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Variants search result for Homo sapiens
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62 records found for search term Tmem104
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
156263637CV2289696single nucleotide variantNM_017728.4(TMEM104):c.16A>G (p.Thr6Ala)not specified [RCV004150394]uncertain significance177477734674777346Humanname
405785737CV3339363single nucleotide variantNM_017728.4(TMEM104):c.25G>A (p.Gly9Arg)not specified [RCV004472791]uncertain significance177477735574777355Humanname
15186737CV704363single nucleotide variantNM_017728.4(TMEM104):c.288C>T (p.Ser96=)not provided [RCV000953374]benign177479023874790238Humanname
598177767CV3921007single nucleotide variantNM_017728.4(TMEM104):c.88G>A (p.Ala30Thr)not specified [RCV005285873]uncertain significance177478552474785524Humanname
156143548CV2200096single nucleotide variantNM_017728.4(TMEM104):c.139G>A (p.Val47Ile)not specified [RCV004069675]uncertain significance177478557574785575Humanname
156202278CV2300620single nucleotide variantNM_017728.4(TMEM104):c.118G>A (p.Ala40Thr)not specified [RCV004155576]uncertain significance177478555474785554Humanname
156175082CV2327068single nucleotide variantNM_017728.4(TMEM104):c.265G>A (p.Asp89Asn)not specified [RCV004178653]uncertain significance177479021574790215Humanname
401887293CV2771866single nucleotide variantNM_017728.4(TMEM104):c.127C>G (p.Leu43Val)not specified [RCV004344582]uncertain significance177478556374785563Humanname
401869659CV2772479single nucleotide variantNM_017728.4(TMEM104):c.163A>C (p.Met55Leu)not specified [RCV004355258]uncertain significance177478559974785599Humanname
597784852CV3620384single nucleotide variantNM_017728.4(TMEM104):c.214G>A (p.Ala72Thr)not specified [RCV004874935]uncertain significance177478883574788835Humanname
598211673CV3921006single nucleotide variantNM_017728.4(TMEM104):c.121G>T (p.Gly41Trp)not specified [RCV005292047]uncertain significance177478555774785557Humanname
156188475CV2205817single nucleotide variantNM_017728.4(TMEM104):c.739G>A (p.Val247Ile)not specified [RCV004076217]likely benign177483593574835935Humanname
156039839CV2219417single nucleotide variantNM_017728.4(TMEM104):c.386G>A (p.Arg129Gln)not specified [RCV004095218]uncertain significance177479099574790995Humanname
156286327CV2292074single nucleotide variantNM_017728.4(TMEM104):c.366C>G (p.Asn122Lys)not specified [RCV004160346]uncertain significance177479097574790975Humanname
156053258CV2320370single nucleotide variantNM_017728.4(TMEM104):c.496G>A (p.Ala166Thr)not specified [RCV004178531]uncertain significance177479508074795080Humanname
156059372CV2323005single nucleotide variantNM_017728.4(TMEM104):c.991G>A (p.Gly331Ser)not specified [RCV004185435]uncertain significance177483618774836187Humanname
155917521CV2332833single nucleotide variantNM_017728.4(TMEM104):c.902G>A (p.Arg301His)not specified [RCV004192097]uncertain significance177483609874836098Humanname
155909031CV2350417single nucleotide variantNM_017728.4(TMEM104):c.302G>A (p.Arg101Gln)not specified [RCV004204794]likely benign177479025274790252Humanname
156197755CV2357722single nucleotide variantNM_017728.4(TMEM104):c.553G>A (p.Gly185Ser)not specified [RCV004205020]uncertain significance177479554974795549Humanname
156146187CV2357918single nucleotide variantNM_017728.4(TMEM104):c.316C>T (p.Arg106Trp)not specified [RCV004209704]uncertain significance177479026674790266Humanname
156103160CV2363313single nucleotide variantNM_017728.4(TMEM104):c.812C>T (p.Ser271Leu)not specified [RCV004213865]uncertain significance177483600874836008Humanname
156391665CV2382487single nucleotide variantNM_017728.4(TMEM104):c.932A>G (p.Tyr311Cys)not specified [RCV004232827]uncertain significance177483612874836128Humanname
155904467CV2385514single nucleotide variantNM_017728.4(TMEM104):c.589C>T (p.Arg197Trp)not specified [RCV004233158]uncertain significance177479558574795585Humanname
401769021CV2686473single nucleotide variantNM_017728.4(TMEM104):c.426A>C (p.Lys142Asn)not specified [RCV004290627]uncertain significance177479103574791035Humanname
401758153CV2704203single nucleotide variantNM_017728.4(TMEM104):c.937C>A (p.Leu313Met)not specified [RCV004311207]uncertain significance177483613374836133Humanname
401760869CV2706127single nucleotide variantNM_017728.4(TMEM104):c.569C>T (p.Thr190Ile)not specified [RCV004314815]uncertain significance177479556574795565Humanname
401864150CV2760825single nucleotide variantNM_017728.4(TMEM104):c.626G>A (p.Arg209His)not specified [RCV004336463]uncertain significance177479562274795622Humanname
401869569CV2782411single nucleotide variantNM_017728.4(TMEM104):c.396G>A (p.Met132Ile)not specified [RCV004365147]uncertain significance177479100574791005Humanname
405785742CV3339364single nucleotide variantNM_017728.4(TMEM104):c.385C>T (p.Arg129Trp)not specified [RCV004472792]uncertain significance177479099474790994Humanname
405785747CV3339365single nucleotide variantNM_017728.4(TMEM104):c.481G>A (p.Ala161Thr)not specified [RCV004472793]uncertain significance177479506574795065Humanname
405785751CV3339366single nucleotide variantNM_017728.4(TMEM104):c.538G>C (p.Gly180Arg)not specified [RCV004472794]uncertain significance177479553474795534Humanname
405785757CV3339367single nucleotide variantNM_017728.4(TMEM104):c.566A>T (p.Asp189Val)not specified [RCV004472795]uncertain significance177479556274795562Humanname
405785761CV3339368single nucleotide variantNM_017728.4(TMEM104):c.775G>A (p.Gly259Arg)not specified [RCV004472796]uncertain significance177483597174835971Humanname
405785766CV3339369single nucleotide variantNM_017728.4(TMEM104):c.821G>A (p.Arg274Gln)not specified [RCV004472797]uncertain significance177483601774836017Humanname
407453023CV3486221single nucleotide variantNM_017728.4(TMEM104):c.989G>A (p.Arg330His)not specified [RCV004684343]uncertain significance177483618574836185Humanname
407453025CV3486222single nucleotide variantNM_017728.4(TMEM104):c.817G>A (p.Val273Ile)not specified [RCV004684344]uncertain significance177483601374836013Humanname
407453029CV3486225single nucleotide variantNM_017728.4(TMEM104):c.434T>C (p.Val145Ala)not specified [RCV004684346]uncertain significance177479501874795018Humanname
597784825CV3620378single nucleotide variantNM_017728.4(TMEM104):c.562G>A (p.Ala188Thr)not specified [RCV004874929]uncertain significance177479555874795558Humanname
597784834CV3620380single nucleotide variantNM_017728.4(TMEM104):c.352C>T (p.Arg118Cys)not specified [RCV004874931]uncertain significance177479096174790961Humanname
597784842CV3620382single nucleotide variantNM_017728.4(TMEM104):c.520G>C (p.Val174Leu)not specified [RCV004874933]uncertain significance177479510474795104Humanname
597784856CV3620385single nucleotide variantNM_017728.4(TMEM104):c.368C>G (p.Pro123Arg)not specified [RCV004874936]uncertain significance177479097774790977Humanname
598211662CV3921003single nucleotide variantNM_017728.4(TMEM104):c.421A>T (p.Asn141Tyr)not specified [RCV005292045]uncertain significance177479103074791030Humanname
598177762CV3921005single nucleotide variantNM_017728.4(TMEM104):c.353G>T (p.Arg118Leu)not specified [RCV005285872]uncertain significance177479096274790962Humanname
15125058CV715694single nucleotide variantNM_017728.4(TMEM104):c.604C>G (p.Leu202Val)not provided [RCV000963517]benign177479560074795600Humanname
8636340CV91563single nucleotide variantNM_017728.3(TMEM104):c.509C>T (p.Ser170Phe)Malignant melanoma [RCV000071661]not provided177479509374795093Humanname
156146903CV2212796single nucleotide variantNM_017728.4(TMEM104):c.1027G>A (p.Ala343Thr)not specified [RCV004091484]uncertain significance177483622374836223Humanname
156283225CV2291805single nucleotide variantNM_017728.4(TMEM104):c.1189C>T (p.Arg397Cys)not specified [RCV004158341]uncertain significance177483638574836385Humanname
156075293CV2321771single nucleotide variantNM_017728.4(TMEM104):c.1103A>G (p.Asn368Ser)not specified [RCV004179764]uncertain significance177483629974836299Humanname
156273216CV2323555single nucleotide variantNM_017728.4(TMEM104):c.1097G>A (p.Ser366Asn)not specified [RCV004165752]uncertain significance177483629374836293Humanname
156174048CV2377143single nucleotide variantNM_017728.4(TMEM104):c.1195G>A (p.Val399Met)not specified [RCV004231820]uncertain significance177483639174836391Humanname
156151438CV2394750single nucleotide variantNM_017728.4(TMEM104):c.1169C>T (p.Thr390Met)not specified [RCV004234424]uncertain significance177483636574836365Humanname
405785721CV3339360single nucleotide variantNM_017728.4(TMEM104):c.1039G>A (p.Val347Ile)not specified [RCV004472788]uncertain significance177483623574836235Humanname
405785727CV3339361single nucleotide variantNM_017728.4(TMEM104):c.1190G>A (p.Arg397His)not specified [RCV004472789]uncertain significance177483638674836386Humanname
405785732CV3339362single nucleotide variantNM_017728.4(TMEM104):c.1294G>A (p.Gly432Ser)not specified [RCV004472790]uncertain significance177483649074836490Humanname
407453027CV3486223single nucleotide variantNM_017728.4(TMEM104):c.1157G>T (p.Arg386Leu)not specified [RCV004684345]uncertain significance177483635374836353Humanname
407458601CV3486224single nucleotide variantNM_017728.4(TMEM104):c.1192G>A (p.Val398Ile)not specified [RCV004686877]uncertain significance177483638874836388Humanname
407453031CV3486226single nucleotide variantNM_017728.4(TMEM104):c.1397G>A (p.Arg466His)not specified [RCV004684347]uncertain significance177483659374836593Humanname
597784830CV3620379single nucleotide variantNM_017728.4(TMEM104):c.1457C>T (p.Thr486Met)not specified [RCV004874930]uncertain significance177483665374836653Humanname
597784838CV3620381single nucleotide variantNM_017728.4(TMEM104):c.1084G>A (p.Val362Ile)not specified [RCV004874932]uncertain significance177483628074836280Humanname
598177756CV3921001single nucleotide variantNM_017728.4(TMEM104):c.1102A>G (p.Asn368Asp)not specified [RCV005285871]uncertain significance177483629874836298Humanname
598211655CV3921002single nucleotide variantNM_017728.4(TMEM104):c.1117G>T (p.Ala373Ser)not specified [RCV005292044]uncertain significance177483631374836313Humanname
598211668CV3921004single nucleotide variantNM_017728.4(TMEM104):c.1406T>C (p.Phe469Ser)not specified [RCV005292046]uncertain significance177483660274836602Humanname