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82 records found for search term Mtmr4
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
8585464CV120051single nucleotide variantNM_004687.4(MTMR4):c.674G>C (p.Arg225Pro)Lung cancer [RCV000100571]uncertain significance175850731158507311Humanname
15107475CV715595single nucleotide variantNM_001378067.1(MTMR4):c.690T>C (p.Ile230=)not provided [RCV000960297]benign175850817858508178Humanname
15107478CV715596single nucleotide variantNM_001378067.1(MTMR4):c.426T>C (p.Phe142=)not provided [RCV000960298]benign175850875158508751Humanname
156387958CV2221671single nucleotide variantNM_001378067.1(MTMR4):c.101C>A (p.Pro34His)not specified [RCV004096910]uncertain significance175851288658512886Humanname
401739413CV2684075single nucleotide variantNM_001378067.1(MTMR4):c.100C>A (p.Pro34Thr)not specified [RCV004295669]uncertain significance175851288758512887Humanname
401859931CV2765210single nucleotide variantNM_001378067.1(MTMR4):c.100C>G (p.Pro34Ala)not specified [RCV004339737]uncertain significance175851288758512887Humanname
401900063CV2780303single nucleotide variantNM_001378067.1(MTMR4):c.199A>C (p.Ile67Leu)not specified [RCV004355927]uncertain significance175851244358512443Humanname
405659276CV3373452single nucleotide variantNM_001378067.1(MTMR4):c.101C>G (p.Pro34Arg)not specified [RCV004512313]uncertain significance175851288658512886Humanname
598263415CV3986425single nucleotide variantNM_001378067.1(MTMR4):c.125A>G (p.Glu42Gly)not specified [RCV005387446]uncertain significance175851286258512862Humanname
155971710CV2334248single nucleotide variantNM_001378067.1(MTMR4):c.524C>T (p.Ala175Val)not specified [RCV004186232]uncertain significance175850853758508537Humanname
156042537CV2387845single nucleotide variantNM_001378067.1(MTMR4):c.436T>C (p.Tyr146His)not specified [RCV004234356]uncertain significance175850874158508741Humanname
156265431CV2389062single nucleotide variantNM_001378067.1(MTMR4):c.713T>C (p.Leu238Ser)not specified [RCV004235400]uncertain significance175850731458507314Humanname
401733116CV2685431single nucleotide variantNM_001378067.1(MTMR4):c.715C>T (p.Arg239Cys)not specified [RCV004294463]uncertain significance175850731258507312Humanname
405659316CV3373440single nucleotide variantNM_001378067.1(MTMR4):c.409A>C (p.Lys137Gln)not specified [RCV004512301]uncertain significance175850876858508768Humanname
405659301CV3373445single nucleotide variantNM_001378067.1(MTMR4):c.555G>C (p.Gln185His)not specified [RCV004512306]uncertain significance175850850658508506Humanname
598263411CV3986424single nucleotide variantNM_001378067.1(MTMR4):c.529C>T (p.Leu177Phe)not specified [RCV005387445]uncertain significance175850853258508532Humanname
15107469CV715594single nucleotide variantNM_001378067.1(MTMR4):c.3081A>T (p.Gly1027=)not provided [RCV000960296]benign175849510358495103Humanname
155978473CV2222692single nucleotide variantNM_001378067.1(MTMR4):c.2519T>C (p.Leu840Pro)not specified [RCV004101552]likely benign175849566558495665Humanname
156226963CV2222693single nucleotide variantNM_001378067.1(MTMR4):c.2693C>T (p.Pro898Leu)not specified [RCV004101553]uncertain significance175849549158495491Humanname
156382465CV2227374single nucleotide variantNM_001378067.1(MTMR4):c.2365G>A (p.Val789Ile)not specified [RCV004091880]likely benign175849581958495819Humanname
155950460CV2242920single nucleotide variantNM_001378067.1(MTMR4):c.1661A>C (p.Asn554Thr)not specified [RCV004107507]uncertain significance175850408758504087Humanname
155963519CV2282749single nucleotide variantNM_001378067.1(MTMR4):c.1618C>T (p.Arg540Trp)not specified [RCV004141607]uncertain significance175850413058504130Humanname
156045430CV2308084single nucleotide variantNM_001378067.1(MTMR4):c.2501C>T (p.Ala834Val)not specified [RCV004170506]uncertain significance175849568358495683Humanname
156280867CV2348488single nucleotide variantNM_001378067.1(MTMR4):c.2870G>A (p.Arg957Gln)not specified [RCV004193675]uncertain significance175849531458495314Humanname
156275212CV2351806single nucleotide variantNM_001378067.1(MTMR4):c.2696T>C (p.Leu899Ser)not specified [RCV004197957]uncertain significance175849548858495488Humanname
155917336CV2362279single nucleotide variantNM_001378067.1(MTMR4):c.1697T>G (p.Met566Arg)not specified [RCV004212922]uncertain significance175850405158504051Humanname
156402026CV2367839single nucleotide variantNM_001378067.1(MTMR4):c.2270G>C (p.Arg757Thr)not specified [RCV004222950]uncertain significance175849591458495914Humanname
155908515CV2387351single nucleotide variantNM_001378067.1(MTMR4):c.1604G>A (p.Arg535His)not specified [RCV004238433]uncertain significance175850414458504144Humanname
156007439CV2394357single nucleotide variantNM_001378067.1(MTMR4):c.1858C>T (p.Pro620Ser)not specified [RCV004238576]uncertain significance175849632658496326Humanname
329358543CV2425218single nucleotide variantNM_001378067.1(MTMR4):c.1057G>A (p.Val353Met)not specified [RCV004250891]uncertain significance175850556058505560Humanname
329360310CV2446669single nucleotide variantNM_001378067.1(MTMR4):c.2024C>G (p.Ser675Cys)not specified [RCV004251555]uncertain significance175849616058496160Humanname
329396506CV2459608single nucleotide variantNM_001378067.1(MTMR4):c.2702T>G (p.Leu901Trp)not specified [RCV004277053]uncertain significance175849548258495482Humanname
401783286CV2716244single nucleotide variantNM_001378067.1(MTMR4):c.1152G>C (p.Leu384Phe)not specified [RCV004323465]uncertain significance175850496858504968Humanname
401743646CV2726136single nucleotide variantNM_001378067.1(MTMR4):c.2939G>A (p.Ser980Asn)not specified [RCV004326619]uncertain significance175849524558495245Humanname
401899730CV2762056single nucleotide variantNM_001378067.1(MTMR4):c.2730G>C (p.Gln910His)not specified [RCV004341874]uncertain significance175849545458495454Humanname
401891593CV2780562single nucleotide variantNM_001378067.1(MTMR4):c.2539C>T (p.Leu847Phe)not specified [RCV004351938]uncertain significance175849564558495645Humanname
401888537CV2785061single nucleotide variantNM_001378067.1(MTMR4):c.1120T>C (p.Cys374Arg)not specified [RCV004355077]uncertain significance175850549758505497Humanname
405658864CV3373351single nucleotide variantNM_001378067.1(MTMR4):c.1520C>T (p.Ala507Val)not specified [RCV004512212]uncertain significance175850431058504310Humanname
405658867CV3373352single nucleotide variantNM_001378067.1(MTMR4):c.1619G>A (p.Arg540Gln)not specified [RCV004512213]uncertain significance175850412958504129Humanname
405658886CV3373357single nucleotide variantNM_001378067.1(MTMR4):c.1723C>T (p.Arg575Trp)not specified [RCV004512218]uncertain significance175850387458503874Humanname
405658896CV3373360single nucleotide variantNM_001378067.1(MTMR4):c.1810C>T (p.Pro604Ser)not specified [RCV004512221]uncertain significance175850378758503787Humanname
405658915CV3373365single nucleotide variantNM_001378067.1(MTMR4):c.1952G>T (p.Cys651Phe)not specified [RCV004512226]uncertain significance175849623258496232Humanname
405658937CV3373372single nucleotide variantNM_001378067.1(MTMR4):c.2174G>A (p.Arg725Gln)not specified [RCV004512233]likely benign175849601058496010Humanname
405658951CV3373378single nucleotide variantNM_001378067.1(MTMR4):c.2359G>C (p.Asp787His)not specified [RCV004512239]uncertain significance175849582558495825Humanname
405658966CV3373384single nucleotide variantNM_001378067.1(MTMR4):c.2423A>T (p.Gln808Leu)not specified [RCV004512245]uncertain significance175849576158495761Humanname
405659022CV3373405single nucleotide variantNM_001378067.1(MTMR4):c.2800G>T (p.Gly934Trp)not specified [RCV004512266]uncertain significance175849538458495384Humanname
407507347CV3447534single nucleotide variantNM_001378067.1(MTMR4):c.2932T>C (p.Cys978Arg)not specified [RCV004646784]uncertain significance175849525258495252Humanname
407507350CV3447535single nucleotide variantNM_001378067.1(MTMR4):c.2420C>G (p.Ala807Gly)not specified [RCV004646785]uncertain significance175849576458495764Humanname
407507357CV3447537single nucleotide variantNM_001378067.1(MTMR4):c.2434A>G (p.Met812Val)not specified [RCV004646787]likely benign175849575058495750Humanname
407507360CV3447538single nucleotide variantNM_001378067.1(MTMR4):c.2555C>T (p.Ser852Leu)not specified [RCV004646788]uncertain significance175849562958495629Humanname
407507364CV3457634single nucleotide variantNM_001378067.1(MTMR4):c.2092A>G (p.Lys698Glu)not specified [RCV004646789]uncertain significance175849609258496092Humanname
597651360CV3561197single nucleotide variantNM_001378067.1(MTMR4):c.2313A>C (p.Glu771Asp)not specified [RCV004833565]uncertain significance175849587158495871Humanname
597650054CV3561198single nucleotide variantNM_001378067.1(MTMR4):c.2490C>G (p.Asn830Lys)not specified [RCV004833566]uncertain significance175849569458495694Humanname
597650063CV3561199single nucleotide variantNM_001378067.1(MTMR4):c.2818C>T (p.Arg940Trp)not specified [RCV004833567]uncertain significance175849536658495366Humanname
597639239CV3561200single nucleotide variantNM_001378067.1(MTMR4):c.1234C>T (p.Arg412Trp)not specified [RCV004825077]uncertain significance175850488658504886Humanname
597650073CV3561201single nucleotide variantNM_001378067.1(MTMR4):c.2314A>G (p.Thr772Ala)not specified [RCV004833568]uncertain significance175849587058495870Humanname
597650083CV3561202single nucleotide variantNM_001378067.1(MTMR4):c.2640A>C (p.Arg880Ser)not specified [RCV004833569]uncertain significance175849554458495544Humanname
597650091CV3561203single nucleotide variantNM_001378067.1(MTMR4):c.2210A>G (p.Lys737Arg)not specified [RCV004833570]uncertain significance175849597458495974Humanname
597650099CV3561204single nucleotide variantNM_001378067.1(MTMR4):c.2985G>A (p.Met995Ile)not specified [RCV004833571]uncertain significance175849519958495199Humanname
597650107CV3561206single nucleotide variantNM_001378067.1(MTMR4):c.1154C>T (p.Ser385Leu)not specified [RCV004833572]uncertain significance175850496658504966Humanname
597650117CV3561207single nucleotide variantNM_001378067.1(MTMR4):c.2819G>A (p.Arg940Gln)not specified [RCV004833573]uncertain significance175849536558495365Humanname
597650123CV3561208single nucleotide variantNM_001378067.1(MTMR4):c.2924C>T (p.Ser975Leu)not specified [RCV004833574]uncertain significance175849526058495260Humanname
597650131CV3561209single nucleotide variantNM_001378067.1(MTMR4):c.1453C>T (p.Leu485Phe)not specified [RCV004833575]uncertain significance175850437758504377Humanname
598227418CV3986420single nucleotide variantNM_001378067.1(MTMR4):c.2869C>T (p.Arg957Trp)not specified [RCV005380722]uncertain significance175849531558495315Humanname
598263407CV3986421single nucleotide variantNM_001378067.1(MTMR4):c.2495C>T (p.Pro832Leu)not specified [RCV005387444]likely benign175849568958495689Humanname
598227431CV3986423single nucleotide variantNM_001378067.1(MTMR4):c.1979C>A (p.Pro660His)not specified [RCV005380724]uncertain significance175849620558496205Humanname
598227441CV3986426single nucleotide variantNM_001378067.1(MTMR4):c.2234C>G (p.Pro745Arg)not specified [RCV005380725]uncertain significance175849595058495950Humanname
156137913CV2236545single nucleotide variantNM_001378067.1(MTMR4):c.3078T>G (p.Asp1026Glu)not specified [RCV004110541]uncertain significance175849510658495106Humanname
155904216CV2275852single nucleotide variantNM_001378067.1(MTMR4):c.3289G>A (p.Asp1097Asn)not specified [RCV004139514]uncertain significance175849291658492916Humanname
156214366CV2385914single nucleotide variantNM_001378067.1(MTMR4):c.3370C>T (p.Arg1124Cys)not specified [RCV004226952]uncertain significance175849259358492593Humanname
401769012CV2686467single nucleotide variantNM_001378067.1(MTMR4):c.3164G>A (p.Arg1055Gln)not specified [RCV004290622]uncertain significance175849502058495020Humanname
401774055CV2727716single nucleotide variantNM_001378067.1(MTMR4):c.3028G>A (p.Val1010Ile)not specified [RCV004323753]uncertain significance175849515658495156Humanname
405659031CV3373408single nucleotide variantNM_001378067.1(MTMR4):c.3011T>A (p.Val1004Asp)not specified [RCV004512269]uncertain significance175849517358495173Humanname
405659070CV3373423single nucleotide variantNM_001378067.1(MTMR4):c.3172C>T (p.Arg1058Cys)not specified [RCV004512284]uncertain significance175849501258495012Humanname
405659082CV3373427single nucleotide variantNM_001378067.1(MTMR4):c.3173G>A (p.Arg1058His)not specified [RCV004512288]uncertain significance175849501158495011Humanname
405659089CV3373429single nucleotide variantNM_001378067.1(MTMR4):c.3200G>A (p.Arg1067His)not specified [RCV004512290]uncertain significance175849498458494984Humanname
405659095CV3373431single nucleotide variantNM_001378067.1(MTMR4):c.3233T>C (p.Met1078Thr)not specified [RCV004512292]uncertain significance175849495158494951Humanname
405659325CV3373437single nucleotide variantNM_001378067.1(MTMR4):c.3307A>G (p.Ser1103Gly)not specified [RCV004512298]uncertain significance175849289858492898Humanname
407507354CV3447536single nucleotide variantNM_001378067.1(MTMR4):c.3121C>A (p.Gln1041Lys)not specified [RCV004646786]uncertain significance175849506358495063Humanname
598263404CV3986419single nucleotide variantNM_001378067.1(MTMR4):c.3535G>A (p.Val1179Ile)not specified [RCV005387443]uncertain significance175849175858491758Humanname
598227424CV3986422single nucleotide variantNM_001378067.1(MTMR4):c.3431C>T (p.Ala1144Val)not specified [RCV005380723]uncertain significance175849253258492532Humanname
598227444CV3986427single nucleotide variantNM_001378067.1(MTMR4):c.3386A>G (p.His1129Arg)not specified [RCV005380726]uncertain significance175849257758492577Humanname