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53 records found for search term Mark1
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
8575657CV110005single nucleotide variantNM_001286124.1(MARK1):c.1470+6232A>GLung cancer [RCV000090530]uncertain significance1220642258220642258Humanname
8575658CV110006single nucleotide variantNM_001286124.1(MARK1):c.1471-3980C>GLung cancer [RCV000090531]uncertain significance1220646640220646640Humanname
402517647CV2936412deletionNM_018650.5(MARK1):c.552+24_552+25delnot provided [RCV003662978]benign1220616014220616015Humanname
156124971CV2350153single nucleotide variantNM_018650.5(MARK1):c.44C>T (p.Thr15Met)not specified [RCV004200073]uncertain significance1220528866220528866Humanname
598198897CV3985498single nucleotide variantNM_018650.5(MARK1):c.50A>G (p.Asn17Ser)not specified [RCV005375619]uncertain significance1220528872220528872Humanname
15106555CV707102single nucleotide variantNM_018650.5(MARK1):c.771C>T (p.Phe257=)not provided [RCV000960104]likely benign1220618528220618528Humanname
15203333CV746162single nucleotide variantNM_018650.5(MARK1):c.606T>C (p.Gly202=)not provided [RCV000913877]likely benign1220618363220618363Humanname
155903673CV2298660single nucleotide variantNM_018650.5(MARK1):c.239T>C (p.Val80Ala)not specified [RCV004162581]uncertain significance1220579541220579541Humanname
156222903CV2399864single nucleotide variantNM_018650.5(MARK1):c.181C>T (p.Arg61Cys)not specified [RCV004246809]uncertain significance1220579483220579483Humanname
329356290CV2430675single nucleotide variantNM_018650.5(MARK1):c.151A>G (p.Thr51Ala)not specified [RCV004253864]uncertain significance1220579453220579453Humanname
329377929CV2458975single nucleotide variantNM_018650.5(MARK1):c.247G>C (p.Gly83Arg)not specified [RCV004272462]uncertain significance1220579549220579549Humanname
401936766CV2816058single nucleotide variantNM_018650.5(MARK1):c.1140G>A (p.Ser380=)not provided [RCV003414784]likely benign1220635393220635393Humanname
405658599CV3281639single nucleotide variantNM_018650.5(MARK1):c.124C>T (p.Arg42Trp)not specified [RCV004416460]uncertain significance1220579426220579426Humanname
597636574CV3697612single nucleotide variantNM_018650.5(MARK1):c.143C>T (p.Thr48Met)not specified [RCV004940809]uncertain significance1220579445220579445Humanname
15194429CV761649single nucleotide variantNM_018650.5(MARK1):c.1299T>C (p.Ala433=)not provided [RCV000933642]likely benign1220635855220635855Humanname
8624898CV80014single nucleotide variantNM_018650.4(MARK1):c.230C>A (p.Ala77Glu)Malignant melanoma [RCV000060090]not provided1220579532220579532Humanname
156333017CV2220773single nucleotide variantNM_018650.5(MARK1):c.733G>A (p.Val245Ile)not specified [RCV004092225]uncertain significance1220618490220618490Humanname
156028890CV2238266single nucleotide variantNM_018650.5(MARK1):c.836A>G (p.Tyr279Cys)not specified [RCV004113349]uncertain significance1220618682220618682Humanname
155930462CV2299921single nucleotide variantNM_018650.5(MARK1):c.803G>A (p.Arg268Gln)not specified [RCV004149056]uncertain significance1220618649220618649Humanname
155970565CV2392269single nucleotide variantNM_018650.5(MARK1):c.992A>G (p.Asn331Ser)not specified [RCV004243875]uncertain significance1220631117220631117Humanname
401898502CV2787960single nucleotide variantNM_018650.5(MARK1):c.676G>A (p.Glu226Lys)not specified [RCV004358618]uncertain significance1220618433220618433Humanname
405866916CV2842432single nucleotide variantNM_018650.5(MARK1):c.823C>T (p.Arg275Cys)EBV-positive nodal T- and NK-cell lymphoma [RCV004557789]likely benign1220618669220618669Humanname
405658492CV3281644single nucleotide variantNM_018650.5(MARK1):c.848A>T (p.Asp283Val)not specified [RCV004416465]uncertain significance1220618694220618694Humanname
155917649CV2199040single nucleotide variantNM_018650.5(MARK1):c.2045G>C (p.Gly682Ala)not specified [RCV004080444]uncertain significance1220661823220661823Humanname
155934167CV2229096single nucleotide variantNM_018650.5(MARK1):c.2257G>A (p.Val753Met)not specified [RCV004098866]uncertain significance1220662035220662035Humanname
155976279CV2324656single nucleotide variantNM_018650.5(MARK1):c.1718C>T (p.Ser573Phe)not specified [RCV004172904]uncertain significance1220652132220652132Humanname
329374937CV2430988single nucleotide variantNM_018650.5(MARK1):c.1750G>A (p.Val584Met)not specified [RCV004250367]uncertain significance1220653114220653114Humanname
329397708CV2463925single nucleotide variantNM_018650.5(MARK1):c.1280G>A (p.Gly427Asp)not specified [RCV004279991]uncertain significance1220635836220635836Humanname
401746690CV2691961single nucleotide variantNM_018650.5(MARK1):c.1172G>A (p.Arg391Gln)not specified [RCV004301691]uncertain significance1220635425220635425Humanname
401757715CV2707927single nucleotide variantNM_018650.5(MARK1):c.1534G>T (p.Asp512Tyr)not specified [RCV004309192]uncertain significance1220650683220650683Humanname
401781768CV2722264single nucleotide variantNM_018650.5(MARK1):c.1054G>A (p.Ala352Thr)not specified [RCV004328821]uncertain significance1220632245220632245Humanname
401757393CV2734992single nucleotide variantNM_018650.5(MARK1):c.1397T>C (p.Val466Ala)not specified [RCV004333696]uncertain significance1220635953220635953Humanname
401857131CV2759980single nucleotide variantNM_018650.5(MARK1):c.1730G>A (p.Arg577Gln)not provided [RCV004691586]|not specified [RCV004345398]uncertain significance1220652144220652144Humanname
401881054CV2763226single nucleotide variantNM_018650.5(MARK1):c.1739C>T (p.Thr580Ile)not specified [RCV004336261]uncertain significance1220653103220653103Humanname
405658594CV3281640single nucleotide variantNM_018650.5(MARK1):c.1543G>A (p.Val515Ile)not specified [RCV004416461]uncertain significance1220650692220650692Humanname
405658591CV3281641single nucleotide variantNM_018650.5(MARK1):c.1591A>G (p.Ser531Gly)not specified [RCV004416462]uncertain significance1220652005220652005Humanname
405658588CV3281642single nucleotide variantNM_018650.5(MARK1):c.1943C>T (p.Thr648Met)not specified [RCV004416463]uncertain significance1220653307220653307Humanname
405658585CV3281643single nucleotide variantNM_018650.5(MARK1):c.1985G>A (p.Arg662His)not specified [RCV004416464]uncertain significance1220653349220653349Humanname
407494835CV3456891single nucleotide variantNM_018650.5(MARK1):c.2323A>G (p.Ile775Val)not specified [RCV004643081]uncertain significance1220662101220662101Humanname
597636543CV3697606single nucleotide variantNM_018650.5(MARK1):c.1085T>C (p.Met362Thr)not specified [RCV004940803]uncertain significance1220632276220632276Humanname
597636547CV3697607single nucleotide variantNM_018650.5(MARK1):c.1365A>C (p.Lys455Asn)not specified [RCV004940804]uncertain significance1220635921220635921Humanname
597636551CV3697608single nucleotide variantNM_018650.5(MARK1):c.1891C>T (p.Pro631Ser)not specified [RCV004940805]uncertain significance1220653255220653255Humanname
597636557CV3697609single nucleotide variantNM_018650.5(MARK1):c.1469G>A (p.Ser490Asn)not specified [RCV004940806]uncertain significance1220636025220636025Humanname
597636564CV3697610single nucleotide variantNM_018650.5(MARK1):c.2084C>G (p.Ser695Cys)not specified [RCV004940807]uncertain significance1220661862220661862Humanname
597636570CV3697611single nucleotide variantNM_018650.5(MARK1):c.1160G>A (p.Cys387Tyr)not specified [RCV004940808]uncertain significance1220635413220635413Humanname
598198888CV3985497single nucleotide variantNM_018650.5(MARK1):c.1325C>A (p.Ala442Asp)not specified [RCV005375618]uncertain significance1220635881220635881Humanname
598198906CV3985499single nucleotide variantNM_018650.5(MARK1):c.1651C>T (p.His551Tyr)not specified [RCV005375620]uncertain significance1220652065220652065Humanname
598176934CV3985500single nucleotide variantNM_018650.5(MARK1):c.2285T>G (p.Leu762Trp)not specified [RCV005371506]uncertain significance1220662063220662063Humanname
598176939CV3985501single nucleotide variantNM_018650.5(MARK1):c.2066A>G (p.Lys689Arg)not specified [RCV005371507]uncertain significance1220661844220661844Humanname
598198922CV3985503single nucleotide variantNM_018650.5(MARK1):c.2146G>A (p.Asp716Asn)not specified [RCV005375622]uncertain significance1220661924220661924Humanname
598176945CV3985504single nucleotide variantNM_018650.5(MARK1):c.1193A>G (p.Asn398Ser)not specified [RCV005371508]uncertain significance1220635446220635446Humanname
15144084CV707103single nucleotide variantNM_018650.5(MARK1):c.1621G>C (p.Ala541Pro)not provided [RCV000966780]benign1220652035220652035Humanname
8624899CV80015single nucleotide variantNM_018650.4(MARK1):c.1295C>T (p.Pro432Leu)Malignant melanoma [RCV000060091]not provided1220635851220635851Humanname