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64 records found for search term Baiap2l1
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
402517919CV2936425deletionNM_018842.5(BAIAP2L1):c.487-6_487-3delnot provided [RCV003662991]benign79831561598315618Humanname
12896633CV389849insertionNM_018842.5(BAIAP2L1):c.487-10_487-9insAnot specified [RCV000455616]benign79831562198315622Humanname
156380960CV2219070single nucleotide variantNM_018842.5(BAIAP2L1):c.21G>C (p.Glu7Asp)not specified [RCV004087233]uncertain significance79840083298400832Humanname
156342188CV2226032single nucleotide variantNM_018842.5(BAIAP2L1):c.27C>G (p.Asn9Lys)not specified [RCV004105188]uncertain significance79840082698400826Humanname
597755281CV3635439single nucleotide variantNM_018842.5(BAIAP2L1):c.83G>A (p.Arg28Gln)not specified [RCV004893654]uncertain significance79836240198362401Humanname
155975834CV2235944single nucleotide variantNM_018842.5(BAIAP2L1):c.179A>T (p.Glu60Val)not specified [RCV004113827]uncertain significance79835507798355077Humanname
401883640CV2758045single nucleotide variantNM_018842.5(BAIAP2L1):c.227T>G (p.Ile76Arg)not specified [RCV004339211]uncertain significance79832028698320286Humanname
401922582CV2825889single nucleotide variantNM_018842.5(BAIAP2L1):c.1347C>T (p.Ala449=)not provided [RCV003433949]likely benign79830427198304271Humanname
407499809CV3417339single nucleotide variantNM_018842.5(BAIAP2L1):c.220G>A (p.Val74Ile)not specified [RCV004606966]uncertain significance79832029398320293Humanname
407494242CV3417340single nucleotide variantNM_018842.5(BAIAP2L1):c.191G>T (p.Gly64Val)not specified [RCV004605545]uncertain significance79835506598355065Humanname
597755425CV3635450single nucleotide variantNM_018842.5(BAIAP2L1):c.187A>T (p.Thr63Ser)not specified [RCV004893665]uncertain significance79835506998355069Humanname
597728368CV3635471single nucleotide variantNM_018842.5(BAIAP2L1):c.246C>G (p.His82Gln)not specified [RCV004888651]uncertain significance79832026798320267Humanname
598275635CV3937360single nucleotide variantNM_018842.5(BAIAP2L1):c.1461C>T (p.Ser487=)not specified [RCV005304769]likely benign79829359698293596Humanname
598275645CV3937371single nucleotide variantNM_018842.5(BAIAP2L1):c.130A>G (p.Met44Val)not specified [RCV005304779]uncertain significance79835512698355126Humanname
156400575CV2199276single nucleotide variantNM_018842.5(BAIAP2L1):c.623A>G (p.His208Arg)not specified [RCV004082630]uncertain significance79831547698315476Humanname
156133504CV2235413single nucleotide variantNM_018842.5(BAIAP2L1):c.743C>A (p.Thr248Asn)not specified [RCV004109470]uncertain significance79831216198312161Humanname
156056495CV2243310single nucleotide variantNM_018842.5(BAIAP2L1):c.730G>A (p.Glu244Lys)not specified [RCV004112010]uncertain significance79831217498312174Humanname
156234914CV2271277single nucleotide variantNM_018842.5(BAIAP2L1):c.755C>T (p.Thr252Ile)not specified [RCV004136406]uncertain significance79831214998312149Humanname
155927938CV2280970single nucleotide variantNM_018842.5(BAIAP2L1):c.986C>T (p.Ser329Leu)not specified [RCV004145475]uncertain significance79830786698307866Humanname
156281622CV2288758single nucleotide variantNM_018842.5(BAIAP2L1):c.998C>T (p.Ala333Val)not specified [RCV004147980]uncertain significance79830785498307854Humanname
155902388CV2301428single nucleotide variantNM_018842.5(BAIAP2L1):c.856C>T (p.Pro286Ser)not specified [RCV004162363]uncertain significance79831054498310544Humanname
156339886CV2351663single nucleotide variantNM_018842.5(BAIAP2L1):c.509G>A (p.Arg170His)not specified [RCV004195374]uncertain significance79831559098315590Humanname
329387729CV2446698single nucleotide variantNM_018842.5(BAIAP2L1):c.671G>A (p.Arg224Gln)not specified [RCV004253745]uncertain significance79831223398312233Humanname
329396674CV2458927single nucleotide variantNM_018842.5(BAIAP2L1):c.581G>C (p.Cys194Ser)not specified [RCV004272424]uncertain significance79831551898315518Humanname
401780437CV2674024single nucleotide variantNM_018842.5(BAIAP2L1):c.490G>A (p.Val164Met)not specified [RCV004293389]uncertain significance79831560998315609Humanname
401754891CV2682327single nucleotide variantNM_018842.5(BAIAP2L1):c.515G>C (p.Ser172Thr)not specified [RCV004290365]uncertain significance79831558498315584Humanname
405691661CV3290867single nucleotide variantNM_018842.5(BAIAP2L1):c.452G>A (p.Arg151Gln)not specified [RCV004423780]uncertain significance79831725398317253Humanname
405691666CV3290868single nucleotide variantNM_018842.5(BAIAP2L1):c.714A>C (p.Lys238Asn)not specified [RCV004423781]uncertain significance79831219098312190Humanname
407494223CV3417334single nucleotide variantNM_018842.5(BAIAP2L1):c.548A>G (p.Lys183Arg)not specified [RCV004605540]uncertain significance79831555198315551Humanname
407494238CV3417338single nucleotide variantNM_018842.5(BAIAP2L1):c.983G>A (p.Arg328Gln)not specified [RCV004605544]uncertain significance79830786998307869Humanname
597755198CV3635420single nucleotide variantNM_018842.5(BAIAP2L1):c.845C>G (p.Pro282Arg)not specified [RCV004893635]uncertain significance79831055598310555Humanname
597728520CV3635489single nucleotide variantNM_018842.5(BAIAP2L1):c.785C>T (p.Pro262Leu)not specified [RCV004888669]uncertain significance79831211998312119Humanname
597728597CV3635499single nucleotide variantNM_018842.5(BAIAP2L1):c.368A>G (p.Gln123Arg)not specified [RCV004888679]uncertain significance79831733798317337Humanname
12896930CV389807insertionNM_018842.5(BAIAP2L1):c.487-14_487-13insATTAnot specified [RCV000456008]benign79831562598315626Humanname
598275627CV3937349single nucleotide variantNM_018842.5(BAIAP2L1):c.859G>A (p.Ala287Thr)not specified [RCV005304761]uncertain significance79831054198310541Humanname
598275651CV3937378single nucleotide variantNM_018842.5(BAIAP2L1):c.917C>T (p.Thr306Met)not specified [RCV005304785]uncertain significance79831048398310483Humanname
598275658CV3937389single nucleotide variantNM_018842.5(BAIAP2L1):c.618C>G (p.His206Gln)not specified [RCV005304792]uncertain significance79831548198315481Humanname
598182645CV3937399single nucleotide variantNM_018842.5(BAIAP2L1):c.925C>T (p.Pro309Ser)not specified [RCV005311272]uncertain significance79831047598310475Humanname
598275671CV3937409single nucleotide variantNM_018842.5(BAIAP2L1):c.841T>C (p.Ser281Pro)not specified [RCV005304805]uncertain significance79831055998310559Humanname
598182689CV3937419single nucleotide variantNM_018842.5(BAIAP2L1):c.513G>C (p.Gln171His)not specified [RCV005311279]uncertain significance79831558698315586Humanname
156230550CV2199581single nucleotide variantNM_018842.5(BAIAP2L1):c.1373C>T (p.Thr458Met)not specified [RCV004072330]uncertain significance79830424598304245Humanname
156149291CV2212984single nucleotide variantNM_018842.5(BAIAP2L1):c.1190C>T (p.Thr397Met)not specified [RCV004091584]uncertain significance79830649098306490Humanname
156248264CV2215411single nucleotide variantNM_018842.5(BAIAP2L1):c.1152C>A (p.Asp384Glu)not specified [RCV004089215]uncertain significance79830770098307700Humanname
156122032CV2241008single nucleotide variantNM_018842.5(BAIAP2L1):c.1307C>A (p.Pro436Gln)not specified [RCV004102274]uncertain significance79830431198304311Humanname
155959745CV2252582single nucleotide variantNM_018842.5(BAIAP2L1):c.1226C>A (p.Thr409Asn)not specified [RCV004118465]uncertain significance79830645498306454Humanname
155931528CV2370942single nucleotide variantNM_018842.5(BAIAP2L1):c.1348G>A (p.Asp450Asn)not specified [RCV004218669]uncertain significance79830427098304270Humanname
156095034CV2377879single nucleotide variantNM_018842.5(BAIAP2L1):c.1350C>A (p.Asp450Glu)not specified [RCV004230450]uncertain significance79830426898304268Humanname
329390945CV2437461single nucleotide variantNM_018842.5(BAIAP2L1):c.1068G>T (p.Lys356Asn)not specified [RCV004256326]uncertain significance79830778498307784Humanname
401729532CV2690314single nucleotide variantNM_018842.5(BAIAP2L1):c.1282G>A (p.Glu428Lys)not specified [RCV004302309]uncertain significance79830433698304336Humanname
401746669CV2691957single nucleotide variantNM_018842.5(BAIAP2L1):c.1157C>G (p.Ser386Cys)not specified [RCV004301687]uncertain significance79830769598307695Humanname
404988941CV2849699single nucleotide variantNM_018842.5(BAIAP2L1):c.1442C>T (p.Ala481Val)not provided [RCV003490509]uncertain significance79829409298294092Humanname
405691642CV3290864single nucleotide variantNM_018842.5(BAIAP2L1):c.1150G>A (p.Asp384Asn)not specified [RCV004423777]uncertain significance79830770298307702Humanname
405691647CV3290865single nucleotide variantNM_018842.5(BAIAP2L1):c.1270G>A (p.Val424Met)not specified [RCV004423778]uncertain significance79830434898304348Humanname
405691654CV3290866single nucleotide variantNM_018842.5(BAIAP2L1):c.1364C>T (p.Ser455Leu)not specified [RCV004423779]uncertain significance79830425498304254Humanname
407494230CV3417336single nucleotide variantNM_018842.5(BAIAP2L1):c.1508A>G (p.Asn503Ser)not specified [RCV004605542]uncertain significance79829354998293549Humanname
407494234CV3417337single nucleotide variantNM_018842.5(BAIAP2L1):c.1294G>A (p.Val432Ile)not specified [RCV004605543]uncertain significance79830432498304324Humanname
597755377CV3635390single nucleotide variantNM_018842.5(BAIAP2L1):c.1408G>A (p.Glu470Lys)not specified [RCV004893605]uncertain significance79830421098304210Humanname
597755333CV3635401single nucleotide variantNM_018842.5(BAIAP2L1):c.1505C>T (p.Thr502Met)not specified [RCV004893616]uncertain significance79829355298293552Humanname
597755166CV3635411single nucleotide variantNM_018842.5(BAIAP2L1):c.1448C>T (p.Pro483Leu)not specified [RCV004893626]uncertain significance79829408698294086Humanname
597755468CV3635461single nucleotide variantNM_018842.5(BAIAP2L1):c.1048C>T (p.His350Tyr)not specified [RCV004893676]uncertain significance79830780498307804Humanname
597728444CV3635480single nucleotide variantNM_018842.5(BAIAP2L1):c.1125G>T (p.Lys375Asn)not specified [RCV004888660]uncertain significance79830772798307727Humanname
598275614CV3937329single nucleotide variantNM_018842.5(BAIAP2L1):c.1529T>C (p.Ile510Thr)not specified [RCV005304748]uncertain significance79829352898293528Humanname
598275621CV3937339single nucleotide variantNM_018842.5(BAIAP2L1):c.1153G>A (p.Val385Met)not specified [RCV005304755]uncertain significance79830769998307699Humanname
402516541CV2936426insertionNM_018842.5(BAIAP2L1):c.487-14_487-13insATTATTATTAnot provided [RCV003662992]likely benign79831562598315626Humanname