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Variants search result for Homo sapiens
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43 records found for search term Arsj
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
156281015CV2224314single nucleotide variantNM_024590.4(ARSJ):c.20C>A (p.Ala7Glu)not specified [RCV004096133]uncertain significance4113978815113978815Humanname
329385530CV2461996single nucleotide variantNM_024590.4(ARSJ):c.23G>C (p.Gly8Ala)not specified [RCV004272184]uncertain significance4113978812113978812Humanname
401781148CV2732302single nucleotide variantNM_024590.4(ARSJ):c.23G>A (p.Gly8Glu)not specified [RCV004331487]uncertain significance4113978812113978812Humanname
156268912CV2240021single nucleotide variantNM_024590.4(ARSJ):c.286T>G (p.Ser96Ala)not specified [RCV004110804]uncertain significance4113978549113978549Humanname
156051284CV2336651single nucleotide variantNM_024590.4(ARSJ):c.232C>G (p.Leu78Val)not specified [RCV004196893]uncertain significance4113978603113978603Humanname
156397658CV2197381single nucleotide variantNM_024590.4(ARSJ):c.598C>T (p.Leu200Phe)not specified [RCV004081123]uncertain significance4113903476113903476Humanname
155921278CV2276279single nucleotide variantNM_024590.4(ARSJ):c.980A>G (p.Asp327Gly)not specified [RCV004144037]uncertain significance4113903094113903094Humanname
156266817CV2304915single nucleotide variantNM_024590.4(ARSJ):c.883G>T (p.Ala295Ser)not specified [RCV004168830]uncertain significance4113903191113903191Humanname
156077259CV2375092single nucleotide variantNM_024590.4(ARSJ):c.998C>T (p.Thr333Met)not specified [RCV004230138]uncertain significance4113903076113903076Humanname
156147371CV2377243single nucleotide variantNM_024590.4(ARSJ):c.520G>A (p.Val174Ile)not specified [RCV004232302]uncertain significance4113903554113903554Humanname
155952765CV2393831single nucleotide variantNM_024590.4(ARSJ):c.853A>G (p.Ile285Val)not specified [RCV004233659]uncertain significance4113903221113903221Humanname
329355072CV2448990single nucleotide variantNM_024590.4(ARSJ):c.736G>A (p.Val246Ile)not specified [RCV004264072]uncertain significance4113903338113903338Humanname
401762635CV2720004single nucleotide variantNM_024590.4(ARSJ):c.974C>T (p.Ser325Phe)not specified [RCV004323584]uncertain significance4113903100113903100Humanname
405664636CV3286536single nucleotide variantNM_024590.4(ARSJ):c.331G>A (p.Val111Ile)not specified [RCV004418274]uncertain significance4113978504113978504Humanname
405664758CV3286537single nucleotide variantNM_024590.4(ARSJ):c.725A>G (p.Tyr242Cys)not specified [RCV004418275]uncertain significance4113903349113903349Humanname
405664763CV3286538single nucleotide variantNM_024590.4(ARSJ):c.767C>T (p.Thr256Ile)not specified [RCV004418276]uncertain significance4113903307113903307Humanname
405664769CV3286539single nucleotide variantNM_024590.4(ARSJ):c.838G>A (p.Glu280Lys)not specified [RCV004418277]uncertain significance4113903236113903236Humanname
405664776CV3286540single nucleotide variantNM_024590.4(ARSJ):c.838G>C (p.Glu280Gln)not specified [RCV004418278]uncertain significance4113903236113903236Humanname
405664780CV3286541single nucleotide variantNM_024590.4(ARSJ):c.848G>T (p.Arg283Leu)not specified [RCV004418279]uncertain significance4113903226113903226Humanname
407461705CV3480161single nucleotide variantNM_024590.4(ARSJ):c.536T>G (p.Leu179Trp)not specified [RCV004658807]uncertain significance4113903538113903538Humanname
597765913CV3589923single nucleotide variantNM_024590.4(ARSJ):c.785A>G (p.Tyr262Cys)not specified [RCV004850156]uncertain significance4113903289113903289Humanname
597787561CV3589934single nucleotide variantNM_024590.4(ARSJ):c.848G>A (p.Arg283Gln)not specified [RCV004855272]uncertain significance4113903226113903226Humanname
597787580CV3589964single nucleotide variantNM_024590.4(ARSJ):c.689G>C (p.Trp230Ser)not specified [RCV004855276]uncertain significance4113903385113903385Humanname
597765946CV3589971single nucleotide variantNM_024590.4(ARSJ):c.319G>A (p.Ala107Thr)not specified [RCV004850164]uncertain significance4113978516113978516Humanname
597787624CV3589990single nucleotide variantNM_024590.4(ARSJ):c.347A>G (p.Tyr116Cys)not specified [RCV004855287]uncertain significance4113978488113978488Humanname
598254518CV3898877single nucleotide variantNM_024590.4(ARSJ):c.837C>G (p.Phe279Leu)not specified [RCV005259750]uncertain significance4113903237113903237Humanname
156249552CV2215571single nucleotide variantNM_024590.4(ARSJ):c.1772C>G (p.Thr591Ser)not specified [RCV004089339]uncertain significance4113902302113902302Humanname
155926462CV2258787single nucleotide variantNM_024590.4(ARSJ):c.1154T>C (p.Ile385Thr)not specified [RCV004118016]uncertain significance4113902920113902920Humanname
156148359CV2265272single nucleotide variantNM_024590.4(ARSJ):c.1796G>T (p.Gly599Val)not specified [RCV004126377]uncertain significance4113902278113902278Humanname
155995024CV2286484single nucleotide variantNM_024590.4(ARSJ):c.1759G>C (p.Val587Leu)not specified [RCV004139989]uncertain significance4113902315113902315Humanname
156052577CV2329033single nucleotide variantNM_024590.4(ARSJ):c.1465A>G (p.Thr489Ala)not specified [RCV004180315]uncertain significance4113902609113902609Humanname
156047085CV2340295single nucleotide variantNM_024590.4(ARSJ):c.1532G>A (p.Arg511Lys)not specified [RCV004194561]uncertain significance4113902542113902542Humanname
156104530CV2352458single nucleotide variantNM_024590.4(ARSJ):c.1219A>G (p.Ile407Val)not specified [RCV004202967]uncertain significance4113902855113902855Humanname
401875957CV2789246single nucleotide variantNM_024590.4(ARSJ):c.1781C>T (p.Ser594Leu)not specified [RCV004365278]uncertain significance4113902293113902293Humanname
405664612CV3286531single nucleotide variantNM_024590.4(ARSJ):c.1004G>A (p.Gly335Glu)not specified [RCV004418269]uncertain significance4113903070113903070Humanname
405664616CV3286532single nucleotide variantNM_024590.4(ARSJ):c.1309G>C (p.Gly437Arg)not specified [RCV004418270]uncertain significance4113902765113902765Humanname
405664622CV3286533single nucleotide variantNM_024590.4(ARSJ):c.1358A>G (p.His453Arg)not specified [RCV004418271]uncertain significance4113902716113902716Humanname
405664626CV3286534single nucleotide variantNM_024590.4(ARSJ):c.1531A>T (p.Arg511Trp)not specified [RCV004418272]uncertain significance4113902543113902543Humanname
405664631CV3286535single nucleotide variantNM_024590.4(ARSJ):c.1607C>A (p.Pro536His)not specified [RCV004418273]uncertain significance4113902467113902467Humanname
597765963CV3589980single nucleotide variantNM_024590.4(ARSJ):c.1645G>A (p.Gly549Arg)not specified [RCV004850168]uncertain significance4113902429113902429Humanname
598254446CV3898867single nucleotide variantNM_024590.4(ARSJ):c.1120C>T (p.Leu374Phe)not specified [RCV005259740]uncertain significance4113902954113902954Humanname
15173211CV734411single nucleotide variantNM_024590.4(ARSJ):c.1244G>A (p.Arg415Gln)not provided [RCV000905819]likely benign4113902830113902830Humanname
8638980CV94207single nucleotide variantNM_024590.3(ARSJ):c.1157C>T (p.Ser386Leu)Malignant melanoma [RCV000074315]not provided4113902917113902917Humanname