Tgm7 Variant Search Result - Rat Genome Database

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78 records found for search term Tgm7

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
596947702	CV3547284	single nucleotide variant	NM_052955.3(TGM7):c.439+8G>A	not provided [RCV004811588]	benign	15	43292701	43292701	Human		name
156169096	CV2320142	single nucleotide variant	NM_052955.3(TGM7):c.41T>C (p.Leu14Pro)	not specified [RCV004167983]	uncertain significance	15	43293601	43293601	Human		name
401773602	CV2709402	single nucleotide variant	NM_052955.3(TGM7):c.74C>T (p.Thr25Met)	not specified [RCV004316538]	uncertain significance	15	43293568	43293568	Human		name
405792680	CV3339039	single nucleotide variant	NM_052955.3(TGM7):c.52A>G (p.Arg18Gly)	not specified [RCV004474641]	uncertain significance	15	43293590	43293590	Human		name
401740080	CV2683253	single nucleotide variant	NM_052955.3(TGM7):c.256G>A (p.Gly86Arg)	not specified [RCV004288038]	uncertain significance	15	43292892	43292892	Human		name
401761579	CV2699350	single nucleotide variant	NM_052955.3(TGM7):c.268A>C (p.Ser90Arg)	not specified [RCV004305936]	uncertain significance	15	43292880	43292880	Human		name
401864482	CV2781783	single nucleotide variant	NM_052955.3(TGM7):c.274T>A (p.Ser92Thr)	not specified [RCV004356745]	uncertain significance	15	43292874	43292874	Human		name
401916230	CV2817512	single nucleotide variant	NM_052955.3(TGM7):c.1965A>T (p.Ile655=)	not provided [RCV003400930]	likely benign	15	43276870	43276870	Human		name
401934430	CV2817513	single nucleotide variant	NM_052955.3(TGM7):c.1752G>A (p.Val584=)	not provided [RCV003411181]	likely benign	15	43279204	43279204	Human		name
401916232	CV2817514	single nucleotide variant	NM_052955.3(TGM7):c.1287C>T (p.Ile429=)	not provided [RCV003400931]	likely benign	15	43281908	43281908	Human		name
405792669	CV3339035	single nucleotide variant	NM_052955.3(TGM7):c.244C>T (p.Arg82Trp)	not specified [RCV004474637]	uncertain significance	15	43292904	43292904	Human		name
405792672	CV3339036	single nucleotide variant	NM_052955.3(TGM7):c.295A>C (p.Asn99His)	not specified [RCV004474638]	uncertain significance	15	43292853	43292853	Human		name
407520012	CV3478780	single nucleotide variant	NM_052955.3(TGM7):c.107G>A (p.Arg36His)	not specified [RCV004676805]	uncertain significance	15	43293535	43293535	Human		name
597752158	CV3616273	single nucleotide variant	NM_052955.3(TGM7):c.196C>A (p.Pro66Thr)	not specified [RCV004867084]	uncertain significance	15	43292952	43292952	Human		name
8635464	CV90685	single nucleotide variant	NM_052955.2(TGM7):c.1170C>T (p.Ala390=)	Malignant melanoma [RCV000070783]	not provided	15	43282025	43282025	Human		name
8635465	CV90686	single nucleotide variant	NM_052955.2(TGM7):c.202C>T (p.Pro68Ser)	Malignant melanoma [RCV000070784]	not provided	15	43292946	43292946	Human		name
156139685	CV2202924	single nucleotide variant	NM_052955.3(TGM7):c.512A>T (p.Lys171Met)	not specified [RCV004069194]	uncertain significance	15	43292025	43292025	Human		name
155918456	CV2205877	single nucleotide variant	NM_052955.3(TGM7):c.671G>T (p.Arg224Met)	not specified [RCV004078314]	uncertain significance	15	43287557	43287557	Human		name
156076219	CV2251276	single nucleotide variant	NM_052955.3(TGM7):c.514G>A (p.Gly172Ser)	not specified [RCV004115492]	uncertain significance	15	43292023	43292023	Human		name
156315089	CV2253354	single nucleotide variant	NM_052955.3(TGM7):c.652G>A (p.Asp218Asn)	not specified [RCV004123181]	uncertain significance	15	43287576	43287576	Human		name
156152258	CV2265896	single nucleotide variant	NM_052955.3(TGM7):c.742T>C (p.Ser248Pro)	not specified [RCV004126751]	uncertain significance	15	43287403	43287403	Human		name
155903785	CV2298681	single nucleotide variant	NM_052955.3(TGM7):c.374G>A (p.Gly125Asp)	not specified [RCV004156257]	uncertain significance	15	43292774	43292774	Human		name
156320444	CV2400434	single nucleotide variant	NM_052955.3(TGM7):c.811G>A (p.Gly271Arg)	not specified [RCV004244479]	uncertain significance	15	43287334	43287334	Human		name
401741082	CV2680325	single nucleotide variant	NM_052955.3(TGM7):c.674T>C (p.Val225Ala)	not specified [RCV004288578]	uncertain significance	15	43287554	43287554	Human		name
401752241	CV2682752	single nucleotide variant	NM_052955.3(TGM7):c.394T>C (p.Tyr132His)	not specified [RCV004281727]	likely benign	15	43292754	43292754	Human		name
401888878	CV2765019	single nucleotide variant	NM_052955.3(TGM7):c.325G>A (p.Ala109Thr)	not specified [RCV004337142]	uncertain significance	15	43292823	43292823	Human		name
405792674	CV3339037	single nucleotide variant	NM_052955.3(TGM7):c.323C>A (p.Pro108Gln)	not specified [RCV004474639]	uncertain significance	15	43292825	43292825	Human		name
405792677	CV3339038	single nucleotide variant	NM_052955.3(TGM7):c.338T>C (p.Ile113Thr)	not specified [RCV004474640]	uncertain significance	15	43292810	43292810	Human		name
407497649	CV3478783	single nucleotide variant	NM_052955.3(TGM7):c.846C>A (p.Phe282Leu)	not specified [RCV004668456]	uncertain significance	15	43287299	43287299	Human		name
597752117	CV3616264	single nucleotide variant	NM_052955.3(TGM7):c.646C>T (p.Arg216Trp)	not specified [RCV004867075]	uncertain significance	15	43287582	43287582	Human		name
597752132	CV3616267	single nucleotide variant	NM_052955.3(TGM7):c.646C>G (p.Arg216Gly)	not specified [RCV004867078]	uncertain significance	15	43287582	43287582	Human		name
597752154	CV3616272	single nucleotide variant	NM_052955.3(TGM7):c.371A>G (p.Gln124Arg)	not specified [RCV004867083]	uncertain significance	15	43292777	43292777	Human		name
597752168	CV3616275	single nucleotide variant	NM_052955.3(TGM7):c.829G>C (p.Gly277Arg)	not specified [RCV004867086]	uncertain significance	15	43287316	43287316	Human		name
598184161	CV3913384	single nucleotide variant	NM_052955.3(TGM7):c.518A>T (p.His173Leu)	not specified [RCV005287240]	uncertain significance	15	43292019	43292019	Human		name
156028869	CV2205876	single nucleotide variant	NM_052955.3(TGM7):c.2062A>G (p.Ile688Val)	not specified [RCV004078313]	uncertain significance	15	43276526	43276526	Human		name
156262091	CV2216529	single nucleotide variant	NM_052955.3(TGM7):c.1531C>T (p.Arg511Cys)	not specified [RCV004097321]	uncertain significance	15	43279772	43279772	Human		name
155928194	CV2227459	single nucleotide variant	NM_052955.3(TGM7):c.1625C>T (p.Thr542Ile)	not specified [RCV004092118]	uncertain significance	15	43279678	43279678	Human		name
155958508	CV2282210	single nucleotide variant	NM_052955.3(TGM7):c.1148G>T (p.Arg383Met)	not specified [RCV004132792]	uncertain significance	15	43282047	43282047	Human		name
156193506	CV2301989	single nucleotide variant	NM_052955.3(TGM7):c.1955A>G (p.Asn652Ser)	not specified [RCV004158761]	uncertain significance	15	43276880	43276880	Human		name
155956521	CV2304046	single nucleotide variant	NM_052955.3(TGM7):c.1573A>G (p.Ile525Val)	not specified [RCV004170095]	uncertain significance	15	43279730	43279730	Human		name
156359905	CV2328331	single nucleotide variant	NM_052955.3(TGM7):c.1447G>C (p.Gly483Arg)	not specified [RCV004175448]	uncertain significance	15	43279856	43279856	Human		name
156298433	CV2329221	single nucleotide variant	NM_052955.3(TGM7):c.1789A>T (p.Met597Leu)	not specified [RCV004173967]	uncertain significance	15	43279167	43279167	Human		name
156167533	CV2337232	single nucleotide variant	NM_052955.3(TGM7):c.1747C>T (p.Arg583Cys)	not specified [RCV004185686]	uncertain significance	15	43279209	43279209	Human		name
156051257	CV2367724	single nucleotide variant	NM_052955.3(TGM7):c.1774G>A (p.Glu592Lys)	not specified [RCV004213686]	uncertain significance	15	43279182	43279182	Human		name
155934852	CV2372553	single nucleotide variant	NM_052955.3(TGM7):c.1769T>C (p.Val590Ala)	not specified [RCV004219345]	uncertain significance	15	43279187	43279187	Human		name
156320370	CV2400399	single nucleotide variant	NM_052955.3(TGM7):c.1826A>T (p.His609Leu)	not specified [RCV004244448]	uncertain significance	15	43279130	43279130	Human		name
329368059	CV2442623	single nucleotide variant	NM_052955.3(TGM7):c.2111T>A (p.Val704Asp)	not specified [RCV004264980]	uncertain significance	15	43276477	43276477	Human		name
329382719	CV2445430	single nucleotide variant	NM_052955.3(TGM7):c.2074G>A (p.Glu692Lys)	not specified [RCV004257493]	uncertain significance	15	43276514	43276514	Human		name
329400854	CV2449768	single nucleotide variant	NM_052955.3(TGM7):c.1213G>T (p.Val405Phe)	not specified [RCV004270443]	uncertain significance	15	43281982	43281982	Human		name
329371586	CV2458910	single nucleotide variant	NM_052955.3(TGM7):c.1208A>G (p.Asp403Gly)	not specified [RCV004270317]	uncertain significance	15	43281987	43281987	Human		name
329356455	CV2460335	single nucleotide variant	NM_052955.3(TGM7):c.1135G>C (p.Val379Leu)	not specified [RCV004268662]	uncertain significance	15	43282060	43282060	Human		name
401725260	CV2697336	single nucleotide variant	NM_052955.3(TGM7):c.1372G>A (p.Val458Ile)	not specified [RCV004304091]	uncertain significance	15	43279931	43279931	Human		name
401759792	CV2701719	single nucleotide variant	NM_052955.3(TGM7):c.1207G>T (p.Asp403Tyr)	not specified [RCV004314126]	uncertain significance	15	43281988	43281988	Human		name
401761412	CV2702326	single nucleotide variant	NM_052955.3(TGM7):c.1211A>G (p.Glu404Gly)	not specified [RCV004316858]	uncertain significance	15	43281984	43281984	Human		name
401736508	CV2703164	single nucleotide variant	NM_052955.3(TGM7):c.1655G>A (p.Arg552Gln)	not specified [RCV004321443]	uncertain significance	15	43279648	43279648	Human		name
401882381	CV2774826	single nucleotide variant	NM_052955.3(TGM7):c.1634C>T (p.Pro545Leu)	not specified [RCV004343915]	uncertain significance	15	43279669	43279669	Human		name
401876150	CV2777678	single nucleotide variant	NM_052955.3(TGM7):c.1226T>C (p.Leu409Pro)	not specified [RCV004343514]	uncertain significance	15	43281969	43281969	Human		name
405792648	CV3339027	single nucleotide variant	NM_052955.3(TGM7):c.1066G>A (p.Gly356Arg)	not specified [RCV004474629]	uncertain significance	15	43282559	43282559	Human		name
405792651	CV3339028	single nucleotide variant	NM_052955.3(TGM7):c.1130C>A (p.Ala377Asp)	not specified [RCV004474630]	uncertain significance	15	43282065	43282065	Human		name
405792653	CV3339029	single nucleotide variant	NM_052955.3(TGM7):c.1216A>C (p.Ile406Leu)	not specified [RCV004474631]	uncertain significance	15	43281979	43281979	Human		name
405792659	CV3339031	single nucleotide variant	NM_052955.3(TGM7):c.1255G>C (p.Ala419Pro)	not specified [RCV004474633]	uncertain significance	15	43281940	43281940	Human		name
405792662	CV3339032	single nucleotide variant	NM_052955.3(TGM7):c.1451G>A (p.Gly484Asp)	not specified [RCV004474634]	likely benign	15	43279852	43279852	Human		name
405792663	CV3339033	single nucleotide variant	NM_052955.3(TGM7):c.1564C>T (p.Arg522Trp)	not specified [RCV004474635]	uncertain significance	15	43279739	43279739	Human		name
407520016	CV3478781	single nucleotide variant	NM_052955.3(TGM7):c.1727T>G (p.Leu576Arg)	not specified [RCV004676806]	uncertain significance	15	43279229	43279229	Human		name
407497645	CV3478782	single nucleotide variant	NM_052955.3(TGM7):c.1868C>T (p.Ala623Val)	not specified [RCV004668455]	uncertain significance	15	43276967	43276967	Human		name
407520018	CV3478784	single nucleotide variant	NM_052955.3(TGM7):c.1702C>T (p.Pro568Ser)	not specified [RCV004676807]	uncertain significance	15	43279254	43279254	Human		name
407497653	CV3478785	single nucleotide variant	NM_052955.3(TGM7):c.1808T>A (p.Ile603Asn)	not specified [RCV004668457]	uncertain significance	15	43279148	43279148	Human		name
597752112	CV3616263	single nucleotide variant	NM_052955.3(TGM7):c.1654C>T (p.Arg552Trp)	not specified [RCV004867074]	uncertain significance	15	43279649	43279649	Human		name
597752122	CV3616265	single nucleotide variant	NM_052955.3(TGM7):c.2113A>G (p.Thr705Ala)	not specified [RCV004867076]	likely benign	15	43276475	43276475	Human		name
597752127	CV3616266	single nucleotide variant	NM_052955.3(TGM7):c.1925C>T (p.Thr642Met)	not specified [RCV004867077]	likely benign	15	43276910	43276910	Human		name
597752137	CV3616268	single nucleotide variant	NM_052955.3(TGM7):c.1567G>A (p.Gly523Arg)	not specified [RCV004867079]	uncertain significance	15	43279736	43279736	Human		name
597752145	CV3616270	single nucleotide variant	NM_052955.3(TGM7):c.1111C>G (p.Leu371Val)	not specified [RCV004867081]	uncertain significance	15	43282084	43282084	Human		name
597752149	CV3616271	single nucleotide variant	NM_052955.3(TGM7):c.2041C>A (p.Pro681Thr)	not specified [RCV004867082]	uncertain significance	15	43276547	43276547	Human		name
597752163	CV3616274	single nucleotide variant	NM_052955.3(TGM7):c.1298T>C (p.Met433Thr)	not specified [RCV004867085]	uncertain significance	15	43281897	43281897	Human		name
598184169	CV3913385	single nucleotide variant	NM_052955.3(TGM7):c.1589G>A (p.Arg530His)	not specified [RCV005287241]	uncertain significance	15	43279714	43279714	Human		name
598184176	CV3913386	single nucleotide variant	NM_052955.3(TGM7):c.1759A>G (p.Ile587Val)	not specified [RCV005287242]	uncertain significance	15	43279197	43279197	Human		name
598175714	CV3913388	single nucleotide variant	NM_052955.3(TGM7):c.1646A>T (p.His549Leu)	not specified [RCV005285532]	uncertain significance	15	43279657	43279657	Human		name
8635463	CV90684	single nucleotide variant	NM_052955.2(TGM7):c.2041C>T (p.Pro681Ser)	Malignant melanoma [RCV000070782]	not provided	15	43276547	43276547	Human		name

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