Trim63 Variant Search Result - Rat Genome Database

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122 records found for search term Trim63

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
150450848	CV1275061	single nucleotide variant	NM_032588.4(TRIM63):c.*2G>A	not provided [RCV003407774]\|not specified [RCV001702315]	benign\|likely benign\|conflicting interpretations of pathogenicity\|uncertain significance	1	26051871	26051871	Human		name
616937633	CV4011249	single nucleotide variant	NM_032588.4(TRIM63):c.*1G>T	not specified [RCV005405095]	likely benign	1	26051872	26051872	Human		name
150436230	CV1275035	single nucleotide variant	NM_032588.4(TRIM63):c.597+7G>A	TRIM63-related disorder [RCV003948683]\|not provided [RCV001724416]\|not specified [RCV001703282]	benign\|likely benign	1	26060259	26060259	Human	1	name , trait , alternate_id
401867277	CV2748816	single nucleotide variant	NM_032588.4(TRIM63):c.332+4G>T	not specified [RCV003331638]	uncertain significance	1	26066264	26066264	Human		name
401905940	CV2804833	single nucleotide variant	NM_032588.4(TRIM63):c.831+2T>G	TRIM63-related disorder [RCV003420952]	uncertain significance	1	26058388	26058388	Human		name , trait , alternate_id
405068810	CV2875528	single nucleotide variant	NM_032588.4(TRIM63):c.855-7C>G	not provided [RCV003548328]	likely benign	1	26057334	26057334	Human		name
598123469	CV3884837	single nucleotide variant	NM_032588.4(TRIM63):c.832-7C>G	not specified [RCV005238445]	uncertain significance	1	26057657	26057657	Human		name
15117796	CV695045	single nucleotide variant	NM_032588.4(TRIM63):c.502-8C>T	TRIM63-related disorder [RCV003920420]\|not provided [RCV000873566]\|not specified [RCV003230603]	benign	1	26060369	26060369	Human	1	name , trait , alternate_id
150466199	CV1218149	single nucleotide variant	NM_032588.4(TRIM63):c.598-36C>G	not provided [RCV001614275]	benign	1	26058659	26058659	Human		name
150506200	CV1226287	single nucleotide variant	NM_032588.4(TRIM63):c.979+76G>C	not provided [RCV001635655]	benign	1	26057127	26057127	Human		name
150471123	CV1248157	single nucleotide variant	NM_032588.4(TRIM63):c.332+96T>A	not provided [RCV001671194]	benign	1	26066172	26066172	Human		name
150499750	CV1254412	single nucleotide variant	NM_032588.4(TRIM63):c.855-57T>C	not provided [RCV001676586]	benign	1	26057384	26057384	Human		name
150484011	CV1263089	single nucleotide variant	NM_032588.4(TRIM63):c.501+32T>G	not provided [RCV001686489]	benign	1	26061134	26061134	Human		name
150499444	CV1270823	single nucleotide variant	NM_032588.4(TRIM63):c.160-43A>G	not provided [RCV001689373]	benign	1	26066483	26066483	Human		name
150495419	CV1272627	single nucleotide variant	NM_032588.4(TRIM63):c.160-40T>G	not provided [RCV001688550]	benign	1	26066480	26066480	Human		name
155799056	CV1862305	single nucleotide variant	NM_032588.4(TRIM63):c.1051+1G>A	Hypertrophic cardiomyopathy [RCV002471709]	uncertain significance	1	26053892	26053892	Human	2	name
401963895	CV2843381	single nucleotide variant	NM_032588.4(TRIM63):c.980-16T>C	not specified [RCV003479723]	likely benign	1	26053980	26053980	Human		name
596942343	CV3544059	single nucleotide variant	NM_032588.4(TRIM63):c.597+14A>G	not specified [RCV004800049]	likely benign	1	26060252	26060252	Human		name
150333990	CV1168830	single nucleotide variant	NM_032588.4(TRIM63):c.501+234C>T	not provided [RCV001537567]	benign	1	26060932	26060932	Human	1	name
150335514	CV1170710	single nucleotide variant	NM_032588.4(TRIM63):c.598-192C>A	not provided [RCV001540600]	benign	1	26058815	26058815	Human		name
150472985	CV1217554	single nucleotide variant	NM_032588.4(TRIM63):c.831+191A>C	not provided [RCV001615565]	benign	1	26058199	26058199	Human		name
150482769	CV1247508	single nucleotide variant	NM_032588.4(TRIM63):c.332+224G>A	not provided [RCV001673334]	benign	1	26066044	26066044	Human		name
150460148	CV1268451	single nucleotide variant	NM_032588.4(TRIM63):c.333-144A>T	not provided [RCV001693448]	benign	1	26061478	26061478	Human		name
150465705	CV1277283	single nucleotide variant	NM_032588.4(TRIM63):c.854+106T>C	not provided [RCV001710577]	benign	1	26057522	26057522	Human		name
616937080	CV4011247	single nucleotide variant	NM_032588.4(TRIM63):c.1051+29C>T	not specified [RCV005405093]	likely benign	1	26053864	26053864	Human		name
616937632	CV4011248	single nucleotide variant	NM_032588.4(TRIM63):c.1051+60G>A	not specified [RCV005405094]	likely benign	1	26053833	26053833	Human		name
150444634	CV1288051	single nucleotide variant	NM_032588.4(TRIM63):c.12G>A (p.Lys4=)	not provided [RCV001725773]\|not specified [RCV003230691]	benign	1	26067483	26067483	Human		name
150442498	CV1264443	deletion	NM_032588.4(TRIM63):c.979+42_979+48del	not provided [RCV001679426]	benign	1	26057155	26057161	Human		name
401797430	CV2742068	single nucleotide variant	NM_032588.4(TRIM63):c.72T>C (p.Pro24=)	not specified [RCV003324245]	likely benign	1	26067423	26067423	Human		name
150501448	CV1256302	single nucleotide variant	NM_032588.4(TRIM63):c.267G>T (p.Val89=)	not provided [RCV001676926]\|not specified [RCV003230687]	benign	1	26066333	26066333	Human		name
15117955	CV690580	single nucleotide variant	NM_032588.4(TRIM63):c.162T>G (p.Ala54=)	not provided [RCV000873596]\|not specified [RCV004800625]	benign\|likely benign\|conflicting interpretations of pathogenicity\|uncertain significance	1	26066438	26066438	Human		name
15143060	CV690581	single nucleotide variant	NM_032588.4(TRIM63):c.135G>C (p.Arg45=)	TRIM63-related disorder [RCV004756062]\|not provided [RCV000877985]\|not specified [RCV001702060]	benign\|likely benign	1	26067360	26067360	Human	1	name , trait , alternate_id
150447580	CV1274789	deletion	NM_032588.4(TRIM63):c.1052-21_1052-20del	not provided [RCV001699911]\|not specified [RCV003487729]	likely benign	1	26051903	26051904	Human		name
401867051	CV2748818	single nucleotide variant	NM_032588.4(TRIM63):c.951C>T (p.Asp317=)	not specified [RCV003331640]	likely benign	1	26057231	26057231	Human		name
405275799	CV3196434	single nucleotide variant	NM_032588.4(TRIM63):c.624G>A (p.Glu208=)	TRIM63-related disorder [RCV003974268]	likely benign	1	26058597	26058597	Human		name , trait , alternate_id
405268911	CV3201152	single nucleotide variant	NM_032588.4(TRIM63):c.420C>A (p.Pro140=)	TRIM63-related disorder [RCV003899259]	likely benign	1	26061247	26061247	Human		name , trait , alternate_id
405797066	CV3337193	single nucleotide variant	NM_032588.4(TRIM63):c.41T>C (p.Met14Thr)	Inborn genetic diseases [RCV004476054]	uncertain significance	1	26067454	26067454	Human	1	name
405797076	CV3337196	single nucleotide variant	NM_032588.4(TRIM63):c.97C>G (p.Pro33Ala)	Inborn genetic diseases [RCV004476057]	uncertain significance	1	26067398	26067398	Human	1	name
408395130	CV3522330	single nucleotide variant	NM_032588.4(TRIM63):c.68G>A (p.Cys23Tyr)	Cardiovascular phenotype [RCV005406129]\|Hypertrophic cardiomyopathy [RCV004765407]	uncertain significance	1	26067427	26067427	Human	2	name
596943940	CV3544448	single nucleotide variant	NM_032588.4(TRIM63):c.306C>T (p.Ile102=)	not specified [RCV004800928]	likely benign	1	26066294	26066294	Human		name
597625160	CV3614484	single nucleotide variant	NM_032588.4(TRIM63):c.30T>G (p.Asp10Glu)	Inborn genetic diseases [RCV004964396]	uncertain significance	1	26067465	26067465	Human	1	name
616936818	CV4010790	single nucleotide variant	NM_032588.4(TRIM63):c.32G>C (p.Gly11Ala)	Cardiovascular phenotype [RCV005404137]	uncertain significance	1	26067463	26067463	Human		name
616937430	CV4010928	single nucleotide variant	NM_032588.4(TRIM63):c.807G>A (p.Glu269=)	not specified [RCV005404771]	likely benign	1	26058414	26058414	Human		name
617152814	CV4018420	single nucleotide variant	NM_032588.4(TRIM63):c.699G>A (p.Gln233=)	not specified [RCV005418680]	likely benign	1	26058522	26058522	Human		name
15117814	CV690579	single nucleotide variant	NM_032588.4(TRIM63):c.375C>T (p.His125=)	not provided [RCV000873569]\|not specified [RCV003230604]	benign\|likely benign	1	26061292	26061292	Human		name
150338320	CV1166961	single nucleotide variant	NM_032588.4(TRIM63):c.115T>G (p.Cys39Gly)	Hypertrophic cardiomyopathy [RCV001533451]	uncertain significance	1	26067380	26067380	Human	2	name
150451929	CV1260322	insertion	NM_032588.4(TRIM63):c.980-274_980-273insA	not provided [RCV001680812]	benign	1	26054237	26054238	Human		name
150499224	CV1270785	single nucleotide variant	NM_032588.4(TRIM63):c.1041G>A (p.Gly347=)	TRIM63-related disorder [RCV003941082]\|not provided [RCV001689335]\|not specified [RCV003230689]	benign	1	26053903	26053903	Human	1	name , trait , alternate_id
150550699	CV1305091	deletion	NM_032588.4(TRIM63):c.888del (p.Lys297fs)	not provided [RCV001765871]	uncertain significance	1	26057294	26057294	Human		name
9832560	CV178468	single nucleotide variant	NM_032588.4(TRIM63):c.143C>T (p.Ala48Val)	Cardiovascular phenotype [RCV005404285]\|Primary familial hypertrophic cardiomyopathy [RCV000157545]\|TRIM63-related disorder [RCV004755782]\|not provided [RCV001701625]	likely benign\|conflicting interpretations of pathogenicity\|uncertain significance	1	26067352	26067352	Human	3	name , trait , alternate_id
156401123	CV2213937	single nucleotide variant	NM_032588.4(TRIM63):c.185G>A (p.Arg62Gln)	Inborn genetic diseases [RCV002656823]\|not specified [RCV003988068]	uncertain significance	1	26066415	26066415	Human	1	name
11040129	CV224215	single nucleotide variant	NM_032588.4(TRIM63):c.224G>A (p.Cys75Tyr)	Cardiovascular phenotype [RCV005404396]\|Hypertrophic cardiomyopathy [RCV001533453]\|Primary familial hypertrophic cardiomyopathy [RCV000208412]\|not specified [RCV003401117]	likely pathogenic\|likely benign\|conflicting interpretations of pathogenicity\|uncertain significance	1	26066376	26066376	Human	4	name
156284886	CV2360713	single nucleotide variant	NM_032588.4(TRIM63):c.235C>T (p.Arg79Cys)	Inborn genetic diseases [RCV002670391]\|not specified [RCV003331450]	uncertain significance	1	26066365	26066365	Human	1	name
156071247	CV2365290	single nucleotide variant	NM_032588.4(TRIM63):c.149A>G (p.Asp50Gly)	Inborn genetic diseases [RCV003000749]	uncertain significance	1	26067346	26067346	Human	1	name
156052655	CV2388476	single nucleotide variant	NM_032588.4(TRIM63):c.184C>T (p.Arg62Trp)	Inborn genetic diseases [RCV002759439]	uncertain significance	1	26066416	26066416	Human	1	name
329376881	CV2460618	single nucleotide variant	NM_032588.4(TRIM63):c.148G>T (p.Asp50Tyr)	Inborn genetic diseases [RCV003186196]	uncertain significance	1	26067347	26067347	Human	1	name
401748007	CV2687659	single nucleotide variant	NM_032588.4(TRIM63):c.221G>A (p.Arg74His)	Cardiovascular phenotype [RCV005406013]\|Inborn genetic diseases [RCV003252977]\|Primary familial hypertrophic cardiomyopathy [RCV003883212]	uncertain significance	1	26066379	26066379	Human	3	name
401867056	CV2748820	single nucleotide variant	NM_032588.4(TRIM63):c.170C>G (p.Pro57Arg)	Inborn genetic diseases [RCV004963618]\|not specified [RCV003331642]	uncertain significance	1	26066430	26066430	Human	1	name
401899927	CV2765687	single nucleotide variant	NM_032588.4(TRIM63):c.251T>G (p.Met84Arg)	Inborn genetic diseases [RCV003378251]	uncertain significance	1	26066349	26066349	Human	1	name
405256254	CV3222454	single nucleotide variant	NM_032588.4(TRIM63):c.277C>T (p.Gln93Ter)	Idiopathic cardiomyopathy [RCV003985950]	pathogenic	1	26066323	26066323	Human	1	name
405797051	CV3337189	single nucleotide variant	NM_032588.4(TRIM63):c.113C>T (p.Pro38Leu)	Inborn genetic diseases [RCV004476050]	uncertain significance	1	26067382	26067382	Human	1	name
405797055	CV3337190	single nucleotide variant	NM_032588.4(TRIM63):c.140G>A (p.Cys47Tyr)	Inborn genetic diseases [RCV004476051]	uncertain significance	1	26067355	26067355	Human	1	name
405797058	CV3337191	single nucleotide variant	NM_032588.4(TRIM63):c.229A>G (p.Thr77Ala)	Inborn genetic diseases [RCV004476052]	uncertain significance	1	26066371	26066371	Human	1	name
405855061	CV3395582	single nucleotide variant	NM_032588.4(TRIM63):c.265G>A (p.Val89Met)	Primary familial hypertrophic cardiomyopathy [RCV004555918]	uncertain significance	1	26066335	26066335	Human	1	name
596930119	CV3538696	single nucleotide variant	NM_032588.4(TRIM63):c.280A>G (p.Arg94Gly)	not provided [RCV004792165]	uncertain significance	1	26066320	26066320	Human		name
12740700	CV359258	single nucleotide variant	NM_032588.4(TRIM63):c.206C>T (p.Ser69Phe)	not specified [RCV000412856]	uncertain significance	1	26066394	26066394	Human		name
598274334	CV3935616	single nucleotide variant	NM_032588.4(TRIM63):c.170C>T (p.Pro57Leu)	Inborn genetic diseases [RCV005303872]	uncertain significance	1	26066430	26066430	Human	1	name
598274336	CV3935618	single nucleotide variant	NM_032588.4(TRIM63):c.187G>A (p.Gly63Ser)	Inborn genetic diseases [RCV005303873]	uncertain significance	1	26066413	26066413	Human	1	name
598274337	CV3935619	single nucleotide variant	NM_032588.4(TRIM63):c.262G>A (p.Gly88Arg)	Inborn genetic diseases [RCV005303874]	uncertain significance	1	26066338	26066338	Human	1	name
616935471	CV4009565	single nucleotide variant	NM_032588.4(TRIM63):c.256C>T (p.Arg86Cys)	not provided [RCV005402734]	uncertain significance	1	26066344	26066344	Human		name
616937431	CV4010927	deletion	NM_032588.4(TRIM63):c.713del (p.Lys238fs)	Cardiovascular phenotype [RCV005404770]	likely pathogenic	1	26058508	26058508	Human		name
616937227	CV4011086	single nucleotide variant	NM_032588.4(TRIM63):c.175T>C (p.Trp59Arg)	Cardiovascular phenotype [RCV005404930]	uncertain significance	1	26066425	26066425	Human		name
42723127	CV966809	single nucleotide variant	NM_032588.4(TRIM63):c.220C>T (p.Arg74Cys)	Hypertrophic cardiomyopathy [RCV001293153]	uncertain significance	1	26066380	26066380	Human	2	name
150460665	CV1231373	single nucleotide variant	NM_032588.4(TRIM63):c.709A>G (p.Lys237Glu)	not provided [RCV001640938]\|not specified [RCV003230685]	benign\|likely benign	1	26058512	26058512	Human		name
150439133	CV1274945	single nucleotide variant	NM_032588.4(TRIM63):c.644C>T (p.Thr215Met)	not provided [RCV001703263]	likely benign	1	26058577	26058577	Human		name
150441178	CV1287317	single nucleotide variant	NM_032588.4(TRIM63):c.609C>A (p.His203Gln)	not provided [RCV001725248]	likely benign	1	26058612	26058612	Human		name
153346001	CV1691531	single nucleotide variant	NM_032588.4(TRIM63):c.427T>C (p.Ser143Pro)	Hypertrophic cardiomyopathy [RCV002273014]	uncertain significance	1	26061240	26061240	Human	2	name
153346006	CV1691533	single nucleotide variant	NM_032588.4(TRIM63):c.335G>A (p.Arg112Gln)	Cardiovascular phenotype [RCV005405879]\|Hypertrophic cardiomyopathy [RCV002273016]\|Inborn genetic diseases [RCV005288744]	uncertain significance	1	26061332	26061332	Human	3	name
9832561	CV178467	single nucleotide variant	NM_032588.4(TRIM63):c.650A>G (p.Tyr217Cys)	Primary familial hypertrophic cardiomyopathy [RCV000157546]	uncertain significance	1	26058571	26058571	Human	1	name
156329301	CV2213811	single nucleotide variant	NM_032588.4(TRIM63):c.587G>A (p.Arg196Gln)	Inborn genetic diseases [RCV002673110]	uncertain significance	1	26060276	26060276	Human	1	name
156044646	CV2237739	single nucleotide variant	NM_032588.4(TRIM63):c.688C>T (p.Arg230Trp)	Inborn genetic diseases [RCV002781654]	uncertain significance	1	26058533	26058533	Human	1	name
11040040	CV224213	single nucleotide variant	NM_032588.4(TRIM63):c.739C>T (p.Gln247Ter)	Cardiovascular phenotype [RCV005404397]\|Hypertrophic cardiomyopathy [RCV000850351]\|Inborn genetic diseases [RCV000623023]\|Primary familial hypertrophic cardiomyopathy [RCV000208240]\|not provided [RCV000873634]	pathogenic\|likely pathogenic\|likely benign\|conflicting interpretations of pathogenicity\|uncertain significance	1	26058482	26058482	Human	5	name
11039930	CV224214	single nucleotide variant	NM_032588.4(TRIM63):c.325T>A (p.Cys109Ser)	not specified [RCV000208021]	likely benign	1	26066275	26066275	Human		name
155999640	CV2287293	single nucleotide variant	NM_032588.4(TRIM63):c.532G>C (p.Val178Leu)	Inborn genetic diseases [RCV002865237]	uncertain significance	1	26060331	26060331	Human	1	name
156338370	CV2343180	single nucleotide variant	NM_032588.4(TRIM63):c.338C>T (p.Pro113Leu)	Inborn genetic diseases [RCV002964997]\|not specified [RCV003479493]	uncertain significance	1	26061329	26061329	Human	1	name
156254980	CV2397599	single nucleotide variant	NM_032588.4(TRIM63):c.568C>A (p.Gln190Lys)	Inborn genetic diseases [RCV002769098]	uncertain significance	1	26060295	26060295	Human	1	name
329366923	CV2441979	single nucleotide variant	NM_032588.4(TRIM63):c.551T>G (p.Val184Gly)	Inborn genetic diseases [RCV003208021]	uncertain significance	1	26060312	26060312	Human	1	name
329370982	CV2461905	single nucleotide variant	NM_032588.4(TRIM63):c.589G>T (p.Val197Leu)	Inborn genetic diseases [RCV003209589]	uncertain significance	1	26060274	26060274	Human	1	name
329951998	CV2668747	single nucleotide variant	NM_032588.4(TRIM63):c.866C>T (p.Ala289Val)	not provided [RCV003481474]\|not specified [RCV003230828]	uncertain significance	1	26057316	26057316	Human		name
401731080	CV2674253	single nucleotide variant	NM_032588.4(TRIM63):c.965T>C (p.Ile322Thr)	Hypertrophic cardiomyopathy [RCV004765383]\|Inborn genetic diseases [RCV003248476]	uncertain significance	1	26057217	26057217	Human	3	name
401720500	CV2701927	single nucleotide variant	NM_032588.4(TRIM63):c.376G>A (p.Glu126Lys)	Inborn genetic diseases [RCV003267235]	uncertain significance	1	26061291	26061291	Human	1	name
401778882	CV2705832	single nucleotide variant	NM_032588.4(TRIM63):c.407C>T (p.Thr136Met)	Inborn genetic diseases [RCV003287287]	uncertain significance	1	26061260	26061260	Human	1	name
401779264	CV2709635	single nucleotide variant	NM_032588.4(TRIM63):c.548G>A (p.Arg183His)	Inborn genetic diseases [RCV003287494]	uncertain significance	1	26060315	26060315	Human	1	name
401867054	CV2748819	single nucleotide variant	NM_032588.4(TRIM63):c.625C>G (p.Leu209Val)	not specified [RCV003331641]	uncertain significance	1	26058596	26058596	Human		name
405797061	CV3337192	single nucleotide variant	NM_032588.4(TRIM63):c.357C>A (p.His119Gln)	Inborn genetic diseases [RCV004476053]	uncertain significance	1	26061310	26061310	Human	1	name
405797069	CV3337194	single nucleotide variant	NM_032588.4(TRIM63):c.680T>C (p.Leu227Ser)	Inborn genetic diseases [RCV004476055]	uncertain significance	1	26058541	26058541	Human	1	name
405797073	CV3337195	single nucleotide variant	NM_032588.4(TRIM63):c.857T>C (p.Ile286Thr)	Inborn genetic diseases [RCV004476056]	uncertain significance	1	26057325	26057325	Human	1	name
407454094	CV3490659	single nucleotide variant	NM_032588.4(TRIM63):c.731C>T (p.Ala244Val)	Cardiovascular phenotype [RCV005406115]\|Inborn genetic diseases [RCV004684788]	uncertain significance	1	26058490	26058490	Human	1	name
407454095	CV3490660	single nucleotide variant	NM_032588.4(TRIM63):c.453C>G (p.His151Gln)	Inborn genetic diseases [RCV004684789]	uncertain significance	1	26061214	26061214	Human	1	name
407454096	CV3490661	single nucleotide variant	NM_032588.4(TRIM63):c.900G>C (p.Gln300His)	Inborn genetic diseases [RCV004684790]	uncertain significance	1	26057282	26057282	Human	1	name
407454097	CV3490662	single nucleotide variant	NM_032588.4(TRIM63):c.404T>C (p.Leu135Pro)	Inborn genetic diseases [RCV004684791]	uncertain significance	1	26061263	26061263	Human	1	name
407454099	CV3490664	single nucleotide variant	NM_032588.4(TRIM63):c.304A>T (p.Ile102Phe)	Inborn genetic diseases [RCV004684793]	uncertain significance	1	26066296	26066296	Human	1	name
407454100	CV3490665	single nucleotide variant	NM_032588.4(TRIM63):c.961G>A (p.Ala321Thr)	Inborn genetic diseases [RCV004684794]	uncertain significance	1	26057221	26057221	Human	1	name
407454101	CV3490666	single nucleotide variant	NM_032588.4(TRIM63):c.962C>T (p.Ala321Val)	Inborn genetic diseases [RCV004684795]	uncertain significance	1	26057220	26057220	Human	1	name
407454102	CV3490667	single nucleotide variant	NM_032588.4(TRIM63):c.785C>T (p.Thr262Ile)	Hypertrophic cardiomyopathy [RCV004765390]\|Inborn genetic diseases [RCV004684796]	uncertain significance	1	26058436	26058436	Human	3	name
408395131	CV3522331	single nucleotide variant	NM_032588.4(TRIM63):c.781G>T (p.Glu261Ter)	Hypertrophic cardiomyopathy [RCV004765408]	uncertain significance	1	26058440	26058440	Human	2	name
597625157	CV3614482	single nucleotide variant	NM_032588.4(TRIM63):c.614T>C (p.Val205Ala)	Inborn genetic diseases [RCV004964394]	uncertain significance	1	26058607	26058607	Human	1	name
597625159	CV3614483	single nucleotide variant	NM_032588.4(TRIM63):c.362T>A (p.Met121Lys)	Inborn genetic diseases [RCV004964395]	uncertain significance	1	26061305	26061305	Human	1	name
597625162	CV3614485	single nucleotide variant	NM_032588.4(TRIM63):c.895G>C (p.Glu299Gln)	Inborn genetic diseases [RCV004964397]	uncertain significance	1	26057287	26057287	Human	1	name
597625164	CV3614486	single nucleotide variant	NM_032588.4(TRIM63):c.686A>C (p.Gln229Pro)	Inborn genetic diseases [RCV004964398]	uncertain significance	1	26058535	26058535	Human	1	name
597849018	CV3762289	single nucleotide variant	NM_032588.4(TRIM63):c.653C>T (p.Ala218Val)	not specified [RCV005087709]	uncertain significance	1	26058568	26058568	Human		name
598123023	CV3884663	single nucleotide variant	NM_032588.4(TRIM63):c.314A>G (p.Tyr105Cys)	not specified [RCV005238269]	uncertain significance	1	26066286	26066286	Human		name
598203195	CV3935620	single nucleotide variant	NM_032588.4(TRIM63):c.547C>T (p.Arg183Cys)	Inborn genetic diseases [RCV005290495]	uncertain significance	1	26060316	26060316	Human	1	name
598203202	CV3935621	single nucleotide variant	NM_032588.4(TRIM63):c.748C>G (p.Gln250Glu)	Inborn genetic diseases [RCV005290496]	uncertain significance	1	26058473	26058473	Human	1	name
616937432	CV4010926	single nucleotide variant	NM_032588.4(TRIM63):c.434G>A (p.Cys145Tyr)	Cardiovascular phenotype [RCV005404769]	uncertain significance	1	26061233	26061233	Human		name
616937631	CV4011246	single nucleotide variant	NM_032588.4(TRIM63):c.726C>G (p.Ile242Met)	not specified [RCV005405092]	likely benign	1	26058495	26058495	Human		name
14396656	CV612529	single nucleotide variant	NM_032588.4(TRIM63):c.395T>C (p.Ile132Thr)	not provided [RCV000761645]	uncertain significance	1	26061272	26061272	Human		name
21071370	CV794654	single nucleotide variant	NM_032588.4(TRIM63):c.805G>A (p.Glu269Lys)	Hypertrophic cardiomyopathy [RCV004765342]\|not provided [RCV000993957]\|not specified [RCV004526059]	likely benign\|conflicting interpretations of pathogenicity\|uncertain significance	1	26058416	26058416	Human	2	name
42723129	CV966808	single nucleotide variant	NM_032588.4(TRIM63):c.390C>G (p.Ile130Met)	Hypertrophic cardiomyopathy [RCV001293154]\|not specified [RCV003331094]	pathogenic\|uncertain significance	1	26061277	26061277	Human	2	name
407454098	CV3490663	single nucleotide variant	NM_032588.4(TRIM63):c.1013A>C (p.Asp338Ala)	Inborn genetic diseases [RCV004684792]	uncertain significance	1	26053931	26053931	Human	1	name
40886805	CV973195	microsatellite	NM_032588.4(TRIM63):c.481_482del (p.Ser161fs)	Hypertrophic cardiomyopathy [RCV001533452]\|Inborn genetic diseases [RCV001266049]\|See cases [RCV002254720]	pathogenic	1	26061185	26061186	Human		name
405867481	CV3396510	indel	NM_032588.4(TRIM63):c.437_442delinsCC (p.Lys146fs)	not provided [RCV004560381]	uncertain significance	1	26061225	26061230	Human		name

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