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50 records found for search term Pex11g
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
156356366CV2320770single nucleotide variantNM_080662.4(PEX11G):c.11T>C (p.Leu4Pro)not specified [RCV004172608]uncertain significance1974890007489000Humanname
401928428CV2815326single nucleotide variantNM_080662.4(PEX11G):c.297T>C (p.Ala99=)not provided [RCV003406814]likely benign1974821647482164Humanname
156260375CV2381141single nucleotide variantNM_080662.4(PEX11G):c.56G>A (p.Arg19His)not specified [RCV004225171]uncertain significance1974889557488955Humanname
156155099CV2388759single nucleotide variantNM_080662.4(PEX11G):c.59T>C (p.Leu20Pro)not specified [RCV004239620]uncertain significance1974889527488952Humanname
155901374CV2294461single nucleotide variantNM_080662.4(PEX11G):c.244G>C (p.Ala82Pro)not specified [RCV004159960]uncertain significance1974858437485843Humanname
156199040CV2362835single nucleotide variantNM_080662.4(PEX11G):c.226A>G (p.Lys76Glu)not specified [RCV004208947]uncertain significance1974858617485861Humanname
401762091CV2699516single nucleotide variantNM_080662.4(PEX11G):c.125G>A (p.Arg42Lys)not specified [RCV004299725]uncertain significance1974859627485962Humanname
401779550CV2731882single nucleotide variantNM_080662.4(PEX11G):c.193C>T (p.Leu65Phe)not specified [RCV004333127]uncertain significance1974858947485894Humanname
401856000CV2754202single nucleotide variantNM_080662.4(PEX11G):c.143G>A (p.Arg48His)not specified [RCV004334391]uncertain significance1974859447485944Humanname
407464102CV3470698single nucleotide variantNM_080662.4(PEX11G):c.201T>A (p.Asp67Glu)not specified [RCV004659866]uncertain significance1974858867485886Humanname
407528833CV3470699single nucleotide variantNM_080662.4(PEX11G):c.258C>A (p.Asp86Glu)not specified [RCV004655729]uncertain significance1974822037482203Humanname
407528835CV3470702single nucleotide variantNM_080662.4(PEX11G):c.134T>C (p.Val45Ala)not specified [RCV004655730]uncertain significance1974859537485953Humanname
597723846CV3575694single nucleotide variantNM_080662.4(PEX11G):c.250G>A (p.Glu84Lys)not specified [RCV004842141]uncertain significance1974822117482211Humanname
597723857CV3575696single nucleotide variantNM_080662.4(PEX11G):c.244G>A (p.Ala82Thr)not specified [RCV004842142]uncertain significance1974858437485843Humanname
597723869CV3575697single nucleotide variantNM_080662.4(PEX11G):c.200A>G (p.Asp67Gly)not specified [RCV004842143]uncertain significance1974858877485887Humanname
598261840CV3999666single nucleotide variantNM_080662.4(PEX11G):c.130G>A (p.Glu44Lys)not specified [RCV005386969]uncertain significance1974859577485957Humanname
155972095CV2214240single nucleotide variantNM_080662.4(PEX11G):c.571G>A (p.Asp191Asn)not specified [RCV004086233]uncertain significance1974773577477357Humanname
155997350CV2250544single nucleotide variantNM_080662.4(PEX11G):c.370C>T (p.Arg124Trp)not specified [RCV004127402]uncertain significance1974820917482091Humanname
156318523CV2260701single nucleotide variantNM_080662.4(PEX11G):c.383T>C (p.Leu128Pro)not specified [RCV004125633]uncertain significance1974820787482078Humanname
155901377CV2294462single nucleotide variantNM_080662.4(PEX11G):c.722C>A (p.Pro241His)not specified [RCV004159961]uncertain significance1974772067477206Humanname
156089628CV2344463single nucleotide variantNM_080662.4(PEX11G):c.586G>A (p.Val196Met)not specified [RCV004195207]uncertain significance1974773427477342Humanname
156218199CV2344716single nucleotide variantNM_080662.4(PEX11G):c.302A>G (p.Gln101Arg)not specified [RCV004190874]uncertain significance1974821597482159Humanname
156338202CV2370594single nucleotide variantNM_080662.4(PEX11G):c.346C>T (p.Arg116Trp)not specified [RCV004215920]uncertain significance1974821157482115Humanname
156084164CV2381962single nucleotide variantNM_080662.4(PEX11G):c.629C>T (p.Pro210Leu)not specified [RCV004225894]uncertain significance1974772997477299Humanname
156095960CV2399022single nucleotide variantNM_080662.4(PEX11G):c.482C>T (p.Pro161Leu)not specified [RCV004245326]uncertain significance1974783237478323Humanname
155932987CV2399244single nucleotide variantNM_080662.4(PEX11G):c.536A>C (p.Gln179Pro)not specified [RCV004247033]uncertain significance1974773927477392Humanname
329385625CV2432135single nucleotide variantNM_080662.4(PEX11G):c.467G>A (p.Arg156Gln)not specified [RCV004249281]uncertain significance1974783387478338Humanname
401780752CV2685704single nucleotide variantNM_080662.4(PEX11G):c.512G>A (p.Arg171Gln)not specified [RCV004296752]uncertain significance1974774167477416Humanname
401782351CV2686737single nucleotide variantNM_080662.4(PEX11G):c.466C>T (p.Arg156Trp)not specified [RCV004301930]uncertain significance1974783397478339Humanname
401772740CV2719744single nucleotide variantNM_080662.4(PEX11G):c.686C>T (p.Ala229Val)not specified [RCV004329180]uncertain significance1974772427477242Humanname
401728649CV2729714single nucleotide variantNM_080662.4(PEX11G):c.611T>A (p.Leu204Gln)not specified [RCV004331969]uncertain significance1974773177477317Humanname
401767553CV2729743single nucleotide variantNM_080662.4(PEX11G):c.700G>A (p.Gly234Ser)not specified [RCV004332764]uncertain significance1974772287477228Humanname
401778806CV2732895single nucleotide variantNM_080662.4(PEX11G):c.539C>T (p.Ser180Leu)not specified [RCV004331074]uncertain significance1974773897477389Humanname
401778838CV2732921single nucleotide variantNM_080662.4(PEX11G):c.494C>T (p.Pro165Leu)not specified [RCV004331100]uncertain significance1974774347477434Humanname
401869932CV2772567single nucleotide variantNM_080662.4(PEX11G):c.706G>A (p.Ala236Thr)not specified [RCV004355325]uncertain significance1974772227477222Humanname
401886494CV2780385single nucleotide variantNM_080662.4(PEX11G):c.479C>T (p.Ala160Val)not specified [RCV004357784]uncertain significance1974783267478326Humanname
401871960CV2783645single nucleotide variantNM_080662.4(PEX11G):c.623G>A (p.Arg208His)not specified [RCV004360291]uncertain significance1974773057477305Humanname
405745572CV3368460single nucleotide variantNM_080662.4(PEX11G):c.334G>A (p.Ala112Thr)not specified [RCV004498358]uncertain significance1974821277482127Humanname
405745583CV3368461single nucleotide variantNM_080662.4(PEX11G):c.401C>T (p.Ala134Val)not specified [RCV004498359]uncertain significance1974820607482060Humanname
405745592CV3368462single nucleotide variantNM_080662.4(PEX11G):c.503G>A (p.Arg168Gln)not specified [RCV004498360]uncertain significance1974774257477425Humanname
405745611CV3368464single nucleotide variantNM_080662.4(PEX11G):c.623G>T (p.Arg208Leu)not specified [RCV004498362]uncertain significance1974773057477305Humanname
405745621CV3368465single nucleotide variantNM_080662.4(PEX11G):c.697G>A (p.Gly233Ser)not specified [RCV004498363]uncertain significance1974772317477231Humanname
405745627CV3368466single nucleotide variantNM_080662.4(PEX11G):c.710A>T (p.Glu237Val)not specified [RCV004498364]uncertain significance1974772187477218Humanname
407464099CV3470697single nucleotide variantNM_080662.4(PEX11G):c.371G>A (p.Arg124Gln)not specified [RCV004659865]uncertain significance1974820907482090Humanname
407464108CV3470700single nucleotide variantNM_080662.4(PEX11G):c.320A>T (p.Glu107Val)not specified [RCV004659867]uncertain significance1974821417482141Humanname
407464112CV3470701single nucleotide variantNM_080662.4(PEX11G):c.502C>T (p.Arg168Trp)not specified [RCV004659868]uncertain significance1974774267477426Humanname
407528837CV3470703single nucleotide variantNM_080662.4(PEX11G):c.404T>G (p.Leu135Arg)not specified [RCV004655731]uncertain significance1974820577482057Humanname
407528841CV3470705single nucleotide variantNM_080662.4(PEX11G):c.691C>G (p.Arg231Gly)not specified [RCV004655733]uncertain significance1974772377477237Humanname
598261830CV3999664single nucleotide variantNM_080662.4(PEX11G):c.553C>T (p.Leu185Phe)not specified [RCV005386967]uncertain significance1974773757477375Humanname
15161898CV728482duplicationNM_080662.4(PEX11G):c.638_639dup (p.Val214Ter)not provided [RCV000881657]benign1974772887477289Humanname