Exoc4 Variant Search Result - Rat Genome Database

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110 records found for search term Exoc4

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
8590419	CV125111	single nucleotide variant	NM_021807.3(EXOC4):c.1872-1988A>G	Lung cancer [RCV000105630]	uncertain significance	7	133915595	133915595	Human		name
8590420	CV125112	single nucleotide variant	NM_021807.3(EXOC4):c.2207-1042T>G	Lung cancer [RCV000105631]	uncertain significance	7	133996450	133996450	Human		name
8590417	CV125109	single nucleotide variant	NM_021807.3(EXOC4):c.1515-66401G>C	Lung cancer [RCV000105628]	uncertain significance	7	133750924	133750924	Human		name
8590418	CV125110	single nucleotide variant	NM_021807.3(EXOC4):c.1515-27639C>G	Lung cancer [RCV000105629]	uncertain significance	7	133789686	133789686	Human		name
598203605	CV3896439	single nucleotide variant	NM_021807.4(EXOC4):c.1417+54940G>A	Familial colorectal cancer type X [RCV005356686]	uncertain significance	7	133535078	133535078	Human	1	name
8590416	CV125108	single nucleotide variant	NM_001037126.1(EXOC4):c.471+4526C>T	Lung cancer [RCV000105627]	uncertain significance	7	133293642	133293642	Human		name
15118027	CV710783	single nucleotide variant	NM_021807.4(EXOC4):c.60C>T (p.Pro20=)	not provided [RCV000962302]	benign	7	133253161	133253161	Human	2	name
15118027	CV710783	single nucleotide variant	NM_021807.4(EXOC4):c.60C>T (p.Pro20=)	not provided [RCV000962302]	benign	7	133253161	133253162	Human	2	name
401778320	CV2709011	single nucleotide variant	NM_021807.4(EXOC4):c.61T>C (p.Ser21Pro)	not specified [RCV004314365]	uncertain significance	7	133253162	133253162	Human		name
405773318	CV3252623	single nucleotide variant	NM_021807.4(EXOC4):c.45C>G (p.Ser15Arg)	not specified [RCV004385507]	uncertain significance	7	133253146	133253146	Human		name
597715701	CV3675189	single nucleotide variant	NM_021807.4(EXOC4):c.51C>G (p.Ser17Arg)	not specified [RCV004918249]	uncertain significance	7	133253152	133253152	Human		name
598210734	CV3954814	single nucleotide variant	NM_021807.4(EXOC4):c.68T>A (p.Leu23Gln)	not specified [RCV005338791]	uncertain significance	7	133253169	133253169	Human		name
156153878	CV2395026	single nucleotide variant	NM_021807.4(EXOC4):c.133G>T (p.Gly45Cys)	not specified [RCV004236716]	uncertain significance	7	133275028	133275028	Human		name
329364921	CV2444039	single nucleotide variant	NM_021807.4(EXOC4):c.167G>C (p.Arg56Pro)	not specified [RCV004258358]	uncertain significance	7	133275062	133275062	Human		name
401909012	CV2823172	single nucleotide variant	NM_021807.4(EXOC4):c.1395T>C (p.Tyr465=)	not provided [RCV003423769]	likely benign	7	133480116	133480116	Human		name
401922875	CV2823173	single nucleotide variant	NM_021807.4(EXOC4):c.2298G>A (p.Ser766=)	not provided [RCV003434137]	likely benign	7	133997583	133997583	Human		name
405773281	CV3252616	single nucleotide variant	NM_021807.4(EXOC4):c.166C>T (p.Arg56Cys)	not specified [RCV004385500]	uncertain significance	7	133275061	133275061	Human		name
405773286	CV3252617	single nucleotide variant	NM_021807.4(EXOC4):c.233G>A (p.Ser78Asn)	not specified [RCV004385501]	uncertain significance	7	133275128	133275128	Human		name
405773299	CV3252620	single nucleotide variant	NM_021807.4(EXOC4):c.244C>T (p.Arg82Cys)	not specified [RCV004385504]	uncertain significance	7	133275139	133275139	Human		name
597715670	CV3675186	single nucleotide variant	NM_021807.4(EXOC4):c.285G>T (p.Glu95Asp)	not specified [RCV004918246]	uncertain significance	7	133288930	133288930	Human		name
15187960	CV699856	single nucleotide variant	NM_021807.4(EXOC4):c.2247C>T (p.Leu749=)	not provided [RCV000953742]	benign	7	133997532	133997532	Human		name
15112313	CV722329	single nucleotide variant	NM_021807.4(EXOC4):c.2778C>T (p.Ile926=)	not provided [RCV000894445]	benign	7	134064381	134064381	Human		name
8632350	CV87558	single nucleotide variant	NM_021807.3(EXOC4):c.2763G>A (p.Thr921=)	Malignant melanoma [RCV000067649]	not provided	7	134064366	134064366	Human		name
155974992	CV2211228	single nucleotide variant	NM_021807.4(EXOC4):c.745A>G (p.Thr249Ala)	not specified [RCV004088378]	uncertain significance	7	133317372	133317372	Human		name
156068303	CV2222025	single nucleotide variant	NM_021807.4(EXOC4):c.563T>C (p.Leu188Pro)	not specified [RCV004103012]	uncertain significance	7	133305968	133305968	Human		name
156357415	CV2253993	single nucleotide variant	NM_021807.4(EXOC4):c.346A>G (p.Ile116Val)	not specified [RCV004127661]	uncertain significance	7	133288991	133288991	Human		name
156000877	CV2257793	single nucleotide variant	NM_021807.4(EXOC4):c.968A>C (p.Tyr323Ser)	not specified [RCV004127855]	uncertain significance	7	133356534	133356534	Human		name
156052408	CV2269422	single nucleotide variant	NM_021807.4(EXOC4):c.985G>A (p.Val329Ile)	not specified [RCV004124543]	uncertain significance	7	133356551	133356551	Human		name
156020355	CV2309514	single nucleotide variant	NM_021807.4(EXOC4):c.322C>T (p.Arg108Trp)	not specified [RCV004158908]	uncertain significance	7	133288967	133288967	Human		name
156189311	CV2342396	single nucleotide variant	NM_021807.4(EXOC4):c.843C>G (p.Ile281Met)	not specified [RCV004194009]	uncertain significance	7	133356409	133356409	Human		name
156055316	CV2361375	single nucleotide variant	NM_021807.4(EXOC4):c.458C>T (p.Ala153Val)	not specified [RCV004218577]	uncertain significance	7	133289103	133289103	Human		name
329402388	CV2454231	single nucleotide variant	NM_021807.4(EXOC4):c.860C>T (p.Ala287Val)	not specified [RCV004265709]	uncertain significance	7	133356426	133356426	Human		name
401757586	CV2675395	single nucleotide variant	NM_021807.4(EXOC4):c.996G>C (p.Glu332Asp)	not specified [RCV004292198]	uncertain significance	7	133356562	133356562	Human		name
401892117	CV2777249	single nucleotide variant	NM_021807.4(EXOC4):c.611C>T (p.Ser204Leu)	not specified [RCV004354275]	uncertain significance	7	133306016	133306016	Human		name
405773324	CV3252624	single nucleotide variant	NM_021807.4(EXOC4):c.632G>A (p.Arg211His)	not specified [RCV004385508]	uncertain significance	7	133306037	133306037	Human		name
405773330	CV3252625	single nucleotide variant	NM_021807.4(EXOC4):c.659C>A (p.Ser220Tyr)	not specified [RCV004385509]	uncertain significance	7	133317286	133317286	Human		name
405773336	CV3252626	single nucleotide variant	NM_021807.4(EXOC4):c.695T>C (p.Val232Ala)	not specified [RCV004385510]	uncertain significance	7	133317322	133317322	Human		name
405773342	CV3252627	single nucleotide variant	NM_021807.4(EXOC4):c.748G>A (p.Ala250Thr)	not specified [RCV004385511]	uncertain significance	7	133317375	133317375	Human		name
405773350	CV3252628	single nucleotide variant	NM_021807.4(EXOC4):c.974G>C (p.Arg325Pro)	not specified [RCV004385512]	uncertain significance	7	133356540	133356540	Human		name
597715596	CV3675178	single nucleotide variant	NM_021807.4(EXOC4):c.853G>T (p.Gly285Cys)	not specified [RCV004918238]	uncertain significance	7	133356419	133356419	Human		name
597715644	CV3675183	single nucleotide variant	NM_021807.4(EXOC4):c.883A>G (p.Thr295Ala)	not specified [RCV004918243]	uncertain significance	7	133356449	133356449	Human		name
597715651	CV3675184	single nucleotide variant	NM_021807.4(EXOC4):c.361C>A (p.His121Asn)	not specified [RCV004918244]	uncertain significance	7	133289006	133289006	Human		name
597715720	CV3675191	single nucleotide variant	NM_021807.4(EXOC4):c.407A>G (p.Gln136Arg)	not specified [RCV004918251]	uncertain significance	7	133289052	133289052	Human		name
598210713	CV3954811	single nucleotide variant	NM_021807.4(EXOC4):c.793G>A (p.Glu265Lys)	not specified [RCV005338788]	uncertain significance	7	133356359	133356359	Human		name
598210726	CV3954813	single nucleotide variant	NM_021807.4(EXOC4):c.431G>A (p.Cys144Tyr)	not specified [RCV005338790]	uncertain significance	7	133289076	133289076	Human		name
598210756	CV3954818	single nucleotide variant	NM_021807.4(EXOC4):c.303G>C (p.Lys101Asn)	not specified [RCV005338794]	uncertain significance	7	133288948	133288948	Human		name
9850345	CV181425	single nucleotide variant	NM_021807.4(EXOC4):c.1733A>G (p.Gln578Arg)	Meckel-Gruber syndrome [RCV000162153]	likely pathogenic	7	133817543	133817543	Human	1	name
156092967	CV2216898	single nucleotide variant	NM_021807.4(EXOC4):c.2139G>C (p.Met713Ile)	not specified [RCV004083311]	uncertain significance	7	133938002	133938002	Human		name
156326592	CV2219642	single nucleotide variant	NM_021807.4(EXOC4):c.2782G>A (p.Ala928Thr)	not specified [RCV004093751]	uncertain significance	7	134064385	134064385	Human		name
156390011	CV2222946	single nucleotide variant	NM_021807.4(EXOC4):c.2339T>A (p.Leu780Gln)	not specified [RCV004101753]	uncertain significance	7	133997624	133997624	Human		name
156036307	CV2243519	single nucleotide variant	NM_021807.4(EXOC4):c.1432A>G (p.Asn478Asp)	not specified [RCV004112472]	uncertain significance	7	133630059	133630059	Human		name
156023758	CV2245510	single nucleotide variant	NM_021807.4(EXOC4):c.1966A>G (p.Met656Val)	not specified [RCV004109283]	uncertain significance	7	133917677	133917677	Human		name
156370011	CV2263458	single nucleotide variant	NM_021807.4(EXOC4):c.1783C>G (p.His595Asp)	not specified [RCV004133703]	uncertain significance	7	133895647	133895647	Human		name
155904101	CV2282359	single nucleotide variant	NM_021807.4(EXOC4):c.1108C>G (p.Pro370Ala)	not specified [RCV004133181]	uncertain significance	7	133374928	133374928	Human		name
156255589	CV2307727	single nucleotide variant	NM_021807.4(EXOC4):c.2104C>T (p.Arg702Cys)	not specified [RCV004168421]	uncertain significance	7	133937967	133937967	Human		name
156271949	CV2308702	single nucleotide variant	NM_021807.4(EXOC4):c.2482A>G (p.Met828Val)	not specified [RCV004169031]	uncertain significance	7	134005045	134005045	Human		name
156043030	CV2311019	single nucleotide variant	NM_021807.4(EXOC4):c.1840G>A (p.Glu614Lys)	not specified [RCV004164039]	uncertain significance	7	133895704	133895704	Human		name
156257628	CV2322079	single nucleotide variant	NM_021807.4(EXOC4):c.2045A>C (p.Glu682Ala)	not specified [RCV004173822]	uncertain significance	7	133937908	133937908	Human		name
156303932	CV2341334	single nucleotide variant	NM_021807.4(EXOC4):c.2656A>G (p.Met886Val)	not specified [RCV004186739]	uncertain significance	7	134007804	134007804	Human		name
156005704	CV2394044	single nucleotide variant	NM_021807.4(EXOC4):c.1255G>A (p.Ala419Thr)	not specified [RCV004236261]	uncertain significance	7	133475400	133475400	Human		name
156166235	CV2398912	single nucleotide variant	NM_021807.4(EXOC4):c.1876A>G (p.Ile626Val)	not specified [RCV004245227]	uncertain significance	7	133917587	133917587	Human		name
329382829	CV2424568	single nucleotide variant	NM_021807.4(EXOC4):c.1759G>A (p.Val587Ile)	not specified [RCV004254069]	uncertain significance	7	133895623	133895623	Human		name
329400242	CV2437475	single nucleotide variant	NM_021807.4(EXOC4):c.1400G>A (p.Arg467Gln)	not specified [RCV004258766]	uncertain significance	7	133480121	133480121	Human		name
329400103	CV2440580	single nucleotide variant	NM_021807.4(EXOC4):c.1165A>G (p.Ile389Val)	not specified [RCV004256493]	uncertain significance	7	133374985	133374985	Human		name
329357331	CV2457515	single nucleotide variant	NM_021807.4(EXOC4):c.2774A>G (p.Tyr925Cys)	not specified [RCV004267326]	uncertain significance	7	134064377	134064377	Human		name
329395900	CV2463053	single nucleotide variant	NM_021807.4(EXOC4):c.1862C>T (p.Ala621Val)	not specified [RCV004272868]	uncertain significance	7	133895726	133895726	Human		name
401739649	CV2684131	single nucleotide variant	NM_021807.4(EXOC4):c.2560A>G (p.Asn854Asp)	not specified [RCV004288809]	uncertain significance	7	134007708	134007708	Human		name
401771441	CV2686174	single nucleotide variant	NM_021807.4(EXOC4):c.2198C>T (p.Thr733Ile)	not specified [RCV004297272]	uncertain significance	7	133938061	133938061	Human		name
401748182	CV2700023	single nucleotide variant	NM_021807.4(EXOC4):c.2920G>A (p.Val974Ile)	not specified [RCV004310448]	uncertain significance	7	134064523	134064523	Human		name
401717999	CV2704124	single nucleotide variant	NM_021807.4(EXOC4):c.1813C>G (p.Leu605Val)	not specified [RCV004308988]	uncertain significance	7	133895677	133895677	Human		name
401749345	CV2706557	single nucleotide variant	NM_021807.4(EXOC4):c.2366A>G (p.Tyr789Cys)	not specified [RCV004319147]	uncertain significance	7	134004929	134004929	Human		name
401889468	CV2758133	single nucleotide variant	NM_021807.4(EXOC4):c.1220G>A (p.Arg407His)	not specified [RCV004341511]	uncertain significance	7	133475365	133475365	Human		name
401944844	CV2840649	single nucleotide variant	NM_021807.4(EXOC4):c.1613A>G (p.Asn538Ser)	not provided [RCV003457522]	likely benign	7	133817423	133817423	Human		name
405773117	CV3252611	single nucleotide variant	NM_021807.4(EXOC4):c.1111C>G (p.Leu371Val)	not specified [RCV004385495]	uncertain significance	7	133374931	133374931	Human		name
405773122	CV3252612	single nucleotide variant	NM_021807.4(EXOC4):c.1226C>A (p.Ala409Asp)	not specified [RCV004385496]	uncertain significance	7	133475371	133475371	Human		name
405773127	CV3252613	single nucleotide variant	NM_021807.4(EXOC4):c.1279G>C (p.Ala427Pro)	not specified [RCV004385497]	uncertain significance	7	133475424	133475424	Human		name
405773135	CV3252614	single nucleotide variant	NM_021807.4(EXOC4):c.1462G>T (p.Val488Phe)	not specified [RCV004385498]	uncertain significance	7	133630089	133630089	Human		name
405773290	CV3252618	single nucleotide variant	NM_021807.4(EXOC4):c.2413G>C (p.Val805Leu)	not specified [RCV004385502]	uncertain significance	7	134004976	134004976	Human		name
405773294	CV3252619	single nucleotide variant	NM_021807.4(EXOC4):c.2434C>G (p.Pro812Ala)	not specified [RCV004385503]	uncertain significance	7	134004997	134004997	Human		name
405773306	CV3252621	single nucleotide variant	NM_021807.4(EXOC4):c.2834A>G (p.Gln945Arg)	not specified [RCV004385505]	uncertain significance	7	134064437	134064437	Human		name
405773310	CV3252622	single nucleotide variant	NM_021807.4(EXOC4):c.2857A>C (p.Lys953Gln)	not specified [RCV004385506]	uncertain significance	7	134064460	134064460	Human		name
407500341	CV3438603	single nucleotide variant	NM_021807.4(EXOC4):c.1588G>A (p.Val530Met)	not specified [RCV004622922]	likely benign	7	133817398	133817398	Human		name
407500336	CV3438604	single nucleotide variant	NM_021807.4(EXOC4):c.1343C>T (p.Ser448Phe)	not specified [RCV004622923]	uncertain significance	7	133480064	133480064	Human		name
407500332	CV3438605	single nucleotide variant	NM_021807.4(EXOC4):c.2138T>C (p.Met713Thr)	not specified [RCV004622924]	uncertain significance	7	133938001	133938001	Human		name
407500207	CV3438606	single nucleotide variant	NM_021807.4(EXOC4):c.2492G>C (p.Ser831Thr)	not specified [RCV004622925]	uncertain significance	7	134005055	134005055	Human		name
407500109	CV3438607	single nucleotide variant	NM_021807.4(EXOC4):c.2864T>G (p.Ile955Ser)	not specified [RCV004622926]	uncertain significance	7	134064467	134064467	Human		name
407500019	CV3438608	single nucleotide variant	NM_021807.4(EXOC4):c.1909G>T (p.Ala637Ser)	not specified [RCV004622927]	uncertain significance	7	133917620	133917620	Human		name
597715607	CV3675179	single nucleotide variant	NM_021807.4(EXOC4):c.1663T>C (p.Ser555Pro)	not specified [RCV004918239]	uncertain significance	7	133817473	133817473	Human		name
597715616	CV3675180	single nucleotide variant	NM_021807.4(EXOC4):c.1214A>G (p.Asn405Ser)	not specified [RCV004918240]	uncertain significance	7	133475359	133475359	Human		name
597715624	CV3675181	single nucleotide variant	NM_021807.4(EXOC4):c.1280C>G (p.Ala427Gly)	not specified [RCV004918241]	uncertain significance	7	133475425	133475425	Human		name
597715634	CV3675182	single nucleotide variant	NM_021807.4(EXOC4):c.2317C>T (p.Arg773Cys)	not specified [RCV004918242]	uncertain significance	7	133997602	133997602	Human		name
597715660	CV3675185	single nucleotide variant	NM_021807.4(EXOC4):c.2165G>A (p.Ser722Asn)	not specified [RCV004918245]	uncertain significance	7	133938028	133938028	Human		name
597715679	CV3675187	single nucleotide variant	NM_021807.4(EXOC4):c.2449C>T (p.Leu817Phe)	not specified [RCV004918247]	uncertain significance	7	134005012	134005012	Human		name
597715710	CV3675190	single nucleotide variant	NM_021807.4(EXOC4):c.1843T>C (p.Tyr615His)	not specified [RCV004918250]	uncertain significance	7	133895707	133895707	Human		name
597715730	CV3675192	single nucleotide variant	NM_021807.4(EXOC4):c.1253A>C (p.Tyr418Ser)	not specified [RCV004918252]	uncertain significance	7	133475398	133475398	Human		name
598210688	CV3954808	single nucleotide variant	NM_021807.4(EXOC4):c.2320T>C (p.Cys774Arg)	not specified [RCV005338785]	uncertain significance	7	133997605	133997605	Human		name
598210698	CV3954809	single nucleotide variant	NM_021807.4(EXOC4):c.1123G>A (p.Glu375Lys)	not specified [RCV005338786]	uncertain significance	7	133374943	133374943	Human		name
598210705	CV3954810	single nucleotide variant	NM_021807.4(EXOC4):c.2137A>G (p.Met713Val)	not specified [RCV005338787]	uncertain significance	7	133938000	133938000	Human		name
598210719	CV3954812	single nucleotide variant	NM_021807.4(EXOC4):c.1735A>T (p.Ser579Cys)	not specified [RCV005338789]	uncertain significance	7	133895599	133895599	Human		name
598210741	CV3954815	single nucleotide variant	NM_021807.4(EXOC4):c.1454C>G (p.Thr485Arg)	not specified [RCV005338792]	uncertain significance	7	133630081	133630081	Human		name
598194686	CV3954816	single nucleotide variant	NM_021807.4(EXOC4):c.1067A>G (p.His356Arg)	not specified [RCV005335439]	uncertain significance	7	133374887	133374887	Human		name
598210749	CV3954817	single nucleotide variant	NM_021807.4(EXOC4):c.2542A>C (p.Ile848Leu)	not specified [RCV005338793]	uncertain significance	7	134007690	134007690	Human		name
598210764	CV3954819	single nucleotide variant	NM_021807.4(EXOC4):c.1052C>G (p.Ala351Gly)	not specified [RCV005338795]	uncertain significance	7	133374872	133374872	Human		name
15108798	CV722328	single nucleotide variant	NM_021807.4(EXOC4):c.1648G>A (p.Gly550Arg)	not provided [RCV000893737]	benign	7	133817458	133817458	Human		name
8632351	CV87559	single nucleotide variant	NM_021807.3(EXOC4):c.2764G>A (p.Glu922Lys)	Malignant melanoma [RCV000067650]	not provided	7	134064367	134064367	Human		name
8626338	CV81482	single nucleotide variant	NM_001037126.1(EXOC4):c.532C>T (p.Arg178Ter)	Malignant melanoma [RCV000061560]	not provided	7	133305937	133305937	Human		name
598245563	CV3896438	duplication	NM_021807.4(EXOC4):c.1417+45990_1417+46001dup	Familial colorectal cancer type X [RCV005365818]	uncertain significance	7	133526126	133526127	Human	1	name
598203599	CV3896440	deletion	NM_021807.4(EXOC4):c.1417+55217_1417+55218del	Familial colorectal cancer type X [RCV005356687]	uncertain significance	7	133535355	133535356	Human	1	name
598245571	CV3896441	duplication	NM_021807.4(EXOC4):c.1417+70974_1417+70999dup	Familial colorectal cancer type X [RCV005365819]	likely benign	7	133551111	133551112	Human	1	name
598210631	CV4008041	indel	NM_021807.4(EXOC4):c.1418-70589_1418-70578delinsA	Colorectal cancer, susceptibility to, 12 [RCV005400355]	uncertain significance	7	133559456	133559467	Human		name

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