Rnf10 Variant Search Result - Rat Genome Database

Advanced Search (OLGA)

Variants search result for All species
(View Results for all Objects and Ontologies)

135 records found for search term Rnf10

Refine Term:

Sort By:

Export

CSV

TAB

RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
156055581	CV2320550	single nucleotide variant	NM_014868.5(RNF10):c.57C>A (p.Ser19Arg)	not specified [RCV004172174]	uncertain significance	12	120534868	120534868	Human		name
401748485	CV2696476	single nucleotide variant	NM_014868.5(RNF10):c.65A>G (p.Asn22Ser)	not specified [RCV004312550]	likely benign	12	120534876	120534876	Human		name
401877619	CV2779885	single nucleotide variant	NM_014868.5(RNF10):c.82T>A (p.Ser28Thr)	not specified [RCV004353500]	uncertain significance	12	120534893	120534893	Human		name
405754239	CV3316369	single nucleotide variant	NM_014868.5(RNF10):c.31A>G (p.Thr11Ala)	not specified [RCV004454254]	uncertain significance	12	120534842	120534842	Human		name
405754255	CV3316371	single nucleotide variant	NM_014868.5(RNF10):c.53A>G (p.Asn18Ser)	not specified [RCV004454256]	uncertain significance	12	120534864	120534864	Human		name
407485700	CV3483453	single nucleotide variant	NM_014868.5(RNF10):c.59G>C (p.Gly20Ala)	not specified [RCV004663366]	uncertain significance	12	120534870	120534870	Human		name
15154675	CV738492	single nucleotide variant	NM_014868.5(RNF10):c.333T>C (p.Phe111=)	not provided [RCV000902000]	likely benign	12	120546580	120546580	Human		name
156130296	CV2209991	single nucleotide variant	NM_014868.5(RNF10):c.142T>G (p.Ser48Ala)	not specified [RCV004076429]	uncertain significance	12	120534953	120534953	Human		name
155917198	CV2236493	single nucleotide variant	NM_014868.5(RNF10):c.185G>A (p.Arg62His)	not specified [RCV004110495]	uncertain significance	12	120546432	120546432	Human		name
156296607	CV2319104	single nucleotide variant	NM_014868.5(RNF10):c.247C>T (p.Arg83Cys)	not specified [RCV004178181]	uncertain significance	12	120546494	120546494	Human		name
401721338	CV2709921	single nucleotide variant	NM_014868.5(RNF10):c.194G>A (p.Arg65His)	not specified [RCV004314996]	uncertain significance	12	120546441	120546441	Human		name
405754221	CV3316366	single nucleotide variant	NM_014868.5(RNF10):c.221A>G (p.Asn74Ser)	not specified [RCV004454251]	uncertain significance	12	120546468	120546468	Human		name
405754226	CV3316367	single nucleotide variant	NM_014868.5(RNF10):c.287C>T (p.Pro96Leu)	not specified [RCV004454252]	uncertain significance	12	120546534	120546534	Human		name
405754232	CV3316368	single nucleotide variant	NM_014868.5(RNF10):c.292C>G (p.Gln98Glu)	not specified [RCV004454253]	uncertain significance	12	120546539	120546539	Human		name
407475996	CV3483452	single nucleotide variant	NM_014868.5(RNF10):c.184C>T (p.Arg62Cys)	not specified [RCV004663365]	uncertain significance	12	120546431	120546431	Human		name
597754420	CV3593914	single nucleotide variant	NM_014868.5(RNF10):c.244C>T (p.Arg82Cys)	not specified [RCV004847358]	uncertain significance	12	120546491	120546491	Human		name
597686118	CV3593922	single nucleotide variant	NM_014868.5(RNF10):c.194G>T (p.Arg65Leu)	not specified [RCV004858349]	uncertain significance	12	120546441	120546441	Human		name
597754436	CV3593923	single nucleotide variant	NM_014868.5(RNF10):c.217A>C (p.Lys73Gln)	not specified [RCV004847362]	uncertain significance	12	120546464	120546464	Human		name
598230529	CV3899369	single nucleotide variant	NM_014868.5(RNF10):c.142T>C (p.Ser48Pro)	not specified [RCV005274361]	uncertain significance	12	120534953	120534953	Human		name
598230541	CV3899371	single nucleotide variant	NM_014868.5(RNF10):c.202G>C (p.Glu68Gln)	not specified [RCV005274363]	uncertain significance	12	120546449	120546449	Human		name
598230562	CV3899375	single nucleotide variant	NM_014868.5(RNF10):c.167A>G (p.Asn56Ser)	not specified [RCV005274367]	uncertain significance	12	120546414	120546414	Human		name
156122993	CV2233907	single nucleotide variant	NM_014868.5(RNF10):c.304G>A (p.Gly102Ser)	not specified [RCV004104260]	uncertain significance	12	120546551	120546551	Human		name
155987575	CV2275639	single nucleotide variant	NM_014868.5(RNF10):c.904G>A (p.Gly302Arg)	not specified [RCV004137265]	uncertain significance	12	120557619	120557619	Human		name
156341883	CV2368475	single nucleotide variant	NM_014868.5(RNF10):c.850C>T (p.His284Tyr)	not specified [RCV004221277]	uncertain significance	12	120557565	120557565	Human		name
329358707	CV2450671	single nucleotide variant	NM_014868.5(RNF10):c.878C>T (p.Thr293Met)	not specified [RCV004267625]	uncertain significance	12	120557593	120557593	Human		name
401732803	CV2691114	single nucleotide variant	NM_014868.5(RNF10):c.679A>G (p.Ile227Val)	not specified [RCV004301109]	uncertain significance	12	120557315	120557315	Human		name
401861688	CV2756415	single nucleotide variant	NM_014868.5(RNF10):c.413T>A (p.Ile138Asn)	not specified [RCV004342955]	uncertain significance	12	120552557	120552557	Human		name
401893112	CV2758498	single nucleotide variant	NM_014868.5(RNF10):c.461C>T (p.Thr154Met)	not specified [RCV004335142]	uncertain significance	12	120552605	120552605	Human		name
405754248	CV3316370	single nucleotide variant	NM_014868.5(RNF10):c.388G>A (p.Ala130Thr)	not specified [RCV004454255]	uncertain significance	12	120552532	120552532	Human		name
405754262	CV3316372	single nucleotide variant	NM_014868.5(RNF10):c.560A>G (p.Gln187Arg)	not specified [RCV004454257]	uncertain significance	12	120554723	120554723	Human		name
405754268	CV3316373	single nucleotide variant	NM_014868.5(RNF10):c.692C>T (p.Pro231Leu)	not specified [RCV004454258]	uncertain significance	12	120557328	120557328	Human		name
405754273	CV3316374	single nucleotide variant	NM_014868.5(RNF10):c.884A>G (p.Gln295Arg)	not specified [RCV004454259]	uncertain significance	12	120557599	120557599	Human		name
597686079	CV3593916	single nucleotide variant	NM_014868.5(RNF10):c.531C>G (p.Asn177Lys)	not specified [RCV004858345]	uncertain significance	12	120552675	120552675	Human		name
597754427	CV3593918	single nucleotide variant	NM_014868.5(RNF10):c.593C>T (p.Ala198Val)	not specified [RCV004847360]	likely benign	12	120554756	120554756	Human		name
598230522	CV3899368	single nucleotide variant	NM_014868.5(RNF10):c.689A>G (p.Tyr230Cys)	not specified [RCV005274360]	uncertain significance	12	120557325	120557325	Human		name
598230545	CV3899372	single nucleotide variant	NM_014868.5(RNF10):c.535G>C (p.Glu179Gln)	not specified [RCV005274364]	uncertain significance	12	120552679	120552679	Human		name
156145504	CV2218800	single nucleotide variant	NM_014868.5(RNF10):c.1924T>C (p.Phe642Leu)	not specified [RCV004085046]	uncertain significance	12	120566863	120566863	Human		name
155972727	CV2238838	single nucleotide variant	NM_014868.5(RNF10):c.1421A>G (p.Asp474Gly)	not specified [RCV004109753]	uncertain significance	12	120563513	120563513	Human		name
156073483	CV2240712	single nucleotide variant	NM_014868.5(RNF10):c.1232A>G (p.Glu411Gly)	not specified [RCV004119333]	uncertain significance	12	120563048	120563048	Human		name
156359456	CV2257702	single nucleotide variant	NM_014868.5(RNF10):c.2378A>G (p.Lys793Arg)	not specified [RCV004127783]	uncertain significance	12	120576608	120576608	Human		name
155951695	CV2309747	single nucleotide variant	NM_014868.5(RNF10):c.2011C>T (p.Pro671Ser)	not specified [RCV004160873]	uncertain significance	12	120566950	120566950	Human		name
156058705	CV2343642	single nucleotide variant	NM_014868.5(RNF10):c.2227C>T (p.Pro743Ser)	not specified [RCV004190670]	uncertain significance	12	120575818	120575818	Human		name
155903757	CV2353661	single nucleotide variant	NM_014868.5(RNF10):c.1973C>T (p.Pro658Leu)	not specified [RCV004201679]	uncertain significance	12	120566912	120566912	Human		name
156017399	CV2370101	single nucleotide variant	NM_014868.5(RNF10):c.1384G>A (p.Gly462Arg)	not specified [RCV004210992]	uncertain significance	12	120563476	120563476	Human		name
156064096	CV2389445	single nucleotide variant	NM_014868.5(RNF10):c.1036C>G (p.Leu346Val)	not specified [RCV004238171]	uncertain significance	12	120560794	120560794	Human		name
329395675	CV2462926	single nucleotide variant	NM_014868.5(RNF10):c.1442C>G (p.Thr481Ser)	not specified [RCV004272766]	uncertain significance	12	120563534	120563534	Human		name
401767412	CV2681655	single nucleotide variant	NM_014868.5(RNF10):c.1942T>C (p.Tyr648His)	not specified [RCV004294210]	uncertain significance	12	120566881	120566881	Human		name
401884781	CV2766238	single nucleotide variant	NM_014868.5(RNF10):c.2239G>A (p.Asp747Asn)	not specified [RCV004340674]	uncertain significance	12	120575830	120575830	Human		name
401864499	CV2777863	single nucleotide variant	NM_014868.5(RNF10):c.2210G>A (p.Ser737Asn)	not specified [RCV004347837]	uncertain significance	12	120575801	120575801	Human		name
401884885	CV2786608	single nucleotide variant	NM_014868.5(RNF10):c.1138G>A (p.Glu380Lys)	not specified [RCV004363747]	uncertain significance	12	120562954	120562954	Human		name
405754159	CV3316357	single nucleotide variant	NM_014868.5(RNF10):c.1018G>T (p.Val340Leu)	not specified [RCV004454242]	uncertain significance	12	120560776	120560776	Human		name
405754166	CV3316358	single nucleotide variant	NM_014868.5(RNF10):c.1148C>G (p.Ser383Trp)	not specified [RCV004454243]	uncertain significance	12	120562964	120562964	Human		name
405754173	CV3316359	single nucleotide variant	NM_014868.5(RNF10):c.1370A>T (p.Glu457Val)	not specified [RCV004454244]	uncertain significance	12	120563462	120563462	Human		name
405754179	CV3316360	single nucleotide variant	NM_014868.5(RNF10):c.1501A>C (p.Ser501Arg)	not specified [RCV004454245]	uncertain significance	12	120563593	120563593	Human		name
405754186	CV3316361	single nucleotide variant	NM_014868.5(RNF10):c.1523T>A (p.Phe508Tyr)	not specified [RCV004454246]	uncertain significance	12	120563615	120563615	Human		name
405754194	CV3316362	single nucleotide variant	NM_014868.5(RNF10):c.1631C>T (p.Thr544Ile)	not specified [RCV004454247]	uncertain significance	12	120563909	120563909	Human		name
405754199	CV3316363	single nucleotide variant	NM_014868.5(RNF10):c.1838G>A (p.Arg613His)	not specified [RCV004454248]	uncertain significance	12	120565482	120565482	Human		name
405754206	CV3316364	single nucleotide variant	NM_014868.5(RNF10):c.2000T>A (p.Leu667His)	not specified [RCV004454249]	uncertain significance	12	120566939	120566939	Human		name
405754212	CV3316365	single nucleotide variant	NM_014868.5(RNF10):c.2047C>A (p.Leu683Met)	not specified [RCV004454250]	uncertain significance	12	120571196	120571196	Human		name
407475981	CV3483449	single nucleotide variant	NM_014868.5(RNF10):c.1937A>G (p.Asn646Ser)	not specified [RCV004663362]	uncertain significance	12	120566876	120566876	Human		name
407475987	CV3483450	single nucleotide variant	NM_014868.5(RNF10):c.2171A>G (p.Asp724Gly)	not specified [RCV004663363]	uncertain significance	12	120575659	120575659	Human		name
597686071	CV3593913	single nucleotide variant	NM_014868.5(RNF10):c.2087C>T (p.Pro696Leu)	not specified [RCV004858344]	uncertain significance	12	120571236	120571236	Human		name
597754423	CV3593915	single nucleotide variant	NM_014868.5(RNF10):c.2127C>G (p.Phe709Leu)	not specified [RCV004847359]	uncertain significance	12	120571276	120571276	Human		name
597686090	CV3593917	single nucleotide variant	NM_014868.5(RNF10):c.1226C>T (p.Ala409Val)	not specified [RCV004858346]	uncertain significance	12	120563042	120563042	Human		name
597686100	CV3593919	single nucleotide variant	NM_014868.5(RNF10):c.1477A>G (p.Thr493Ala)	not specified [RCV004858347]	uncertain significance	12	120563569	120563569	Human		name
597686109	CV3593920	single nucleotide variant	NM_014868.5(RNF10):c.1624T>G (p.Ser542Ala)	not specified [RCV004858348]	uncertain significance	12	120563902	120563902	Human		name
598230517	CV3899367	single nucleotide variant	NM_014868.5(RNF10):c.1427A>G (p.Asn476Ser)	not specified [RCV005274359]	likely benign	12	120563519	120563519	Human		name
598230534	CV3899370	single nucleotide variant	NM_014868.5(RNF10):c.2023A>C (p.Ser675Arg)	not specified [RCV005274362]	uncertain significance	12	120566962	120566962	Human		name
598230552	CV3899373	single nucleotide variant	NM_014868.5(RNF10):c.2167G>A (p.Ala723Thr)	not specified [RCV005274365]	uncertain significance	12	120575655	120575655	Human		name
598230569	CV3899376	single nucleotide variant	NM_014868.5(RNF10):c.1993G>T (p.Gly665Trp)	not specified [RCV005274368]	uncertain significance	12	120566932	120566932	Human		name
598230576	CV3899377	single nucleotide variant	NM_014868.5(RNF10):c.2311G>C (p.Ala771Pro)	not specified [RCV005274369]	uncertain significance	12	120575902	120575902	Human		name
598230582	CV3899378	single nucleotide variant	NM_014868.5(RNF10):c.2074A>G (p.Ser692Gly)	not specified [RCV005274370]	uncertain significance	12	120571223	120571223	Human		name
598230589	CV3899379	single nucleotide variant	NM_014868.5(RNF10):c.1574G>A (p.Arg525His)	not specified [RCV005274371]	uncertain significance	12	120563852	120563852	Human		name
15140588	CV713383	single nucleotide variant	NM_014868.5(RNF10):c.1159G>A (p.Gly387Arg)	not provided [RCV000966163]	benign	12	120562975	120562975	Human		name
8577623	CV111999	single nucleotide variant	NM_001198954.1(RNF103-CHMP3):c.-102-4642G>T	Lung cancer [RCV000092522]	uncertain significance	2	86692967	86692967	Human		name
156303686	CV2258897	single nucleotide variant	NM_005667.4(RNF103):c.94A>G (p.Ile32Val)	not specified [RCV004118102]	uncertain significance	2	86622793	86622793	Human		name
401891928	CV2775823	single nucleotide variant	NM_005667.4(RNF103):c.94A>C (p.Ile32Leu)	not specified [RCV004344862]	uncertain significance	2	86622793	86622793	Human		name
597686173	CV3593935	single nucleotide variant	NM_005667.4(RNF103):c.76G>A (p.Val26Met)	not specified [RCV004858355]	uncertain significance	2	86622811	86622811	Human		name
156329531	CV2213852	single nucleotide variant	NM_005667.4(RNF103):c.133T>C (p.Phe45Leu)	not specified [RCV004089905]	uncertain significance	2	86622754	86622754	Human		name
155990686	CV2276495	single nucleotide variant	NM_005667.4(RNF103):c.138G>C (p.Lys46Asn)	not specified [RCV004144211]	uncertain significance	2	86622749	86622749	Human		name
156094520	CV2377745	single nucleotide variant	NM_005667.4(RNF103):c.280G>A (p.Glu94Lys)	not specified [RCV004230331]	uncertain significance	2	86620416	86620416	Human		name
401728629	CV2729704	single nucleotide variant	NM_005667.4(RNF103):c.198G>C (p.Lys66Asn)	not specified [RCV004331959]	uncertain significance	2	86622689	86622689	Human		name
405754280	CV3316375	single nucleotide variant	NM_005667.4(RNF103):c.108G>T (p.Gln36His)	not specified [RCV004454260]	uncertain significance	2	86622779	86622779	Human		name
156284622	CV2231270	single nucleotide variant	NM_005667.4(RNF103):c.521T>C (p.Ile174Thr)	not specified [RCV004094462]	uncertain significance	2	86605380	86605380	Human		name
156238963	CV2235865	single nucleotide variant	NM_005667.4(RNF103):c.761G>C (p.Ser254Thr)	not specified [RCV004111976]	uncertain significance	2	86605140	86605140	Human		name
156351829	CV2323843	single nucleotide variant	NM_005667.4(RNF103):c.548C>T (p.Ser183Leu)	not specified [RCV004176376]	uncertain significance	2	86605353	86605353	Human		name
156170784	CV2354905	single nucleotide variant	NM_005667.4(RNF103):c.692A>G (p.Asp231Gly)	not specified [RCV004191401]	uncertain significance	2	86605209	86605209	Human		name
156197688	CV2357704	single nucleotide variant	NM_005667.4(RNF103):c.684T>A (p.Asn228Lys)	not specified [RCV004205004]	uncertain significance	2	86605217	86605217	Human		name
155967149	CV2391312	single nucleotide variant	NM_005667.4(RNF103):c.397G>C (p.Gly133Arg)	not specified [RCV004237676]	uncertain significance	2	86612244	86612244	Human		name
401768552	CV2675431	single nucleotide variant	NM_005667.4(RNF103):c.584G>A (p.Arg195His)	not specified [RCV004292231]	uncertain significance	2	86605317	86605317	Human		name
401751399	CV2716376	single nucleotide variant	NM_005667.4(RNF103):c.416A>G (p.Lys139Arg)	not specified [RCV004325369]	uncertain significance	2	86612225	86612225	Human		name
401882220	CV2774744	single nucleotide variant	NM_005667.4(RNF103):c.810T>A (p.Asn270Lys)	not specified [RCV004343844]	uncertain significance	2	86605091	86605091	Human		name
401883695	CV2785738	single nucleotide variant	NM_005667.4(RNF103):c.578G>A (p.Ser193Asn)	not specified [RCV004364993]	uncertain significance	2	86605323	86605323	Human		name
405754307	CV3316379	single nucleotide variant	NM_005667.4(RNF103):c.464A>G (p.Asn155Ser)	not specified [RCV004454264]	uncertain significance	2	86612177	86612177	Human		name
405754312	CV3316380	single nucleotide variant	NM_005667.4(RNF103):c.712T>C (p.Tyr238His)	not specified [RCV004454265]	uncertain significance	2	86605189	86605189	Human		name
405754321	CV3316381	single nucleotide variant	NM_005667.4(RNF103):c.819C>G (p.Asn273Lys)	not specified [RCV004454266]	uncertain significance	2	86605082	86605082	Human		name
407487131	CV3479512	single nucleotide variant	NM_005667.4(RNF103):c.821A>G (p.Lys274Arg)	not specified [RCV004672082]	uncertain significance	2	86605080	86605080	Human		name
407487136	CV3479513	single nucleotide variant	NM_005667.4(RNF103):c.981T>G (p.Phe327Leu)	not specified [RCV004672083]	uncertain significance	2	86604920	86604920	Human		name
407485717	CV3479514	single nucleotide variant	NM_005667.4(RNF103):c.515C>T (p.Thr172Ile)	not specified [RCV004663368]	uncertain significance	2	86605386	86605386	Human		name
597686137	CV3593928	single nucleotide variant	NM_005667.4(RNF103):c.409T>G (p.Trp137Gly)	not specified [RCV004858351]	uncertain significance	2	86612232	86612232	Human		name
597754457	CV3593931	single nucleotide variant	NM_005667.4(RNF103):c.715C>G (p.Leu239Val)	not specified [RCV004847367]	uncertain significance	2	86605186	86605186	Human		name
598230596	CV3899380	single nucleotide variant	NM_005667.4(RNF103):c.844A>C (p.Ile282Leu)	not specified [RCV005274372]	uncertain significance	2	86605057	86605057	Human		name
598230617	CV3899383	single nucleotide variant	NM_005667.4(RNF103):c.786G>C (p.Glu262Asp)	not specified [RCV005274375]	uncertain significance	2	86605115	86605115	Human		name
156132473	CV2195883	single nucleotide variant	NM_005667.4(RNF103):c.1319G>A (p.Arg440His)	not specified [RCV004072147]	uncertain significance	2	86604582	86604582	Human		name
155975685	CV2235919	single nucleotide variant	NM_005667.4(RNF103):c.1815A>C (p.Glu605Asp)	not specified [RCV004113807]	uncertain significance	2	86604086	86604086	Human		name
156269025	CV2240047	single nucleotide variant	NM_005667.4(RNF103):c.1589A>C (p.Glu530Ala)	not specified [RCV004110826]	uncertain significance	2	86604312	86604312	Human		name
156090062	CV2256475	single nucleotide variant	NM_005667.4(RNF103):c.1547G>A (p.Arg516Gln)	not specified [RCV004118684]	uncertain significance	2	86604354	86604354	Human		name
156061930	CV2263173	single nucleotide variant	NM_005667.4(RNF103):c.1480G>A (p.Ala494Thr)	not specified [RCV004131406]	uncertain significance	2	86604421	86604421	Human		name
156293342	CV2321301	single nucleotide variant	NM_005667.4(RNF103):c.1306A>G (p.Lys436Glu)	not specified [RCV004177314]	uncertain significance	2	86604595	86604595	Human		name
156281664	CV2348796	single nucleotide variant	NM_005667.4(RNF103):c.1616C>G (p.Ser539Trp)	not specified [RCV004203242]	uncertain significance	2	86604285	86604285	Human		name
156108346	CV2355395	single nucleotide variant	NM_005667.4(RNF103):c.1343A>G (p.Asn448Ser)	not specified [RCV004205254]	uncertain significance	2	86604558	86604558	Human		name
329368017	CV2427669	single nucleotide variant	NM_005667.4(RNF103):c.1967G>A (p.Arg656Gln)	not specified [RCV004250292]	uncertain significance	2	86603934	86603934	Human		name
401777753	CV2718324	single nucleotide variant	NM_005667.4(RNF103):c.1814A>G (p.Glu605Gly)	not specified [RCV004318162]	uncertain significance	2	86604087	86604087	Human		name
401870185	CV2792301	single nucleotide variant	NM_005667.4(RNF103):c.1724C>T (p.Ala575Val)	not specified [RCV004361485]	uncertain significance	2	86604177	86604177	Human		name
405754290	CV3316377	single nucleotide variant	NM_005667.4(RNF103):c.1584G>A (p.Met528Ile)	not specified [RCV004454262]	uncertain significance	2	86604317	86604317	Human		name
407485726	CV3479515	single nucleotide variant	NM_005667.4(RNF103):c.1338A>T (p.Glu446Asp)	not specified [RCV004663369]	uncertain significance	2	86604563	86604563	Human		name
407485734	CV3479516	single nucleotide variant	NM_005667.4(RNF103):c.1165T>A (p.Tyr389Asn)	not specified [RCV004663370]	uncertain significance	2	86604736	86604736	Human		name
407485709	CV3483454	single nucleotide variant	NM_005667.4(RNF103):c.1311G>T (p.Lys437Asn)	not specified [RCV004663367]	uncertain significance	2	86604590	86604590	Human		name
597754440	CV3593924	single nucleotide variant	NM_005667.4(RNF103):c.1808A>T (p.Asp603Val)	not specified [RCV004847363]	uncertain significance	2	86604093	86604093	Human		name
597686127	CV3593925	single nucleotide variant	NM_005667.4(RNF103):c.1220G>A (p.Arg407Lys)	not specified [RCV004858350]	uncertain significance	2	86604681	86604681	Human		name
597754444	CV3593926	single nucleotide variant	NM_005667.4(RNF103):c.1614C>G (p.Asp538Glu)	not specified [RCV004847364]	uncertain significance	2	86604287	86604287	Human		name
597754447	CV3593927	single nucleotide variant	NM_005667.4(RNF103):c.1465T>C (p.Phe489Leu)	not specified [RCV004847365]	uncertain significance	2	86604436	86604436	Human		name
597754452	CV3593929	single nucleotide variant	NM_005667.4(RNF103):c.1888A>G (p.Asn630Asp)	not specified [RCV004847366]	uncertain significance	2	86604013	86604013	Human		name
597686146	CV3593930	single nucleotide variant	NM_005667.4(RNF103):c.1878G>T (p.Glu626Asp)	not specified [RCV004858352]	uncertain significance	2	86604023	86604023	Human		name
597754460	CV3593933	single nucleotide variant	NM_005667.4(RNF103):c.1604C>G (p.Thr535Ser)	not specified [RCV004847368]	uncertain significance	2	86604297	86604297	Human		name
597686166	CV3593934	single nucleotide variant	NM_005667.4(RNF103):c.1054C>G (p.Arg352Gly)	not specified [RCV004858354]	uncertain significance	2	86604847	86604847	Human		name
597754464	CV3593936	single nucleotide variant	NM_005667.4(RNF103):c.1137G>C (p.Gln379His)	not specified [RCV004847369]	uncertain significance	2	86604764	86604764	Human		name
597754468	CV3593937	single nucleotide variant	NM_005667.4(RNF103):c.1595C>T (p.Ser532Phe)	not specified [RCV004847370]	uncertain significance	2	86604306	86604306	Human		name
598230603	CV3899381	single nucleotide variant	NM_005667.4(RNF103):c.1009A>G (p.Met337Val)	not specified [RCV005274373]	uncertain significance	2	86604892	86604892	Human		name
598230610	CV3899382	single nucleotide variant	NM_005667.4(RNF103):c.1291A>G (p.Ile431Val)	not specified [RCV005274374]	uncertain significance	2	86604610	86604610	Human		name
598230623	CV3899384	single nucleotide variant	NM_005667.4(RNF103):c.1088A>G (p.Tyr363Cys)	not specified [RCV005274376]	uncertain significance	2	86604813	86604813	Human		name
598230637	CV3899386	single nucleotide variant	NM_005667.4(RNF103):c.1819G>A (p.Asp607Asn)	not specified [RCV005274378]	uncertain significance	2	86604082	86604082	Human		name
598230644	CV3899387	single nucleotide variant	NM_005667.4(RNF103):c.1414T>G (p.Ser472Ala)	not specified [RCV005274379]	uncertain significance	2	86604487	86604487	Human		name
598230650	CV3899388	single nucleotide variant	NM_001198954.1(RNF103-CHMP3):c.236A>G (p.Asp79Gly)	not specified [RCV005274380]	uncertain significance	2	86529355	86529355	Human		name
597754472	CV3593938	single nucleotide variant	NM_001198954.1(RNF103-CHMP3):c.463A>G (p.Thr155Ala)	not specified [RCV004847371]	uncertain significance	2	86510390	86510390	Human		name

Gene Annotator (Functional Annotation) unavailable	Gene Annotator (Annotation Distribution) unavailable	Variant Visualizer (Genomic Variants) unavailble Variant Visualizer (Genomic Variants) unavailable
Gene Annotator (Functional Annotation)	Gene Annotator (Annotation Distribution)	Variant Visualizer (Genomic Variants)

InterViewer (Protein-Protein Interactions) unavailable	Gviewer (Genome Viewer) unavailable	Variant Visualizer (Damaging Variants) unavailble Variant Visualizer (Damaging Variants) unavailable
InterViewer (Protein-Protein Interactions)	GViewer (Genome Viewer)	Variant Visualizer (Damaging Variants)

Gene Annotator (Annotation Comparison) unavailable	OLGA (Gene List Generator) unavailable
Gene Annotator (Annotation Comparison)	OLGA (Gene List Generator)	Excel (Download)

MOET (Multi-Ontology Enrichement) unavailable	GOLF (Gene-Ortholog Location Finder) unavailable
MOET (Multi-Ontology Enrichement)	GOLF (Gene-Ortholog Location Finder)

Create Name:

Description:

Send us a Message