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Pathways
Variants search result for Homo sapiens
(View Results for all Objects and Ontologies)


35 records found for search term Nek6
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
401751323CV2716354single nucleotide variantNM_014397.6(NEK6):c.-26G>Anot specified [RCV004325350]uncertain significance9124301939124301939Humanname
156090592CV2206621single nucleotide variantNM_014397.6(NEK6):c.-29-8925G>Tnot specified [RCV004080962]uncertain significance9124293011124293011Humanname
156186738CV2236258single nucleotide variantNM_014397.6(NEK6):c.-29-8974T>Anot specified [RCV004107958]uncertain significance9124292962124292962Humanname
401752572CV2707054single nucleotide variantNM_014397.6(NEK6):c.-29-8925G>Anot specified [RCV004321640]uncertain significance9124293011124293011Humanname
407489584CV3454882single nucleotide variantNM_014397.6(NEK6):c.-29-8971G>Anot specified [RCV004641494]uncertain significance9124292965124292965Humanname
598231849CV3990719single nucleotide variantNM_014397.6(NEK6):c.11A>G (p.Gln4Arg)not specified [RCV005381432]uncertain significance9124301975124301975Humanname
15199972CV723328single nucleotide variantNM_014397.6(NEK6):c.270T>C (p.Cys90=)not provided [RCV000890783]benign9124313961124313961Humanname
156312965CV2196442single nucleotide variantNM_014397.6(NEK6):c.29A>G (p.His10Arg)not specified [RCV004073743]uncertain significance9124301993124301993Humanname
155978610CV2247091single nucleotide variantNM_014397.6(NEK6):c.37A>T (p.Ser13Cys)not specified [RCV004114630]uncertain significance9124302001124302001Humanname
156265962CV2247092single nucleotide variantNM_014397.6(NEK6):c.40T>C (p.Ser14Pro)not specified [RCV004114631]likely benign9124302004124302004Humanname
401768778CV2686368single nucleotide variantNM_014397.6(NEK6):c.64G>T (p.Gly22Trp)not specified [RCV004297442]uncertain significance9124302028124302028Humanname
405808425CV3353149single nucleotide variantNM_014397.6(NEK6):c.48C>A (p.Asn16Lys)not specified [RCV004481175]uncertain significance9124302012124302012Humanname
156388192CV2221771single nucleotide variantNM_014397.6(NEK6):c.142G>A (p.Glu48Lys)not specified [RCV004098528]uncertain significance9124312560124312560Humanname
156210568CV2370247single nucleotide variantNM_014397.6(NEK6):c.104C>T (p.Thr35Met)not specified [RCV004213167]uncertain significance9124312522124312522Humanname
405808439CV3353156single nucleotide variantNM_014397.6(NEK6):c.103A>G (p.Thr35Ala)not specified [RCV004481182]likely benign9124312521124312521Humanname
405808472CV3353172single nucleotide variantNM_014397.6(NEK6):c.282C>G (p.Ile94Met)not specified [RCV004481198]uncertain significance9124313973124313973Humanname
407489579CV3454881single nucleotide variantNM_014397.6(NEK6):c.172G>A (p.Glu58Lys)not specified [RCV004641493]uncertain significance9124312590124312590Humanname
156245679CV2310411single nucleotide variantNM_014397.6(NEK6):c.478G>A (p.Val160Met)not specified [RCV004163452]uncertain significance9124326402124326402Humanname
156069820CV2341147single nucleotide variantNM_014397.6(NEK6):c.895G>A (p.Val299Met)not specified [RCV004181623]uncertain significance9124350900124350900Humanname
155935485CV2371809single nucleotide variantNM_014397.6(NEK6):c.496C>T (p.Arg166Cys)not specified [RCV004219466]uncertain significance9124326420124326420Humanname
156178368CV2374591single nucleotide variantNM_014397.6(NEK6):c.826G>A (p.Glu276Lys)not specified [RCV004225217]uncertain significance9124347817124347817Humanname
156066837CV2381039single nucleotide variantNM_014397.6(NEK6):c.434C>T (p.Pro145Leu)not specified [RCV004225078]uncertain significance9124326358124326358Humanname
329399135CV2469958single nucleotide variantNM_014397.6(NEK6):c.920A>G (p.His307Arg)not specified [RCV004285415]uncertain significance9124350925124350925Humanname
401730287CV2680083single nucleotide variantNM_014397.6(NEK6):c.811G>A (p.Gly271Arg)not specified [RCV004286575]uncertain significance9124347802124347802Humanname
401782983CV2716073single nucleotide variantNM_014397.6(NEK6):c.402C>G (p.Ile134Met)not specified [RCV004323320]uncertain significance9124321566124321566Humanname
401878308CV2774166single nucleotide variantNM_014397.6(NEK6):c.694T>G (p.Ser232Ala)not specified [RCV004345756]uncertain significance9124339642124339642Humanname
405808529CV3353201single nucleotide variantNM_014397.6(NEK6):c.756G>A (p.Met252Ile)not specified [RCV004481227]uncertain significance9124347747124347747Humanname
597638893CV3555951single nucleotide variantNM_014397.6(NEK6):c.565G>A (p.Gly189Ser)not specified [RCV004831822]uncertain significance9124327388124327388Humanname
597638899CV3555952single nucleotide variantNM_014397.6(NEK6):c.756G>C (p.Met252Ile)not specified [RCV004831823]uncertain significance9124347747124347747Humanname
597638904CV3555953single nucleotide variantNM_014397.6(NEK6):c.406T>C (p.Tyr136His)not specified [RCV004831824]uncertain significance9124326330124326330Humanname
597638910CV3555954single nucleotide variantNM_014397.6(NEK6):c.851T>C (p.Met284Thr)not specified [RCV004831825]uncertain significance9124350856124350856Humanname
597638916CV3555955single nucleotide variantNM_014397.6(NEK6):c.803C>G (p.Pro268Arg)not specified [RCV004831826]uncertain significance9124347794124347794Humanname
597638921CV3555956single nucleotide variantNM_014397.6(NEK6):c.715G>A (p.Glu239Lys)not specified [RCV004831827]uncertain significance9124339663124339663Humanname
598231854CV3990720single nucleotide variantNM_014397.6(NEK6):c.299T>G (p.Leu100Arg)not specified [RCV005381433]uncertain significance9124321463124321463Humanname
598231861CV3990721single nucleotide variantNM_014397.6(NEK6):c.919C>T (p.His307Tyr)not specified [RCV005381434]uncertain significance9124350924124350924Humanname