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Variants search result for Homo sapiens
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68 records found for search term Ecm2
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
401734497CV2709518single nucleotide variantNM_001393.4(ECM2):c.65A>C (p.Asn22Thr)not specified [RCV004318757]uncertain significance99252280292522802Humanname
156169836CV2197830single nucleotide variantNM_001393.4(ECM2):c.145T>A (p.Ser49Thr)not specified [RCV004077067]uncertain significance99252272292522722Humanname
155998512CV2373299single nucleotide variantNM_001393.4(ECM2):c.144A>T (p.Arg48Ser)not specified [RCV004220010]uncertain significance99252272392522723Humanname
329352993CV2468152single nucleotide variantNM_001393.4(ECM2):c.205A>G (p.Ile69Val)not specified [RCV004275742]likely benign99252266292522662Humanname
597803190CV3667318single nucleotide variantNM_001393.4(ECM2):c.199C>T (p.Leu67Phe)not specified [RCV004907068]likely benign99252266892522668Humanname
597735889CV3667325single nucleotide variantNM_001393.4(ECM2):c.243A>C (p.Glu81Asp)not specified [RCV004920549]uncertain significance99252262492522624Humanname
598165459CV3954011single nucleotide variantNM_001393.4(ECM2):c.259C>T (p.Pro87Ser)not specified [RCV005329710]uncertain significance99252260892522608Humanname
598165472CV3954013single nucleotide variantNM_001393.4(ECM2):c.122G>T (p.Ser41Ile)not specified [RCV005329712]uncertain significance99252274592522745Humanname
156003328CV2258057single nucleotide variantNM_001393.4(ECM2):c.767A>T (p.Glu256Val)not specified [RCV004129852]uncertain significance99251491892514918Humanname
156134683CV2260185single nucleotide variantNM_001393.4(ECM2):c.368C>T (p.Thr123Ile)not specified [RCV004120962]uncertain significance99251780092517800Humanname
156179055CV2287974single nucleotide variantNM_001393.4(ECM2):c.944G>A (p.Arg315His)not specified [RCV004147746]uncertain significance99251474192514741Humanname
156286234CV2360887single nucleotide variantNM_001393.4(ECM2):c.466G>C (p.Val156Leu)not specified [RCV004213656]uncertain significance99251770292517702Humanname
156165344CV2376343single nucleotide variantNM_001393.4(ECM2):c.877G>A (p.Val293Ile)not specified [RCV004222603]uncertain significance99251480892514808Humanname
401778735CV2705594single nucleotide variantNM_001393.4(ECM2):c.865G>C (p.Glu289Gln)not specified [RCV004318458]uncertain significance99251482092514820Humanname
401770100CV2719036single nucleotide variantNM_001393.4(ECM2):c.439G>C (p.Val147Leu)not specified [RCV004322618]uncertain significance99251772992517729Humanname
401857476CV2759257single nucleotide variantNM_001393.4(ECM2):c.623A>G (p.Lys208Arg)not specified [RCV004335854]uncertain significance99251506292515062Humanname
405753831CV3238494single nucleotide variantNM_001393.4(ECM2):c.496C>T (p.Leu166Phe)not specified [RCV004382370]uncertain significance99251518992515189Humanname
405753837CV3238495single nucleotide variantNM_001393.4(ECM2):c.560C>G (p.Pro187Arg)not specified [RCV004382371]uncertain significance99251512592515125Humanname
405753844CV3238496single nucleotide variantNM_001393.4(ECM2):c.664G>A (p.Glu222Lys)not specified [RCV004382372]uncertain significance99251502192515021Humanname
405753851CV3238497single nucleotide variantNM_001393.4(ECM2):c.776G>A (p.Arg259Lys)not specified [RCV004382373]uncertain significance99251490992514909Humanname
405753863CV3238499single nucleotide variantNM_001393.4(ECM2):c.796C>T (p.Arg266Cys)not specified [RCV004382375]uncertain significance99251488992514889Humanname
405753870CV3238500single nucleotide variantNM_001393.4(ECM2):c.820G>C (p.Asp274His)not specified [RCV004382376]uncertain significance99251486592514865Humanname
407478532CV3441494single nucleotide variantNM_001393.4(ECM2):c.697T>C (p.Ser233Pro)not specified [RCV004617542]likely benign99251498892514988Humanname
597803189CV3667317single nucleotide variantNM_001393.4(ECM2):c.944G>T (p.Arg315Leu)not specified [RCV004907067]uncertain significance99251474192514741Humanname
597803200CV3667323single nucleotide variantNM_001393.4(ECM2):c.466G>A (p.Val156Ile)not specified [RCV004907073]uncertain significance99251770292517702Humanname
597803202CV3667324single nucleotide variantNM_001393.4(ECM2):c.390A>C (p.Arg130Ser)not specified [RCV004907074]uncertain significance99251777892517778Humanname
597803203CV3667326single nucleotide variantNM_001393.4(ECM2):c.766G>A (p.Glu256Lys)not specified [RCV004907075]uncertain significance99251491992514919Humanname
597735910CV3667329single nucleotide variantNM_001393.4(ECM2):c.560C>A (p.Pro187His)not specified [RCV004920552]uncertain significance99251512592515125Humanname
597803207CV3667331single nucleotide variantNM_001393.4(ECM2):c.586C>T (p.Pro196Ser)not specified [RCV004907077]uncertain significance99251509992515099Humanname
598165439CV3954008single nucleotide variantNM_001393.4(ECM2):c.519T>A (p.Asp173Glu)not specified [RCV005329707]uncertain significance99251516692515166Humanname
156080504CV2194587single nucleotide variantNM_001393.4(ECM2):c.1066G>A (p.Ala356Thr)not specified [RCV004081999]likely benign99251211592512115Humanname
156181344CV2226069single nucleotide variantNM_001393.4(ECM2):c.1186A>T (p.Met396Leu)not specified [RCV004105217]uncertain significance99251001992510019Humanname
156073056CV2263703single nucleotide variantNM_001393.4(ECM2):c.1397T>C (p.Leu466Pro)not specified [RCV004135995]uncertain significance99250560092505600Humanname
156365224CV2272077single nucleotide variantNM_001393.4(ECM2):c.1412T>C (p.Leu471Pro)not specified [RCV004124871]uncertain significance99250558592505585Humanname
155931685CV2293658single nucleotide variantNM_001393.4(ECM2):c.1898T>G (p.Leu633Arg)not specified [RCV004153162]uncertain significance99250076092500760Humanname
156046867CV2315636single nucleotide variantNM_001393.4(ECM2):c.1930C>T (p.Arg644Trp)not specified [RCV004169669]uncertain significance99250072892500728Humanname
155900976CV2345708single nucleotide variantNM_001393.4(ECM2):c.1882C>A (p.Gln628Lys)not specified [RCV004205647]uncertain significance99250077692500776Humanname
155903393CV2353573single nucleotide variantNM_001393.4(ECM2):c.1811A>G (p.Tyr604Cys)not specified [RCV004199553]uncertain significance99250084792500847Humanname
156012658CV2358937single nucleotide variantNM_001393.4(ECM2):c.1016C>T (p.Pro339Leu)not specified [RCV004212272]uncertain significance99251466992514669Humanname
156112931CV2387966single nucleotide variantNM_001393.4(ECM2):c.1559A>G (p.Lys520Arg)not specified [RCV004236504]uncertain significance99250255892502558Humanname
156008087CV2392689single nucleotide variantNM_001393.4(ECM2):c.1785T>A (p.Asp595Glu)not specified [RCV004247065]uncertain significance99250087392500873Humanname
156004920CV2397010single nucleotide variantNM_001393.4(ECM2):c.1521T>A (p.His507Gln)not specified [RCV004236162]uncertain significance99250259692502596Humanname
329374298CV2434767single nucleotide variantNM_001393.4(ECM2):c.1060T>C (p.Ser354Pro)not specified [RCV004248468]uncertain significance99251212192512121Humanname
329381049CV2440614single nucleotide variantNM_001393.4(ECM2):c.1708C>T (p.Arg570Trp)not specified [RCV004256526]uncertain significance99250095092500950Humanname
329398810CV2442872single nucleotide variantNM_001393.4(ECM2):c.1460T>C (p.Ile487Thr)not specified [RCV004253480]uncertain significance99250553792505537Humanname
329379242CV2443345single nucleotide variantNM_001393.4(ECM2):c.1288G>A (p.Asp430Asn)not specified [RCV004260144]uncertain significance99250991792509917Humanname
329401756CV2457373single nucleotide variantNM_001393.4(ECM2):c.1075C>A (p.Pro359Thr)not specified [RCV004267206]uncertain significance99251210692512106Humanname
329370181CV2461333single nucleotide variantNM_001393.4(ECM2):c.2036C>T (p.Ser679Phe)not specified [RCV004267497]uncertain significance99249637992496379Humanname
329359706CV2462227single nucleotide variantNM_001393.4(ECM2):c.1439C>T (p.Pro480Leu)not specified [RCV004266229]uncertain significance99250555892505558Humanname
401898683CV2782589single nucleotide variantNM_001393.4(ECM2):c.1532T>C (p.Ile511Thr)not specified [RCV004359619]uncertain significance99250258592502585Humanname
401896891CV2788913single nucleotide variantNM_001393.4(ECM2):c.1283C>T (p.Ala428Val)not specified [RCV004362949]uncertain significance99250992292509922Humanname
405753803CV3238490single nucleotide variantNM_001393.4(ECM2):c.1408C>A (p.Arg470Ser)not specified [RCV004382366]uncertain significance99250558992505589Humanname
405753810CV3238491single nucleotide variantNM_001393.4(ECM2):c.1502C>T (p.Thr501Ile)not specified [RCV004382367]uncertain significance99250261592502615Humanname
405753815CV3238492single nucleotide variantNM_001393.4(ECM2):c.1652C>T (p.Pro551Leu)not specified [RCV004382368]uncertain significance99250100692501006Humanname
405753822CV3238493single nucleotide variantNM_001393.4(ECM2):c.1799G>A (p.Arg600His)not specified [RCV004382369]uncertain significance99250085992500859Humanname
407478527CV3441493single nucleotide variantNM_001393.4(ECM2):c.1151T>C (p.Ile384Thr)not specified [RCV004617541]uncertain significance99251203092512030Humanname
407478537CV3441495single nucleotide variantNM_001393.4(ECM2):c.1757T>G (p.Leu586Trp)not specified [RCV004617543]uncertain significance99250090192500901Humanname
597803192CV3667319single nucleotide variantNM_001393.4(ECM2):c.1394G>T (p.Ser465Ile)not specified [RCV004907069]uncertain significance99250560392505603Humanname
597803194CV3667320single nucleotide variantNM_001393.4(ECM2):c.1189C>A (p.Arg397Ser)not specified [RCV004907070]uncertain significance99251001692510016Humanname
597803196CV3667321single nucleotide variantNM_001393.4(ECM2):c.1874C>T (p.Pro625Leu)not specified [RCV004907071]uncertain significance99250078492500784Humanname
597735896CV3667327single nucleotide variantNM_001393.4(ECM2):c.1577T>C (p.Ile526Thr)not specified [RCV004920550]uncertain significance99250254092502540Humanname
597735903CV3667328single nucleotide variantNM_001393.4(ECM2):c.1798C>T (p.Arg600Cys)not specified [RCV004920551]uncertain significance99250086092500860Humanname
597803205CV3667330single nucleotide variantNM_001393.4(ECM2):c.1145C>T (p.Ser382Leu)not specified [RCV004907076]uncertain significance99251203692512036Humanname
598165432CV3954007single nucleotide variantNM_001393.4(ECM2):c.2044T>C (p.Phe682Leu)not specified [RCV005329706]uncertain significance99249637192496371Humanname
598165446CV3954009single nucleotide variantNM_001393.4(ECM2):c.1364T>C (p.Val455Ala)not specified [RCV005329708]uncertain significance99250563392505633Humanname
598165452CV3954010single nucleotide variantNM_001393.4(ECM2):c.1643A>G (p.Tyr548Cys)not specified [RCV005329709]uncertain significance99250101592501015Humanname
598165478CV3954014single nucleotide variantNM_001393.4(ECM2):c.1647C>G (p.His549Gln)not specified [RCV005329713]uncertain significance99250101192501011Humanname
8633438CV88653single nucleotide variantNM_001197295.1(ECM2):c.717A>C (p.Ala239=)Malignant melanoma [RCV000068746]not provided99251490292514902Humanname