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Variants search result for Homo sapiens
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80 records found for search term Arhgef19
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
407507582CV3465211single nucleotide variantNM_153213.5(ARHGEF19):c.90G>C (p.Glu30Asp)not specified [RCV004671771]uncertain significance11620896516208965Humanname
156061784CV2323195single nucleotide variantNM_153213.5(ARHGEF19):c.145G>C (p.Asp49His)not specified [RCV004187594]uncertain significance11620891016208910Humanname
156194139CV2398186single nucleotide variantNM_153213.5(ARHGEF19):c.115G>A (p.Ala39Thr)not specified [RCV004241759]likely benign11620894016208940Humanname
329352982CV2468139single nucleotide variantNM_153213.5(ARHGEF19):c.137T>C (p.Val46Ala)not specified [RCV004275731]uncertain significance11620891816208918Humanname
401898728CV2782635single nucleotide variantNM_153213.5(ARHGEF19):c.191G>A (p.Arg64His)not specified [RCV004359658]uncertain significance11620886416208864Humanname
401935359CV2805837single nucleotide variantNM_153213.5(ARHGEF19):c.1080C>T (p.Asp360=)not provided [RCV003412783]likely benign11620700516207005Humanname
405698914CV3279395single nucleotide variantNM_153213.5(ARHGEF19):c.160G>A (p.Ala54Thr)not specified [RCV004425047]likely benign11620889516208895Humanname
405698931CV3279398single nucleotide variantNM_153213.5(ARHGEF19):c.190C>T (p.Arg64Cys)not specified [RCV004425050]uncertain significance11620886516208865Humanname
405698950CV3279401single nucleotide variantNM_153213.5(ARHGEF19):c.206C>T (p.Thr69Ile)not specified [RCV004425053]uncertain significance11620884916208849Humanname
405698964CV3279403single nucleotide variantNM_153213.5(ARHGEF19):c.262G>A (p.Glu88Lys)not specified [RCV004425055]uncertain significance11620879316208793Humanname
407458987CV3465221single nucleotide variantNM_153213.5(ARHGEF19):c.108G>C (p.Glu36Asp)not specified [RCV004658026]uncertain significance11620894716208947Humanname
598169999CV3907698single nucleotide variantNM_153213.5(ARHGEF19):c.133C>G (p.Pro45Ala)not specified [RCV005262965]uncertain significance11620892216208922Humanname
598170083CV3907726single nucleotide variantNM_153213.5(ARHGEF19):c.221A>G (p.Gln74Arg)not specified [RCV005262992]uncertain significance11620883416208834Humanname
156247043CV2219167single nucleotide variantNM_153213.5(ARHGEF19):c.526C>A (p.Pro176Thr)not specified [RCV004087322]uncertain significance11620811216208112Humanname
156332227CV2220647single nucleotide variantNM_153213.5(ARHGEF19):c.388C>T (p.His130Tyr)not specified [RCV004097827]uncertain significance11620866716208667Humanname
156242582CV2231444single nucleotide variantNM_153213.5(ARHGEF19):c.975G>T (p.Glu325Asp)not specified [RCV004096523]uncertain significance11620711016207110Humanname
156038081CV2239641single nucleotide variantNM_153213.5(ARHGEF19):c.995G>T (p.Arg332Leu)not specified [RCV004108193]uncertain significance11620709016207090Humanname
156024535CV2242139single nucleotide variantNM_153213.5(ARHGEF19):c.719G>T (p.Arg240Leu)not specified [RCV004109354]uncertain significance11620775316207753Humanname
156244778CV2243202single nucleotide variantNM_153213.5(ARHGEF19):c.731T>C (p.Met244Thr)not specified [RCV004110095]likely benign11620774116207741Humanname
156074549CV2248182single nucleotide variantNM_153213.5(ARHGEF19):c.698A>G (p.Lys233Arg)not specified [RCV004117576]uncertain significance11620777416207774Humanname
156269780CV2293350single nucleotide variantNM_153213.5(ARHGEF19):c.462G>T (p.Glu154Asp)not specified [RCV004150830]uncertain significance11620817616208176Humanname
156064190CV2340737single nucleotide variantNM_153213.5(ARHGEF19):c.307C>G (p.Pro103Ala)not specified [RCV004188102]uncertain significance11620874816208748Humanname
156283967CV2360620single nucleotide variantNM_153213.5(ARHGEF19):c.629G>A (p.Arg210His)not specified [RCV004213422]uncertain significance11620800916208009Humanname
155933491CV2372290single nucleotide variantNM_153213.5(ARHGEF19):c.377G>A (p.Arg126His)not specified [RCV004217065]uncertain significance11620867816208678Humanname
329395887CV2463042single nucleotide variantNM_153213.5(ARHGEF19):c.581G>A (p.Arg194Lys)not specified [RCV004272858]uncertain significance11620805716208057Humanname
401723842CV2725055single nucleotide variantNM_153213.5(ARHGEF19):c.571C>T (p.Pro191Ser)not specified [RCV004319808]uncertain significance11620806716208067Humanname
401893963CV2770164single nucleotide variantNM_153213.5(ARHGEF19):c.451G>C (p.Gly151Arg)not specified [RCV004356061]uncertain significance11620818716208187Humanname
405698970CV3279404single nucleotide variantNM_153213.5(ARHGEF19):c.391G>A (p.Gly131Ser)not specified [RCV004425056]uncertain significance11620866416208664Humanname
405698975CV3279405single nucleotide variantNM_153213.5(ARHGEF19):c.409G>C (p.Ala137Pro)not specified [RCV004425057]uncertain significance11620864616208646Humanname
405698981CV3279406single nucleotide variantNM_153213.5(ARHGEF19):c.469G>T (p.Ala157Ser)not specified [RCV004425058]uncertain significance11620816916208169Humanname
405698990CV3279408single nucleotide variantNM_153213.5(ARHGEF19):c.836G>T (p.Ser279Ile)not specified [RCV004425060]uncertain significance11620756016207560Humanname
405698996CV3279409single nucleotide variantNM_153213.5(ARHGEF19):c.845A>T (p.Glu282Val)not specified [RCV004425061]uncertain significance11620755116207551Humanname
405852897CV3393325single nucleotide variantNM_153213.5(ARHGEF19):c.610C>T (p.Arg204Trp)not provided [RCV004546055]likely benign11620802816208028Humanname
407507589CV3465216single nucleotide variantNM_153213.5(ARHGEF19):c.896G>A (p.Ser299Asn)not specified [RCV004671773]uncertain significance11620718916207189Humanname
597749994CV3592054single nucleotide variantNM_153213.5(ARHGEF19):c.947G>T (p.Gly316Val)not specified [RCV004846342]uncertain significance11620713816207138Humanname
597750165CV3592097single nucleotide variantNM_153213.5(ARHGEF19):c.881T>C (p.Leu294Pro)not specified [RCV004846380]uncertain significance11620720416207204Humanname
597750796CV3592107single nucleotide variantNM_153213.5(ARHGEF19):c.838A>T (p.Thr280Ser)not specified [RCV004846390]uncertain significance11620755816207558Humanname
597750747CV3592118single nucleotide variantNM_153213.5(ARHGEF19):c.427G>A (p.Val143Met)not specified [RCV004846401]uncertain significance11620821116208211Humanname
598169937CV3907676single nucleotide variantNM_153213.5(ARHGEF19):c.314G>C (p.Cys105Ser)not specified [RCV005262944]uncertain significance11620874116208741Humanname
598169973CV3907688single nucleotide variantNM_153213.5(ARHGEF19):c.995G>C (p.Arg332Pro)not specified [RCV005262956]uncertain significance11620709016207090Humanname
598170052CV3907716single nucleotide variantNM_153213.5(ARHGEF19):c.425G>A (p.Arg142Gln)not specified [RCV005262982]uncertain significance11620821316208213Humanname
156145724CV2196820single nucleotide variantNM_153213.5(ARHGEF19):c.1024C>G (p.Arg342Gly)not specified [RCV004069829]uncertain significance11620706116207061Humanname
155972295CV2214279single nucleotide variantNM_153213.5(ARHGEF19):c.1443G>T (p.Gln481His)not specified [RCV004086270]uncertain significance11620593916205939Humanname
156330771CV2224316single nucleotide variantNM_153213.5(ARHGEF19):c.1328A>T (p.Glu443Val)not specified [RCV004096134]uncertain significance11620605416206054Humanname
156386424CV2228213single nucleotide variantNM_153213.5(ARHGEF19):c.1013G>T (p.Ser338Ile)not specified [RCV004097948]uncertain significance11620707216207072Humanname
156125948CV2283668single nucleotide variantNM_153213.5(ARHGEF19):c.1554G>C (p.Arg518Ser)not specified [RCV004142206]uncertain significance11620556516205565Humanname
156060757CV2323123single nucleotide variantNM_153213.5(ARHGEF19):c.1862A>G (p.Tyr621Cys)not specified [RCV004187531]uncertain significance11620480416204804Humanname
156054255CV2326492single nucleotide variantNM_153213.5(ARHGEF19):c.2195A>G (p.Asp732Gly)not specified [RCV004183051]uncertain significance11619920616199206Humanname
155914609CV2342038single nucleotide variantNM_153213.5(ARHGEF19):c.1900C>T (p.Arg634Trp)not specified [RCV004187019]uncertain significance11620476616204766Humanname
155977266CV2342870single nucleotide variantNM_153213.5(ARHGEF19):c.2361T>A (p.Asn787Lys)not specified [RCV004189904]uncertain significance11619863516198635Humanname
156338225CV2343159single nucleotide variantNM_153213.5(ARHGEF19):c.1289C>T (p.Thr430Ile)not specified [RCV004194791]uncertain significance11620618916206189Humanname
156304090CV2359516single nucleotide variantNM_153213.5(ARHGEF19):c.1382C>T (p.Ala461Val)not specified [RCV004214825]uncertain significance11620600016206000Humanname
329366035CV2438024single nucleotide variantNM_153213.5(ARHGEF19):c.1486C>T (p.Arg496Cys)not specified [RCV004263730]uncertain significance11620563316205633Humanname
329388668CV2469461single nucleotide variantNM_153213.5(ARHGEF19):c.2150G>A (p.Cys717Tyr)not specified [RCV004282918]uncertain significance11619925116199251Humanname
401771451CV2686178single nucleotide variantNM_153213.5(ARHGEF19):c.2059C>T (p.Arg687Trp)not specified [RCV004297276]uncertain significance11620242316202423Humanname
401725407CV2697399single nucleotide variantNM_153213.5(ARHGEF19):c.2023G>A (p.Gly675Arg)not specified [RCV004304149]uncertain significance11620245916202459Humanname
401725467CV2697424single nucleotide variantNM_153213.5(ARHGEF19):c.2081G>A (p.Arg694Gln)not specified [RCV004304172]uncertain significance11620184716201847Humanname
401778926CV2705892single nucleotide variantNM_153213.5(ARHGEF19):c.2038C>T (p.His680Tyr)not specified [RCV004320498]uncertain significance11620244416202444Humanname
401782842CV2707522single nucleotide variantNM_153213.5(ARHGEF19):c.1121A>C (p.Asp374Ala)not specified [RCV004312893]uncertain significance11620696416206964Humanname
401864257CV2760867single nucleotide variantNM_153213.5(ARHGEF19):c.1073T>C (p.Ile358Thr)not specified [RCV004336502]uncertain significance11620701216207012Humanname
401884457CV2789689single nucleotide variantNM_153213.5(ARHGEF19):c.1096G>A (p.Val366Ile)not specified [RCV004360280]uncertain significance11620698916206989Humanname
405698896CV3279392single nucleotide variantNM_153213.5(ARHGEF19):c.1006T>A (p.Ser336Thr)not specified [RCV004425044]uncertain significance11620707916207079Humanname
405698903CV3279393single nucleotide variantNM_153213.5(ARHGEF19):c.1150C>G (p.Leu384Val)not specified [RCV004425045]uncertain significance11620632816206328Humanname
405698920CV3279396single nucleotide variantNM_153213.5(ARHGEF19):c.1733A>G (p.His578Arg)not specified [RCV004425048]uncertain significance11620510016205100Humanname
405698922CV3279397single nucleotide variantNM_153213.5(ARHGEF19):c.1790G>C (p.Gly597Ala)not specified [RCV004425049]uncertain significance11620487616204876Humanname
405698944CV3279400single nucleotide variantNM_153213.5(ARHGEF19):c.2053C>T (p.Arg685Trp)not specified [RCV004425052]uncertain significance11620242916202429Humanname
405698956CV3279402single nucleotide variantNM_153213.5(ARHGEF19):c.2129T>C (p.Val710Ala)not specified [RCV004425054]uncertain significance11620179916201799Humanname
407459057CV3465197single nucleotide variantNM_153213.5(ARHGEF19):c.1930G>A (p.Val644Ile)not specified [RCV004658012]uncertain significance11620255216202552Humanname
407459031CV3465206single nucleotide variantNM_153213.5(ARHGEF19):c.1467G>T (p.Arg489Ser)not specified [RCV004658017]uncertain significance11620565216205652Humanname
407459004CV3465213single nucleotide variantNM_153213.5(ARHGEF19):c.1013G>A (p.Ser338Asn)not specified [RCV004658022]uncertain significance11620707216207072Humanname
597749858CV3592016single nucleotide variantNM_153213.5(ARHGEF19):c.2360A>G (p.Asn787Ser)not specified [RCV004846311]uncertain significance11619863616198636Humanname
597749946CV3592044single nucleotide variantNM_153213.5(ARHGEF19):c.1118G>A (p.Arg373Gln)not specified [RCV004846332]uncertain significance11620696716206967Humanname
597750018CV3592064single nucleotide variantNM_153213.5(ARHGEF19):c.1897C>T (p.Arg633Trp)not specified [RCV004846347]uncertain significance11620476916204769Humanname
597750061CV3592074single nucleotide variantNM_153213.5(ARHGEF19):c.2252G>C (p.Gly751Ala)not specified [RCV004846357]uncertain significance11619874416198744Humanname
597750112CV3592085single nucleotide variantNM_153213.5(ARHGEF19):c.2152C>A (p.Pro718Thr)not specified [RCV004846368]uncertain significance11619924916199249Humanname
598169847CV3897709single nucleotide variantNM_153213.5(ARHGEF19):c.1561C>T (p.Arg521Cys)not specified [RCV005262916]uncertain significance11620555816205558Humanname
598169878CV3897718single nucleotide variantNM_153213.5(ARHGEF19):c.1487G>A (p.Arg496His)not specified [RCV005262925]uncertain significance11620563216205632Humanname
598169911CV3897728single nucleotide variantNM_153213.5(ARHGEF19):c.1669T>C (p.Cys557Arg)not specified [RCV005262935]uncertain significance11620516416205164Humanname
598170025CV3907708single nucleotide variantNM_153213.5(ARHGEF19):c.1302C>G (p.Phe434Leu)not specified [RCV005262974]uncertain significance11620608016206080Humanname
15155700CV706817single nucleotide variantNM_153213.5(ARHGEF19):c.1898G>A (p.Arg633Gln)not provided [RCV000968972]benign11620476816204768Humanname