Rtn3 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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100 records found for search term Rtn3

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
156038496	CV2313647	single nucleotide variant	NM_001265589.2(RTN3):c.5C>T (p.Ala2Val)	not specified [RCV004157578]	uncertain significance	11	63681641	63681641	Human		name
15201581	CV701849	single nucleotide variant	NM_001265589.2(RTN3):c.30C>T (p.Ser10=)	not provided [RCV000957663]	benign	11	63681666	63681666	Human		name
15098073	CV724544	single nucleotide variant	NM_001265589.2(RTN3):c.177A>C (p.Val59=)	not provided [RCV000891650]	benign	11	63704885	63704885	Human		name
8634265	CV89483	single nucleotide variant	NM_201428.2(RTN3):c.829C>A (p.Pro277Thr)	Malignant melanoma [RCV000069580]	not provided	11	63719388	63719388	Human		name
8634266	CV89484	single nucleotide variant	NM_201428.2(RTN3):c.830C>T (p.Pro277Leu)	Malignant melanoma [RCV000069581]	not provided	11	63719389	63719389	Human		name
155973621	CV2332422	single nucleotide variant	NM_001265589.2(RTN3):c.44C>T (p.Ser15Leu)	not specified [RCV004196153]	uncertain significance	11	63681680	63681680	Human		name
401775104	CV2696219	single nucleotide variant	NM_001265589.2(RTN3):c.64C>T (p.Pro22Ser)	not specified [RCV004310261]	uncertain significance	11	63681700	63681700	Human		name
401905339	CV2813288	single nucleotide variant	NM_001265589.2(RTN3):c.1011C>T (p.Asn337=)	not provided [RCV003395885]	likely benign	11	63719513	63719513	Human		name
407514060	CV3473112	single nucleotide variant	NM_001265589.2(RTN3):c.104C>G (p.Pro35Arg)	not specified [RCV004674350]	uncertain significance	11	63681740	63681740	Human		name
156308754	CV2249555	single nucleotide variant	NM_001265589.2(RTN3):c.418G>A (p.Val140Ile)	not specified [RCV004120583]	likely benign	11	63718920	63718920	Human		name
156361175	CV2269185	single nucleotide variant	NM_001265589.2(RTN3):c.677A>T (p.Tyr226Phe)	not specified [RCV004130346]	uncertain significance	11	63719179	63719179	Human		name
156169947	CV2315494	single nucleotide variant	NM_001265589.2(RTN3):c.844G>A (p.Glu282Lys)	not specified [RCV004167438]	uncertain significance	11	63719346	63719346	Human		name
156260575	CV2322311	single nucleotide variant	NM_001265589.2(RTN3):c.919A>G (p.Met307Val)	not specified [RCV004176072]	uncertain significance	11	63719421	63719421	Human		name
155926894	CV2345289	single nucleotide variant	NM_001265589.2(RTN3):c.892A>G (p.Arg298Gly)	not specified [RCV004196024]	uncertain significance	11	63719394	63719394	Human		name
401751200	CV2696259	single nucleotide variant	NM_001265589.2(RTN3):c.463C>T (p.Arg155Cys)	not specified [RCV004310600]	uncertain significance	11	63718965	63718965	Human		name
401764242	CV2708769	single nucleotide variant	NM_001265589.2(RTN3):c.952A>G (p.Thr318Ala)	not specified [RCV004307733]	uncertain significance	11	63719454	63719454	Human		name
401891629	CV2780600	single nucleotide variant	NM_001265589.2(RTN3):c.863C>T (p.Ser288Leu)	not specified [RCV004351965]	likely benign	11	63719365	63719365	Human		name
405699726	CV3313680	single nucleotide variant	NM_001265589.2(RTN3):c.452T>A (p.Val151Asp)	not specified [RCV004446866]	uncertain significance	11	63718954	63718954	Human		name
405699731	CV3313681	single nucleotide variant	NM_001265589.2(RTN3):c.908G>C (p.Gly303Ala)	not specified [RCV004446867]	uncertain significance	11	63719410	63719410	Human		name
405699738	CV3313682	single nucleotide variant	NM_001265589.2(RTN3):c.921G>A (p.Met307Ile)	not specified [RCV004446868]	uncertain significance	11	63719423	63719423	Human		name
405699744	CV3313683	single nucleotide variant	NM_001265589.2(RTN3):c.922T>C (p.Ser308Pro)	not specified [RCV004446869]	uncertain significance	11	63719424	63719424	Human		name
407468472	CV3473111	single nucleotide variant	NM_001265589.2(RTN3):c.776A>G (p.Lys259Arg)	not specified [RCV004661132]	likely benign	11	63719278	63719278	Human		name
597712600	CV3601292	single nucleotide variant	NM_001265589.2(RTN3):c.868A>T (p.Thr290Ser)	not specified [RCV004861193]	likely benign	11	63719370	63719370	Human		name
597712610	CV3601294	single nucleotide variant	NM_001265589.2(RTN3):c.910C>T (p.Arg304Cys)	not specified [RCV004861194]	uncertain significance	11	63719412	63719412	Human		name
597712647	CV3601298	single nucleotide variant	NM_001265589.2(RTN3):c.766G>A (p.Ala256Thr)	not specified [RCV004861197]	uncertain significance	11	63719268	63719268	Human		name
597712669	CV3601300	single nucleotide variant	NM_001265589.2(RTN3):c.649T>A (p.Tyr217Asn)	not specified [RCV004861199]	uncertain significance	11	63719151	63719151	Human		name
597712700	CV3601305	single nucleotide variant	NM_001265589.2(RTN3):c.685T>C (p.Ser229Pro)	not specified [RCV004861202]	uncertain significance	11	63719187	63719187	Human		name
597712711	CV3601306	single nucleotide variant	NM_001265589.2(RTN3):c.317A>G (p.His106Arg)	not specified [RCV004861203]	uncertain significance	11	63718819	63718819	Human		name
598232764	CV3909886	single nucleotide variant	NM_001265589.2(RTN3):c.664G>A (p.Gly222Ser)	not specified [RCV005274750]	uncertain significance	11	63719166	63719166	Human		name
598232784	CV3909889	single nucleotide variant	NM_001265589.2(RTN3):c.472A>G (p.Ile158Val)	not specified [RCV005274753]	uncertain significance	11	63718974	63718974	Human		name
156365743	CV2193264	single nucleotide variant	NM_001265589.2(RTN3):c.1694A>C (p.His565Pro)	not specified [RCV004071245]	uncertain significance	11	63720196	63720196	Human		name
156165053	CV2195984	single nucleotide variant	NM_001265589.2(RTN3):c.2099G>T (p.Gly700Val)	not specified [RCV004072235]	uncertain significance	11	63720601	63720601	Human		name
155963047	CV2197733	single nucleotide variant	NM_001265589.2(RTN3):c.1993G>A (p.Gly665Arg)	not specified [RCV004074936]	uncertain significance	11	63720495	63720495	Human		name
156399545	CV2205183	single nucleotide variant	NM_001265589.2(RTN3):c.1285A>G (p.Lys429Glu)	not specified [RCV004077777]	uncertain significance	11	63719787	63719787	Human		name
156118414	CV2209256	single nucleotide variant	NM_001265589.2(RTN3):c.2847T>G (p.Phe949Leu)	not specified [RCV004093442]	uncertain significance	11	63752615	63752615	Human		name
156381590	CV2215640	single nucleotide variant	NM_001265589.2(RTN3):c.1759G>T (p.Asp587Tyr)	not specified [RCV004089390]	uncertain significance	11	63720261	63720261	Human		name
156082470	CV2249131	single nucleotide variant	NM_001265589.2(RTN3):c.2845T>C (p.Phe949Leu)	not specified [RCV004118185]	uncertain significance	11	63752613	63752613	Human		name
156255894	CV2264764	single nucleotide variant	NM_001265589.2(RTN3):c.2210A>T (p.Asp737Val)	not specified [RCV004132741]	uncertain significance	11	63720712	63720712	Human		name
155954676	CV2274359	single nucleotide variant	NM_001265589.2(RTN3):c.2751C>A (p.Asp917Glu)	not specified [RCV004136742]	uncertain significance	11	63752519	63752519	Human		name
156279614	CV2285093	single nucleotide variant	NM_001265589.2(RTN3):c.1915C>T (p.His639Tyr)	not specified [RCV004145323]	uncertain significance	11	63720417	63720417	Human		name
156179592	CV2288024	single nucleotide variant	NM_001265589.2(RTN3):c.1282A>G (p.Thr428Ala)	not specified [RCV004147784]	uncertain significance	11	63719784	63719784	Human		name
155939724	CV2293959	single nucleotide variant	NM_001265589.2(RTN3):c.1843G>T (p.Val615Leu)	not specified [RCV004149360]	uncertain significance	11	63720345	63720345	Human		name
156006944	CV2299633	single nucleotide variant	NM_001265589.2(RTN3):c.1864G>A (p.Glu622Lys)	not specified [RCV004154950]	uncertain significance	11	63720366	63720366	Human		name
156091151	CV2302633	single nucleotide variant	NM_001265589.2(RTN3):c.1277A>T (p.Asn426Ile)	not specified [RCV004160792]	uncertain significance	11	63719779	63719779	Human		name
156051749	CV2304679	single nucleotide variant	NM_001265589.2(RTN3):c.2057C>T (p.Thr686Ile)	not specified [RCV004166560]	uncertain significance	11	63720559	63720559	Human		name
156094423	CV2310010	single nucleotide variant	NM_001265589.2(RTN3):c.1148C>T (p.Thr383Ile)	not specified [RCV004163151]	uncertain significance	11	63719650	63719650	Human		name
156283477	CV2318863	single nucleotide variant	NM_001265589.2(RTN3):c.1302A>C (p.Lys434Asn)	not specified [RCV004175770]	uncertain significance	11	63719804	63719804	Human		name
156050608	CV2323288	single nucleotide variant	NM_001265589.2(RTN3):c.1373G>A (p.Cys458Tyr)	not specified [RCV004171704]	uncertain significance	11	63719875	63719875	Human		name
156067466	CV2324105	single nucleotide variant	NM_001265589.2(RTN3):c.2539C>G (p.Leu847Val)	not specified [RCV004178392]	uncertain significance	11	63749999	63749999	Human		name
155932540	CV2364412	single nucleotide variant	NM_001265589.2(RTN3):c.1343C>G (p.Ala448Gly)	not specified [RCV004223623]	uncertain significance	11	63719845	63719845	Human		name
155996481	CV2373076	single nucleotide variant	NM_001265589.2(RTN3):c.2377C>G (p.Leu793Val)	not specified [RCV004217773]	uncertain significance	11	63720879	63720879	Human		name
155935814	CV2380097	single nucleotide variant	NM_001265589.2(RTN3):c.1261G>C (p.Val421Leu)	not specified [RCV004224478]	uncertain significance	11	63719763	63719763	Human		name
156142219	CV2386010	single nucleotide variant	NM_001265589.2(RTN3):c.2741C>G (p.Ala914Gly)	not specified [RCV004229076]	uncertain significance	11	63752509	63752509	Human		name
329356057	CV2430557	single nucleotide variant	NM_001265589.2(RTN3):c.1936A>G (p.Ile646Val)	not specified [RCV004252139]	uncertain significance	11	63720438	63720438	Human		name
329360906	CV2439870	single nucleotide variant	NM_001265589.2(RTN3):c.1888A>G (p.Thr630Ala)	not specified [RCV004257910]	uncertain significance	11	63720390	63720390	Human		name
329351763	CV2455273	single nucleotide variant	NM_001265589.2(RTN3):c.2483A>C (p.Glu828Ala)	not specified [RCV004274786]	uncertain significance	11	63720985	63720985	Human		name
329390040	CV2457537	single nucleotide variant	NM_001265589.2(RTN3):c.1937T>C (p.Ile646Thr)	not specified [RCV004267344]	uncertain significance	11	63720439	63720439	Human		name
329398736	CV2471681	single nucleotide variant	NM_001265589.2(RTN3):c.1885G>C (p.Val629Leu)	not specified [RCV004286966]	uncertain significance	11	63720387	63720387	Human		name
401757516	CV2675349	single nucleotide variant	NM_001265589.2(RTN3):c.1408G>A (p.Val470Met)	not specified [RCV004292157]	uncertain significance	11	63719910	63719910	Human		name
401735409	CV2687576	single nucleotide variant	NM_001265589.2(RTN3):c.1604G>A (p.Gly535Asp)	not specified [RCV004300800]	likely benign	11	63720106	63720106	Human		name
401748790	CV2709594	single nucleotide variant	NM_001265589.2(RTN3):c.2405A>T (p.Asp802Val)	not specified [RCV004318820]	uncertain significance	11	63720907	63720907	Human		name
401764419	CV2725636	single nucleotide variant	NM_001265589.2(RTN3):c.2291G>A (p.Arg764His)	not specified [RCV004322014]	likely benign	11	63720793	63720793	Human		name
401718113	CV2728439	single nucleotide variant	NM_001265589.2(RTN3):c.1675G>A (p.Val559Ile)	not specified [RCV004333426]	uncertain significance	11	63720177	63720177	Human		name
401877280	CV2764572	single nucleotide variant	NM_001265589.2(RTN3):c.1675G>T (p.Val559Phe)	not specified [RCV004339127]	uncertain significance	11	63720177	63720177	Human		name
401880076	CV2769899	single nucleotide variant	NM_001265589.2(RTN3):c.1736A>C (p.Glu579Ala)	not specified [RCV004353745]	uncertain significance	11	63720238	63720238	Human		name
405758482	CV3313671	single nucleotide variant	NM_001265589.2(RTN3):c.1378T>C (p.Ser460Pro)	not specified [RCV004454876]	uncertain significance	11	63719880	63719880	Human		name
405758490	CV3313672	single nucleotide variant	NM_001265589.2(RTN3):c.1489T>C (p.Ser497Pro)	not specified [RCV004454877]	uncertain significance	11	63719991	63719991	Human		name
405758502	CV3313674	single nucleotide variant	NM_001265589.2(RTN3):c.1792G>T (p.Val598Phe)	not specified [RCV004454879]	uncertain significance	11	63720294	63720294	Human		name
405758510	CV3313675	single nucleotide variant	NM_001265589.2(RTN3):c.2027C>T (p.Ala676Val)	not specified [RCV004454880]	uncertain significance	11	63720529	63720529	Human		name
405758518	CV3313676	single nucleotide variant	NM_001265589.2(RTN3):c.2185C>G (p.Gln729Glu)	not specified [RCV004454881]	uncertain significance	11	63720687	63720687	Human		name
405758527	CV3313677	single nucleotide variant	NM_001265589.2(RTN3):c.2383C>T (p.Arg795Cys)	not specified [RCV004454882]	uncertain significance	11	63720885	63720885	Human		name
405758534	CV3313678	single nucleotide variant	NM_001265589.2(RTN3):c.2477A>G (p.Lys826Arg)	not specified [RCV004454883]	uncertain significance	11	63720979	63720979	Human		name
405758541	CV3313679	single nucleotide variant	NM_001265589.2(RTN3):c.2553A>T (p.Arg851Ser)	not specified [RCV004454884]	uncertain significance	11	63750013	63750013	Human		name
407468452	CV3473103	single nucleotide variant	NM_001265589.2(RTN3):c.1144A>G (p.Ser382Gly)	not specified [RCV004661125]	uncertain significance	11	63719646	63719646	Human		name
407468454	CV3473104	single nucleotide variant	NM_001265589.2(RTN3):c.2384G>A (p.Arg795His)	not specified [RCV004661126]	likely benign	11	63720886	63720886	Human		name
407468460	CV3473106	single nucleotide variant	NM_001265589.2(RTN3):c.1096G>A (p.Asp366Asn)	not specified [RCV004661128]	uncertain significance	11	63719598	63719598	Human		name
407468463	CV3473107	single nucleotide variant	NM_001265589.2(RTN3):c.1006A>G (p.Thr336Ala)	not specified [RCV004661129]	uncertain significance	11	63719508	63719508	Human		name
407514058	CV3473108	single nucleotide variant	NM_001265589.2(RTN3):c.2413A>T (p.Ile805Phe)	not specified [RCV004674349]	uncertain significance	11	63720915	63720915	Human		name
407468466	CV3473109	single nucleotide variant	NM_001265589.2(RTN3):c.2165C>T (p.Pro722Leu)	not specified [RCV004661130]	likely benign	11	63720667	63720667	Human		name
407468469	CV3473110	single nucleotide variant	NM_001265589.2(RTN3):c.1436A>G (p.Asp479Gly)	not specified [RCV004661131]	likely benign	11	63719938	63719938	Human		name
597712592	CV3601290	single nucleotide variant	NM_001265589.2(RTN3):c.1246A>G (p.Ile416Val)	not specified [RCV004861192]	uncertain significance	11	63719748	63719748	Human		name
597766261	CV3601291	single nucleotide variant	NM_001265589.2(RTN3):c.2506G>A (p.Ala836Thr)	not specified [RCV004850237]	uncertain significance	11	63721008	63721008	Human		name
597712622	CV3601295	single nucleotide variant	NM_001265589.2(RTN3):c.1568A>C (p.Lys523Thr)	not specified [RCV004861195]	uncertain significance	11	63720070	63720070	Human		name
597712635	CV3601296	single nucleotide variant	NM_001265589.2(RTN3):c.2336C>T (p.Thr779Ile)	not specified [RCV004861196]	uncertain significance	11	63720838	63720838	Human		name
597766271	CV3601297	single nucleotide variant	NM_001265589.2(RTN3):c.1535C>T (p.Thr512Ile)	not specified [RCV004850239]	uncertain significance	11	63720037	63720037	Human		name
597712659	CV3601299	single nucleotide variant	NM_001265589.2(RTN3):c.1194C>G (p.Ile398Met)	not specified [RCV004861198]	uncertain significance	11	63719696	63719696	Human		name
597766276	CV3601301	single nucleotide variant	NM_001265589.2(RTN3):c.1393G>A (p.Val465Met)	not specified [RCV004850240]	uncertain significance	11	63719895	63719895	Human		name
597712689	CV3601303	single nucleotide variant	NM_001265589.2(RTN3):c.1091G>A (p.Gly364Glu)	not specified [RCV004861201]	uncertain significance	11	63719593	63719593	Human		name
597766281	CV3601304	single nucleotide variant	NM_001265589.2(RTN3):c.2605T>C (p.Ser869Pro)	not specified [RCV004850241]	uncertain significance	11	63750065	63750065	Human		name
597766286	CV3601307	single nucleotide variant	NM_001265589.2(RTN3):c.1873T>G (p.Phe625Val)	not specified [RCV004850242]	uncertain significance	11	63720375	63720375	Human		name
598232730	CV3909881	single nucleotide variant	NM_001265589.2(RTN3):c.1700A>G (p.Asp567Gly)	not specified [RCV005274745]	uncertain significance	11	63720202	63720202	Human		name
598232735	CV3909882	single nucleotide variant	NM_001265589.2(RTN3):c.1970C>T (p.Ala657Val)	not specified [RCV005274746]	uncertain significance	11	63720472	63720472	Human		name
598232741	CV3909883	single nucleotide variant	NM_001265589.2(RTN3):c.1155G>C (p.Gln385His)	not specified [RCV005274747]	uncertain significance	11	63719657	63719657	Human		name
598232748	CV3909884	single nucleotide variant	NM_001265589.2(RTN3):c.2755G>A (p.Asp919Asn)	not specified [RCV005274748]	uncertain significance	11	63752523	63752523	Human		name
598232754	CV3909885	single nucleotide variant	NM_001265589.2(RTN3):c.1941T>A (p.Asp647Glu)	not specified [RCV005274749]	uncertain significance	11	63720443	63720443	Human		name
598232769	CV3909887	single nucleotide variant	NM_001265589.2(RTN3):c.1220A>C (p.Glu407Ala)	not specified [RCV005274751]	uncertain significance	11	63719722	63719722	Human		name
598232777	CV3909888	single nucleotide variant	NM_001265589.2(RTN3):c.2874G>C (p.Leu958Phe)	not specified [RCV005274752]	uncertain significance	11	63752642	63752642	Human		name
598232789	CV3909890	single nucleotide variant	NM_001265589.2(RTN3):c.1087A>G (p.Thr363Ala)	not specified [RCV005274754]	uncertain significance	11	63719589	63719589	Human		name
15183429	CV724545	single nucleotide variant	NM_001265589.2(RTN3):c.1808C>T (p.Pro603Leu)	not provided [RCV000886223]	benign	11	63720310	63720310	Human		name
407468457	CV3473105	single nucleotide variant	NM_001265589.2(RTN3):c.3090G>T (p.Lys1030Asn)	not specified [RCV004661127]	uncertain significance	11	63758192	63758192	Human		name

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