Exd1 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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46 records found for search term Exd1

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
401864289	CV2781632	single nucleotide variant	NM_001286441.2(EXD1):c.-71G>A	not specified [RCV004354836]	uncertain significance	15	41230496	41230496	Human		name
155948871	CV2242581	single nucleotide variant	NM_001286441.2(EXD1):c.251C>G (p.Ser84Cys)	not specified [RCV004113647]	uncertain significance	15	41217106	41217106	Human		name
156200100	CV2365491	single nucleotide variant	NM_001286441.2(EXD1):c.291A>C (p.Lys97Asn)	not specified [RCV004209561]	uncertain significance	15	41216765	41216765	Human		name
156369827	CV2194097	single nucleotide variant	NM_001286441.2(EXD1):c.346C>T (p.Pro116Ser)	not specified [RCV004076855]	uncertain significance	15	41216710	41216710	Human		name
156098945	CV2250634	single nucleotide variant	NM_001286441.2(EXD1):c.721G>A (p.Val241Ile)	not specified [RCV004129267]	uncertain significance	15	41191585	41191585	Human		name
156220514	CV2254159	single nucleotide variant	NM_001286441.2(EXD1):c.861T>G (p.Ile287Met)	not specified [RCV004129589]	uncertain significance	15	41191445	41191445	Human		name
155969420	CV2262110	single nucleotide variant	NM_001286441.2(EXD1):c.755G>A (p.Gly252Asp)	not specified [RCV004126572]	uncertain significance	15	41191551	41191551	Human		name
156254975	CV2264692	single nucleotide variant	NM_001286441.2(EXD1):c.890G>A (p.Arg297Gln)	not specified [RCV004132687]	uncertain significance	15	41190103	41190103	Human		name
156185490	CV2294953	single nucleotide variant	NM_001286441.2(EXD1):c.335C>A (p.Ala112Asp)	not specified [RCV004156101]	uncertain significance	15	41216721	41216721	Human		name
156357251	CV2318263	single nucleotide variant	NM_001286441.2(EXD1):c.928G>A (p.Glu310Lys)	not specified [RCV004179437]	uncertain significance	15	41190065	41190065	Human		name
156199088	CV2331222	single nucleotide variant	NM_001286441.2(EXD1):c.952C>T (p.Arg318Cys)	not specified [RCV004181825]	uncertain significance	15	41190041	41190041	Human		name
156116644	CV2349401	single nucleotide variant	NM_001286441.2(EXD1):c.923C>T (p.Ala308Val)	not specified [RCV004199331]	uncertain significance	15	41190070	41190070	Human		name
156145750	CV2384027	single nucleotide variant	NM_001286441.2(EXD1):c.598A>G (p.Asn200Asp)	not specified [RCV004224997]	uncertain significance	15	41195974	41195974	Human		name
329367096	CV2430891	single nucleotide variant	NM_001286441.2(EXD1):c.877G>T (p.Val293Leu)	not specified [RCV004248088]	uncertain significance	15	41190116	41190116	Human		name
329366047	CV2438042	single nucleotide variant	NM_001286441.2(EXD1):c.752C>T (p.Thr251Met)	not specified [RCV004263744]	uncertain significance	15	41191554	41191554	Human		name
329402782	CV2451365	single nucleotide variant	NM_001286441.2(EXD1):c.670T>C (p.Cys224Arg)	not specified [RCV004272053]	uncertain significance	15	41195825	41195825	Human		name
401751530	CV2727030	single nucleotide variant	NM_001286441.2(EXD1):c.781A>G (p.Thr261Ala)	not specified [RCV004325408]	uncertain significance	15	41191525	41191525	Human		name
401866103	CV2775416	single nucleotide variant	NM_001286441.2(EXD1):c.848G>A (p.Arg283Lys)	not specified [RCV004348814]	uncertain significance	15	41191458	41191458	Human		name
405760263	CV3252442	single nucleotide variant	NM_001286441.2(EXD1):c.788A>C (p.Gln263Pro)	not specified [RCV004383343]	uncertain significance	15	41191518	41191518	Human		name
405760273	CV3252444	single nucleotide variant	NM_001286441.2(EXD1):c.997G>A (p.Val333Met)	not specified [RCV004383345]	uncertain significance	15	41189996	41189996	Human		name
597693862	CV3675037	single nucleotide variant	NM_001286441.2(EXD1):c.830T>C (p.Leu277Pro)	not specified [RCV004915617]	uncertain significance	15	41191476	41191476	Human		name
597693883	CV3675039	single nucleotide variant	NM_001286441.2(EXD1):c.865G>A (p.Glu289Lys)	not specified [RCV004915619]	uncertain significance	15	41190128	41190128	Human		name
598210095	CV3954714	single nucleotide variant	NM_001286441.2(EXD1):c.319G>A (p.Glu107Lys)	not specified [RCV005338699]	uncertain significance	15	41216737	41216737	Human		name
598210112	CV3954716	single nucleotide variant	NM_001286441.2(EXD1):c.902C>G (p.Pro301Arg)	not specified [RCV005338701]	uncertain significance	15	41190091	41190091	Human		name
598210127	CV3954718	single nucleotide variant	NM_001286441.2(EXD1):c.946C>T (p.Pro316Ser)	not specified [RCV005338703]	uncertain significance	15	41190047	41190047	Human		name
156034299	CV2211750	single nucleotide variant	NM_001286441.2(EXD1):c.1561A>G (p.Lys521Glu)	not specified [RCV004084627]	uncertain significance	15	41184089	41184089	Human		name
156077915	CV2281696	single nucleotide variant	NM_001286441.2(EXD1):c.1042C>T (p.Leu348Phe)	not specified [RCV004147847]	uncertain significance	15	41189951	41189951	Human		name
155958219	CV2304256	single nucleotide variant	NM_001286441.2(EXD1):c.1378G>A (p.Glu460Lys)	not specified [RCV004170270]	uncertain significance	15	41184272	41184272	Human		name
155926997	CV2345315	single nucleotide variant	NM_001286441.2(EXD1):c.1512G>T (p.Glu504Asp)	not specified [RCV004198095]	uncertain significance	15	41184138	41184138	Human		name
401777909	CV2704443	single nucleotide variant	NM_001286441.2(EXD1):c.1670C>G (p.Ala557Gly)	not specified [RCV004313194]	uncertain significance	15	41183980	41183980	Human		name
401891568	CV2769040	single nucleotide variant	NM_001286441.2(EXD1):c.1576A>G (p.Met526Val)	not specified [RCV004348909]	likely benign	15	41184074	41184074	Human		name
405760241	CV3252438	single nucleotide variant	NM_001286441.2(EXD1):c.1178T>C (p.Leu393Pro)	not specified [RCV004383339]	uncertain significance	15	41184472	41184472	Human		name
405760247	CV3252439	single nucleotide variant	NM_001286441.2(EXD1):c.1244G>C (p.Gly415Ala)	not specified [RCV004383340]	uncertain significance	15	41184406	41184406	Human		name
405760251	CV3252440	single nucleotide variant	NM_001286441.2(EXD1):c.1516G>A (p.Glu506Lys)	not specified [RCV004383341]	uncertain significance	15	41184134	41184134	Human		name
405760256	CV3252441	single nucleotide variant	NM_001286441.2(EXD1):c.1680G>T (p.Lys560Asn)	not specified [RCV004383342]	uncertain significance	15	41183970	41183970	Human		name
405760278	CV3252445	single nucleotide variant	NM_001286441.2(EXD1):c.1022G>A (p.Arg341His)	not specified [RCV004383346]	uncertain significance	15	41189971	41189971	Human		name
405760284	CV3252446	single nucleotide variant	NM_001286441.2(EXD1):c.1052C>T (p.Thr351Ile)	not specified [RCV004383347]	uncertain significance	15	41189941	41189941	Human		name
405760289	CV3252447	single nucleotide variant	NM_001286441.2(EXD1):c.1104C>G (p.Phe368Leu)	not specified [RCV004383348]	uncertain significance	15	41184546	41184546	Human		name
407499805	CV3438544	single nucleotide variant	NM_001286441.2(EXD1):c.1111C>G (p.Gln371Glu)	not specified [RCV004622863]	uncertain significance	15	41184539	41184539	Human		name
597693822	CV3675033	single nucleotide variant	NM_001286441.2(EXD1):c.1040G>A (p.Arg347Gln)	not specified [RCV004915613]	uncertain significance	15	41189953	41189953	Human		name
597693832	CV3675034	single nucleotide variant	NM_001286441.2(EXD1):c.1603G>A (p.Val535Met)	not specified [RCV004915614]	likely benign	15	41184047	41184047	Human		name
597693843	CV3675035	single nucleotide variant	NM_001286441.2(EXD1):c.1481A>T (p.Glu494Val)	not specified [RCV004915615]	uncertain significance	15	41184169	41184169	Human		name
597693853	CV3675036	single nucleotide variant	NM_001286441.2(EXD1):c.1021C>T (p.Arg341Cys)	not specified [RCV004915616]	uncertain significance	15	41189972	41189972	Human		name
597693872	CV3675038	single nucleotide variant	NM_001286441.2(EXD1):c.1232G>C (p.Gly411Ala)	not specified [RCV004915618]	uncertain significance	15	41184418	41184418	Human		name
598210104	CV3954715	single nucleotide variant	NM_001286441.2(EXD1):c.1443A>C (p.Arg481Ser)	not specified [RCV005338700]	uncertain significance	15	41184207	41184207	Human		name
598210121	CV3954717	single nucleotide variant	NM_001286441.2(EXD1):c.1002T>G (p.Asp334Glu)	not specified [RCV005338702]	uncertain significance	15	41189991	41189991	Human		name

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