Fam186b Variant Search Result - Rat Genome Database

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152 records found for search term Fam186b

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
150485083	CV1250154	single nucleotide variant	NM_032130.3(FAM186B):c.-15A>G	not provided [RCV001673767]	benign	12	49605492	49605492	Human		name
152165777	CV1612667	single nucleotide variant	NM_032130.3(FAM186B):c.323-5T>G	not provided [RCV002160515]	benign\|likely benign	12	49603372	49603372	Human		name
13704944	CV539149	single nucleotide variant	NM_032130.3(FAM186B):c.506-2A>G	Nephronophthisis [RCV000662275]	likely pathogenic	12	49601136	49601136	Human	2	name
152105190	CV1572414	single nucleotide variant	NM_032130.3(FAM186B):c.323-18C>A	not provided [RCV002152307]	benign	12	49603385	49603385	Human		name
156365764	CV2010719	single nucleotide variant	NM_032130.3(FAM186B):c.2364+6C>T	not provided [RCV002676548]	uncertain significance	12	49598749	49598749	Human		name
156175540	CV2022966	single nucleotide variant	NM_032130.3(FAM186B):c.2534+5G>A	not provided [RCV002765451]	uncertain significance	12	49588449	49588449	Human		name
150454156	CV1232222	single nucleotide variant	NM_032130.3(FAM186B):c.2171+80A>G	not provided [RCV001648235]	benign	12	49599389	49599389	Human		name
156290613	CV2155180	single nucleotide variant	NM_032130.3(FAM186B):c.2364+13C>T	not provided [RCV003009954]	likely benign	12	49598742	49598742	Human		name
150494892	CV1267430	single nucleotide variant	NM_032130.3(FAM186B):c.2535-187A>G	not provided [RCV001688458]	benign	12	49587939	49587939	Human		name
8654035	CV130610	single nucleotide variant	NM_032130.2(FAM186B):c.2364+1913T>C	Lung cancer [RCV000111097]	uncertain significance	12	49596842	49596842	Human		name
156326373	CV2098321	single nucleotide variant	NM_032130.3(FAM186B):c.87G>A (p.Arg29=)	not provided [RCV002899654]	benign	12	49605391	49605391	Human		name
156058223	CV2008108	single nucleotide variant	NM_032130.3(FAM186B):c.105T>C (p.Ser35=)	not provided [RCV002705294]	likely benign	12	49604530	49604530	Human		name
405199643	CV3041116	single nucleotide variant	NM_032130.3(FAM186B):c.114C>G (p.Leu38=)	not provided [RCV003707318]	likely benign	12	49604521	49604521	Human		name
597738995	CV3665363	single nucleotide variant	NM_032130.3(FAM186B):c.20C>A (p.Pro7Gln)	not specified [RCV004921149]	uncertain significance	12	49605458	49605458	Human		name
152084117	CV1554841	single nucleotide variant	NM_032130.3(FAM186B):c.804G>A (p.Ala268=)	not provided [RCV002211810]	likely benign	12	49600836	49600836	Human		name
156269641	CV2026835	single nucleotide variant	NM_032130.3(FAM186B):c.312G>A (p.Leu104=)	not provided [RCV002746593]	uncertain significance	12	49604323	49604323	Human		name
156313452	CV2120170	single nucleotide variant	NM_032130.3(FAM186B):c.86G>A (p.Arg29Gln)	not provided [RCV002962753]	uncertain significance	12	49605392	49605392	Human		name
597852055	CV3737598	single nucleotide variant	NM_032130.3(FAM186B):c.684G>T (p.Gly228=)	not provided [RCV005066371]	likely benign	12	49600956	49600956	Human		name
597929403	CV3789179	single nucleotide variant	NM_032130.3(FAM186B):c.384C>T (p.Asp128=)	not provided [RCV005131460]	likely benign	12	49603306	49603306	Human		name
597952779	CV3798833	single nucleotide variant	NM_032130.3(FAM186B):c.630G>A (p.Ser210=)	not provided [RCV005136407]	likely benign	12	49601010	49601010	Human		name
15192879	CV738688	single nucleotide variant	NM_032130.3(FAM186B):c.882G>A (p.Leu294=)	not provided [RCV000910674]	benign	12	49600758	49600758	Human		name
152027822	CV1521056	single nucleotide variant	NM_032130.3(FAM186B):c.1927C>A (p.Arg643=)	not provided [RCV002085257]	likely benign	12	49599713	49599713	Human		name
152085162	CV1645157	single nucleotide variant	NM_032130.3(FAM186B):c.1410G>A (p.Gln470=)	not provided [RCV002131333]	likely benign	12	49600230	49600230	Human		name
156358340	CV1904083	single nucleotide variant	NM_032130.3(FAM186B):c.281A>T (p.Glu94Val)	not provided [RCV002581550]	uncertain significance	12	49604354	49604354	Human		name
156170424	CV2016114	single nucleotide variant	NM_032130.3(FAM186B):c.2157C>G (p.Arg719=)	not provided [RCV002710468]	likely benign	12	49599483	49599483	Human		name
155915024	CV2091675	single nucleotide variant	NM_032130.3(FAM186B):c.2592C>T (p.Tyr864=)	not provided [RCV002903027]	benign	12	49587695	49587695	Human		name
156224904	CV2203007	single nucleotide variant	NM_032130.3(FAM186B):c.107C>T (p.Thr36Ile)	not specified [RCV004069261]	uncertain significance	12	49604528	49604528	Human		name
156240381	CV2213614	single nucleotide variant	NM_032130.3(FAM186B):c.156C>A (p.Phe52Leu)	not specified [RCV004089700]	uncertain significance	12	49604479	49604479	Human		name
405116182	CV2951683	single nucleotide variant	NM_032130.3(FAM186B):c.163G>T (p.Glu55Ter)	not provided [RCV003670973]	uncertain significance	12	49604472	49604472	Human		name
405178308	CV3027548	single nucleotide variant	NM_032130.3(FAM186B):c.1038C>T (p.Thr346=)	not provided [RCV003705292]	likely benign	12	49600602	49600602	Human		name
405745007	CV3260165	single nucleotide variant	NM_032130.3(FAM186B):c.274A>G (p.Met92Val)	not specified [RCV004381120]	uncertain significance	12	49604361	49604361	Human		name
597739017	CV3665368	single nucleotide variant	NM_032130.3(FAM186B):c.151C>T (p.Arg51Cys)	not specified [RCV004921154]	uncertain significance	12	49604484	49604484	Human		name
597960420	CV3756204	single nucleotide variant	NM_032130.3(FAM186B):c.2109C>T (p.Gly703=)	not provided [RCV005081521]	likely benign	12	49599531	49599531	Human		name
597943175	CV3847431	single nucleotide variant	NM_032130.3(FAM186B):c.1392T>C (p.Ser464=)	not provided [RCV005188350]	likely benign	12	49600248	49600248	Human		name
15158968	CV713558	single nucleotide variant	NM_032130.3(FAM186B):c.1281G>A (p.Lys427=)	not provided [RCV000969623]	benign	12	49600359	49600359	Human		name
150461112	CV1234736	single nucleotide variant	NM_032130.3(FAM186B):c.765G>C (p.Arg255Ser)	not provided [RCV001649318]	benign	12	49600875	49600875	Human		name
151746655	CV1462262	single nucleotide variant	NM_032130.3(FAM186B):c.977G>A (p.Gly326Asp)	not provided [RCV001968718]	uncertain significance	12	49600663	49600663	Human		name
152147569	CV1618721	single nucleotide variant	NM_032130.3(FAM186B):c.321G>C (p.Trp107Cys)	not provided [RCV002121287]	benign	12	49604314	49604314	Human		name
152134443	CV1645961	single nucleotide variant	NM_032130.3(FAM186B):c.385G>A (p.Glu129Lys)	not provided [RCV002177236]	likely benign	12	49603305	49603305	Human		name
152091841	CV1662294	single nucleotide variant	NM_032130.3(FAM186B):c.638C>T (p.Thr213Met)	not provided [RCV002132141]	benign	12	49601002	49601002	Human		name
156352051	CV1965521	single nucleotide variant	NM_032130.3(FAM186B):c.707T>G (p.Met236Arg)	not provided [RCV002581133]	uncertain significance	12	49600933	49600933	Human		name
156298305	CV2075727	single nucleotide variant	NM_032130.3(FAM186B):c.702G>T (p.Arg234Ser)	not provided [RCV002857045]	uncertain significance	12	49600938	49600938	Human		name
156103290	CV2099372	single nucleotide variant	NM_032130.3(FAM186B):c.416C>T (p.Pro139Leu)	not provided [RCV002913486]	likely benign	12	49603274	49603274	Human		name
156315682	CV2130332	single nucleotide variant	NM_032130.3(FAM186B):c.325G>A (p.Asp109Asn)	not provided [RCV002962888]	likely benign	12	49603365	49603365	Human		name
156064390	CV2200158	single nucleotide variant	NM_032130.3(FAM186B):c.663C>A (p.Asp221Glu)	not specified [RCV004069728]	uncertain significance	12	49600977	49600977	Human		name
156380252	CV2208036	single nucleotide variant	NM_032130.3(FAM186B):c.886C>G (p.Gln296Glu)	not specified [RCV004086732]	uncertain significance	12	49600754	49600754	Human		name
156093950	CV2213254	single nucleotide variant	NM_032130.3(FAM186B):c.803C>T (p.Ala268Val)	not provided [RCV005099508]\|not specified [RCV004085473]	uncertain significance	12	49600837	49600837	Human		name
156335144	CV2272762	single nucleotide variant	NM_032130.3(FAM186B):c.890T>C (p.Val297Ala)	not specified [RCV004135683]	uncertain significance	12	49600750	49600750	Human		name
156259155	CV2304924	single nucleotide variant	NM_032130.3(FAM186B):c.394G>C (p.Glu132Gln)	not specified [RCV004168834]	uncertain significance	12	49603296	49603296	Human		name
329399561	CV2443255	single nucleotide variant	NM_032130.3(FAM186B):c.305G>A (p.Arg102His)	not specified [RCV004260062]	likely benign	12	49604330	49604330	Human		name
329391918	CV2463763	single nucleotide variant	NM_032130.3(FAM186B):c.952C>G (p.Leu318Val)	not specified [RCV004279599]	uncertain significance	12	49600688	49600688	Human		name
401771260	CV2675518	single nucleotide variant	NM_032130.3(FAM186B):c.514C>T (p.Arg172Cys)	not specified [RCV004295135]	uncertain significance	12	49601126	49601126	Human		name
401783327	CV2716287	single nucleotide variant	NM_032130.3(FAM186B):c.731A>G (p.Asn244Ser)	not specified [RCV004325289]	uncertain significance	12	49600909	49600909	Human		name
401779357	CV2718514	single nucleotide variant	NM_032130.3(FAM186B):c.542G>A (p.Arg181Lys)	not specified [RCV004318321]	likely benign	12	49601098	49601098	Human		name
401757390	CV2734991	single nucleotide variant	NM_032130.3(FAM186B):c.498G>T (p.Arg166Ser)	not specified [RCV004333695]	uncertain significance	12	49603192	49603192	Human		name
405745014	CV3260166	single nucleotide variant	NM_032130.3(FAM186B):c.545G>A (p.Ser182Asn)	not specified [RCV004381121]	uncertain significance	12	49601095	49601095	Human		name
405745021	CV3260167	single nucleotide variant	NM_032130.3(FAM186B):c.655C>T (p.Leu219Phe)	not specified [RCV004381122]	uncertain significance	12	49600985	49600985	Human		name
405745031	CV3260168	single nucleotide variant	NM_032130.3(FAM186B):c.745C>T (p.Leu249Phe)	not specified [RCV004381123]	uncertain significance	12	49600895	49600895	Human		name
407508500	CV3435627	single nucleotide variant	NM_032130.3(FAM186B):c.631G>A (p.Glu211Lys)	not specified [RCV004625432]	uncertain significance	12	49601009	49601009	Human		name
597739025	CV3665370	single nucleotide variant	NM_032130.3(FAM186B):c.779A>G (p.Lys260Arg)	not specified [RCV004921156]	uncertain significance	12	49600861	49600861	Human		name
597739030	CV3665371	single nucleotide variant	NM_032130.3(FAM186B):c.326A>C (p.Asp109Ala)	not specified [RCV004921157]	uncertain significance	12	49603364	49603364	Human		name
597739035	CV3665372	single nucleotide variant	NM_032130.3(FAM186B):c.361G>A (p.Glu121Lys)	not specified [RCV004921158]	uncertain significance	12	49603329	49603329	Human		name
597889302	CV3739390	single nucleotide variant	NM_032130.3(FAM186B):c.595C>G (p.Leu199Val)	not provided [RCV005070937]	uncertain significance	12	49601045	49601045	Human		name
597970124	CV3821950	single nucleotide variant	NM_032130.3(FAM186B):c.823C>T (p.Gln275Ter)	not provided [RCV005166413]	uncertain significance	12	49600817	49600817	Human		name
597940331	CV3836661	deletion	NM_032130.3(FAM186B):c.1969del (p.Ile657fs)	not provided [RCV005187682]	uncertain significance	12	49599671	49599671	Human		name
598195104	CV3962150	single nucleotide variant	NM_032130.3(FAM186B):c.904G>A (p.Gly302Arg)	not specified [RCV005335515]	uncertain significance	12	49600736	49600736	Human		name
598226008	CV3962153	single nucleotide variant	NM_032130.3(FAM186B):c.964C>G (p.Gln322Glu)	not specified [RCV005341543]	uncertain significance	12	49600676	49600676	Human		name
15180473	CV738687	deletion	NM_032130.3(FAM186B):c.1603del (p.Val535fs)	not provided [RCV000907362]	likely benign	12	49600037	49600037	Human		name
150434706	CV1215956	single nucleotide variant	NM_032130.3(FAM186B):c.1745G>A (p.Arg582Gln)	not provided [RCV001609145]	benign	12	49599895	49599895	Human		name
150501300	CV1223669	single nucleotide variant	NM_032130.3(FAM186B):c.1657G>C (p.Glu553Gln)	not provided [RCV001620790]	benign	12	49599983	49599983	Human		name
151723483	CV1414156	single nucleotide variant	NM_032130.3(FAM186B):c.1777C>T (p.His593Tyr)	not provided [RCV002020495]	uncertain significance	12	49599863	49599863	Human		name
151883242	CV1443415	single nucleotide variant	NM_032130.3(FAM186B):c.1868G>A (p.Arg623His)	not provided [RCV002037300]	uncertain significance	12	49599772	49599772	Human		name
151797838	CV1467807	single nucleotide variant	NM_032130.3(FAM186B):c.1867C>T (p.Arg623Cys)	not provided [RCV001952641]\|not specified [RCV004041989]	uncertain significance	12	49599773	49599773	Human		name
151753214	CV1508963	single nucleotide variant	NM_032130.3(FAM186B):c.2374G>T (p.Glu792Ter)	not provided [RCV002043504]	uncertain significance	12	49588614	49588614	Human		name
152114602	CV1537360	single nucleotide variant	NM_032130.3(FAM186B):c.2556G>C (p.Glu852Asp)	not provided [RCV002134934]	benign	12	49587731	49587731	Human		name
152084680	CV1554936	single nucleotide variant	NM_032130.3(FAM186B):c.2452C>T (p.Arg818Trp)	not provided [RCV002211882]	benign	12	49588536	49588536	Human		name
152118904	CV1600737	single nucleotide variant	NM_032130.3(FAM186B):c.2529G>A (p.Met843Ile)	not provided [RCV002154002]	likely benign	12	49588459	49588459	Human		name
152131949	CV1604670	single nucleotide variant	NM_032130.3(FAM186B):c.1369T>G (p.Phe457Val)	not provided [RCV002099608]	benign	12	49600271	49600271	Human		name
152034261	CV1610555	single nucleotide variant	NM_032130.3(FAM186B):c.2533C>T (p.Arg845Cys)	not provided [RCV002125069]	benign	12	49588455	49588455	Human		name
152073331	CV1633276	single nucleotide variant	NM_032130.3(FAM186B):c.2507G>A (p.Arg836Gln)	not provided [RCV002129884]	benign	12	49588481	49588481	Human		name
156362125	CV1905047	single nucleotide variant	NM_032130.3(FAM186B):c.1729G>A (p.Val577Met)	not provided [RCV002602574]\|not specified [RCV004068768]	uncertain significance	12	49599911	49599911	Human		name
156068256	CV1927985	single nucleotide variant	NM_032130.3(FAM186B):c.1204G>A (p.Ala402Thr)	not provided [RCV002638515]\|not specified [RCV004072070]	uncertain significance	12	49600436	49600436	Human		name
156440292	CV1946653	single nucleotide variant	NM_032130.3(FAM186B):c.2326C>T (p.Arg776Ter)	not provided [RCV003110323]	uncertain significance	12	49598793	49598793	Human		name
156018257	CV2044258	single nucleotide variant	NM_032130.3(FAM186B):c.1607A>G (p.Gln536Arg)	not provided [RCV002795456]	uncertain significance	12	49600033	49600033	Human		name
156157156	CV2063378	single nucleotide variant	NM_032130.3(FAM186B):c.1429G>A (p.Glu477Lys)	not provided [RCV002851074]	uncertain significance	12	49600211	49600211	Human		name
156244354	CV2105532	single nucleotide variant	NM_032130.3(FAM186B):c.2135A>G (p.His712Arg)	not provided [RCV002933318]	uncertain significance	12	49599505	49599505	Human		name
156080850	CV2138181	single nucleotide variant	NM_032130.3(FAM186B):c.2528T>C (p.Met843Thr)	not provided [RCV002979255]	likely benign	12	49588460	49588460	Human		name
156258485	CV2204664	single nucleotide variant	NM_032130.3(FAM186B):c.1418C>G (p.Ser473Cys)	not specified [RCV004081768]	uncertain significance	12	49600222	49600222	Human		name
156037593	CV2218641	single nucleotide variant	NM_032130.3(FAM186B):c.2626C>T (p.Arg876Trp)	not specified [RCV004090896]	likely benign	12	49587661	49587661	Human		name
156333519	CV2220846	single nucleotide variant	NM_032130.3(FAM186B):c.1890G>T (p.Lys630Asn)	not specified [RCV004092277]	uncertain significance	12	49599750	49599750	Human		name
155975794	CV2270110	single nucleotide variant	NM_032130.3(FAM186B):c.1418C>T (p.Ser473Phe)	not specified [RCV004129066]	uncertain significance	12	49600222	49600222	Human		name
156070039	CV2295782	single nucleotide variant	NM_032130.3(FAM186B):c.1087A>G (p.Lys363Glu)	not specified [RCV004151708]	likely benign	12	49600553	49600553	Human		name
156066220	CV2317823	single nucleotide variant	NM_032130.3(FAM186B):c.2022G>T (p.Gln674His)	not specified [RCV004175065]	uncertain significance	12	49599618	49599618	Human		name
156357476	CV2318305	single nucleotide variant	NM_032130.3(FAM186B):c.1566T>A (p.Asn522Lys)	not specified [RCV004179473]	likely benign	12	49600074	49600074	Human		name
156176329	CV2327096	single nucleotide variant	NM_032130.3(FAM186B):c.1966A>G (p.Asn656Asp)	not specified [RCV004178673]	uncertain significance	12	49599674	49599674	Human		name
156331274	CV2339613	single nucleotide variant	NM_032130.3(FAM186B):c.2029A>G (p.Ser677Gly)	not provided [RCV005099915]\|not specified [RCV004196323]	uncertain significance	12	49599611	49599611	Human		name
156085641	CV2340810	single nucleotide variant	NM_032130.3(FAM186B):c.1771A>T (p.Arg591Trp)	not specified [RCV004188170]	uncertain significance	12	49599869	49599869	Human		name
156120868	CV2354208	single nucleotide variant	NM_032130.3(FAM186B):c.1231G>A (p.Glu411Lys)	not specified [RCV004206636]	likely benign	12	49600409	49600409	Human		name
156246918	CV2357018	single nucleotide variant	NM_032130.3(FAM186B):c.1741A>G (p.Ser581Gly)	not specified [RCV004206823]	uncertain significance	12	49599899	49599899	Human		name
156085047	CV2366127	single nucleotide variant	NM_032130.3(FAM186B):c.1744C>T (p.Arg582Trp)	not specified [RCV004210161]	uncertain significance	12	49599896	49599896	Human		name
155990897	CV2372111	single nucleotide variant	NM_032130.3(FAM186B):c.1508G>T (p.Arg503Leu)	not specified [RCV004221769]	uncertain significance	12	49600132	49600132	Human		name
156041175	CV2384417	single nucleotide variant	NM_032130.3(FAM186B):c.2411C>T (p.Ser804Leu)	not specified [RCV004229835]	uncertain significance	12	49588577	49588577	Human		name
329374122	CV2434706	single nucleotide variant	NM_032130.3(FAM186B):c.2597T>C (p.Ile866Thr)	not provided [RCV003720779]\|not specified [RCV004248419]	uncertain significance	12	49587690	49587690	Human		name
329400227	CV2440787	single nucleotide variant	NM_032130.3(FAM186B):c.2066G>A (p.Arg689His)	not specified [RCV004258730]	uncertain significance	12	49599574	49599574	Human		name
329362071	CV2456711	single nucleotide variant	NM_032130.3(FAM186B):c.2219C>T (p.Ser740Phe)	not specified [RCV004277878]	uncertain significance	12	49598900	49598900	Human		name
401730812	CV2677352	single nucleotide variant	NM_032130.3(FAM186B):c.2660G>A (p.Arg887Gln)	not specified [RCV004289060]	uncertain significance	12	49587627	49587627	Human		name
401736535	CV2689367	single nucleotide variant	NM_032130.3(FAM186B):c.1958C>T (p.Ser653Phe)	not specified [RCV004306188]	uncertain significance	12	49599682	49599682	Human		name
401782069	CV2719161	single nucleotide variant	NM_032130.3(FAM186B):c.1093G>A (p.Glu365Lys)	not specified [RCV004324825]	uncertain significance	12	49600547	49600547	Human		name
401888571	CV2757716	single nucleotide variant	NM_032130.3(FAM186B):c.1595G>A (p.Arg532Gln)	not specified [RCV004336869]	likely benign	12	49600045	49600045	Human		name
401885241	CV2759653	single nucleotide variant	NM_032130.3(FAM186B):c.1466G>A (p.Arg489Gln)	not specified [RCV004338619]	uncertain significance	12	49600174	49600174	Human		name
401886183	CV2774592	single nucleotide variant	NM_032130.3(FAM186B):c.1928G>A (p.Arg643Gln)	not specified [RCV004350066]	likely benign	12	49599712	49599712	Human		name
401886813	CV2776755	single nucleotide variant	NM_032130.3(FAM186B):c.1852T>A (p.Tyr618Asn)	not specified [RCV004357907]	uncertain significance	12	49599788	49599788	Human		name
401891331	CV2779367	single nucleotide variant	NM_032130.3(FAM186B):c.1981G>A (p.Val661Met)	not specified [RCV004351021]	uncertain significance	12	49599659	49599659	Human		name
401891333	CV2779368	single nucleotide variant	NM_032130.3(FAM186B):c.1982T>A (p.Val661Glu)	not specified [RCV004351022]	uncertain significance	12	49599658	49599658	Human		name
405196116	CV2868880	single nucleotide variant	NM_032130.3(FAM186B):c.1956A>G (p.Ile652Met)	not provided [RCV003550849]	benign	12	49599684	49599684	Human		name
405220822	CV2884340	single nucleotide variant	NM_032130.3(FAM186B):c.1633C>T (p.Arg545Trp)	not provided [RCV003553853]	uncertain significance	12	49600007	49600007	Human		name
405239704	CV2979968	single nucleotide variant	NM_032130.3(FAM186B):c.1199G>C (p.Arg400Thr)	not provided [RCV003683787]	uncertain significance	12	49600441	49600441	Human		name
405212292	CV3063193	single nucleotide variant	NM_032130.3(FAM186B):c.1922C>T (p.Ser641Phe)	not provided [RCV003732179]	uncertain significance	12	49599718	49599718	Human		name
405205366	CV3068163	single nucleotide variant	NM_032130.3(FAM186B):c.1273T>C (p.Phe425Leu)	not provided [RCV003731264]	uncertain significance	12	49600367	49600367	Human		name
405744955	CV3260158	single nucleotide variant	NM_032130.3(FAM186B):c.1621C>G (p.Gln541Glu)	not specified [RCV004381113]	uncertain significance	12	49600019	49600019	Human		name
405744961	CV3260159	single nucleotide variant	NM_032130.3(FAM186B):c.1634G>A (p.Arg545Gln)	not specified [RCV004381114]	uncertain significance	12	49600006	49600006	Human		name
405744969	CV3260160	single nucleotide variant	NM_032130.3(FAM186B):c.1759C>T (p.His587Tyr)	not specified [RCV004381115]	uncertain significance	12	49599881	49599881	Human		name
405744985	CV3260162	single nucleotide variant	NM_032130.3(FAM186B):c.2065C>T (p.Arg689Cys)	not specified [RCV004381117]	uncertain significance	12	49599575	49599575	Human		name
405744993	CV3260163	single nucleotide variant	NM_032130.3(FAM186B):c.2294C>T (p.Thr765Met)	not specified [RCV004381118]	uncertain significance	12	49598825	49598825	Human		name
405745000	CV3260164	single nucleotide variant	NM_032130.3(FAM186B):c.2359C>G (p.Pro787Ala)	not specified [RCV004381119]	uncertain significance	12	49598760	49598760	Human		name
407508493	CV3435625	single nucleotide variant	NM_032130.3(FAM186B):c.2156G>A (p.Arg719His)	not specified [RCV004625430]	likely benign	12	49599484	49599484	Human		name
407508503	CV3435628	single nucleotide variant	NM_032130.3(FAM186B):c.1384C>A (p.Gln462Lys)	not specified [RCV004625433]	uncertain significance	12	49600256	49600256	Human		name
407508506	CV3435629	single nucleotide variant	NM_032130.3(FAM186B):c.1225G>A (p.Asp409Asn)	not specified [RCV004625434]	uncertain significance	12	49600415	49600415	Human		name
597738981	CV3665360	single nucleotide variant	NM_032130.3(FAM186B):c.1216G>A (p.Gly406Ser)	not specified [RCV004921146]	likely benign	12	49600424	49600424	Human		name
597738986	CV3665361	single nucleotide variant	NM_032130.3(FAM186B):c.1591C>A (p.Gln531Lys)	not specified [RCV004921147]	uncertain significance	12	49600049	49600049	Human		name
597738999	CV3665364	single nucleotide variant	NM_032130.3(FAM186B):c.2602A>G (p.Lys868Glu)	not provided [RCV005110243]\|not specified [RCV004921150]	uncertain significance	12	49587685	49587685	Human		name
597739004	CV3665365	single nucleotide variant	NM_032130.3(FAM186B):c.2102A>T (p.Glu701Val)	not provided [RCV005110244]\|not specified [RCV004921151]	uncertain significance	12	49599538	49599538	Human		name
597739009	CV3665366	single nucleotide variant	NM_032130.3(FAM186B):c.2166C>A (p.Ser722Arg)	not specified [RCV004921152]	uncertain significance	12	49599474	49599474	Human		name
597739013	CV3665367	single nucleotide variant	NM_032130.3(FAM186B):c.1748C>A (p.Thr583Asn)	not specified [RCV004921153]	uncertain significance	12	49599892	49599892	Human		name
597739040	CV3665373	single nucleotide variant	NM_032130.3(FAM186B):c.2429G>C (p.Cys810Ser)	not specified [RCV004921159]	likely benign	12	49588559	49588559	Human		name
597964381	CV3754344	single nucleotide variant	NM_032130.3(FAM186B):c.1498T>C (p.Trp500Arg)	not provided [RCV005082451]	uncertain significance	12	49600142	49600142	Human		name
597886097	CV3800045	single nucleotide variant	NM_032130.3(FAM186B):c.1132A>G (p.Met378Val)	not provided [RCV005150524]	uncertain significance	12	49600508	49600508	Human		name
597974024	CV3801700	single nucleotide variant	NM_032130.3(FAM186B):c.2023C>T (p.Leu675Phe)	not provided [RCV005143689]	uncertain significance	12	49599617	49599617	Human		name
598225975	CV3962147	single nucleotide variant	NM_032130.3(FAM186B):c.1831A>G (p.Met611Val)	not specified [RCV005341538]	uncertain significance	12	49599809	49599809	Human		name
598225981	CV3962148	single nucleotide variant	NM_032130.3(FAM186B):c.1075C>G (p.Gln359Glu)	not specified [RCV005341539]	uncertain significance	12	49600565	49600565	Human		name
598225988	CV3962149	single nucleotide variant	NM_032130.3(FAM186B):c.1148G>T (p.Gly383Val)	not specified [RCV005341540]	uncertain significance	12	49600492	49600492	Human		name
598226001	CV3962152	single nucleotide variant	NM_032130.3(FAM186B):c.1655G>A (p.Gly552Glu)	not specified [RCV005341542]	uncertain significance	12	49599985	49599985	Human		name
15189780	CV702346	single nucleotide variant	NM_032130.3(FAM186B):c.2180C>T (p.Ala727Val)	not provided [RCV000954281]	benign	12	49598939	49598939	Human		name
15139002	CV713559	single nucleotide variant	NM_032130.3(FAM186B):c.1192C>T (p.Arg398Cys)	not provided [RCV000965889]	benign	12	49600448	49600448	Human		name
15179138	CV725133	single nucleotide variant	NM_032130.3(FAM186B):c.2210C>T (p.Thr737Met)	not provided [RCV000885223]	benign	12	49598909	49598909	Human		name
15165858	CV738685	single nucleotide variant	NM_032130.3(FAM186B):c.2453G>A (p.Arg818Gln)	not provided [RCV000904316]	likely benign	12	49588535	49588535	Human		name
15190985	CV738686	single nucleotide variant	NM_032130.3(FAM186B):c.1790C>G (p.Ser597Cys)	not provided [RCV000910112]	benign	12	49599850	49599850	Human		name
151717045	CV1346258	microsatellite	NM_032130.3(FAM186B):c.1513AAG[1] (p.Lys506del)	not provided [RCV001965382]	uncertain significance	12	49600122	49600124	Human		name
156444351	CV1938209	microsatellite	NM_032130.3(FAM186B):c.1972AAG[2] (p.Lys660del)	not provided [RCV003115275]	uncertain significance	12	49599660	49599662	Human		name
156043252	CV1977927	microsatellite	NM_032130.3(FAM186B):c.2314GAG[1] (p.Glu773del)	not provided [RCV002590408]	uncertain significance	12	49598800	49598802	Human		name
156326358	CV2098320	duplication	NM_032130.3(FAM186B):c.1342_1360dup (p.Gln454fs)	not provided [RCV002899653]	uncertain significance	12	49600279	49600280	Human		name
597933602	CV3858644	deletion	NM_032130.3(FAM186B):c.1510_1513del (p.Gln504fs)	not provided [RCV005207114]	uncertain significance	12	49600127	49600130	Human		name

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