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114 records found for search term Anks1a
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
15115606CV744117single nucleotide variantNM_015245.3(ANKS1A):c.1424-8A>Gnot provided [RCV000895056]likely benign63501746535017465Humanname
15192640CV730424single nucleotide variantNM_015245.3(ANKS1A):c.2437-10C>Tnot provided [RCV000888718]benign63507981135079811Humanname
8581865CV116313single nucleotide variantNM_015245.2(ANKS1A):c.198-18282G>CLung cancer [RCV000096836]uncertain significance63494895734948957Humanname
8581866CV116314single nucleotide variantNM_015245.2(ANKS1A):c.2011-10478G>ALung cancer [RCV000096837]uncertain significance63504362135043621Humanname
156155035CV2328714single nucleotide variantNM_015245.3(ANKS1A):c.4G>A (p.Gly2Arg)not specified [RCV004177949]uncertain significance63488940634889406Humanname
401885758CV2775077single nucleotide variantNM_015245.3(ANKS1A):c.198C>T (p.Ser66=)not specified [RCV004346445]likely benign63496723934967239Humanname
405694756CV3226516single nucleotide variantNM_015245.3(ANKS1A):c.249C>G (p.Pro83=)not provided [RCV003992909]likely benign63496729034967290Humanname
15115600CV735637single nucleotide variantNM_015245.3(ANKS1A):c.321C>T (p.Asn107=)not provided [RCV000895055]likely benign63497005234970052Humanname
405684016CV3282354single nucleotide variantNM_015245.3(ANKS1A):c.179C>T (p.Pro60Leu)not specified [RCV004422333]uncertain significance63488958134889581Humanname
597650954CV3561373single nucleotide variantNM_015245.3(ANKS1A):c.167C>T (p.Ser56Phe)not specified [RCV004833678]uncertain significance63488956934889569Humanname
597651189CV3561419single nucleotide variantNM_015245.3(ANKS1A):c.119C>G (p.Ser40Cys)not specified [RCV004833706]uncertain significance63488952134889521Humanname
598168646CV3982592single nucleotide variantNM_015245.3(ANKS1A):c.289G>C (p.Glu97Gln)not specified [RCV005369741]uncertain significance63497002034970020Humanname
15174611CV710468single nucleotide variantNM_015245.3(ANKS1A):c.1890C>T (p.Leu630=)not provided [RCV000972753]benign63501793935017939Humanname
15195708CV722008single nucleotide variantNM_015245.3(ANKS1A):c.2835T>C (p.Asn945=)not provided [RCV000889579]benign63508281635082816Humanname
156375062CV2204995single nucleotide variantNM_015245.3(ANKS1A):c.952A>C (p.Thr318Pro)not specified [RCV004077613]uncertain significance63498336534983365Humanname
156224095CV2219276single nucleotide variantNM_015245.3(ANKS1A):c.700C>A (p.Leu234Ile)not specified [RCV004095153]uncertain significance63498195434981954Humanname
401748446CV2704296single nucleotide variantNM_015245.3(ANKS1A):c.545T>G (p.Phe182Cys)not specified [RCV004311283]uncertain significance63498179934981799Humanname
401860334CV2762399single nucleotide variantNM_015245.3(ANKS1A):c.343T>C (p.Tyr115His)not specified [RCV004335505]uncertain significance63497007434970074Humanname
401920606CV2822977single nucleotide variantNM_015245.3(ANKS1A):c.3267G>A (p.Pro1089=)not provided [RCV003431820]|not specified [RCV005363114]likely benign63508590035085900Humanname
405260874CV3185955single nucleotide variantNM_015245.3(ANKS1A):c.3225C>T (p.Gly1075=)not provided [RCV003885031]likely benign63508585835085858Humanname
405684085CV3282368single nucleotide variantNM_015245.3(ANKS1A):c.600G>A (p.Met200Ile)not specified [RCV004422347]uncertain significance63498185434981854Humanname
405684091CV3282369single nucleotide variantNM_015245.3(ANKS1A):c.739A>G (p.Met247Val)not specified [RCV004422348]uncertain significance63498275834982758Humanname
407505264CV3447687single nucleotide variantNM_015245.3(ANKS1A):c.437A>G (p.Asn146Ser)not specified [RCV004646061]uncertain significance63498169134981691Humanname
407505298CV3447718single nucleotide variantNM_015245.3(ANKS1A):c.347C>G (p.Pro116Arg)not specified [RCV004646071]uncertain significance63497007834970078Humanname
597651434CV3561341single nucleotide variantNM_015245.3(ANKS1A):c.891A>C (p.Gln297His)not specified [RCV004833664]uncertain significance63498319534983195Humanname
597639423CV3561380single nucleotide variantNM_015245.3(ANKS1A):c.857C>T (p.Thr286Ile)not specified [RCV004825112]uncertain significance63498316134983161Humanname
597651570CV3561451single nucleotide variantNM_015245.3(ANKS1A):c.302G>A (p.Arg101Lys)not specified [RCV004833726]uncertain significance63497003334970033Humanname
597639822CV3561472single nucleotide variantNM_015245.3(ANKS1A):c.865G>A (p.Glu289Lys)not specified [RCV004825136]uncertain significance63498316934983169Humanname
598168499CV3982531single nucleotide variantNM_015245.3(ANKS1A):c.388C>T (p.Arg130Trp)not specified [RCV005369715]uncertain significance63497011934970119Humanname
598201697CV3982550single nucleotide variantNM_015245.3(ANKS1A):c.959C>A (p.Pro320Gln)not specified [RCV005376087]uncertain significance63498337234983372Humanname
15110554CV722009single nucleotide variantNM_015245.3(ANKS1A):c.3285C>T (p.Val1095=)not provided [RCV000894090]benign63508591835085918Humanname
8632027CV87233single nucleotide variantNM_015245.2(ANKS1A):c.688G>A (p.Val230Met)Malignant melanoma [RCV000067324]not provided63498194234981942Humanname
156027673CV2195538single nucleotide variantNM_015245.3(ANKS1A):c.1433G>A (p.Arg478Gln)not specified [RCV004082753]uncertain significance63501748235017482Humanname
156263181CV2201144single nucleotide variantNM_015245.3(ANKS1A):c.1982C>T (p.Ser661Leu)not specified [RCV004077302]uncertain significance63501803135018031Humanname
156373725CV2201356single nucleotide variantNM_015245.3(ANKS1A):c.2062C>T (p.Arg688Trp)not specified [RCV004077481]uncertain significance63505415035054150Humanname
156381918CV2212471single nucleotide variantNM_015245.3(ANKS1A):c.2266G>T (p.Ala756Ser)not specified [RCV004091365]uncertain significance63507863935078639Humanname
156249476CV2215559single nucleotide variantNM_015245.3(ANKS1A):c.1567G>A (p.Ala523Thr)not specified [RCV004089330]likely benign63501761635017616Humanname
156380019CV2218024single nucleotide variantNM_015245.3(ANKS1A):c.1567G>C (p.Ala523Pro)not specified [RCV004086466]likely benign63501761635017616Humanname
156028155CV2238203single nucleotide variantNM_015245.3(ANKS1A):c.2216G>A (p.Arg739Gln)not specified [RCV004113295]uncertain significance63507858935078589Humanname
156297370CV2240849single nucleotide variantNM_015245.3(ANKS1A):c.2495G>A (p.Arg832Lys)not specified [RCV004102138]uncertain significance63507987935079879Humanname
156081799CV2244351single nucleotide variantNM_015245.3(ANKS1A):c.1432C>T (p.Arg478Trp)not specified [RCV004100335]uncertain significance63501748135017481Humanname
155919764CV2254924single nucleotide variantNM_015245.3(ANKS1A):c.2189C>G (p.Ser730Cys)not specified [RCV004117163]uncertain significance63507856235078562Humanname
156339271CV2271392single nucleotide variantNM_015245.3(ANKS1A):c.1948A>T (p.Asn650Tyr)not specified [RCV004136502]uncertain significance63501799735017997Humanname
156251776CV2273434single nucleotide variantNM_015245.3(ANKS1A):c.2980G>A (p.Asp994Asn)not specified [RCV004132191]uncertain significance63508348935083489Humanname
156068086CV2280608single nucleotide variantNM_015245.3(ANKS1A):c.2890G>A (p.Ala964Thr)not specified [RCV004143085]uncertain significance63508320935083209Humanname
156257539CV2322073single nucleotide variantNM_015245.3(ANKS1A):c.2170G>A (p.Asp724Asn)not specified [RCV004173816]uncertain significance63506023935060239Humanname
156255451CV2325750single nucleotide variantNM_015245.3(ANKS1A):c.2123T>C (p.Ile708Thr)not specified [RCV004173643]uncertain significance63506019235060192Humanname
155919055CV2333124single nucleotide variantNM_015245.3(ANKS1A):c.2773G>T (p.Val925Leu)not specified [RCV004194417]uncertain significance63508275435082754Humanname
156197475CV2334279single nucleotide variantNM_015245.3(ANKS1A):c.1695A>C (p.Arg565Ser)not specified [RCV004188262]uncertain significance63501774435017744Humanname
156230628CV2348695single nucleotide variantNM_015245.3(ANKS1A):c.1814G>A (p.Ser605Asn)not specified [RCV004201108]uncertain significance63501786335017863Humanname
155925913CV2365665single nucleotide variantNM_015245.3(ANKS1A):c.1579C>T (p.His527Tyr)not specified [RCV004214219]uncertain significance63501762835017628Humanname
155906561CV2379063single nucleotide variantNM_015245.3(ANKS1A):c.1219C>T (p.Pro407Ser)not specified [RCV004233820]uncertain significance63498923334989233Humanname
156046589CV2382295single nucleotide variantNM_015245.3(ANKS1A):c.2063G>A (p.Arg688Gln)not specified [RCV004230645]likely benign63505415135054151Humanname
155902839CV2386349single nucleotide variantNM_015245.3(ANKS1A):c.1463C>T (p.Ala488Val)not specified [RCV004228684]uncertain significance63501751235017512Humanname
329354502CV2448304single nucleotide variantNM_015245.3(ANKS1A):c.2741G>A (p.Arg914Gln)not specified [RCV004256594]uncertain significance63508272235082722Humanname
329391772CV2453116single nucleotide variantNM_015245.3(ANKS1A):c.1798C>T (p.Arg600Trp)not specified [RCV004279507]uncertain significance63501784735017847Humanname
329395586CV2454374single nucleotide variantNM_015245.3(ANKS1A):c.1135G>A (p.Gly379Arg)not specified [RCV004267893]uncertain significance63498520434985204Humanname
329363870CV2460244single nucleotide variantNM_015245.3(ANKS1A):c.1001A>G (p.Gln334Arg)not specified [RCV004266802]uncertain significance63498341434983414Humanname
401720902CV2702182single nucleotide variantNM_015245.3(ANKS1A):c.2758G>A (p.Ala920Thr)not specified [RCV004314532]uncertain significance63508273935082739Humanname
401777263CV2707837single nucleotide variantNM_015245.3(ANKS1A):c.2215C>T (p.Arg739Trp)not specified [RCV004309120]uncertain significance63507858835078588Humanname
401757626CV2707883single nucleotide variantNM_015245.3(ANKS1A):c.2097G>C (p.Gln699His)not specified [RCV004309159]uncertain significance63506016635060166Humanname
401763418CV2720314single nucleotide variantNM_015245.3(ANKS1A):c.2005G>A (p.Asp669Asn)not specified [RCV004325638]uncertain significance63501805435018054Humanname
401780675CV2727506single nucleotide variantNM_015245.3(ANKS1A):c.1531G>A (p.Glu511Lys)not specified [RCV004329703]uncertain significance63501758035017580Humanname
401900047CV2780253single nucleotide variantNM_015245.3(ANKS1A):c.1379C>G (p.Thr460Arg)not specified [RCV004355886]uncertain significance63499437834994378Humanname
405684347CV3282348single nucleotide variantNM_015245.3(ANKS1A):c.1514G>A (p.Gly505Asp)not specified [RCV004422327]uncertain significance63501756335017563Humanname
405684216CV3282349single nucleotide variantNM_015245.3(ANKS1A):c.1588G>A (p.Gly530Arg)not specified [RCV004422328]uncertain significance63501763735017637Humanname
405684095CV3282350single nucleotide variantNM_015245.3(ANKS1A):c.1613A>C (p.His538Pro)not specified [RCV004422329]uncertain significance63501766235017662Humanname
405684002CV3282351single nucleotide variantNM_015245.3(ANKS1A):c.1661C>A (p.Ala554Asp)not specified [RCV004422330]uncertain significance63501771035017710Humanname
405684007CV3282352single nucleotide variantNM_015245.3(ANKS1A):c.1769C>T (p.Pro590Leu)not specified [RCV004422331]uncertain significance63501781835017818Humanname
405684011CV3282353single nucleotide variantNM_015245.3(ANKS1A):c.1795G>A (p.Asp599Asn)not specified [RCV004422332]uncertain significance63501784435017844Humanname
405684020CV3282355single nucleotide variantNM_015245.3(ANKS1A):c.1828A>G (p.Thr610Ala)not specified [RCV004422334]uncertain significance63501787735017877Humanname
405684027CV3282356single nucleotide variantNM_015245.3(ANKS1A):c.2083C>T (p.Arg695Trp)not specified [RCV004422335]uncertain significance63506015235060152Humanname
405684032CV3282357single nucleotide variantNM_015245.3(ANKS1A):c.2116G>A (p.Glu706Lys)not specified [RCV004422336]uncertain significance63506018535060185Humanname
405684039CV3282359single nucleotide variantNM_015245.3(ANKS1A):c.2270G>A (p.Arg757His)not specified [RCV004422338]uncertain significance63507864335078643Humanname
405684045CV3282360single nucleotide variantNM_015245.3(ANKS1A):c.2438T>G (p.Val813Gly)not specified [RCV004422339]uncertain significance63507982235079822Humanname
405684050CV3282361single nucleotide variantNM_015245.3(ANKS1A):c.2509C>G (p.Pro837Ala)not specified [RCV004422340]uncertain significance63507989335079893Humanname
405684056CV3282362single nucleotide variantNM_015245.3(ANKS1A):c.2567C>T (p.Thr856Met)not specified [RCV004422341]uncertain significance63508101635081016Humanname
405684063CV3282364single nucleotide variantNM_015245.3(ANKS1A):c.2867G>A (p.Arg956Gln)not specified [RCV004422343]uncertain significance63508318635083186Humanname
405684068CV3282365single nucleotide variantNM_015245.3(ANKS1A):c.2946C>G (p.Ile982Met)not specified [RCV004422344]uncertain significance63508345535083455Humanname
407505208CV3447658single nucleotide variantNM_015245.3(ANKS1A):c.2696G>A (p.Arg899His)not specified [RCV004646044]uncertain significance63508114535081145Humanname
407505215CV3447662single nucleotide variantNM_015245.3(ANKS1A):c.2812G>A (p.Glu938Lys)not specified [RCV004646047]uncertain significance63508279335082793Humanname
407505219CV3447667single nucleotide variantNM_015245.3(ANKS1A):c.1387A>G (p.Thr463Ala)not specified [RCV004646048]uncertain significance63499438634994386Humanname
407520276CV3447676single nucleotide variantNM_015245.3(ANKS1A):c.1328A>G (p.His443Arg)not specified [RCV004652135]uncertain significance63499432734994327Humanname
407520304CV3447698single nucleotide variantNM_015245.3(ANKS1A):c.1073A>C (p.Glu358Ala)not specified [RCV004652147]uncertain significance63498514234985142Humanname
407505283CV3447708single nucleotide variantNM_015245.3(ANKS1A):c.2773G>C (p.Val925Leu)not specified [RCV004646067]uncertain significance63508275435082754Humanname
597650838CV3561345single nucleotide variantNM_015245.3(ANKS1A):c.1526T>C (p.Val509Ala)not specified [RCV004833665]uncertain significance63501757535017575Humanname
597639369CV3561353single nucleotide variantNM_015245.3(ANKS1A):c.2104G>A (p.Gly702Arg)not specified [RCV004825102]uncertain significance63506017335060173Humanname
597651051CV3561390single nucleotide variantNM_015245.3(ANKS1A):c.1291A>C (p.Thr431Pro)not specified [RCV004833689]uncertain significance63498930534989305Humanname
597651163CV3561408single nucleotide variantNM_015245.3(ANKS1A):c.1997C>T (p.Ser666Leu)not specified [RCV004833703]uncertain significance63501804635018046Humanname
597639896CV3561428single nucleotide variantNM_015245.3(ANKS1A):c.1192C>T (p.Pro398Ser)not specified [RCV004825124]uncertain significance63498526134985261Humanname
597651469CV3561436single nucleotide variantNM_015245.3(ANKS1A):c.1139G>A (p.Arg380Gln)not specified [RCV004833714]uncertain significance63498520834985208Humanname
597651523CV3561443single nucleotide variantNM_015245.3(ANKS1A):c.2704A>G (p.Ile902Val)not specified [RCV004833720]uncertain significance63508115335081153Humanname
597639843CV3561461single nucleotide variantNM_015245.3(ANKS1A):c.1343G>A (p.Arg448Gln)not specified [RCV004825132]likely benign63499434234994342Humanname
597639807CV3561481single nucleotide variantNM_015245.3(ANKS1A):c.2245C>T (p.Arg749Trp)not specified [RCV004825139]uncertain significance63507861835078618Humanname
598201612CV3982495single nucleotide variantNM_015245.3(ANKS1A):c.1477G>A (p.Gly493Arg)not specified [RCV005376066]uncertain significance63501752635017526Humanname
598201616CV3982504single nucleotide variantNM_015245.3(ANKS1A):c.2600C>T (p.Thr867Ile)not specified [RCV005376067]uncertain significance63508104935081049Humanname
598201624CV3982514single nucleotide variantNM_015245.3(ANKS1A):c.2606G>A (p.Arg869Gln)not specified [RCV005376069]uncertain significance63508105535081055Humanname
598201643CV3982523single nucleotide variantNM_015245.3(ANKS1A):c.1817G>A (p.Arg606Gln)not specified [RCV005376074]uncertain significance63501786635017866Humanname
598201738CV3982562single nucleotide variantNM_015245.3(ANKS1A):c.1612C>A (p.His538Asn)not specified [RCV005376096]uncertain significance63501766135017661Humanname
598168598CV3982570single nucleotide variantNM_015245.3(ANKS1A):c.1915G>A (p.Ala639Thr)not specified [RCV005369732]likely benign63501796435017964Humanname
598168667CV3982598single nucleotide variantNM_015245.3(ANKS1A):c.1313T>C (p.Met438Thr)not specified [RCV005369745]uncertain significance63499431234994312Humanname
598168700CV3982608single nucleotide variantNM_015245.3(ANKS1A):c.1958T>C (p.Ile653Thr)not specified [RCV005369751]uncertain significance63501800735018007Humanname
15157722CV699558single nucleotide variantNM_015245.3(ANKS1A):c.1417A>G (p.Thr473Ala)not provided [RCV000946937]benign63499441634994416Humanname
15123025CV710467single nucleotide variantNM_015245.3(ANKS1A):c.1732C>G (p.Arg578Gly)not provided [RCV000963170]benign63501778135017781Humanname
156384965CV2231238single nucleotide variantNM_015245.3(ANKS1A):c.3201G>C (p.Gln1067His)not specified [RCV004094437]uncertain significance63508583435085834Humanname
156155252CV2266128single nucleotide variantNM_015245.3(ANKS1A):c.3301G>A (p.Ala1101Thr)not specified [RCV004128717]uncertain significance63508593435085934Humanname
156149215CV2307396single nucleotide variantNM_015245.3(ANKS1A):c.3090G>T (p.Gln1030His)not specified [RCV004166076]uncertain significance63508421635084216Humanname
156336189CV2333638single nucleotide variantNM_015245.3(ANKS1A):c.3124G>A (p.Val1042Met)not specified [RCV004192479]uncertain significance63508425035084250Humanname
155924972CV2348259single nucleotide variantNM_015245.3(ANKS1A):c.3226G>A (p.Ala1076Thr)not specified [RCV004191297]uncertain significance63508585935085859Humanname
156269071CV2372155single nucleotide variantNM_015245.3(ANKS1A):c.3020G>A (p.Arg1007Gln)not specified [RCV004223677]uncertain significance63508414635084146Humanname
155952759CV2393830single nucleotide variantNM_015245.3(ANKS1A):c.3266C>G (p.Pro1089Arg)not specified [RCV004233658]uncertain significance63508589935085899Humanname
405684081CV3282367single nucleotide variantNM_015245.3(ANKS1A):c.3320T>C (p.Met1107Thr)not specified [RCV004422346]likely benign63508696835086968Humanname
597651443CV3561362single nucleotide variantNM_015245.3(ANKS1A):c.3047C>T (p.Pro1016Leu)not specified [RCV004833671]uncertain significance63508417335084173Humanname
598168627CV3982581single nucleotide variantNM_015245.3(ANKS1A):c.3112G>A (p.Val1038Met)not specified [RCV005369737]uncertain significance63508423835084238Humanname