Ttll12 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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105 records found for search term Ttll12

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
15112111	CV780058	single nucleotide variant	NM_015140.4(TTLL12):c.1645-5C>A	not provided [RCV000961239]	benign	22	43168917	43168917	Human		name
156175410	CV2355683	single nucleotide variant	NM_015140.4(TTLL12):c.10G>C (p.Glu4Gln)	not specified [RCV004199045]	uncertain significance	22	43187060	43187060	Human		name
329380658	CV2444497	single nucleotide variant	NM_015140.4(TTLL12):c.14G>A (p.Arg5Gln)	not specified [RCV004263226]	uncertain significance	22	43187056	43187056	Human		name
15203146	CV705974	single nucleotide variant	NM_015140.4(TTLL12):c.252G>A (p.Arg84=)	not provided [RCV000958246]	benign	22	43183075	43183075	Human		name
156277841	CV2252035	single nucleotide variant	NM_015140.4(TTLL12):c.77A>C (p.Gln26Pro)	not specified [RCV004122071]	uncertain significance	22	43186993	43186993	Human		name
156112903	CV2261232	single nucleotide variant	NM_015140.4(TTLL12):c.28C>G (p.Arg10Gly)	not specified [RCV004128108]	uncertain significance	22	43187042	43187042	Human		name
155931477	CV2293533	single nucleotide variant	NM_015140.4(TTLL12):c.74C>T (p.Ala25Val)	not specified [RCV004153064]	uncertain significance	22	43186996	43186996	Human		name
401926148	CV2819643	single nucleotide variant	NM_015140.4(TTLL12):c.711G>A (p.Glu237=)	not provided [RCV003437633]	likely benign	22	43179748	43179748	Human		name
401926150	CV2819644	single nucleotide variant	NM_015140.4(TTLL12):c.597G>A (p.Ser199=)	not provided [RCV003437634]	likely benign	22	43179950	43179950	Human		name
405808928	CV3347743	single nucleotide variant	NM_015140.4(TTLL12):c.89A>C (p.Glu30Ala)	not specified [RCV004481438]	uncertain significance	22	43186981	43186981	Human		name
405808930	CV3347744	single nucleotide variant	NM_015140.4(TTLL12):c.95C>T (p.Ala32Val)	not specified [RCV004481439]	uncertain significance	22	43186975	43186975	Human		name
407531984	CV3487383	single nucleotide variant	NM_015140.4(TTLL12):c.47G>A (p.Ser16Asn)	not specified [RCV004682778]	uncertain significance	22	43187023	43187023	Human		name
407531990	CV3487386	single nucleotide variant	NM_015140.4(TTLL12):c.88G>A (p.Glu30Lys)	not specified [RCV004682781]	uncertain significance	22	43186982	43186982	Human		name
597797407	CV3622212	single nucleotide variant	NM_015140.4(TTLL12):c.37G>A (p.Glu13Lys)	not specified [RCV004878847]	uncertain significance	22	43187033	43187033	Human		name
15124285	CV742962	single nucleotide variant	NM_015140.4(TTLL12):c.630C>T (p.Ala210=)	not provided [RCV000896559]	likely benign	22	43179917	43179917	Human		name
156277326	CV2300146	single nucleotide variant	NM_015140.4(TTLL12):c.256G>A (p.Val86Met)	not specified [RCV004151336]	uncertain significance	22	43183071	43183071	Human		name
156167087	CV2330171	single nucleotide variant	NM_015140.4(TTLL12):c.278C>T (p.Pro93Leu)	not specified [RCV004185656]	uncertain significance	22	43183049	43183049	Human		name
156198359	CV2400857	single nucleotide variant	NM_015140.4(TTLL12):c.172C>G (p.His58Asp)	not specified [RCV004242510]	uncertain significance	22	43186898	43186898	Human		name
401721545	CV2683552	single nucleotide variant	NM_015140.4(TTLL12):c.251G>A (p.Arg84Gln)	not specified [RCV004282484]	likely benign	22	43183076	43183076	Human		name
401752760	CV2723346	single nucleotide variant	NM_015140.4(TTLL12):c.191G>C (p.Gly64Ala)	not specified [RCV004329560]	uncertain significance	22	43183136	43183136	Human		name
401881957	CV2774608	single nucleotide variant	NM_015140.4(TTLL12):c.256G>T (p.Val86Leu)	not specified [RCV004350078]	uncertain significance	22	43183071	43183071	Human		name
401926147	CV2819642	single nucleotide variant	NM_015140.4(TTLL12):c.1272G>A (p.Ala424=)	not provided [RCV003437632]	likely benign	22	43173784	43173784	Human		name
405808916	CV3347736	single nucleotide variant	NM_015140.4(TTLL12):c.235G>A (p.Glu79Lys)	not specified [RCV004481431]	uncertain significance	22	43183092	43183092	Human		name
405808918	CV3347737	single nucleotide variant	NM_015140.4(TTLL12):c.260G>A (p.Arg87Gln)	not specified [RCV004481432]	uncertain significance	22	43183067	43183067	Human		name
597797412	CV3622214	single nucleotide variant	NM_015140.4(TTLL12):c.155T>C (p.Leu52Pro)	not specified [RCV004878849]	uncertain significance	22	43186915	43186915	Human		name
598231175	CV3935839	single nucleotide variant	NM_015140.4(TTLL12):c.148G>A (p.Gly50Ser)	not specified [RCV005295159]	uncertain significance	22	43186922	43186922	Human		name
15143550	CV717497	single nucleotide variant	NM_015140.4(TTLL12):c.1749C>T (p.Val583=)	not provided [RCV000966686]	benign	22	43168808	43168808	Human		name
15196784	CV729237	single nucleotide variant	NM_015140.4(TTLL12):c.1539G>A (p.Thr513=)	not provided [RCV000889868]	benign	22	43171855	43171855	Human		name
15124279	CV742959	single nucleotide variant	NM_015140.4(TTLL12):c.1854C>T (p.Tyr618=)	not provided [RCV000896558]	likely benign	22	43168089	43168089	Human		name
15165928	CV742960	single nucleotide variant	NM_015140.4(TTLL12):c.1287C>G (p.Thr429=)	not provided [RCV000904331]	likely benign	22	43173769	43173769	Human		name
15153937	CV742961	single nucleotide variant	NM_015140.4(TTLL12):c.1143C>T (p.Pro381=)	not provided [RCV000901857]	benign	22	43174295	43174295	Human		name
156107499	CV2214212	single nucleotide variant	NM_015140.4(TTLL12):c.363C>G (p.Asp121Glu)	not specified [RCV004086207]	uncertain significance	22	43180925	43180925	Human		name
156334050	CV2230859	single nucleotide variant	NM_015140.4(TTLL12):c.994G>A (p.Ala332Thr)	not specified [RCV004092339]	uncertain significance	22	43174539	43174539	Human		name
155967229	CV2261136	single nucleotide variant	NM_015140.4(TTLL12):c.911T>C (p.Ile304Thr)	not specified [RCV004128034]	uncertain significance	22	43176326	43176326	Human		name
156111034	CV2387731	single nucleotide variant	NM_015140.4(TTLL12):c.478A>G (p.Thr160Ala)	not specified [RCV004234266]	likely benign	22	43180810	43180810	Human		name
156148820	CV2394524	single nucleotide variant	NM_015140.4(TTLL12):c.865A>C (p.Lys289Gln)	not specified [RCV004240882]	uncertain significance	22	43176372	43176372	Human		name
329369616	CV2424867	single nucleotide variant	NM_015140.4(TTLL12):c.841G>A (p.Ala281Thr)	not specified [RCV004248751]	uncertain significance	22	43176396	43176396	Human		name
401742917	CV2673906	single nucleotide variant	NM_015140.4(TTLL12):c.599G>A (p.Arg200Gln)	not specified [RCV004293281]	uncertain significance	22	43179948	43179948	Human		name
401755495	CV2682502	single nucleotide variant	NM_015140.4(TTLL12):c.598C>T (p.Arg200Trp)	not specified [RCV004290522]	uncertain significance	22	43179949	43179949	Human		name
401775246	CV2692310	single nucleotide variant	NM_015140.4(TTLL12):c.879C>A (p.Asp293Glu)	not specified [RCV004310299]	uncertain significance	22	43176358	43176358	Human		name
401749457	CV2694654	single nucleotide variant	NM_015140.4(TTLL12):c.491C>A (p.Ala164Asp)	not specified [RCV004298764]	likely benign	22	43180797	43180797	Human		name
401752049	CV2713957	single nucleotide variant	NM_015140.4(TTLL12):c.973C>T (p.Leu325Phe)	not specified [RCV004315376]	likely benign	22	43174560	43174560	Human		name
401763143	CV2720211	single nucleotide variant	NM_015140.4(TTLL12):c.620C>T (p.Pro207Leu)	not specified [RCV004325550]	uncertain significance	22	43179927	43179927	Human		name
401864711	CV2791328	single nucleotide variant	NM_015140.4(TTLL12):c.962C>T (p.Pro321Leu)	not specified [RCV004356948]	uncertain significance	22	43174571	43174571	Human		name
405808920	CV3347738	single nucleotide variant	NM_015140.4(TTLL12):c.340C>T (p.Pro114Ser)	not specified [RCV004481433]	uncertain significance	22	43182987	43182987	Human		name
405808923	CV3347740	single nucleotide variant	NM_015140.4(TTLL12):c.627C>A (p.Phe209Leu)	not specified [RCV004481435]	uncertain significance	22	43179920	43179920	Human		name
405808925	CV3347741	single nucleotide variant	NM_015140.4(TTLL12):c.821C>T (p.Pro274Leu)	not specified [RCV004481436]	uncertain significance	22	43179638	43179638	Human		name
405808927	CV3347742	single nucleotide variant	NM_015140.4(TTLL12):c.881T>C (p.Ile294Thr)	not specified [RCV004481437]	uncertain significance	22	43176356	43176356	Human		name
407531974	CV3487377	single nucleotide variant	NM_015140.4(TTLL12):c.544G>A (p.Gly182Arg)	not specified [RCV004682773]	uncertain significance	22	43180744	43180744	Human		name
407531978	CV3487379	single nucleotide variant	NM_015140.4(TTLL12):c.394C>T (p.Arg132Cys)	not specified [RCV004682775]	uncertain significance	22	43180894	43180894	Human		name
407531980	CV3487380	single nucleotide variant	NM_015140.4(TTLL12):c.591C>A (p.Phe197Leu)	not specified [RCV004682776]	uncertain significance	22	43179956	43179956	Human		name
597797381	CV3622202	single nucleotide variant	NM_015140.4(TTLL12):c.308T>C (p.Val103Ala)	not specified [RCV004878838]	uncertain significance	22	43183019	43183019	Human		name
597797384	CV3622203	single nucleotide variant	NM_015140.4(TTLL12):c.899C>T (p.Pro300Leu)	not specified [RCV004878839]	uncertain significance	22	43176338	43176338	Human		name
597797392	CV3622206	single nucleotide variant	NM_015140.4(TTLL12):c.436G>A (p.Ala146Thr)	not specified [RCV004878842]	uncertain significance	22	43180852	43180852	Human		name
597797398	CV3622209	single nucleotide variant	NM_015140.4(TTLL12):c.718C>G (p.Arg240Gly)	not specified [RCV004878844]	uncertain significance	22	43179741	43179741	Human		name
597797401	CV3622210	single nucleotide variant	NM_015140.4(TTLL12):c.754C>T (p.Arg252Trp)	not specified [RCV004878845]	uncertain significance	22	43179705	43179705	Human		name
597797404	CV3622211	single nucleotide variant	NM_015140.4(TTLL12):c.430C>T (p.Arg144Cys)	not specified [RCV004878846]	uncertain significance	22	43180858	43180858	Human		name
598254009	CV3935829	single nucleotide variant	NM_015140.4(TTLL12):c.306C>G (p.Ile102Met)	not specified [RCV005299167]	uncertain significance	22	43183021	43183021	Human		name
598231150	CV3935834	single nucleotide variant	NM_015140.4(TTLL12):c.731A>G (p.Tyr244Cys)	not specified [RCV005295156]	uncertain significance	22	43179728	43179728	Human		name
598231190	CV3935842	single nucleotide variant	NM_015140.4(TTLL12):c.526A>C (p.Thr176Pro)	not specified [RCV005295161]	uncertain significance	22	43180762	43180762	Human		name
155975482	CV2211284	single nucleotide variant	NM_015140.4(TTLL12):c.1651A>G (p.Ile551Val)	not specified [RCV004090216]	uncertain significance	22	43168906	43168906	Human		name
156331271	CV2218137	single nucleotide variant	NM_015140.4(TTLL12):c.1677C>A (p.Phe559Leu)	not specified [RCV004086563]	uncertain significance	22	43168880	43168880	Human		name
156360104	CV2254211	single nucleotide variant	NM_015140.4(TTLL12):c.1658G>A (p.Arg553Gln)	not specified [RCV004129890]	likely benign	22	43168899	43168899	Human		name
155963648	CV2254591	single nucleotide variant	NM_015140.4(TTLL12):c.1057G>C (p.Gly353Arg)	not specified [RCV004123937]	uncertain significance	22	43174381	43174381	Human		name
156333233	CV2335952	single nucleotide variant	NM_015140.4(TTLL12):c.1459G>A (p.Val487Met)	not specified [RCV004189562]	uncertain significance	22	43172437	43172437	Human		name
155978024	CV2338900	single nucleotide variant	NM_015140.4(TTLL12):c.1382G>A (p.Arg461Gln)	not specified [RCV004184493]	uncertain significance	22	43172514	43172514	Human		name
155920518	CV2350522	single nucleotide variant	NM_015140.4(TTLL12):c.1019A>G (p.His340Arg)	not specified [RCV004204881]	uncertain significance	22	43174514	43174514	Human		name
155905735	CV2357173	single nucleotide variant	NM_015140.4(TTLL12):c.1301G>A (p.Ser434Asn)	not specified [RCV004206961]	likely benign	22	43173755	43173755	Human		name
156003545	CV2357469	single nucleotide variant	NM_015140.4(TTLL12):c.1273C>T (p.Arg425Cys)	not specified [RCV004202757]	uncertain significance	22	43173783	43173783	Human		name
156225547	CV2390626	single nucleotide variant	NM_015140.4(TTLL12):c.1509C>G (p.Asn503Lys)	not specified [RCV004239149]	uncertain significance	22	43171885	43171885	Human		name
155928212	CV2391677	single nucleotide variant	NM_015140.4(TTLL12):c.1601A>T (p.Glu534Val)	not specified [RCV004241835]	uncertain significance	22	43169543	43169543	Human		name
401740297	CV2684321	single nucleotide variant	NM_015140.4(TTLL12):c.1312A>G (p.Ile438Val)	not specified [RCV004288972]	uncertain significance	22	43173744	43173744	Human		name
401754096	CV2715546	single nucleotide variant	NM_015140.4(TTLL12):c.1559A>G (p.Asp520Gly)	not specified [RCV004326946]	uncertain significance	22	43171835	43171835	Human		name
405808895	CV3347724	single nucleotide variant	NM_015140.4(TTLL12):c.1118C>A (p.Ser373Tyr)	not specified [RCV004481419]	uncertain significance	22	43174320	43174320	Human		name
405808897	CV3347725	single nucleotide variant	NM_015140.4(TTLL12):c.1291G>A (p.Val431Ile)	not specified [RCV004481420]	likely benign	22	43173765	43173765	Human		name
405808901	CV3347727	single nucleotide variant	NM_015140.4(TTLL12):c.1294A>G (p.Thr432Ala)	not specified [RCV004481422]	uncertain significance	22	43173762	43173762	Human		name
405808902	CV3347728	single nucleotide variant	NM_015140.4(TTLL12):c.1375T>C (p.Phe459Leu)	not specified [RCV004481423]	uncertain significance	22	43172521	43172521	Human		name
405808904	CV3347729	single nucleotide variant	NM_015140.4(TTLL12):c.1600G>A (p.Glu534Lys)	not specified [RCV004481424]	uncertain significance	22	43169544	43169544	Human		name
405808907	CV3347731	single nucleotide variant	NM_015140.4(TTLL12):c.1626T>G (p.Phe542Leu)	not specified [RCV004481426]	uncertain significance	22	43169518	43169518	Human		name
405808909	CV3347732	single nucleotide variant	NM_015140.4(TTLL12):c.1773C>A (p.Asn591Lys)	not specified [RCV004481427]	uncertain significance	22	43168784	43168784	Human		name
405808911	CV3347733	single nucleotide variant	NM_015140.4(TTLL12):c.1774G>C (p.Gly592Arg)	not specified [RCV004481428]	likely benign	22	43168783	43168783	Human		name
405808913	CV3347734	single nucleotide variant	NM_015140.4(TTLL12):c.1795A>G (p.Met599Val)	not specified [RCV004481429]	uncertain significance	22	43168148	43168148	Human		name
405808914	CV3347735	single nucleotide variant	NM_015140.4(TTLL12):c.1918G>A (p.Val640Ile)	not specified [RCV004481430]	uncertain significance	22	43168025	43168025	Human		name
407462064	CV3487381	single nucleotide variant	NM_015140.4(TTLL12):c.1166G>A (p.Arg389Gln)	not specified [RCV004687837]	uncertain significance	22	43174272	43174272	Human		name
407531982	CV3487382	single nucleotide variant	NM_015140.4(TTLL12):c.1274G>T (p.Arg425Leu)	not specified [RCV004682777]	uncertain significance	22	43173782	43173782	Human		name
407531986	CV3487384	single nucleotide variant	NM_015140.4(TTLL12):c.1435T>A (p.Ser479Thr)	not specified [RCV004682779]	uncertain significance	22	43172461	43172461	Human		name
407531988	CV3487385	single nucleotide variant	NM_015140.4(TTLL12):c.1756A>G (p.Met586Val)	not specified [RCV004682780]	uncertain significance	22	43168801	43168801	Human		name
407531993	CV3487387	single nucleotide variant	NM_015140.4(TTLL12):c.1274G>A (p.Arg425His)	not specified [RCV004682782]	uncertain significance	22	43173782	43173782	Human		name
597797368	CV3622197	single nucleotide variant	NM_015140.4(TTLL12):c.1774G>A (p.Gly592Ser)	not specified [RCV004878833]	uncertain significance	22	43168783	43168783	Human		name
597797750	CV3622198	single nucleotide variant	NM_015140.4(TTLL12):c.1351A>G (p.Lys451Glu)	not specified [RCV004878834]	uncertain significance	22	43172545	43172545	Human		name
597797372	CV3622199	single nucleotide variant	NM_015140.4(TTLL12):c.1408G>A (p.Asp470Asn)	not specified [RCV004878835]	uncertain significance	22	43172488	43172488	Human		name
597797375	CV3622200	single nucleotide variant	NM_015140.4(TTLL12):c.1181G>A (p.Arg394His)	not specified [RCV004878836]	uncertain significance	22	43174257	43174257	Human		name
597797378	CV3622201	single nucleotide variant	NM_015140.4(TTLL12):c.1114G>A (p.Ala372Thr)	not specified [RCV004878837]	uncertain significance	22	43174324	43174324	Human		name
597797387	CV3622204	single nucleotide variant	NM_015140.4(TTLL12):c.1540G>A (p.Val514Ile)	not specified [RCV004878840]	uncertain significance	22	43171854	43171854	Human		name
597797389	CV3622205	single nucleotide variant	NM_015140.4(TTLL12):c.1841G>A (p.Arg614Gln)	not specified [RCV004878841]	uncertain significance	22	43168102	43168102	Human		name
597797395	CV3622207	single nucleotide variant	NM_015140.4(TTLL12):c.1123G>A (p.Ala375Thr)	not specified [RCV004878843]	uncertain significance	22	43174315	43174315	Human		name
597797409	CV3622213	single nucleotide variant	NM_015140.4(TTLL12):c.1162C>T (p.Pro388Ser)	not specified [RCV004878848]	uncertain significance	22	43174276	43174276	Human		name
598231122	CV3935830	single nucleotide variant	NM_015140.4(TTLL12):c.1418A>G (p.Tyr473Cys)	not specified [RCV005295152]	uncertain significance	22	43172478	43172478	Human		name
598231136	CV3935832	single nucleotide variant	NM_015140.4(TTLL12):c.1230G>T (p.Trp410Cys)	not specified [RCV005295154]	uncertain significance	22	43173826	43173826	Human		name
598231143	CV3935833	single nucleotide variant	NM_015140.4(TTLL12):c.1634C>T (p.Thr545Met)	not specified [RCV005295155]	uncertain significance	22	43169510	43169510	Human		name
598231157	CV3935835	single nucleotide variant	NM_015140.4(TTLL12):c.1399G>A (p.Val467Ile)	not specified [RCV005295157]	uncertain significance	22	43172497	43172497	Human		name
598231166	CV3935836	single nucleotide variant	NM_015140.4(TTLL12):c.1423G>A (p.Val475Met)	not specified [RCV005295158]	uncertain significance	22	43172473	43172473	Human		name
598254013	CV3935837	single nucleotide variant	NM_015140.4(TTLL12):c.1226G>C (p.Arg409Thr)	not specified [RCV005299168]	uncertain significance	22	43174212	43174212	Human		name
598254018	CV3935838	single nucleotide variant	NM_015140.4(TTLL12):c.1120A>G (p.Ile374Val)	not specified [RCV005299169]	uncertain significance	22	43174318	43174318	Human		name
598254025	CV3935840	single nucleotide variant	NM_015140.4(TTLL12):c.1915C>T (p.His639Tyr)	not specified [RCV005299170]	uncertain significance	22	43168028	43168028	Human		name

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