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


42 records found for search term Fzd7
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
15120124CV781109single nucleotide variantNM_003507.2(FZD7):c.789G>A (p.Leu263=)not provided [RCV000979237]likely benign2202035436202035436Humanname
156087374CV2241320single nucleotide variantNM_003507.2(FZD7):c.164C>A (p.Pro55Gln)not specified [RCV004102460]uncertain significance2202034811202034811Humanname
156395855CV2325965single nucleotide variantNM_003507.2(FZD7):c.133G>A (p.Asp45Asn)not specified [RCV004176178]uncertain significance2202034780202034780Humanname
405731057CV3257834single nucleotide variantNM_003507.2(FZD7):c.130C>T (p.Pro44Ser)not specified [RCV004390007]uncertain significance2202034777202034777Humanname
407485626CV3439483single nucleotide variantNM_003507.2(FZD7):c.114G>C (p.Glu38Asp)not specified [RCV004618952]uncertain significance2202034761202034761Humanname
597779159CV3676979single nucleotide variantNM_003507.2(FZD7):c.199C>A (p.Leu67Met)not specified [RCV004930306]uncertain significance2202034846202034846Humanname
15121459CV733076single nucleotide variantNM_003507.2(FZD7):c.1227G>A (p.Gly409=)not provided [RCV000896068]benign2202035874202035874Humanname
156264113CV2201223single nucleotide variantNM_003507.2(FZD7):c.814G>A (p.Val272Ile)not specified [RCV004077364]uncertain significance2202035461202035461Humanname
156231090CV2227576single nucleotide variantNM_003507.2(FZD7):c.613G>C (p.Ala205Pro)not specified [RCV004092216]uncertain significance2202035260202035260Humanname
156218912CV2253996single nucleotide variantNM_003507.2(FZD7):c.947T>C (p.Val316Ala)not specified [RCV004127664]uncertain significance2202035594202035594Humanname
156245318CV2267476single nucleotide variantNM_003507.2(FZD7):c.325G>A (p.Val109Met)not specified [RCV004135902]uncertain significance2202034972202034972Humanname
156068768CV2270938single nucleotide variantNM_003507.2(FZD7):c.572C>G (p.Thr191Ser)not specified [RCV004131973]uncertain significance2202035219202035219Humanname
329353788CV2439685single nucleotide variantNM_003507.2(FZD7):c.608G>A (p.Arg203His)not specified [RCV004255699]uncertain significance2202035255202035255Humanname
401881222CV2789492single nucleotide variantNM_003507.2(FZD7):c.757G>A (p.Ala253Thr)not specified [RCV004360108]uncertain significance2202035404202035404Humanname
405731096CV3257839single nucleotide variantNM_003507.2(FZD7):c.530C>A (p.Thr177Asn)not specified [RCV004390012]uncertain significance2202035177202035177Humanname
405731103CV3257840single nucleotide variantNM_003507.2(FZD7):c.736A>G (p.Lys246Glu)not specified [RCV004390013]uncertain significance2202035383202035383Humanname
407485640CV3439485single nucleotide variantNM_003507.2(FZD7):c.538C>T (p.Pro180Ser)not specified [RCV004618954]uncertain significance2202035185202035185Humanname
597743085CV3676978single nucleotide variantNM_003507.2(FZD7):c.634C>T (p.Arg212Cys)not specified [RCV004921990]uncertain significance2202035281202035281Humanname
597743092CV3676980single nucleotide variantNM_003507.2(FZD7):c.361C>G (p.Arg121Gly)not specified [RCV004921991]uncertain significance2202035008202035008Humanname
597779163CV3676981single nucleotide variantNM_003507.2(FZD7):c.599G>A (p.Gly200Asp)not specified [RCV004930307]uncertain significance2202035246202035246Humanname
598244144CV3977241single nucleotide variantNM_003507.2(FZD7):c.964G>T (p.Asp322Tyr)not specified [RCV005344821]uncertain significance2202035611202035611Humanname
598244152CV3977242single nucleotide variantNM_003507.2(FZD7):c.365C>T (p.Ser122Phe)not specified [RCV005344822]uncertain significance2202035012202035012Humanname
598244159CV3977243single nucleotide variantNM_003507.2(FZD7):c.646G>C (p.Val216Leu)not specified [RCV005344823]uncertain significance2202035293202035293Humanname
598244174CV3977245single nucleotide variantNM_003507.2(FZD7):c.934C>A (p.Arg312Ser)not specified [RCV005344825]uncertain significance2202035581202035581Humanname
598244181CV3977247single nucleotide variantNM_003507.2(FZD7):c.385C>A (p.Gln129Lys)not specified [RCV005344826]uncertain significance2202035032202035032Humanname
15171744CV697252single nucleotide variantNM_003507.2(FZD7):c.587G>A (p.Gly196Glu)not provided [RCV000949888]benign2202035234202035234Humanname
8630134CV85281single nucleotide variantNM_003507.1(FZD7):c.853C>T (p.Pro285Ser)Malignant melanoma [RCV000065363]not provided2202035500202035500Humanname
155975635CV2211295single nucleotide variantNM_003507.2(FZD7):c.1715C>T (p.Thr572Ile)not specified [RCV004090227]uncertain significance2202036362202036362Humanname
156388526CV2231874single nucleotide variantNM_003507.2(FZD7):c.1127C>T (p.Ala376Val)not specified [RCV004098672]uncertain significance2202035774202035774Humanname
156206301CV2249943single nucleotide variantNM_003507.2(FZD7):c.1621G>C (p.Gly541Arg)not specified [RCV004122915]uncertain significance2202036268202036268Humanname
156121608CV2276022single nucleotide variantNM_003507.2(FZD7):c.1613T>C (p.Met538Thr)not specified [RCV004141699]uncertain significance2202036260202036260Humanname
401768754CV2716719single nucleotide variantNM_003507.2(FZD7):c.1258G>T (p.Ala420Ser)not specified [RCV004327767]uncertain significance2202035905202035905Humanname
401863851CV2773492single nucleotide variantNM_003507.2(FZD7):c.1097G>A (p.Gly366Asp)not specified [RCV004354122]uncertain significance2202035744202035744Humanname
401892574CV2782230single nucleotide variantNM_003507.2(FZD7):c.1162G>T (p.Val388Leu)not specified [RCV004359200]uncertain significance2202035809202035809Humanname
405731065CV3257835single nucleotide variantNM_003507.2(FZD7):c.1351C>T (p.Arg451Cys)not specified [RCV004390008]uncertain significance2202035998202035998Humanname
405731073CV3257836single nucleotide variantNM_003507.2(FZD7):c.1591A>G (p.Met531Val)not specified [RCV004390009]uncertain significance2202036238202036238Humanname
405731080CV3257837single nucleotide variantNM_003507.2(FZD7):c.1598A>C (p.Lys533Thr)not specified [RCV004390010]uncertain significance2202036245202036245Humanname
407485647CV3439486single nucleotide variantNM_003507.2(FZD7):c.1417G>A (p.Val473Ile)not specified [RCV004618955]uncertain significance2202036064202036064Humanname
597743098CV3676983single nucleotide variantNM_003507.2(FZD7):c.1151C>A (p.Ala384Asp)not specified [RCV004921992]uncertain significance2202035798202035798Humanname
598158693CV3977246single nucleotide variantNM_003507.2(FZD7):c.1376C>G (p.Thr459Ser)not specified [RCV005328104]uncertain significance2202036023202036023Humanname
598244187CV3977248single nucleotide variantNM_003507.2(FZD7):c.1039G>A (p.Gly347Ser)not specified [RCV005344827]uncertain significance2202035686202035686Humanname
598244194CV3977249single nucleotide variantNM_003507.2(FZD7):c.1700G>A (p.Ser567Asn)not specified [RCV005344828]uncertain significance2202036347202036347Humanname