Rtl1 Variant Search Result - Rat Genome Database

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156 records found for search term Rtl1

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
156187481	CV2292467	single nucleotide variant	NM_001134888.3(RTL1):c.10C>T (p.Pro4Ser)	not specified [RCV004150256]	uncertain significance	14	100884779	100884779	Human		name
401902309	CV2807271	single nucleotide variant	NM_001134888.3(RTL1):c.153A>T (p.Pro51=)	not provided [RCV003393635]	likely benign	14	100884636	100884636	Human		name
401902311	CV2807272	single nucleotide variant	NM_001134888.3(RTL1):c.135A>T (p.Ala45=)	not provided [RCV003393636]	likely benign	14	100884654	100884654	Human		name
151347978	CV1325205	single nucleotide variant	NM_001134888.3(RTL1):c.828A>G (p.Glu276=)	not provided [RCV001813847]	benign	14	100883961	100883961	Human		name
401902307	CV2807269	single nucleotide variant	NM_001134888.3(RTL1):c.726C>T (p.Ile242=)	not provided [RCV003393633]	likely benign	14	100884063	100884063	Human		name
401902308	CV2807270	single nucleotide variant	NM_001134888.3(RTL1):c.651C>T (p.Ile217=)	not provided [RCV003393634]	likely benign	14	100884138	100884138	Human		name
598129404	CV3888701	single nucleotide variant	NM_001134888.3(RTL1):c.624C>A (p.Gly208=)	not provided [RCV005244875]	likely benign	14	100884165	100884165	Human		name
126732003	CV1000853	single nucleotide variant	NM_001134888.3(RTL1):c.2214C>T (p.Tyr738=)	not provided [RCV001310720]	likely benign	14	100882575	100882575	Human		name
155905218	CV2285893	single nucleotide variant	NM_001134888.3(RTL1):c.253C>T (p.Arg85Cys)	not specified [RCV004143825]	uncertain significance	14	100884536	100884536	Human		name
155957175	CV2304126	single nucleotide variant	NM_001134888.3(RTL1):c.173C>T (p.Pro58Leu)	not specified [RCV004170161]	uncertain significance	14	100884616	100884616	Human		name
401902304	CV2807267	single nucleotide variant	NM_001134888.3(RTL1):c.1260C>T (p.Tyr420=)	not provided [RCV003393631]	likely benign	14	100883529	100883529	Human		name
405757525	CV3313529	single nucleotide variant	NM_001134888.3(RTL1):c.124C>T (p.Arg42Trp)	not specified [RCV004454734]	uncertain significance	14	100884665	100884665	Human		name
597787295	CV3601199	single nucleotide variant	NM_001134888.3(RTL1):c.155C>A (p.Ala52Asp)	not specified [RCV004855203]	uncertain significance	14	100884634	100884634	Human		name
15101924	CV725559	single nucleotide variant	NM_001134888.3(RTL1):c.115A>C (p.Ser39Arg)	not provided [RCV000892376]	likely benign	14	100884674	100884674	Human		name
15187432	CV739115	single nucleotide variant	NM_001134888.3(RTL1):c.1395G>A (p.Ser465=)	not provided [RCV000909089]	likely benign	14	100883394	100883394	Human		name
15172350	CV769642	single nucleotide variant	NM_001134888.3(RTL1):c.1611G>A (p.Pro537=)	not provided [RCV000928096]	likely benign	14	100883178	100883178	Human		name
155929898	CV2224634	single nucleotide variant	NM_001134888.3(RTL1):c.994G>A (p.Glu332Lys)	not specified [RCV004092483]	uncertain significance	14	100883795	100883795	Human		name
155962377	CV2285648	single nucleotide variant	NM_001134888.3(RTL1):c.382C>T (p.Pro128Ser)	not specified [RCV004141509]	uncertain significance	14	100884407	100884407	Human		name
156180774	CV2288119	single nucleotide variant	NM_001134888.3(RTL1):c.330G>C (p.Arg110Ser)	not specified [RCV004149650]	uncertain significance	14	100884459	100884459	Human		name
155940802	CV2294142	single nucleotide variant	NM_001134888.3(RTL1):c.334G>A (p.Asp112Asn)	not specified [RCV004149511]	uncertain significance	14	100884455	100884455	Human		name
156105119	CV2307295	single nucleotide variant	NM_001134888.3(RTL1):c.785C>G (p.Pro262Arg)	not specified [RCV004165990]	uncertain significance	14	100884004	100884004	Human		name
156356198	CV2320743	single nucleotide variant	NM_001134888.3(RTL1):c.785C>T (p.Pro262Leu)	not specified [RCV004179088]	uncertain significance	14	100884004	100884004	Human		name
155963196	CV2330302	single nucleotide variant	NM_001134888.3(RTL1):c.722T>G (p.Val241Gly)	not specified [RCV004180886]	uncertain significance	14	100884067	100884067	Human		name
156273785	CV2344160	single nucleotide variant	NM_001134888.3(RTL1):c.643G>A (p.Glu215Lys)	not specified [RCV004195758]	uncertain significance	14	100884146	100884146	Human		name
329353058	CV2471416	single nucleotide variant	NM_001134888.3(RTL1):c.977T>C (p.Leu326Ser)	not specified [RCV004280417]	uncertain significance	14	100883812	100883812	Human		name
401902302	CV2807266	single nucleotide variant	NM_001134888.3(RTL1):c.3492T>G (p.Ala1164=)	not provided [RCV003393630]	likely benign	14	100881297	100881297	Human		name
401902305	CV2807268	single nucleotide variant	NM_001134888.3(RTL1):c.784C>A (p.Pro262Thr)	not provided [RCV003393632]	likely benign	14	100884005	100884005	Human		name
405757581	CV3313538	single nucleotide variant	NM_001134888.3(RTL1):c.313G>T (p.Gly105Cys)	not specified [RCV004454743]	uncertain significance	14	100884476	100884476	Human		name
405757616	CV3313543	single nucleotide variant	NM_001134888.3(RTL1):c.499G>A (p.Val167Met)	not specified [RCV004454748]	uncertain significance	14	100884290	100884290	Human		name
405757623	CV3313544	single nucleotide variant	NM_001134888.3(RTL1):c.793G>A (p.Gly265Arg)	not specified [RCV004454749]	uncertain significance	14	100883996	100883996	Human		name
407468262	CV3473045	single nucleotide variant	NM_001134888.3(RTL1):c.395G>A (p.Arg132Gln)	not specified [RCV004661085]	likely benign	14	100884394	100884394	Human		name
407514019	CV3473049	single nucleotide variant	NM_001134888.3(RTL1):c.854G>A (p.Arg285His)	not specified [RCV004674333]	uncertain significance	14	100883935	100883935	Human		name
407468274	CV3473052	single nucleotide variant	NM_001134888.3(RTL1):c.751G>C (p.Glu251Gln)	not specified [RCV004661089]	uncertain significance	14	100884038	100884038	Human		name
596948017	CV3547609	single nucleotide variant	NM_001134888.3(RTL1):c.3786C>T (p.Asn1262=)	not provided [RCV004811914]	likely benign	14	100881003	100881003	Human		name
597712198	CV3601197	single nucleotide variant	NM_001134888.3(RTL1):c.527G>A (p.Arg176Gln)	not specified [RCV004861155]	uncertain significance	14	100884262	100884262	Human		name
597787291	CV3601198	single nucleotide variant	NM_001134888.3(RTL1):c.386C>T (p.Ser129Leu)	not specified [RCV004855202]	uncertain significance	14	100884403	100884403	Human		name
597712210	CV3601200	single nucleotide variant	NM_001134888.3(RTL1):c.974A>G (p.His325Arg)	not specified [RCV004861156]	uncertain significance	14	100883815	100883815	Human		name
597712282	CV3601215	single nucleotide variant	NM_001134888.3(RTL1):c.956A>G (p.Asp319Gly)	not specified [RCV004861163]	uncertain significance	14	100883833	100883833	Human		name
597787339	CV3601218	single nucleotide variant	NM_001134888.3(RTL1):c.668C>G (p.Thr223Ser)	not specified [RCV004855212]	uncertain significance	14	100884121	100884121	Human		name
597787357	CV3601222	single nucleotide variant	NM_001134888.3(RTL1):c.461A>C (p.Asn154Thr)	not specified [RCV004855216]	uncertain significance	14	100884328	100884328	Human		name
598232250	CV3899855	single nucleotide variant	NM_001134888.3(RTL1):c.829G>C (p.Val277Leu)	not specified [RCV005274660]	uncertain significance	14	100883960	100883960	Human		name
15180307	CV713998	single nucleotide variant	NM_001134888.3(RTL1):c.3561G>A (p.Gln1187=)	not provided [RCV000974120]	benign	14	100881228	100881228	Human		name
15169268	CV725555	single nucleotide variant	NM_001134888.3(RTL1):c.3771G>A (p.Gln1257=)	not provided [RCV000883232]	benign	14	100881018	100881018	Human		name
15177108	CV725556	single nucleotide variant	NM_001134888.3(RTL1):c.3600C>T (p.Phe1200=)	not provided [RCV000884744]	likely benign	14	100881189	100881189	Human		name
15115381	CV784639	single nucleotide variant	NM_001134888.3(RTL1):c.3678T>C (p.Gly1226=)	not provided [RCV000978393]	likely benign	14	100881111	100881111	Human		name
150411008	CV1196111	single nucleotide variant	NM_001134888.3(RTL1):c.2554G>A (p.Ala852Thr)	not provided [RCV001573430]\|not specified [RCV001703126]	benign\|likely benign	14	100882235	100882235	Human		name
150411152	CV1196112	single nucleotide variant	NM_001134888.3(RTL1):c.1672C>A (p.Pro558Thr)	not provided [RCV001573521]	likely benign	14	100883117	100883117	Human	1	name
156269918	CV2195121	single nucleotide variant	NM_001134888.3(RTL1):c.1520G>A (p.Arg507His)	not specified [RCV004078027]	uncertain significance	14	100883269	100883269	Human		name
156318355	CV2200301	single nucleotide variant	NM_001134888.3(RTL1):c.1445T>C (p.Ile482Thr)	not specified [RCV004076638]	uncertain significance	14	100883344	100883344	Human		name
156139516	CV2212083	single nucleotide variant	NM_001134888.3(RTL1):c.2710G>A (p.Ala904Thr)	not specified [RCV004088992]	uncertain significance	14	100882079	100882079	Human		name
155927007	CV2230717	single nucleotide variant	NM_001134888.3(RTL1):c.1447C>T (p.His483Tyr)	not specified [RCV004097659]	uncertain significance	14	100883342	100883342	Human		name
156202974	CV2234562	single nucleotide variant	NM_001134888.3(RTL1):c.1952C>T (p.Pro651Leu)	not specified [RCV004102539]	uncertain significance	14	100882837	100882837	Human		name
156067553	CV2236983	single nucleotide variant	NM_001134888.3(RTL1):c.1119G>C (p.Glu373Asp)	not specified [RCV004112976]	uncertain significance	14	100883670	100883670	Human		name
156252401	CV2286968	single nucleotide variant	NM_001134888.3(RTL1):c.1139C>T (p.Thr380Ile)	not specified [RCV004144569]	uncertain significance	14	100883650	100883650	Human		name
156184306	CV2292222	single nucleotide variant	NM_001134888.3(RTL1):c.2684A>G (p.Asp895Gly)	not specified [RCV004148264]	uncertain significance	14	100882105	100882105	Human		name
156284780	CV2334790	single nucleotide variant	NM_001134888.3(RTL1):c.2581C>T (p.Arg861Cys)	not specified [RCV004181906]	uncertain significance	14	100882208	100882208	Human		name
156075886	CV2350912	single nucleotide variant	NM_001134888.3(RTL1):c.1571C>T (p.Thr524Ile)	not specified [RCV004211746]	uncertain significance	14	100883218	100883218	Human		name
156103140	CV2363311	single nucleotide variant	NM_001134888.3(RTL1):c.2564G>A (p.Cys855Tyr)	not specified [RCV004213863]	uncertain significance	14	100882225	100882225	Human		name
156153383	CV2394965	single nucleotide variant	NM_001134888.3(RTL1):c.1690G>A (p.Asp564Asn)	not specified [RCV004234613]	uncertain significance	14	100883099	100883099	Human		name
329382472	CV2424479	single nucleotide variant	NM_001134888.3(RTL1):c.2344G>C (p.Val782Leu)	not specified [RCV004252368]	uncertain significance	14	100882445	100882445	Human		name
329383128	CV2441720	single nucleotide variant	NM_001134888.3(RTL1):c.1840G>A (p.Ala614Thr)	not specified [RCV004259889]	uncertain significance	14	100882949	100882949	Human		name
401766850	CV2680171	single nucleotide variant	NM_001134888.3(RTL1):c.2269C>A (p.Arg757Ser)	not specified [RCV004286652]	uncertain significance	14	100882520	100882520	Human		name
401773717	CV2695340	single nucleotide variant	NM_001134888.3(RTL1):c.2434T>A (p.Phe812Ile)	not specified [RCV004305248]	uncertain significance	14	100882355	100882355	Human		name
401756772	CV2696478	single nucleotide variant	NM_001134888.3(RTL1):c.1719T>G (p.Asp573Glu)	not specified [RCV004312552]	likely benign	14	100883070	100883070	Human		name
401766356	CV2725380	single nucleotide variant	NM_001134888.3(RTL1):c.1986G>C (p.Trp662Cys)	not specified [RCV004320026]	uncertain significance	14	100882803	100882803	Human		name
401855852	CV2757550	single nucleotide variant	NM_001134888.3(RTL1):c.1519C>T (p.Arg507Cys)	not specified [RCV004340924]	uncertain significance	14	100883270	100883270	Human		name
401883514	CV2757954	single nucleotide variant	NM_001134888.3(RTL1):c.2455T>C (p.Tyr819His)	not specified [RCV004337087]	uncertain significance	14	100882334	100882334	Human		name
401864724	CV2778002	single nucleotide variant	NM_001134888.3(RTL1):c.1130G>A (p.Arg377Gln)	not specified [RCV004347960]	uncertain significance	14	100883659	100883659	Human		name
401883541	CV2785691	single nucleotide variant	NM_001134888.3(RTL1):c.1418G>C (p.Trp473Ser)	not specified [RCV004364955]	uncertain significance	14	100883371	100883371	Human		name
401898340	CV2787681	single nucleotide variant	NM_001134888.3(RTL1):c.1270G>A (p.Ala424Thr)	not specified [RCV004356603]	uncertain significance	14	100883519	100883519	Human		name
401896865	CV2788886	single nucleotide variant	NM_001134888.3(RTL1):c.2107T>C (p.Phe703Leu)	not specified [RCV004362925]	uncertain significance	14	100882682	100882682	Human		name
405757517	CV3313528	single nucleotide variant	NM_001134888.3(RTL1):c.1017C>G (p.Phe339Leu)	not specified [RCV004454733]	uncertain significance	14	100883772	100883772	Human		name
405757533	CV3313530	single nucleotide variant	NM_001134888.3(RTL1):c.1528C>G (p.Arg510Gly)	not specified [RCV004454735]	uncertain significance	14	100883261	100883261	Human		name
405757538	CV3313531	single nucleotide variant	NM_001134888.3(RTL1):c.1543G>A (p.Glu515Lys)	not specified [RCV004454736]	uncertain significance	14	100883246	100883246	Human		name
405757543	CV3313532	single nucleotide variant	NM_001134888.3(RTL1):c.1703C>G (p.Pro568Arg)	not specified [RCV004454737]	uncertain significance	14	100883086	100883086	Human		name
405757549	CV3313533	single nucleotide variant	NM_001134888.3(RTL1):c.1985G>C (p.Trp662Ser)	not specified [RCV004454738]	uncertain significance	14	100882804	100882804	Human		name
405757556	CV3313534	single nucleotide variant	NM_001134888.3(RTL1):c.2142C>A (p.Asn714Lys)	not specified [RCV004454739]	uncertain significance	14	100882647	100882647	Human		name
405757563	CV3313535	single nucleotide variant	NM_001134888.3(RTL1):c.2155A>G (p.Ile719Val)	not specified [RCV004454740]	uncertain significance	14	100882634	100882634	Human		name
407468259	CV3473044	single nucleotide variant	NM_001134888.3(RTL1):c.1217G>A (p.Arg406His)	not specified [RCV004661084]	uncertain significance	14	100883572	100883572	Human		name
407514014	CV3473046	single nucleotide variant	NM_001134888.3(RTL1):c.2467G>A (p.Val823Met)	not specified [RCV004674331]	uncertain significance	14	100882322	100882322	Human		name
407514016	CV3473047	single nucleotide variant	NM_001134888.3(RTL1):c.1384G>A (p.Val462Met)	not specified [RCV004674332]	uncertain significance	14	100883405	100883405	Human		name
407468268	CV3473050	single nucleotide variant	NM_001134888.3(RTL1):c.1004G>A (p.Arg335Lys)	not specified [RCV004661087]	uncertain significance	14	100883785	100883785	Human		name
407468271	CV3473051	single nucleotide variant	NM_001134888.3(RTL1):c.2438T>C (p.Ile813Thr)	not specified [RCV004661088]	uncertain significance	14	100882351	100882351	Human		name
407468277	CV3473053	single nucleotide variant	NM_001134888.3(RTL1):c.1866G>T (p.Arg622Ser)	not specified [RCV004661090]	uncertain significance	14	100882923	100882923	Human		name
597787283	CV3601191	single nucleotide variant	NM_001134888.3(RTL1):c.2605C>T (p.Pro869Ser)	not specified [RCV004855200]	uncertain significance	14	100882184	100882184	Human		name
597712169	CV3601193	single nucleotide variant	NM_001134888.3(RTL1):c.1576C>A (p.His526Asn)	not specified [RCV004861152]	uncertain significance	14	100883213	100883213	Human		name
597787287	CV3601194	single nucleotide variant	NM_001134888.3(RTL1):c.1219G>A (p.Ala407Thr)	not specified [RCV004855201]	uncertain significance	14	100883570	100883570	Human		name
597712217	CV3601202	single nucleotide variant	NM_001134888.3(RTL1):c.1642G>C (p.Gly548Arg)	not specified [RCV004861157]	uncertain significance	14	100883147	100883147	Human		name
597787304	CV3601203	single nucleotide variant	NM_001134888.3(RTL1):c.2574G>C (p.Arg858Ser)	not specified [RCV004855205]	uncertain significance	14	100882215	100882215	Human		name
597712228	CV3601204	single nucleotide variant	NM_001134888.3(RTL1):c.1225C>T (p.Leu409Phe)	not specified [RCV004861158]	uncertain significance	14	100883564	100883564	Human		name
597787319	CV3601207	single nucleotide variant	NM_001134888.3(RTL1):c.1373C>T (p.Pro458Leu)	not specified [RCV004855207]	uncertain significance	14	100883416	100883416	Human		name
597787325	CV3601208	single nucleotide variant	NM_001134888.3(RTL1):c.2638G>A (p.Gly880Ser)	not specified [RCV004855208]	uncertain significance	14	100882151	100882151	Human		name
597787337	CV3601211	single nucleotide variant	NM_001134888.3(RTL1):c.2326G>C (p.Glu776Gln)	not specified [RCV004855211]	uncertain significance	14	100882463	100882463	Human		name
597712260	CV3601213	single nucleotide variant	NM_001134888.3(RTL1):c.1912G>C (p.Asp638His)	not specified [RCV004861161]	uncertain significance	14	100882877	100882877	Human		name
597712269	CV3601214	single nucleotide variant	NM_001134888.3(RTL1):c.2453C>A (p.Pro818His)	not specified [RCV004861162]	uncertain significance	14	100882336	100882336	Human		name
597712305	CV3601217	single nucleotide variant	NM_001134888.3(RTL1):c.2389A>G (p.Ile797Val)	not specified [RCV004861165]	likely benign	14	100882400	100882400	Human		name
597787345	CV3601219	single nucleotide variant	NM_001134888.3(RTL1):c.1573T>C (p.Phe525Leu)	not specified [RCV004855213]	uncertain significance	14	100883216	100883216	Human		name
597787353	CV3601221	single nucleotide variant	NM_001134888.3(RTL1):c.2059A>G (p.Lys687Glu)	not specified [RCV004855215]	uncertain significance	14	100882730	100882730	Human		name
598232255	CV3899856	single nucleotide variant	NM_001134888.3(RTL1):c.1616C>T (p.Pro539Leu)	not specified [RCV005274661]	uncertain significance	14	100883173	100883173	Human		name
598232260	CV3899857	single nucleotide variant	NM_001134888.3(RTL1):c.1323G>C (p.Lys441Asn)	not specified [RCV005274662]	uncertain significance	14	100883466	100883466	Human		name
598232272	CV3899859	single nucleotide variant	NM_001134888.3(RTL1):c.2065G>A (p.Ala689Thr)	not specified [RCV005274664]	uncertain significance	14	100882724	100882724	Human		name
598232277	CV3899860	single nucleotide variant	NM_001134888.3(RTL1):c.1117G>A (p.Glu373Lys)	not specified [RCV005274665]	uncertain significance	14	100883672	100883672	Human		name
598232291	CV3899863	single nucleotide variant	NM_001134888.3(RTL1):c.1692C>G (p.Asp564Glu)	not specified [RCV005274668]	uncertain significance	14	100883097	100883097	Human		name
598232301	CV3899865	single nucleotide variant	NM_001134888.3(RTL1):c.2436C>A (p.Phe812Leu)	not specified [RCV005274670]	likely benign	14	100882353	100882353	Human		name
598232316	CV3899868	single nucleotide variant	NM_001134888.3(RTL1):c.1354G>A (p.Glu452Lys)	not specified [RCV005274673]	uncertain significance	14	100883435	100883435	Human		name
598232321	CV3899869	single nucleotide variant	NM_001134888.3(RTL1):c.2386A>G (p.Ile796Val)	not specified [RCV005274674]	uncertain significance	14	100882403	100882403	Human		name
15201793	CV725558	single nucleotide variant	NM_001134888.3(RTL1):c.1195G>A (p.Glu399Lys)	not provided [RCV000891293]	likely benign	14	100883594	100883594	Human		name
15180869	CV739116	single nucleotide variant	NM_001134888.3(RTL1):c.1202A>G (p.His401Arg)	not provided [RCV000907456]\|not specified [RCV004028578]	likely benign\|uncertain significance	14	100883587	100883587	Human		name
15138366	CV753917	single nucleotide variant	NM_001134888.3(RTL1):c.2968G>A (p.Gly990Ser)	not provided [RCV000921320]	likely benign	14	100881821	100881821	Human		name
150409920	CV1196110	single nucleotide variant	NM_001134888.3(RTL1):c.3323G>A (p.Arg1108Gln)	not provided [RCV001572847]\|not specified [RCV001702124]	benign\|likely benign	14	100881466	100881466	Human		name
155979479	CV2222869	single nucleotide variant	NM_001134888.3(RTL1):c.3842G>A (p.Arg1281His)	not specified [RCV004101691]	likely benign	14	100880947	100880947	Human		name
156271100	CV2237105	single nucleotide variant	NM_001134888.3(RTL1):c.3643C>T (p.Arg1215Cys)	not specified [RCV004114862]	uncertain significance	14	100881146	100881146	Human		name
156364904	CV2272017	single nucleotide variant	NM_001134888.3(RTL1):c.3836G>A (p.Arg1279His)	not specified [RCV004124822]	uncertain significance	14	100880953	100880953	Human		name
156267031	CV2296529	single nucleotide variant	NM_001134888.3(RTL1):c.4015C>A (p.Pro1339Thr)	not specified [RCV004154604]	uncertain significance	14	100880774	100880774	Human		name
155968358	CV2312828	single nucleotide variant	NM_001134888.3(RTL1):c.3883C>T (p.Arg1295Cys)	not specified [RCV004171326]	uncertain significance	14	100880906	100880906	Human		name
156185617	CV2335893	single nucleotide variant	NM_001134888.3(RTL1):c.3535C>T (p.His1179Tyr)	not specified [RCV004196112]	uncertain significance	14	100881254	100881254	Human		name
156118269	CV2346025	single nucleotide variant	NM_001134888.3(RTL1):c.4000G>A (p.Ala1334Thr)	not specified [RCV004201505]	uncertain significance	14	100880789	100880789	Human		name
156131881	CV2365634	single nucleotide variant	NM_001134888.3(RTL1):c.3529G>C (p.Ala1177Pro)	not specified [RCV004214195]	uncertain significance	14	100881260	100881260	Human		name
156193003	CV2397899	single nucleotide variant	NM_001134888.3(RTL1):c.3524G>A (p.Arg1175Gln)	not specified [RCV004239724]	uncertain significance	14	100881265	100881265	Human		name
329373641	CV2434561	single nucleotide variant	NM_001134888.3(RTL1):c.3133A>C (p.Ile1045Leu)	not specified [RCV004254261]	uncertain significance	14	100881656	100881656	Human		name
329362749	CV2439206	single nucleotide variant	NM_001134888.3(RTL1):c.3301G>A (p.Val1101Met)	not specified [RCV004266478]	uncertain significance	14	100881488	100881488	Human		name
329389521	CV2445191	single nucleotide variant	NM_001134888.3(RTL1):c.3983G>A (p.Arg1328Gln)	not specified [RCV004263826]	likely benign	14	100880806	100880806	Human		name
329385684	CV2462190	single nucleotide variant	NM_001134888.3(RTL1):c.3419C>G (p.Thr1140Arg)	not specified [RCV004266200]	uncertain significance	14	100881370	100881370	Human		name
329392035	CV2470315	single nucleotide variant	NM_001134888.3(RTL1):c.3322C>T (p.Arg1108Trp)	not specified [RCV004279709]	uncertain significance	14	100881467	100881467	Human		name
401774182	CV2702634	single nucleotide variant	NM_001134888.3(RTL1):c.3830C>G (p.Pro1277Arg)	not specified [RCV004318903]	uncertain significance	14	100880959	100880959	Human		name
401742472	CV2715238	single nucleotide variant	NM_001134888.3(RTL1):c.3029C>T (p.Ala1010Val)	not specified [RCV004324587]	uncertain significance	14	100881760	100881760	Human		name
401860786	CV2758628	single nucleotide variant	NM_001134888.3(RTL1):c.3613A>C (p.Thr1205Pro)	not specified [RCV004337703]	uncertain significance	14	100881176	100881176	Human		name
401893678	CV2760099	single nucleotide variant	NM_001134888.3(RTL1):c.3724C>T (p.Arg1242Cys)	not specified [RCV004345506]	uncertain significance	14	100881065	100881065	Human		name
405757568	CV3313536	single nucleotide variant	NM_001134888.3(RTL1):c.2999G>A (p.Arg1000Gln)	not specified [RCV004454741]	uncertain significance	14	100881790	100881790	Human		name
405757575	CV3313537	single nucleotide variant	NM_001134888.3(RTL1):c.3068C>G (p.Pro1023Arg)	not specified [RCV004454742]	uncertain significance	14	100881721	100881721	Human		name
405757590	CV3313539	single nucleotide variant	NM_001134888.3(RTL1):c.3538T>C (p.Ser1180Pro)	not specified [RCV004454744]	likely benign	14	100881251	100881251	Human		name
405757595	CV3313540	single nucleotide variant	NM_001134888.3(RTL1):c.3592G>A (p.Glu1198Lys)	not specified [RCV004454745]	uncertain significance	14	100881197	100881197	Human		name
405757604	CV3313541	single nucleotide variant	NM_001134888.3(RTL1):c.3805C>T (p.Pro1269Ser)	not specified [RCV004454746]	uncertain significance	14	100880984	100880984	Human		name
405757610	CV3313542	single nucleotide variant	NM_001134888.3(RTL1):c.3982C>T (p.Arg1328Trp)	not specified [RCV004454747]	uncertain significance	14	100880807	100880807	Human		name
407468280	CV3473054	single nucleotide variant	NM_001134888.3(RTL1):c.3875T>C (p.Leu1292Pro)	not specified [RCV004661091]	uncertain significance	14	100880914	100880914	Human		name
597712178	CV3601195	single nucleotide variant	NM_001134888.3(RTL1):c.3317C>G (p.Ser1106Trp)	not specified [RCV004861153]	uncertain significance	14	100881472	100881472	Human		name
597712188	CV3601196	single nucleotide variant	NM_001134888.3(RTL1):c.3223G>A (p.Val1075Ile)	not specified [RCV004861154]	uncertain significance	14	100881566	100881566	Human		name
597712238	CV3601205	single nucleotide variant	NM_001134888.3(RTL1):c.3020G>T (p.Arg1007Met)	not specified [RCV004861159]	uncertain significance	14	100881769	100881769	Human		name
597787308	CV3601206	single nucleotide variant	NM_001134888.3(RTL1):c.3778C>G (p.Gln1260Glu)	not specified [RCV004855206]	uncertain significance	14	100881011	100881011	Human		name
597787328	CV3601209	single nucleotide variant	NM_001134888.3(RTL1):c.3970C>G (p.Leu1324Val)	not specified [RCV004855209]	uncertain significance	14	100880819	100880819	Human		name
597787333	CV3601210	single nucleotide variant	NM_001134888.3(RTL1):c.3955A>G (p.Ser1319Gly)	not specified [RCV004855210]	uncertain significance	14	100880834	100880834	Human		name
597712296	CV3601216	single nucleotide variant	NM_001134888.3(RTL1):c.3611T>C (p.Val1204Ala)	not specified [RCV004861164]	uncertain significance	14	100881178	100881178	Human		name
597787349	CV3601220	single nucleotide variant	NM_001134888.3(RTL1):c.3514C>G (p.Arg1172Gly)	not specified [RCV004855214]	uncertain significance	14	100881275	100881275	Human		name
598232267	CV3899858	single nucleotide variant	NM_001134888.3(RTL1):c.3325C>T (p.Pro1109Ser)	not specified [RCV005274663]	uncertain significance	14	100881464	100881464	Human		name
598232286	CV3899862	single nucleotide variant	NM_001134888.3(RTL1):c.3790G>A (p.Val1264Met)	not specified [RCV005274667]	uncertain significance	14	100880999	100880999	Human		name
598232296	CV3899864	single nucleotide variant	NM_001134888.3(RTL1):c.3560A>C (p.Gln1187Pro)	not specified [RCV005274669]	uncertain significance	14	100881229	100881229	Human		name
598232306	CV3899866	single nucleotide variant	NM_001134888.3(RTL1):c.3350G>A (p.Arg1117Gln)	not specified [RCV005274671]	uncertain significance	14	100881439	100881439	Human		name
598232311	CV3899867	single nucleotide variant	NM_001134888.3(RTL1):c.3895A>T (p.Ile1299Phe)	not specified [RCV005274672]	uncertain significance	14	100880894	100880894	Human		name
598232326	CV3899870	single nucleotide variant	NM_001134888.3(RTL1):c.3145G>A (p.Glu1049Lys)	not specified [RCV005274675]	uncertain significance	14	100881644	100881644	Human		name
598232331	CV3899871	single nucleotide variant	NM_001134888.3(RTL1):c.3953T>A (p.Leu1318Gln)	not specified [RCV005274676]	uncertain significance	14	100880836	100880836	Human		name
15131007	CV713997	single nucleotide variant	NM_001134888.3(RTL1):c.3644G>A (p.Arg1215His)	not provided [RCV000964531]	benign\|likely benign	14	100881145	100881145	Human		name
15153113	CV713999	single nucleotide variant	NM_001134888.3(RTL1):c.3340C>T (p.Arg1114Trp)	not provided [RCV000968484]	likely benign	14	100881449	100881449	Human		name
15166481	CV714000	single nucleotide variant	NM_001134888.3(RTL1):c.3301G>C (p.Val1101Leu)	not provided [RCV000971189]	benign	14	100881488	100881488	Human		name
15173582	CV725557	single nucleotide variant	NM_001134888.3(RTL1):c.3364C>T (p.Arg1122Cys)	not provided [RCV000884037]	benign	14	100881425	100881425	Human		name
15105738	CV753916	single nucleotide variant	NM_001134888.3(RTL1):c.3457G>A (p.Val1153Ile)	not provided [RCV000915608]	benign	14	100881332	100881332	Human		name
405757632	CV3313545	single nucleotide variant	NM_024627.6(RTL10):c.367G>A (p.Asp123Asn)	not specified [RCV004454750]	uncertain significance	22	19851895	19851895	Human		name

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