Mon2 Variant Search Result - Rat Genome Database

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93 records found for search term Mon2

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
405703652	CV3361648	single nucleotide variant	NM_015026.3(MON2):c.13A>G (p.Ser5Gly)	not specified [RCV004492828]	uncertain significance	12	62467220	62467220	Human		name
405690655	CV3351675	single nucleotide variant	NM_015026.3(MON2):c.54G>C (p.Gln18His)	not specified [RCV004490625]	uncertain significance	12	62467261	62467261	Human		name
15160367	CV778109	microsatellite	NM_015026.3(MON2):c.2466+10_2466+11del	not provided [RCV000947470]	benign	12	62543205	62543206	Human		name
156033045	CV2236151	single nucleotide variant	NM_015026.3(MON2):c.242A>G (p.Lys81Arg)	not specified [RCV004114294]	uncertain significance	12	62493981	62493981	Human		name
329366477	CV2445764	single nucleotide variant	NM_015026.3(MON2):c.155G>A (p.Arg52Gln)	not specified [RCV004259825]	uncertain significance	12	62484213	62484213	Human		name
329393996	CV2472256	single nucleotide variant	NM_015026.3(MON2):c.124G>A (p.Gly42Arg)	not specified [RCV004283362]	uncertain significance	12	62484182	62484182	Human		name
405722052	CV3358629	single nucleotide variant	NM_015026.3(MON2):c.2604G>A (p.Pro868=)	not specified [RCV004495317]	likely benign	12	62546923	62546923	Human		name
407495833	CV3453840	single nucleotide variant	NM_015026.3(MON2):c.286C>T (p.His96Tyr)	not specified [RCV004643319]	uncertain significance	12	62494025	62494025	Human		name
15127965	CV753537	single nucleotide variant	NM_015026.3(MON2):c.2580G>A (p.Arg860=)	not provided [RCV000919577]	likely benign	12	62546899	62546899	Human		name
155980679	CV2212012	single nucleotide variant	NM_015026.3(MON2):c.902C>A (p.Pro301Gln)	not specified [RCV004088925]	uncertain significance	12	62508398	62508398	Human		name
156170203	CV2273488	single nucleotide variant	NM_015026.3(MON2):c.925A>G (p.Ile309Val)	not specified [RCV004132233]	uncertain significance	12	62508421	62508421	Human		name
401767888	CV2677849	single nucleotide variant	NM_015026.3(MON2):c.773C>T (p.Pro258Leu)	not specified [RCV004294345]	uncertain significance	12	62501682	62501682	Human		name
405690640	CV3351678	single nucleotide variant	NM_015026.3(MON2):c.611G>A (p.Arg204Lys)	not specified [RCV004490628]	uncertain significance	12	62500828	62500828	Human		name
405690617	CV3351682	single nucleotide variant	NM_015026.3(MON2):c.683A>C (p.Asn228Thr)	not specified [RCV004490632]	uncertain significance	12	62501592	62501592	Human		name
598201071	CV3986255	single nucleotide variant	NM_015026.3(MON2):c.801T>G (p.Phe267Leu)	not specified [RCV005375964]	uncertain significance	12	62508297	62508297	Human		name
598201076	CV3986256	single nucleotide variant	NM_015026.3(MON2):c.933G>A (p.Met311Ile)	not specified [RCV005375965]	uncertain significance	12	62508429	62508429	Human		name
156178099	CV2201562	single nucleotide variant	NM_015026.3(MON2):c.2549A>G (p.Asn850Ser)	not specified [RCV004080052]	uncertain significance	12	62544980	62544980	Human		name
155918508	CV2362623	single nucleotide variant	NM_015026.3(MON2):c.2173G>A (p.Gly725Arg)	not specified [RCV004215275]	uncertain significance	12	62538150	62538150	Human		name
156101715	CV2367688	single nucleotide variant	NM_015026.3(MON2):c.1210C>T (p.Pro404Ser)	not specified [RCV004211606]	uncertain significance	12	62525184	62525184	Human		name
156214770	CV2385943	single nucleotide variant	NM_015026.3(MON2):c.1817C>T (p.Thr606Ile)	not specified [RCV004226976]	uncertain significance	12	62535626	62535626	Human		name
329402523	CV2454759	single nucleotide variant	NM_015026.3(MON2):c.2813C>T (p.Pro938Leu)	not specified [RCV004269990]	uncertain significance	12	62549727	62549727	Human		name
401719677	CV2675655	single nucleotide variant	NM_015026.3(MON2):c.1909G>A (p.Val637Ile)	not specified [RCV004287908]	likely benign	12	62537159	62537159	Human		name
401757953	CV2708046	single nucleotide variant	NM_015026.3(MON2):c.2416A>G (p.Met806Val)	not specified [RCV004309289]	uncertain significance	12	62543148	62543148	Human		name
401750309	CV2715585	single nucleotide variant	NM_015026.3(MON2):c.2401A>G (p.Thr801Ala)	not specified [RCV004326976]	uncertain significance	12	62543133	62543133	Human		name
401764702	CV2721473	single nucleotide variant	NM_015026.3(MON2):c.1937G>A (p.Ser646Asn)	not specified [RCV004322203]	uncertain significance	12	62537187	62537187	Human		name
401780795	CV2723617	single nucleotide variant	NM_015026.3(MON2):c.2063A>G (p.His688Arg)	not specified [RCV004325799]	uncertain significance	12	62537651	62537651	Human		name
401872325	CV2754341	single nucleotide variant	NM_015026.3(MON2):c.2489G>A (p.Arg830Gln)	not specified [RCV004334517]	uncertain significance	12	62544920	62544920	Human		name
401888754	CV2754974	single nucleotide variant	NM_015026.3(MON2):c.1862T>C (p.Val621Ala)	not specified [RCV004341439]	uncertain significance	12	62535671	62535671	Human		name
401892271	CV2777380	single nucleotide variant	NM_015026.3(MON2):c.2566T>C (p.Ser856Pro)	not specified [RCV004354385]	uncertain significance	12	62544997	62544997	Human		name
405720681	CV3358455	single nucleotide variant	NM_015026.3(MON2):c.2418G>A (p.Met806Ile)	not specified [RCV004495143]	uncertain significance	12	62543150	62543150	Human		name
405722295	CV3358660	single nucleotide variant	NM_015026.3(MON2):c.2621A>G (p.Asn874Ser)	not specified [RCV004495348]	likely benign	12	62546940	62546940	Human		name
405674845	CV3358721	single nucleotide variant	NM_015026.3(MON2):c.2825G>C (p.Cys942Ser)	not specified [RCV004487393]	uncertain significance	12	62549739	62549739	Human		name
405674980	CV3358754	single nucleotide variant	NM_015026.3(MON2):c.2982G>C (p.Glu994Asp)	not specified [RCV004487426]	uncertain significance	12	62552946	62552946	Human		name
405702586	CV3361533	single nucleotide variant	NM_015026.3(MON2):c.1055G>A (p.Arg352Gln)	not specified [RCV004492713]	uncertain significance	12	62524585	62524585	Human		name
405703389	CV3361615	single nucleotide variant	NM_015026.3(MON2):c.1318A>G (p.Thr440Ala)	not specified [RCV004492795]	uncertain significance	12	62526020	62526020	Human		name
405720243	CV3361851	single nucleotide variant	NM_015026.3(MON2):c.2030T>C (p.Ile677Thr)	not specified [RCV004495014]	uncertain significance	12	62537618	62537618	Human		name
407495817	CV3453836	single nucleotide variant	NM_015026.3(MON2):c.2417T>A (p.Met806Lys)	not specified [RCV004643316]	uncertain significance	12	62543149	62543149	Human		name
407495823	CV3453837	single nucleotide variant	NM_015026.3(MON2):c.1928T>C (p.Met643Thr)	not specified [RCV004643317]	uncertain significance	12	62537178	62537178	Human		name
407495843	CV3453842	single nucleotide variant	NM_015026.3(MON2):c.2635G>A (p.Asp879Asn)	not specified [RCV004643321]	uncertain significance	12	62546954	62546954	Human		name
407495856	CV3453845	single nucleotide variant	NM_015026.3(MON2):c.2519C>T (p.Thr840Ile)	not specified [RCV004643324]	uncertain significance	12	62544950	62544950	Human		name
407495865	CV3453848	single nucleotide variant	NM_015026.3(MON2):c.1886C>T (p.Thr629Ile)	not specified [RCV004643326]	uncertain significance	12	62535695	62535695	Human		name
407495875	CV3453850	single nucleotide variant	NM_015026.3(MON2):c.2243A>G (p.Asn748Ser)	not specified [RCV004643328]	uncertain significance	12	62538295	62538295	Human		name
597660172	CV3563857	single nucleotide variant	NM_015026.3(MON2):c.1211C>T (p.Pro404Leu)	not specified [RCV004828335]	uncertain significance	12	62525185	62525185	Human		name
597660179	CV3563858	single nucleotide variant	NM_015026.3(MON2):c.1160G>A (p.Arg387His)	not specified [RCV004828336]	uncertain significance	12	62525134	62525134	Human		name
597660197	CV3563861	single nucleotide variant	NM_015026.3(MON2):c.1381G>T (p.Gly461Cys)	not specified [RCV004828339]	uncertain significance	12	62526083	62526083	Human		name
597660205	CV3563862	single nucleotide variant	NM_015026.3(MON2):c.1294A>G (p.Met432Val)	not specified [RCV004828340]	uncertain significance	12	62525996	62525996	Human		name
597637026	CV3563865	single nucleotide variant	NM_015026.3(MON2):c.2818A>G (p.Met940Val)	not specified [RCV004824670]	uncertain significance	12	62549732	62549732	Human		name
598201082	CV3986257	single nucleotide variant	NM_015026.3(MON2):c.1768G>A (p.Ala590Thr)	not specified [RCV005375966]	uncertain significance	12	62535577	62535577	Human		name
156251820	CV2196606	single nucleotide variant	NM_015026.3(MON2):c.4333G>C (p.Val1445Leu)	not specified [RCV004073879]	uncertain significance	12	62571401	62571401	Human		name
156146256	CV2196866	single nucleotide variant	NM_015026.3(MON2):c.4036A>G (p.Ile1346Val)	not specified [RCV004069870]	uncertain significance	12	62565240	62565240	Human		name
156380525	CV2218794	single nucleotide variant	NM_015026.3(MON2):c.3790C>G (p.Leu1264Val)	not specified [RCV004085040]	uncertain significance	12	62560871	62560871	Human		name
156138896	CV2236795	single nucleotide variant	NM_015026.3(MON2):c.4672A>G (p.Ile1558Val)	not specified [RCV004112562]	uncertain significance	12	62580393	62580393	Human		name
155981380	CV2272845	single nucleotide variant	NM_015026.3(MON2):c.4807A>G (p.Ile1603Val)	not specified [RCV004135750]	uncertain significance	12	62585401	62585401	Human		name
156296881	CV2297617	single nucleotide variant	NM_015026.3(MON2):c.4573G>A (p.Glu1525Lys)	not specified [RCV004155314]	uncertain significance	12	62578503	62578503	Human		name
155901856	CV2301337	single nucleotide variant	NM_015026.3(MON2):c.4927A>T (p.Ile1643Leu)	not specified [RCV004160495]	uncertain significance	12	62588093	62588093	Human		name
155976007	CV2328019	single nucleotide variant	NM_015026.3(MON2):c.3973G>A (p.Glu1325Lys)	not specified [RCV004179324]	uncertain significance	12	62561054	62561054	Human		name
156264508	CV2329444	single nucleotide variant	NM_015026.3(MON2):c.4579G>A (p.Val1527Ile)	not specified [RCV004187449]	uncertain significance	12	62580300	62580300	Human		name
329371197	CV2431916	single nucleotide variant	NM_015026.3(MON2):c.5125G>C (p.Ala1709Pro)	not specified [RCV004255048]	uncertain significance	12	62592720	62592720	Human		name
329395045	CV2457793	single nucleotide variant	NM_015026.3(MON2):c.4627A>G (p.Lys1543Glu)	not specified [RCV004269620]	uncertain significance	12	62580348	62580348	Human		name
329398318	CV2465013	single nucleotide variant	NM_015026.3(MON2):c.4865A>C (p.Tyr1622Ser)	not specified [RCV004284918]	uncertain significance	12	62585459	62585459	Human		name
401735595	CV2672693	single nucleotide variant	NM_015026.3(MON2):c.3429G>C (p.Trp1143Cys)	not specified [RCV004287707]	uncertain significance	12	62560510	62560510	Human		name
401757630	CV2675424	single nucleotide variant	NM_015026.3(MON2):c.3835A>G (p.Ile1279Val)	not specified [RCV004292224]	uncertain significance	12	62560916	62560916	Human		name
401760127	CV2694932	single nucleotide variant	NM_015026.3(MON2):c.3290A>G (p.Asn1097Ser)	not specified [RCV004301321]	uncertain significance	12	62556073	62556073	Human		name
405690195	CV3351644	single nucleotide variant	NM_015026.3(MON2):c.4868T>A (p.Ile1623Lys)	not specified [RCV004490594]	uncertain significance	12	62585462	62585462	Human		name
405675197	CV3354855	single nucleotide variant	NM_015026.3(MON2):c.3109C>T (p.Arg1037Cys)	not specified [RCV004487482]	uncertain significance	12	62553073	62553073	Human		name
405675639	CV3354941	single nucleotide variant	NM_015026.3(MON2):c.3452A>T (p.Gln1151Leu)	not specified [RCV004487568]	uncertain significance	12	62560533	62560533	Human		name
405675768	CV3354966	single nucleotide variant	NM_015026.3(MON2):c.3710T>G (p.Leu1237Trp)	not specified [RCV004487593]	uncertain significance	12	62560791	62560791	Human		name
405676442	CV3355106	single nucleotide variant	NM_015026.3(MON2):c.4084G>C (p.Asp1362His)	not specified [RCV004487733]	uncertain significance	12	62565288	62565288	Human		name
405676626	CV3355144	single nucleotide variant	NM_015026.3(MON2):c.4092G>T (p.Leu1364Phe)	not specified [RCV004487771]	uncertain significance	12	62565296	62565296	Human		name
405676784	CV3355175	single nucleotide variant	NM_015026.3(MON2):c.4097C>T (p.Ala1366Val)	not specified [RCV004487802]	uncertain significance	12	62565301	62565301	Human		name
405676948	CV3355207	single nucleotide variant	NM_015026.3(MON2):c.4241T>C (p.Leu1414Ser)	not specified [RCV004487834]	uncertain significance	12	62566368	62566368	Human		name
405689277	CV3355274	single nucleotide variant	NM_015026.3(MON2):c.4537A>C (p.Ile1513Leu)	not specified [RCV004490379]	uncertain significance	12	62578467	62578467	Human		name
407518938	CV3453838	single nucleotide variant	NM_015026.3(MON2):c.4100T>C (p.Phe1367Ser)	not specified [RCV004629057]	uncertain significance	12	62565304	62565304	Human		name
407495827	CV3453839	single nucleotide variant	NM_015026.3(MON2):c.4408C>G (p.Leu1470Val)	not specified [RCV004643318]	uncertain significance	12	62571476	62571476	Human		name
407495837	CV3453841	single nucleotide variant	NM_015026.3(MON2):c.4415T>C (p.Ile1472Thr)	not specified [RCV004643320]	uncertain significance	12	62571483	62571483	Human		name
407518940	CV3453846	single nucleotide variant	NM_015026.3(MON2):c.4444T>G (p.Ser1482Ala)	not specified [RCV004629058]	uncertain significance	12	62571512	62571512	Human		name
407495862	CV3453847	single nucleotide variant	NM_015026.3(MON2):c.4584A>C (p.Gln1528His)	not specified [RCV004643325]	uncertain significance	12	62580305	62580305	Human		name
407495869	CV3453849	single nucleotide variant	NM_015026.3(MON2):c.4589T>C (p.Ile1530Thr)	not specified [RCV004643327]	uncertain significance	12	62580310	62580310	Human		name
407495879	CV3453851	single nucleotide variant	NM_015026.3(MON2):c.4518A>G (p.Ile1506Met)	not specified [RCV004643329]	uncertain significance	12	62578448	62578448	Human		name
597660165	CV3563856	single nucleotide variant	NM_015026.3(MON2):c.4396C>T (p.Leu1466Phe)	not specified [RCV004828334]	uncertain significance	12	62571464	62571464	Human		name
597660186	CV3563859	single nucleotide variant	NM_015026.3(MON2):c.3845C>G (p.Ala1282Gly)	not specified [RCV004828337]	uncertain significance	12	62560926	62560926	Human		name
597660192	CV3563860	single nucleotide variant	NM_015026.3(MON2):c.3697G>A (p.Glu1233Lys)	not specified [RCV004828338]	uncertain significance	12	62560778	62560778	Human		name
597660212	CV3563863	single nucleotide variant	NM_015026.3(MON2):c.3673T>G (p.Ser1225Ala)	not specified [RCV004828341]	uncertain significance	12	62560754	62560754	Human		name
597660218	CV3563864	single nucleotide variant	NM_015026.3(MON2):c.4130A>G (p.Tyr1377Cys)	not specified [RCV004828342]	uncertain significance	12	62565334	62565334	Human		name
597660226	CV3563866	single nucleotide variant	NM_015026.3(MON2):c.3712A>C (p.Asn1238His)	not specified [RCV004828343]	uncertain significance	12	62560793	62560793	Human		name
597660232	CV3563867	single nucleotide variant	NM_015026.3(MON2):c.3155T>C (p.Ile1052Thr)	not specified [RCV004828344]	uncertain significance	12	62553119	62553119	Human		name
598167897	CV3986254	single nucleotide variant	NM_015026.3(MON2):c.3712A>G (p.Asn1238Asp)	not specified [RCV005369606]	uncertain significance	12	62560793	62560793	Human		name
598167902	CV3986258	single nucleotide variant	NM_015026.3(MON2):c.4432C>T (p.Arg1478Trp)	not specified [RCV005369607]	uncertain significance	12	62571500	62571500	Human		name
598167909	CV3986259	single nucleotide variant	NM_015026.3(MON2):c.4715T>C (p.Ile1572Thr)	not specified [RCV005369608]	uncertain significance	12	62585309	62585309	Human		name
598167915	CV3986260	single nucleotide variant	NM_015026.3(MON2):c.3915T>A (p.Ser1305Arg)	not specified [RCV005369609]	uncertain significance	12	62560996	62560996	Human		name
598167921	CV3986261	single nucleotide variant	NM_015026.3(MON2):c.3586C>T (p.Pro1196Ser)	not specified [RCV005369610]	uncertain significance	12	62560667	62560667	Human		name
598201095	CV3986263	single nucleotide variant	NM_015026.3(MON2):c.4498T>A (p.Phe1500Ile)	not specified [RCV005375968]	uncertain significance	12	62571566	62571566	Human		name
598201099	CV3986264	single nucleotide variant	NM_015026.3(MON2):c.3157G>A (p.Gly1053Ser)	not specified [RCV005375969]	uncertain significance	12	62553121	62553121	Human		name

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