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Variants search result for Homo sapiens
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56 records found for search term Angpt4
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
8586645CV121249single nucleotide variantNM_015985.2(ANGPT4):c.310-966T>CLung cancer [RCV000101769]uncertain significance20891334891334Humanname
8586650CV121254single nucleotide variantNM_015985.2(ANGPT4):c.309+5777A>GLung cancer [RCV000101774]uncertain significance20910129910129Humanname
156292989CV2321264single nucleotide variantNM_015985.4(ANGPT4):c.37C>T (p.Leu13Phe)not specified [RCV004175376]uncertain significance20916178916178Humanname
598235312CV3976195single nucleotide variantNM_015985.4(ANGPT4):c.384G>A (p.Thr128=)not specified [RCV005363646]likely benign20890294890294Humanname
15165975CV728828single nucleotide variantNM_015985.4(ANGPT4):c.351G>A (p.Glu117=)not provided [RCV000882530]benign20890327890327Humanname
8637442CV92668single nucleotide variantNM_015985.2(ANGPT4):c.531G>A (p.Leu177=)Malignant melanoma [RCV000072766]not provided20888374888374Humanname
155910199CV2303542single nucleotide variantNM_015985.4(ANGPT4):c.232C>T (p.His78Tyr)not specified [RCV004161638]uncertain significance20915983915983Humanname
401720711CV2673457single nucleotide variantNM_015985.4(ANGPT4):c.100G>A (p.Glu34Lys)not specified [RCV004288428]uncertain significance20916115916115Humanname
401734744CV2688606single nucleotide variantNM_015985.4(ANGPT4):c.293C>T (p.Thr98Met)not specified [RCV004301560]uncertain significance20915922915922Humanname
401743540CV2696814single nucleotide variantNM_015985.4(ANGPT4):c.121G>A (p.Gly41Ser)not specified [RCV004290783]uncertain significance20916094916094Humanname
401770000CV2710801single nucleotide variantNM_015985.4(ANGPT4):c.109G>C (p.Val37Leu)not specified [RCV004308729]uncertain significance20916106916106Humanname
407502430CV3449736single nucleotide variantNM_015985.4(ANGPT4):c.106C>G (p.Leu36Val)not specified [RCV004645146]uncertain significance20916109916109Humanname
597641609CV3696174single nucleotide variantNM_015985.4(ANGPT4):c.122G>A (p.Gly41Asp)not specified [RCV004941724]uncertain significance20916093916093Humanname
597641664CV3696185single nucleotide variantNM_015985.4(ANGPT4):c.260T>C (p.Val87Ala)not specified [RCV004941734]uncertain significance20915955915955Humanname
15178729CV705623single nucleotide variantNM_015985.4(ANGPT4):c.1305A>C (p.Ser435=)not provided [RCV000951349]benign20874330874330Humanname
156092822CV2216863single nucleotide variantNM_015985.4(ANGPT4):c.811G>A (p.Glu271Lys)not specified [RCV004083286]uncertain significance20885102885102Humanname
156383592CV2220122single nucleotide variantNM_015985.4(ANGPT4):c.677C>G (p.Thr226Arg)not specified [RCV004093977]uncertain significance20885236885236Humanname
156032922CV2259704single nucleotide variantNM_015985.4(ANGPT4):c.374A>G (p.Gln125Arg)not specified [RCV004116723]uncertain significance20890304890304Humanname
156267849CV2296720single nucleotide variantNM_015985.4(ANGPT4):c.350A>G (p.Glu117Gly)not specified [RCV004148632]uncertain significance20890328890328Humanname
156072353CV2325319single nucleotide variantNM_015985.4(ANGPT4):c.943C>T (p.Pro315Ser)not specified [RCV004177705]uncertain significance20881179881179Humanname
156070706CV2337701single nucleotide variantNM_015985.4(ANGPT4):c.329C>T (p.Thr110Met)not specified [RCV004183728]likely benign20890349890349Humanname
329352349CV2452901single nucleotide variantNM_015985.4(ANGPT4):c.790T>G (p.Leu264Val)not specified [RCV004277541]likely benign20885123885123Humanname
329385651CV2462136single nucleotide variantNM_015985.4(ANGPT4):c.925G>A (p.Val309Met)not specified [RCV004266160]uncertain significance20881197881197Humanname
329374121CV2463327single nucleotide variantNM_015985.4(ANGPT4):c.836C>A (p.Ala279Asp)not specified [RCV004275384]uncertain significance20881286881286Humanname
329389295CV2467250single nucleotide variantNM_015985.4(ANGPT4):c.626A>T (p.Gln209Leu)not specified [RCV004285059]uncertain significance20885287885287Humanname
401760512CV2705961single nucleotide variantNM_015985.4(ANGPT4):c.989C>G (p.Thr330Ser)not specified [RCV004320883]uncertain significance20879811879811Humanname
405817752CV3280255single nucleotide variantNM_015985.4(ANGPT4):c.524A>G (p.Asn175Ser)not specified [RCV004412762]uncertain significance20888381888381Humanname
405817754CV3280257single nucleotide variantNM_015985.4(ANGPT4):c.648C>G (p.Ile216Met)not specified [RCV004412764]uncertain significance20885265885265Humanname
405817760CV3280263single nucleotide variantNM_015985.4(ANGPT4):c.712G>C (p.Glu238Gln)not specified [RCV004412770]uncertain significance20885201885201Humanname
405817762CV3280265single nucleotide variantNM_015985.4(ANGPT4):c.730G>A (p.Val244Ile)not specified [RCV004412772]uncertain significance20885183885183Humanname
407502456CV3449743single nucleotide variantNM_015985.4(ANGPT4):c.781C>G (p.Leu261Val)not specified [RCV004645152]uncertain significance20885132885132Humanname
407502336CV3453656single nucleotide variantNM_015985.4(ANGPT4):c.938C>T (p.Thr313Met)not specified [RCV004645123]uncertain significance20881184881184Humanname
407518014CV3453666single nucleotide variantNM_015985.4(ANGPT4):c.421C>A (p.Gln141Lys)not specified [RCV004628722]uncertain significance20890257890257Humanname
597641445CV3696127single nucleotide variantNM_015985.4(ANGPT4):c.739A>G (p.Asn247Asp)not specified [RCV004941696]uncertain significance20885174885174Humanname
597641491CV3696138single nucleotide variantNM_015985.4(ANGPT4):c.502C>T (p.Pro168Ser)not specified [RCV004941704]uncertain significance20888403888403Humanname
597795748CV3696164single nucleotide variantNM_015985.4(ANGPT4):c.697G>T (p.Ala233Ser)not specified [RCV004934956]uncertain significance20885216885216Humanname
597641700CV3696196single nucleotide variantNM_015985.4(ANGPT4):c.525C>A (p.Asn175Lys)not specified [RCV004941740]uncertain significance20888380888380Humanname
598213098CV3976202single nucleotide variantNM_015985.4(ANGPT4):c.298T>G (p.Trp100Gly)not specified [RCV005358929]uncertain significance20915917915917Humanname
598235345CV3976205single nucleotide variantNM_015985.4(ANGPT4):c.917C>T (p.Thr306Ile)not specified [RCV005363651]uncertain significance20881205881205Humanname
598259973CV3976225single nucleotide variantNM_015985.4(ANGPT4):c.985T>A (p.Trp329Arg)not specified [RCV005347531]uncertain significance20879815879815Humanname
15174566CV728827single nucleotide variantNM_015985.4(ANGPT4):c.515T>G (p.Leu172Arg)not provided [RCV000884159]benign20888390888390Humanname
156188603CV2205826single nucleotide variantNM_015985.4(ANGPT4):c.1393G>A (p.Val465Ile)not specified [RCV004076226]likely benign20873079873079Humanname
156064383CV2272426single nucleotide variantNM_015985.4(ANGPT4):c.1130C>G (p.Ser377Cys)not specified [RCV004133347]uncertain significance20878251878251Humanname
155973396CV2321017single nucleotide variantNM_015985.4(ANGPT4):c.1389C>A (p.Asn463Lys)not specified [RCV004172809]uncertain significance20873083873083Humanname
156067081CV2340945single nucleotide variantNM_015985.4(ANGPT4):c.1495C>T (p.Arg499Trp)not specified [RCV004181439]uncertain significance20872977872977Humanname
156308653CV2369965single nucleotide variantNM_015985.4(ANGPT4):c.1243G>A (p.Gly415Ser)not specified [RCV004208428]uncertain significance20874392874392Humanname
401725065CV2697263single nucleotide variantNM_015985.4(ANGPT4):c.1000C>T (p.Arg334Cys)not specified [RCV004304028]uncertain significance20879800879800Humanname
401780621CV2727477single nucleotide variantNM_015985.4(ANGPT4):c.1411G>A (p.Asp471Asn)not specified [RCV004329679]likely benign20873061873061Humanname
401876985CV2793307single nucleotide variantNM_015985.4(ANGPT4):c.1018G>A (p.Val340Met)not specified [RCV004362127]uncertain significance20879782879782Humanname
405817860CV3280224single nucleotide variantNM_015985.4(ANGPT4):c.1262G>A (p.Ser421Asn)not specified [RCV004412731]uncertain significance20874373874373Humanname
407502461CV3449746single nucleotide variantNM_015985.4(ANGPT4):c.1187A>G (p.His396Arg)not specified [RCV004645153]uncertain significance20878194878194Humanname
407502390CV3453674single nucleotide variantNM_015985.4(ANGPT4):c.1060G>A (p.Gly354Arg)not specified [RCV004645137]uncertain significance20878321878321Humanname
597795743CV3696153single nucleotide variantNM_015985.4(ANGPT4):c.1312G>A (p.Asp438Asn)not specified [RCV004934954]uncertain significance20874323874323Humanname
598235253CV3976175single nucleotide variantNM_015985.4(ANGPT4):c.1075G>A (p.Glu359Lys)not specified [RCV005363638]uncertain significance20878306878306Humanname
598235280CV3976185single nucleotide variantNM_015985.4(ANGPT4):c.1135C>T (p.Arg379Cys)not specified [RCV005363642]uncertain significance20878246878246Humanname
598235389CV3976215single nucleotide variantNM_015985.4(ANGPT4):c.1185A>T (p.Glu395Asp)not specified [RCV005363657]uncertain significance20878196878196Humanname