Tbl3 Variant Search Result - Rat Genome Database

Advanced Search (OLGA)

Variants search result for Homo sapiens
(View Results for all Objects and Ontologies)

146 records found for search term Tbl3

Refine Term:

Assembly:

Chr

Sort By:

Export

CSV

TAB

RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
15193342	CV731051	single nucleotide variant	NM_006453.3(TBL3):c.1742+8G>C	not provided [RCV000888920]	benign	16	1977434	1977434	Human		name
156161511	CV2272602	single nucleotide variant	NM_006453.3(TBL3):c.13G>T (p.Ala5Ser)	not specified [RCV004133485]	uncertain significance	16	1972177	1972177	Human		name
15154357	CV714788	single nucleotide variant	NM_006453.3(TBL3):c.258G>A (p.Arg86=)	not provided [RCV000968722]	benign	16	1974558	1974558	Human		name
405791378	CV3335461	single nucleotide variant	NM_006453.3(TBL3):c.97G>A (p.Asp33Asn)	not specified [RCV004474223]	uncertain significance	16	1974200	1974200	Human		name
597762119	CV3619260	single nucleotide variant	NM_006453.3(TBL3):c.40A>G (p.Asn14Asp)	not specified [RCV004869564]	uncertain significance	16	1972204	1972204	Human		name
597762155	CV3619270	single nucleotide variant	NM_006453.3(TBL3):c.82G>A (p.Gly28Arg)	not specified [RCV004869572]	uncertain significance	16	1974096	1974096	Human		name
15165304	CV726481	single nucleotide variant	NM_006453.3(TBL3):c.483G>A (p.Pro161=)	not provided [RCV000882382]	benign	16	1974946	1974946	Human		name
156096768	CV2294402	single nucleotide variant	NM_006453.3(TBL3):c.212C>T (p.Ala71Val)	not specified [RCV004159912]	uncertain significance	16	1974398	1974398	Human		name
155972249	CV2309388	single nucleotide variant	NM_006453.3(TBL3):c.227C>T (p.Pro76Leu)	not specified [RCV004165536]	uncertain significance	16	1974413	1974413	Human		name
156187683	CV2378095	single nucleotide variant	NM_006453.3(TBL3):c.101A>G (p.Gln34Arg)	not specified [RCV004232653]	uncertain significance	16	1974204	1974204	Human		name
156135906	CV2380003	single nucleotide variant	NM_006453.3(TBL3):c.280G>A (p.Ala94Thr)	not specified [RCV004222143]	uncertain significance	16	1974580	1974580	Human		name
401758033	CV2685683	single nucleotide variant	NM_006453.3(TBL3):c.296G>T (p.Ser99Ile)	not specified [RCV004296736]	uncertain significance	16	1974596	1974596	Human		name
401904764	CV2810839	single nucleotide variant	NM_006453.3(TBL3):c.1071C>T (p.Pro357=)	not provided [RCV003395221]	likely benign	16	1975891	1975891	Human		name
401904765	CV2810840	single nucleotide variant	NM_006453.3(TBL3):c.1581C>T (p.Val527=)	not provided [RCV003395222]	likely benign	16	1977194	1977194	Human		name
405791284	CV3335427	single nucleotide variant	NM_006453.3(TBL3):c.124G>A (p.Val42Ile)	not specified [RCV004474189]	likely benign	16	1974227	1974227	Human		name
405791340	CV3335447	single nucleotide variant	NM_006453.3(TBL3):c.257G>A (p.Arg86Gln)	not specified [RCV004474209]	uncertain significance	16	1974557	1974557	Human		name
405791343	CV3335448	single nucleotide variant	NM_006453.3(TBL3):c.296G>C (p.Ser99Thr)	not specified [RCV004474210]	uncertain significance	16	1974596	1974596	Human		name
597762084	CV3619252	single nucleotide variant	NM_006453.3(TBL3):c.161C>T (p.Ser54Leu)	not specified [RCV004869556]	uncertain significance	16	1974264	1974264	Human		name
598208663	CV3913016	single nucleotide variant	NM_006453.3(TBL3):c.195C>G (p.Asp65Glu)	not specified [RCV005291534]	uncertain significance	16	1974381	1974381	Human		name
15192823	CV740007	single nucleotide variant	NM_006453.3(TBL3):c.1254C>T (p.Ser418=)	not provided [RCV000910657]	likely benign	16	1976276	1976276	Human		name
156398328	CV2200671	single nucleotide variant	NM_006453.3(TBL3):c.400C>T (p.Arg134Cys)	not specified [RCV004081332]	uncertain significance	16	1974783	1974783	Human		name
156129401	CV2209771	single nucleotide variant	NM_006453.3(TBL3):c.715G>A (p.Val239Met)	not specified [RCV004083085]	uncertain significance	16	1975348	1975348	Human		name
156172184	CV2286828	single nucleotide variant	NM_006453.3(TBL3):c.832T>C (p.Ser278Pro)	not specified [RCV004142630]	uncertain significance	16	1975555	1975555	Human		name
156101663	CV2291392	single nucleotide variant	NM_006453.3(TBL3):c.874G>A (p.Gly292Arg)	not specified [RCV004155731]	uncertain significance	16	1975597	1975597	Human		name
156251961	CV2311334	single nucleotide variant	NM_006453.3(TBL3):c.391G>A (p.Gly131Arg)	not specified [RCV004166403]	uncertain significance	16	1974774	1974774	Human		name
156219788	CV2344937	single nucleotide variant	NM_006453.3(TBL3):c.991G>A (p.Ala331Thr)	not specified [RCV004193232]	uncertain significance	16	1975811	1975811	Human		name
156382604	CV2362758	single nucleotide variant	NM_006453.3(TBL3):c.331C>T (p.Pro111Ser)	not specified [RCV004208876]	uncertain significance	16	1974631	1974631	Human		name
156074826	CV2365554	single nucleotide variant	NM_006453.3(TBL3):c.619G>A (p.Gly207Ser)	not specified [RCV004211668]	uncertain significance	16	1975082	1975082	Human		name
155931447	CV2370923	single nucleotide variant	NM_006453.3(TBL3):c.701C>T (p.Pro234Leu)	not specified [RCV004218651]	uncertain significance	16	1975252	1975252	Human		name
156168372	CV2373787	single nucleotide variant	NM_006453.3(TBL3):c.514G>A (p.Ala172Thr)	not specified [RCV004224727]	uncertain significance	16	1974977	1974977	Human		name
156149947	CV2394614	single nucleotide variant	NM_006453.3(TBL3):c.449C>T (p.Ser150Leu)	not specified [RCV004240958]	uncertain significance	16	1974832	1974832	Human		name
156185915	CV2397520	single nucleotide variant	NM_006453.3(TBL3):c.644G>A (p.Arg215His)	not specified [RCV004236988]	uncertain significance	16	1975195	1975195	Human		name
329363624	CV2442358	single nucleotide variant	NM_006453.3(TBL3):c.552C>A (p.Asp184Glu)	not specified [RCV004266617]	uncertain significance	16	1975015	1975015	Human		name
329359428	CV2446258	single nucleotide variant	NM_006453.3(TBL3):c.913G>A (p.Gly305Ser)	not specified [RCV004249397]	uncertain significance	16	1975636	1975636	Human		name
329358255	CV2450239	single nucleotide variant	NM_006453.3(TBL3):c.512C>T (p.Ser171Leu)	not specified [RCV004271344]	uncertain significance	16	1974975	1974975	Human		name
329395518	CV2458433	single nucleotide variant	NM_006453.3(TBL3):c.958G>A (p.Glu320Lys)	not specified [RCV004266062]	uncertain significance	16	1975681	1975681	Human		name
329395637	CV2462891	single nucleotide variant	NM_006453.3(TBL3):c.317C>T (p.Ala106Val)	not specified [RCV004272734]	uncertain significance	16	1974617	1974617	Human		name
401742004	CV2676872	single nucleotide variant	NM_006453.3(TBL3):c.814C>T (p.Arg272Cys)	not specified [RCV004291037]	uncertain significance	16	1975537	1975537	Human		name
401719895	CV2705559	single nucleotide variant	NM_006453.3(TBL3):c.916G>A (p.Val306Met)	not specified [RCV004318427]	uncertain significance	16	1975639	1975639	Human		name
401893472	CV2763463	single nucleotide variant	NM_006453.3(TBL3):c.334G>A (p.Val112Met)	not specified [RCV004349347]	uncertain significance	16	1974634	1974634	Human		name
401858279	CV2774270	single nucleotide variant	NM_006453.3(TBL3):c.460G>C (p.Val154Leu)	not specified [RCV004347635]	uncertain significance	16	1974843	1974843	Human		name
401871723	CV2783582	single nucleotide variant	NM_006453.3(TBL3):c.535G>A (p.Val179Met)	not specified [RCV004365906]	uncertain significance	16	1974998	1974998	Human		name
401904763	CV2810838	single nucleotide variant	NM_006453.3(TBL3):c.703G>A (p.Val235Met)	not provided [RCV003395220]	likely benign	16	1975254	1975254	Human		name
405791346	CV3335449	single nucleotide variant	NM_006453.3(TBL3):c.316G>A (p.Ala106Thr)	not specified [RCV004474211]	uncertain significance	16	1974616	1974616	Human		name
405791349	CV3335450	single nucleotide variant	NM_006453.3(TBL3):c.356C>T (p.Pro119Leu)	not specified [RCV004474212]	uncertain significance	16	1974656	1974656	Human		name
405791352	CV3335451	single nucleotide variant	NM_006453.3(TBL3):c.427G>A (p.Gly143Arg)	not specified [RCV004474213]	uncertain significance	16	1974810	1974810	Human		name
405791354	CV3335452	single nucleotide variant	NM_006453.3(TBL3):c.472G>A (p.Ala158Thr)	not specified [RCV004474214]	uncertain significance	16	1974935	1974935	Human		name
405791356	CV3335453	single nucleotide variant	NM_006453.3(TBL3):c.535G>C (p.Val179Leu)	not specified [RCV004474215]	uncertain significance	16	1974998	1974998	Human		name
405791362	CV3335455	single nucleotide variant	NM_006453.3(TBL3):c.721G>A (p.Ala241Thr)	not specified [RCV004474217]	uncertain significance	16	1975354	1975354	Human		name
405791365	CV3335456	single nucleotide variant	NM_006453.3(TBL3):c.823G>A (p.Glu275Lys)	not specified [RCV004474218]	uncertain significance	16	1975546	1975546	Human		name
405791368	CV3335457	single nucleotide variant	NM_006453.3(TBL3):c.868G>A (p.Gly290Ser)	not specified [RCV004474219]	uncertain significance	16	1975591	1975591	Human		name
405791373	CV3335459	single nucleotide variant	NM_006453.3(TBL3):c.910G>A (p.Ala304Thr)	not specified [RCV004474221]	uncertain significance	16	1975633	1975633	Human		name
405791376	CV3335460	single nucleotide variant	NM_006453.3(TBL3):c.960G>C (p.Glu320Asp)	not specified [RCV004474222]	uncertain significance	16	1975683	1975683	Human		name
407512687	CV3485700	single nucleotide variant	NM_006453.3(TBL3):c.518C>T (p.Thr173Met)	not specified [RCV004673516]	uncertain significance	16	1974981	1974981	Human		name
407512690	CV3485701	single nucleotide variant	NM_006453.3(TBL3):c.473C>G (p.Ala158Gly)	not specified [RCV004673517]	uncertain significance	16	1974936	1974936	Human		name
407512693	CV3485702	single nucleotide variant	NM_006453.3(TBL3):c.589G>A (p.Ala197Thr)	not specified [RCV004673518]	uncertain significance	16	1975052	1975052	Human		name
407512696	CV3485704	single nucleotide variant	NM_006453.3(TBL3):c.974G>A (p.Arg325Gln)	not specified [RCV004673519]	likely benign	16	1975697	1975697	Human		name
407530696	CV3485707	single nucleotide variant	NM_006453.3(TBL3):c.763G>A (p.Val255Met)	not specified [RCV004682040]	uncertain significance	16	1975396	1975396	Human		name
597762093	CV3619254	single nucleotide variant	NM_006453.3(TBL3):c.583T>C (p.Tyr195His)	not specified [RCV004869558]	uncertain significance	16	1975046	1975046	Human		name
597762110	CV3619258	single nucleotide variant	NM_006453.3(TBL3):c.628A>G (p.Met210Val)	not specified [RCV004869562]	uncertain significance	16	1975091	1975091	Human		name
597762130	CV3619262	single nucleotide variant	NM_006453.3(TBL3):c.851C>G (p.Thr284Arg)	not specified [RCV004869566]	uncertain significance	16	1975574	1975574	Human		name
597794860	CV3619263	single nucleotide variant	NM_006453.3(TBL3):c.607T>C (p.Phe203Leu)	not specified [RCV004877999]	uncertain significance	16	1975070	1975070	Human		name
597762138	CV3619265	single nucleotide variant	NM_006453.3(TBL3):c.923T>G (p.Leu308Arg)	not specified [RCV004869568]	uncertain significance	16	1975646	1975646	Human		name
597762148	CV3619268	single nucleotide variant	NM_006453.3(TBL3):c.314A>G (p.Lys105Arg)	not specified [RCV004869570]	uncertain significance	16	1974614	1974614	Human		name
597762175	CV3619274	single nucleotide variant	NM_006453.3(TBL3):c.643C>T (p.Arg215Cys)	not specified [RCV004869576]	uncertain significance	16	1975194	1975194	Human		name
598208623	CV3913004	single nucleotide variant	NM_006453.3(TBL3):c.937G>A (p.Asp313Asn)	not specified [RCV005291525]	uncertain significance	16	1975660	1975660	Human		name
598208636	CV3913009	single nucleotide variant	NM_006453.3(TBL3):c.817G>A (p.Val273Met)	not specified [RCV005291528]	uncertain significance	16	1975540	1975540	Human		name
598208649	CV3913012	single nucleotide variant	NM_006453.3(TBL3):c.500T>C (p.Leu167Pro)	not specified [RCV005291531]	uncertain significance	16	1974963	1974963	Human		name
598163272	CV3913019	single nucleotide variant	NM_006453.3(TBL3):c.767A>C (p.Lys256Thr)	not specified [RCV005283085]	uncertain significance	16	1975400	1975400	Human		name
156369272	CV2193933	single nucleotide variant	NM_006453.3(TBL3):c.2114G>A (p.Arg705Gln)	not specified [RCV004074663]	likely benign	16	1978200	1978200	Human		name
156169108	CV2197755	single nucleotide variant	NM_006453.3(TBL3):c.1496A>G (p.Gln499Arg)	not specified [RCV004074954]	uncertain significance	16	1977109	1977109	Human		name
156027312	CV2199333	single nucleotide variant	NM_006453.3(TBL3):c.1807G>A (p.Ala603Thr)	not specified [RCV004082679]	uncertain significance	16	1977578	1977578	Human		name
156034586	CV2282907	single nucleotide variant	NM_006453.3(TBL3):c.2395C>T (p.Pro799Ser)	not specified [RCV004143549]	uncertain significance	16	1978653	1978653	Human		name
156275242	CV2287584	single nucleotide variant	NM_006453.3(TBL3):c.1504A>G (p.Thr502Ala)	not specified [RCV004141028]	uncertain significance	16	1977117	1977117	Human		name
156263260	CV2287707	single nucleotide variant	NM_006453.3(TBL3):c.1331G>A (p.Cys444Tyr)	not specified [RCV004141125]	uncertain significance	16	1976852	1976852	Human		name
156004557	CV2295972	single nucleotide variant	NM_006453.3(TBL3):c.2228C>T (p.Ala743Val)	not specified [RCV004151864]	uncertain significance	16	1978406	1978406	Human		name
156205973	CV2297924	single nucleotide variant	NM_006453.3(TBL3):c.2158A>C (p.Thr720Pro)	not specified [RCV004157852]	uncertain significance	16	1978336	1978336	Human		name
156292615	CV2306245	single nucleotide variant	NM_006453.3(TBL3):c.1120G>A (p.Gly374Ser)	not specified [RCV004162976]	uncertain significance	16	1975940	1975940	Human		name
156348335	CV2312723	single nucleotide variant	NM_006453.3(TBL3):c.2147G>A (p.Arg716His)	not specified [RCV004169447]	uncertain significance	16	1978325	1978325	Human		name
155964850	CV2330502	single nucleotide variant	NM_006453.3(TBL3):c.2237A>T (p.Glu746Val)	not specified [RCV004181067]	uncertain significance	16	1978415	1978415	Human		name
156087605	CV2337751	single nucleotide variant	NM_006453.3(TBL3):c.1994G>A (p.Arg665Gln)	not specified [RCV004183772]	uncertain significance	16	1977993	1977993	Human		name
156102346	CV2352278	single nucleotide variant	NM_006453.3(TBL3):c.2392A>C (p.Thr798Pro)	not specified [RCV004200753]	uncertain significance	16	1978650	1978650	Human		name
155988228	CV2355036	single nucleotide variant	NM_006453.3(TBL3):c.2044G>A (p.Val682Met)	not specified [RCV004198431]	uncertain significance	16	1978043	1978043	Human		name
156391810	CV2382624	single nucleotide variant	NM_006453.3(TBL3):c.1535A>G (p.Gln512Arg)	not specified [RCV004232947]	uncertain significance	16	1977148	1977148	Human		name
155902975	CV2386394	single nucleotide variant	NM_006453.3(TBL3):c.1082T>C (p.Val361Ala)	not specified [RCV004228725]	uncertain significance	16	1975902	1975902	Human		name
329366522	CV2445798	single nucleotide variant	NM_006453.3(TBL3):c.1048G>A (p.Val350Ile)	not specified [RCV004259855]	likely benign	16	1975868	1975868	Human		name
401753005	CV2677765	single nucleotide variant	NM_006453.3(TBL3):c.1579G>A (p.Val527Ile)	not specified [RCV004291837]	uncertain significance	16	1977192	1977192	Human		name
401768712	CV2686347	single nucleotide variant	NM_006453.3(TBL3):c.1852G>A (p.Asp618Asn)	not specified [RCV004297423]	uncertain significance	16	1977623	1977623	Human		name
401782360	CV2686746	single nucleotide variant	NM_006453.3(TBL3):c.1133T>C (p.Ile378Thr)	not specified [RCV004301936]	uncertain significance	16	1976059	1976059	Human		name
401764228	CV2711179	single nucleotide variant	NM_006453.3(TBL3):c.1457C>G (p.Ala486Gly)	not specified [RCV004312978]	uncertain significance	16	1977070	1977070	Human		name
401754693	CV2719711	single nucleotide variant	NM_006453.3(TBL3):c.2323C>T (p.Leu775Phe)	not specified [RCV004329151]	uncertain significance	16	1978581	1978581	Human		name
401783594	CV2723746	single nucleotide variant	NM_006453.3(TBL3):c.1687G>C (p.Asp563His)	not specified [RCV004325906]	uncertain significance	16	1977371	1977371	Human		name
401728816	CV2729825	single nucleotide variant	NM_006453.3(TBL3):c.2222G>A (p.Arg741Gln)	not specified [RCV004332835]	uncertain significance	16	1978400	1978400	Human		name
405791271	CV3335422	single nucleotide variant	NM_006453.3(TBL3):c.1009G>A (p.Val337Ile)	not specified [RCV004474184]	uncertain significance	16	1975829	1975829	Human		name
405791276	CV3335424	single nucleotide variant	NM_006453.3(TBL3):c.1072T>C (p.Cys358Arg)	not specified [RCV004474186]	uncertain significance	16	1975892	1975892	Human		name
405791278	CV3335425	single nucleotide variant	NM_006453.3(TBL3):c.1135G>A (p.Val379Ile)	not specified [RCV004474187]	uncertain significance	16	1976061	1976061	Human		name
405791281	CV3335426	single nucleotide variant	NM_006453.3(TBL3):c.1157G>A (p.Arg386Gln)	not specified [RCV004474188]	uncertain significance	16	1976083	1976083	Human		name
405791287	CV3335428	single nucleotide variant	NM_006453.3(TBL3):c.1264C>T (p.His422Tyr)	not specified [RCV004474190]	uncertain significance	16	1976286	1976286	Human		name
405791290	CV3335429	single nucleotide variant	NM_006453.3(TBL3):c.1279G>C (p.Val427Leu)	not specified [RCV004474191]	uncertain significance	16	1976301	1976301	Human		name
405791292	CV3335430	single nucleotide variant	NM_006453.3(TBL3):c.1370C>T (p.Ser457Phe)	not specified [RCV004474192]	uncertain significance	16	1976891	1976891	Human		name
405791295	CV3335431	single nucleotide variant	NM_006453.3(TBL3):c.1427G>A (p.Arg476His)	not specified [RCV004474193]	uncertain significance	16	1976948	1976948	Human		name
405791298	CV3335432	single nucleotide variant	NM_006453.3(TBL3):c.1502G>A (p.Arg501His)	not specified [RCV004474194]	uncertain significance	16	1977115	1977115	Human		name
405791301	CV3335433	single nucleotide variant	NM_006453.3(TBL3):c.1594A>G (p.Met532Val)	not specified [RCV004474195]	uncertain significance	16	1977207	1977207	Human		name
405791303	CV3335434	single nucleotide variant	NM_006453.3(TBL3):c.1681G>C (p.Gly561Arg)	not specified [RCV004474196]	uncertain significance	16	1977365	1977365	Human		name
405791306	CV3335435	single nucleotide variant	NM_006453.3(TBL3):c.1709C>T (p.Ala570Val)	not specified [RCV004474197]	uncertain significance	16	1977393	1977393	Human		name
405791309	CV3335436	single nucleotide variant	NM_006453.3(TBL3):c.1858G>A (p.Ala620Thr)	not specified [RCV004474198]	uncertain significance	16	1977629	1977629	Human		name
405791312	CV3335437	single nucleotide variant	NM_006453.3(TBL3):c.1901A>G (p.Asp634Gly)	not specified [RCV004474199]	uncertain significance	16	1977743	1977743	Human		name
405791315	CV3335438	single nucleotide variant	NM_006453.3(TBL3):c.1921G>A (p.Ala641Thr)	not specified [RCV004474200]	uncertain significance	16	1977763	1977763	Human		name
405791317	CV3335439	single nucleotide variant	NM_006453.3(TBL3):c.2002C>T (p.Arg668Trp)	not specified [RCV004474201]	uncertain significance	16	1978001	1978001	Human		name
405791482	CV3335440	single nucleotide variant	NM_006453.3(TBL3):c.2140C>G (p.Leu714Val)	not specified [RCV004474202]	uncertain significance	16	1978318	1978318	Human		name
405791323	CV3335441	single nucleotide variant	NM_006453.3(TBL3):c.2165A>T (p.Asn722Ile)	not specified [RCV004474203]	uncertain significance	16	1978343	1978343	Human		name
405791326	CV3335442	single nucleotide variant	NM_006453.3(TBL3):c.2236G>A (p.Glu746Lys)	not specified [RCV004474204]	uncertain significance	16	1978414	1978414	Human		name
405791329	CV3335443	single nucleotide variant	NM_006453.3(TBL3):c.2261G>A (p.Arg754Gln)	not specified [RCV004474205]	likely benign	16	1978439	1978439	Human		name
405791332	CV3335444	single nucleotide variant	NM_006453.3(TBL3):c.2285C>A (p.Pro762His)	not specified [RCV004474206]	uncertain significance	16	1978463	1978463	Human		name
405791335	CV3335445	single nucleotide variant	NM_006453.3(TBL3):c.2335G>A (p.Ala779Thr)	not specified [RCV004474207]	likely benign	16	1978593	1978593	Human		name
405791337	CV3335446	single nucleotide variant	NM_006453.3(TBL3):c.2422C>G (p.Pro808Ala)	not specified [RCV004474208]	uncertain significance	16	1978680	1978680	Human		name
407512684	CV3485699	single nucleotide variant	NM_006453.3(TBL3):c.2033G>A (p.Arg678Gln)	not specified [RCV004673515]	uncertain significance	16	1978032	1978032	Human		name
407530695	CV3485703	single nucleotide variant	NM_006453.3(TBL3):c.1127C>T (p.Thr376Met)	not specified [RCV004682039]	uncertain significance	16	1975947	1975947	Human		name
407512698	CV3485705	single nucleotide variant	NM_006453.3(TBL3):c.1086T>G (p.Phe362Leu)	not specified [RCV004673520]	uncertain significance	16	1975906	1975906	Human		name
407512701	CV3485706	single nucleotide variant	NM_006453.3(TBL3):c.1240G>A (p.Val414Met)	not specified [RCV004673521]	uncertain significance	16	1976262	1976262	Human		name
407530698	CV3485708	single nucleotide variant	NM_006453.3(TBL3):c.2122C>T (p.Arg708Cys)	not specified [RCV004682041]	uncertain significance	16	1978208	1978208	Human		name
597762088	CV3619253	single nucleotide variant	NM_006453.3(TBL3):c.2305C>G (p.Gln769Glu)	not specified [RCV004869557]	uncertain significance	16	1978563	1978563	Human		name
597762096	CV3619255	single nucleotide variant	NM_006453.3(TBL3):c.1748C>T (p.Ser583Leu)	not specified [RCV004869559]	uncertain significance	16	1977519	1977519	Human		name
597762101	CV3619256	single nucleotide variant	NM_006453.3(TBL3):c.2089G>A (p.Glu697Lys)	not specified [RCV004869560]	uncertain significance	16	1978175	1978175	Human		name
597762106	CV3619257	single nucleotide variant	NM_006453.3(TBL3):c.2233G>A (p.Glu745Lys)	not specified [RCV004869561]	uncertain significance	16	1978411	1978411	Human		name
597762115	CV3619259	single nucleotide variant	NM_006453.3(TBL3):c.2065A>G (p.Ile689Val)	not specified [RCV004869563]	uncertain significance	16	1978151	1978151	Human		name
597762134	CV3619264	single nucleotide variant	NM_006453.3(TBL3):c.2368C>T (p.Leu790Phe)	not specified [RCV004869567]	uncertain significance	16	1978626	1978626	Human		name
597762143	CV3619266	single nucleotide variant	NM_006453.3(TBL3):c.2413G>A (p.Gly805Ser)	not specified [RCV004869569]	uncertain significance	16	1978671	1978671	Human		name
597794863	CV3619267	single nucleotide variant	NM_006453.3(TBL3):c.1010T>A (p.Val337Asp)	not specified [RCV004878000]	uncertain significance	16	1975830	1975830	Human		name
597762152	CV3619269	single nucleotide variant	NM_006453.3(TBL3):c.1547T>C (p.Val516Ala)	not specified [RCV004869571]	uncertain significance	16	1977160	1977160	Human		name
597762160	CV3619271	single nucleotide variant	NM_006453.3(TBL3):c.1565G>A (p.Arg522His)	not specified [RCV004869573]	uncertain significance	16	1977178	1977178	Human		name
597762171	CV3619273	single nucleotide variant	NM_006453.3(TBL3):c.1952T>G (p.Val651Gly)	not specified [RCV004869575]	uncertain significance	16	1977794	1977794	Human		name
597762179	CV3619275	single nucleotide variant	NM_006453.3(TBL3):c.1325A>G (p.Gln442Arg)	not specified [RCV004869577]	uncertain significance	16	1976846	1976846	Human		name
597762184	CV3619276	single nucleotide variant	NM_006453.3(TBL3):c.2006C>T (p.Ala669Val)	not specified [RCV004869578]	uncertain significance	16	1978005	1978005	Human		name
598208628	CV3913005	single nucleotide variant	NM_006453.3(TBL3):c.2159C>T (p.Thr720Met)	not specified [RCV005291526]	uncertain significance	16	1978337	1978337	Human		name
598163255	CV3913006	single nucleotide variant	NM_006453.3(TBL3):c.1054G>A (p.Val352Met)	not specified [RCV005283082]	uncertain significance	16	1975874	1975874	Human		name
598208631	CV3913008	single nucleotide variant	NM_006453.3(TBL3):c.1459A>G (p.Ile487Val)	not specified [RCV005291527]	likely benign	16	1977072	1977072	Human		name
598208640	CV3913010	single nucleotide variant	NM_006453.3(TBL3):c.1194G>C (p.Gln398His)	not specified [RCV005291529]	uncertain significance	16	1976216	1976216	Human		name
598208644	CV3913011	single nucleotide variant	NM_006453.3(TBL3):c.1795C>G (p.Arg599Gly)	not specified [RCV005291530]	uncertain significance	16	1977566	1977566	Human		name
598208653	CV3913013	single nucleotide variant	NM_006453.3(TBL3):c.1505C>A (p.Thr502Lys)	not specified [RCV005291532]	uncertain significance	16	1977118	1977118	Human		name
598163267	CV3913014	single nucleotide variant	NM_006453.3(TBL3):c.1193A>G (p.Gln398Arg)	not specified [RCV005283084]	uncertain significance	16	1976215	1976215	Human		name
598208659	CV3913015	single nucleotide variant	NM_006453.3(TBL3):c.2125G>C (p.Asp709His)	not specified [RCV005291533]	uncertain significance	16	1978211	1978211	Human		name
598208668	CV3913017	single nucleotide variant	NM_006453.3(TBL3):c.2396C>G (p.Pro799Arg)	not specified [RCV005291535]	uncertain significance	16	1978654	1978654	Human		name
598208672	CV3913018	single nucleotide variant	NM_006453.3(TBL3):c.1730A>G (p.Gln577Arg)	not specified [RCV005291536]	uncertain significance	16	1977414	1977414	Human		name
598208677	CV3913020	single nucleotide variant	NM_006453.3(TBL3):c.1750G>C (p.Asp584His)	not specified [RCV005291537]	uncertain significance	16	1977521	1977521	Human		name
598208683	CV3913021	single nucleotide variant	NM_006453.3(TBL3):c.1706T>C (p.Val569Ala)	not specified [RCV005291538]	uncertain significance	16	1977390	1977390	Human		name

Gene Annotator (Functional Annotation) unavailable	Gene Annotator (Annotation Distribution) unavailable	Variant Visualizer (Genomic Variants) unavailble Variant Visualizer (Genomic Variants) unavailable
Gene Annotator (Functional Annotation)	Gene Annotator (Annotation Distribution)	Variant Visualizer (Genomic Variants)

InterViewer (Protein-Protein Interactions) unavailable	Gviewer (Genome Viewer) unavailable	Variant Visualizer (Damaging Variants) unavailble Variant Visualizer (Damaging Variants) unavailable
InterViewer (Protein-Protein Interactions)	GViewer (Genome Viewer)	Variant Visualizer (Damaging Variants)

Gene Annotator (Annotation Comparison) unavailable	OLGA (Gene List Generator) unavailable
Gene Annotator (Annotation Comparison)	OLGA (Gene List Generator)	Excel (Download)

MOET (Multi-Ontology Enrichement) unavailable	GOLF (Gene-Ortholog Location Finder) unavailable
MOET (Multi-Ontology Enrichement)	GOLF (Gene-Ortholog Location Finder)

Create Name:

Description:

Send us a Message