Eno4 Variant Search Result - Rat Genome Database

Advanced Search (OLGA)

Variants search result for Homo sapiens
(View Results for all Objects and Ontologies)

58 records found for search term Eno4

Refine Term:

Assembly:

Chr

Sort By:

Export

CSV

TAB

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

Gene Annotator (Functional Annotation) unavailable	Gene Annotator (Annotation Distribution) unavailable	Variant Visualizer (Genomic Variants) unavailble Variant Visualizer (Genomic Variants) unavailable
Gene Annotator (Functional Annotation)	Gene Annotator (Annotation Distribution)	Variant Visualizer (Genomic Variants)

InterViewer (Protein-Protein Interactions) unavailable	Gviewer (Genome Viewer) unavailable	Variant Visualizer (Damaging Variants) unavailble Variant Visualizer (Damaging Variants) unavailable
InterViewer (Protein-Protein Interactions)	GViewer (Genome Viewer)	Variant Visualizer (Damaging Variants)

Gene Annotator (Annotation Comparison) unavailable	OLGA (Gene List Generator) unavailable
Gene Annotator (Annotation Comparison)	OLGA (Gene List Generator)	Excel (Download)

MOET (Multi-Ontology Enrichement) unavailable	GOLF (Gene-Ortholog Location Finder) unavailable
MOET (Multi-Ontology Enrichement)	GOLF (Gene-Ortholog Location Finder)

Create Name:

Description:

Send us a Message