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Variants search result for Homo sapiens
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62 records found for search term Xpo4
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
34890637CV904580single nucleotide variantNM_022459.5(XPO4):c.645C>G (p.Leu215=)not provided [RCV001171669]likely benign132084297720842977Humanname
15181610CV725418single nucleotide variantNM_022459.5(XPO4):c.1146T>C (p.Phe382=)not provided [RCV000885804]benign132082173120821731Humanname
8634990CV90212single nucleotide variantNM_022459.4(XPO4):c.2397G>A (p.Glu799=)Malignant melanoma [RCV000070309]not provided132079698320796983Humanname
155921856CV2240588single nucleotide variantNM_022459.5(XPO4):c.946C>G (p.Gln316Glu)not specified [RCV004119236]uncertain significance132082218420822184Humanname
156151605CV2245186single nucleotide variantNM_022459.5(XPO4):c.742A>G (p.Ile248Val)not specified [RCV004106966]uncertain significance132082716520827165Humanname
156071850CV2267365single nucleotide variantNM_022459.5(XPO4):c.346C>A (p.Leu116Ile)not specified [RCV004134022]uncertain significance132085573720855737Humanname
156063296CV2272346single nucleotide variantNM_022459.5(XPO4):c.525C>G (p.Asn175Lys)not specified [RCV004131487]uncertain significance132084381820843818Humanname
155918971CV2360117single nucleotide variantNM_022459.5(XPO4):c.580G>T (p.Asp194Tyr)not specified [RCV004215392]uncertain significance132084304220843042Humanname
401872193CV2793007single nucleotide variantNM_022459.5(XPO4):c.875C>T (p.Ala292Val)not specified [RCV004360343]uncertain significance132082225520822255Humanname
405666728CV3349604single nucleotide variantNM_022459.5(XPO4):c.991A>G (p.Ile331Val)not specified [RCV004485631]uncertain significance132082213920822139Humanname
597804670CV3630392single nucleotide variantNM_022459.5(XPO4):c.761C>T (p.Ser254Leu)not specified [RCV004882369]uncertain significance132082714620827146Humanname
597804672CV3630393single nucleotide variantNM_022459.5(XPO4):c.380C>T (p.Ser127Leu)not specified [RCV004882370]uncertain significance132085570320855703Humanname
597751663CV3630396single nucleotide variantNM_022459.5(XPO4):c.995A>G (p.Asn332Ser)not specified [RCV004892796]uncertain significance132082213520822135Humanname
597804677CV3630397single nucleotide variantNM_022459.5(XPO4):c.652C>G (p.Gln218Glu)not specified [RCV004882372]uncertain significance132084297020842970Humanname
597804681CV3630399single nucleotide variantNM_022459.5(XPO4):c.692A>G (p.Asn231Ser)not specified [RCV004882374]uncertain significance132084293020842930Humanname
597804685CV3630401single nucleotide variantNM_022459.5(XPO4):c.673C>T (p.Arg225Cys)not specified [RCV004882376]uncertain significance132084294920842949Humanname
598275801CV3933733single nucleotide variantNM_022459.5(XPO4):c.587G>A (p.Arg196His)not specified [RCV005304935]uncertain significance132084303520843035Humanname
156282695CV2220876single nucleotide variantNM_022459.5(XPO4):c.2074G>A (p.Val692Ile)not specified [RCV004092303]uncertain significance132080022920800229Humanname
156211581CV2259891single nucleotide variantNM_022459.5(XPO4):c.2841A>T (p.Arg947Ser)not specified [RCV004118926]uncertain significance132079053720790537Humanname
156039785CV2261240single nucleotide variantNM_022459.5(XPO4):c.2924C>G (p.Thr975Ser)not specified [RCV004128115]uncertain significance132078860920788609Humanname
156087655CV2295440single nucleotide variantNM_022459.5(XPO4):c.2550G>T (p.Glu850Asp)not specified [RCV004160560]uncertain significance132079683020796830Humanname
155911484CV2303828single nucleotide variantNM_022459.5(XPO4):c.1470A>T (p.Glu490Asp)not specified [RCV004163665]uncertain significance132080910620809106Humanname
155962925CV2308211single nucleotide variantNM_022459.5(XPO4):c.2728G>T (p.Asp910Tyr)not specified [RCV004164712]uncertain significance132079614520796145Humanname
156064150CV2316064single nucleotide variantNM_022459.5(XPO4):c.2543C>A (p.Thr848Asn)not specified [RCV004165941]uncertain significance132079683720796837Humanname
156185556CV2324669single nucleotide variantNM_022459.5(XPO4):c.1123C>T (p.Leu375Phe)not specified [RCV004172914]uncertain significance132082175420821754Humanname
156299319CV2326031single nucleotide variantNM_022459.5(XPO4):c.1333G>C (p.Asp445His)not specified [RCV004176237]uncertain significance132080980820809808Humanname
156071009CV2328461single nucleotide variantNM_022459.5(XPO4):c.1277C>T (p.Thr426Ile)not specified [RCV004175846]uncertain significance132080986420809864Humanname
156169721CV2337387single nucleotide variantNM_022459.5(XPO4):c.2662G>C (p.Val888Leu)not specified [RCV004187832]uncertain significance132079621120796211Humanname
156002549CV2347701single nucleotide variantNM_022459.5(XPO4):c.1849G>A (p.Val617Ile)not specified [RCV004200627]uncertain significance132080095920800959Humanname
329361176CV2436746single nucleotide variantNM_022459.5(XPO4):c.2090A>G (p.Gln697Arg)not specified [RCV004258113]uncertain significance132080021320800213Humanname
329400280CV2437561single nucleotide variantNM_022459.5(XPO4):c.2537A>G (p.Lys846Arg)not specified [RCV004258844]uncertain significance132079684320796843Humanname
329402770CV2451348single nucleotide variantNM_022459.5(XPO4):c.1030A>C (p.Ile344Leu)not specified [RCV004272037]uncertain significance132082184720821847Humanname
329382063CV2467487single nucleotide variantNM_022459.5(XPO4):c.2036T>C (p.Ile679Thr)not specified [RCV004287091]uncertain significance132080026720800267Humanname
401745904CV2693374single nucleotide variantNM_022459.5(XPO4):c.1138T>G (p.Cys380Gly)not specified [RCV004295332]uncertain significance132082173920821739Humanname
401772792CV2697984single nucleotide variantNM_022459.5(XPO4):c.2059A>G (p.Ile687Val)not specified [RCV004302796]uncertain significance132080024420800244Humanname
401759707CV2705687single nucleotide variantNM_022459.5(XPO4):c.1024G>A (p.Val342Met)not specified [RCV004318540]uncertain significance132082185320821853Humanname
405666687CV3349595single nucleotide variantNM_022459.5(XPO4):c.1151G>A (p.Arg384Gln)not specified [RCV004485622]uncertain significance132082172620821726Humanname
405666690CV3349596single nucleotide variantNM_022459.5(XPO4):c.1154G>A (p.Ser385Asn)not specified [RCV004485623]uncertain significance132082172320821723Humanname
405666695CV3349597single nucleotide variantNM_022459.5(XPO4):c.1189A>G (p.Met397Val)not specified [RCV004485624]uncertain significance132080995220809952Humanname
405666701CV3349598single nucleotide variantNM_022459.5(XPO4):c.1559C>T (p.Ala520Val)not specified [RCV004485625]uncertain significance132080851620808516Humanname
405666706CV3349599single nucleotide variantNM_022459.5(XPO4):c.1676C>T (p.Pro559Leu)not specified [RCV004485626]uncertain significance132080759820807598Humanname
405666721CV3349602single nucleotide variantNM_022459.5(XPO4):c.2530G>T (p.Val844Phe)not specified [RCV004485629]uncertain significance132079685020796850Humanname
405666724CV3349603single nucleotide variantNM_022459.5(XPO4):c.2686C>T (p.Arg896Trp)not specified [RCV004485630]uncertain significance132079618720796187Humanname
407456005CV3488245single nucleotide variantNM_022459.5(XPO4):c.2167T>A (p.Cys723Ser)not specified [RCV004685782]uncertain significance132079932020799320Humanname
407456011CV3488247single nucleotide variantNM_022459.5(XPO4):c.1104C>G (p.Phe368Leu)not specified [RCV004685784]uncertain significance132082177320821773Humanname
407456013CV3488248single nucleotide variantNM_022459.5(XPO4):c.1585A>G (p.Asn529Asp)not specified [RCV004685785]uncertain significance132080849020808490Humanname
407465637CV3488249single nucleotide variantNM_022459.5(XPO4):c.1808C>G (p.Ser603Cys)not specified [RCV004688822]uncertain significance132080746620807466Humanname
597804666CV3630390single nucleotide variantNM_022459.5(XPO4):c.2701G>A (p.Val901Ile)not specified [RCV004882367]uncertain significance132079617220796172Humanname
597804668CV3630391single nucleotide variantNM_022459.5(XPO4):c.1930C>T (p.Arg644Cys)not specified [RCV004882368]uncertain significance132080087820800878Humanname
597751657CV3630394single nucleotide variantNM_022459.5(XPO4):c.2470G>T (p.Val824Leu)not specified [RCV004892795]uncertain significance132079691020796910Humanname
597804674CV3630395single nucleotide variantNM_022459.5(XPO4):c.1955T>C (p.Val652Ala)not specified [RCV004882371]uncertain significance132080085320800853Humanname
597804683CV3630400single nucleotide variantNM_022459.5(XPO4):c.2522T>G (p.Leu841Trp)not specified [RCV004882375]uncertain significance132079685820796858Humanname
598275798CV3933730single nucleotide variantNM_022459.5(XPO4):c.2234G>A (p.Ser745Asn)not specified [RCV005304932]uncertain significance132079925320799253Humanname
598275800CV3933732single nucleotide variantNM_022459.5(XPO4):c.2558A>G (p.Asn853Ser)not specified [RCV005304934]uncertain significance132079682220796822Humanname
598275802CV3933734single nucleotide variantNM_022459.5(XPO4):c.1065C>A (p.Phe355Leu)not specified [RCV005304936]uncertain significance132082181220821812Humanname
8634989CV90211single nucleotide variantNM_022459.4(XPO4):c.2398G>A (p.Glu800Lys)Malignant melanoma [RCV000070308]not provided132079698220796982Humanname
156243525CV2210952single nucleotide variantNM_022459.5(XPO4):c.3370A>G (p.Thr1124Ala)not specified [RCV004086025]uncertain significance132078380820783808Humanname
156383685CV2220165single nucleotide variantNM_022459.5(XPO4):c.3333T>A (p.Asp1111Glu)not specified [RCV004095643]uncertain significance132078384520783845Humanname
155905920CV2357212single nucleotide variantNM_022459.5(XPO4):c.3371C>T (p.Thr1124Met)not specified [RCV004206995]uncertain significance132078380720783807Humanname
401869022CV2767444single nucleotide variantNM_022459.5(XPO4):c.3436G>C (p.Gly1146Arg)not specified [RCV004349593]uncertain significance132078374220783742Humanname
407456008CV3488246single nucleotide variantNM_022459.5(XPO4):c.3232T>C (p.Phe1078Leu)not specified [RCV004685783]uncertain significance132078699120786991Humanname
598275799CV3933731single nucleotide variantNM_022459.5(XPO4):c.3331G>C (p.Asp1111His)not specified [RCV005304933]uncertain significance132078384720783847Humanname