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56 records found for search term Crtc3
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
8584656CV119232single nucleotide variantNM_001042574.2(CRTC3):c.*2534C>ALung cancer [RCV000099752]uncertain significance159064467490644674Humanname
401904491CV2814490single nucleotide variantNM_022769.5(CRTC3):c.126G>A (p.Leu42=)not provided [RCV003395035]likely benign159053019790530197Humanname
405675648CV3239132single nucleotide variantNM_022769.5(CRTC3):c.51G>C (p.Glu17Asp)not specified [RCV004370014]uncertain significance159053012290530122Humanname
15098643CV726349single nucleotide variantNM_022769.5(CRTC3):c.663G>A (p.Pro221=)not provided [RCV000891784]benign159061793290617932Humanname
401727180CV2715011single nucleotide variantNM_022769.5(CRTC3):c.166A>C (p.Thr56Pro)not specified [RCV004322326]uncertain significance159054007290540072Humanname
407464384CV3429753single nucleotide variantNM_022769.5(CRTC3):c.268C>T (p.Arg90Cys)not specified [RCV004613440]uncertain significance159059367290593672Humanname
598260090CV3963004single nucleotide variantNM_022769.5(CRTC3):c.155A>G (p.Gln52Arg)not specified [RCV005324909]uncertain significance159054006190540061Humanname
15098647CV726350single nucleotide variantNM_022769.5(CRTC3):c.1692G>A (p.Ala564=)not provided [RCV000891785]benign159064197290641972Humanname
156048553CV2241679single nucleotide variantNM_022769.5(CRTC3):c.355G>A (p.Asp119Asn)not specified [RCV004106626]uncertain significance159060232790602327Humanname
156197346CV2334255single nucleotide variantNM_022769.5(CRTC3):c.377A>G (p.Asn126Ser)not specified [RCV004186238]uncertain significance159060234990602349Humanname
329392170CV2441285single nucleotide variantNM_022769.5(CRTC3):c.552G>C (p.Gln184His)not specified [RCV004257104]uncertain significance159060745390607453Humanname
329374674CV2444013single nucleotide variantNM_022769.5(CRTC3):c.965C>T (p.Ser322Phe)not specified [RCV004258335]uncertain significance159062599190625991Humanname
401759469CV2701566single nucleotide variantNM_022769.5(CRTC3):c.458T>C (p.Leu153Pro)not specified [RCV004314006]uncertain significance159060442990604429Humanname
405675643CV3239131single nucleotide variantNM_022769.5(CRTC3):c.467C>T (p.Ala156Val)not specified [RCV004370013]uncertain significance159060443890604438Humanname
405675653CV3239133single nucleotide variantNM_022769.5(CRTC3):c.779G>A (p.Gly260Asp)not specified [RCV004370015]uncertain significance159062580590625805Humanname
407464370CV3429749single nucleotide variantNM_022769.5(CRTC3):c.404G>A (p.Ser135Asn)not specified [RCV004613436]uncertain significance159060237690602376Humanname
597799683CV3657694single nucleotide variantNM_022769.5(CRTC3):c.901A>T (p.Ser301Cys)not specified [RCV004905346]uncertain significance159062592790625927Humanname
597799689CV3657697single nucleotide variantNM_022769.5(CRTC3):c.709C>A (p.Leu237Met)not specified [RCV004905349]uncertain significance159061975090619750Humanname
597799692CV3657698single nucleotide variantNM_022769.5(CRTC3):c.424C>G (p.Pro142Ala)not specified [RCV004905350]uncertain significance159060439590604395Humanname
598260058CV3962998single nucleotide variantNM_022769.5(CRTC3):c.725G>A (p.Arg242Gln)not specified [RCV005324903]uncertain significance159061976690619766Humanname
598260080CV3963002single nucleotide variantNM_022769.5(CRTC3):c.490T>C (p.Ser164Pro)not specified [RCV005324907]uncertain significance159060739190607391Humanname
598260085CV3963003single nucleotide variantNM_022769.5(CRTC3):c.952A>T (p.Ile318Leu)not specified [RCV005324908]uncertain significance159062597890625978Humanname
9687079CV171565single nucleotide variantNM_022769.5(CRTC3):c.1387C>A (p.Arg463Ser)Prostate cancer [RCV000149298]uncertain significance159063856690638566Human2name
155901156CV2275332single nucleotide variantNM_022769.5(CRTC3):c.1678G>T (p.Asp560Tyr)not specified [RCV004137100]uncertain significance159064195890641958Humanname
155918873CV2279307single nucleotide variantNM_022769.5(CRTC3):c.1501G>C (p.Gly501Arg)not specified [RCV004139824]uncertain significance159063876890638768Humanname
155944074CV2294968single nucleotide variantNM_022769.5(CRTC3):c.1568G>A (p.Gly523Asp)not specified [RCV004156114]uncertain significance159064111690641116Humanname
156002025CV2296474single nucleotide variantNM_022769.5(CRTC3):c.1007C>T (p.Thr336Met)not specified [RCV004148212]uncertain significance159062927390629273Humanname
156206654CV2297984single nucleotide variantNM_022769.5(CRTC3):c.1181C>T (p.Thr394Met)not specified [RCV004157900]uncertain significance159062944790629447Humanname
156047557CV2304348single nucleotide variantNM_022769.5(CRTC3):c.1253A>G (p.Tyr418Cys)not specified [RCV004164462]uncertain significance159062951990629519Humanname
156030375CV2379607single nucleotide variantNM_022769.5(CRTC3):c.1058C>T (p.Ser353Phe)not specified [RCV004217306]uncertain significance159062932490629324Humanname
156043972CV2381589single nucleotide variantNM_022769.5(CRTC3):c.1610C>T (p.Pro537Leu)not specified [RCV004232065]likely benign159064115890641158Humanname
156201179CV2392472single nucleotide variantNM_022769.5(CRTC3):c.1310A>C (p.Glu437Ala)not specified [RCV004244044]uncertain significance159063848990638489Humanname
329399469CV2436174single nucleotide variantNM_022769.5(CRTC3):c.1439A>T (p.Gln480Leu)not specified [RCV004249807]uncertain significance159063861890638618Humanname
329381157CV2464537single nucleotide variantNM_022769.5(CRTC3):c.1267A>G (p.Met423Val)not specified [RCV004278235]uncertain significance159063844690638446Humanname
401745181CV2693200single nucleotide variantNM_022769.5(CRTC3):c.1624G>A (p.Gly542Arg)not specified [RCV004293128]uncertain significance159064117290641172Humanname
401768764CV2735421single nucleotide variantNM_022769.5(CRTC3):c.1460C>T (p.Pro487Leu)not specified [RCV004330983]uncertain significance159063863990638639Humanname
401888763CV2764659single nucleotide variantNM_022769.5(CRTC3):c.1584G>T (p.Gln528His)not specified [RCV004341462]uncertain significance159064113290641132Humanname
405675602CV3239123single nucleotide variantNM_022769.5(CRTC3):c.1168G>A (p.Val390Ile)not specified [RCV004370005]uncertain significance159062943490629434Humanname
405675607CV3239124single nucleotide variantNM_022769.5(CRTC3):c.1424C>G (p.Ala475Gly)not specified [RCV004370006]uncertain significance159063860390638603Humanname
405675611CV3239125single nucleotide variantNM_022769.5(CRTC3):c.1427C>T (p.Ser476Phe)not specified [RCV004370007]uncertain significance159063860690638606Humanname
405675621CV3239127single nucleotide variantNM_022769.5(CRTC3):c.1485C>G (p.Asn495Lys)not specified [RCV004370009]uncertain significance159063875290638752Humanname
405675627CV3239128single nucleotide variantNM_022769.5(CRTC3):c.1630C>G (p.Leu544Val)not specified [RCV004370010]uncertain significance159064117890641178Humanname
405675638CV3239130single nucleotide variantNM_022769.5(CRTC3):c.1787A>G (p.Asn596Ser)not specified [RCV004370012]uncertain significance159064206790642067Humanname
407464377CV3429751single nucleotide variantNM_022769.5(CRTC3):c.1555C>G (p.Leu519Val)not specified [RCV004613438]uncertain significance159064110390641103Humanname
407464380CV3429752single nucleotide variantNM_022769.5(CRTC3):c.1234A>G (p.Thr412Ala)not specified [RCV004613439]uncertain significance159062950090629500Humanname
597799676CV3657691single nucleotide variantNM_022769.5(CRTC3):c.1150C>T (p.Arg384Trp)not specified [RCV004905343]uncertain significance159062941690629416Humanname
597799679CV3657692single nucleotide variantNM_022769.5(CRTC3):c.1514A>G (p.Gln505Arg)not specified [RCV004905344]uncertain significance159063878190638781Humanname
597799681CV3657693single nucleotide variantNM_022769.5(CRTC3):c.1303C>T (p.Pro435Ser)not specified [RCV004905345]uncertain significance159063848290638482Humanname
597799685CV3657695single nucleotide variantNM_022769.5(CRTC3):c.1291C>G (p.Leu431Val)not specified [RCV004905347]uncertain significance159063847090638470Humanname
597799687CV3657696single nucleotide variantNM_022769.5(CRTC3):c.1723G>A (p.Val575Met)not specified [RCV004905348]likely benign159064200390642003Humanname
598260064CV3962999single nucleotide variantNM_022769.5(CRTC3):c.1594C>T (p.His532Tyr)not specified [RCV005324904]uncertain significance159064114290641142Humanname
598260070CV3963000single nucleotide variantNM_022769.5(CRTC3):c.1448T>A (p.Phe483Tyr)not specified [RCV005324905]uncertain significance159063862790638627Humanname
598260075CV3963001single nucleotide variantNM_022769.5(CRTC3):c.1564C>G (p.Gln522Glu)not specified [RCV005324906]uncertain significance159064111290641112Humanname
8635636CV90858single nucleotide variantNM_001042574.2(CRTC3):c.321C>T (p.His107=)Malignant melanoma [RCV000070956]not provided159059372590593725Humanname
8635637CV90859single nucleotide variantNM_001042574.2(CRTC3):c.1290A>T (p.Gln430His)Malignant melanoma [RCV000070957]not provided159063846990638469Humanname
8635638CV90860single nucleotide variantNM_001042574.2(CRTC3):c.1291C>T (p.Leu431Phe)Malignant melanoma [RCV000070958]not provided159063847090638470Humanname