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Variants search result for Homo sapiens
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62 records found for search term Serpina4
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
405747241CV3310935single nucleotide variantNM_006215.4(SERPINA4):c.70G>A (p.Val24Ile)not specified [RCV004453235]uncertain significance149456355294563552Humanname
155997421CV2250552single nucleotide variantNM_006215.4(SERPINA4):c.235C>T (p.Pro79Ser)not specified [RCV004127410]uncertain significance149456371794563717Humanname
329372511CV2424117single nucleotide variantNM_006215.4(SERPINA4):c.271C>A (p.Leu91Met)not specified [RCV004248016]uncertain significance149456375394563753Humanname
401749432CV2694647single nucleotide variantNM_006215.4(SERPINA4):c.199G>A (p.Ala67Thr)not specified [RCV004298758]uncertain significance149456368194563681Humanname
405747193CV3310927single nucleotide variantNM_006215.4(SERPINA4):c.199G>T (p.Ala67Ser)not specified [RCV004453227]uncertain significance149456368194563681Humanname
405747197CV3310928single nucleotide variantNM_006215.4(SERPINA4):c.293G>A (p.Arg98His)not specified [RCV004453228]uncertain significance149456377594563775Humanname
597738049CV3598512single nucleotide variantNM_006215.4(SERPINA4):c.236C>T (p.Pro79Leu)not specified [RCV004864169]uncertain significance149456371894563718Humanname
597738071CV3598518single nucleotide variantNM_006215.4(SERPINA4):c.280T>C (p.Cys94Arg)not specified [RCV004864174]likely benign149456376294563762Humanname
598225622CV3900416single nucleotide variantNM_006215.4(SERPINA4):c.212C>T (p.Pro71Leu)not specified [RCV005273383]uncertain significance149456369494563694Humanname
15140653CV714281single nucleotide variantNM_006215.4(SERPINA4):c.1116G>A (p.Glu372=)not provided [RCV000966174]benign149456942794569427Human1name
15140653CV714281single nucleotide variantNM_006215.4(SERPINA4):c.1116G>A (p.Glu372=)not provided [RCV000966174]benign149456942794569428Human1name
8627602CV82746single nucleotide variantNM_006215.3(SERPINA4):c.1275G>A (p.Thr425=)Malignant melanoma [RCV000062826]not provided149456958694569586Humanname
155917550CV2198983single nucleotide variantNM_006215.4(SERPINA4):c.520G>A (p.Asp174Asn)not specified [RCV004080393]uncertain significance149456400294564002Humanname
156226276CV2203120single nucleotide variantNM_006215.4(SERPINA4):c.410C>A (p.Thr137Lys)not specified [RCV004069360]uncertain significance149456389294563892Humanname
155969860CV2213392single nucleotide variantNM_006215.4(SERPINA4):c.497A>G (p.Lys166Arg)not specified [RCV004087375]uncertain significance149456397994563979Humanname
156163243CV2246622single nucleotide variantNM_006215.4(SERPINA4):c.415G>A (p.Val139Met)not specified [RCV004110364]likely benign149456389794563897Humanname
156043467CV2268454single nucleotide variantNM_006215.4(SERPINA4):c.470A>G (p.Asn157Ser)not specified [RCV004130153]uncertain significance149456395294563952Humanname
156014973CV2269736single nucleotide variantNM_006215.4(SERPINA4):c.475A>G (p.Thr159Ala)not specified [RCV004126987]uncertain significance149456395794563957Humanname
156094300CV2300290single nucleotide variantNM_006215.4(SERPINA4):c.914T>G (p.Leu305Trp)not specified [RCV004153245]uncertain significance149456723494567234Humanname
156158924CV2322691single nucleotide variantNM_006215.4(SERPINA4):c.451T>C (p.Phe151Leu)not specified [RCV004182817]likely benign149456393394563933Humanname
329352200CV2452214single nucleotide variantNM_006215.4(SERPINA4):c.482C>A (p.Ala161Asp)not specified [RCV004278915]uncertain significance149456396494563964Humanname
401719559CV2675615single nucleotide variantNM_006215.4(SERPINA4):c.999G>C (p.Leu333Phe)not specified [RCV004287875]uncertain significance149456820494568204Humanname
401883288CV2760865single nucleotide variantNM_006215.4(SERPINA4):c.800G>A (p.Arg267Gln)not specified [RCV004336500]uncertain significance149456712094567120Humanname
401866008CV2775377single nucleotide variantNM_006215.4(SERPINA4):c.359G>A (p.Gly120Asp)not specified [RCV004348781]uncertain significance149456384194563841Humanname
401866010CV2775378single nucleotide variantNM_006215.4(SERPINA4):c.711G>C (p.Glu237Asp)not specified [RCV004348782]uncertain significance149456703194567031Humanname
405747203CV3310929single nucleotide variantNM_006215.4(SERPINA4):c.340G>C (p.Glu114Gln)not specified [RCV004453229]uncertain significance149456382294563822Humanname
405747210CV3310930single nucleotide variantNM_006215.4(SERPINA4):c.343T>A (p.Ser115Thr)not specified [RCV004453230]uncertain significance149456382594563825Humanname
405747217CV3310931single nucleotide variantNM_006215.4(SERPINA4):c.386A>G (p.Asn129Ser)not specified [RCV004453231]likely benign149456386894563868Humanname
405747223CV3310932single nucleotide variantNM_006215.4(SERPINA4):c.471T>A (p.Asn157Lys)not specified [RCV004453232]uncertain significance149456395394563953Humanname
405747234CV3310934single nucleotide variantNM_006215.4(SERPINA4):c.538C>G (p.Gln180Glu)not specified [RCV004453234]uncertain significance149456402094564020Humanname
405747248CV3310936single nucleotide variantNM_006215.4(SERPINA4):c.799C>T (p.Arg267Trp)not specified [RCV004453236]uncertain significance149456711994567119Humanname
405747254CV3310937single nucleotide variantNM_006215.4(SERPINA4):c.977C>T (p.Ser326Phe)not specified [RCV004453237]uncertain significance149456818294568182Humanname
407488864CV3473632single nucleotide variantNM_006215.4(SERPINA4):c.724C>T (p.Arg242Trp)not specified [RCV004665945]uncertain significance149456704494567044Humanname
407488870CV3473633single nucleotide variantNM_006215.4(SERPINA4):c.346G>T (p.Asp116Tyr)not specified [RCV004665946]uncertain significance149456382894563828Humanname
407488876CV3473634single nucleotide variantNM_006215.4(SERPINA4):c.419G>C (p.Gly140Ala)not specified [RCV004665947]uncertain significance149456390194563901Humanname
407492464CV3473635single nucleotide variantNM_006215.4(SERPINA4):c.892C>G (p.Leu298Val)not specified [RCV004667133]uncertain significance149456721294567212Humanname
597738028CV3598507single nucleotide variantNM_006215.4(SERPINA4):c.803T>G (p.Met268Arg)not specified [RCV004864164]uncertain significance149456712394567123Humanname
597738041CV3598510single nucleotide variantNM_006215.4(SERPINA4):c.643T>C (p.Phe215Leu)not specified [RCV004864167]uncertain significance149456412594564125Humanname
597738045CV3598511single nucleotide variantNM_006215.4(SERPINA4):c.596G>T (p.Ser199Ile)not specified [RCV004864168]uncertain significance149456407894564078Humanname
597738054CV3598514single nucleotide variantNM_006215.4(SERPINA4):c.791C>T (p.Ser264Leu)not specified [RCV004864170]uncertain significance149456711194567111Humanname
597738058CV3598515single nucleotide variantNM_006215.4(SERPINA4):c.346G>A (p.Asp116Asn)not specified [RCV004864171]uncertain significance149456382894563828Humanname
597738068CV3598517single nucleotide variantNM_006215.4(SERPINA4):c.692A>G (p.Lys231Arg)not specified [RCV004864173]uncertain significance149456701294567012Humanname
597738075CV3598519single nucleotide variantNM_006215.4(SERPINA4):c.826G>A (p.Val276Met)not specified [RCV004864175]uncertain significance149456714694567146Humanname
598225629CV3900417single nucleotide variantNM_006215.4(SERPINA4):c.737T>C (p.Met246Thr)not specified [RCV005273384]uncertain significance149456705794567057Humanname
598225635CV3900418single nucleotide variantNM_006215.4(SERPINA4):c.963C>A (p.Phe321Leu)not specified [RCV005273385]uncertain significance149456816894568168Humanname
598225640CV3900419single nucleotide variantNM_006215.4(SERPINA4):c.418G>A (p.Gly140Ser)not specified [RCV005273386]uncertain significance149456390094563900Humanname
598225646CV3900420single nucleotide variantNM_006215.4(SERPINA4):c.415G>C (p.Val139Leu)not specified [RCV005273387]uncertain significance149456389794563897Humanname
598225652CV3900421single nucleotide variantNM_006215.4(SERPINA4):c.955C>A (p.Pro319Thr)not specified [RCV005273388]uncertain significance149456816094568160Humanname
598225658CV3900422single nucleotide variantNM_006215.4(SERPINA4):c.990T>A (p.Asp330Glu)not specified [RCV005273389]uncertain significance149456819594568195Humanname
15162459CV714280single nucleotide variantNM_006215.4(SERPINA4):c.412C>T (p.Arg138Cys)not provided [RCV000970274]benign149456389494563894Humanname
156380638CV2218856single nucleotide variantNM_006215.4(SERPINA4):c.1108G>A (p.Val370Met)not specified [RCV004085097]uncertain significance149456941994569419Humanname
156246936CV2221836single nucleotide variantNM_006215.4(SERPINA4):c.1229C>T (p.Thr410Ile)not specified [RCV004102862]uncertain significance149456954094569540Humanname
156088888CV2241434single nucleotide variantNM_006215.4(SERPINA4):c.1235C>A (p.Thr412Asn)not specified [RCV004104347]uncertain significance149456954694569546Humanname
156151494CV2377557single nucleotide variantNM_006215.4(SERPINA4):c.1202G>A (p.Arg401Gln)not specified [RCV004227754]uncertain significance149456951394569513Humanname
401895363CV2786404single nucleotide variantNM_006215.4(SERPINA4):c.1241G>A (p.Ser414Asn)not specified [RCV004361994]uncertain significance149456955294569552Humanname
405747165CV3310923single nucleotide variantNM_006215.4(SERPINA4):c.1016C>A (p.Thr339Lys)not specified [RCV004453223]uncertain significance149456822194568221Humanname
405747171CV3310924single nucleotide variantNM_006215.4(SERPINA4):c.1175C>T (p.Thr392Ile)not specified [RCV004453224]uncertain significance149456948694569486Humanname
405747180CV3310925single nucleotide variantNM_006215.4(SERPINA4):c.1181G>T (p.Arg394Leu)not specified [RCV004453225]uncertain significance149456949294569492Humanname
597738033CV3598508single nucleotide variantNM_006215.4(SERPINA4):c.1180C>A (p.Arg394Ser)not specified [RCV004864165]uncertain significance149456949194569491Humanname
597738038CV3598509single nucleotide variantNM_006215.4(SERPINA4):c.1009G>A (p.Gly337Ser)not specified [RCV004864166]uncertain significance149456821494568214Humanname
597738063CV3598516single nucleotide variantNM_006215.4(SERPINA4):c.1246C>T (p.Leu416Phe)not specified [RCV004864172]uncertain significance149456955794569557Humanname
598225666CV3900423single nucleotide variantNM_006215.4(SERPINA4):c.1259A>G (p.Lys420Arg)not specified [RCV005273390]uncertain significance149456957094569570Humanname