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Variants search result for Homo sapiens
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97 records found for search term Bcan
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
597759929CV3643013single nucleotide variantNM_021948.5(BCAN):c.19C>T (p.Pro7Ser)not specified [RCV004894655]uncertain significance1156646073156646073Humanname
8574921CV109260single nucleotide variantNM_021948.4(BCAN):c.945C>T (p.Ile315=)Lung cancer [RCV000089785]uncertain significance1156648743156648743Humanname
405706307CV3301698single nucleotide variantNM_021948.5(BCAN):c.71T>C (p.Val24Ala)not specified [RCV004426125]likely benign1156646125156646125Humanname
407500289CV3417604single nucleotide variantNM_021948.5(BCAN):c.97C>A (p.Arg33Ser)not specified [RCV004606998]uncertain significance1156646806156646806Humanname
598262773CV3949037single nucleotide variantNM_021948.5(BCAN):c.696C>T (p.Pro232=)not specified [RCV005300860]likely benign1156648037156648037Humanname
156150823CV2197801single nucleotide variantNM_021948.5(BCAN):c.290G>A (p.Arg97His)not specified [RCV004077041]uncertain significance1156646999156646999Humanname
156283674CV2360597single nucleotide variantNM_021948.5(BCAN):c.256C>T (p.Arg86Trp)not specified [RCV004211354]uncertain significance1156646965156646965Humanname
401728738CV2693774single nucleotide variantNM_021948.5(BCAN):c.284G>A (p.Gly95Glu)not specified [RCV004298096]uncertain significance1156646993156646993Humanname
401933082CV2806067single nucleotide variantNM_021948.5(BCAN):c.1377T>C (p.Tyr459=)not provided [RCV003409153]likely benign1156652327156652327Humanname
401933083CV2806068single nucleotide variantNM_021948.5(BCAN):c.1545G>A (p.Leu515=)not provided [RCV003409154]likely benign1156652495156652495Humanname
598185580CV3949069single nucleotide variantNM_021948.5(BCAN):c.106C>T (p.Arg36Cys)not specified [RCV005311729]uncertain significance1156646815156646815Humanname
15185691CV731773single nucleotide variantNM_021948.5(BCAN):c.1953C>T (p.Val651=)not provided [RCV000908598]benign1156656292156656292Humanname
8628980CV84123single nucleotide variantNM_021948.4(BCAN):c.2568C>T (p.Ile856=)Malignant melanoma [RCV000064204]not provided1156658673156658673Humanname
156315876CV2250833single nucleotide variantNM_021948.5(BCAN):c.410G>T (p.Cys137Phe)not specified [RCV004129691]uncertain significance1156647119156647119Humanname
156208904CV2370048single nucleotide variantNM_021948.5(BCAN):c.500G>A (p.Arg167His)not specified [RCV004210944]uncertain significance1156647541156647541Humanname
401755471CV2732872single nucleotide variantNM_021948.5(BCAN):c.725C>T (p.Pro242Leu)not specified [RCV004332625]uncertain significance1156648066156648066Humanname
405706271CV3301693single nucleotide variantNM_021948.5(BCAN):c.304G>C (p.Glu102Gln)not specified [RCV004426120]uncertain significance1156647013156647013Humanname
405706279CV3301694single nucleotide variantNM_021948.5(BCAN):c.385C>T (p.Pro129Ser)not specified [RCV004426121]uncertain significance1156647094156647094Humanname
405706287CV3301695single nucleotide variantNM_021948.5(BCAN):c.424G>A (p.Gly142Ser)not specified [RCV004426122]uncertain significance1156647133156647133Humanname
405706295CV3301696single nucleotide variantNM_021948.5(BCAN):c.497C>T (p.Ala166Val)not specified [RCV004426123]uncertain significance1156647538156647538Humanname
405706301CV3301697single nucleotide variantNM_021948.5(BCAN):c.505G>A (p.Ala169Thr)not specified [RCV004426124]uncertain significance1156647546156647546Humanname
407495220CV3417599single nucleotide variantNM_021948.5(BCAN):c.390C>A (p.Asn130Lys)not specified [RCV004605774]uncertain significance1156647099156647099Humanname
597759925CV3643012single nucleotide variantNM_021948.5(BCAN):c.541C>G (p.Arg181Gly)not specified [RCV004894654]uncertain significance1156647582156647582Humanname
597759947CV3643017single nucleotide variantNM_021948.5(BCAN):c.676G>A (p.Gly226Arg)not specified [RCV004894660]uncertain significance1156648017156648017Humanname
12896563CV389328single nucleotide variantNM_021948.5(BCAN):c.313C>G (p.Arg105Gly)not provided [RCV004713975]|not specified [RCV000455522]benign1156647022156647022Humanname
598262751CV3949027single nucleotide variantNM_021948.5(BCAN):c.900C>G (p.His300Gln)not specified [RCV005300856]uncertain significance1156648698156648698Humanname
598185634CV3949089single nucleotide variantNM_021948.5(BCAN):c.673T>C (p.Tyr225His)not specified [RCV005311738]uncertain significance1156648014156648014Humanname
156290406CV2226171single nucleotide variantNM_021948.5(BCAN):c.1711G>A (p.Gly571Ser)not specified [RCV004105573]uncertain significance1156652661156652661Humanname
156340493CV2229501single nucleotide variantNM_021948.5(BCAN):c.2179A>C (p.Ser727Arg)not specified [RCV004101258]uncertain significance1156657066156657066Humanname
155975318CV2231306single nucleotide variantNM_021948.5(BCAN):c.2498G>A (p.Arg833His)not specified [RCV004096411]uncertain significance1156658603156658603Humanname
156190786CV2255187single nucleotide variantNM_021948.5(BCAN):c.1778C>T (p.Ser593Phe)not specified [RCV004115801]uncertain significance1156652728156652728Humanname
156002304CV2257944single nucleotide variantNM_021948.5(BCAN):c.1796G>A (p.Arg599Gln)not specified [RCV004129759]uncertain significance1156652746156652746Humanname
155969364CV2262105single nucleotide variantNM_021948.5(BCAN):c.2245G>A (p.Asp749Asn)not specified [RCV004126568]uncertain significance1156657710156657710Humanname
156252848CV2283996single nucleotide variantNM_021948.5(BCAN):c.2578G>A (p.Glu860Lys)not specified [RCV004144613]uncertain significance1156658683156658683Humanname
155910208CV2303545single nucleotide variantNM_021948.5(BCAN):c.1070C>T (p.Ala357Val)not specified [RCV004161640]uncertain significance1156651462156651462Humanname
156052229CV2320286single nucleotide variantNM_021948.5(BCAN):c.1151C>G (p.Thr384Arg)not specified [RCV004178454]uncertain significance1156651543156651543Humanname
156221600CV2343864single nucleotide variantNM_021948.5(BCAN):c.1765G>A (p.Glu589Lys)not specified [RCV004193447]uncertain significance1156652715156652715Humanname
156215875CV2347919single nucleotide variantNM_021948.5(BCAN):c.2360T>C (p.Met787Thr)not specified [RCV004197612]uncertain significance1156658194156658194Humanname
156224123CV2355633single nucleotide variantNM_021948.5(BCAN):c.2687G>A (p.Arg896His)not specified [RCV004205471]likely benign1156659085156659085Humanname
156161916CV2371572single nucleotide variantNM_021948.5(BCAN):c.1456C>T (p.Leu486Phe)not specified [RCV004216820]likely benign1156652406156652406Humanname
156387033CV2372612single nucleotide variantNM_021948.5(BCAN):c.1204C>T (p.Arg402Cys)not specified [RCV004221817]uncertain significance1156651596156651596Humanname
155991654CV2379223single nucleotide variantNM_021948.5(BCAN):c.1753A>G (p.Thr585Ala)not specified [RCV004223704]uncertain significance1156652703156652703Humanname
156043642CV2381563single nucleotide variantNM_021948.5(BCAN):c.2248A>G (p.Arg750Gly)not specified [RCV004230033]uncertain significance1156657713156657713Humanname
156133358CV2382935single nucleotide variantNM_021948.5(BCAN):c.1466C>T (p.Pro489Leu)not specified [RCV004217528]likely benign1156652416156652416Humanname
329383724CV2434858single nucleotide variantNM_021948.5(BCAN):c.2456C>T (p.Pro819Leu)not specified [RCV004250735]uncertain significance1156658561156658561Humanname
329391454CV2452354single nucleotide variantNM_021948.5(BCAN):c.1732C>T (p.Pro578Ser)not specified [RCV004272681]uncertain significance1156652682156652682Humanname
401757530CV2675359single nucleotide variantNM_021948.5(BCAN):c.1771G>A (p.Ala591Thr)not specified [RCV004292167]uncertain significance1156652721156652721Humanname
401730304CV2680092single nucleotide variantNM_021948.5(BCAN):c.1205G>A (p.Arg402His)not specified [RCV004286583]uncertain significance1156651597156651597Humanname
401760890CV2695199single nucleotide variantNM_021948.5(BCAN):c.1697G>A (p.Gly566Glu)not specified [RCV004303340]uncertain significance1156652647156652647Humanname
401771334CV2722793single nucleotide variantNM_021948.5(BCAN):c.1795C>T (p.Arg599Trp)not specified [RCV004325217]uncertain significance1156652745156652745Humanname
401885272CV2768036single nucleotide variantNM_021948.5(BCAN):c.2594A>G (p.Glu865Gly)not specified [RCV004348278]uncertain significance1156658699156658699Humanname
401867687CV2780788single nucleotide variantNM_021948.5(BCAN):c.1123G>C (p.Asp375His)not specified [RCV004352110]uncertain significance1156651515156651515Humanname
401879277CV2791337single nucleotide variantNM_021948.5(BCAN):c.2489C>G (p.Pro830Arg)not specified [RCV004356956]uncertain significance1156658594156658594Humanname
401879372CV2791506single nucleotide variantNM_021948.5(BCAN):c.1463G>C (p.Ser488Thr)not specified [RCV004358888]uncertain significance1156652413156652413Humanname
405706145CV3301675single nucleotide variantNM_021948.5(BCAN):c.1081G>A (p.Ala361Thr)not specified [RCV004426102]uncertain significance1156651473156651473Humanname
405706154CV3301676single nucleotide variantNM_021948.5(BCAN):c.1123G>A (p.Asp375Asn)not specified [RCV004426103]uncertain significance1156651515156651515Humanname
405706161CV3301677single nucleotide variantNM_021948.5(BCAN):c.1253G>A (p.Ser418Asn)not specified [RCV004426104]uncertain significance1156651645156651645Humanname
405706168CV3301678single nucleotide variantNM_021948.5(BCAN):c.1258A>G (p.Thr420Ala)not specified [RCV004426105]uncertain significance1156651650156651650Humanname
405706175CV3301679single nucleotide variantNM_021948.5(BCAN):c.1453G>A (p.Glu485Lys)not specified [RCV004426106]uncertain significance1156652403156652403Humanname
405706182CV3301680single nucleotide variantNM_021948.5(BCAN):c.1490C>G (p.Thr497Ser)not specified [RCV004426107]uncertain significance1156652440156652440Humanname
405706199CV3301682single nucleotide variantNM_021948.5(BCAN):c.1927G>A (p.Val643Met)not specified [RCV004426109]uncertain significance1156652877156652877Humanname
405706205CV3301683single nucleotide variantNM_021948.5(BCAN):c.2005C>T (p.Arg669Cys)not specified [RCV004426110]uncertain significance1156656344156656344Humanname
405706213CV3301684single nucleotide variantNM_021948.5(BCAN):c.2006G>A (p.Arg669His)not specified [RCV004426111]uncertain significance1156656345156656345Humanname
405706219CV3301685single nucleotide variantNM_021948.5(BCAN):c.2035G>C (p.Asp679His)not specified [RCV004426112]uncertain significance1156656374156656374Humanname
405706231CV3301687single nucleotide variantNM_021948.5(BCAN):c.2450C>T (p.Pro817Leu)not specified [RCV004426114]uncertain significance1156658555156658555Humanname
405706239CV3301688single nucleotide variantNM_021948.5(BCAN):c.2482G>A (p.Gly828Ser)not specified [RCV004426115]uncertain significance1156658587156658587Humanname
405706244CV3301689single nucleotide variantNM_021948.5(BCAN):c.2515G>C (p.Val839Leu)not specified [RCV004426116]uncertain significance1156658620156658620Humanname
405706258CV3301691single nucleotide variantNM_021948.5(BCAN):c.2627C>G (p.Pro876Arg)not specified [RCV004426118]uncertain significance1156658732156658732Humanname
405706264CV3301692single nucleotide variantNM_021948.5(BCAN):c.2643C>A (p.His881Gln)not specified [RCV004426119]uncertain significance1156659041156659041Humanname
407495211CV3417597single nucleotide variantNM_021948.5(BCAN):c.1733C>G (p.Pro578Arg)not specified [RCV004605772]uncertain significance1156652683156652683Humanname
407495216CV3417598single nucleotide variantNM_021948.5(BCAN):c.1096T>G (p.Ser366Ala)not specified [RCV004605773]uncertain significance1156651488156651488Humanname
407500293CV3417600single nucleotide variantNM_021948.5(BCAN):c.1885C>A (p.Pro629Thr)not specified [RCV004606997]uncertain significance1156652835156652835Humanname
407495225CV3417601single nucleotide variantNM_021948.5(BCAN):c.2371G>A (p.Asp791Asn)not specified [RCV004605775]uncertain significance1156658205156658205Humanname
407495230CV3417602single nucleotide variantNM_021948.5(BCAN):c.1418A>T (p.Glu473Val)not specified [RCV004605776]uncertain significance1156652368156652368Humanname
407495233CV3417603single nucleotide variantNM_021948.5(BCAN):c.1873G>T (p.Val625Leu)not specified [RCV004605777]uncertain significance1156652823156652823Humanname
597759914CV3643009single nucleotide variantNM_021948.5(BCAN):c.2584G>A (p.Gly862Ser)not specified [RCV004894652]uncertain significance1156658689156658689Humanname
597759919CV3643010single nucleotide variantNM_021948.5(BCAN):c.1289C>T (p.Thr430Met)not specified [RCV004894653]uncertain significance1156651681156651681Humanname
597759933CV3643014single nucleotide variantNM_021948.5(BCAN):c.1847G>A (p.Gly616Glu)not specified [RCV004894657]uncertain significance1156652797156652797Humanname
597759938CV3643015single nucleotide variantNM_021948.5(BCAN):c.1117G>T (p.Ala373Ser)not specified [RCV004894658]uncertain significance1156651509156651509Humanname
597759942CV3643016single nucleotide variantNM_021948.5(BCAN):c.2068C>T (p.Pro690Ser)not specified [RCV004894659]uncertain significance1156656955156656955Humanname
597759951CV3643018single nucleotide variantNM_021948.5(BCAN):c.1825G>A (p.Ala609Thr)not specified [RCV004894661]uncertain significance1156652775156652775Humanname
597759956CV3643019single nucleotide variantNM_021948.5(BCAN):c.2284G>A (p.Val762Ile)not specified [RCV004894662]uncertain significance1156657749156657749Humanname
598262600CV3948979single nucleotide variantNM_021948.5(BCAN):c.1353G>C (p.Lys451Asn)not specified [RCV005300823]uncertain significance1156652303156652303Humanname
598185409CV3948989single nucleotide variantNM_021948.5(BCAN):c.2092G>A (p.Ala698Thr)not specified [RCV005311702]uncertain significance1156656979156656979Humanname
598262647CV3948998single nucleotide variantNM_021948.5(BCAN):c.2131G>A (p.Glu711Lys)not specified [RCV005300834]uncertain significance1156657018156657018Humanname
598185450CV3949008single nucleotide variantNM_021948.5(BCAN):c.2588G>A (p.Arg863His)not specified [RCV005311709]uncertain significance1156658693156658693Humanname
598262708CV3949017single nucleotide variantNM_021948.5(BCAN):c.1936G>C (p.Ala646Pro)not specified [RCV005300847]uncertain significance1156652886156652886Humanname
598262819CV3949048single nucleotide variantNM_021948.5(BCAN):c.2653G>C (p.Asp885His)not specified [RCV005300869]uncertain significance1156659051156659051Humanname
598262845CV3949058single nucleotide variantNM_021948.5(BCAN):c.1573G>A (p.Gly525Arg)not specified [RCV005300874]uncertain significance1156652523156652523Humanname
598185597CV3949080single nucleotide variantNM_021948.5(BCAN):c.2176A>G (p.Ile726Val)not specified [RCV005311732]uncertain significance1156657063156657063Humanname
598262954CV3949099single nucleotide variantNM_021948.5(BCAN):c.2392G>A (p.Val798Met)not specified [RCV005300900]uncertain significance1156658226156658226Humanname
14696189CV612363single nucleotide variantNM_021948.5(BCAN):c.2518C>T (p.Leu840Phe)High myopia [RCV000785737]|not specified [RCV004027187]uncertain significance1156658623156658623Human2name
15098167CV696161single nucleotide variantNM_021948.5(BCAN):c.1783C>A (p.Leu595Ile)not provided [RCV000958493]benign1156652733156652733Humanname
15160109CV706735single nucleotide variantNM_021948.5(BCAN):c.2117G>T (p.Arg706Leu)not provided [RCV000969836]likely benign1156657004156657004Human1name
15160109CV706735single nucleotide variantNM_021948.5(BCAN):c.2117G>T (p.Arg706Leu)not provided [RCV000969836]likely benign1156657004156657005Human1name
15114119CV731774single nucleotide variantNM_021948.5(BCAN):c.2695G>A (p.Ala899Thr)not provided [RCV000894795]likely benign1156659093156659093Humanname
8628981CV84124single nucleotide variantNM_021948.5(BCAN):c.2714C>T (p.Ser905Phe)not specified [RCV004894656]uncertain significance|not provided1156659112156659112Humanname