified [RCV004669880]	uncertain significance	14	71724737	71724737	Human		name
407502035	CV3480800	single nucleotide variant	NM_001386936.1(SIPA1L1):c.4510C>T (p.Leu1504Phe)	not specified [RCV004669881]	uncertain significance	14	71724731	71724731	Human		name
597738375	CV3595894	single nucleotide variant	NM_001386936.1(SIPA1L1):c.4514G>A (p.Arg1505Gln)	not specified [RCV004864239]	uncertain significance	14	71724735	71724735	Human		name
597738380	CV3595896	single nucleotide variant	NM_001386936.1(SIPA1L1):c.4813C>T (p.Leu1605Phe)	not specified [RCV004864240]	uncertain significance	14	71730253	71730253	Human		name
597738391	CV3595898	single nucleotide variant	NM_001386936.1(SIPA1L1):c.3988C>T (p.Arg1330Cys)	not specified [RCV004864242]	uncertain significance	14	71709444	71709444	Human		name
597738417	CV3595903	single nucleotide variant	NM_001386936.1(SIPA1L1):c.4621G>C (p.Ala1541Pro)	not specified [RCV004864247]	uncertain significance	14	71730061	71730061	Human		name
597738431	CV3595907	single nucleotide variant	NM_001386936.1(SIPA1L1):c.3980C>T (p.Ser1327Leu)	not specified [RCV004864250]	uncertain significance	14	71709436	71709436	Human		name
597738440	CV3595909	single nucleotide variant	NM_001386936.1(SIPA1L1):c.3703C>A (p.Pro1235Thr)	not specified [RCV004864252]	uncertain significance	14	71705278	71705278	Human		name
597738445	CV3595910	single nucleotide variant	NM_001386936.1(SIPA1L1):c.3815A>G (p.Asn1272Ser)	not specified [RCV004864253]	uncertain significance	14	71709271	71709271	Human		name
597738449	CV3595911	single nucleotide variant	NM_001386936.1(SIPA1L1):c.4067T>C (p.Leu1356Ser)	not specified [RCV004864254]	uncertain significance	14	71709523	71709523	Human		name
597738453	CV3595912	single nucleotide variant	NM_001386936.1(SIPA1L1):c.4474A>G (p.Ile1492Val)	not specified [RCV004864255]	uncertain significance	14	71724695	71724695	Human		name
598257711	CV3910735	single nucleotide variant	NM_001386936.1(SIPA1L1):c.4625T>A (p.Leu1542His)	not specified [RCV005279261]	uncertain significance	14	71730065	71730065	Human		name
598257732	CV3910739	single nucleotide variant	NM_001386936.1(SIPA1L1):c.3874C>G (p.Leu1292Val)	not specified [RCV005279265]	uncertain significance	14	71709330	71709330	Human		name
598257748	CV3910742	single nucleotide variant	NM_001386936.1(SIPA1L1):c.5113C>G (p.Pro1705Ala)	not specified [RCV005279268]	uncertain significance	14	71735381	71735381	Human		name
598257759	CV3910744	single nucleotide variant	NM_001386936.1(SIPA1L1):c.4196C>T (p.Ala1399Val)	not specified [RCV005279270]	uncertain significance	14	71709652	71709652	Human		name
598257770	CV3910746	single nucleotide variant	NM_001386936.1(SIPA1L1):c.3385G>T (p.Gly1129Cys)	not specified [RCV005279272]	uncertain significance	14	71698991	71698991	Human		name
598257777	CV3910747	single nucleotide variant	NM_001386936.1(SIPA1L1):c.4667G>C (p.Arg1556Pro)	not specified [RCV005279273]	uncertain significance	14	71730107	71730107	Human		name
598257784	CV3910748	single nucleotide variant	NM_001386936.1(SIPA1L1):c.3544C>T (p.Pro1182Ser)	not specified [RCV005279274]	uncertain significance	14	71702403	71702403	Human		name
598257803	CV3910751	single nucleotide variant	NM_001386936.1(SIPA1L1):c.4774G>A (p.Val1592Ile)	not specified [RCV005279277]	uncertain significance	14	71730214	71730214	Human		name
598257825	CV3910755	single nucleotide variant	NM_001386936.1(SIPA1L1):c.3008C>T (p.Ala1003Val)	not specified [RCV005279281]	uncertain significance	14	71672526	71672526	Human		name

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