Ttc16 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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112 records found for search term Ttc16

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
598252954	CV3925120	single nucleotide variant	NM_144965.3(TTC16):c.4A>G (p.Thr2Ala)	not specified [RCV005298985]	uncertain significance	9	127716149	127716149	Human		name
401783453	CV2723587	single nucleotide variant	NM_144965.3(TTC16):c.69G>C (p.Trp23Cys)	not specified [RCV004323984]	uncertain significance	9	127716894	127716894	Human		name
401918455	CV2826404	single nucleotide variant	NM_144965.3(TTC16):c.369A>G (p.Ser123=)	not provided [RCV003430252]	likely benign	9	127717715	127717715	Human		name
156078185	CV2198293	single nucleotide variant	NM_144965.3(TTC16):c.130A>T (p.Ser44Cys)	not specified [RCV004081848]	uncertain significance	9	127716955	127716955	Human		name
156336644	CV2360783	single nucleotide variant	NM_144965.3(TTC16):c.101A>C (p.His34Pro)	not specified [RCV004213560]	uncertain significance	9	127716926	127716926	Human		name
329398615	CV2471610	single nucleotide variant	NM_144965.3(TTC16):c.129A>T (p.Gln43His)	not specified [RCV004286907]	uncertain significance	9	127716954	127716954	Human		name
405803854	CV3337334	single nucleotide variant	NM_144965.3(TTC16):c.173C>T (p.Pro58Leu)	not specified [RCV004478982]	uncertain significance	9	127716998	127716998	Human		name
405803872	CV3337342	single nucleotide variant	NM_144965.3(TTC16):c.259G>A (p.Ala87Thr)	not specified [RCV004478990]	uncertain significance	9	127717401	127717401	Human		name
598252904	CV3925109	single nucleotide variant	NM_144965.3(TTC16):c.286G>C (p.Asp96His)	not specified [RCV005298977]	uncertain significance	9	127717632	127717632	Human		name
156330208	CV2339443	single nucleotide variant	NM_144965.3(TTC16):c.890G>A (p.Arg297Gln)	not specified [RCV004194113]	uncertain significance	9	127724137	127724137	Human		name
156192099	CV2356931	single nucleotide variant	NM_144965.3(TTC16):c.773C>T (p.Ala258Val)	not specified [RCV004204302]	uncertain significance	9	127723234	127723234	Human		name
155991533	CV2379212	single nucleotide variant	NM_144965.3(TTC16):c.761C>T (p.Ala254Val)	not specified [RCV004223695]	uncertain significance	9	127723222	127723222	Human		name
156388509	CV2380485	single nucleotide variant	NM_144965.3(TTC16):c.628C>T (p.Arg210Trp)	not specified [RCV004218079]	uncertain significance	9	127720366	127720366	Human		name
329359184	CV2450910	single nucleotide variant	NM_144965.3(TTC16):c.599A>G (p.Asp200Gly)	not specified [RCV004267809]	likely benign	9	127720337	127720337	Human		name
329371103	CV2461948	single nucleotide variant	NM_144965.3(TTC16):c.995T>C (p.Leu332Pro)	not specified [RCV004271848]	uncertain significance	9	127724242	127724242	Human		name
329361765	CV2468285	single nucleotide variant	NM_144965.3(TTC16):c.803A>G (p.Gln268Arg)	not specified [RCV004275844]	uncertain significance	9	127723264	127723264	Human		name
401722505	CV2677009	single nucleotide variant	NM_144965.3(TTC16):c.764G>A (p.Arg255His)	not specified [RCV004293610]	uncertain significance	9	127723225	127723225	Human		name
401874668	CV2781108	single nucleotide variant	NM_144965.3(TTC16):c.928A>G (p.Lys310Glu)	not specified [RCV004358476]	uncertain significance	9	127724175	127724175	Human		name
405803874	CV3337343	single nucleotide variant	NM_144965.3(TTC16):c.322C>T (p.Leu108Phe)	not specified [RCV004478991]	uncertain significance	9	127717668	127717668	Human		name
405803877	CV3337344	single nucleotide variant	NM_144965.3(TTC16):c.352C>G (p.Leu118Val)	not specified [RCV004478992]	uncertain significance	9	127717698	127717698	Human		name
405803879	CV3337345	single nucleotide variant	NM_144965.3(TTC16):c.596A>T (p.Gln199Leu)	not specified [RCV004478993]	uncertain significance	9	127720334	127720334	Human		name
405803881	CV3337346	single nucleotide variant	NM_144965.3(TTC16):c.622A>G (p.Ile208Val)	not specified [RCV004478994]	uncertain significance	9	127720360	127720360	Human		name
405803883	CV3337347	single nucleotide variant	NM_144965.3(TTC16):c.626T>C (p.Phe209Ser)	not specified [RCV004478995]	uncertain significance	9	127720364	127720364	Human		name
405803885	CV3337348	single nucleotide variant	NM_144965.3(TTC16):c.815A>G (p.Gln272Arg)	not specified [RCV004478996]	uncertain significance	9	127723276	127723276	Human		name
405803888	CV3337349	single nucleotide variant	NM_144965.3(TTC16):c.854C>T (p.Pro285Leu)	not specified [RCV004478997]	uncertain significance	9	127723315	127723315	Human		name
405803890	CV3337350	single nucleotide variant	NM_144965.3(TTC16):c.977C>T (p.Ala326Val)	not specified [RCV004478998]	uncertain significance	9	127724224	127724224	Human		name
407528786	CV3487169	single nucleotide variant	NM_144965.3(TTC16):c.344C>T (p.Ala115Val)	not specified [RCV004680568]	uncertain significance	9	127717690	127717690	Human		name
597789078	CV3625219	single nucleotide variant	NM_144965.3(TTC16):c.594G>C (p.Lys198Asn)	not specified [RCV004876009]	uncertain significance	9	127720332	127720332	Human		name
597789112	CV3625228	single nucleotide variant	NM_144965.3(TTC16):c.610G>A (p.Ala204Thr)	not specified [RCV004876017]	uncertain significance	9	127720348	127720348	Human		name
597789116	CV3625230	single nucleotide variant	NM_144965.3(TTC16):c.911C>T (p.Ala304Val)	not specified [RCV004876018]	uncertain significance	9	127724158	127724158	Human		name
597789120	CV3625231	single nucleotide variant	NM_144965.3(TTC16):c.620A>G (p.Tyr207Cys)	not specified [RCV004876019]	uncertain significance	9	127720358	127720358	Human		name
597789132	CV3625234	single nucleotide variant	NM_144965.3(TTC16):c.596A>G (p.Gln199Arg)	not specified [RCV004876022]	uncertain significance	9	127720334	127720334	Human		name
598230077	CV3925108	single nucleotide variant	NM_144965.3(TTC16):c.673C>T (p.Arg225Trp)	not specified [RCV005294992]	uncertain significance	9	127723134	127723134	Human		name
598252910	CV3925110	single nucleotide variant	NM_144965.3(TTC16):c.818G>A (p.Arg273Gln)	not specified [RCV005298978]	uncertain significance	9	127723279	127723279	Human		name
598252922	CV3925113	single nucleotide variant	NM_144965.3(TTC16):c.555G>T (p.Gln185His)	not specified [RCV005298980]	uncertain significance	9	127720293	127720293	Human		name
14399883	CV610457	single nucleotide variant	NM_144965.3(TTC16):c.356G>A (p.Arg119Gln)	Premature ovarian insufficiency [RCV000766152]\|not provided [RCV004692218]	uncertain significance	9	127717702	127717702	Human	2	name
156368292	CV2199812	single nucleotide variant	NM_144965.3(TTC16):c.1348C>T (p.Arg450Trp)	not specified [RCV004074012]	uncertain significance	9	127726327	127726327	Human		name
156017571	CV2222914	single nucleotide variant	NM_144965.3(TTC16):c.1379G>T (p.Arg460Leu)	not specified [RCV004101727]	uncertain significance	9	127726358	127726358	Human		name
156123012	CV2227191	single nucleotide variant	NM_144965.3(TTC16):c.1945T>C (p.Ser649Pro)	not specified [RCV004091800]	uncertain significance	9	127730728	127730728	Human		name
155926173	CV2258704	single nucleotide variant	NM_144965.3(TTC16):c.1237G>A (p.Gly413Ser)	not specified [RCV004117945]	uncertain significance	9	127724875	127724875	Human		name
156257155	CV2277635	single nucleotide variant	NM_144965.3(TTC16):c.1133T>G (p.Leu378Arg)	not specified [RCV004147099]	uncertain significance	9	127724771	127724771	Human		name
155929520	CV2278171	single nucleotide variant	NM_144965.3(TTC16):c.1228G>C (p.Glu410Gln)	not specified [RCV004141369]	uncertain significance	9	127724866	127724866	Human		name
156245551	CV2283430	single nucleotide variant	NM_144965.3(TTC16):c.1029G>C (p.Arg343Ser)	not specified [RCV004139653]	uncertain significance	9	127724276	127724276	Human		name
156180532	CV2288097	single nucleotide variant	NM_144965.3(TTC16):c.2453C>G (p.Thr818Ser)	not specified [RCV004149632]	uncertain significance	9	127731236	127731236	Human		name
156007503	CV2289128	single nucleotide variant	NM_144965.3(TTC16):c.1208C>T (p.Thr403Met)	not specified [RCV004150061]	uncertain significance	9	127724846	127724846	Human		name
156173743	CV2290160	single nucleotide variant	NM_144965.3(TTC16):c.1292C>T (p.Thr431Met)	not specified [RCV004152823]	likely benign	9	127726271	127726271	Human		name
155901640	CV2294583	single nucleotide variant	NM_144965.3(TTC16):c.1081G>A (p.Glu361Lys)	not specified [RCV004161846]	uncertain significance	9	127724328	127724328	Human		name
156184457	CV2294877	single nucleotide variant	NM_144965.3(TTC16):c.1303C>T (p.His435Tyr)	not specified [RCV004156033]	uncertain significance	9	127726282	127726282	Human		name
155960926	CV2314081	single nucleotide variant	NM_144965.3(TTC16):c.2338G>A (p.Gly780Ser)	not specified [RCV004164354]	uncertain significance	9	127731121	127731121	Human		name
156047982	CV2319200	single nucleotide variant	NM_144965.3(TTC16):c.1051G>A (p.Val351Met)	not specified [RCV004178256]	uncertain significance	9	127724298	127724298	Human		name
156166538	CV2319946	single nucleotide variant	NM_144965.3(TTC16):c.1100T>G (p.Leu367Arg)	not specified [RCV004167823]	uncertain significance	9	127724347	127724347	Human		name
156281642	CV2321909	single nucleotide variant	NM_144965.3(TTC16):c.1171G>A (p.Ala391Thr)	not specified [RCV004173376]	uncertain significance	9	127724809	127724809	Human		name
156066819	CV2323976	single nucleotide variant	NM_144965.3(TTC16):c.1613T>C (p.Leu538Pro)	not specified [RCV004176496]	uncertain significance	9	127727314	127727314	Human		name
156253365	CV2325499	single nucleotide variant	NM_144965.3(TTC16):c.1256G>A (p.Arg419His)	not specified [RCV004179944]	likely benign	9	127724894	127724894	Human		name
155972133	CV2335755	single nucleotide variant	NM_144965.3(TTC16):c.1552C>G (p.Pro518Ala)	not specified [RCV004193951]	uncertain significance	9	127727096	127727096	Human		name
155913698	CV2341839	single nucleotide variant	NM_144965.3(TTC16):c.1689G>T (p.Gln563His)	not specified [RCV004184791]	uncertain significance	9	127727390	127727390	Human		name
156184991	CV2346475	single nucleotide variant	NM_144965.3(TTC16):c.2246T>C (p.Ile749Thr)	not specified [RCV004206399]	likely benign	9	127731029	127731029	Human		name
156229466	CV2352987	single nucleotide variant	NM_144965.3(TTC16):c.2297G>A (p.Arg766Gln)	not specified [RCV004201019]	likely benign	9	127731080	127731080	Human		name
329371327	CV2431961	single nucleotide variant	NM_144965.3(TTC16):c.1594C>T (p.Arg532Cys)	not specified [RCV004249116]	uncertain significance	9	127727295	127727295	Human		name
329392998	CV2449429	single nucleotide variant	NM_144965.3(TTC16):c.1112G>A (p.Arg371Gln)	not specified [RCV004266588]	uncertain significance	9	127724359	127724359	Human		name
329352021	CV2455626	single nucleotide variant	NM_144965.3(TTC16):c.2201G>A (p.Ser734Asn)	not specified [RCV004276872]	uncertain significance	9	127730984	127730984	Human		name
401773338	CV2709253	single nucleotide variant	NM_144965.3(TTC16):c.1519C>A (p.Gln507Lys)	not specified [RCV004316417]	uncertain significance	9	127727063	127727063	Human		name
401717674	CV2717725	single nucleotide variant	NM_144965.3(TTC16):c.1994T>C (p.Leu665Pro)	not specified [RCV004333405]	uncertain significance	9	127730777	127730777	Human		name
401718904	CV2731035	single nucleotide variant	NM_144965.3(TTC16):c.2105T>C (p.Ile702Thr)	not specified [RCV004332642]	uncertain significance	9	127730888	127730888	Human		name
401883552	CV2757983	single nucleotide variant	NM_144965.3(TTC16):c.1115G>T (p.Gly372Val)	not specified [RCV004339157]	uncertain significance	9	127724362	127724362	Human		name
401871491	CV2763768	single nucleotide variant	NM_144965.3(TTC16):c.1657G>A (p.Glu553Lys)	not specified [RCV004343251]	likely benign	9	127727358	127727358	Human		name
401882119	CV2774704	single nucleotide variant	NM_144965.3(TTC16):c.2043C>A (p.Ser681Arg)	not specified [RCV004343809]	likely benign	9	127730826	127730826	Human		name
401885573	CV2783336	single nucleotide variant	NM_144965.3(TTC16):c.1018C>A (p.His340Asn)	not specified [RCV004365700]	uncertain significance	9	127724265	127724265	Human		name
401896933	CV2785419	single nucleotide variant	NM_144965.3(TTC16):c.2073G>T (p.Gln691His)	not specified [RCV004362963]	uncertain significance	9	127730856	127730856	Human		name
401897441	CV2787046	single nucleotide variant	NM_144965.3(TTC16):c.1223T>C (p.Leu408Pro)	not specified [RCV004366162]	uncertain significance	9	127724861	127724861	Human		name
401870828	CV2792467	single nucleotide variant	NM_144965.3(TTC16):c.1628A>G (p.Lys543Arg)	not specified [RCV004363209]	uncertain significance	9	127727329	127727329	Human		name
405803835	CV3337325	single nucleotide variant	NM_144965.3(TTC16):c.1033G>T (p.Gly345Cys)	not specified [RCV004478973]	uncertain significance	9	127724280	127724280	Human		name
405803837	CV3337326	single nucleotide variant	NM_144965.3(TTC16):c.1103A>G (p.Tyr368Cys)	not specified [RCV004478974]	uncertain significance	9	127724350	127724350	Human		name
405803839	CV3337327	single nucleotide variant	NM_144965.3(TTC16):c.1223T>G (p.Leu408Arg)	not specified [RCV004478975]	uncertain significance	9	127724861	127724861	Human		name
405803844	CV3337329	single nucleotide variant	NM_144965.3(TTC16):c.1370T>C (p.Phe457Ser)	not specified [RCV004478977]	uncertain significance	9	127726349	127726349	Human		name
405803846	CV3337330	single nucleotide variant	NM_144965.3(TTC16):c.1379G>A (p.Arg460His)	not specified [RCV004478978]	uncertain significance	9	127726358	127726358	Human		name
405803848	CV3337331	single nucleotide variant	NM_144965.3(TTC16):c.1411C>T (p.Pro471Ser)	not specified [RCV004478979]	uncertain significance	9	127726390	127726390	Human		name
405803850	CV3337332	single nucleotide variant	NM_144965.3(TTC16):c.1460T>A (p.Met487Lys)	not specified [RCV004478980]	uncertain significance	9	127727004	127727004	Human		name
405803852	CV3337333	single nucleotide variant	NM_144965.3(TTC16):c.1599G>C (p.Gln533His)	not specified [RCV004478981]	uncertain significance	9	127727300	127727300	Human		name
405803857	CV3337335	single nucleotide variant	NM_144965.3(TTC16):c.1845C>A (p.Ser615Arg)	not specified [RCV004478983]	uncertain significance	9	127729661	127729661	Human		name
405803861	CV3337337	single nucleotide variant	NM_144965.3(TTC16):c.1990G>A (p.Ala664Thr)	not specified [RCV004478985]	uncertain significance	9	127730773	127730773	Human		name
405803863	CV3337338	single nucleotide variant	NM_144965.3(TTC16):c.2341C>T (p.Arg781Trp)	not specified [RCV004478986]	uncertain significance	9	127731124	127731124	Human		name
405803868	CV3337340	single nucleotide variant	NM_144965.3(TTC16):c.2342G>A (p.Arg781Gln)	not specified [RCV004478988]	likely benign	9	127731125	127731125	Human		name
405803870	CV3337341	single nucleotide variant	NM_144965.3(TTC16):c.2588T>C (p.Val863Ala)	not specified [RCV004478989]	uncertain significance	9	127731371	127731371	Human		name
407528788	CV3487170	single nucleotide variant	NM_144965.3(TTC16):c.1310C>T (p.Pro437Leu)	not specified [RCV004680569]	uncertain significance	9	127726289	127726289	Human		name
407528790	CV3487171	single nucleotide variant	NM_144965.3(TTC16):c.1583A>T (p.His528Leu)	not specified [RCV004680570]	uncertain significance	9	127727284	127727284	Human		name
407528792	CV3487172	single nucleotide variant	NM_144965.3(TTC16):c.2428G>C (p.Asp810His)	not specified [RCV004680571]	uncertain significance	9	127731211	127731211	Human		name
407528794	CV3487173	single nucleotide variant	NM_144965.3(TTC16):c.1768A>G (p.Lys590Glu)	not specified [RCV004680572]	likely benign	9	127729584	127729584	Human		name
597789065	CV3625216	single nucleotide variant	NM_144965.3(TTC16):c.1685C>T (p.Pro562Leu)	not specified [RCV004876006]	likely benign	9	127727386	127727386	Human		name
597789068	CV3625217	single nucleotide variant	NM_144965.3(TTC16):c.1646T>C (p.Ile549Thr)	not specified [RCV004876007]	uncertain significance	9	127727347	127727347	Human		name
597789072	CV3625218	single nucleotide variant	NM_144965.3(TTC16):c.1618C>T (p.His540Tyr)	not specified [RCV004876008]	uncertain significance	9	127727319	127727319	Human		name
597789087	CV3625222	single nucleotide variant	NM_144965.3(TTC16):c.1958C>T (p.Thr653Met)	not specified [RCV004876011]	uncertain significance	9	127730741	127730741	Human		name
597789091	CV3625223	single nucleotide variant	NM_144965.3(TTC16):c.2407A>G (p.Thr803Ala)	not specified [RCV004876012]	uncertain significance	9	127731190	127731190	Human		name
597789095	CV3625224	single nucleotide variant	NM_144965.3(TTC16):c.1670C>T (p.Ala557Val)	not specified [RCV004876013]	uncertain significance	9	127727371	127727371	Human		name
597789098	CV3625225	single nucleotide variant	NM_144965.3(TTC16):c.1034G>A (p.Gly345Asp)	not specified [RCV004876014]	uncertain significance	9	127724281	127724281	Human		name
597789103	CV3625226	single nucleotide variant	NM_144965.3(TTC16):c.1162T>C (p.Tyr388His)	not specified [RCV004876015]	uncertain significance	9	127724800	127724800	Human		name
597789107	CV3625227	single nucleotide variant	NM_144965.3(TTC16):c.1210C>G (p.Arg404Gly)	not specified [RCV004876016]	uncertain significance	9	127724848	127724848	Human		name
597789125	CV3625232	single nucleotide variant	NM_144965.3(TTC16):c.2114G>C (p.Arg705Thr)	not specified [RCV004876020]	uncertain significance	9	127730897	127730897	Human		name
597789128	CV3625233	single nucleotide variant	NM_144965.3(TTC16):c.1465G>A (p.Val489Met)	not specified [RCV004876021]	uncertain significance	9	127727009	127727009	Human		name
598252882	CV3925101	single nucleotide variant	NM_144965.3(TTC16):c.2275C>G (p.Pro759Ala)	not specified [RCV005298973]	uncertain significance	9	127731058	127731058	Human		name
598252888	CV3925102	single nucleotide variant	NM_144965.3(TTC16):c.2336G>A (p.Arg779His)	not specified [RCV005298974]	likely benign	9	127731119	127731119	Human		name
598230056	CV3925103	single nucleotide variant	NM_144965.3(TTC16):c.2063C>T (p.Thr688Ile)	not specified [RCV005294989]	uncertain significance	9	127730846	127730846	Human		name
598230063	CV3925104	single nucleotide variant	NM_144965.3(TTC16):c.2152C>T (p.Arg718Trp)	not specified [RCV005294990]	uncertain significance	9	127730935	127730935	Human		name
598252892	CV3925106	single nucleotide variant	NM_144965.3(TTC16):c.2078G>A (p.Arg693Gln)	not specified [RCV005298975]	likely benign	9	127730861	127730861	Human		name
598252898	CV3925107	single nucleotide variant	NM_144965.3(TTC16):c.1411C>G (p.Pro471Ala)	not specified [RCV005298976]	uncertain significance	9	127726390	127726390	Human		name
598230086	CV3925111	single nucleotide variant	NM_144965.3(TTC16):c.2122A>G (p.Ser708Gly)	not specified [RCV005294993]	uncertain significance	9	127730905	127730905	Human		name
598252916	CV3925112	single nucleotide variant	NM_144965.3(TTC16):c.2263C>T (p.Pro755Ser)	not specified [RCV005298979]	uncertain significance	9	127731046	127731046	Human		name
598230092	CV3925114	single nucleotide variant	NM_144965.3(TTC16):c.1558G>A (p.Gly520Ser)	not specified [RCV005294994]	uncertain significance	9	127727102	127727102	Human		name
598252928	CV3925115	single nucleotide variant	NM_144965.3(TTC16):c.2366A>C (p.Asp789Ala)	not specified [RCV005298981]	uncertain significance	9	127731149	127731149	Human		name
598230099	CV3925117	single nucleotide variant	NM_144965.3(TTC16):c.1982A>G (p.Asn661Ser)	not specified [RCV005294995]	uncertain significance	9	127730765	127730765	Human		name
598252942	CV3925118	single nucleotide variant	NM_144965.3(TTC16):c.2598C>A (p.Asp866Glu)	not specified [RCV005298983]	uncertain significance	9	127731381	127731381	Human		name
598252948	CV3925119	single nucleotide variant	NM_144965.3(TTC16):c.1223T>A (p.Leu408Gln)	not specified [RCV005298984]	uncertain significance	9	127724861	127724861	Human		name

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