Accs Variant Search Result - Rat Genome Database

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111 records found for search term Accs

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
156169427	CV2400480	single nucleotide variant	NM_032592.4(ACCS):c.58T>C (p.Cys20Arg)	not specified [RCV004246681]	uncertain significance	11	44067685	44067685	Human		name
15160998	CV724430	single nucleotide variant	NM_032592.4(ACCS):c.606G>A (p.Val202=)	not provided [RCV000881490]	benign	11	44077328	44077328	Human		name
156048779	CV2304453	single nucleotide variant	NM_032592.4(ACCS):c.110C>T (p.Ser37Phe)	not specified [RCV004164548]	uncertain significance	11	44067737	44067737	Human		name
156075173	CV2350854	single nucleotide variant	NM_032592.4(ACCS):c.142C>T (p.Arg48Cys)	not specified [RCV004211692]	uncertain significance	11	44067769	44067769	Human		name
401743858	CV2688043	single nucleotide variant	NM_032592.4(ACCS):c.260A>T (p.Asp87Val)	not specified [RCV004305114]	uncertain significance	11	44067887	44067887	Human		name
405750019	CV3291457	single nucleotide variant	NM_032592.4(ACCS):c.143G>A (p.Arg48His)	not specified [RCV004431958]	uncertain significance	11	44067770	44067770	Human		name
597745522	CV3635783	single nucleotide variant	NM_032592.4(ACCS):c.238G>A (p.Gly80Ser)	not specified [RCV004891569]	uncertain significance	11	44067865	44067865	Human		name
15191939	CV724432	single nucleotide variant	NM_032592.4(ACCS):c.1035C>T (p.Ala345=)	not provided [RCV000888520]	benign	11	44081244	44081244	Human		name
156270019	CV2195128	single nucleotide variant	NM_032592.4(ACCS):c.950T>A (p.Val317Glu)	not specified [RCV004078034]	uncertain significance	11	44081046	44081046	Human		name
156141647	CV2288555	single nucleotide variant	NM_032592.4(ACCS):c.709G>A (p.Ala237Thr)	not specified [RCV004152080]	uncertain significance	11	44077899	44077899	Human		name
156058789	CV2305276	single nucleotide variant	NM_032592.4(ACCS):c.485A>T (p.Glu162Val)	not specified [RCV004171197]	uncertain significance	11	44074677	44074677	Human		name
156274325	CV2320005	single nucleotide variant	NM_032592.4(ACCS):c.997G>C (p.Gly333Arg)	not specified [RCV004167873]	uncertain significance	11	44081206	44081206	Human		name
156306788	CV2360050	single nucleotide variant	NM_032592.4(ACCS):c.976G>A (p.Gly326Arg)	not specified [RCV004212883]	uncertain significance	11	44081185	44081185	Human		name
329381736	CV2471245	single nucleotide variant	NM_032592.4(ACCS):c.608G>A (p.Cys203Tyr)	not specified [RCV004280274]	likely benign	11	44077330	44077330	Human		name
401719606	CV2675632	single nucleotide variant	NM_032592.4(ACCS):c.445C>G (p.Leu149Val)	not specified [RCV004287888]	uncertain significance	11	44074637	44074637	Human		name
405750044	CV3291461	single nucleotide variant	NM_032592.4(ACCS):c.307A>G (p.Thr103Ala)	not specified [RCV004431962]	uncertain significance	11	44071274	44071274	Human		name
405750105	CV3291471	single nucleotide variant	NM_032592.4(ACCS):c.614A>G (p.Tyr205Cys)	not specified [RCV004431972]	uncertain significance	11	44077336	44077336	Human		name
405750156	CV3291478	single nucleotide variant	NM_032592.4(ACCS):c.859G>A (p.Glu287Lys)	not specified [RCV004431979]	uncertain significance	11	44079556	44079556	Human		name
407480279	CV3424187	single nucleotide variant	NM_032592.4(ACCS):c.425G>A (p.Arg142Gln)	not specified [RCV004602189]	uncertain significance	11	44074617	44074617	Human		name
407480305	CV3424194	single nucleotide variant	NM_032592.4(ACCS):c.400G>A (p.Asp134Asn)	not specified [RCV004602194]	uncertain significance	11	44073498	44073498	Human		name
407480330	CV3424200	single nucleotide variant	NM_032592.4(ACCS):c.595A>G (p.Thr199Ala)	not specified [RCV004602199]	uncertain significance	11	44077317	44077317	Human		name
597745079	CV3635687	single nucleotide variant	NM_032592.4(ACCS):c.763A>G (p.Ser255Gly)	not specified [RCV004891474]	uncertain significance	11	44078714	44078714	Human		name
597744160	CV3638997	single nucleotide variant	NM_032592.4(ACCS):c.625C>T (p.Arg209Trp)	not specified [RCV004891294]	uncertain significance	11	44077347	44077347	Human		name
598275882	CV3927264	single nucleotide variant	NM_032592.4(ACCS):c.424C>T (p.Arg142Trp)	not specified [RCV005305016]	uncertain significance	11	44074616	44074616	Human		name
598275941	CV3927358	single nucleotide variant	NM_032592.4(ACCS):c.950T>G (p.Val317Gly)	not specified [RCV005305075]	uncertain significance	11	44081046	44081046	Human		name
598275991	CV3927440	single nucleotide variant	NM_032592.4(ACCS):c.726C>A (p.His242Gln)	not specified [RCV005305125]	uncertain significance	11	44077916	44077916	Human		name
15172969	CV724431	single nucleotide variant	NM_032592.4(ACCS):c.662G>A (p.Gly221Glu)	not provided [RCV000883947]	benign	11	44077852	44077852	Human		name
155963429	CV2282739	single nucleotide variant	NM_032592.4(ACCS):c.1225G>A (p.Gly409Ser)	not specified [RCV004141598]	uncertain significance	11	44083282	44083282	Human		name
156297949	CV2297728	single nucleotide variant	NM_032592.4(ACCS):c.1390G>A (p.Val464Ile)	not specified [RCV004155406]	uncertain significance	11	44083559	44083559	Human		name
155903517	CV2301655	single nucleotide variant	NM_032592.4(ACCS):c.1121A>G (p.Asn374Ser)	not specified [RCV004162557]	uncertain significance	11	44083178	44083178	Human		name
156270383	CV2379504	single nucleotide variant	NM_032592.4(ACCS):c.1136C>T (p.Pro379Leu)	not specified [RCV004217219]	uncertain significance	11	44083193	44083193	Human		name
156270399	CV2379505	single nucleotide variant	NM_032592.4(ACCS):c.1216C>T (p.Arg406Cys)	not specified [RCV004217220]	uncertain significance	11	44083273	44083273	Human		name
329375456	CV2440934	single nucleotide variant	NM_032592.4(ACCS):c.1300C>T (p.Arg434Cys)	not specified [RCV004261323]	uncertain significance	11	44083469	44083469	Human		name
329361110	CV2463289	single nucleotide variant	NM_032592.4(ACCS):c.1120A>G (p.Asn374Asp)	not specified [RCV004275047]	uncertain significance	11	44083177	44083177	Human		name
401751498	CV2708660	single nucleotide variant	NM_032592.4(ACCS):c.1172A>G (p.Tyr391Cys)	not specified [RCV004307643]	uncertain significance	11	44083229	44083229	Human		name
401885136	CV2771257	single nucleotide variant	NM_032592.4(ACCS):c.1229T>C (p.Phe410Ser)	not specified [RCV004346235]	uncertain significance	11	44083286	44083286	Human		name
401885719	CV2774485	single nucleotide variant	NM_032592.4(ACCS):c.1102C>T (p.Arg368Trp)	not specified [RCV004349977]	uncertain significance	11	44081311	44081311	Human		name
405749948	CV3291446	single nucleotide variant	NM_032592.4(ACCS):c.1301G>A (p.Arg434His)	not specified [RCV004431947]	uncertain significance	11	44083470	44083470	Human		name
405749962	CV3291448	single nucleotide variant	NM_032592.4(ACCS):c.1328C>T (p.Ser443Phe)	not specified [RCV004431949]	uncertain significance	11	44083497	44083497	Human		name
405749985	CV3291452	single nucleotide variant	NM_032592.4(ACCS):c.1418G>A (p.Arg473Lys)	not specified [RCV004431953]	uncertain significance	11	44083704	44083704	Human		name
405750026	CV3291458	single nucleotide variant	NM_032592.4(ACCS):c.1466G>A (p.Arg489His)	not specified [RCV004431959]	uncertain significance	11	44083752	44083752	Human		name
597745834	CV3635872	single nucleotide variant	NM_032592.4(ACCS):c.1498C>T (p.Arg500Cys)	not specified [RCV004891657]	likely benign	11	44083784	44083784	Human		name
597709550	CV3638810	single nucleotide variant	NM_032592.4(ACCS):c.1103G>A (p.Arg368Gln)	not specified [RCV004886581]	uncertain significance	11	44081312	44081312	Human		name
597743772	CV3638904	single nucleotide variant	NM_032592.4(ACCS):c.1150C>T (p.Arg384Trp)	not specified [RCV004891202]	uncertain significance	11	44083207	44083207	Human		name
597744673	CV3639086	single nucleotide variant	NM_032592.4(ACCS):c.1052G>A (p.Arg351His)	not specified [RCV004891382]	uncertain significance	11	44081261	44081261	Human		name
598276051	CV3927538	single nucleotide variant	NM_032592.4(ACCS):c.1151G>A (p.Arg384Gln)	not specified [RCV005305185]	uncertain significance	11	44083208	44083208	Human		name
598276110	CV3938002	single nucleotide variant	NM_032592.4(ACCS):c.1103G>T (p.Arg368Leu)	not specified [RCV005305244]	uncertain significance	11	44081312	44081312	Human		name
15161078	CV724433	single nucleotide variant	NM_032592.4(ACCS):c.1465C>T (p.Arg489Cys)	not provided [RCV000881505]	benign	11	44083751	44083751	Human		name
405750248	CV3291492	single nucleotide variant	NM_001031854.2(ACCSL):c.11G>A (p.Arg4Gln)	not specified [RCV004431993]	uncertain significance	11	44048047	44048047	Human		name
598244959	CV3934570	single nucleotide variant	NM_001031854.2(ACCSL):c.31C>T (p.Pro11Ser)	not specified [RCV005297537]	uncertain significance	11	44048067	44048067	Human		name
8634039	CV89257	single nucleotide variant	NM_001031854.2(ACCSL):c.660C>T (p.Phe220=)	Malignant melanoma [RCV000069354]	not provided	11	44051359	44051359	Human		name
156298057	CV2297741	single nucleotide variant	NM_001031854.2(ACCSL):c.259G>A (p.Ala87Thr)	not specified [RCV004155418]	likely benign	11	44048295	44048295	Human		name
156115395	CV2397285	single nucleotide variant	NM_001031854.2(ACCSL):c.229C>T (p.Arg77Trp)	not specified [RCV004238817]	uncertain significance	11	44048265	44048265	Human		name
401740429	CV2679724	single nucleotide variant	NM_001031854.2(ACCSL):c.122C>T (p.Thr41Met)	not specified [RCV004282192]	uncertain significance	11	44048158	44048158	Human		name
401778004	CV2734388	single nucleotide variant	NM_001031854.2(ACCSL):c.1050G>A (p.Arg350=)	not specified [RCV004332539]	likely benign	11	44055202	44055202	Human		name
401904271	CV2816573	single nucleotide variant	NM_001031854.2(ACCSL):c.166G>T (p.Glu56Ter)	not provided [RCV003394820]	uncertain significance	11	44048202	44048202	Human		name
407480349	CV3424206	single nucleotide variant	NM_001031854.2(ACCSL):c.260C>T (p.Ala87Val)	not specified [RCV004602203]	uncertain significance	11	44048296	44048296	Human		name
597756396	CV3645716	single nucleotide variant	NM_001031854.2(ACCSL):c.143C>T (p.Thr48Met)	not specified [RCV004893901]	uncertain significance	11	44048179	44048179	Human		name
156076262	CV2198157	single nucleotide variant	NM_001031854.2(ACCSL):c.619T>C (p.Trp207Arg)	not specified [RCV004079746]	uncertain significance	11	44050606	44050606	Human		name
156186115	CV2236123	single nucleotide variant	NM_001031854.2(ACCSL):c.332C>T (p.Ala111Val)	not specified [RCV004114269]	uncertain significance	11	44048368	44048368	Human		name
155948005	CV2245834	single nucleotide variant	NM_001031854.2(ACCSL):c.891T>A (p.His297Gln)	not specified [RCV004111684]	likely benign	11	44053011	44053011	Human		name
156197454	CV2306802	single nucleotide variant	NM_001031854.2(ACCSL):c.706G>A (p.Val236Met)	not specified [RCV004159372]	uncertain significance	11	44051653	44051653	Human		name
156079490	CV2341257	single nucleotide variant	NM_001031854.2(ACCSL):c.481T>C (p.Tyr161His)	not specified [RCV004186670]	uncertain significance	11	44048517	44048517	Human		name
156057158	CV2371214	single nucleotide variant	NM_001031854.2(ACCSL):c.412C>T (p.Arg138Cys)	not specified [RCV004220952]	uncertain significance	11	44048448	44048448	Human		name
401719417	CV2679526	single nucleotide variant	NM_001031854.2(ACCSL):c.551T>C (p.Leu184Pro)	not specified [RCV004287829]	uncertain significance	11	44050108	44050108	Human		name
401748882	CV2708389	single nucleotide variant	NM_001031854.2(ACCSL):c.641G>A (p.Arg214Gln)	not specified [RCV004313504]	uncertain significance	11	44051340	44051340	Human		name
401879030	CV2780899	single nucleotide variant	NM_001031854.2(ACCSL):c.991C>G (p.Pro331Ala)	not specified [RCV004354444]	uncertain significance	11	44053448	44053448	Human		name
405750570	CV3291538	single nucleotide variant	NM_001031854.2(ACCSL):c.298G>A (p.Asp100Asn)	not specified [RCV004432039]	uncertain significance	11	44048334	44048334	Human		name
405750602	CV3291543	single nucleotide variant	NM_001031854.2(ACCSL):c.308G>T (p.Gly103Val)	not specified [RCV004432044]	uncertain significance	11	44048344	44048344	Human		name
405750669	CV3291553	single nucleotide variant	NM_001031854.2(ACCSL):c.506G>A (p.Gly169Asp)	not specified [RCV004432054]	uncertain significance	11	44050063	44050063	Human		name
405750692	CV3291557	single nucleotide variant	NM_001031854.2(ACCSL):c.599C>T (p.Thr200Ile)	not specified [RCV004432058]	uncertain significance	11	44050586	44050586	Human		name
405750718	CV3291561	single nucleotide variant	NM_001031854.2(ACCSL):c.616G>C (p.Asp206His)	not specified [RCV004432062]	uncertain significance	11	44050603	44050603	Human		name
405750830	CV3291576	single nucleotide variant	NM_001031854.2(ACCSL):c.764A>G (p.Asp255Gly)	not specified [RCV004432077]	uncertain significance	11	44051711	44051711	Human		name
407480354	CV3424207	single nucleotide variant	NM_001031854.2(ACCSL):c.443C>T (p.Ser148Leu)	not specified [RCV004602204]	uncertain significance	11	44048479	44048479	Human		name
407500401	CV3424209	single nucleotide variant	NM_001031854.2(ACCSL):c.800A>C (p.Tyr267Ser)	not specified [RCV004607109]	uncertain significance	11	44052689	44052689	Human		name
597756007	CV3635136	single nucleotide variant	NM_001031854.2(ACCSL):c.656G>A (p.Arg219Gln)	not specified [RCV004893814]	uncertain significance	11	44051355	44051355	Human		name
597755866	CV3635965	single nucleotide variant	NM_001031854.2(ACCSL):c.961C>G (p.Arg321Gly)	not specified [RCV004893729]	uncertain significance	11	44053418	44053418	Human		name
597710338	CV3639195	single nucleotide variant	NM_001031854.2(ACCSL):c.421G>C (p.Asp141His)	not specified [RCV004886696]	uncertain significance	11	44048457	44048457	Human		name
597734413	CV3642317	single nucleotide variant	NM_001031854.2(ACCSL):c.377G>A (p.Cys126Tyr)	not specified [RCV004889309]	uncertain significance	11	44048413	44048413	Human		name
597735145	CV3642502	single nucleotide variant	NM_001031854.2(ACCSL):c.671A>G (p.Tyr224Cys)	not specified [RCV004889484]	uncertain significance	11	44051370	44051370	Human		name
597756842	CV3645811	single nucleotide variant	NM_001031854.2(ACCSL):c.901C>T (p.Leu301Phe)	not specified [RCV004893991]	uncertain significance	11	44053021	44053021	Human		name
597757281	CV3645915	single nucleotide variant	NM_001031854.2(ACCSL):c.931C>A (p.Leu311Ile)	not specified [RCV004894090]	uncertain significance	11	44053051	44053051	Human		name
597733363	CV3646009	single nucleotide variant	NM_001031854.2(ACCSL):c.965G>A (p.Gly322Asp)	not specified [RCV004889144]	uncertain significance	11	44053422	44053422	Human		name
598246733	CV3931066	single nucleotide variant	NM_001031854.2(ACCSL):c.461A>G (p.Asn154Ser)	not specified [RCV005297786]	uncertain significance	11	44048497	44048497	Human		name
598245480	CV3934669	single nucleotide variant	NM_001031854.2(ACCSL):c.371G>A (p.Ser124Asn)	not specified [RCV005297608]	uncertain significance	11	44048407	44048407	Human		name
598171916	CV3934766	single nucleotide variant	NM_001031854.2(ACCSL):c.867T>A (p.Ser289Arg)	not specified [RCV005309301]	uncertain significance	11	44052756	44052756	Human		name
598171185	CV3938183	single nucleotide variant	NM_001031854.2(ACCSL):c.962G>A (p.Arg321Gln)	not specified [RCV005309130]	uncertain significance	11	44053419	44053419	Human		name
155994962	CV2250294	single nucleotide variant	NM_001031854.2(ACCSL):c.1622T>C (p.Leu541Ser)	not specified [RCV004127192]	uncertain significance	11	44058697	44058697	Human		name
156277481	CV2300195	single nucleotide variant	NM_001031854.2(ACCSL):c.1233C>G (p.Asn411Lys)	not specified [RCV004151383]	uncertain significance	11	44056232	44056232	Human		name
156047394	CV2304337	single nucleotide variant	NM_001031854.2(ACCSL):c.1674A>G (p.Ile558Met)	not specified [RCV004164453]	uncertain significance	11	44059887	44059887	Human		name
156042460	CV2381457	single nucleotide variant	NM_001031854.2(ACCSL):c.1613G>A (p.Arg538Gln)	not specified [RCV004229942]	uncertain significance	11	44058688	44058688	Human		name
156223081	CV2399928	single nucleotide variant	NM_001031854.2(ACCSL):c.1366C>T (p.Arg456Trp)	not specified [RCV004246864]	uncertain significance	11	44058355	44058355	Human		name
329395644	CV2462901	single nucleotide variant	NM_001031854.2(ACCSL):c.1057C>A (p.Leu353Ile)	not specified [RCV004272743]	uncertain significance	11	44055209	44055209	Human		name
401721322	CV2673677	single nucleotide variant	NM_001031854.2(ACCSL):c.1546C>T (p.Arg516Cys)	not specified [RCV004282408]	likely benign	11	44058621	44058621	Human		name
401755945	CV2686168	single nucleotide variant	NM_001031854.2(ACCSL):c.1612C>T (p.Arg538Trp)	not specified [RCV004297267]	uncertain significance	11	44058687	44058687	Human		name
401764937	CV2701587	single nucleotide variant	NM_001031854.2(ACCSL):c.1379C>T (p.Ala460Val)	not specified [RCV004314015]	uncertain significance	11	44058368	44058368	Human		name
401773790	CV2702435	single nucleotide variant	NM_001031854.2(ACCSL):c.1286G>T (p.Gly429Val)	not specified [RCV004316948]	uncertain significance	11	44056285	44056285	Human		name
401767288	CV2718446	single nucleotide variant	NM_001031854.2(ACCSL):c.1533G>T (p.Lys511Asn)	not specified [RCV004318262]	uncertain significance	11	44058608	44058608	Human		name
405750223	CV3291488	single nucleotide variant	NM_001031854.2(ACCSL):c.1055A>G (p.Asn352Ser)	not specified [RCV004431989]	uncertain significance	11	44055207	44055207	Human		name
405750234	CV3291490	single nucleotide variant	NM_001031854.2(ACCSL):c.1100A>C (p.Asp367Ala)	not specified [RCV004431991]	uncertain significance	11	44055252	44055252	Human		name
405750256	CV3291493	single nucleotide variant	NM_001031854.2(ACCSL):c.1207C>T (p.Arg403Cys)	not specified [RCV004431994]	uncertain significance	11	44056206	44056206	Human		name
405750342	CV3291506	single nucleotide variant	NM_001031854.2(ACCSL):c.1516C>T (p.Arg506Cys)	not specified [RCV004432007]	uncertain significance	11	44058591	44058591	Human		name
405750480	CV3291526	single nucleotide variant	NM_001031854.2(ACCSL):c.1664A>C (p.Glu555Ala)	not specified [RCV004432027]	uncertain significance	11	44059877	44059877	Human		name
407480360	CV3424208	single nucleotide variant	NM_001031854.2(ACCSL):c.1066A>G (p.Ile356Val)	not specified [RCV004602205]	uncertain significance	11	44055218	44055218	Human		name
597735815	CV3639101	single nucleotide variant	NM_001031854.2(ACCSL):c.1261T>C (p.Phe421Leu)	not specified [RCV004889578]	uncertain significance	11	44056260	44056260	Human		name
597711316	CV3639284	single nucleotide variant	NM_001031854.2(ACCSL):c.1069A>G (p.Ile357Val)	not specified [RCV004886785]	uncertain significance	11	44055221	44055221	Human		name
597734811	CV3642409	single nucleotide variant	NM_001031854.2(ACCSL):c.1364A>G (p.Tyr455Cys)	not specified [RCV004889391]	uncertain significance	11	44058353	44058353	Human		name
598244802	CV3934506	single nucleotide variant	NM_001031854.2(ACCSL):c.1276A>G (p.Ser426Gly)	not specified [RCV005297500]	likely benign	11	44056275	44056275	Human		name
598246318	CV3934859	single nucleotide variant	NM_001031854.2(ACCSL):c.1106C>T (p.Ser369Phe)	not specified [RCV005297725]	uncertain significance	11	44055258	44055258	Human		name
598276296	CV3938282	single nucleotide variant	NM_001031854.2(ACCSL):c.1442G>A (p.Gly481Asp)	not specified [RCV005305430]	uncertain significance	11	44058431	44058431	Human		name
598244565	CV3938322	single nucleotide variant	NM_001031854.2(ACCSL):c.1432C>T (p.Arg478Cys)	not specified [RCV005297451]	uncertain significance	11	44058421	44058421	Human		name

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