Eno4 Variant Search Result - Rat Genome Database

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58 records found for search term Eno4

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
156239539	CV2221265	single nucleotide variant	NM_001242699.2(ENO4):c.41G>C (p.Arg14Thr)	not specified [RCV004094698]	uncertain significance	10	116849607	116849607	Human		name
156294353	CV2293182	single nucleotide variant	NM_001242699.2(ENO4):c.65A>G (p.Gln22Arg)	not specified [RCV004150696]	uncertain significance	10	116849631	116849631	Human		name
598269519	CV3954274	single nucleotide variant	NM_001242699.2(ENO4):c.73G>A (p.Glu25Lys)	not specified [RCV005327349]	uncertain significance	10	116849639	116849639	Human		name
156398657	CV2194706	single nucleotide variant	NM_001242699.2(ENO4):c.202A>C (p.Ile68Leu)	not specified [RCV004075263]	uncertain significance	10	116855659	116855659	Human		name
156032254	CV2239379	single nucleotide variant	NM_001242699.2(ENO4):c.112G>A (p.Glu38Lys)	not specified [RCV004114113]	uncertain significance	10	116849678	116849678	Human		name
156038602	CV2384187	single nucleotide variant	NM_001242699.2(ENO4):c.150C>A (p.Asp50Glu)	not specified [RCV004227583]	uncertain significance	10	116849716	116849716	Human		name
401722163	CV2680847	single nucleotide variant	NM_001242699.2(ENO4):c.212T>C (p.Ile71Thr)	not specified [RCV004293494]	uncertain significance	10	116855669	116855669	Human		name
401857477	CV2779162	single nucleotide variant	NM_001242699.2(ENO4):c.152T>C (p.Val51Ala)	not specified [RCV004349074]	uncertain significance	10	116849718	116849718	Human		name
407483181	CV3435070	single nucleotide variant	NM_001242699.2(ENO4):c.162C>A (p.His54Gln)	not specified [RCV004625045]	uncertain significance	10	116849728	116849728	Human		name
15135832	CV737354	single nucleotide variant	NM_001242699.2(ENO4):c.1455C>T (p.Ile485=)	not provided [RCV000898528]	benign	10	116876178	116876178	Human		name
8633512	CV88727	single nucleotide variant	NM_001242699.1(ENO4):c.1857A>G (p.Glu619=)	Malignant melanoma [RCV000068822]	not provided	10	116881648	116881648	Human		name
156236957	CV2193527	single nucleotide variant	NM_001242699.2(ENO4):c.298G>A (p.Val100Ile)	not specified [RCV004073007]	likely benign	10	116856495	116856495	Human		name
156193667	CV2214145	single nucleotide variant	NM_001242699.2(ENO4):c.493T>C (p.Phe165Leu)	not specified [RCV004086146]	uncertain significance	10	116858997	116858997	Human		name
155930828	CV2220920	single nucleotide variant	NM_001242699.2(ENO4):c.685G>C (p.Glu229Gln)	not specified [RCV004092620]	uncertain significance	10	116860844	116860844	Human		name
155981392	CV2233074	single nucleotide variant	NM_001242699.2(ENO4):c.716G>A (p.Gly239Glu)	not specified [RCV004103703]	uncertain significance	10	116860875	116860875	Human		name
156317891	CV2251109	single nucleotide variant	NM_001242699.2(ENO4):c.685G>A (p.Glu229Lys)	not specified [RCV004123650]	uncertain significance	10	116860844	116860844	Human		name
156221181	CV2345122	single nucleotide variant	NM_001242699.2(ENO4):c.454T>C (p.Ser152Pro)	not specified [RCV004193393]	uncertain significance	10	116856651	116856651	Human		name
156188513	CV2395453	single nucleotide variant	NM_001242699.2(ENO4):c.496G>A (p.Ala166Thr)	not specified [RCV004241322]	uncertain significance	10	116859000	116859000	Human		name
156146580	CV2397428	single nucleotide variant	NM_001242699.2(ENO4):c.533T>C (p.Leu178Ser)	not specified [RCV004238945]	uncertain significance	10	116859037	116859037	Human		name
401760910	CV2706143	single nucleotide variant	NM_001242699.2(ENO4):c.700G>A (p.Gly234Ser)	not specified [RCV004314827]	uncertain significance	10	116860859	116860859	Human		name
401782637	CV2719915	single nucleotide variant	NM_001242699.2(ENO4):c.388G>A (p.Ala130Thr)	not specified [RCV004329315]	uncertain significance	10	116856585	116856585	Human		name
401872670	CV2764285	single nucleotide variant	NM_001242699.2(ENO4):c.943G>A (p.Glu315Lys)	not specified [RCV004336817]	uncertain significance	10	116862805	116862805	Human		name
405756818	CV3245174	single nucleotide variant	NM_001242699.2(ENO4):c.428C>T (p.Thr143Met)	not specified [RCV004382806]	uncertain significance	10	116856625	116856625	Human		name
405756823	CV3245175	single nucleotide variant	NM_001242699.2(ENO4):c.742G>C (p.Ala248Pro)	not specified [RCV004382807]	uncertain significance	10	116860901	116860901	Human		name
407507260	CV3435071	single nucleotide variant	NM_001242699.2(ENO4):c.883A>C (p.Asn295His)	not specified [RCV004625046]	uncertain significance	10	116861137	116861137	Human		name
597747301	CV3664547	single nucleotide variant	NM_001242699.2(ENO4):c.389C>T (p.Ala130Val)	not specified [RCV004922900]	uncertain significance	10	116856586	116856586	Human		name
598269530	CV3954276	single nucleotide variant	NM_001242699.2(ENO4):c.707T>C (p.Met236Thr)	not specified [RCV005327351]	uncertain significance	10	116860866	116860866	Human		name
598269536	CV3954277	single nucleotide variant	NM_001242699.2(ENO4):c.656A>G (p.Glu219Gly)	not specified [RCV005327352]	uncertain significance	10	116860815	116860815	Human		name
598269542	CV3954278	single nucleotide variant	NM_001242699.2(ENO4):c.721G>T (p.Val241Leu)	not specified [RCV005327353]	uncertain significance	10	116860880	116860880	Human		name
598269547	CV3954279	single nucleotide variant	NM_001242699.2(ENO4):c.418A>G (p.Ser140Gly)	not specified [RCV005327354]	likely benign	10	116856615	116856615	Human		name
598269565	CV3954282	single nucleotide variant	NM_001242699.2(ENO4):c.811C>T (p.Pro271Ser)	not specified [RCV005327357]	uncertain significance	10	116861065	116861065	Human		name
598269571	CV3954283	single nucleotide variant	NM_001242699.2(ENO4):c.472G>C (p.Asp158His)	not specified [RCV005327358]	uncertain significance	10	116856669	116856669	Human		name
155920744	CV2210874	single nucleotide variant	NM_001242699.2(ENO4):c.1057A>T (p.Thr353Ser)	not specified [RCV004085959]	uncertain significance	10	116871134	116871134	Human		name
155972723	CV2214360	single nucleotide variant	NM_001242699.2(ENO4):c.1681C>T (p.Leu561Phe)	not specified [RCV004088135]	uncertain significance	10	116879944	116879944	Human		name
155916016	CV2281844	single nucleotide variant	NM_001242699.2(ENO4):c.1635G>C (p.Lys545Asn)	not specified [RCV004136849]	uncertain significance	10	116879898	116879898	Human		name
156160024	CV2311633	single nucleotide variant	NM_001242699.2(ENO4):c.1786C>T (p.Leu596Phe)	not specified [RCV004168730]	uncertain significance	10	116881577	116881577	Human		name
156078063	CV2318654	single nucleotide variant	NM_001242699.2(ENO4):c.1022G>A (p.Gly341Glu)	not specified [RCV004173551]	uncertain significance	10	116868681	116868681	Human		name
156165302	CV2319855	single nucleotide variant	NM_001242699.2(ENO4):c.1679G>A (p.Arg560His)	not specified [RCV004167739]	uncertain significance	10	116879942	116879942	Human		name
329396558	CV2462745	single nucleotide variant	NM_001242699.2(ENO4):c.1676A>G (p.Asn559Ser)	not specified [RCV004278669]	uncertain significance	10	116879939	116879939	Human		name
401779989	CV2676765	single nucleotide variant	NM_001242699.2(ENO4):c.1745T>C (p.Phe582Ser)	not specified [RCV004290937]	uncertain significance	10	116881536	116881536	Human		name
401731526	CV2701408	single nucleotide variant	NM_001242699.2(ENO4):c.1712A>G (p.Asn571Ser)	not specified [RCV004311768]	uncertain significance	10	116879975	116879975	Human		name
401777563	CV2704155	single nucleotide variant	NM_001242699.2(ENO4):c.1262C>T (p.Ala421Val)	not specified [RCV004311168]	uncertain significance	10	116874122	116874122	Human		name
401772895	CV2709008	single nucleotide variant	NM_001242699.2(ENO4):c.1837G>C (p.Gly613Arg)	not specified [RCV004314362]	uncertain significance	10	116881628	116881628	Human		name
401877033	CV2764458	single nucleotide variant	NM_001242699.2(ENO4):c.1532T>C (p.Ile511Thr)	not specified [RCV004339023]	uncertain significance	10	116876255	116876255	Human		name
405756780	CV3245169	single nucleotide variant	NM_001242699.2(ENO4):c.1088C>T (p.Thr363Ile)	not specified [RCV004382801]	uncertain significance	10	116871165	116871165	Human		name
405756789	CV3245170	single nucleotide variant	NM_001242699.2(ENO4):c.1145A>G (p.Asn382Ser)	not specified [RCV004382802]	uncertain significance	10	116871222	116871222	Human		name
405756795	CV3245171	single nucleotide variant	NM_001242699.2(ENO4):c.1551C>G (p.Ile517Met)	not specified [RCV004382803]	uncertain significance	10	116879304	116879304	Human		name
405756805	CV3245172	single nucleotide variant	NM_001242699.2(ENO4):c.1625G>A (p.Arg542Gln)	not specified [RCV004382804]	uncertain significance	10	116879888	116879888	Human		name
405756813	CV3245173	single nucleotide variant	NM_001242699.2(ENO4):c.1690A>G (p.Ile564Val)	not specified [RCV004382805]	uncertain significance	10	116879953	116879953	Human		name
407507262	CV3435072	single nucleotide variant	NM_001242699.2(ENO4):c.1314T>G (p.Ile438Met)	not specified [RCV004625047]	uncertain significance	10	116874174	116874174	Human		name
407507265	CV3435073	single nucleotide variant	NM_001242699.2(ENO4):c.1065G>T (p.Lys355Asn)	not specified [RCV004625048]	uncertain significance	10	116871142	116871142	Human		name
597747297	CV3664544	single nucleotide variant	NM_001242699.2(ENO4):c.1855G>A (p.Glu619Lys)	not specified [RCV004922899]	likely benign	10	116881646	116881646	Human		name
597686488	CV3664546	single nucleotide variant	NM_001242699.2(ENO4):c.1097G>A (p.Cys366Tyr)	not specified [RCV004914896]	likely benign	10	116871174	116871174	Human		name
597686498	CV3664548	single nucleotide variant	NM_001242699.2(ENO4):c.1799C>T (p.Ala600Val)	not specified [RCV004914897]	uncertain significance	10	116881590	116881590	Human		name
597686507	CV3664549	single nucleotide variant	NM_001242699.2(ENO4):c.1546C>G (p.His516Asp)	not specified [RCV004914898]	uncertain significance	10	116879299	116879299	Human		name
597686516	CV3664550	single nucleotide variant	NM_001242699.2(ENO4):c.1379G>C (p.Gly460Ala)	not specified [RCV004914899]	uncertain significance	10	116876102	116876102	Human		name
598269525	CV3954275	single nucleotide variant	NM_001242699.2(ENO4):c.1778C>T (p.Ala593Val)	not specified [RCV005327350]	uncertain significance	10	116881569	116881569	Human		name
598269559	CV3954281	single nucleotide variant	NM_001242699.2(ENO4):c.1208T>G (p.Met403Arg)	not specified [RCV005327356]	uncertain significance	10	116871285	116871285	Human		name

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