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Variants search result for Homo sapiens
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66 records found for search term Tysnd1
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
156294733CV2293236single nucleotide variantNM_173555.4(TYSND1):c.40C>G (p.Gln14Glu)not specified [RCV004150739]uncertain significance107014654770146547Humanname
329392692CV2471504single nucleotide variantNM_173555.4(TYSND1):c.74G>C (p.Gly25Ala)not specified [RCV004280496]uncertain significance107014651370146513Humanname
401938369CV2813242single nucleotide variantNM_173555.4(TYSND1):c.642C>T (p.Pro214=)not provided [RCV003417465]likely benign107014594570145945Humanname
405813982CV3344998single nucleotide variantNM_173555.4(TYSND1):c.263C>T (p.Ala88Val)not specified [RCV004484131]uncertain significance107014632470146324Humanname
156118434CV2209258single nucleotide variantNM_173555.4(TYSND1):c.958C>G (p.Leu320Val)not specified [RCV004093444]uncertain significance107014562970145629Humanname
156119017CV2228802single nucleotide variantNM_173555.4(TYSND1):c.464C>T (p.Ala155Val)not specified [RCV004095049]uncertain significance107014612370146123Humanname
155990019CV2276412single nucleotide variantNM_173555.4(TYSND1):c.338T>G (p.Leu113Arg)not specified [RCV004144140]uncertain significance107014624970146249Humanname
155919118CV2279359single nucleotide variantNM_173555.4(TYSND1):c.322C>T (p.Pro108Ser)not specified [RCV004139873]uncertain significance107014626570146265Humanname
155922489CV2284369single nucleotide variantNM_173555.4(TYSND1):c.397G>A (p.Glu133Lys)not specified [RCV004146711]uncertain significance107014619070146190Humanname
156255637CV2307730single nucleotide variantNM_173555.4(TYSND1):c.974C>T (p.Pro325Leu)not specified [RCV004168424]uncertain significance107014561370145613Humanname
155972527CV2334346single nucleotide variantNM_173555.4(TYSND1):c.526G>A (p.Ala176Thr)not specified [RCV004188324]uncertain significance107014606170146061Humanname
156126459CV2350292single nucleotide variantNM_173555.4(TYSND1):c.996G>T (p.Trp332Cys)not specified [RCV004202246]uncertain significance107014559170145591Humanname
156085779CV2390688single nucleotide variantNM_173555.4(TYSND1):c.764C>T (p.Ala255Val)not specified [RCV004239202]uncertain significance107014582370145823Humanname
329359042CV2450812single nucleotide variantNM_173555.4(TYSND1):c.803C>T (p.Thr268Ile)not specified [RCV004267729]uncertain significance107014578470145784Humanname
401719664CV2701223single nucleotide variantNM_173555.4(TYSND1):c.924C>A (p.Asp308Glu)not specified [RCV004309797]uncertain significance107014566370145663Humanname
401739005CV2708278single nucleotide variantNM_173555.4(TYSND1):c.997G>T (p.Gly333Cys)not specified [RCV004311619]uncertain significance107014559070145590Humanname
401783431CV2723565single nucleotide variantNM_173555.4(TYSND1):c.311G>A (p.Gly104Glu)not specified [RCV004323966]uncertain significance107014627670146276Humanname
405813984CV3344999single nucleotide variantNM_173555.4(TYSND1):c.317G>A (p.Cys106Tyr)not specified [RCV004484132]uncertain significance107014627070146270Humanname
405813986CV3345000single nucleotide variantNM_173555.4(TYSND1):c.320C>A (p.Thr107Lys)not specified [RCV004484133]uncertain significance107014626770146267Humanname
405813988CV3345001single nucleotide variantNM_173555.4(TYSND1):c.356C>G (p.Ala119Gly)not specified [RCV004484134]uncertain significance107014623170146231Humanname
405813990CV3345002single nucleotide variantNM_173555.4(TYSND1):c.632G>T (p.Gly211Val)not specified [RCV004484135]uncertain significance107014595570145955Humanname
405813991CV3345003single nucleotide variantNM_173555.4(TYSND1):c.852T>G (p.Cys284Trp)not specified [RCV004484136]uncertain significance107014573570145735Humanname
407462240CV3490909single nucleotide variantNM_173555.4(TYSND1):c.933C>A (p.His311Gln)not specified [RCV004687897]uncertain significance107014565470145654Humanname
407522403CV3490911single nucleotide variantNM_173555.4(TYSND1):c.947G>A (p.Ser316Asn)not specified [RCV004677673]uncertain significance107014564070145640Humanname
407522405CV3490912single nucleotide variantNM_173555.4(TYSND1):c.398A>G (p.Glu133Gly)not specified [RCV004677674]uncertain significance107014618970146189Humanname
407522408CV3490913single nucleotide variantNM_173555.4(TYSND1):c.556G>A (p.Ala186Thr)not specified [RCV004677675]uncertain significance107014603170146031Humanname
597802854CV3629024single nucleotide variantNM_173555.4(TYSND1):c.928C>T (p.Leu310Phe)not specified [RCV004881448]uncertain significance107014565970145659Humanname
597802860CV3629027single nucleotide variantNM_173555.4(TYSND1):c.683C>T (p.Ala228Val)not specified [RCV004881451]uncertain significance107014590470145904Humanname
597802862CV3629028single nucleotide variantNM_173555.4(TYSND1):c.745C>T (p.Pro249Ser)not specified [RCV004881452]uncertain significance107014584270145842Humanname
597802865CV3629030single nucleotide variantNM_173555.4(TYSND1):c.586G>A (p.Glu196Lys)not specified [RCV004881454]uncertain significance107014600170146001Humanname
598264367CV3932499single nucleotide variantNM_173555.4(TYSND1):c.454G>C (p.Gly152Arg)not specified [RCV005301531]uncertain significance107014613370146133Humanname
598264373CV3932500single nucleotide variantNM_173555.4(TYSND1):c.796G>A (p.Val266Met)not specified [RCV005301532]uncertain significance107014579170145791Humanname
598232418CV3932502single nucleotide variantNM_173555.4(TYSND1):c.794G>C (p.Gly265Ala)not specified [RCV005295402]uncertain significance107014579370145793Humanname
598264387CV3932504single nucleotide variantNM_173555.4(TYSND1):c.959T>C (p.Leu320Pro)not specified [RCV005301535]uncertain significance107014562870145628Humanname
15192061CV701420single nucleotide variantNM_173555.4(TYSND1):c.338T>C (p.Leu113Pro)not provided [RCV000954957]benign107014624970146249Humanname
156153411CV2209440single nucleotide variantNM_173555.4(TYSND1):c.1402G>A (p.Val468Ile)not specified [RCV004093590]uncertain significance107014274970142749Humanname
156252851CV2212485single nucleotide variantNM_173555.4(TYSND1):c.1344C>G (p.Cys448Trp)not specified [RCV004091376]uncertain significance107014280770142807Humanname
155918607CV2236866single nucleotide variantNM_173555.4(TYSND1):c.1271C>T (p.Pro424Leu)not specified [RCV004112623]uncertain significance107014386870143868Humanname
156156486CV2238487single nucleotide variantNM_173555.4(TYSND1):c.1214G>A (p.Cys405Tyr)not specified [RCV004113538]uncertain significance107014392570143925Humanname
156335882CV2273060single nucleotide variantNM_173555.4(TYSND1):c.1511A>G (p.Asn504Ser)not specified [RCV004137710]uncertain significance107014011470140114Humanname
156281308CV2295105single nucleotide variantNM_173555.4(TYSND1):c.1612C>T (p.Leu538Phe)not specified [RCV004156209]uncertain significance107014001370140013Humanname
156101511CV2352181single nucleotide variantNM_173555.4(TYSND1):c.1666C>T (p.Arg556Trp)not specified [RCV004200669]uncertain significance107013995970139959Humanname
156157201CV2363605single nucleotide variantNM_173555.4(TYSND1):c.1616G>A (p.Arg539His)not specified [RCV004216560]uncertain significance107014000970140009Humanname
156216912CV2386100single nucleotide variantNM_173555.4(TYSND1):c.1184G>C (p.Gly395Ala)not specified [RCV004229154]uncertain significance107014395570143955Humanname
329373660CV2447315single nucleotide variantNM_173555.4(TYSND1):c.1433G>C (p.Ser478Thr)not specified [RCV004262600]uncertain significance107014271870142718Humanname
401739742CV2684160single nucleotide variantNM_173555.4(TYSND1):c.1682C>T (p.Ala561Val)not specified [RCV004288833]uncertain significance107013994370139943Humanname
401740348CV2684335single nucleotide variantNM_173555.4(TYSND1):c.1638G>C (p.Glu546Asp)not specified [RCV004288984]uncertain significance107013998770139987Humanname
401779646CV2714660single nucleotide variantNM_173555.4(TYSND1):c.1316T>C (p.Val439Ala)not specified [RCV004320241]uncertain significance107014283570142835Humanname
405813967CV3344990single nucleotide variantNM_173555.4(TYSND1):c.1220A>G (p.Tyr407Cys)not specified [RCV004484123]uncertain significance107014391970143919Humanname
405813969CV3344991single nucleotide variantNM_173555.4(TYSND1):c.1397C>T (p.Thr466Met)not specified [RCV004484124]likely benign107014275470142754Humanname
405813971CV3344992single nucleotide variantNM_173555.4(TYSND1):c.1429C>T (p.His477Tyr)not specified [RCV004484125]uncertain significance107014272270142722Humanname
405813973CV3344993single nucleotide variantNM_173555.4(TYSND1):c.1466A>C (p.His489Pro)not specified [RCV004484126]uncertain significance107014268570142685Humanname
405813975CV3344994single nucleotide variantNM_173555.4(TYSND1):c.1502C>G (p.Thr501Ser)not specified [RCV004484127]uncertain significance107014012370140123Humanname
405813977CV3344995single nucleotide variantNM_173555.4(TYSND1):c.1505G>A (p.Arg502Gln)not specified [RCV004484128]uncertain significance107014012070140120Humanname
405813978CV3344996single nucleotide variantNM_173555.4(TYSND1):c.1559C>T (p.Thr520Met)not specified [RCV004484129]uncertain significance107014006670140066Humanname
405813980CV3344997single nucleotide variantNM_173555.4(TYSND1):c.1667G>A (p.Arg556Gln)not specified [RCV004484130]uncertain significance107013995870139958Humanname
407522411CV3490914single nucleotide variantNM_173555.4(TYSND1):c.1072T>C (p.Ser358Pro)not specified [RCV004677676]uncertain significance107014551570145515Humanname
407522395CV3493207single nucleotide variantNM_173555.4(TYSND1):c.1418C>T (p.Thr473Met)not specified [RCV004677670]uncertain significance107014273370142733Humanname
407522397CV3493208single nucleotide variantNM_173555.4(TYSND1):c.1685C>T (p.Pro562Leu)not specified [RCV004677671]uncertain significance107013994070139940Humanname
597802850CV3629022single nucleotide variantNM_173555.4(TYSND1):c.1261G>A (p.Val421Ile)not specified [RCV004881446]uncertain significance107014387870143878Humanname
597802852CV3629023single nucleotide variantNM_173555.4(TYSND1):c.1517C>T (p.Thr506Met)not specified [RCV004881447]uncertain significance107014010870140108Humanname
597802856CV3629025single nucleotide variantNM_173555.4(TYSND1):c.1040C>T (p.Ala347Val)not specified [RCV004881449]uncertain significance107014554770145547Humanname
597802863CV3629029single nucleotide variantNM_173555.4(TYSND1):c.1630G>A (p.Ala544Thr)not specified [RCV004881453]uncertain significance107013999570139995Humanname
597802867CV3629031single nucleotide variantNM_173555.4(TYSND1):c.1357A>G (p.Thr453Ala)not specified [RCV004881455]uncertain significance107014279470142794Humanname
598264378CV3932501single nucleotide variantNM_173555.4(TYSND1):c.1475A>G (p.Asn492Ser)not specified [RCV005301533]uncertain significance107014267670142676Humanname
598264382CV3932503single nucleotide variantNM_173555.4(TYSND1):c.1561G>A (p.Val521Met)not specified [RCV005301534]uncertain significance107014006470140064Humanname