R3hdm2 Variant Search Result - Rat Genome Database

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55 records found for search term R3hdm2

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
155967150	CV2261129	single nucleotide variant	NM_001394031.1(R3HDM2):c.938+130C>T	not specified [RCV004128027]	uncertain significance	12	57288879	57288879	Human		name
598163437	CV3898445	single nucleotide variant	NM_001394031.1(R3HDM2):c.938+100C>A	not specified [RCV005261548]	uncertain significance	12	57288909	57288909	Human		name
8634814	CV90034	single nucleotide variant	NM_014925.3(R3HDM2):c.1252C>T (p.Pro418Ser)	Malignant melanoma [RCV000070131]	not provided	12	57280408	57280408	Human		name
407499694	CV3465067	single nucleotide variant	NM_001394031.1(R3HDM2):c.272C>T (p.Ala91Val)	not specified [RCV004669374]	uncertain significance	12	57300117	57300117	Human		name
407499699	CV3465069	single nucleotide variant	NM_001394031.1(R3HDM2):c.121A>G (p.Ile41Val)	not specified [RCV004669375]	uncertain significance	12	57310308	57310308	Human		name
407499703	CV3465072	single nucleotide variant	NM_001394031.1(R3HDM2):c.285A>T (p.Leu95Phe)	not specified [RCV004669376]	uncertain significance	12	57300104	57300104	Human		name
597774658	CV3588910	single nucleotide variant	NM_001394031.1(R3HDM2):c.233G>A (p.Arg78His)	not specified [RCV004852039]	uncertain significance	12	57300156	57300156	Human		name
598163408	CV3898440	single nucleotide variant	NM_001394031.1(R3HDM2):c.110G>A (p.Ser37Asn)	not specified [RCV005261543]	uncertain significance	12	57310319	57310319	Human		name
598163449	CV3898447	single nucleotide variant	NM_001394031.1(R3HDM2):c.265C>T (p.Pro89Ser)	not specified [RCV005261550]	uncertain significance	12	57300124	57300124	Human		name
15117808	CV713673	single nucleotide variant	NM_001394031.1(R3HDM2):c.2073C>T (p.Tyr691=)	not provided [RCV000962267]	benign	12	57266789	57266789	Human		name
401724123	CV2725144	single nucleotide variant	NM_001394031.1(R3HDM2):c.943A>T (p.Asn315Tyr)	not specified [RCV004319886]	uncertain significance	12	57284052	57284052	Human		name
405678877	CV3308468	single nucleotide variant	NM_001394031.1(R3HDM2):c.756A>T (p.Gln252His)	not specified [RCV004442924]	uncertain significance	12	57295453	57295453	Human		name
597774654	CV3588909	single nucleotide variant	NM_001394031.1(R3HDM2):c.955C>G (p.Leu319Val)	not specified [RCV004852038]	uncertain significance	12	57284040	57284040	Human		name
598163400	CV3898439	single nucleotide variant	NM_001394031.1(R3HDM2):c.961C>T (p.Arg321Cys)	not specified [RCV005261542]	uncertain significance	12	57284034	57284034	Human		name
598163454	CV3898448	single nucleotide variant	NM_001394031.1(R3HDM2):c.482C>T (p.Thr161Ile)	not specified [RCV005261551]	uncertain significance	12	57298108	57298108	Human		name
156222681	CV2232797	single nucleotide variant	NM_001394031.1(R3HDM2):c.2730G>C (p.Lys910Asn)	not specified [RCV004101429]	uncertain significance	12	57255016	57255016	Human		name
156243264	CV2283254	single nucleotide variant	NM_001394031.1(R3HDM2):c.1362C>A (p.Asn454Lys)	not specified [RCV004145924]	uncertain significance	12	57269977	57269977	Human		name
156293239	CV2306304	single nucleotide variant	NM_001394031.1(R3HDM2):c.2416A>T (p.Thr806Ser)	not specified [RCV004163019]	uncertain significance	12	57258023	57258023	Human		name
155912704	CV2308962	single nucleotide variant	NM_001394031.1(R3HDM2):c.1228C>T (p.Arg410Trp)	not specified [RCV004169245]	uncertain significance	12	57280474	57280474	Human		name
156146139	CV2311067	single nucleotide variant	NM_001394031.1(R3HDM2):c.1738C>A (p.Gln580Lys)	not specified [RCV004164072]	uncertain significance	12	57269059	57269059	Human		name
156276082	CV2318458	single nucleotide variant	NM_001394031.1(R3HDM2):c.2515C>T (p.Leu839Phe)	not specified [RCV004173105]	uncertain significance	12	57256446	57256446	Human		name
156340124	CV2351717	single nucleotide variant	NM_001394031.1(R3HDM2):c.2479C>T (p.Pro827Ser)	not specified [RCV004195422]	uncertain significance	12	57256482	57256482	Human		name
156189814	CV2375643	single nucleotide variant	NM_001394031.1(R3HDM2):c.1643G>A (p.Arg548Gln)	not specified [RCV004226121]	uncertain significance	12	57269394	57269394	Human		name
156073505	CV2376904	single nucleotide variant	NM_001394031.1(R3HDM2):c.2239T>C (p.Tyr747His)	not specified [RCV004229597]	uncertain significance	12	57258952	57258952	Human		name
156172763	CV2380848	single nucleotide variant	NM_001394031.1(R3HDM2):c.2773G>T (p.Gly925Trp)	not specified [RCV004218403]	uncertain significance	12	57254973	57254973	Human		name
156045882	CV2381749	single nucleotide variant	NM_001394031.1(R3HDM2):c.2008C>G (p.Pro670Ala)	not specified [RCV004232203]	uncertain significance	12	57268325	57268325	Human		name
329393215	CV2449568	single nucleotide variant	NM_001394031.1(R3HDM2):c.1726A>T (p.Met576Leu)	not specified [RCV004268497]	uncertain significance	12	57269071	57269071	Human		name
329395504	CV2458425	single nucleotide variant	NM_001394031.1(R3HDM2):c.1066C>A (p.Pro356Thr)	not specified [RCV004266057]	uncertain significance	12	57283929	57283929	Human		name
401782528	CV2719862	single nucleotide variant	NM_001394031.1(R3HDM2):c.1345G>C (p.Ala449Pro)	not specified [RCV004329275]	uncertain significance	12	57269994	57269994	Human		name
401861313	CV2759500	single nucleotide variant	NM_001394031.1(R3HDM2):c.1126A>T (p.Ile376Phe)	not specified [RCV004338490]	uncertain significance	12	57283869	57283869	Human		name
401877615	CV2779884	single nucleotide variant	NM_001394031.1(R3HDM2):c.1781C>T (p.Pro594Leu)	not specified [RCV004353499]	uncertain significance	12	57269016	57269016	Human		name
405678834	CV3308460	single nucleotide variant	NM_001394031.1(R3HDM2):c.1066C>T (p.Pro356Ser)	not specified [RCV004442916]	uncertain significance	12	57283929	57283929	Human		name
405678839	CV3308461	single nucleotide variant	NM_001394031.1(R3HDM2):c.1282C>T (p.Leu428Phe)	not specified [RCV004442917]	uncertain significance	12	57280420	57280420	Human		name
405678845	CV3308462	single nucleotide variant	NM_001394031.1(R3HDM2):c.1301C>T (p.Thr434Met)	not specified [RCV004442918]	uncertain significance	12	57280401	57280401	Human		name
405678851	CV3308463	single nucleotide variant	NM_001394031.1(R3HDM2):c.1780C>G (p.Pro594Ala)	not specified [RCV004442919]	uncertain significance	12	57269017	57269017	Human		name
405678857	CV3308464	single nucleotide variant	NM_001394031.1(R3HDM2):c.2537C>T (p.Thr846Met)	not specified [RCV004442920]	uncertain significance	12	57256424	57256424	Human		name
405678861	CV3308465	single nucleotide variant	NM_001394031.1(R3HDM2):c.2756G>T (p.Gly919Val)	not specified [RCV004442921]	uncertain significance	12	57254990	57254990	Human		name
405679170	CV3308466	single nucleotide variant	NM_001394031.1(R3HDM2):c.2813C>T (p.Ser938Leu)	not specified [RCV004442922]	uncertain significance	12	57254933	57254933	Human		name
405678873	CV3308467	single nucleotide variant	NM_001394031.1(R3HDM2):c.2906G>A (p.Arg969His)	not specified [RCV004442923]	uncertain significance	12	57254840	57254840	Human		name
407483355	CV3465064	single nucleotide variant	NM_001394031.1(R3HDM2):c.2705C>T (p.Thr902Met)	not specified [RCV004664936]	uncertain significance	12	57255041	57255041	Human		name
407483362	CV3465065	single nucleotide variant	NM_001394031.1(R3HDM2):c.1903G>A (p.Val635Met)	not specified [RCV004664937]	uncertain significance	12	57268430	57268430	Human		name
407483369	CV3465066	single nucleotide variant	NM_001394031.1(R3HDM2):c.1406C>T (p.Ala469Val)	not specified [RCV004664938]	uncertain significance	12	57269933	57269933	Human		name
407483380	CV3465070	single nucleotide variant	NM_001394031.1(R3HDM2):c.1417T>C (p.Ser473Pro)	not specified [RCV004664940]	uncertain significance	12	57269922	57269922	Human		name
407483388	CV3465071	single nucleotide variant	NM_001394031.1(R3HDM2):c.1646C>T (p.Pro549Leu)	not specified [RCV004664941]	uncertain significance	12	57269391	57269391	Human		name
597774643	CV3588905	single nucleotide variant	NM_001394031.1(R3HDM2):c.1105A>G (p.Ile369Val)	not specified [RCV004852035]	uncertain significance	12	57283890	57283890	Human		name
597774647	CV3588906	single nucleotide variant	NM_001394031.1(R3HDM2):c.1885G>A (p.Gly629Ser)	not specified [RCV004852036]	uncertain significance	12	57268448	57268448	Human		name
597774650	CV3588907	single nucleotide variant	NM_001394031.1(R3HDM2):c.1981G>T (p.Val661Leu)	not specified [RCV004852037]	uncertain significance	12	57268352	57268352	Human		name
597774662	CV3588911	single nucleotide variant	NM_001394031.1(R3HDM2):c.2552A>G (p.Gln851Arg)	not specified [RCV004852040]	uncertain significance	12	57256070	57256070	Human		name
597774666	CV3588912	single nucleotide variant	NM_001394031.1(R3HDM2):c.2487G>C (p.Gln829His)	not specified [RCV004852041]	uncertain significance	12	57256474	57256474	Human		name
597774670	CV3588913	single nucleotide variant	NM_001394031.1(R3HDM2):c.2809C>A (p.His937Asn)	not specified [RCV004852042]	uncertain significance	12	57254937	57254937	Human		name
598163413	CV3898441	single nucleotide variant	NM_001394031.1(R3HDM2):c.1868C>T (p.Ser623Phe)	not specified [RCV005261544]	uncertain significance	12	57268929	57268929	Human		name
598163419	CV3898442	single nucleotide variant	NM_001394031.1(R3HDM2):c.1010T>C (p.Leu337Pro)	not specified [RCV005261545]	uncertain significance	12	57283985	57283985	Human		name
598163426	CV3898443	single nucleotide variant	NM_001394031.1(R3HDM2):c.2506C>T (p.Pro836Ser)	not specified [RCV005261546]	uncertain significance	12	57256455	57256455	Human		name
598163432	CV3898444	single nucleotide variant	NM_001394031.1(R3HDM2):c.1054C>T (p.Arg352Trp)	not specified [RCV005261547]	uncertain significance	12	57283941	57283941	Human		name
598163460	CV3898449	single nucleotide variant	NM_001394031.1(R3HDM2):c.2419C>G (p.Gln807Glu)	not specified [RCV005261552]	uncertain significance	12	57258020	57258020	Human		name

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