Ttll3 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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113 records found for search term Ttll3

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
156229371	CV2352980	single nucleotide variant	NM_001387446.1(TTLL3):c.-77C>T	not specified [RCV004201013]	uncertain significance	3	9810359	9810359	Human		name
401771612	CV2686261	single nucleotide variant	NM_001387446.1(TTLL3):c.-87C>T	not specified [RCV004297346]	uncertain significance	3	9810349	9810349	Human		name
401720201	CV2705750	single nucleotide variant	NM_001387446.1(TTLL3):c.-20G>A	not specified [RCV004318588]	uncertain significance	3	9810642	9810642	Human		name
405808976	CV3347768	single nucleotide variant	NM_001387446.1(TTLL3):c.-89C>T	not specified [RCV004481463]	uncertain significance	3	9810347	9810347	Human		name
405808977	CV3347769	single nucleotide variant	NM_001387446.1(TTLL3):c.-84G>A	not specified [RCV004481464]	uncertain significance	3	9810352	9810352	Human		name
597797468	CV3622234	single nucleotide variant	NM_001387446.1(TTLL3):c.-80C>G	not specified [RCV004878869]	uncertain significance	3	9810356	9810356	Human		name
156131365	CV2235231	single nucleotide variant	NM_001387446.1(TTLL3):c.-153C>T	not specified [RCV004107279]	uncertain significance	3	9810283	9810283	Human		name
156292950	CV2321259	single nucleotide variant	NM_001387446.1(TTLL3):c.-168G>A	not specified [RCV004175373]	uncertain significance	3	9810268	9810268	Human		name
156174764	CV2345966	single nucleotide variant	NM_001387446.1(TTLL3):c.-134C>T	not specified [RCV004199000]	uncertain significance	3	9810302	9810302	Human		name
407488707	CV3487396	single nucleotide variant	NM_001387446.1(TTLL3):c.-105G>A	not specified [RCV004682790]	uncertain significance	3	9810331	9810331	Human		name
597797458	CV3622230	single nucleotide variant	NM_001387446.1(TTLL3):c.-170C>G	not specified [RCV004878865]	uncertain significance	3	9810266	9810266	Human		name
598254064	CV3935855	single nucleotide variant	NM_001387446.1(TTLL3):c.-171C>T	not specified [RCV005299177]	uncertain significance	3	9810265	9810265	Human		name
15113136	CV778928	single nucleotide variant	NM_001387446.1(TTLL3):c.1004-4G>A	not provided [RCV000961432]	benign	3	9826993	9826993	Human		name
156156584	CV2322501	single nucleotide variant	NM_001025930.5(TTLL3):c.71C>A (p.Ser24Tyr)	not specified [RCV004180622]	uncertain significance	3	9810077	9810077	Human		name
405808979	CV3347770	single nucleotide variant	NM_001387446.1(TTLL3):c.40G>A (p.Ala14Thr)	not specified [RCV004481465]	uncertain significance	3	9810701	9810701	Human		name
15202156	CV706360	single nucleotide variant	NM_001387446.1(TTLL3):c.855C>T (p.His285=)	not provided [RCV000957834]	benign	3	9825800	9825800	Human		name
156185682	CV2195590	single nucleotide variant	NM_001025930.5(TTLL3):c.118C>G (p.Pro40Ala)	not specified [RCV004082800]	uncertain significance	3	9810124	9810124	Human		name
156027786	CV2195591	single nucleotide variant	NM_001025930.5(TTLL3):c.119C>A (p.Pro40Gln)	not specified [RCV004082801]	uncertain significance	3	9810125	9810125	Human		name
156373887	CV2198048	single nucleotide variant	NM_001025930.5(TTLL3):c.238G>A (p.Gly80Ser)	not specified [RCV004079651]	uncertain significance	3	9810244	9810244	Human		name
401743767	CV2696977	single nucleotide variant	NM_001025930.5(TTLL3):c.130G>A (p.Glu44Lys)	not specified [RCV004292969]	uncertain significance	3	9810136	9810136	Human		name
405808963	CV3347761	single nucleotide variant	NM_001025930.5(TTLL3):c.104A>C (p.Asn35Thr)	not specified [RCV004481456]	uncertain significance	3	9810110	9810110	Human		name
405808967	CV3347763	single nucleotide variant	NM_001025930.5(TTLL3):c.185G>A (p.Arg62Lys)	not specified [RCV004481458]	uncertain significance	3	9810191	9810191	Human		name
405808972	CV3347766	single nucleotide variant	NM_001025930.5(TTLL3):c.239G>T (p.Gly80Val)	not specified [RCV004481461]	uncertain significance	3	9810245	9810245	Human		name
407451850	CV3487393	single nucleotide variant	NM_001025930.5(TTLL3):c.173G>T (p.Arg58Leu)	not specified [RCV004682787]	uncertain significance	3	9810179	9810179	Human		name
407451852	CV3492773	single nucleotide variant	NM_001025930.5(TTLL3):c.137G>A (p.Arg46His)	not specified [RCV004682791]	uncertain significance	3	9810143	9810143	Human		name
597689954	CV3622232	single nucleotide variant	NM_001025930.5(TTLL3):c.110T>C (p.Leu37Pro)	not specified [RCV004878867]	likely benign	3	9810116	9810116	Human		name
598231224	CV3935851	single nucleotide variant	NM_001025930.5(TTLL3):c.119C>T (p.Pro40Leu)	not specified [RCV005295166]	uncertain significance	3	9810125	9810125	Human		name
156185831	CV2232580	single nucleotide variant	NM_001387446.1(TTLL3):c.584G>T (p.Arg195Leu)	not specified [RCV004101259]	uncertain significance	3	9818846	9818846	Human		name
407488689	CV3487392	single nucleotide variant	NM_001387446.1(TTLL3):c.583C>T (p.Arg195Cys)	not specified [RCV004682786]	uncertain significance	3	9818845	9818845	Human		name
407488701	CV3487395	single nucleotide variant	NM_001387446.1(TTLL3):c.584G>A (p.Arg195His)	not specified [RCV004682789]	uncertain significance	3	9818846	9818846	Human		name
597797453	CV3622228	single nucleotide variant	NM_001387446.1(TTLL3):c.563A>T (p.Asp188Val)	not specified [RCV004878863]	uncertain significance	3	9818825	9818825	Human		name
598254048	CV3935849	single nucleotide variant	NM_001387446.1(TTLL3):c.589G>A (p.Val197Ile)	not specified [RCV005299174]	uncertain significance	3	9818851	9818851	Human		name
156094983	CV2213521	single nucleotide variant	NM_001387446.1(TTLL3):c.2368G>T (p.Gly790Trp)	not specified [RCV004087485]	uncertain significance	3	9835409	9835409	Human		name
156239360	CV2217249	single nucleotide variant	NM_001387446.1(TTLL3):c.1973T>C (p.Leu658Pro)	not specified [RCV004087700]	uncertain significance	3	9834828	9834828	Human		name
156241829	CV2231387	single nucleotide variant	NM_001387446.1(TTLL3):c.2426C>T (p.Pro809Leu)	not specified [RCV004096474]	uncertain significance	3	9835467	9835467	Human		name
156029124	CV2238287	single nucleotide variant	NM_001387446.1(TTLL3):c.1999C>T (p.Leu667Phe)	not specified [RCV004113365]	likely benign	3	9834854	9834854	Human		name
156281061	CV2316034	single nucleotide variant	NM_001387446.1(TTLL3):c.2172G>T (p.Arg724Ser)	not specified [RCV004165915]	uncertain significance	3	9835213	9835213	Human		name
156350623	CV2316240	single nucleotide variant	NM_001387446.1(TTLL3):c.1690G>A (p.Val564Met)	not specified [RCV004174273]	uncertain significance	3	9833110	9833110	Human		name
156173613	CV2326863	single nucleotide variant	NM_001387446.1(TTLL3):c.2069G>C (p.Cys690Ser)	not specified [RCV004176689]	uncertain significance	3	9835110	9835110	Human		name
156183973	CV2335493	single nucleotide variant	NM_001387446.1(TTLL3):c.2417C>T (p.Pro806Leu)	not specified [RCV004191663]	uncertain significance	3	9835458	9835458	Human		name
155923092	CV2340736	single nucleotide variant	NM_001387446.1(TTLL3):c.1906A>G (p.Arg636Gly)	not specified [RCV004190403]	uncertain significance	3	9834761	9834761	Human		name
156173073	CV2355137	single nucleotide variant	NM_001387446.1(TTLL3):c.2317G>A (p.Ala773Thr)	not specified [RCV004198528]	uncertain significance	3	9835358	9835358	Human		name
156248850	CV2358762	single nucleotide variant	NM_001387446.1(TTLL3):c.1784G>A (p.Arg595His)	not specified [RCV004210070]	uncertain significance	3	9833204	9833204	Human		name
156050767	CV2391192	single nucleotide variant	NM_001387446.1(TTLL3):c.1035G>A (p.Met345Ile)	not specified [RCV004237210]	uncertain significance	3	9827028	9827028	Human		name
329362824	CV2449396	single nucleotide variant	NM_001387446.1(TTLL3):c.1828C>T (p.Arg610Cys)	not specified [RCV004266556]	uncertain significance	3	9834683	9834683	Human		name
401729365	CV2690179	single nucleotide variant	NM_001387446.1(TTLL3):c.2311C>T (p.Pro771Ser)	not specified [RCV004302191]	uncertain significance	3	9835352	9835352	Human		name
401741469	CV2713516	single nucleotide variant	NM_001387446.1(TTLL3):c.2027C>T (p.Ala676Val)	not specified [RCV004319116]	uncertain significance	3	9834882	9834882	Human		name
401779113	CV2733132	single nucleotide variant	NM_001387446.1(TTLL3):c.2306G>A (p.Arg769Gln)	not specified [RCV004332062]	uncertain significance	3	9835347	9835347	Human		name
405808968	CV3347764	single nucleotide variant	NM_001387446.1(TTLL3):c.1717C>T (p.Arg573Trp)	not specified [RCV004481459]	uncertain significance	3	9833137	9833137	Human		name
405808970	CV3347765	single nucleotide variant	NM_001387446.1(TTLL3):c.1772G>A (p.Arg591Gln)	not specified [RCV004481460]	uncertain significance	3	9833192	9833192	Human		name
405808974	CV3347767	single nucleotide variant	NM_001387446.1(TTLL3):c.2264G>A (p.Arg755His)	not specified [RCV004481462]	likely benign	3	9835305	9835305	Human		name
407488695	CV3487394	single nucleotide variant	NM_001387446.1(TTLL3):c.2176G>C (p.Asp726His)	not specified [RCV004682788]	uncertain significance	3	9835217	9835217	Human		name
597797456	CV3622229	single nucleotide variant	NM_001387446.1(TTLL3):c.2132T>C (p.Leu711Pro)	not specified [RCV004878864]	uncertain significance	3	9835173	9835173	Human		name
597797461	CV3622231	single nucleotide variant	NM_001387446.1(TTLL3):c.1715T>C (p.Ile572Thr)	not specified [RCV004878866]	uncertain significance	3	9833135	9833135	Human		name
597797465	CV3622233	single nucleotide variant	NM_001387446.1(TTLL3):c.2102G>C (p.Cys701Ser)	not specified [RCV004878868]	uncertain significance	3	9835143	9835143	Human		name
597797471	CV3622235	single nucleotide variant	NM_001387446.1(TTLL3):c.2115G>C (p.Leu705Phe)	not specified [RCV004878870]	uncertain significance	3	9835156	9835156	Human		name
597797474	CV3622236	single nucleotide variant	NM_001387446.1(TTLL3):c.1741A>G (p.Ile581Val)	not specified [RCV004878871]	uncertain significance	3	9833161	9833161	Human		name
597797477	CV3622238	single nucleotide variant	NM_001387446.1(TTLL3):c.1712G>T (p.Gly571Val)	not specified [RCV004878872]	uncertain significance	3	9833132	9833132	Human		name
598254054	CV3935852	single nucleotide variant	NM_001387446.1(TTLL3):c.2029C>A (p.Pro677Thr)	not specified [RCV005299175]	uncertain significance	3	9834884	9834884	Human		name
598231232	CV3935853	single nucleotide variant	NM_001387446.1(TTLL3):c.1757C>T (p.Ala586Val)	not specified [RCV005295167]	uncertain significance	3	9833177	9833177	Human		name
598254058	CV3935854	single nucleotide variant	NM_001387446.1(TTLL3):c.1786C>T (p.Pro596Ser)	not specified [RCV005299176]	uncertain significance	3	9833206	9833206	Human		name
597729884	CV3583025	single nucleotide variant	NM_001198793.1(ARPC4-TTLL3):c.75C>G (p.Phe25Leu)	not specified [RCV004862975]	uncertain significance	3	9797730	9797730	Human		name
156177482	CV2278355	single nucleotide variant	NM_001198793.1(ARPC4-TTLL3):c.619C>T (p.Arg207Trp)	not specified [RCV004147646]	uncertain significance	3	9817666	9817666	Human		name
405663930	CV3290361	single nucleotide variant	NM_001198793.1(ARPC4-TTLL3):c.371T>C (p.Ile124Thr)	not specified [RCV004418134]	uncertain significance	3	9812983	9812983	Human		name
405663937	CV3290362	single nucleotide variant	NM_001198793.1(ARPC4-TTLL3):c.373C>T (p.Arg125Trp)	not specified [RCV004418135]	uncertain significance	3	9812985	9812985	Human		name
405664723	CV3290363	single nucleotide variant	NM_001198793.1(ARPC4-TTLL3):c.386G>A (p.Arg129His)	not specified [RCV004418136]	uncertain significance	3	9812998	9812998	Human		name
405663945	CV3290364	single nucleotide variant	NM_001198793.1(ARPC4-TTLL3):c.479A>G (p.Asp160Gly)	not specified [RCV004418137]	uncertain significance	3	9813091	9813091	Human		name
405663950	CV3290365	single nucleotide variant	NM_001198793.1(ARPC4-TTLL3):c.482G>A (p.Ser161Asn)	not specified [RCV004418138]	uncertain significance	3	9813094	9813094	Human		name
405663957	CV3290366	single nucleotide variant	NM_001198793.1(ARPC4-TTLL3):c.519G>C (p.Glu173Asp)	not specified [RCV004418139]	uncertain significance	3	9813267	9813267	Human		name
405663963	CV3290367	single nucleotide variant	NM_001198793.1(ARPC4-TTLL3):c.580G>A (p.Gly194Arg)	not specified [RCV004418140]	uncertain significance	3	9813328	9813328	Human		name
405663968	CV3290368	single nucleotide variant	NM_001198793.1(ARPC4-TTLL3):c.584C>T (p.Thr195Ile)	not specified [RCV004418141]	uncertain significance	3	9813332	9813332	Human		name
405663974	CV3290369	single nucleotide variant	NM_001198793.1(ARPC4-TTLL3):c.629C>T (p.Pro210Leu)	not specified [RCV004418142]	uncertain significance	3	9817676	9817676	Human		name
405663979	CV3290370	single nucleotide variant	NM_001198793.1(ARPC4-TTLL3):c.814G>C (p.Ala272Pro)	not specified [RCV004418143]	uncertain significance	3	9820647	9820647	Human		name
405663984	CV3290371	single nucleotide variant	NM_001198793.1(ARPC4-TTLL3):c.829G>A (p.Asp277Asn)	not specified [RCV004418144]	uncertain significance	3	9820662	9820662	Human		name
405663990	CV3290372	single nucleotide variant	NM_001198793.1(ARPC4-TTLL3):c.845C>T (p.Ala282Val)	not specified [RCV004418145]	uncertain significance	3	9820678	9820678	Human		name
405663995	CV3290373	single nucleotide variant	NM_001198793.1(ARPC4-TTLL3):c.899A>G (p.Gln300Arg)	not specified [RCV004418146]	uncertain significance	3	9820732	9820732	Human		name
156186422	CV2236196	single nucleotide variant	NM_001198793.1(ARPC4-TTLL3):c.1763C>T (p.Thr588Ile)	not specified [RCV004107906]	uncertain significance	3	9834706	9834706	Human		name
156119230	CV2275784	single nucleotide variant	NM_001198793.1(ARPC4-TTLL3):c.1862C>G (p.Pro621Arg)	not specified [RCV004139464]	uncertain significance	3	9834805	9834805	Human		name
401890239	CV2758914	single nucleotide variant	NM_001198793.1(ARPC4-TTLL3):c.1703G>C (p.Cys568Ser)	not specified [RCV004339994]	uncertain significance	3	9829361	9829361	Human		name
401882031	CV2774673	single nucleotide variant	NM_001198793.1(ARPC4-TTLL3):c.1546G>A (p.Ala516Thr)	not specified [RCV004350133]	uncertain significance	3	9829204	9829204	Human		name
405664665	CV3290328	single nucleotide variant	NM_001198793.1(ARPC4-TTLL3):c.1010A>G (p.Asp337Gly)	not specified [RCV004418101]	uncertain significance	3	9825901	9825901	Human		name
405664661	CV3290329	single nucleotide variant	NM_001198793.1(ARPC4-TTLL3):c.1051G>A (p.Gly351Arg)	not specified [RCV004418102]	uncertain significance	3	9825942	9825942	Human		name
405664657	CV3290330	single nucleotide variant	NM_001198793.1(ARPC4-TTLL3):c.1066T>C (p.Cys356Arg)	not specified [RCV004418103]	uncertain significance	3	9827005	9827005	Human		name
405664651	CV3290331	single nucleotide variant	NM_001198793.1(ARPC4-TTLL3):c.1088T>C (p.Met363Thr)	not specified [RCV004418104]	uncertain significance	3	9827027	9827027	Human		name
405664645	CV3290332	single nucleotide variant	NM_001198793.1(ARPC4-TTLL3):c.1110C>A (p.Asn370Lys)	not specified [RCV004418105]	uncertain significance	3	9827049	9827049	Human		name
405664639	CV3290333	single nucleotide variant	NM_001198793.1(ARPC4-TTLL3):c.1160G>A (p.Arg387Gln)	not specified [RCV004418106]	uncertain significance	3	9827099	9827099	Human		name
405664484	CV3290334	single nucleotide variant	NM_001198793.1(ARPC4-TTLL3):c.1225C>G (p.Pro409Ala)	not specified [RCV004418107]	uncertain significance	3	9827164	9827164	Human		name
405664413	CV3290335	single nucleotide variant	NM_001198793.1(ARPC4-TTLL3):c.1246C>T (p.Arg416Cys)	not specified [RCV004418108]	uncertain significance	3	9827185	9827185	Human		name
405664409	CV3290336	single nucleotide variant	NM_001198793.1(ARPC4-TTLL3):c.1247G>A (p.Arg416His)	not specified [RCV004418109]	uncertain significance	3	9827186	9827186	Human		name
405664371	CV3290337	single nucleotide variant	NM_001198793.1(ARPC4-TTLL3):c.1249G>A (p.Asp417Asn)	not specified [RCV004418110]	uncertain significance	3	9827188	9827188	Human		name
405664242	CV3290338	single nucleotide variant	NM_001198793.1(ARPC4-TTLL3):c.1261C>T (p.Arg421Cys)	not specified [RCV004418111]	uncertain significance	3	9827200	9827200	Human		name
405664089	CV3290339	single nucleotide variant	NM_001198793.1(ARPC4-TTLL3):c.1262G>A (p.Arg421His)	not specified [RCV004418112]	uncertain significance	3	9827201	9827201	Human		name
405663943	CV3290340	single nucleotide variant	NM_001198793.1(ARPC4-TTLL3):c.1271C>T (p.Thr424Met)	not specified [RCV004418113]	uncertain significance	3	9827210	9827210	Human		name
405663833	CV3290341	single nucleotide variant	NM_001198793.1(ARPC4-TTLL3):c.1315T>C (p.Cys439Arg)	not specified [RCV004418114]	uncertain significance	3	9828973	9828973	Human		name
405663836	CV3290342	single nucleotide variant	NM_001198793.1(ARPC4-TTLL3):c.1342G>C (p.Glu448Gln)	not specified [RCV004418115]	uncertain significance	3	9829000	9829000	Human		name
405663844	CV3290344	single nucleotide variant	NM_001198793.1(ARPC4-TTLL3):c.1358G>A (p.Arg453Gln)	not specified [RCV004418117]	uncertain significance	3	9829016	9829016	Human		name
405663849	CV3290345	single nucleotide variant	NM_001198793.1(ARPC4-TTLL3):c.1363C>T (p.Pro455Ser)	not specified [RCV004418118]	uncertain significance	3	9829021	9829021	Human		name
405663853	CV3290346	single nucleotide variant	NM_001198793.1(ARPC4-TTLL3):c.1385T>C (p.Met462Thr)	not specified [RCV004418119]	uncertain significance	3	9829043	9829043	Human		name
405663858	CV3290347	single nucleotide variant	NM_001198793.1(ARPC4-TTLL3):c.1445C>A (p.Ser482Tyr)	not specified [RCV004418120]	uncertain significance	3	9829103	9829103	Human		name
405663864	CV3290348	single nucleotide variant	NM_001198793.1(ARPC4-TTLL3):c.1555G>A (p.Val519Met)	not specified [RCV004418121]	uncertain significance	3	9829213	9829213	Human		name
405663870	CV3290349	single nucleotide variant	NM_001198793.1(ARPC4-TTLL3):c.1597G>A (p.Ala533Thr)	not specified [RCV004418122]	uncertain significance	3	9829255	9829255	Human		name
405663874	CV3290350	single nucleotide variant	NM_001198793.1(ARPC4-TTLL3):c.1602C>A (p.Ser534Arg)	not specified [RCV004418123]	uncertain significance	3	9829260	9829260	Human		name
405663879	CV3290351	single nucleotide variant	NM_001198793.1(ARPC4-TTLL3):c.1631C>A (p.Thr544Asn)	not specified [RCV004418124]	uncertain significance	3	9829289	9829289	Human		name
405663883	CV3290352	single nucleotide variant	NM_001198793.1(ARPC4-TTLL3):c.1649G>C (p.Gly550Ala)	not specified [RCV004418125]	uncertain significance	3	9829307	9829307	Human		name
405663892	CV3290354	single nucleotide variant	NM_001198793.1(ARPC4-TTLL3):c.1651G>A (p.Val551Met)	not specified [RCV004418127]	uncertain significance	3	9829309	9829309	Human		name
405663897	CV3290355	single nucleotide variant	NM_001198793.1(ARPC4-TTLL3):c.1669C>T (p.Arg557Cys)	not specified [RCV004418128]	uncertain significance	3	9829327	9829327	Human		name
405663904	CV3290356	single nucleotide variant	NM_001198793.1(ARPC4-TTLL3):c.1696C>T (p.Arg566Cys)	not specified [RCV004418129]	uncertain significance	3	9829354	9829354	Human		name
405663910	CV3290357	single nucleotide variant	NM_001198793.1(ARPC4-TTLL3):c.1697G>A (p.Arg566His)	not specified [RCV004418130]	uncertain significance	3	9829355	9829355	Human		name
405663915	CV3290358	single nucleotide variant	NM_001198793.1(ARPC4-TTLL3):c.1697G>C (p.Arg566Pro)	not specified [RCV004418131]	uncertain significance	3	9829355	9829355	Human		name
405663920	CV3290359	single nucleotide variant	NM_001198793.1(ARPC4-TTLL3):c.1712G>C (p.Gly571Ala)	not specified [RCV004418132]	uncertain significance	3	9829370	9829370	Human		name
405663925	CV3290360	single nucleotide variant	NM_001198793.1(ARPC4-TTLL3):c.1726A>G (p.Ile576Val)	not specified [RCV004418133]	uncertain significance	3	9829384	9829384	Human		name
598175515	CV3905337	single nucleotide variant	NM_001198793.1(ARPC4-TTLL3):c.1510G>A (p.Val504Met)	not specified [RCV005264015]	uncertain significance	3	9829168	9829168	Human		name
598175591	CV3905347	single nucleotide variant	NM_001198793.1(ARPC4-TTLL3):c.1742T>C (p.Val581Ala)	not specified [RCV005264025]	uncertain significance	3	9834685	9834685	Human		name

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