Eepd1 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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61 records found for search term Eepd1

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
156145581	CV2218811	single nucleotide variant	NM_030636.3(EEPD1):c.59A>G (p.His20Arg)	not specified [RCV004085057]	uncertain significance	7	36154383	36154383	Human		name
156383410	CV2223917	single nucleotide variant	NM_030636.3(EEPD1):c.95A>G (p.Asn32Ser)	not specified [RCV004093911]	uncertain significance	7	36154419	36154419	Human		name
597645178	CV3664122	single nucleotide variant	NM_030636.3(EEPD1):c.92G>A (p.Ser31Asn)	not specified [RCV004909752]	uncertain significance	7	36154416	36154416	Human		name
8632563	CV87771	single nucleotide variant	NM_030636.2(EEPD1):c.456C>T (p.Gly152=)	Malignant melanoma [RCV000067863]	not provided	7	36154780	36154780	Human		name
156044208	CV2381614	single nucleotide variant	NM_030636.3(EEPD1):c.256G>A (p.Val86Ile)	not specified [RCV004232087]	uncertain significance	7	36154580	36154580	Human		name
155993058	CV2381676	single nucleotide variant	NM_030636.3(EEPD1):c.130A>G (p.Thr44Ala)	not specified [RCV004232142]	uncertain significance	7	36154454	36154454	Human		name
405768751	CV3248459	single nucleotide variant	NM_030636.3(EEPD1):c.170C>T (p.Thr57Met)	not specified [RCV004384752]	uncertain significance	7	36154494	36154494	Human		name
407497459	CV3441658	single nucleotide variant	NM_030636.3(EEPD1):c.1164C>T (p.Leu388=)	not specified [RCV004622205]	likely benign	7	36284808	36284808	Human		name
597736241	CV3664123	single nucleotide variant	NM_030636.3(EEPD1):c.188G>A (p.Ser63Asn)	not specified [RCV004920606]	uncertain significance	7	36154512	36154512	Human		name
597645186	CV3664124	single nucleotide variant	NM_030636.3(EEPD1):c.143A>G (p.Glu48Gly)	not specified [RCV004909753]	uncertain significance	7	36154467	36154467	Human		name
155972778	CV2335843	single nucleotide variant	NM_030636.3(EEPD1):c.359C>G (p.Ala120Gly)	not specified [RCV004196072]	uncertain significance	7	36154683	36154683	Human		name
156205867	CV2385259	single nucleotide variant	NM_030636.3(EEPD1):c.389C>T (p.Ala130Val)	not specified [RCV004228500]	uncertain significance	7	36154713	36154713	Human		name
156052265	CV2386569	single nucleotide variant	NM_030636.3(EEPD1):c.551A>G (p.Asn184Ser)	not specified [RCV004230921]	uncertain significance	7	36154875	36154875	Human		name
156093703	CV2389730	single nucleotide variant	NM_030636.3(EEPD1):c.313A>G (p.Ser105Gly)	not specified [RCV004243776]	uncertain significance	7	36154637	36154637	Human		name
156251001	CV2394263	single nucleotide variant	NM_030636.3(EEPD1):c.475C>G (p.Leu159Val)	not specified [RCV004238496]	likely benign	7	36154799	36154799	Human		name
401768618	CV2685295	single nucleotide variant	NM_030636.3(EEPD1):c.305G>T (p.Ser102Ile)	not specified [RCV004292295]	uncertain significance	7	36154629	36154629	Human		name
401762428	CV2714136	single nucleotide variant	NM_030636.3(EEPD1):c.556G>A (p.Ala186Thr)	not specified [RCV004317390]	uncertain significance	7	36154880	36154880	Human		name
401776981	CV2721556	single nucleotide variant	NM_030636.3(EEPD1):c.845G>A (p.Arg282Gln)	not specified [RCV004316071]	uncertain significance	7	36155169	36155169	Human		name
401870555	CV2769290	single nucleotide variant	NM_030636.3(EEPD1):c.831C>A (p.Asn277Lys)	not specified [RCV004357294]	uncertain significance	7	36155155	36155155	Human		name
401876182	CV2777692	single nucleotide variant	NM_030636.3(EEPD1):c.455G>A (p.Gly152Asp)	not specified [RCV004343527]	uncertain significance	7	36154779	36154779	Human		name
405768758	CV3248460	single nucleotide variant	NM_030636.3(EEPD1):c.329C>T (p.Ser110Phe)	not specified [RCV004384753]	uncertain significance	7	36154653	36154653	Human		name
405768764	CV3248461	single nucleotide variant	NM_030636.3(EEPD1):c.442A>G (p.Met148Val)	not specified [RCV004384754]	uncertain significance	7	36154766	36154766	Human		name
405768777	CV3248463	single nucleotide variant	NM_030636.3(EEPD1):c.952C>G (p.Pro318Ala)	not specified [RCV004384756]	uncertain significance	7	36281136	36281136	Human		name
405768782	CV3248464	single nucleotide variant	NM_030636.3(EEPD1):c.953C>T (p.Pro318Leu)	not specified [RCV004384757]	uncertain significance	7	36281137	36281137	Human		name
407497450	CV3441656	single nucleotide variant	NM_030636.3(EEPD1):c.533T>C (p.Val178Ala)	not specified [RCV004622203]	uncertain significance	7	36154857	36154857	Human		name
407497454	CV3441657	single nucleotide variant	NM_030636.3(EEPD1):c.640A>G (p.Thr214Ala)	not specified [RCV004622204]	uncertain significance	7	36154964	36154964	Human		name
597645193	CV3664125	single nucleotide variant	NM_030636.3(EEPD1):c.670C>G (p.Leu224Val)	not specified [RCV004909754]	uncertain significance	7	36154994	36154994	Human		name
597736250	CV3664126	single nucleotide variant	NM_030636.3(EEPD1):c.556G>C (p.Ala186Pro)	not specified [RCV004920607]	uncertain significance	7	36154880	36154880	Human		name
597736262	CV3664128	single nucleotide variant	NM_030636.3(EEPD1):c.620C>T (p.Thr207Met)	not specified [RCV004920609]	uncertain significance	7	36154944	36154944	Human		name
598166606	CV3964728	single nucleotide variant	NM_030636.3(EEPD1):c.500A>G (p.Glu167Gly)	not specified [RCV005329903]	uncertain significance	7	36154824	36154824	Human		name
598166612	CV3964729	single nucleotide variant	NM_030636.3(EEPD1):c.577C>T (p.His193Tyr)	not specified [RCV005329904]	uncertain significance	7	36154901	36154901	Human		name
598166628	CV3964731	single nucleotide variant	NM_030636.3(EEPD1):c.611C>G (p.Ser204Cys)	not specified [RCV005329906]	uncertain significance	7	36154935	36154935	Human		name
598166638	CV3964732	single nucleotide variant	NM_030636.3(EEPD1):c.996C>G (p.Cys332Trp)	not specified [RCV005329907]	uncertain significance	7	36281180	36281180	Human		name
598166646	CV3964733	single nucleotide variant	NM_030636.3(EEPD1):c.624C>A (p.Asn208Lys)	not specified [RCV005329908]	uncertain significance	7	36154948	36154948	Human		name
8632564	CV87772	single nucleotide variant	NM_030636.2(EEPD1):c.457C>T (p.Leu153Phe)	Malignant melanoma [RCV000067864]	not provided	7	36154781	36154781	Human		name
155996371	CV2288503	single nucleotide variant	NM_030636.3(EEPD1):c.1247C>A (p.Pro416His)	not specified [RCV004152038]	uncertain significance	7	36287709	36287709	Human		name
156017446	CV2295605	single nucleotide variant	NM_030636.3(EEPD1):c.1645G>A (p.Ala549Thr)	not specified [RCV004160690]	uncertain significance	7	36299141	36299141	Human		name
156283808	CV2317488	single nucleotide variant	NM_030636.3(EEPD1):c.1006G>A (p.Val336Ile)	not specified [RCV004172451]	uncertain significance	7	36281190	36281190	Human		name
156343144	CV2353352	single nucleotide variant	NM_030636.3(EEPD1):c.1073C>T (p.Ala358Val)	not specified [RCV004205815]	uncertain significance	7	36284717	36284717	Human		name
156161533	CV2371481	single nucleotide variant	NM_030636.3(EEPD1):c.1135G>A (p.Gly379Arg)	not specified [RCV004216734]	uncertain significance	7	36284779	36284779	Human		name
156209276	CV2382605	single nucleotide variant	NM_030636.3(EEPD1):c.1100C>T (p.Ala367Val)	not specified [RCV004232930]	uncertain significance	7	36284744	36284744	Human		name
155957730	CV2387544	single nucleotide variant	NM_030636.3(EEPD1):c.1151C>G (p.Pro384Arg)	not specified [RCV004240392]	uncertain significance	7	36284795	36284795	Human		name
329393854	CV2472166	single nucleotide variant	NM_030636.3(EEPD1):c.1687G>A (p.Ala563Thr)	not specified [RCV004283290]	uncertain significance	7	36299183	36299183	Human		name
401738664	CV2712041	single nucleotide variant	NM_030636.3(EEPD1):c.1262G>T (p.Ser421Ile)	not specified [RCV004311460]	uncertain significance	7	36287724	36287724	Human		name
401743500	CV2715496	single nucleotide variant	NM_030636.3(EEPD1):c.1583C>G (p.Ala528Gly)	not specified [RCV004326590]	uncertain significance	7	36299079	36299079	Human		name
401879725	CV2755245	single nucleotide variant	NM_030636.3(EEPD1):c.1706G>A (p.Arg569Gln)	not specified [RCV004337428]	uncertain significance	7	36299202	36299202	Human		name
401893930	CV2770101	single nucleotide variant	NM_030636.3(EEPD1):c.1046C>T (p.Ala349Val)	not specified [RCV004356010]	uncertain significance	7	36284690	36284690	Human		name
405768715	CV3248453	single nucleotide variant	NM_030636.3(EEPD1):c.1414G>A (p.Ala472Thr)	not specified [RCV004384746]	uncertain significance	7	36297091	36297091	Human		name
405768722	CV3248454	single nucleotide variant	NM_030636.3(EEPD1):c.1415C>T (p.Ala472Val)	not specified [RCV004384747]	uncertain significance	7	36297092	36297092	Human		name
405768728	CV3248455	single nucleotide variant	NM_030636.3(EEPD1):c.1519G>A (p.Ala507Thr)	not specified [RCV004384748]	uncertain significance	7	36299015	36299015	Human		name
405768734	CV3248456	single nucleotide variant	NM_030636.3(EEPD1):c.1563C>G (p.Asn521Lys)	not specified [RCV004384749]	uncertain significance	7	36299059	36299059	Human		name
405768740	CV3248457	single nucleotide variant	NM_030636.3(EEPD1):c.1652G>A (p.Arg551Gln)	not specified [RCV004384750]	uncertain significance	7	36299148	36299148	Human		name
405768745	CV3248458	single nucleotide variant	NM_030636.3(EEPD1):c.1679G>A (p.Arg560Gln)	not specified [RCV004384751]	uncertain significance	7	36299175	36299175	Human		name
407497442	CV3441654	single nucleotide variant	NM_030636.3(EEPD1):c.1099G>A (p.Ala367Thr)	not specified [RCV004622201]	uncertain significance	7	36284743	36284743	Human		name
407497446	CV3441655	single nucleotide variant	NM_030636.3(EEPD1):c.1466T>C (p.Leu489Pro)	not specified [RCV004622202]	uncertain significance	7	36297143	36297143	Human		name
407497463	CV3441659	single nucleotide variant	NM_030636.3(EEPD1):c.1069G>A (p.Asp357Asn)	not specified [RCV004622206]	uncertain significance	7	36284713	36284713	Human		name
597645170	CV3664121	single nucleotide variant	NM_030636.3(EEPD1):c.1274G>A (p.Arg425Gln)	not specified [RCV004909751]	uncertain significance	7	36287736	36287736	Human		name
597736256	CV3664127	single nucleotide variant	NM_030636.3(EEPD1):c.1307C>T (p.Thr436Ile)	not specified [RCV004920608]	uncertain significance	7	36287769	36287769	Human		name
598166597	CV3964727	single nucleotide variant	NM_030636.3(EEPD1):c.1025C>T (p.Ser342Leu)	not specified [RCV005329902]	uncertain significance	7	36281209	36281209	Human		name
598166619	CV3964730	single nucleotide variant	NM_030636.3(EEPD1):c.1682G>T (p.Ser561Ile)	not specified [RCV005329905]	uncertain significance	7	36299178	36299178	Human		name
598166653	CV3964734	single nucleotide variant	NM_030636.3(EEPD1):c.1262G>A (p.Ser421Asn)	not specified [RCV005329909]	uncertain significance	7	36287724	36287724	Human		name

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