Nedd9 Variant Search Result - Rat Genome Database

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86 records found for search term Nedd9

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
156085481	CV2295259	single nucleotide variant	NM_006403.4(NEDD9):c.99A>G (p.Ile33Met)	not specified [RCV004158633]	uncertain significance	6	11213641	11213641	Human		name
598231462	CV3990632	single nucleotide variant	NM_006403.4(NEDD9):c.74G>A (p.Arg25His)	not specified [RCV005381375]	uncertain significance	6	11213666	11213666	Human		name
156342041	CV2225992	single nucleotide variant	NM_006403.4(NEDD9):c.223G>C (p.Glu75Gln)	not specified [RCV004105154]	uncertain significance	6	11213517	11213517	Human		name
401925429	CV2822699	single nucleotide variant	NM_006403.4(NEDD9):c.2037C>T (p.Pro679=)	not provided [RCV003436496]	likely benign	6	11185630	11185630	Human		name
405812384	CV3353064	single nucleotide variant	NM_006403.4(NEDD9):c.224A>T (p.Glu75Val)	not specified [RCV004483264]	uncertain significance	6	11213516	11213516	Human		name
407526129	CV3454804	single nucleotide variant	NM_006403.4(NEDD9):c.289C>G (p.Pro97Ala)	not specified [RCV004654700]	uncertain significance	6	11213451	11213451	Human		name
597670543	CV3555823	single nucleotide variant	NM_006403.4(NEDD9):c.247C>G (p.Gln83Glu)	not specified [RCV004829678]	uncertain significance	6	11213493	11213493	Human		name
597670525	CV3555825	single nucleotide variant	NM_006403.4(NEDD9):c.152G>T (p.Arg51Leu)	not specified [RCV004829680]	uncertain significance	6	11213588	11213588	Human		name
598254198	CV3990637	single nucleotide variant	NM_006403.4(NEDD9):c.148G>A (p.Gly50Ser)	not specified [RCV005385465]	uncertain significance	6	11213592	11213592	Human		name
15149416	CV710129	single nucleotide variant	NM_006403.4(NEDD9):c.1743C>T (p.His581=)	not provided [RCV000967749]	benign	6	11190126	11190126	Human		name
15164974	CV721677	single nucleotide variant	NM_006403.4(NEDD9):c.1899C>T (p.His633=)	not provided [RCV000882313]	benign\|likely benign	6	11189970	11189970	Human		name
155975025	CV2235805	single nucleotide variant	NM_006403.4(NEDD9):c.580T>A (p.Ser194Thr)	not specified [RCV004111927]	uncertain significance	6	11192428	11192428	Human		name
156036322	CV2243534	single nucleotide variant	NM_006403.4(NEDD9):c.871G>A (p.Ala291Thr)	not specified [RCV004112487]	uncertain significance	6	11190998	11190998	Human		name
156135148	CV2256834	single nucleotide variant	NM_006403.4(NEDD9):c.739A>G (p.Met247Val)	not specified [RCV004121050]	uncertain significance	6	11191130	11191130	Human		name
155904612	CV2276038	single nucleotide variant	NM_006403.4(NEDD9):c.623T>G (p.Ile208Arg)	not specified [RCV004141714]	uncertain significance	6	11192385	11192385	Human		name
156161920	CV2319510	single nucleotide variant	NM_006403.4(NEDD9):c.997A>T (p.Ser333Cys)	not specified [RCV004185080]	uncertain significance	6	11190872	11190872	Human		name
156114308	CV2397151	single nucleotide variant	NM_006403.4(NEDD9):c.770C>T (p.Pro257Leu)	not specified [RCV004236651]	uncertain significance	6	11191099	11191099	Human		name
329387253	CV2436336	single nucleotide variant	NM_006403.4(NEDD9):c.811G>C (p.Ala271Pro)	not specified [RCV004251735]	uncertain significance	6	11191058	11191058	Human		name
329374530	CV2443919	single nucleotide variant	NM_006403.4(NEDD9):c.664G>A (p.Val222Ile)	not specified [RCV004258249]	uncertain significance	6	11191205	11191205	Human		name
329375133	CV2444906	single nucleotide variant	NM_006403.4(NEDD9):c.452G>A (p.Gly151Asp)	not specified [RCV004259142]	uncertain significance	6	11213288	11213288	Human		name
329397471	CV2456207	single nucleotide variant	NM_006403.4(NEDD9):c.713A>C (p.Glu238Ala)	not specified [RCV004273392]	uncertain significance	6	11191156	11191156	Human		name
401769986	CV2710786	single nucleotide variant	NM_006403.4(NEDD9):c.373G>A (p.Gly125Ser)	not specified [RCV004308715]	uncertain significance	6	11213367	11213367	Human		name
401784363	CV2717298	single nucleotide variant	NM_006403.4(NEDD9):c.866C>T (p.Pro289Leu)	not specified [RCV004330194]	likely benign	6	11191003	11191003	Human		name
401775820	CV2724231	single nucleotide variant	NM_006403.4(NEDD9):c.593G>A (p.Gly198Asp)	not specified [RCV004328126]	uncertain significance	6	11192415	11192415	Human		name
405812478	CV3349271	single nucleotide variant	NM_006403.4(NEDD9):c.947C>T (p.Ala316Val)	not specified [RCV004483316]	uncertain significance	6	11190922	11190922	Human		name
405812489	CV3349277	single nucleotide variant	NM_006403.4(NEDD9):c.967G>A (p.Val323Ile)	not specified [RCV004483322]	uncertain significance	6	11190902	11190902	Human		name
405812404	CV3353075	single nucleotide variant	NM_006403.4(NEDD9):c.359T>C (p.Val120Ala)	not specified [RCV004483275]	uncertain significance	6	11213381	11213381	Human		name
405812413	CV3353080	single nucleotide variant	NM_006403.4(NEDD9):c.433A>G (p.Thr145Ala)	not specified [RCV004483280]	likely benign	6	11213307	11213307	Human		name
405812428	CV3353088	single nucleotide variant	NM_006403.4(NEDD9):c.568G>A (p.Asp190Asn)	not specified [RCV004483288]	uncertain significance	6	11192440	11192440	Human		name
405812462	CV3353107	single nucleotide variant	NM_006403.4(NEDD9):c.692G>A (p.Arg231Gln)	not specified [RCV004483307]	uncertain significance	6	11191177	11191177	Human		name
407489440	CV3454803	single nucleotide variant	NM_006403.4(NEDD9):c.425T>C (p.Ile142Thr)	not specified [RCV004641467]	uncertain significance	6	11213315	11213315	Human		name
597670576	CV3555819	single nucleotide variant	NM_006403.4(NEDD9):c.919G>A (p.Gly307Arg)	not specified [RCV004829674]	uncertain significance	6	11190950	11190950	Human		name
597670559	CV3555821	single nucleotide variant	NM_006403.4(NEDD9):c.945C>G (p.Asp315Glu)	not specified [RCV004829676]	uncertain significance	6	11190924	11190924	Human		name
597670551	CV3555822	single nucleotide variant	NM_006403.4(NEDD9):c.656C>T (p.Thr219Ile)	not specified [RCV004829677]	uncertain significance	6	11192352	11192352	Human		name
597670534	CV3555824	single nucleotide variant	NM_006403.4(NEDD9):c.646A>T (p.Ile216Phe)	not specified [RCV004829679]	uncertain significance	6	11192362	11192362	Human		name
597670514	CV3555826	single nucleotide variant	NM_006403.4(NEDD9):c.565T>A (p.Tyr189Asn)	not specified [RCV004829681]	uncertain significance	6	11192443	11192443	Human		name
597670243	CV3555827	single nucleotide variant	NM_006403.4(NEDD9):c.962G>A (p.Arg321Gln)	not specified [RCV004829682]	uncertain significance	6	11190907	11190907	Human		name
597670274	CV3555831	single nucleotide variant	NM_006403.4(NEDD9):c.526G>A (p.Val176Ile)	not specified [RCV004829686]	likely benign	6	11193626	11193626	Human		name
598231653	CV3990630	single nucleotide variant	NM_006403.4(NEDD9):c.727T>G (p.Phe243Val)	not specified [RCV005381373]	uncertain significance	6	11191142	11191142	Human		name
598254187	CV3990636	single nucleotide variant	NM_006403.4(NEDD9):c.352T>C (p.Tyr118His)	not specified [RCV005385464]	uncertain significance	6	11213388	11213388	Human		name
598254207	CV3990638	single nucleotide variant	NM_006403.4(NEDD9):c.722A>G (p.Tyr241Cys)	not specified [RCV005385466]	uncertain significance	6	11191147	11191147	Human		name
598231489	CV3990640	single nucleotide variant	NM_006403.4(NEDD9):c.355C>G (p.Gln119Glu)	not specified [RCV005381379]	uncertain significance	6	11213385	11213385	Human		name
156098045	CV2206978	single nucleotide variant	NM_006403.4(NEDD9):c.2476C>T (p.Arg826Cys)	not specified [RCV004085598]	uncertain significance	6	11185191	11185191	Human		name
155968950	CV2213244	single nucleotide variant	NM_006403.4(NEDD9):c.1279C>A (p.Leu427Ile)	not specified [RCV004085466]	uncertain significance	6	11190590	11190590	Human		name
156245373	CV2231675	single nucleotide variant	NM_006403.4(NEDD9):c.1694A>G (p.His565Arg)	not specified [RCV004098237]	uncertain significance	6	11190175	11190175	Human		name
155980140	CV2243911	single nucleotide variant	NM_006403.4(NEDD9):c.1837C>T (p.Pro613Ser)	not specified [RCV004108423]	uncertain significance	6	11190032	11190032	Human		name
155927237	CV2285089	single nucleotide variant	NM_006403.4(NEDD9):c.2396T>G (p.Leu799Arg)	not specified [RCV004145319]	uncertain significance	6	11185271	11185271	Human		name
156270980	CV2290223	single nucleotide variant	NM_006403.4(NEDD9):c.1988A>G (p.His663Arg)	not specified [RCV004152875]	uncertain significance	6	11188225	11188225	Human		name
156246290	CV2310557	single nucleotide variant	NM_006403.4(NEDD9):c.2318G>A (p.Arg773His)	not specified [RCV004163575]	uncertain significance	6	11185349	11185349	Human		name
156100974	CV2313451	single nucleotide variant	NM_006403.4(NEDD9):c.1310G>A (p.Cys437Tyr)	not specified [RCV004163765]	uncertain significance	6	11190559	11190559	Human		name
156249103	CV2314122	single nucleotide variant	NM_006403.4(NEDD9):c.2114G>T (p.Arg705Leu)	not specified [RCV004166212]	uncertain significance	6	11185553	11185553	Human		name
156298190	CV2329144	single nucleotide variant	NM_006403.4(NEDD9):c.1914G>C (p.Glu638Asp)	not specified [RCV004173902]	uncertain significance	6	11188299	11188299	Human		name
156098702	CV2370809	single nucleotide variant	NM_006403.4(NEDD9):c.2177T>C (p.Ile726Thr)	not specified [RCV004209203]	uncertain significance	6	11185490	11185490	Human		name
156264429	CV2388952	single nucleotide variant	NM_006403.4(NEDD9):c.1054C>A (p.Pro352Thr)	not specified [RCV004241953]	uncertain significance	6	11190815	11190815	Human		name
329400294	CV2437589	single nucleotide variant	NM_006403.4(NEDD9):c.2152C>T (p.His718Tyr)	not specified [RCV004258868]	uncertain significance	6	11185515	11185515	Human		name
329359979	CV2446505	single nucleotide variant	NM_006403.4(NEDD9):c.1075C>T (p.Arg359Trp)	not specified [RCV004251407]	uncertain significance	6	11190794	11190794	Human		name
329382860	CV2465444	single nucleotide variant	NM_006403.4(NEDD9):c.2237G>T (p.Ser746Ile)	not specified [RCV004281214]	uncertain significance	6	11185430	11185430	Human		name
401726491	CV2674158	single nucleotide variant	NM_006403.4(NEDD9):c.2221A>C (p.Ile741Leu)	not specified [RCV004295560]	uncertain significance	6	11185446	11185446	Human		name
401780928	CV2681822	single nucleotide variant	NM_006403.4(NEDD9):c.2086A>C (p.Thr696Pro)	not specified [RCV004296823]	uncertain significance	6	11185581	11185581	Human		name
401751199	CV2716319	single nucleotide variant	NM_006403.4(NEDD9):c.2038G>A (p.Val680Met)	not specified [RCV004325317]	uncertain significance	6	11185629	11185629	Human		name
401771069	CV2726352	single nucleotide variant	NM_006403.4(NEDD9):c.2368A>G (p.Ile790Val)	not specified [RCV004326789]	uncertain significance	6	11185299	11185299	Human		name
405812259	CV3352996	single nucleotide variant	NM_006403.4(NEDD9):c.1012C>T (p.Pro338Ser)	not specified [RCV004483196]	uncertain significance	6	11190857	11190857	Human		name
405812274	CV3353004	single nucleotide variant	NM_006403.4(NEDD9):c.1130G>A (p.Arg377Gln)	not specified [RCV004483204]	uncertain significance	6	11190739	11190739	Human		name
405812280	CV3353007	single nucleotide variant	NM_006403.4(NEDD9):c.1184C>T (p.Ser395Phe)	not specified [RCV004483207]	uncertain significance	6	11190685	11190685	Human		name
405812298	CV3353017	single nucleotide variant	NM_006403.4(NEDD9):c.1484C>A (p.Ser495Tyr)	not specified [RCV004483217]	uncertain significance	6	11190385	11190385	Human		name
405812306	CV3353021	single nucleotide variant	NM_006403.4(NEDD9):c.1588C>G (p.Arg530Gly)	not specified [RCV004483221]	uncertain significance	6	11190281	11190281	Human		name
405812317	CV3353027	single nucleotide variant	NM_006403.4(NEDD9):c.1894G>A (p.Val632Ile)	not specified [RCV004483227]	uncertain significance	6	11189975	11189975	Human		name
405812339	CV3353039	single nucleotide variant	NM_006403.4(NEDD9):c.2080C>T (p.Pro694Ser)	not specified [RCV004483239]	uncertain significance	6	11185587	11185587	Human		name
407526126	CV3454802	single nucleotide variant	NM_006403.4(NEDD9):c.1709C>T (p.Pro570Leu)	not specified [RCV004654699]	uncertain significance	6	11190160	11190160	Human		name
407526133	CV3454805	single nucleotide variant	NM_006403.4(NEDD9):c.2185C>T (p.Leu729Phe)	not specified [RCV004654701]	uncertain significance	6	11185482	11185482	Human		name
597670567	CV3555820	single nucleotide variant	NM_006403.4(NEDD9):c.2072A>G (p.Gln691Arg)	not specified [RCV004829675]	uncertain significance	6	11185595	11185595	Human		name
597670250	CV3555828	single nucleotide variant	NM_006403.4(NEDD9):c.2293C>T (p.Arg765Trp)	not specified [RCV004829683]	uncertain significance	6	11185374	11185374	Human		name
597670258	CV3555829	single nucleotide variant	NM_006403.4(NEDD9):c.1139T>C (p.Met380Thr)	not specified [RCV004829684]	uncertain significance	6	11190730	11190730	Human		name
597670266	CV3555830	single nucleotide variant	NM_006403.4(NEDD9):c.1213G>C (p.Asp405His)	not specified [RCV004829685]	uncertain significance	6	11190656	11190656	Human		name
597670281	CV3555832	single nucleotide variant	NM_006403.4(NEDD9):c.1058C>A (p.Pro353Gln)	not specified [RCV004829687]	uncertain significance	6	11190811	11190811	Human		name
598254166	CV3990628	single nucleotide variant	NM_006403.4(NEDD9):c.1618G>A (p.Asp540Asn)	not specified [RCV005385462]	uncertain significance	6	11190251	11190251	Human		name
598231659	CV3990629	single nucleotide variant	NM_006403.4(NEDD9):c.1987C>T (p.His663Tyr)	not specified [RCV005381372]	uncertain significance	6	11188226	11188226	Human		name
598231646	CV3990631	single nucleotide variant	NM_006403.4(NEDD9):c.1744G>A (p.Gly582Ser)	not specified [RCV005381374]	likely benign	6	11190125	11190125	Human		name
598254176	CV3990633	single nucleotide variant	NM_006403.4(NEDD9):c.1363G>A (p.Val455Met)	not specified [RCV005385463]	uncertain significance	6	11190506	11190506	Human		name
598231468	CV3990634	single nucleotide variant	NM_006403.4(NEDD9):c.2299G>T (p.Val767Leu)	not specified [RCV005381376]	uncertain significance	6	11185368	11185368	Human		name
598231476	CV3990635	single nucleotide variant	NM_006403.4(NEDD9):c.1231G>A (p.Glu411Lys)	not specified [RCV005381377]	uncertain significance	6	11190638	11190638	Human		name
598231483	CV3990639	single nucleotide variant	NM_006403.4(NEDD9):c.1267G>A (p.Gly423Ser)	not specified [RCV005381378]	uncertain significance	6	11190602	11190602	Human		name
598254213	CV3990641	single nucleotide variant	NM_006403.4(NEDD9):c.1844G>C (p.Cys615Ser)	not specified [RCV005385467]	uncertain significance	6	11190025	11190025	Human		name
598254220	CV3990642	single nucleotide variant	NM_006403.4(NEDD9):c.1766T>G (p.Leu589Arg)	not specified [RCV005385468]	uncertain significance	6	11190103	11190103	Human		name
598231495	CV3990643	single nucleotide variant	NM_006403.4(NEDD9):c.1333A>G (p.Ile445Val)	not specified [RCV005381380]	uncertain significance	6	11190536	11190536	Human		name
15154954	CV735364	single nucleotide variant	NM_006403.4(NEDD9):c.1511A>G (p.His504Arg)	NEDD9-related disorder [RCV003922988]\|not provided [RCV000902050]	likely benign	6	11190358	11190358	Human		name , trait , alternate_id

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