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47 records found for search term Dnaja4
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
405731725CV3244529single nucleotide variantNM_001130182.2(DNAJA4):c.-7A>Gnot specified [RCV004379258]likely benign157826475778264757Humanname
401934339CV2814391single nucleotide variantNM_001130182.2(DNAJA4):c.-14C>Tnot provided [RCV003411196]likely benign157826475078264750Humanname
155926432CV2230614single nucleotide variantNM_018602.4(DNAJA4):c.26G>C (p.Trp9Ser)not specified [RCV004097572]uncertain significance157826433978264339Humanname
156244572CV2243137single nucleotide variantNM_001130182.2(DNAJA4):c.58G>C (p.Glu20Gln)not specified [RCV004110043]uncertain significance157826482178264821Humanname
156083247CV2249186single nucleotide variantNM_001130182.2(DNAJA4):c.94A>C (p.Lys32Gln)not specified [RCV004118233]uncertain significance157826485778264857Humanname
155959669CV2285302single nucleotide variantNM_001130182.2(DNAJA4):c.84G>C (p.Lys28Asn)not specified [RCV004139183]uncertain significance157826484778264847Humanname
405731290CV3244526single nucleotide variantNM_001130182.2(DNAJA4):c.98A>G (p.Tyr33Cys)not specified [RCV004379255]uncertain significance157826486178264861Humanname
597713817CV3662867single nucleotide variantNM_001130182.2(DNAJA4):c.67A>G (p.Lys23Glu)not specified [RCV004918066]uncertain significance157826483078264830Humanname
156333471CV2220841single nucleotide variantNM_001130182.2(DNAJA4):c.205G>C (p.Glu69Gln)not specified [RCV004092272]uncertain significance157827056978270569Humanname
156212207CV2259936single nucleotide variantNM_001130182.2(DNAJA4):c.115C>G (p.Pro39Ala)not specified [RCV004118961]uncertain significance157826487878264878Humanname
156144509CV2383935single nucleotide variantNM_001130182.2(DNAJA4):c.292C>T (p.Arg98Trp)not specified [RCV004231787]uncertain significance157827065678270656Humanname
597643565CV3662872single nucleotide variantNM_001130182.2(DNAJA4):c.143T>C (p.Ile48Thr)not specified [RCV004909508]uncertain significance157827050778270507Humanname
156256385CV2194567single nucleotide variantNM_001130182.2(DNAJA4):c.830C>T (p.Thr277Met)not specified [RCV004081627]uncertain significance157827568178275681Humanname
155931491CV2221042single nucleotide variantNM_001130182.2(DNAJA4):c.337T>C (p.Ser113Pro)not specified [RCV004092719]uncertain significance157827311878273118Humanname
155924814CV2248875single nucleotide variantNM_001130182.2(DNAJA4):c.856C>G (p.Leu286Val)not specified [RCV004115883]uncertain significance157827570778275707Humanname
156248946CV2277053single nucleotide variantNM_001130182.2(DNAJA4):c.727G>A (p.Val243Met)not specified [RCV004140373]uncertain significance157827557878275578Humanname
155970717CV2335609single nucleotide variantNM_001130182.2(DNAJA4):c.620A>T (p.Lys207Met)not specified [RCV004193814]uncertain significance157827439878274398Humanname
156013440CV2359101single nucleotide variantNM_001130182.2(DNAJA4):c.469C>T (p.Arg157Trp)not specified [RCV004214467]uncertain significance157827424778274247Humanname
155926367CV2365741single nucleotide variantNM_001130182.2(DNAJA4):c.968T>C (p.Ile323Thr)not specified [RCV004214283]uncertain significance157828013578280135Humanname
156338157CV2370580single nucleotide variantNM_001130182.2(DNAJA4):c.371C>T (p.Thr124Met)not specified [RCV004215909]uncertain significance157827315278273152Humanname
156077274CV2375093single nucleotide variantNM_001130182.2(DNAJA4):c.602A>G (p.Lys201Arg)not specified [RCV004230139]uncertain significance157827438078274380Humanname
156347999CV2375613single nucleotide variantNM_001130182.2(DNAJA4):c.797A>C (p.Gln266Pro)not specified [RCV004226096]uncertain significance157827564878275648Humanname
156195188CV2400471single nucleotide variantNM_001130182.2(DNAJA4):c.772G>T (p.Asp258Tyr)not specified [RCV004246673]uncertain significance157827562378275623Humanname
156004286CV2400970single nucleotide variantNM_001130182.2(DNAJA4):c.559C>T (p.Arg187Cys)not specified [RCV004244255]uncertain significance157827433778274337Humanname
329355106CV2449083single nucleotide variantNM_001130182.2(DNAJA4):c.322G>A (p.Val108Ile)not specified [RCV004264149]uncertain significance157827310378273103Humanname
405731297CV3244527single nucleotide variantNM_001130182.2(DNAJA4):c.522C>G (p.Ile174Met)not specified [RCV004379256]uncertain significance157827430078274300Humanname
405731306CV3244528single nucleotide variantNM_001130182.2(DNAJA4):c.583G>A (p.Glu195Lys)not specified [RCV004379257]uncertain significance157827436178274361Humanname
407497176CV3437470single nucleotide variantNM_001130182.2(DNAJA4):c.498C>G (p.Ile166Met)not specified [RCV004622133]uncertain significance157827427678274276Humanname
407497188CV3437473single nucleotide variantNM_001130182.2(DNAJA4):c.477G>T (p.Met159Ile)not specified [RCV004622136]uncertain significance157827425578274255Humanname
597713826CV3662868single nucleotide variantNM_001130182.2(DNAJA4):c.913C>T (p.Arg305Cys)not specified [RCV004918067]uncertain significance157828008078280080Humanname
597643558CV3662869single nucleotide variantNM_001130182.2(DNAJA4):c.764G>A (p.Arg255Gln)not specified [RCV004909507]uncertain significance157827561578275615Humanname
597713837CV3662870single nucleotide variantNM_001130182.2(DNAJA4):c.595G>A (p.Gly199Arg)not specified [RCV004918068]uncertain significance157827437378274373Humanname
597713848CV3662871single nucleotide variantNM_001130182.2(DNAJA4):c.578G>T (p.Arg193Leu)not specified [RCV004918069]uncertain significance157827435678274356Humanname
12896812CV390183deletionNM_001130182.2(DNAJA4):c.132+1348_132+1349delnot specified [RCV000455856]likely benign157826624378266244Humanname
598162995CV3953419single nucleotide variantNM_001130182.2(DNAJA4):c.725T>C (p.Ile242Thr)not specified [RCV005329286]uncertain significance157827557678275576Humanname
598163008CV3953421single nucleotide variantNM_001130182.2(DNAJA4):c.538G>A (p.Glu180Lys)not specified [RCV005329288]uncertain significance157827431678274316Humanname
598163015CV3953422single nucleotide variantNM_001130182.2(DNAJA4):c.854T>C (p.Ile285Thr)not specified [RCV005329289]uncertain significance157827570578275705Humanname
156030492CV2238410single nucleotide variantNM_001130182.2(DNAJA4):c.1187C>T (p.Thr396Met)not specified [RCV004113474]uncertain significance157828045378280453Humanname
155950995CV2238695single nucleotide variantNM_001130182.2(DNAJA4):c.1049G>C (p.Arg350Pro)not specified [RCV004107589]uncertain significance157828031578280315Humanname
401774838CV2688305single nucleotide variantNM_001130182.2(DNAJA4):c.1131C>A (p.His377Gln)not specified [RCV004299313]uncertain significance157828039778280397Humanname
401766417CV2725528single nucleotide variantNM_001130182.2(DNAJA4):c.1021C>T (p.Pro341Ser)not specified [RCV004320144]uncertain significance157828028778280287Humanname
405731265CV3244523single nucleotide variantNM_001130182.2(DNAJA4):c.1017G>T (p.Lys339Asn)not specified [RCV004379252]uncertain significance157828028378280283Humanname
405731278CV3244525single nucleotide variantNM_001130182.2(DNAJA4):c.1151A>G (p.Asp384Gly)not specified [RCV004379254]uncertain significance157828041778280417Humanname
407497171CV3437469single nucleotide variantNM_001130182.2(DNAJA4):c.1027C>G (p.Leu343Val)not specified [RCV004622132]uncertain significance157828029378280293Humanname
407497184CV3437472single nucleotide variantNM_001130182.2(DNAJA4):c.1048C>G (p.Arg350Gly)not specified [RCV004622135]uncertain significance157828031478280314Humanname
597643572CV3662873single nucleotide variantNM_001130182.2(DNAJA4):c.1076T>C (p.Met359Thr)not specified [RCV004909509]uncertain significance157828034278280342Humanname
598163001CV3953420single nucleotide variantNM_001130182.2(DNAJA4):c.1159G>A (p.Gly387Arg)not specified [RCV005329287]uncertain significance157828042578280425Humanname