Odf2 Variant Search Result - Rat Genome Database

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111 records found for search term Odf2

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
407425007	CV3409301	single nucleotide variant	NM_001351578.2(ODF2):c.830+7T>C	not provided [RCV004585232]	likely benign	9	128471475	128471475	Human		name
156388857	CV2229693	single nucleotide variant	NM_001351578.2(ODF2):c.197G>A (p.Ser66Asn)	not specified [RCV004103499]	uncertain significance	9	128459599	128459599	Human		name
156033099	CV2236156	single nucleotide variant	NM_001351578.2(ODF2):c.131G>A (p.Arg44Lys)	not specified [RCV004114297]	uncertain significance	9	128456222	128456222	Human		name
156272972	CV2333975	single nucleotide variant	NM_001351578.2(ODF2):c.235G>A (p.Ala79Thr)	not specified [RCV004183505]	uncertain significance	9	128459637	128459637	Human		name
155910760	CV2366637	single nucleotide variant	NM_001351578.2(ODF2):c.203C>T (p.Thr68Met)	not specified [RCV004210649]	uncertain significance	9	128459605	128459605	Human		name
401918475	CV2826428	single nucleotide variant	NM_001351578.2(ODF2):c.1200G>A (p.Glu400=)	not provided [RCV003430268]	likely benign	9	128482851	128482851	Human		name
401911151	CV2826429	single nucleotide variant	NM_001351578.2(ODF2):c.2193G>A (p.Ala731=)	not provided [RCV003425800]	likely benign	9	128496073	128496073	Human		name
597732972	CV3577513	single nucleotide variant	NM_001351578.2(ODF2):c.254C>T (p.Thr85Met)	not specified [RCV004843134]	uncertain significance	9	128459656	128459656	Human		name
597732984	CV3577514	single nucleotide variant	NM_001351578.2(ODF2):c.223G>C (p.Ala75Pro)	not specified [RCV004843135]	uncertain significance	9	128459625	128459625	Human		name
597660316	CV3577516	single nucleotide variant	NM_001351578.2(ODF2):c.262A>G (p.Thr88Ala)	not specified [RCV004834907]	uncertain significance	9	128460556	128460556	Human		name
617152796	CV4021002	single nucleotide variant	NM_001351578.2(ODF2):c.2460G>A (p.Glu820=)	not provided [RCV005428755]	likely benign	9	128499036	128499036	Human		name
156249693	CV2273199	single nucleotide variant	NM_001351578.2(ODF2):c.647C>T (p.Ala216Val)	not specified [RCV004138132]	uncertain significance	9	128469331	128469331	Human		name
155906759	CV2279408	single nucleotide variant	NM_001351578.2(ODF2):c.890C>T (p.Ala297Val)	not specified [RCV004141954]	uncertain significance	9	128472972	128472972	Human		name
156132120	CV2280024	single nucleotide variant	NM_001351578.2(ODF2):c.779C>T (p.Thr260Met)	not specified [RCV004146386]	uncertain significance	9	128471417	128471417	Human		name
156103562	CV2291624	single nucleotide variant	NM_001351578.2(ODF2):c.799G>A (p.Glu267Lys)	not specified [RCV004155915]	uncertain significance	9	128471437	128471437	Human		name
156276818	CV2330784	single nucleotide variant	NM_001351578.2(ODF2):c.524C>T (p.Thr175Met)	not specified [RCV004185844]	uncertain significance	9	128469208	128469208	Human		name
155969392	CV2339419	single nucleotide variant	NM_001351578.2(ODF2):c.427C>T (p.Arg143Trp)	not specified [RCV004191635]	uncertain significance	9	128460996	128460996	Human		name
156200556	CV2350864	single nucleotide variant	NM_001351578.2(ODF2):c.959C>T (p.Thr320Ile)	not specified [RCV004211701]	uncertain significance	9	128473041	128473041	Human		name
156275842	CV2351874	single nucleotide variant	NM_001351578.2(ODF2):c.803G>T (p.Arg268Leu)	not specified [RCV004198017]	uncertain significance	9	128471441	128471441	Human		name
156053407	CV2388528	single nucleotide variant	NM_001351578.2(ODF2):c.627G>T (p.Lys209Asn)	not specified [RCV004237379]	uncertain significance	9	128469311	128469311	Human		name
329367476	CV2427314	single nucleotide variant	NM_001351578.2(ODF2):c.988A>C (p.Asn330His)	not specified [RCV004248174]	uncertain significance	9	128473637	128473637	Human		name
401738999	CV2676417	single nucleotide variant	NM_001351578.2(ODF2):c.419G>A (p.Arg140Gln)	not specified [RCV004286438]	uncertain significance	9	128460988	128460988	Human		name
401866633	CV2782900	single nucleotide variant	NM_001351578.2(ODF2):c.865T>C (p.Cys289Arg)	not specified [RCV004361703]	uncertain significance	9	128472947	128472947	Human		name
405734568	CV3370268	single nucleotide variant	NM_001351578.2(ODF2):c.334A>T (p.Ile112Leu)	not specified [RCV004496863]	uncertain significance	9	128460628	128460628	Human		name
405734577	CV3370269	single nucleotide variant	NM_001351578.2(ODF2):c.416G>A (p.Arg139Gln)	not specified [RCV004496864]	uncertain significance	9	128460985	128460985	Human		name
405749978	CV3370270	single nucleotide variant	NM_001351578.2(ODF2):c.691C>G (p.Arg231Gly)	not specified [RCV004498935]	uncertain significance	9	128471329	128471329	Human		name
598160873	CV3998343	single nucleotide variant	NM_001351578.2(ODF2):c.691C>T (p.Arg231Cys)	not specified [RCV005390507]	uncertain significance	9	128471329	128471329	Human		name
598160878	CV3998344	single nucleotide variant	NM_001351578.2(ODF2):c.581A>C (p.Glu194Ala)	not specified [RCV005390508]	uncertain significance	9	128469265	128469265	Human		name
598160894	CV3998347	single nucleotide variant	NM_001351578.2(ODF2):c.347C>T (p.Pro116Leu)	not specified [RCV005390511]	uncertain significance	9	128460641	128460641	Human		name
598160899	CV3998348	single nucleotide variant	NM_001351578.2(ODF2):c.805A>G (p.Met269Val)	not specified [RCV005390512]	uncertain significance	9	128471443	128471443	Human		name
156120916	CV2233813	single nucleotide variant	NM_001351578.2(ODF2):c.2419A>G (p.Arg807Gly)	not specified [RCV004102032]	uncertain significance	9	128498570	128498570	Human		name
156072000	CV2251458	single nucleotide variant	NM_001351578.2(ODF2):c.1054A>T (p.Thr352Ser)	not specified [RCV004117437]	uncertain significance	9	128473703	128473703	Human		name
156238641	CV2268947	single nucleotide variant	NM_001351578.2(ODF2):c.1160A>G (p.Lys387Arg)	not specified [RCV004128351]	uncertain significance	9	128481647	128481647	Human		name
401783627	CV2723780	single nucleotide variant	NM_001351578.2(ODF2):c.1657A>G (p.Thr553Ala)	not specified [RCV004325937]	uncertain significance	9	128487897	128487897	Human		name
401876723	CV2754455	single nucleotide variant	NM_001351578.2(ODF2):c.1368C>A (p.Ser456Arg)	not specified [RCV004336668]	uncertain significance	9	128484715	128484715	Human		name
401898066	CV2780135	single nucleotide variant	NM_001351578.2(ODF2):c.1061G>A (p.Arg354Gln)	not specified [RCV004355791]	uncertain significance	9	128473710	128473710	Human		name
405734537	CV3370264	single nucleotide variant	NM_001351578.2(ODF2):c.1376A>G (p.Gln459Arg)	not specified [RCV004496859]	uncertain significance	9	128484723	128484723	Human		name
405734546	CV3370265	single nucleotide variant	NM_001351578.2(ODF2):c.1537A>G (p.Lys513Glu)	not specified [RCV004496860]	uncertain significance	9	128484884	128484884	Human		name
405734553	CV3370266	single nucleotide variant	NM_001351578.2(ODF2):c.1901T>C (p.Met634Thr)	not specified [RCV004496861]	uncertain significance	9	128492705	128492705	Human		name
405749972	CV3370271	single nucleotide variant	NM_001351578.2(ODF2):c.1052G>A (p.Arg351His)	not specified [RCV004498936]	uncertain significance	9	128473701	128473701	Human		name
407527186	CV3469654	single nucleotide variant	NM_001351578.2(ODF2):c.2122A>G (p.Ile708Val)	not specified [RCV004655090]	uncertain significance	9	128494630	128494630	Human		name
407527189	CV3469655	single nucleotide variant	NM_001351578.2(ODF2):c.1369G>A (p.Gly457Arg)	not specified [RCV004655091]	uncertain significance	9	128484716	128484716	Human		name
407527192	CV3469656	single nucleotide variant	NM_001351578.2(ODF2):c.1064A>G (p.Asp355Gly)	not specified [RCV004655092]	uncertain significance	9	128473713	128473713	Human		name
407527195	CV3469657	single nucleotide variant	NM_001351578.2(ODF2):c.2053A>T (p.Ile685Phe)	not specified [RCV004655093]	uncertain significance	9	128494561	128494561	Human		name
407505397	CV3469658	single nucleotide variant	NM_001351578.2(ODF2):c.1165C>T (p.Arg389Cys)	not specified [RCV004646108]	uncertain significance	9	128482816	128482816	Human		name
597732993	CV3577515	single nucleotide variant	NM_001351578.2(ODF2):c.1166G>A (p.Arg389His)	not specified [RCV004843136]	uncertain significance	9	128482817	128482817	Human		name
598172879	CV3998342	single nucleotide variant	NM_001351578.2(ODF2):c.1756G>A (p.Ala586Thr)	not specified [RCV005393106]	uncertain significance	9	128487996	128487996	Human		name
598160883	CV3998345	single nucleotide variant	NM_001351578.2(ODF2):c.1326G>C (p.Glu442Asp)	not specified [RCV005390509]	uncertain significance	9	128484027	128484027	Human		name
598160889	CV3998346	single nucleotide variant	NM_001351578.2(ODF2):c.1831G>A (p.Glu611Lys)	not specified [RCV005390510]	uncertain significance	9	128492471	128492471	Human		name
15159091	CV700807	single nucleotide variant	NM_001351578.2(ODF2):c.2378C>G (p.Thr793Ser)	not provided [RCV000947204]	benign	9	128498529	128498529	Human		name
15129194	CV751412	single nucleotide variant	NM_001351578.2(ODF2):c.2662G>A (p.Ala888Thr)	not provided [RCV000919784]\|not specified [RCV004029446]	likely benign\|uncertain significance	9	128500178	128500178	Human		name
401748555	CV2698408	single nucleotide variant	NM_001366781.1(ODF2L):c.1806+664C>T	not specified [RCV004304940]	uncertain significance	1	86352195	86352195	Human		name
401892862	CV2758150	single nucleotide variant	NM_001366781.1(ODF2L):c.74A>G (p.Glu25Gly)	not specified [RCV004341526]	uncertain significance	1	86386954	86386954	Human		name
156382688	CV2223591	single nucleotide variant	NM_001366781.1(ODF2L):c.251A>G (p.Asn84Ser)	not specified [RCV004091943]	uncertain significance	1	86384797	86384797	Human		name
597733017	CV3577519	single nucleotide variant	NM_001366781.1(ODF2L):c.103C>T (p.His35Tyr)	not specified [RCV004843138]	uncertain significance	1	86386925	86386925	Human		name
598160911	CV3998350	single nucleotide variant	NM_001366781.1(ODF2L):c.151G>A (p.Glu51Lys)	not specified [RCV005390514]	uncertain significance	1	86385553	86385553	Human		name
15167717	CV707552	single nucleotide variant	NM_001366781.1(ODF2L):c.1332G>A (p.Thr444=)	not provided [RCV000971457]	benign	1	86356543	86356543	Human		name
155993580	CV2252301	single nucleotide variant	NM_001366781.1(ODF2L):c.928A>G (p.Ile310Val)	not specified [RCV004116161]	uncertain significance	1	86371146	86371146	Human		name
156246118	CV2276716	single nucleotide variant	NM_001366781.1(ODF2L):c.685A>G (p.Ile229Val)	not specified [RCV004146506]	likely benign	1	86376358	86376358	Human		name
156038569	CV2278942	single nucleotide variant	NM_001366781.1(ODF2L):c.575A>G (p.Gln192Arg)	not specified [RCV004145635]	uncertain significance	1	86382291	86382291	Human		name
156190413	CV2301728	single nucleotide variant	NM_001366781.1(ODF2L):c.821T>G (p.Leu274Trp)	not specified [RCV004156546]	uncertain significance	1	86372530	86372530	Human		name
156178784	CV2327613	single nucleotide variant	NM_001366781.1(ODF2L):c.980G>A (p.Cys327Tyr)	not specified [RCV004177198]	uncertain significance	1	86371094	86371094	Human		name
155930250	CV2366638	single nucleotide variant	NM_001366781.1(ODF2L):c.857G>A (p.Ser286Asn)	not specified [RCV004210650]	uncertain significance	1	86372494	86372494	Human		name
329398948	CV2428574	single nucleotide variant	NM_001366781.1(ODF2L):c.845A>G (p.Asn282Ser)	not specified [RCV004255385]	uncertain significance	1	86372506	86372506	Human		name
329380159	CV2444244	single nucleotide variant	NM_001366781.1(ODF2L):c.806A>G (p.Asp269Gly)	not specified [RCV004263014]	uncertain significance	1	86376237	86376237	Human		name
401782417	CV2686828	single nucleotide variant	NM_001366781.1(ODF2L):c.595G>A (p.Glu199Lys)	not specified [RCV004302008]	uncertain significance	1	86382271	86382271	Human		name
401772897	CV2720403	single nucleotide variant	NM_001366781.1(ODF2L):c.739A>C (p.Lys247Gln)	not specified [RCV004325707]	uncertain significance	1	86376304	86376304	Human		name
401877350	CV2764604	single nucleotide variant	NM_001366781.1(ODF2L):c.677A>G (p.Asn226Ser)	not specified [RCV004340981]	uncertain significance	1	86376366	86376366	Human		name
405749931	CV3370277	single nucleotide variant	NM_001366781.1(ODF2L):c.529C>T (p.Arg177Cys)	not specified [RCV004498942]	uncertain significance	1	86382337	86382337	Human		name
405749925	CV3370278	single nucleotide variant	NM_001366781.1(ODF2L):c.812A>T (p.Glu271Val)	not specified [RCV004498943]	uncertain significance	1	86372539	86372539	Human		name
405749920	CV3370279	single nucleotide variant	NM_001366781.1(ODF2L):c.813A>T (p.Glu271Asp)	not specified [RCV004498944]	uncertain significance	1	86372538	86372538	Human		name
405749910	CV3370280	single nucleotide variant	NM_001366781.1(ODF2L):c.914T>C (p.Met305Thr)	not specified [RCV004498945]	uncertain significance	1	86372437	86372437	Human		name
405749903	CV3370281	single nucleotide variant	NM_001366781.1(ODF2L):c.949A>G (p.Lys317Glu)	not specified [RCV004498946]	uncertain significance	1	86371125	86371125	Human		name
405749899	CV3370282	single nucleotide variant	NM_001366781.1(ODF2L):c.980G>T (p.Cys327Phe)	not specified [RCV004498947]	uncertain significance	1	86371094	86371094	Human		name
407505407	CV3469662	single nucleotide variant	NM_001366781.1(ODF2L):c.353G>A (p.Arg118Lys)	not specified [RCV004646111]	uncertain significance	1	86384695	86384695	Human		name
597733026	CV3577521	single nucleotide variant	NM_001366781.1(ODF2L):c.601G>A (p.Asp201Asn)	not specified [RCV004843139]	likely benign	1	86382265	86382265	Human		name
597733036	CV3577522	single nucleotide variant	NM_001366781.1(ODF2L):c.346C>G (p.Leu116Val)	not specified [RCV004843140]	uncertain significance	1	86384702	86384702	Human		name
598160906	CV3998349	single nucleotide variant	NM_001366781.1(ODF2L):c.368A>G (p.Lys123Arg)	not specified [RCV005390513]	uncertain significance	1	86384680	86384680	Human		name
598172896	CV3998353	single nucleotide variant	NM_001366781.1(ODF2L):c.320A>G (p.Lys107Arg)	not specified [RCV005393108]	uncertain significance	1	86384728	86384728	Human		name
598160922	CV3998354	single nucleotide variant	NM_001366781.1(ODF2L):c.762C>G (p.Asp254Glu)	not specified [RCV005390516]	likely benign	1	86376281	86376281	Human		name
598172903	CV3998355	single nucleotide variant	NM_001366781.1(ODF2L):c.298A>T (p.Ile100Leu)	not specified [RCV005393109]	uncertain significance	1	86384750	86384750	Human		name
15194866	CV746662	single nucleotide variant	NM_001366781.1(ODF2L):c.882A>T (p.Glu294Asp)	not provided [RCV000911246]	likely benign	1	86372469	86372469	Human		name
156256134	CV2219732	single nucleotide variant	NM_001366781.1(ODF2L):c.1045A>G (p.Thr349Ala)	not specified [RCV004095432]	uncertain significance	1	86371029	86371029	Human		name
156033457	CV2236260	single nucleotide variant	NM_001366781.1(ODF2L):c.1847A>G (p.Asn616Ser)	not specified [RCV004107960]	uncertain significance	1	86348838	86348838	Human		name
156276544	CV2255810	single nucleotide variant	NM_001366781.1(ODF2L):c.1027A>G (p.Thr343Ala)	not specified [RCV004121974]	uncertain significance	1	86371047	86371047	Human		name
156161215	CV2323430	single nucleotide variant	NM_001366781.1(ODF2L):c.1862C>T (p.Ser621Leu)	not specified [RCV004165650]	uncertain significance	1	86348823	86348823	Human		name
156276218	CV2330737	single nucleotide variant	NM_001366781.1(ODF2L):c.1475A>G (p.Glu492Gly)	not specified [RCV004185801]	uncertain significance	1	86354816	86354816	Human		name
156069386	CV2341121	single nucleotide variant	NM_001366781.1(ODF2L):c.1711A>G (p.Arg571Gly)	not specified [RCV004181599]	uncertain significance	1	86352954	86352954	Human		name
155975504	CV2342672	single nucleotide variant	NM_001366781.1(ODF2L):c.1798A>G (p.Met600Val)	not specified [RCV004196754]	uncertain significance	1	86352867	86352867	Human		name
155997510	CV2398724	single nucleotide variant	NM_001366781.1(ODF2L):c.1290G>T (p.Glu430Asp)	not specified [RCV004240063]	uncertain significance	1	86356585	86356585	Human		name
329399336	CV2446782	single nucleotide variant	NM_001366781.1(ODF2L):c.1142C>A (p.Thr381Asn)	not specified [RCV004257645]	uncertain significance	1	86360451	86360451	Human		name
329372743	CV2451633	single nucleotide variant	NM_001366781.1(ODF2L):c.1179G>T (p.Leu393Phe)	not specified [RCV004274553]	uncertain significance	1	86358880	86358880	Human		name
401780357	CV2726013	single nucleotide variant	NM_001366781.1(ODF2L):c.1396G>A (p.Asp466Asn)	not specified [RCV004324374]	uncertain significance	1	86356479	86356479	Human		name
405749965	CV3370272	single nucleotide variant	NM_001366781.1(ODF2L):c.1036C>G (p.Leu346Val)	not specified [RCV004498937]	uncertain significance	1	86371038	86371038	Human		name
405749959	CV3370273	single nucleotide variant	NM_001366781.1(ODF2L):c.1127A>G (p.Glu376Gly)	not specified [RCV004498938]	uncertain significance	1	86360466	86360466	Human		name
405749951	CV3370274	single nucleotide variant	NM_001366781.1(ODF2L):c.1352A>C (p.His451Pro)	not specified [RCV004498939]	uncertain significance	1	86356523	86356523	Human		name
405749938	CV3370276	single nucleotide variant	NM_001366781.1(ODF2L):c.1738T>A (p.Leu580Ile)	not specified [RCV004498941]	uncertain significance	1	86352927	86352927	Human		name
407527198	CV3469659	single nucleotide variant	NM_001366781.1(ODF2L):c.1134A>T (p.Lys378Asn)	not specified [RCV004655094]	likely benign	1	86360459	86360459	Human		name
407505400	CV3469660	single nucleotide variant	NM_001366781.1(ODF2L):c.1789G>T (p.Val597Phe)	not specified [RCV004646109]	uncertain significance	1	86352876	86352876	Human		name
407505404	CV3469661	single nucleotide variant	NM_001366781.1(ODF2L):c.1082A>G (p.Glu361Gly)	not specified [RCV004646110]	uncertain significance	1	86360511	86360511	Human		name
407527201	CV3469663	single nucleotide variant	NM_001366781.1(ODF2L):c.1679A>C (p.Lys560Thr)	not specified [RCV004655095]	uncertain significance	1	86354531	86354531	Human		name
407527204	CV3469664	single nucleotide variant	NM_001366781.1(ODF2L):c.1165C>G (p.Gln389Glu)	not specified [RCV004655096]	uncertain significance	1	86360428	86360428	Human		name
597660312	CV3577517	single nucleotide variant	NM_001366781.1(ODF2L):c.1337C>T (p.Ala446Val)	not specified [RCV004834908]	uncertain significance	1	86356538	86356538	Human		name
597733006	CV3577518	single nucleotide variant	NM_001366781.1(ODF2L):c.1258A>C (p.Lys420Gln)	not specified [RCV004843137]	uncertain significance	1	86358801	86358801	Human		name
597660170	CV3577520	single nucleotide variant	NM_001366781.1(ODF2L):c.1669G>C (p.Gly557Arg)	not specified [RCV004834909]	uncertain significance	1	86354541	86354541	Human		name
597733047	CV3577523	single nucleotide variant	NM_001366781.1(ODF2L):c.1430A>T (p.Gln477Leu)	not specified [RCV004843141]	uncertain significance	1	86356445	86356445	Human		name
597733058	CV3577524	single nucleotide variant	NM_001366781.1(ODF2L):c.1249A>C (p.Thr417Pro)	not specified [RCV004843142]	uncertain significance	1	86358810	86358810	Human		name
598172889	CV3998351	single nucleotide variant	NM_001366781.1(ODF2L):c.1747G>C (p.Glu583Gln)	not specified [RCV005393107]	uncertain significance	1	86352918	86352918	Human		name
598160916	CV3998352	single nucleotide variant	NM_001366781.1(ODF2L):c.1343G>A (p.Arg448Gln)	not specified [RCV005390515]	likely benign	1	86356532	86356532	Human		name
15179812	CV707553	single nucleotide variant	NM_001366781.1(ODF2L):c.1246A>G (p.Lys416Glu)	not provided [RCV000974000]	benign	1	86358813	86358813	Human		name
15161667	CV732627	single nucleotide variant	NM_001366781.1(ODF2L):c.1313G>A (p.Arg438His)	not provided [RCV000903393]	benign	1	86356562	86356562	Human		name

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