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35 records found for search term Vgll3
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
8578868CV113264single nucleotide variantNM_016206.2(VGLL3):c.937+6219G>ALung cancer [RCV000093787]uncertain significance38696237186962371Humanname
401926484CV2827575single nucleotide variantNM_016206.4(VGLL3):c.225A>G (p.Lys75=)not provided [RCV003437918]likely benign38697870486978704Humanname
401926485CV2827576single nucleotide variantNM_016206.4(VGLL3):c.105G>A (p.Pro35=)not provided [RCV003437919]likely benign38699063986990639Humanname
156212394CV2378409single nucleotide variantNM_016206.4(VGLL3):c.29C>T (p.Pro10Leu)not specified [RCV004226428]uncertain significance38699071586990715Humanname
401897528CV2787135single nucleotide variantNM_016206.4(VGLL3):c.53A>G (p.Tyr18Cys)not specified [RCV004360565]uncertain significance38699069186990691Humanname
155971997CV2214217single nucleotide variantNM_016206.4(VGLL3):c.238G>A (p.Glu80Lys)not specified [RCV004086212]uncertain significance38697869186978691Humanname
156347093CV2353867single nucleotide variantNM_016206.4(VGLL3):c.103C>A (p.Pro35Thr)not specified [RCV004201867]uncertain significance38699064186990641Humanname
405806862CV3345631single nucleotide variantNM_016206.4(VGLL3):c.102G>C (p.Gln34His)not specified [RCV004480418]likely benign38699064286990642Humanname
405806864CV3345632single nucleotide variantNM_016206.4(VGLL3):c.227A>C (p.Asp76Ala)not specified [RCV004480419]uncertain significance38697870286978702Humanname
405806866CV3345633single nucleotide variantNM_016206.4(VGLL3):c.229C>A (p.Gln77Lys)not specified [RCV004480420]uncertain significance38697870086978700Humanname
8630959CV86115single nucleotide variantNM_016206.2(VGLL3):c.287G>A (p.Gly96Glu)Malignant melanoma [RCV000066199]not provided38697864286978642Humanname
156255914CV2194540single nucleotide variantNM_016206.4(VGLL3):c.715C>T (p.Arg239Cys)not specified [RCV004081603]uncertain significance38696881286968812Humanname
156237192CV2224191single nucleotide variantNM_016206.4(VGLL3):c.622C>A (p.Pro208Thr)not specified [RCV004096036]uncertain significance38696890586968905Humanname
156222372CV2232713single nucleotide variantNM_016206.4(VGLL3):c.781C>T (p.Pro261Ser)not specified [RCV004101371]uncertain significance38696874686968746Humanname
156098018CV2253234single nucleotide variantNM_016206.4(VGLL3):c.593C>T (p.Ala198Val)not specified [RCV004122778]uncertain significance38696893486968934Humanname
156176423CV2299839single nucleotide variantNM_016206.4(VGLL3):c.381G>T (p.Met127Ile)not specified [RCV004148987]uncertain significance38697854886978548Humanname
155980513CV2343535single nucleotide variantNM_016206.4(VGLL3):c.817C>T (p.Pro273Ser)not specified [RCV004190570]uncertain significance38696871086968710Humanname
156225955CV2390715single nucleotide variantNM_016206.4(VGLL3):c.470C>A (p.Pro157His)not specified [RCV004241014]uncertain significance38696905786969057Humanname
329371997CV2454944single nucleotide variantNM_016206.4(VGLL3):c.751G>T (p.Ala251Ser)not specified [RCV004272224]uncertain significance38696877686968776Humanname
329362603CV2464039single nucleotide variantNM_016206.4(VGLL3):c.407G>A (p.Ser136Asn)not specified [RCV004273745]uncertain significance38696912086969120Humanname
401723465CV2674961single nucleotide variantNM_016206.4(VGLL3):c.877G>A (p.Ala293Thr)not specified [RCV004296269]uncertain significance38696865086968650Humanname
401888357CV2788378single nucleotide variantNM_016206.4(VGLL3):c.670G>A (p.Asp224Asn)not specified [RCV004354916]uncertain significance38696885786968857Humanname
405806868CV3345634single nucleotide variantNM_016206.4(VGLL3):c.427C>T (p.Arg143Trp)not specified [RCV004480421]uncertain significance38696910086969100Humanname
405810703CV3345635single nucleotide variantNM_016206.4(VGLL3):c.643G>A (p.Val215Met)not specified [RCV004482405]uncertain significance38696888486968884Humanname
405810705CV3345636single nucleotide variantNM_016206.4(VGLL3):c.757T>A (p.Ser253Thr)not specified [RCV004482406]uncertain significance38696877086968770Humanname
405810707CV3345637single nucleotide variantNM_016206.4(VGLL3):c.887G>T (p.Gly296Val)not specified [RCV004482407]uncertain significance38696864086968640Humanname
405810708CV3345638single nucleotide variantNM_016206.4(VGLL3):c.890C>G (p.Ala297Gly)not specified [RCV004482408]uncertain significance38696863786968637Humanname
407529630CV3493484single nucleotide variantNM_016206.4(VGLL3):c.428G>A (p.Arg143Gln)not specified [RCV004681012]uncertain significance38696909986969099Humanname
407529632CV3493485single nucleotide variantNM_016206.4(VGLL3):c.470C>T (p.Pro157Leu)not specified [RCV004681013]uncertain significance38696905786969057Humanname
407529636CV3493487single nucleotide variantNM_016206.4(VGLL3):c.364A>T (p.Ile122Phe)not specified [RCV004681015]uncertain significance38697856586978565Humanname
597803888CV3629618single nucleotide variantNM_016206.4(VGLL3):c.911T>A (p.Ile304Lys)not specified [RCV004881998]uncertain significance38696861686968616Humanname
597803890CV3629619single nucleotide variantNM_016206.4(VGLL3):c.490G>A (p.Gly164Arg)not specified [RCV004881999]uncertain significance38696903786969037Humanname
598205992CV3929596single nucleotide variantNM_016206.4(VGLL3):c.563C>T (p.Pro188Leu)not specified [RCV005290940]uncertain significance38696896486968964Humanname
598240701CV3929597single nucleotide variantNM_016206.4(VGLL3):c.637T>A (p.Ser213Thr)not specified [RCV005296807]uncertain significance38696889086968890Humanname
8630958CV86114single nucleotide variantNM_016206.2(VGLL3):c.355G>A (p.Glu119Lys)Malignant melanoma [RCV000066198]not provided38697857486978574Humanname