Ranbp3 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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91 records found for search term Ranbp3

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
405693873	CV3315475	single nucleotide variant	NM_007322.3(RANBP3):c.10C>G (p.Leu4Val)	not specified [RCV004445805]	uncertain significance	19	5978073	5978073	Human		name
156033948	CV2211653	single nucleotide variant	NM_007322.3(RANBP3):c.52G>C (p.Val18Leu)	not specified [RCV004084545]	uncertain significance	19	5957944	5957944	Human		name
405693837	CV3315481	single nucleotide variant	NM_007322.3(RANBP3):c.52G>A (p.Val18Met)	not specified [RCV004445811]	uncertain significance	19	5957944	5957944	Human		name
598175587	CV3905346	single nucleotide variant	NM_007322.3(RANBP3):c.46G>A (p.Val16Ile)	not specified [RCV005264024]	uncertain significance	19	5957950	5957950	Human		name
156019298	CV2272586	single nucleotide variant	NM_007322.3(RANBP3):c.227C>T (p.Pro76Leu)	not specified [RCV004133473]	uncertain significance	19	5951448	5951448	Human		name
156073873	CV2281401	single nucleotide variant	NM_007322.3(RANBP3):c.110C>T (p.Ser37Leu)	not specified [RCV004153738]	uncertain significance	19	5951565	5951565	Human		name
156276304	CV2330743	single nucleotide variant	NM_007322.3(RANBP3):c.277G>A (p.Ala93Thr)	not specified [RCV004185807]	uncertain significance	19	5951398	5951398	Human		name
401753419	CV2722463	single nucleotide variant	NM_007322.3(RANBP3):c.100T>A (p.Leu34Met)	not specified [RCV004322853]	uncertain significance	19	5951575	5951575	Human		name
401723955	CV2725103	single nucleotide variant	NM_007322.3(RANBP3):c.127G>A (p.Gly43Arg)	not specified [RCV004319848]	uncertain significance	19	5951548	5951548	Human		name
401857276	CV2758966	single nucleotide variant	NM_007322.3(RANBP3):c.155C>T (p.Thr52Met)	not specified [RCV004342281]	uncertain significance	19	5951520	5951520	Human		name
401878700	CV2767518	single nucleotide variant	NM_007322.3(RANBP3):c.158G>A (p.Gly53Asp)	not specified [RCV004343679]	uncertain significance	19	5951517	5951517	Human		name
401890695	CV2778297	single nucleotide variant	NM_007322.3(RANBP3):c.295G>A (p.Gly99Ser)	not specified [RCV004350351]	uncertain significance	19	5941823	5941823	Human		name
401891744	CV2779390	single nucleotide variant	NM_007322.3(RANBP3):c.217G>C (p.Ala73Pro)	not specified [RCV004351040]	uncertain significance	19	5951458	5951458	Human		name
401872411	CV2779639	single nucleotide variant	NM_007322.3(RANBP3):c.152G>A (p.Gly51Asp)	not specified [RCV004351342]	uncertain significance	19	5951523	5951523	Human		name
405693860	CV3315477	single nucleotide variant	NM_007322.3(RANBP3):c.124C>T (p.Arg42Trp)	not specified [RCV004445807]	uncertain significance	19	5951551	5951551	Human		name
405693843	CV3315480	single nucleotide variant	NM_007322.3(RANBP3):c.266C>T (p.Pro89Leu)	not specified [RCV004445810]	uncertain significance	19	5951409	5951409	Human		name
598203517	CV3905351	single nucleotide variant	NM_007322.3(RANBP3):c.127G>T (p.Gly43Trp)	not specified [RCV005269388]	uncertain significance	19	5951548	5951548	Human		name
598175628	CV3905354	single nucleotide variant	NM_007322.3(RANBP3):c.163C>T (p.Pro55Ser)	not specified [RCV005264030]	uncertain significance	19	5951512	5951512	Human		name
155906309	CV2303290	single nucleotide variant	NM_007322.3(RANBP3):c.938G>A (p.Ser313Asn)	not specified [RCV004159039]	uncertain significance	19	5924885	5924885	Human		name
156292150	CV2321187	single nucleotide variant	NM_007322.3(RANBP3):c.560A>C (p.Gln187Pro)	not specified [RCV004175309]	uncertain significance	19	5932457	5932457	Human		name
155932156	CV2364345	single nucleotide variant	NM_007322.3(RANBP3):c.829G>A (p.Val277Met)	not specified [RCV004223565]	uncertain significance	19	5925722	5925722	Human		name
155958007	CV2396628	single nucleotide variant	NM_007322.3(RANBP3):c.505C>T (p.Arg169Trp)	not specified [RCV004240450]	uncertain significance	19	5932512	5932512	Human		name
156005670	CV2401117	single nucleotide variant	NM_007322.3(RANBP3):c.859C>T (p.His287Tyr)	not specified [RCV004245686]	uncertain significance	19	5925692	5925692	Human		name
401782380	CV2719788	single nucleotide variant	NM_007322.3(RANBP3):c.469G>A (p.Ala157Thr)	not specified [RCV004329217]	uncertain significance	19	5933417	5933417	Human		name
401898899	CV2792099	single nucleotide variant	NM_007322.3(RANBP3):c.428G>A (p.Arg143Gln)	not specified [RCV004361327]	uncertain significance	19	5933458	5933458	Human		name
405693833	CV3315482	single nucleotide variant	NM_007322.3(RANBP3):c.868G>A (p.Ala290Thr)	not specified [RCV004445812]	uncertain significance	19	5925683	5925683	Human		name
405693829	CV3315483	single nucleotide variant	NM_007322.3(RANBP3):c.883G>A (p.Ala295Thr)	not specified [RCV004445813]	uncertain significance	19	5925668	5925668	Human		name
407466366	CV3472294	single nucleotide variant	NM_007322.3(RANBP3):c.625G>A (p.Ala209Thr)	not specified [RCV004660454]	uncertain significance	19	5931472	5931472	Human		name
407500430	CV3472296	single nucleotide variant	NM_007322.3(RANBP3):c.980T>C (p.Met327Thr)	not specified [RCV004669558]	uncertain significance	19	5924843	5924843	Human		name
597753790	CV3582762	single nucleotide variant	NM_007322.3(RANBP3):c.611C>T (p.Thr204Met)	not specified [RCV004847205]	uncertain significance	19	5931486	5931486	Human		name
597704775	CV3582763	single nucleotide variant	NM_007322.3(RANBP3):c.688C>T (p.Leu230Phe)	not specified [RCV004860331]	uncertain significance	19	5931409	5931409	Human		name
597753793	CV3582764	single nucleotide variant	NM_007322.3(RANBP3):c.323C>G (p.Ser108Cys)	not specified [RCV004847206]	uncertain significance	19	5941704	5941704	Human		name
597753797	CV3582766	single nucleotide variant	NM_007322.3(RANBP3):c.880A>T (p.Thr294Ser)	not specified [RCV004847207]	uncertain significance	19	5925671	5925671	Human		name
597704794	CV3582767	single nucleotide variant	NM_007322.3(RANBP3):c.656G>T (p.Ser219Ile)	not specified [RCV004860333]	uncertain significance	19	5931441	5931441	Human		name
597704804	CV3582768	single nucleotide variant	NM_007322.3(RANBP3):c.914C>T (p.Ser305Phe)	not specified [RCV004860334]	uncertain significance	19	5925637	5925637	Human		name
598203511	CV3905348	single nucleotide variant	NM_007322.3(RANBP3):c.754A>G (p.Lys252Glu)	not specified [RCV005269387]	uncertain significance	19	5928027	5928027	Human		name
598175599	CV3905349	single nucleotide variant	NM_007322.3(RANBP3):c.593G>T (p.Ser198Ile)	not specified [RCV005264026]	uncertain significance	19	5931504	5931504	Human		name
598175606	CV3905350	single nucleotide variant	NM_007322.3(RANBP3):c.845T>C (p.Met282Thr)	not specified [RCV005264027]	uncertain significance	19	5925706	5925706	Human		name
598175613	CV3905352	single nucleotide variant	NM_007322.3(RANBP3):c.386A>G (p.Gln129Arg)	not specified [RCV005264028]	uncertain significance	19	5941641	5941641	Human		name
598175622	CV3905353	single nucleotide variant	NM_007322.3(RANBP3):c.709A>G (p.Lys237Glu)	not specified [RCV005264029]	uncertain significance	19	5928072	5928072	Human		name
15184715	CV705305	single nucleotide variant	NM_007322.3(RANBP3):c.941C>T (p.Ala314Val)	not provided [RCV000952776]	benign	19	5924882	5924882	Human		name
155998229	CV2287123	single nucleotide variant	NM_007322.3(RANBP3):c.1325G>A (p.Arg442Gln)	not specified [RCV004144991]	uncertain significance	19	5921206	5921206	Human		name
155918305	CV2332977	single nucleotide variant	NM_007322.3(RANBP3):c.1672G>A (p.Glu558Lys)	not specified [RCV004194278]	uncertain significance	19	5917642	5917642	Human		name
401721215	CV2673639	single nucleotide variant	NM_007322.3(RANBP3):c.1343A>G (p.Gln448Arg)	not specified [RCV004282373]	uncertain significance	19	5918626	5918626	Human		name
401754287	CV2685222	single nucleotide variant	NM_007322.3(RANBP3):c.1396G>A (p.Asp466Asn)	not specified [RCV004289775]	uncertain significance	19	5918573	5918573	Human		name
405693865	CV3315476	single nucleotide variant	NM_007322.3(RANBP3):c.1144C>T (p.Arg382Trp)	not specified [RCV004445806]	uncertain significance	19	5923259	5923259	Human		name
405693855	CV3315478	single nucleotide variant	NM_007322.3(RANBP3):c.1304A>G (p.Asp435Gly)	not specified [RCV004445808]	uncertain significance	19	5921227	5921227	Human		name
405693849	CV3315479	single nucleotide variant	NM_007322.3(RANBP3):c.1693G>A (p.Gly565Arg)	not specified [RCV004445809]	uncertain significance	19	5917621	5917621	Human		name
407466371	CV3472295	single nucleotide variant	NM_007322.3(RANBP3):c.1018G>A (p.Val340Ile)	not specified [RCV004660455]	uncertain significance	19	5923893	5923893	Human		name
407466376	CV3472297	single nucleotide variant	NM_007322.3(RANBP3):c.1042A>T (p.Asn348Tyr)	not specified [RCV004660456]	uncertain significance	19	5923869	5923869	Human		name
597753786	CV3582761	single nucleotide variant	NM_007322.3(RANBP3):c.1073C>T (p.Ser358Leu)	not specified [RCV004847204]	uncertain significance	19	5923838	5923838	Human		name
597704786	CV3582765	single nucleotide variant	NM_007322.3(RANBP3):c.1608G>C (p.Glu536Asp)	not specified [RCV004860332]	uncertain significance	19	5917846	5917846	Human		name
597704812	CV3582769	single nucleotide variant	NM_007322.3(RANBP3):c.1151G>A (p.Cys384Tyr)	not specified [RCV004860335]	uncertain significance	19	5923252	5923252	Human		name
405081823	CV2941844	single nucleotide variant	NM_145000.5(RANBP3L):c.*1004A>C	not provided [RCV003664635]	benign	5	36248650	36248650	Human		name
8580942	CV115378	single nucleotide variant	NM_001161429.1(RANBP3L):c.659+24C>G	Lung cancer [RCV000095901]	uncertain significance	5	36261915	36261915	Human		name
156361038	CV2269157	single nucleotide variant	NM_145000.5(RANBP3L):c.34C>G (p.Leu12Val)	not specified [RCV004130326]	uncertain significance	5	36301383	36301383	Human		name
156286738	CV2327263	single nucleotide variant	NM_145000.5(RANBP3L):c.40G>A (p.Gly14Ser)	not specified [RCV004174712]	uncertain significance	5	36301377	36301377	Human		name
155919604	CV2333226	single nucleotide variant	NM_145000.5(RANBP3L):c.52A>G (p.Thr18Ala)	not specified [RCV004196559]	uncertain significance	5	36301365	36301365	Human		name
156113229	CV2397023	single nucleotide variant	NM_145000.5(RANBP3L):c.79C>T (p.Arg27Trp)	not specified [RCV004236540]	uncertain significance	5	36301338	36301338	Human		name
401754522	CV2717419	single nucleotide variant	NM_145000.5(RANBP3L):c.44G>A (p.Ser15Asn)	not specified [RCV004330247]	uncertain significance	5	36301373	36301373	Human		name
155928922	CV2281323	single nucleotide variant	NM_145000.5(RANBP3L):c.101T>C (p.Val34Ala)	not specified [RCV004147553]	uncertain significance	5	36271302	36271302	Human		name
401757268	CV2692905	single nucleotide variant	NM_145000.5(RANBP3L):c.205C>T (p.Pro69Ser)	not specified [RCV004306433]	likely benign	5	36269453	36269453	Human		name
401877470	CV2761143	single nucleotide variant	NM_145000.5(RANBP3L):c.115A>G (p.Ile39Val)	not specified [RCV004341031]	uncertain significance	5	36271288	36271288	Human		name
405693797	CV3315489	single nucleotide variant	NM_145000.5(RANBP3L):c.221G>A (p.Arg74Gln)	not specified [RCV004445819]	uncertain significance	5	36269437	36269437	Human		name
407500435	CV3472298	single nucleotide variant	NM_145000.5(RANBP3L):c.220C>T (p.Arg74Trp)	not specified [RCV004669559]	uncertain significance	5	36269438	36269438	Human		name
155990343	CV2255494	single nucleotide variant	NM_145000.5(RANBP3L):c.619A>G (p.Ser207Gly)	not specified [RCV004119931]	uncertain significance	5	36260830	36260830	Human		name
156256868	CV2264834	single nucleotide variant	NM_145000.5(RANBP3L):c.538G>A (p.Val180Ile)	not specified [RCV004134592]	uncertain significance	5	36261985	36261985	Human		name
155992178	CV2281177	single nucleotide variant	NM_145000.5(RANBP3L):c.968C>T (p.Thr323Met)	not specified [RCV004147431]	uncertain significance	5	36255526	36255526	Human		name
401746439	CV2695569	single nucleotide variant	NM_145000.5(RANBP3L):c.707A>T (p.Asp236Val)	not specified [RCV004305739]	uncertain significance	5	36257519	36257519	Human		name
405693822	CV3315484	single nucleotide variant	NM_145000.5(RANBP3L):c.995C>T (p.Thr332Ile)	not specified [RCV004445814]	uncertain significance	5	36255499	36255499	Human		name
405693790	CV3315490	single nucleotide variant	NM_145000.5(RANBP3L):c.485C>T (p.Ser162Phe)	not specified [RCV004445820]	uncertain significance	5	36262038	36262038	Human		name
405693597	CV3315491	single nucleotide variant	NM_145000.5(RANBP3L):c.557A>G (p.Gln186Arg)	not specified [RCV004445821]	uncertain significance	5	36261966	36261966	Human		name
405693526	CV3315492	single nucleotide variant	NM_145000.5(RANBP3L):c.601G>A (p.Asp201Asn)	not specified [RCV004445822]	uncertain significance	5	36260848	36260848	Human		name
405693532	CV3315493	single nucleotide variant	NM_145000.5(RANBP3L):c.845G>A (p.Cys282Tyr)	not specified [RCV004445823]	uncertain significance	5	36256999	36256999	Human		name
405693538	CV3315494	single nucleotide variant	NM_145000.5(RANBP3L):c.860T>C (p.Ile287Thr)	not specified [RCV004445824]	uncertain significance	5	36256984	36256984	Human		name
597753800	CV3582772	single nucleotide variant	NM_145000.5(RANBP3L):c.595A>G (p.Asn199Asp)	not specified [RCV004847208]	uncertain significance	5	36260854	36260854	Human		name
597753804	CV3582773	single nucleotide variant	NM_145000.5(RANBP3L):c.487G>A (p.Glu163Lys)	not specified [RCV004847209]	uncertain significance	5	36262036	36262036	Human		name
597704843	CV3582774	single nucleotide variant	NM_145000.5(RANBP3L):c.476A>G (p.Asn159Ser)	not specified [RCV004860338]	uncertain significance	5	36264963	36264963	Human		name
597704854	CV3582775	single nucleotide variant	NM_145000.5(RANBP3L):c.463G>A (p.Glu155Lys)	not specified [RCV004860339]	uncertain significance	5	36264976	36264976	Human		name
598175639	CV3905356	single nucleotide variant	NM_145000.5(RANBP3L):c.668T>C (p.Leu223Ser)	not specified [RCV005264032]	uncertain significance	5	36260781	36260781	Human		name
156073010	CV2233408	single nucleotide variant	NM_145000.5(RANBP3L):c.1141T>C (p.Tyr381His)	not specified [RCV004105765]	uncertain significance	5	36253673	36253673	Human		name
156037463	CV2243800	single nucleotide variant	NM_145000.5(RANBP3L):c.1133T>C (p.Leu378Ser)	not specified [RCV004114488]	uncertain significance	5	36253681	36253681	Human		name
156017792	CV2262962	single nucleotide variant	NM_145000.5(RANBP3L):c.1003G>A (p.Gly335Arg)	not specified [RCV004125096]	uncertain significance	5	36255491	36255491	Human		name
401894061	CV2770251	single nucleotide variant	NM_145000.5(RANBP3L):c.1382C>T (p.Ser461Leu)	not specified [RCV004356135]	uncertain significance	5	36249670	36249670	Human		name
401886200	CV2770983	single nucleotide variant	NM_145000.5(RANBP3L):c.1034A>G (p.Asn345Ser)	not specified [RCV004344002]	uncertain significance	5	36253780	36253780	Human		name
405693818	CV3315485	single nucleotide variant	NM_145000.5(RANBP3L):c.1097C>A (p.Ala366Glu)	not specified [RCV004445815]	uncertain significance	5	36253717	36253717	Human		name
405693810	CV3315487	single nucleotide variant	NM_145000.5(RANBP3L):c.1256A>G (p.Asn419Ser)	not specified [RCV004445817]	uncertain significance	5	36251411	36251411	Human		name
405693802	CV3315488	single nucleotide variant	NM_145000.5(RANBP3L):c.1314G>C (p.Glu438Asp)	not specified [RCV004445818]	uncertain significance	5	36251353	36251353	Human		name
597704831	CV3582771	single nucleotide variant	NM_145000.5(RANBP3L):c.1237A>G (p.Asn413Asp)	not specified [RCV004860337]	likely benign	5	36251430	36251430	Human		name
598175633	CV3905355	single nucleotide variant	NM_145000.5(RANBP3L):c.1213C>T (p.Arg405Cys)	not specified [RCV005264031]	uncertain significance	5	36251454	36251454	Human		name
8631617	CV86821	single nucleotide variant	NM_001161429.1(RANBP3L):c.475C>T (p.Arg159Ter)	Malignant melanoma [RCV000066912]	not provided	5	36265039	36265039	Human		name

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