Tmtc1 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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87 records found for search term Tmtc1

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
15147013	CV779660	single nucleotide variant	NM_001193451.2(TMTC1):c.1418+9A>G	not provided [RCV000967257]	benign	12	29583398	29583398	Human		name
8653869	CV130444	single nucleotide variant	NM_001193451.1(TMTC1):c.1128+12034C>T	Lung cancer [RCV000110931]	uncertain significance	12	29621113	29621113	Human		name
401906042	CV2806819	single nucleotide variant	NM_001193451.2(TMTC1):c.75G>A (p.Ala25=)	not provided [RCV003396295]	likely benign	12	29783677	29783677	Human		name
401879818	CV2755285	single nucleotide variant	NM_001193451.2(TMTC1):c.16T>C (p.Ser6Pro)	not specified [RCV004337460]	uncertain significance	12	29783736	29783736	Human		name
156201288	CV2256143	single nucleotide variant	NM_001193451.2(TMTC1):c.85G>C (p.Ala29Pro)	not specified [RCV004116422]	uncertain significance	12	29783667	29783667	Human		name
156160629	CV2398207	single nucleotide variant	NM_001193451.2(TMTC1):c.86C>T (p.Ala29Val)	not specified [RCV004241776]	uncertain significance	12	29783666	29783666	Human		name
401756889	CV2696638	single nucleotide variant	NM_001193451.2(TMTC1):c.43A>G (p.Thr15Ala)	not specified [RCV004312655]	likely benign	12	29783709	29783709	Human		name
401732439	CV2708830	single nucleotide variant	NM_001193451.2(TMTC1):c.31G>A (p.Gly11Ser)	not specified [RCV004307779]	uncertain significance	12	29783721	29783721	Human		name
401906041	CV2806818	single nucleotide variant	NM_001193451.2(TMTC1):c.546G>A (p.Ser182=)	not provided [RCV003396294]	likely benign	12	29758712	29758712	Human		name
597801299	CV3620583	single nucleotide variant	NM_001193451.2(TMTC1):c.52C>G (p.Arg18Gly)	not specified [RCV004880667]	uncertain significance	12	29783700	29783700	Human		name
597801308	CV3620587	single nucleotide variant	NM_001193451.2(TMTC1):c.52C>T (p.Arg18Trp)	not specified [RCV004880671]	uncertain significance	12	29783700	29783700	Human		name
598226872	CV3894432	single nucleotide variant	NM_001193451.2(TMTC1):c.588C>T (p.Phe196=)	not provided [RCV005257675]	likely benign	12	29755852	29755852	Human		name
15127701	CV713499	single nucleotide variant	NM_001193451.2(TMTC1):c.366C>T (p.His122=)	not provided [RCV000963951]	benign	12	29768012	29768012	Human		name
156241101	CV2203833	single nucleotide variant	NM_001193451.2(TMTC1):c.256A>C (p.Asn86His)	not specified [RCV004069896]	uncertain significance	12	29783496	29783496	Human		name
329359530	CV2451064	single nucleotide variant	NM_001193451.2(TMTC1):c.101C>T (p.Ala34Val)	not specified [RCV004269720]	uncertain significance	12	29783651	29783651	Human		name
401727114	CV2684475	single nucleotide variant	NM_001193451.2(TMTC1):c.147C>G (p.Phe49Leu)	not specified [RCV004291548]	uncertain significance	12	29783605	29783605	Human		name
401768236	CV2735227	single nucleotide variant	NM_001193451.2(TMTC1):c.223A>T (p.Thr75Ser)	not specified [RCV004333907]	uncertain significance	12	29783529	29783529	Human		name
405786408	CV3343636	single nucleotide variant	NM_001193451.2(TMTC1):c.122A>T (p.Tyr41Phe)	not specified [RCV004472930]	uncertain significance	12	29783630	29783630	Human		name
597801292	CV3620579	single nucleotide variant	NM_001193451.2(TMTC1):c.182C>T (p.Pro61Leu)	not specified [RCV004880663]	uncertain significance	12	29783570	29783570	Human		name
15168092	CV738611	single nucleotide variant	NM_001193451.2(TMTC1):c.1146G>A (p.Glu382=)	not provided [RCV000904782]	benign	12	29604282	29604282	Human		name
156191854	CV2255302	single nucleotide variant	NM_001193451.2(TMTC1):c.662C>T (p.Thr221Ile)	not specified [RCV004117682]	uncertain significance	12	29755778	29755778	Human		name
156366644	CV2269743	single nucleotide variant	NM_001193451.2(TMTC1):c.893G>A (p.Ser298Asn)	not specified [RCV004126993]	uncertain significance	12	29751711	29751711	Human		name
156233074	CV2273868	single nucleotide variant	NM_001193451.2(TMTC1):c.319A>G (p.Thr107Ala)	not specified [RCV004132493]	uncertain significance	12	29768059	29768059	Human		name
156001810	CV2296450	single nucleotide variant	NM_001193451.2(TMTC1):c.745C>T (p.Leu249Phe)	not specified [RCV004148191]	uncertain significance	12	29751859	29751859	Human		name
156062916	CV2316642	single nucleotide variant	NM_001193451.2(TMTC1):c.877C>A (p.Pro293Thr)	not specified [RCV004171882]	uncertain significance	12	29751727	29751727	Human		name
156145782	CV2357887	single nucleotide variant	NM_001193451.2(TMTC1):c.754C>T (p.Arg252Cys)	not specified [RCV004209677]	likely benign	12	29751850	29751850	Human		name
156104722	CV2361038	single nucleotide variant	NM_001193451.2(TMTC1):c.589C>G (p.Pro197Ala)	not specified [RCV004216234]	uncertain significance	12	29755851	29755851	Human		name
329356730	CV2430878	single nucleotide variant	NM_001193451.2(TMTC1):c.913C>T (p.Pro305Ser)	not specified [RCV004248078]	uncertain significance	12	29751691	29751691	Human		name
329386790	CV2452527	single nucleotide variant	NM_001193451.2(TMTC1):c.931A>G (p.Met311Val)	not specified [RCV004273120]	uncertain significance	12	29751673	29751673	Human		name
329376975	CV2455120	single nucleotide variant	NM_001193451.2(TMTC1):c.390G>A (p.Met130Ile)	not specified [RCV004272364]	uncertain significance	12	29767988	29767988	Human		name
329351836	CV2455365	single nucleotide variant	NM_001193451.2(TMTC1):c.967T>A (p.Phe323Ile)	not specified [RCV004274865]	uncertain significance	12	29633308	29633308	Human		name
401752391	CV2706993	single nucleotide variant	NM_001193451.2(TMTC1):c.831G>T (p.Gln277His)	not specified [RCV004321590]	uncertain significance	12	29751773	29751773	Human		name
401766552	CV2732372	single nucleotide variant	NM_001193451.2(TMTC1):c.508G>A (p.Val170Met)	not specified [RCV004331500]	uncertain significance	12	29758750	29758750	Human		name
405786441	CV3343642	single nucleotide variant	NM_001193451.2(TMTC1):c.466A>G (p.Ile156Val)	not specified [RCV004472936]	likely benign	12	29767912	29767912	Human		name
405786446	CV3343643	single nucleotide variant	NM_001193451.2(TMTC1):c.765G>T (p.Gln255His)	not specified [RCV004472937]	uncertain significance	12	29751839	29751839	Human		name
405786456	CV3343645	single nucleotide variant	NM_001193451.2(TMTC1):c.917G>A (p.Arg306Gln)	not specified [RCV004472939]	uncertain significance	12	29751687	29751687	Human		name
407458910	CV3479096	single nucleotide variant	NM_001193451.2(TMTC1):c.811C>T (p.Arg271Trp)	not specified [RCV004686984]	uncertain significance	12	29751793	29751793	Human		name
407527322	CV3479097	single nucleotide variant	NM_001193451.2(TMTC1):c.764A>G (p.Gln255Arg)	not specified [RCV004679998]	uncertain significance	12	29751840	29751840	Human		name
407527329	CV3479099	single nucleotide variant	NM_001193451.2(TMTC1):c.889A>G (p.Lys297Glu)	not specified [RCV004680000]	uncertain significance	12	29751715	29751715	Human		name
407458914	CV3479100	single nucleotide variant	NM_001193451.2(TMTC1):c.440C>T (p.Thr147Met)	not specified [RCV004686985]	uncertain significance	12	29767938	29767938	Human		name
597801284	CV3620574	single nucleotide variant	NM_001193451.2(TMTC1):c.953C>T (p.Ser318Phe)	not specified [RCV004880659]	uncertain significance	12	29633322	29633322	Human		name
597801286	CV3620575	single nucleotide variant	NM_001193451.2(TMTC1):c.772G>A (p.Gly258Arg)	not specified [RCV004880660]	uncertain significance	12	29751832	29751832	Human		name
597801288	CV3620576	single nucleotide variant	NM_001193451.2(TMTC1):c.671C>T (p.Thr224Met)	not specified [RCV004880661]	uncertain significance	12	29755769	29755769	Human		name
597801290	CV3620577	single nucleotide variant	NM_001193451.2(TMTC1):c.871C>T (p.Pro291Ser)	not specified [RCV004880662]	uncertain significance	12	29751733	29751733	Human		name
597801401	CV3620580	single nucleotide variant	NM_001193451.2(TMTC1):c.910T>C (p.Ser304Pro)	not specified [RCV004880664]	uncertain significance	12	29751694	29751694	Human		name
597801298	CV3620582	single nucleotide variant	NM_001193451.2(TMTC1):c.950A>G (p.Tyr317Cys)	not specified [RCV004880666]	uncertain significance	12	29633325	29633325	Human		name
598228642	CV3935008	single nucleotide variant	NM_001193451.2(TMTC1):c.701T>G (p.Leu234Arg)	not specified [RCV005294771]	uncertain significance	12	29755739	29755739	Human		name
598228674	CV3935013	single nucleotide variant	NM_001193451.2(TMTC1):c.421C>T (p.Arg141Cys)	not specified [RCV005294775]	uncertain significance	12	29767957	29767957	Human		name
155961087	CV2204441	single nucleotide variant	NM_001193451.2(TMTC1):c.1505C>T (p.Ala502Val)	not specified [RCV004079248]	uncertain significance	12	29572132	29572132	Human		name
155919321	CV2254846	single nucleotide variant	NM_001193451.2(TMTC1):c.2263C>T (p.Arg755Cys)	not specified [RCV004115307]	uncertain significance	12	29516393	29516393	Human		name
155966333	CV2261901	single nucleotide variant	NM_001193451.2(TMTC1):c.2348A>G (p.Lys783Arg)	not specified [RCV004127952]	uncertain significance	12	29514564	29514564	Human		name
156052026	CV2269398	single nucleotide variant	NM_001193451.2(TMTC1):c.2227A>T (p.Ile743Phe)	not specified [RCV004124525]	uncertain significance	12	29516429	29516429	Human		name
156294829	CV2293256	single nucleotide variant	NM_001193451.2(TMTC1):c.2120A>G (p.Gln707Arg)	not specified [RCV004150757]	likely benign	12	29517476	29517476	Human		name
156302304	CV2311836	single nucleotide variant	NM_001193451.2(TMTC1):c.2530G>A (p.Ala844Thr)	not specified [RCV004170680]	uncertain significance	12	29506965	29506965	Human		name
156199199	CV2312975	single nucleotide variant	NM_001193451.2(TMTC1):c.2023C>T (p.Arg675Cys)	not specified [RCV004159480]	uncertain significance	12	29518473	29518473	Human		name
156283062	CV2317438	single nucleotide variant	NM_001193451.2(TMTC1):c.1067C>G (p.Ala356Gly)	not specified [RCV004172407]	uncertain significance	12	29633208	29633208	Human		name
156078536	CV2318743	single nucleotide variant	NM_001193451.2(TMTC1):c.1492C>T (p.Arg498Trp)	not specified [RCV004175674]	uncertain significance	12	29572145	29572145	Human		name
156255685	CV2325774	single nucleotide variant	NM_001193451.2(TMTC1):c.2299C>T (p.His767Tyr)	not specified [RCV004173665]	uncertain significance	12	29516357	29516357	Human		name
156169832	CV2337396	single nucleotide variant	NM_001193451.2(TMTC1):c.2035G>A (p.Val679Met)	not specified [RCV004187841]	uncertain significance	12	29517561	29517561	Human		name
156329332	CV2342390	single nucleotide variant	NM_001193451.2(TMTC1):c.1027A>G (p.Ile343Val)	not specified [RCV004194003]	uncertain significance	12	29633248	29633248	Human		name
156345666	CV2356312	single nucleotide variant	NM_001193451.2(TMTC1):c.1226C>T (p.Ala409Val)	not specified [RCV004206121]	uncertain significance	12	29604202	29604202	Human		name
156208377	CV2369983	single nucleotide variant	NM_001193451.2(TMTC1):c.1487A>G (p.Gln496Arg)	not specified [RCV004210887]	uncertain significance	12	29572150	29572150	Human		name
156214330	CV2385911	single nucleotide variant	NM_001193451.2(TMTC1):c.2159G>A (p.Arg720His)	not specified [RCV004226949]	uncertain significance	12	29517437	29517437	Human		name
329361792	CV2448028	single nucleotide variant	NM_001193451.2(TMTC1):c.2195A>G (p.Gln732Arg)	not specified [RCV004263261]	uncertain significance	12	29516461	29516461	Human		name
401727050	CV2692136	single nucleotide variant	NM_001193451.2(TMTC1):c.2416G>A (p.Asp806Asn)	not specified [RCV004301839]	uncertain significance	12	29514496	29514496	Human		name
401886141	CV2774861	single nucleotide variant	NM_001193451.2(TMTC1):c.1790G>A (p.Arg597Gln)	not specified [RCV004343945]	uncertain significance	12	29520716	29520716	Human		name
401899132	CV2783684	single nucleotide variant	NM_001193451.2(TMTC1):c.2300A>G (p.His767Arg)	not specified [RCV004360615]	uncertain significance	12	29516356	29516356	Human		name
401865812	CV2786136	single nucleotide variant	NM_001193451.2(TMTC1):c.1445A>G (p.Asn482Ser)	not specified [RCV004359942]	uncertain significance	12	29572192	29572192	Human		name
405786396	CV3343634	single nucleotide variant	NM_001193451.2(TMTC1):c.1087G>A (p.Val363Met)	not specified [RCV004472928]	uncertain significance	12	29633188	29633188	Human		name
405786402	CV3343635	single nucleotide variant	NM_001193451.2(TMTC1):c.1186C>G (p.Pro396Ala)	not specified [RCV004472929]	uncertain significance	12	29604242	29604242	Human		name
405786414	CV3343637	single nucleotide variant	NM_001193451.2(TMTC1):c.1543C>T (p.Arg515Cys)	not specified [RCV004472931]	uncertain significance	12	29556990	29556990	Human		name
405786419	CV3343638	single nucleotide variant	NM_001193451.2(TMTC1):c.1768T>C (p.Ser590Pro)	not specified [RCV004472932]	uncertain significance	12	29536226	29536226	Human		name
405786424	CV3343639	single nucleotide variant	NM_001193451.2(TMTC1):c.2085C>A (p.Asn695Lys)	not specified [RCV004472933]	uncertain significance	12	29517511	29517511	Human		name
405786436	CV3343641	single nucleotide variant	NM_001193451.2(TMTC1):c.2185G>A (p.Val729Met)	not specified [RCV004472935]	uncertain significance	12	29516471	29516471	Human		name
407527326	CV3479098	single nucleotide variant	NM_001193451.2(TMTC1):c.2246G>C (p.Gly749Ala)	not specified [RCV004679999]	uncertain significance	12	29516410	29516410	Human		name
407527331	CV3479101	single nucleotide variant	NM_001193451.2(TMTC1):c.1493G>A (p.Arg498Gln)	not specified [RCV004680001]	uncertain significance	12	29572144	29572144	Human		name
597801282	CV3620573	single nucleotide variant	NM_001193451.2(TMTC1):c.2132C>T (p.Ala711Val)	not specified [RCV004880658]	uncertain significance	12	29517464	29517464	Human		name
597801296	CV3620581	single nucleotide variant	NM_001193451.2(TMTC1):c.1327C>G (p.Leu443Val)	not specified [RCV004880665]	uncertain significance	12	29583498	29583498	Human		name
597801301	CV3620584	single nucleotide variant	NM_001193451.2(TMTC1):c.2344C>T (p.Pro782Ser)	not specified [RCV004880668]	uncertain significance	12	29514568	29514568	Human		name
597801304	CV3620585	single nucleotide variant	NM_001193451.2(TMTC1):c.1346T>C (p.Leu449Ser)	not specified [RCV004880669]	uncertain significance	12	29583479	29583479	Human		name
597801306	CV3620586	single nucleotide variant	NM_001193451.2(TMTC1):c.1276C>A (p.His426Asn)	not specified [RCV004880670]	uncertain significance	12	29583549	29583549	Human		name
598228634	CV3935006	single nucleotide variant	NM_001193451.2(TMTC1):c.2418C>G (p.Asp806Glu)	not specified [RCV005294770]	uncertain significance	12	29514494	29514494	Human		name
598253093	CV3935007	single nucleotide variant	NM_001193451.2(TMTC1):c.1951G>A (p.Val651Met)	not specified [RCV005278191]	uncertain significance	12	29518545	29518545	Human		name
598228651	CV3935009	single nucleotide variant	NM_001193451.2(TMTC1):c.1625A>G (p.Gln542Arg)	not specified [RCV005294772]	uncertain significance	12	29556908	29556908	Human		name
598228659	CV3935010	single nucleotide variant	NM_001193451.2(TMTC1):c.1192A>G (p.Ser398Gly)	not specified [RCV005294773]	uncertain significance	12	29604236	29604236	Human		name
598228667	CV3935011	single nucleotide variant	NM_001193451.2(TMTC1):c.1156G>A (p.Gly386Ser)	not specified [RCV005294774]	uncertain significance	12	29604272	29604272	Human		name
598253099	CV3935012	single nucleotide variant	NM_001193451.2(TMTC1):c.2116T>A (p.Tyr706Asn)	not specified [RCV005278192]	uncertain significance	12	29517480	29517480	Human		name

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