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41 records found for search term Snx15
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
8653160CV129735single nucleotide variantNM_013306.4(SNX15):c.664+1249T>ALung cancer [RCV000110222]uncertain significance116503691265036912Humanname
156073044CV2325394single nucleotide variantNM_013306.5(SNX15):c.88G>C (p.Val30Leu)not specified [RCV004177761]uncertain significance116502762565027625Humanname
401751587CV2727058single nucleotide variantNM_013306.5(SNX15):c.286C>T (p.Arg96Trp)not specified [RCV004325433]uncertain significance116503487665034876Humanname
401861036CV2772681single nucleotide variantNM_013306.5(SNX15):c.157A>G (p.Ser53Gly)not specified [RCV004355418]uncertain significance116503245265032452Humanname
405732500CV3322559single nucleotide variantNM_013306.5(SNX15):c.160G>A (p.Asp54Asn)not specified [RCV004464521]uncertain significance116503245565032455Humanname
405732509CV3322560single nucleotide variantNM_013306.5(SNX15):c.166C>A (p.Arg56Ser)not specified [RCV004464522]uncertain significance116503246165032461Humanname
405732516CV3322561single nucleotide variantNM_013306.5(SNX15):c.200G>A (p.Arg67His)not specified [RCV004464523]uncertain significance116503249565032495Humanname
405732523CV3322562single nucleotide variantNM_013306.5(SNX15):c.275T>G (p.Val92Gly)not specified [RCV004464524]uncertain significance116503486565034865Humanname
597745287CV3607249single nucleotide variantNM_013306.5(SNX15):c.115G>C (p.Asp39His)not specified [RCV004865640]uncertain significance116503218365032183Humanname
597741032CV3607250single nucleotide variantNM_013306.5(SNX15):c.223G>A (p.Glu75Lys)not specified [RCV004864778]uncertain significance116503251865032518Humanname
598171802CV3911668single nucleotide variantNM_013306.5(SNX15):c.242G>A (p.Arg81Gln)not specified [RCV005284903]uncertain significance116503253765032537Humanname
598171634CV3911670single nucleotide variantNM_013306.5(SNX15):c.215G>A (p.Arg72His)not specified [RCV005284905]uncertain significance116503251065032510Humanname
598171638CV3911671single nucleotide variantNM_013306.5(SNX15):c.167G>A (p.Arg56His)not specified [RCV005284906]uncertain significance116503246265032462Humanname
598171653CV3911674single nucleotide variantNM_013306.5(SNX15):c.238C>T (p.Pro80Ser)not specified [RCV005284909]uncertain significance116503253365032533Humanname
156180234CV2225879single nucleotide variantNM_013306.5(SNX15):c.646G>T (p.Asp216Tyr)not specified [RCV004103271]uncertain significance116503564565035645Humanname
155982777CV2273005single nucleotide variantNM_013306.5(SNX15):c.983G>T (p.Arg328Leu)not specified [RCV004137663]uncertain significance116503974665039746Humanname
156248747CV2277024single nucleotide variantNM_013306.5(SNX15):c.430C>T (p.Pro144Ser)not specified [RCV004140344]uncertain significance116503511665035116Humanname
156208386CV2298121single nucleotide variantNM_013306.5(SNX15):c.314G>A (p.Arg105His)not specified [RCV004159787]uncertain significance116503490465034904Humanname
156066580CV2346838single nucleotide variantNM_013306.5(SNX15):c.680G>C (p.Ser227Thr)not specified [RCV004199838]uncertain significance116503858765038587Humanname
156246324CV2347305single nucleotide variantNM_013306.5(SNX15):c.530C>T (p.Pro177Leu)not specified [RCV004206784]uncertain significance116503552965035529Humanname
156283886CV2348976single nucleotide variantNM_013306.5(SNX15):c.706A>G (p.Thr236Ala)not specified [RCV004203407]likely benign116503861365038613Humanname
155909422CV2359727single nucleotide variantNM_013306.5(SNX15):c.689A>C (p.His230Pro)not specified [RCV004210544]uncertain significance116503859665038596Humanname
329394354CV2469828single nucleotide variantNM_013306.5(SNX15):c.866C>T (p.Ala289Val)not specified [RCV004285318]uncertain significance116503877365038773Humanname
401861749CV2756477single nucleotide variantNM_013306.5(SNX15):c.868G>A (p.Ala290Thr)not specified [RCV004343008]uncertain significance116503877565038775Humanname
401864342CV2760791single nucleotide variantNM_013306.5(SNX15):c.464G>A (p.Arg155Gln)not specified [RCV004336433]uncertain significance116503515065035150Humanname
405732533CV3322563single nucleotide variantNM_013306.5(SNX15):c.332C>G (p.Pro111Arg)not specified [RCV004464525]uncertain significance116503492265034922Humanname
405732540CV3322564single nucleotide variantNM_013306.5(SNX15):c.430C>A (p.Pro144Thr)not specified [RCV004464526]uncertain significance116503511665035116Humanname
405732547CV3322565single nucleotide variantNM_013306.5(SNX15):c.452C>G (p.Pro151Arg)not specified [RCV004464527]uncertain significance116503513865035138Humanname
405732555CV3322566single nucleotide variantNM_013306.5(SNX15):c.800C>T (p.Ala267Val)not specified [RCV004464528]uncertain significance116503870765038707Humanname
407525305CV3484794single nucleotide variantNM_013306.5(SNX15):c.983G>A (p.Arg328Gln)not specified [RCV004679127]uncertain significance116503974665039746Humanname
407503941CV3484796single nucleotide variantNM_013306.5(SNX15):c.985G>A (p.Ala329Thr)not specified [RCV004670387]uncertain significance116503974865039748Humanname
407503944CV3484797single nucleotide variantNM_013306.5(SNX15):c.472C>G (p.Gln158Glu)not specified [RCV004670388]uncertain significance116503515865035158Humanname
597745266CV3607245single nucleotide variantNM_013306.5(SNX15):c.945G>C (p.Gln315His)not specified [RCV004865636]uncertain significance116503970865039708Humanname
597745272CV3607246single nucleotide variantNM_013306.5(SNX15):c.901G>A (p.Val301Ile)not specified [RCV004865637]likely benign116503880865038808Humanname
597745277CV3607247single nucleotide variantNM_013306.5(SNX15):c.826A>C (p.Ile276Leu)not specified [RCV004865638]uncertain significance116503873365038733Humanname
597745282CV3607248single nucleotide variantNM_013306.5(SNX15):c.484G>A (p.Ala162Thr)not specified [RCV004865639]uncertain significance116503517065035170Humanname
598171797CV3911669single nucleotide variantNM_013306.5(SNX15):c.895G>A (p.Val299Met)not specified [RCV005284904]uncertain significance116503880265038802Humanname
598171643CV3911672single nucleotide variantNM_013306.5(SNX15):c.997C>G (p.Leu333Val)not specified [RCV005284907]uncertain significance116503976065039760Humanname
598171648CV3911673single nucleotide variantNM_013306.5(SNX15):c.455A>G (p.Asp152Gly)not specified [RCV005284908]uncertain significance116503514165035141Humanname
8634285CV89505single nucleotide variantNM_013306.4(SNX15):c.682C>T (p.Pro228Ser)Malignant melanoma [RCV000069602]not provided116503858965038589Humanname
155978911CV2335229single nucleotide variantNM_013306.5(SNX15):c.1021C>G (p.Pro341Ala)not specified [RCV004186799]uncertain significance116503978465039784Humanname