Trim24 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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65 records found for search term Trim24

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
8590459	CV125151	single nucleotide variant	NM_015905.2(TRIM24):c.1531-3402G>T	Lung cancer [RCV000105670]	uncertain significance	7	138564079	138564079	Human		name
156282230	CV2348839	single nucleotide variant	NM_015905.3(TRIM24):c.44C>T (p.Ala15Val)	not specified [RCV004203282]	uncertain significance	7	138460592	138460592	Human		name
156131813	CV2372920	single nucleotide variant	NM_015905.3(TRIM24):c.55G>C (p.Ala19Pro)	not specified [RCV004223965]	uncertain significance	7	138460603	138460603	Human		name
243054564	CV2418963	single nucleotide variant	NM_015905.3(TRIM24):c.76G>A (p.Ala26Thr)	Ovarian cancer [RCV003154646]	benign	7	138460624	138460624	Human	2	name
156083248	CV2205500	single nucleotide variant	NM_015905.3(TRIM24):c.193A>T (p.Ser65Cys)	not specified [RCV004082435]	uncertain significance	7	138460741	138460741	Human		name
156045361	CV2315518	single nucleotide variant	NM_015905.3(TRIM24):c.257A>T (p.Gln86Leu)	not specified [RCV004169569]	uncertain significance	7	138460805	138460805	Human		name
156344475	CV2364287	single nucleotide variant	NM_015905.3(TRIM24):c.290G>C (p.Gly97Ala)	not specified [RCV004223512]	uncertain significance	7	138460838	138460838	Human		name
243054524	CV2419023	single nucleotide variant	NM_015905.3(TRIM24):c.259C>T (p.Arg87Cys)	Ovarian cancer [RCV003154706]	benign	7	138460807	138460807	Human	2	name
401748661	CV2696651	single nucleotide variant	NM_015905.3(TRIM24):c.133G>A (p.Gly45Ser)	not specified [RCV004312668]	uncertain significance	7	138460681	138460681	Human		name
401748664	CV2696652	single nucleotide variant	NM_015905.3(TRIM24):c.296C>G (p.Ala99Gly)	not specified [RCV004312669]	uncertain significance	7	138460844	138460844	Human		name
405294433	CV3211416	single nucleotide variant	NM_015905.3(TRIM24):c.1254C>T (p.Ile418=)	TRIM24-related disorder [RCV003934372]	likely benign	7	138551173	138551173	Human		name , trait , alternate_id
8626347	CV81491	single nucleotide variant	NM_015905.2(TRIM24):c.2676G>A (p.Lys892=)	Malignant melanoma [RCV000061569]	not provided	7	138580652	138580652	Human		name
156149251	CV2265338	single nucleotide variant	NM_015905.3(TRIM24):c.479A>C (p.Asn160Thr)	not specified [RCV004128228]	uncertain significance	7	138504404	138504404	Human		name
156114484	CV2397181	single nucleotide variant	NM_015905.3(TRIM24):c.341G>T (p.Gly114Val)	not specified [RCV004238721]	uncertain significance	7	138460889	138460889	Human		name
329376773	CV2455059	single nucleotide variant	NM_015905.3(TRIM24):c.748G>A (p.Glu250Lys)	not specified [RCV004272311]	uncertain significance	7	138519305	138519305	Human		name
401773320	CV2716526	single nucleotide variant	NM_015905.3(TRIM24):c.376C>T (p.Arg126Cys)	not specified [RCV004327609]	uncertain significance	7	138504301	138504301	Human		name
405269140	CV3187222	single nucleotide variant	NM_015905.3(TRIM24):c.787T>C (p.Phe263Leu)	not provided [RCV003887306]	uncertain significance	7	138525263	138525263	Human		name
405789947	CV3336839	single nucleotide variant	NM_015905.3(TRIM24):c.352T>G (p.Phe118Val)	not specified [RCV004473718]	uncertain significance	7	138460900	138460900	Human		name
407453637	CV3492754	single nucleotide variant	NM_015905.3(TRIM24):c.785C>T (p.Ala262Val)	not specified [RCV004684616]	uncertain significance	7	138525261	138525261	Human		name
597801625	CV3617631	single nucleotide variant	NM_015905.3(TRIM24):c.329C>T (p.Ser110Leu)	not specified [RCV004880815]	uncertain significance	7	138460877	138460877	Human		name
598274059	CV3935380	single nucleotide variant	NM_015905.3(TRIM24):c.796C>G (p.Gln266Glu)	not specified [RCV005303739]	uncertain significance	7	138525272	138525272	Human		name
598274060	CV3935381	single nucleotide variant	NM_015905.3(TRIM24):c.350C>T (p.Pro117Leu)	not specified [RCV005303740]	uncertain significance	7	138460898	138460898	Human		name
156259226	CV2204720	single nucleotide variant	NM_015905.3(TRIM24):c.1750A>G (p.Thr584Ala)	not specified [RCV004074983]	uncertain significance	7	138570875	138570875	Human		name
155976411	CV2231694	single nucleotide variant	NM_015905.3(TRIM24):c.1078A>G (p.Met360Val)	not specified [RCV004098255]	uncertain significance	7	138538738	138538738	Human		name
155919931	CV2254959	single nucleotide variant	NM_015905.3(TRIM24):c.1544G>A (p.Arg515His)	not specified [RCV004117191]	uncertain significance	7	138567494	138567494	Human		name
156047364	CV2268745	single nucleotide variant	NM_015905.3(TRIM24):c.2810A>C (p.Lys937Thr)	not specified [RCV004124136]	uncertain significance	7	138583866	138583866	Human		name
156043267	CV2307909	single nucleotide variant	NM_015905.3(TRIM24):c.2192A>C (p.Glu731Ala)	not specified [RCV004170362]	uncertain significance	7	138577524	138577524	Human		name
156162785	CV2323558	single nucleotide variant	NM_015905.3(TRIM24):c.1960T>C (p.Ser654Pro)	not specified [RCV004165755]	uncertain significance	7	138573588	138573588	Human		name
156353300	CV2327509	single nucleotide variant	NM_015905.3(TRIM24):c.1807G>T (p.Ala603Ser)	not specified [RCV004176820]	uncertain significance	7	138570932	138570932	Human		name
155935227	CV2371752	single nucleotide variant	NM_015905.3(TRIM24):c.1208C>T (p.Thr403Ile)	not specified [RCV004219418]	uncertain significance	7	138551127	138551127	Human		name
156130670	CV2372659	single nucleotide variant	NM_015905.3(TRIM24):c.1376T>A (p.Phe459Tyr)	not specified [RCV004221859]	uncertain significance	7	138554812	138554812	Human		name
243054457	CV2418974	single nucleotide variant	NM_015905.3(TRIM24):c.2899G>A (p.Ala967Thr)	Ovarian cancer [RCV003154657]	benign	7	138583955	138583955	Human	2	name
243054618	CV2419075	single nucleotide variant	NM_015905.3(TRIM24):c.2050C>T (p.Arg684Cys)	Ovarian cancer [RCV003154759]	likely pathogenic	7	138576408	138576408	Human	2	name
243054650	CV2419097	single nucleotide variant	NM_015905.3(TRIM24):c.2338T>A (p.Ser780Thr)	Ovarian cancer [RCV003154781]	benign	7	138579285	138579285	Human	2	name
401746780	CV2690968	single nucleotide variant	NM_015905.3(TRIM24):c.2939A>G (p.Asn980Ser)	not specified [RCV004300992]	uncertain significance	7	138583995	138583995	Human		name
401735209	CV2699200	single nucleotide variant	NM_015905.3(TRIM24):c.1159C>T (p.Arg387Trp)	not specified [RCV004303694]	uncertain significance	7	138551078	138551078	Human		name
401767858	CV2727302	single nucleotide variant	NM_015905.3(TRIM24):c.1190C>T (p.Ser397Phe)	not specified [RCV004327415]	uncertain significance	7	138551109	138551109	Human		name
401884050	CV2765947	single nucleotide variant	NM_015905.3(TRIM24):c.1822A>G (p.Met608Val)	not specified [RCV004337972]	uncertain significance	7	138570947	138570947	Human		name
401892154	CV2775969	single nucleotide variant	NM_015905.3(TRIM24):c.2657G>A (p.Ser886Asn)	not specified [RCV004344985]	uncertain significance	7	138580633	138580633	Human		name
405789923	CV3336833	single nucleotide variant	NM_015905.3(TRIM24):c.1202A>G (p.Asn401Ser)	not specified [RCV004473712]	uncertain significance	7	138551121	138551121	Human		name
405789927	CV3336834	single nucleotide variant	NM_015905.3(TRIM24):c.1321G>A (p.Val441Met)	not specified [RCV004473713]	uncertain significance	7	138554757	138554757	Human		name
405789931	CV3336835	single nucleotide variant	NM_015905.3(TRIM24):c.1655A>C (p.Lys552Thr)	not specified [RCV004473714]	uncertain significance	7	138567605	138567605	Human		name
405789934	CV3336836	single nucleotide variant	NM_015905.3(TRIM24):c.1721G>T (p.Gly574Val)	not specified [RCV004473715]	uncertain significance	7	138570846	138570846	Human		name
405789939	CV3336837	single nucleotide variant	NM_015905.3(TRIM24):c.2297A>G (p.Asn766Ser)	not specified [RCV004473716]	uncertain significance	7	138579244	138579244	Human		name
597801621	CV3617629	single nucleotide variant	NM_015905.3(TRIM24):c.2189C>T (p.Pro730Leu)	not specified [RCV004880813]	uncertain significance	7	138577521	138577521	Human		name
597801623	CV3617630	single nucleotide variant	NM_015905.3(TRIM24):c.1535C>T (p.Pro512Leu)	not specified [RCV004880814]	uncertain significance	7	138567485	138567485	Human		name
597801627	CV3617633	single nucleotide variant	NM_015905.3(TRIM24):c.1172G>A (p.Arg391His)	not specified [RCV004880816]	uncertain significance	7	138551091	138551091	Human		name
597801629	CV3617634	single nucleotide variant	NM_015905.3(TRIM24):c.1658C>A (p.Pro553Gln)	not specified [RCV004880817]	uncertain significance	7	138567608	138567608	Human		name
597801631	CV3617635	single nucleotide variant	NM_015905.3(TRIM24):c.2647G>A (p.Asp883Asn)	not specified [RCV004880818]	uncertain significance	7	138580623	138580623	Human		name
597801633	CV3617636	single nucleotide variant	NM_015905.3(TRIM24):c.2692G>T (p.Val898Phe)	not specified [RCV004880819]	uncertain significance	7	138580668	138580668	Human		name
597801634	CV3617637	single nucleotide variant	NM_015905.3(TRIM24):c.2395A>C (p.Asn799His)	not specified [RCV004880820]	uncertain significance	7	138579342	138579342	Human		name
598274051	CV3935374	single nucleotide variant	NM_015905.3(TRIM24):c.2665T>G (p.Ser889Ala)	not specified [RCV005303735]	uncertain significance	7	138580641	138580641	Human		name
598274053	CV3935376	single nucleotide variant	NM_015905.3(TRIM24):c.2177A>G (p.Asn726Ser)	not specified [RCV005303736]	uncertain significance	7	138577509	138577509	Human		name
598274055	CV3935377	single nucleotide variant	NM_015905.3(TRIM24):c.2261A>G (p.Asn754Ser)	not specified [RCV005303737]	uncertain significance	7	138579208	138579208	Human		name
598202509	CV3935379	single nucleotide variant	NM_015905.3(TRIM24):c.1493T>G (p.Met498Arg)	not specified [RCV005290389]	uncertain significance	7	138554929	138554929	Human		name
598274062	CV3935382	single nucleotide variant	NM_015905.3(TRIM24):c.1660A>T (p.Asn554Tyr)	not specified [RCV005303741]	uncertain significance	7	138567610	138567610	Human		name
598202515	CV3935383	single nucleotide variant	NM_015905.3(TRIM24):c.2311T>A (p.Ser771Thr)	not specified [RCV005290390]	uncertain significance	7	138579258	138579258	Human		name
598202520	CV3935384	single nucleotide variant	NM_015905.3(TRIM24):c.1607A>T (p.Gln536Leu)	not specified [RCV005290391]	uncertain significance	7	138567557	138567557	Human		name
598274064	CV3935385	single nucleotide variant	NM_015905.3(TRIM24):c.1492A>G (p.Met498Val)	not specified [RCV005303742]	uncertain significance	7	138554928	138554928	Human		name
15190310	CV699867	single nucleotide variant	NM_015905.3(TRIM24):c.2616C>G (p.Asp872Glu)	not provided [RCV000954437]	benign	7	138580592	138580592	Human		name
156088158	CV2337116	single nucleotide variant	NM_015905.3(TRIM24):c.3128T>C (p.Ile1043Thr)	not specified [RCV004192876]	uncertain significance	7	138584926	138584926	Human		name
401898344	CV2787687	single nucleotide variant	NM_015905.3(TRIM24):c.3009C>A (p.Asn1003Lys)	not specified [RCV004356609]	uncertain significance	7	138584807	138584807	Human		name
405789943	CV3336838	single nucleotide variant	NM_015905.3(TRIM24):c.3107G>A (p.Arg1036Gln)	not specified [RCV004473717]	uncertain significance	7	138584905	138584905	Human		name
597801636	CV3617638	single nucleotide variant	NM_015905.3(TRIM24):c.3127A>G (p.Ile1043Val)	not specified [RCV004880821]	uncertain significance	7	138584925	138584925	Human		name
598274057	CV3935378	single nucleotide variant	NM_015905.3(TRIM24):c.3136C>T (p.Arg1046Cys)	not specified [RCV005303738]	uncertain significance	7	138584934	138584934	Human		name

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