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Variants search result for Homo sapiens
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55 records found for search term Tox3
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
8584893CV119470single nucleotide variantNM_001146188.1(TOX3):c.75+5866A>TLung cancer [RCV000099990]uncertain significance165251354052513540Humanname
8584892CV119469single nucleotide variantNM_001146188.1(TOX3):c.76-20579A>TLung cancer [RCV000099989]uncertain significance165248915352489153Humanname
8584894CV119471single nucleotide variantNM_001146188.1(TOX3):c.-100+11611A>TLung cancer [RCV000099991]uncertain significance165253610352536103Humanname
401872617CV2779825single nucleotide variantNM_001080430.4(TOX3):c.17A>G (p.Tyr6Cys)not specified [RCV004353451]uncertain significance165254670752546707Humanname
405758644CV3347124single nucleotide variantNM_001080430.4(TOX3):c.12G>C (p.Arg4Ser)not specified [RCV004468224]uncertain significance165254671252546712Humanname
156254979CV2280936single nucleotide variantNM_001080430.4(TOX3):c.44G>T (p.Ser15Ile)not specified [RCV004145176]uncertain significance165254668052546680Humanname
401756908CV2696645single nucleotide variantNM_001080430.4(TOX3):c.43A>G (p.Ser15Gly)not specified [RCV004312662]likely benign165254668152546681Humanname
156135887CV2213520single nucleotide variantNM_001080430.4(TOX3):c.229C>T (p.Pro77Ser)not specified [RCV004087484]uncertain significance165246411352464113Humanname
329359953CV2462202single nucleotide variantNM_001080430.4(TOX3):c.293A>G (p.Gln98Arg)not specified [RCV004266210]uncertain significance165246404952464049Humanname
407521093CV3486851single nucleotide variantNM_001080430.4(TOX3):c.249T>A (p.Asp83Glu)not specified [RCV004677174]uncertain significance165246409352464093Humanname
597787290CV3611086single nucleotide variantNM_001080430.4(TOX3):c.125C>T (p.Ala42Val)not specified [RCV004875564]uncertain significance165246853752468537Humanname
15200730CV703734single nucleotide variantNM_001080430.4(TOX3):c.1149C>T (p.Ile383=)not provided [RCV000957414]benign165243980752439807Humanname
155926166CV2258702single nucleotide variantNM_001080430.4(TOX3):c.697G>C (p.Ala233Pro)not specified [RCV004117943]uncertain significance165244620352446203Humanname
156053050CV2329064single nucleotide variantNM_001080430.4(TOX3):c.919A>G (p.Lys307Glu)not specified [RCV004180338]uncertain significance165244434452444344Humanname
156083629CV2330711single nucleotide variantNM_001080430.4(TOX3):c.464G>A (p.Arg155Gln)not specified [RCV004185780]uncertain significance165245049152450491Humanname
401755658CV2682545single nucleotide variantNM_001080430.4(TOX3):c.836A>T (p.Asn279Ile)not specified [RCV004290557]uncertain significance165244606452446064Humanname
401772512CV2687717single nucleotide variantNM_001080430.4(TOX3):c.443A>G (p.Gln148Arg)not specified [RCV004302706]uncertain significance165245051252450512Humanname
405758668CV3347128single nucleotide variantNM_001080430.4(TOX3):c.494G>A (p.Arg165His)not specified [RCV004468228]uncertain significance165245046152450461Humanname
407521089CV3486849single nucleotide variantNM_001080430.4(TOX3):c.874A>G (p.Met292Val)not specified [RCV004677172]uncertain significance165244602652446026Humanname
407521102CV3486854single nucleotide variantNM_001080430.4(TOX3):c.584T>C (p.Met195Thr)not specified [RCV004677177]uncertain significance165245037152450371Humanname
597787302CV3611089single nucleotide variantNM_001080430.4(TOX3):c.404A>G (p.His135Arg)not specified [RCV004875567]uncertain significance165246393852463938Humanname
597787306CV3611090single nucleotide variantNM_001080430.4(TOX3):c.905A>G (p.Gln302Arg)not specified [RCV004875568]uncertain significance165244599552445995Humanname
597787312CV3611092single nucleotide variantNM_001080430.4(TOX3):c.836A>G (p.Asn279Ser)not specified [RCV004875570]uncertain significance165244606452446064Humanname
597787316CV3611093single nucleotide variantNM_001080430.4(TOX3):c.664G>T (p.Asp222Tyr)not specified [RCV004875571]uncertain significance165245029152450291Humanname
598188647CV3928195single nucleotide variantNM_001080430.4(TOX3):c.308C>T (p.Thr103Ile)not specified [RCV005287966]uncertain significance165246403452464034Humanname
15197941CV726676single nucleotide variantNM_001080430.4(TOX3):c.550G>A (p.Ala184Thr)not provided [RCV000890211]benign165245040552450405Humanname
8635837CV91060single nucleotide variantNM_001146188.1(TOX3):c.344G>A (p.Arg115Lys)Malignant melanoma [RCV000071158]not provided165246398352463983Humanname
156313778CV2196551single nucleotide variantNM_001080430.4(TOX3):c.1286C>T (p.Ser429Phe)not specified [RCV004073836]uncertain significance165243967052439670Humanname
155989172CV2259665single nucleotide variantNM_001080430.4(TOX3):c.1710A>T (p.Leu570Phe)not specified [RCV004116698]uncertain significance165243924652439246Humanname
155905740CV2303171single nucleotide variantNM_001080430.4(TOX3):c.1058C>T (p.Thr353Ile)not specified [RCV004156936]uncertain significance165243989852439898Humanname
156307149CV2369607single nucleotide variantNM_001080430.4(TOX3):c.1213G>A (p.Ala405Thr)not specified [RCV004215019]uncertain significance165243974352439743Humanname
329400284CV2437571single nucleotide variantNM_001080430.4(TOX3):c.1622C>G (p.Thr541Arg)not specified [RCV004258854]uncertain significance165243933452439334Humanname
329377738CV2450010single nucleotide variantNM_001080430.4(TOX3):c.1452C>A (p.His484Gln)not specified [RCV004269068]uncertain significance165243950452439504Humanname
401721074CV2673591single nucleotide variantNM_001080430.4(TOX3):c.1624T>A (p.Ser542Thr)not specified [RCV004282329]uncertain significance165243933252439332Humanname
401754887CV2682326single nucleotide variantNM_001080430.4(TOX3):c.1217A>G (p.Asn406Ser)not specified [RCV004290364]uncertain significance165243973952439739Humanname
401743202CV2684041single nucleotide variantNM_001080430.4(TOX3):c.1526A>T (p.Gln509Leu)not specified [RCV004295645]uncertain significance165243943052439430Humanname
401771003CV2686136single nucleotide variantNM_001080430.4(TOX3):c.1676C>T (p.Ser559Leu)not specified [RCV004297142]uncertain significance165243928052439280Humanname
401768669CV2716691single nucleotide variantNM_001080430.4(TOX3):c.1523A>T (p.Gln508Leu)not specified [RCV004327742]uncertain significance165243943352439433Humanname
401891828CV2779483single nucleotide variantNM_001080430.4(TOX3):c.1226C>T (p.Ser409Leu)not specified [RCV004351112]uncertain significance165243973052439730Humanname
405758633CV3347122single nucleotide variantNM_001080430.4(TOX3):c.1185C>A (p.Asn395Lys)not specified [RCV004468222]uncertain significance165243977152439771Humanname
405758638CV3347123single nucleotide variantNM_001080430.4(TOX3):c.1238C>A (p.Ala413Asp)not specified [RCV004468223]uncertain significance165243971852439718Humanname
405758651CV3347125single nucleotide variantNM_001080430.4(TOX3):c.1368G>C (p.Met456Ile)not specified [RCV004468225]uncertain significance165243958852439588Humanname
405758654CV3347126single nucleotide variantNM_001080430.4(TOX3):c.1538G>A (p.Arg513His)not specified [RCV004468226]likely benign165243941852439418Humanname
405758662CV3347127single nucleotide variantNM_001080430.4(TOX3):c.1658C>T (p.Ala553Val)not specified [RCV004468227]uncertain significance165243929852439298Humanname
407521092CV3486850single nucleotide variantNM_001080430.4(TOX3):c.1499A>G (p.Gln500Arg)not specified [RCV004677173]uncertain significance165243945752439457Humanname
407521096CV3486852single nucleotide variantNM_001080430.4(TOX3):c.1661C>G (p.Ser554Cys)not specified [RCV004677175]uncertain significance165243929552439295Humanname
407521105CV3486855single nucleotide variantNM_001080430.4(TOX3):c.1094A>G (p.His365Arg)not specified [RCV004677178]uncertain significance165243986252439862Humanname
597787294CV3611087single nucleotide variantNM_001080430.4(TOX3):c.1022G>A (p.Arg341His)not specified [RCV004875565]uncertain significance165243993452439934Humanname
597787298CV3611088single nucleotide variantNM_001080430.4(TOX3):c.1642G>A (p.Gly548Arg)not specified [RCV004875566]uncertain significance165243931452439314Humanname
597787309CV3611091single nucleotide variantNM_001080430.4(TOX3):c.1093C>T (p.His365Tyr)not specified [RCV004875569]uncertain significance165243986352439863Humanname
598254720CV3928191single nucleotide variantNM_001080430.4(TOX3):c.1052A>G (p.Asn351Ser)not specified [RCV005278488]uncertain significance165243990452439904Humanname
598188630CV3928193single nucleotide variantNM_001080430.4(TOX3):c.1262C>T (p.Thr421Met)not specified [RCV005287964]uncertain significance165243969452439694Humanname
598188639CV3928194single nucleotide variantNM_001080430.4(TOX3):c.1237G>C (p.Ala413Pro)not specified [RCV005287965]uncertain significance165243971952439719Humanname
598188653CV3928196single nucleotide variantNM_001080430.4(TOX3):c.1237G>A (p.Ala413Thr)not specified [RCV005287967]uncertain significance165243971952439719Humanname
15182246CV714965single nucleotide variantNM_001080430.4(TOX3):c.1537C>T (p.Arg513Cys)not provided [RCV000974585]benign165243941952439419Humanname