Trim36 Variant Search Result - Rat Genome Database

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85 records found for search term Trim36

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
405287675	CV3217858	single nucleotide variant	NM_001300759.2(TRIM36):c.1211-7C>T	TRIM36-related disorder [RCV003981981]	benign	5	115134154	115134154	Human		name , trait , alternate_id
8580261	CV114691	single nucleotide variant	NM_001017397.1(TRIM36):c.64-3104T>G	Lung cancer [RCV000095214]	uncertain significance	5	115174326	115174326	Human		name
151663234	CV1333844	single nucleotide variant	NM_001300759.2(TRIM36):c.1797-35T>G	Anencephaly 1 [RCV001838945]	benign	5	115126892	115126892	Human	1	name
156377345	CV2207045	single nucleotide variant	NM_018700.4(TRIM36):c.50T>C (p.Ile17Thr)	not specified [RCV004085657]	uncertain significance	5	115179988	115179988	Human		name
156088339	CV2359227	single nucleotide variant	NM_018700.4(TRIM36):c.59G>A (p.Gly20Asp)	not specified [RCV004212521]	uncertain significance	5	115179979	115179979	Human		name
597690131	CV3617716	single nucleotide variant	NM_018700.4(TRIM36):c.35A>G (p.Tyr12Cys)	not specified [RCV004880891]	uncertain significance	5	115180003	115180003	Human		name
598202615	CV3935431	single nucleotide variant	NM_018700.4(TRIM36):c.42G>A (p.Met14Ile)	not specified [RCV005290405]	uncertain significance	5	115179996	115179996	Human		name
405273961	CV3191424	single nucleotide variant	NM_001017397.2(TRIM36):c.78A>G (p.Arg26=)	TRIM36-related disorder [RCV003919580]	benign	5	115171208	115171208	Human		name , trait , alternate_id
15176302	CV721161	single nucleotide variant	NM_001300759.2(TRIM36):c.42T>C (p.Asn14=)	not provided [RCV000884554]	benign	5	115163738	115163738	Human		name
8631351	CV86512	single nucleotide variant	NM_018700.3(TRIM36):c.208G>A (p.Asp70Asn)	Malignant melanoma [RCV000066603]	not provided	5	115163608	115163608	Human		name
15184849	CV721160	single nucleotide variant	NM_001300759.2(TRIM36):c.114T>C (p.His38=)	not provided [RCV000886539]	benign	5	115163666	115163666	Human		name
405272350	CV3199335	single nucleotide variant	NM_001300759.2(TRIM36):c.582A>G (p.Arg194=)	TRIM36-related disorder [RCV003914285]	likely benign	5	115147075	115147075	Human		name , trait , alternate_id
405280303	CV3200688	single nucleotide variant	NM_001300759.2(TRIM36):c.666G>A (p.Leu222=)	TRIM36-related disorder [RCV003977313]	benign	5	115144667	115144667	Human		name , trait , alternate_id
597801763	CV3617715	single nucleotide variant	NM_001300759.2(TRIM36):c.86C>T (p.Thr29Ile)	not specified [RCV004880890]	uncertain significance	5	115163694	115163694	Human		name
15157354	CV698735	single nucleotide variant	NM_001300759.2(TRIM36):c.717T>C (p.Ser239=)	not provided [RCV000946869]	benign	5	115144616	115144616	Human		name
155967690	CV2216887	single nucleotide variant	NM_001300759.2(TRIM36):c.157G>C (p.Asp53His)	not specified [RCV004083302]	uncertain significance	5	115163623	115163623	Human		name
156147006	CV2265172	single nucleotide variant	NM_001300759.2(TRIM36):c.174T>G (p.Asp58Glu)	not specified [RCV004126297]	uncertain significance	5	115163606	115163606	Human		name
329357643	CV2427790	single nucleotide variant	NM_001300759.2(TRIM36):c.248G>A (p.Arg83Gln)	not specified [RCV004252568]	uncertain significance	5	115163532	115163532	Human		name
329391704	CV2453053	single nucleotide variant	NM_001300759.2(TRIM36):c.128A>G (p.Lys43Arg)	not specified [RCV004277664]	uncertain significance	5	115163652	115163652	Human		name
401914990	CV2827946	single nucleotide variant	NM_001300759.2(TRIM36):c.2145C>T (p.Asp715=)	not provided [RCV003428584]	likely benign	5	115126509	115126509	Human		name
405790287	CV3336943	single nucleotide variant	NM_001300759.2(TRIM36):c.215G>A (p.Arg72Gln)	not specified [RCV004473822]	uncertain significance	5	115163565	115163565	Human		name
407453765	CV3490501	single nucleotide variant	NM_001300759.2(TRIM36):c.161A>T (p.Asp54Val)	not specified [RCV004684658]	uncertain significance	5	115163619	115163619	Human		name
598274133	CV3935433	single nucleotide variant	NM_001300759.2(TRIM36):c.209G>T (p.Arg70Leu)	not specified [RCV005303775]	uncertain significance	5	115163571	115163571	Human		name
598274135	CV3935434	single nucleotide variant	NM_001300759.2(TRIM36):c.221C>T (p.Pro74Leu)	not specified [RCV005303776]	uncertain significance	5	115163559	115163559	Human		name
15099394	CV721159	single nucleotide variant	NM_001300759.2(TRIM36):c.2115C>T (p.Ile705=)	not provided [RCV000891938]	likely benign	5	115126539	115126539	Human		name
155959502	CV2193910	single nucleotide variant	NM_001300759.2(TRIM36):c.706A>G (p.Thr236Ala)	not specified [RCV004074644]	uncertain significance	5	115144627	115144627	Human		name
156342478	CV2222283	single nucleotide variant	NM_001300759.2(TRIM36):c.584C>T (p.Pro195Leu)	not specified [RCV004105301]	uncertain significance	5	115147073	115147073	Human		name
155991547	CV2255683	single nucleotide variant	NM_001300759.2(TRIM36):c.483C>G (p.Asp161Glu)	not specified [RCV004120084]	uncertain significance	5	115147174	115147174	Human		name
155925900	CV2287772	single nucleotide variant	NM_001300759.2(TRIM36):c.862A>G (p.Ile288Val)	not specified [RCV004143222]	uncertain significance	5	115137586	115137586	Human		name
155995996	CV2393132	single nucleotide variant	NM_001300759.2(TRIM36):c.965C>T (p.Thr322Ile)	not specified [RCV004226612]	uncertain significance	5	115137483	115137483	Human		name
401779802	CV2676691	single nucleotide variant	NM_001300759.2(TRIM36):c.337G>A (p.Gly113Arg)	not specified [RCV004290869]	uncertain significance	5	115147320	115147320	Human		name
401739536	CV2683096	single nucleotide variant	NM_001300759.2(TRIM36):c.925A>G (p.Ile309Val)	not specified [RCV004286103]	uncertain significance	5	115137523	115137523	Human		name
401773793	CV2691409	single nucleotide variant	NM_001300759.2(TRIM36):c.768T>G (p.Ile256Met)	not specified [RCV004305271]	uncertain significance	5	115141342	115141342	Human		name
401886545	CV2780410	single nucleotide variant	NM_001300759.2(TRIM36):c.481G>C (p.Asp161His)	not specified [RCV004357803]	uncertain significance	5	115147176	115147176	Human		name
405277139	CV3195337	single nucleotide variant	NM_001300759.2(TRIM36):c.745T>A (p.Ser249Thr)	TRIM36-related disorder [RCV003904127]	likely benign	5	115141365	115141365	Human		name , trait , alternate_id
405292898	CV3207044	single nucleotide variant	NM_001300759.2(TRIM36):c.372C>G (p.Phe124Leu)	TRIM36-related disorder [RCV003931460]	likely benign	5	115147285	115147285	Human		name , trait , alternate_id
405790292	CV3336945	single nucleotide variant	NM_001300759.2(TRIM36):c.467C>G (p.Thr156Arg)	not specified [RCV004473824]	uncertain significance	5	115147190	115147190	Human		name
405790295	CV3336946	single nucleotide variant	NM_001300759.2(TRIM36):c.595A>G (p.Met199Val)	not specified [RCV004473825]	uncertain significance	5	115144738	115144738	Human		name
405790298	CV3336947	single nucleotide variant	NM_001300759.2(TRIM36):c.642A>C (p.Leu214Phe)	not specified [RCV004473826]	uncertain significance	5	115144691	115144691	Human		name
407453768	CV3490502	single nucleotide variant	NM_001300759.2(TRIM36):c.871T>C (p.Phe291Leu)	not specified [RCV004684659]	uncertain significance	5	115137577	115137577	Human		name
597801765	CV3617717	single nucleotide variant	NM_001300759.2(TRIM36):c.847G>A (p.Ala283Thr)	not specified [RCV004880892]	uncertain significance	5	115137601	115137601	Human		name
597801769	CV3617719	single nucleotide variant	NM_001300759.2(TRIM36):c.373A>G (p.Thr125Ala)	not specified [RCV004880894]	uncertain significance	5	115147284	115147284	Human		name
151663232	CV1333843	single nucleotide variant	NM_001300759.2(TRIM36):c.1996G>A (p.Asp666Asn)	Anencephaly 1 [RCV001838944]	benign	5	115126658	115126658	Human	1	name
156320267	CV2197263	single nucleotide variant	NM_001300759.2(TRIM36):c.2036G>A (p.Arg679His)	not specified [RCV004079039]	uncertain significance	5	115126618	115126618	Human		name
156169982	CV2197844	single nucleotide variant	NM_001300759.2(TRIM36):c.1768C>T (p.Arg590Cys)	not specified [RCV004077079]	uncertain significance	5	115130620	115130620	Human		name
155917786	CV2199117	single nucleotide variant	NM_001300759.2(TRIM36):c.1916C>G (p.Ser639Cys)	not specified [RCV004080513]	uncertain significance	5	115126738	115126738	Human		name
156070638	CV2204047	single nucleotide variant	NM_001300759.2(TRIM36):c.1279C>G (p.His427Asp)	not specified [RCV004076517]	uncertain significance	5	115134079	115134079	Human		name
155975733	CV2211306	single nucleotide variant	NM_001300759.2(TRIM36):c.1545C>A (p.His515Gln)	not specified [RCV004090236]	uncertain significance	5	115130843	115130843	Human		name
156161348	CV2236457	single nucleotide variant	NM_001300759.2(TRIM36):c.1916C>T (p.Ser639Phe)	not specified [RCV004108126]	uncertain significance	5	115126738	115126738	Human		name
155925165	CV2248967	single nucleotide variant	NM_001300759.2(TRIM36):c.1658G>A (p.Gly553Glu)	not specified [RCV004115965]	uncertain significance	5	115130730	115130730	Human		name
156150579	CV2268888	single nucleotide variant	NM_001300759.2(TRIM36):c.1300G>A (p.Asp434Asn)	not specified [RCV004128303]	uncertain significance	5	115134058	115134058	Human		name
156185124	CV2292296	single nucleotide variant	NM_001300759.2(TRIM36):c.1879G>C (p.Gly627Arg)	not specified [RCV004148327]	uncertain significance	5	115126775	115126775	Human		name
155930676	CV2297014	single nucleotide variant	NM_001300759.2(TRIM36):c.2009T>C (p.Met670Thr)	not specified [RCV004150939]	uncertain significance	5	115126645	115126645	Human		name
156048356	CV2304419	single nucleotide variant	NM_001300759.2(TRIM36):c.1118T>G (p.Phe373Cys)	not specified [RCV004164519]	uncertain significance	5	115137092	115137092	Human		name
156356400	CV2320780	single nucleotide variant	NM_001300759.2(TRIM36):c.1058T>C (p.Val353Ala)	not specified [RCV004172617]	uncertain significance	5	115137390	115137390	Human		name
155937633	CV2373733	single nucleotide variant	NM_001300759.2(TRIM36):c.1447A>G (p.Ile483Val)	not specified [RCV004224677]	uncertain significance	5	115133911	115133911	Human		name
156217170	CV2386126	single nucleotide variant	NM_001300759.2(TRIM36):c.1200T>G (p.Phe400Leu)	not specified [RCV004603407]	uncertain significance	5	115137010	115137010	Human		name
329391174	CV2447857	single nucleotide variant	NM_001300759.2(TRIM36):c.1232A>G (p.Asn411Ser)	not specified [RCV004258629]	uncertain significance	5	115134126	115134126	Human		name
329376903	CV2451570	single nucleotide variant	NM_001300759.2(TRIM36):c.1805A>C (p.Gln602Pro)	not specified [RCV004274507]	uncertain significance	5	115126849	115126849	Human		name
329390330	CV2453745	single nucleotide variant	NM_001300759.2(TRIM36):c.1891T>C (p.Phe631Leu)	not specified [RCV004269378]	uncertain significance	5	115126763	115126763	Human		name
329390049	CV2457551	single nucleotide variant	NM_001300759.2(TRIM36):c.2035C>T (p.Arg679Cys)	not specified [RCV004267355]	uncertain significance	5	115126619	115126619	Human		name
401758337	CV2678623	single nucleotide variant	NM_001300759.2(TRIM36):c.1179A>T (p.Glu393Asp)	not specified [RCV004292624]	uncertain significance	5	115137031	115137031	Human		name
401737614	CV2679926	single nucleotide variant	NM_001300759.2(TRIM36):c.1735G>A (p.Val579Ile)	not specified [RCV004284208]	uncertain significance	5	115130653	115130653	Human		name
401722248	CV2706440	single nucleotide variant	NM_001300759.2(TRIM36):c.1384A>G (p.Ile462Val)	not specified [RCV004317264]	likely benign	5	115133974	115133974	Human		name
405290845	CV3197138	single nucleotide variant	NM_001300759.2(TRIM36):c.1331A>G (p.Asn444Ser)	TRIM36-related disorder [RCV003984700]	benign	5	115134027	115134027	Human		name , trait , alternate_id
405790262	CV3336934	single nucleotide variant	NM_001300759.2(TRIM36):c.1289A>C (p.Lys430Thr)	not specified [RCV004473813]	uncertain significance	5	115134069	115134069	Human		name
405790264	CV3336935	single nucleotide variant	NM_001300759.2(TRIM36):c.1351T>C (p.Trp451Arg)	not specified [RCV004473814]	uncertain significance	5	115134007	115134007	Human		name
405790267	CV3336936	single nucleotide variant	NM_001300759.2(TRIM36):c.1562A>G (p.Lys521Arg)	not specified [RCV004473815]	uncertain significance	5	115130826	115130826	Human		name
405790272	CV3336938	single nucleotide variant	NM_001300759.2(TRIM36):c.1571G>A (p.Arg524His)	not specified [RCV004473817]	uncertain significance	5	115130817	115130817	Human		name
405790275	CV3336939	single nucleotide variant	NM_001300759.2(TRIM36):c.1744A>G (p.Ser582Gly)	not specified [RCV004473818]	uncertain significance	5	115130644	115130644	Human		name
405790278	CV3336940	single nucleotide variant	NM_001300759.2(TRIM36):c.1876A>G (p.Ile626Val)	not specified [RCV004473819]	uncertain significance	5	115126778	115126778	Human		name
405790281	CV3336941	single nucleotide variant	NM_001300759.2(TRIM36):c.1987G>A (p.Gly663Ser)	not specified [RCV004473820]	uncertain significance	5	115126667	115126667	Human		name
405790284	CV3336942	single nucleotide variant	NM_001300759.2(TRIM36):c.2041G>C (p.Val681Leu)	not specified [RCV004473821]	uncertain significance	5	115126613	115126613	Human		name
407461447	CV3490498	single nucleotide variant	NM_001300759.2(TRIM36):c.2019G>T (p.Met673Ile)	not specified [RCV004687655]	uncertain significance	5	115126635	115126635	Human		name
407453759	CV3490499	single nucleotide variant	NM_001300759.2(TRIM36):c.2120C>T (p.Ala707Val)	not specified [RCV004684656]	uncertain significance	5	115126534	115126534	Human		name
407453761	CV3490500	single nucleotide variant	NM_001300759.2(TRIM36):c.2054A>G (p.His685Arg)	not specified [RCV004684657]	uncertain significance	5	115126600	115126600	Human		name
407453771	CV3490503	single nucleotide variant	NM_001300759.2(TRIM36):c.1151A>G (p.Tyr384Cys)	not specified [RCV004684660]	uncertain significance	5	115137059	115137059	Human		name
597801758	CV3617712	single nucleotide variant	NM_001300759.2(TRIM36):c.2026C>A (p.Leu676Ile)	not specified [RCV004880887]	uncertain significance	5	115126628	115126628	Human		name
597801760	CV3617713	single nucleotide variant	NM_001300759.2(TRIM36):c.1762T>C (p.Trp588Arg)	not specified [RCV004880888]	uncertain significance	5	115130626	115130626	Human		name
597801761	CV3617714	single nucleotide variant	NM_001300759.2(TRIM36):c.1451G>A (p.Cys484Tyr)	not specified [RCV004880889]	uncertain significance	5	115133907	115133907	Human		name
597801767	CV3617718	single nucleotide variant	NM_001300759.2(TRIM36):c.1684C>T (p.His562Tyr)	not specified [RCV004880893]	uncertain significance	5	115130704	115130704	Human		name
598274131	CV3935430	single nucleotide variant	NM_001300759.2(TRIM36):c.1778G>A (p.Arg593Gln)	not specified [RCV005303774]	uncertain significance	5	115130610	115130610	Human		name
598202623	CV3935432	single nucleotide variant	NM_001300759.2(TRIM36):c.2144A>G (p.Asp715Gly)	not specified [RCV005290406]	uncertain significance	5	115126510	115126510	Human		name
13210847	CV424689	single nucleotide variant	NM_001300759.2(TRIM36):c.1486C>A (p.Pro496Thr)	Anencephaly [RCV000496691]	pathogenic	5	115133872	115133872	Human	2	name
15114249	CV734807	single nucleotide variant	NM_001300759.2(TRIM36):c.2137C>G (p.Gln713Glu)	TRIM36-related disorder [RCV003922839]\|not provided [RCV000894822]	benign	5	115126517	115126517	Human	1	name , trait , alternate_id

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