Mri1 Variant Search Result - Rat Genome Database

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68 records found for search term Mri1

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
150491204	CV1267739	single nucleotide variant	NM_001031727.4(MRI1):c.*4A>G	not provided [RCV001687763]	benign	19	13772285	13772285	Human		name
15138348	CV745372	single nucleotide variant	NM_001031727.4(MRI1):c.724+10C>G	not provided [RCV000898964]	likely benign	19	13768747	13768747	Human		name
404980350	CV2850481	deletion	NM_001031727.4(MRI1):c.363_371+2del	not provided [RCV003488040]	uncertain significance	19	13765098	13765108	Human		name
156045217	CV2049932	microsatellite	NM_001031727.4(MRI1):c.132+6GCGGGGCG[5]	not provided [RCV002796582]	likely benign	19	13764726	13764765	Human		name
155993273	CV2049933	microsatellite	NM_001031727.4(MRI1):c.132+6GCGGGGCG[7]	not provided [RCV002819305]	likely benign	19	13764726	13764749	Human		name
155940206	CV2071571	microsatellite	NM_001031727.4(MRI1):c.132+6GCGGGGCG[9]	not provided [RCV002861724]	likely benign	19	13764726	13764733	Human		name
156373273	CV2185225	microsatellite	NM_001031727.4(MRI1):c.132+6GCGGGGCG[6]	not provided [RCV003049887]	likely benign	19	13764726	13764757	Human		name
155953330	CV2073311	microsatellite	NM_001031727.4(MRI1):c.132+6GCGGGGCG[11]	not provided [RCV002816388]	benign	19	13764725	13764726	Human		name
15109788	CV727922	single nucleotide variant	NM_001031727.4(MRI1):c.19C>T (p.Arg7Cys)	not provided [RCV000893936]	benign	19	13764607	13764607	Human	1	name
15109788	CV727922	single nucleotide variant	NM_001031727.4(MRI1):c.19C>T (p.Arg7Cys)	not provided [RCV000893936]	benign	19	13764607	13764608	Human	1	name
156278939	CV2297558	single nucleotide variant	NM_001031727.4(MRI1):c.32G>A (p.Gly11Asp)	not specified [RCV004155264]	uncertain significance	19	13764620	13764620	Human		name
401783961	CV2720901	single nucleotide variant	NM_001031727.4(MRI1):c.77G>A (p.Arg26His)	not specified [RCV004328250]	uncertain significance	19	13764665	13764665	Human		name
407519078	CV3450202	single nucleotide variant	NM_001031727.4(MRI1):c.68A>G (p.Lys23Arg)	not specified [RCV004629127]	uncertain significance	19	13764656	13764656	Human		name
597662572	CV3560932	single nucleotide variant	NM_001031727.4(MRI1):c.600A>G (p.Thr200=)	not specified [RCV004828655]	likely benign	19	13768613	13768613	Human		name
15186966	CV727924	single nucleotide variant	NM_001031727.4(MRI1):c.975C>T (p.Phe325=)	not provided [RCV000887123]	benign	19	13772146	13772146	Human		name
15179349	CV741608	single nucleotide variant	NM_001031727.4(MRI1):c.303C>T (p.Arg101=)	not provided [RCV000907087]	likely benign	19	13765041	13765041	Human		name
15180887	CV741609	single nucleotide variant	NM_001031727.4(MRI1):c.474C>T (p.Ser158=)	not provided [RCV000907460]	likely benign	19	13766056	13766056	Human		name
15159148	CV756741	single nucleotide variant	NM_001031727.4(MRI1):c.453C>G (p.Leu151=)	not provided [RCV000925220]	likely benign	19	13766035	13766035	Human		name
155919736	CV2343216	single nucleotide variant	NM_001031727.4(MRI1):c.290C>G (p.Ala97Gly)	not specified [RCV004194845]	uncertain significance	19	13765028	13765028	Human		name
156063323	CV2352743	single nucleotide variant	NM_001031727.4(MRI1):c.286A>G (p.Met96Val)	not specified [RCV004198765]	uncertain significance	19	13765024	13765024	Human		name
156151633	CV2377567	single nucleotide variant	NM_001031727.4(MRI1):c.212G>A (p.Gly71Glu)	not specified [RCV004227763]	uncertain significance	19	13764950	13764950	Human		name
329399681	CV2443486	single nucleotide variant	NM_001031727.4(MRI1):c.154G>T (p.Ala52Ser)	not specified [RCV004262321]	uncertain significance	19	13764892	13764892	Human		name
405767792	CV3363217	single nucleotide variant	NM_001031727.4(MRI1):c.239G>T (p.Arg80Leu)	not specified [RCV004501740]	uncertain significance	19	13764977	13764977	Human		name
407496726	CV3450204	single nucleotide variant	NM_001031727.4(MRI1):c.118A>G (p.Ile40Val)	not specified [RCV004643565]	uncertain significance	19	13764706	13764706	Human		name
598202160	CV3982713	single nucleotide variant	NM_001031727.4(MRI1):c.289G>T (p.Ala97Ser)	not specified [RCV005376183]	uncertain significance	19	13765027	13765027	Human		name
9850326	CV181458	single nucleotide variant	NM_001031727.4(MRI1):c.629G>A (p.Arg210Gln)	Severe cystic degeneration of the brain [RCV000162126]\|not specified [RCV003987382]	likely pathogenic\|uncertain significance\|no classifications from unflagged records	19	13768642	13768642	Human	1	name
156065395	CV2196916	single nucleotide variant	NM_001031727.4(MRI1):c.607C>T (p.Arg203Trp)	not specified [RCV004071380]	uncertain significance	19	13768620	13768620	Human		name
156378758	CV2207798	single nucleotide variant	NM_001031727.4(MRI1):c.682G>A (p.Asp228Asn)	not specified [RCV004084234]	uncertain significance	19	13768695	13768695	Human		name
156076876	CV2230247	single nucleotide variant	NM_001031727.4(MRI1):c.482A>C (p.Lys161Thr)	not specified [RCV004099867]	uncertain significance	19	13766064	13766064	Human		name
156318385	CV2260681	single nucleotide variant	NM_001031727.4(MRI1):c.769G>A (p.Ala257Thr)	not specified [RCV004123703]	uncertain significance	19	13768868	13768868	Human		name
155987765	CV2275687	single nucleotide variant	NM_001031727.4(MRI1):c.533A>G (p.Tyr178Cys)	not specified [RCV004137301]	uncertain significance	19	13766115	13766115	Human		name
156297279	CV2297662	single nucleotide variant	NM_001031727.4(MRI1):c.439G>C (p.Gly147Arg)	not specified [RCV004155348]	uncertain significance	19	13766021	13766021	Human		name
156077542	CV2318563	single nucleotide variant	NM_001031727.4(MRI1):c.467C>T (p.Ala156Val)	not specified [RCV004173469]	uncertain significance	19	13766049	13766049	Human		name
156159542	CV2322747	single nucleotide variant	NM_001031727.4(MRI1):c.325C>T (p.Arg109Trp)	not specified [RCV004182857]	uncertain significance	19	13765063	13765063	Human		name
155906100	CV2357258	single nucleotide variant	NM_001031727.4(MRI1):c.460C>T (p.Arg154Trp)	not specified [RCV004200157]	uncertain significance	19	13766042	13766042	Human		name
156083679	CV2369049	single nucleotide variant	NM_001031727.4(MRI1):c.928G>T (p.Gly310Trp)	not specified [RCV004207982]	uncertain significance	19	13769027	13769027	Human		name
156166896	CV2373641	single nucleotide variant	NM_001031727.4(MRI1):c.991G>A (p.Asp331Asn)	not specified [RCV004222730]	uncertain significance	19	13772162	13772162	Human		name
401859402	CV2771576	single nucleotide variant	NM_001031727.4(MRI1):c.899G>A (p.Arg300Gln)	not specified [RCV004348598]	uncertain significance	19	13768998	13768998	Human		name
401928536	CV2811665	single nucleotide variant	NM_001031727.4(MRI1):c.707C>T (p.Ala236Val)	not provided [RCV003406868]	uncertain significance	19	13768720	13768720	Human		name
404980345	CV2850480	single nucleotide variant	NM_001031727.4(MRI1):c.722C>G (p.Ser241Ter)	not provided [RCV003488039]	uncertain significance	19	13768735	13768735	Human		name
405767910	CV3363235	single nucleotide variant	NM_001031727.4(MRI1):c.460C>G (p.Arg154Gly)	not specified [RCV004501758]	uncertain significance	19	13766042	13766042	Human		name
405767991	CV3363248	single nucleotide variant	NM_001031727.4(MRI1):c.526G>A (p.Ala176Thr)	not specified [RCV004501771]	uncertain significance	19	13766108	13766108	Human		name
405768045	CV3363257	single nucleotide variant	NM_001031727.4(MRI1):c.622G>A (p.Gly208Arg)	not specified [RCV004501780]	uncertain significance	19	13768635	13768635	Human		name
405768064	CV3363260	single nucleotide variant	NM_001031727.4(MRI1):c.664C>T (p.Pro222Ser)	not specified [RCV004501783]	uncertain significance	19	13768677	13768677	Human		name
405768173	CV3363277	single nucleotide variant	NM_001031727.4(MRI1):c.833T>G (p.Val278Gly)	not specified [RCV004501800]	uncertain significance	19	13768932	13768932	Human		name
405768542	CV3363279	single nucleotide variant	NM_001031727.4(MRI1):c.884T>A (p.Ile295Asn)	not specified [RCV004501803]	uncertain significance	19	13768983	13768983	Human		name
405768514	CV3363284	single nucleotide variant	NM_001031727.4(MRI1):c.898C>G (p.Arg300Gly)	not specified [RCV004501808]	uncertain significance	19	13768997	13768997	Human		name
407496718	CV3450200	single nucleotide variant	NM_001031727.4(MRI1):c.667G>A (p.Ala223Thr)	not specified [RCV004643563]	uncertain significance	19	13768680	13768680	Human		name
407496722	CV3450203	single nucleotide variant	NM_001031727.4(MRI1):c.767C>G (p.Thr256Arg)	not specified [RCV004643564]	uncertain significance	19	13768866	13768866	Human		name
407519081	CV3450205	single nucleotide variant	NM_001031727.4(MRI1):c.520G>A (p.Ala174Thr)	not specified [RCV004629128]	uncertain significance	19	13766102	13766102	Human		name
597662566	CV3560931	single nucleotide variant	NM_001031727.4(MRI1):c.758A>G (p.Asn253Ser)	not specified [RCV004828654]	uncertain significance	19	13768857	13768857	Human		name
597637649	CV3560933	single nucleotide variant	NM_001031727.4(MRI1):c.509C>G (p.Thr170Ser)	not specified [RCV004824766]	uncertain significance	19	13766091	13766091	Human		name
597662579	CV3560934	single nucleotide variant	NM_001031727.4(MRI1):c.457G>A (p.Glu153Lys)	not specified [RCV004828656]	uncertain significance	19	13766039	13766039	Human		name
598202131	CV3982708	single nucleotide variant	NM_001031727.4(MRI1):c.517C>G (p.Leu173Val)	not specified [RCV005376178]	uncertain significance	19	13766099	13766099	Human		name
598202137	CV3982709	single nucleotide variant	NM_001031727.4(MRI1):c.733G>A (p.Val245Met)	not specified [RCV005376179]	uncertain significance	19	13768832	13768832	Human		name
598202141	CV3982710	single nucleotide variant	NM_001031727.4(MRI1):c.874G>A (p.Gly292Ser)	not specified [RCV005376180]	uncertain significance	19	13768973	13768973	Human		name
598202147	CV3982711	single nucleotide variant	NM_001031727.4(MRI1):c.617A>G (p.Asn206Ser)	not specified [RCV005376181]	uncertain significance	19	13768630	13768630	Human		name
598202154	CV3982712	single nucleotide variant	NM_001031727.4(MRI1):c.496A>G (p.Thr166Ala)	not specified [RCV005376182]	uncertain significance	19	13766078	13766078	Human		name
15120268	CV716193	single nucleotide variant	NM_001031727.4(MRI1):c.703A>G (p.Met235Val)	not provided [RCV000962694]	benign	19	13768716	13768716	Human		name
15098018	CV727923	single nucleotide variant	NM_001031727.4(MRI1):c.352G>A (p.Glu118Lys)	not provided [RCV000891639]	likely benign	19	13765090	13765090	Human	1	name
15098018	CV727923	single nucleotide variant	NM_001031727.4(MRI1):c.352G>A (p.Glu118Lys)	not provided [RCV000891639]	likely benign	19	13765090	13765091	Human	1	name
156113047	CV2212648	single nucleotide variant	NM_001031727.4(MRI1):c.1064C>A (p.Thr355Asn)	not specified [RCV004085172]	uncertain significance	19	13772235	13772235	Human		name
155907602	CV2302247	single nucleotide variant	NM_001031727.4(MRI1):c.1093G>A (p.Asp365Asn)	not specified [RCV004159235]	uncertain significance	19	13772264	13772264	Human		name
156183202	CV2327952	single nucleotide variant	NM_001031727.4(MRI1):c.1100C>A (p.Pro367His)	not specified [RCV004179267]	uncertain significance	19	13772271	13772271	Human		name
401779914	CV2676731	single nucleotide variant	NM_001031727.4(MRI1):c.1006G>A (p.Gly336Ser)	not specified [RCV004290905]	uncertain significance	19	13772177	13772177	Human		name
405767684	CV3363199	single nucleotide variant	NM_001031727.4(MRI1):c.1009A>G (p.Ile337Val)	not specified [RCV004501722]	uncertain significance	19	13772180	13772180	Human		name
597637643	CV3560930	single nucleotide variant	NM_001031727.4(MRI1):c.1048C>T (p.Arg350Trp)	not specified [RCV004824765]	uncertain significance	19	13772219	13772219	Human		name
15198812	CV727925	single nucleotide variant	NM_001031727.4(MRI1):c.1049G>A (p.Arg350Gln)	not provided [RCV000890463]	likely benign	19	13772220	13772220	Human		name

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