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Variants search result for Homo sapiens
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49 records found for search term Frzb
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
15101725CV730092single nucleotide variantNM_001463.4(FRZB):c.861+6C>Anot provided [RCV000892336]likely benign2182837942182837942Humanname
8576827CV111195single nucleotide variantNM_001463.3(FRZB):c.526+5405A>GLung cancer [RCV000091718]uncertain significance2182853381182853381Humanname
405288097CV3214926single nucleotide variantNM_001463.4(FRZB):c.234C>T (p.Thr78=)FRZB-related disorder [RCV003924707]likely benign2182866319182866319Humanname , trait , alternate_id
401930202CV2819412single nucleotide variantNM_001463.4(FRZB):c.450C>A (p.Pro150=)not provided [RCV003440094]likely benign2182866103182866103Humanname
405293021CV3207125single nucleotide variantNM_001463.4(FRZB):c.450C>T (p.Pro150=)FRZB-related disorder [RCV003931535]likely benign2182866103182866103Humanname , trait , alternate_id
405273052CV3210282single nucleotide variantNM_001463.4(FRZB):c.753T>C (p.Asn251=)FRZB-related disorder [RCV003914512]likely benign2182838453182838453Humanname , trait , alternate_id
405782091CV3261203single nucleotide variantNM_001463.4(FRZB):c.76C>T (p.Arg26Trp)not specified [RCV004386952]uncertain significance2182866477182866477Humanname
13528671CV513520deletionNM_001463.4(FRZB):c.282del (p.Ile95fs)Osteoarthritis [RCV000626077]uncertain significance2182866271182866271Human2name
15189637CV697200single nucleotide variantNM_001463.4(FRZB):c.906T>C (p.Asp302=)not provided [RCV000954238]benign2182834921182834921Humanname
156085457CV2244618single nucleotide variantNM_001463.4(FRZB):c.140C>T (p.Pro47Leu)not specified [RCV004102337]uncertain significance2182866413182866413Humanname
156055170CV2388660single nucleotide variantNM_001463.4(FRZB):c.293T>C (p.Ile98Thr)not specified [RCV004239535]uncertain significance2182866260182866260Humanname
405782069CV3261199single nucleotide variantNM_001463.4(FRZB):c.115C>G (p.Arg39Gly)not specified [RCV004386948]uncertain significance2182866438182866438Humanname
405782074CV3261200single nucleotide variantNM_001463.4(FRZB):c.244C>T (p.Pro82Ser)not specified [RCV004386949]uncertain significance2182866309182866309Humanname
407495494CV3443118single nucleotide variantNM_001463.4(FRZB):c.124C>G (p.Leu42Val)not specified [RCV004621610]uncertain significance2182866429182866429Humanname
597741768CV3677351single nucleotide variantNM_001463.4(FRZB):c.272T>G (p.Met91Arg)not specified [RCV004921742]uncertain significance2182866281182866281Humanname
598158563CV3966484single nucleotide variantNM_001463.4(FRZB):c.122C>G (p.Pro41Arg)not specified [RCV005328062]uncertain significance2182866431182866431Humanname
8558553CV20259single nucleotide variantNM_001463.4(FRZB):c.970C>G (p.Arg324Gly)FRZB-related disorder [RCV003964794]|Osteoarthritis susceptibility 1 [RCV004576877]risk factor|benign2182834857182834857Human3name , trait , alternate_id
8558553CV20259single nucleotide variantNM_001463.4(FRZB):c.970C>G (p.Arg324Gly)FRZB-related disorder [RCV003964794]|Osteoarthritis susceptibility 1 [RCV004576877]risk factor|benign2182834857182834858Human3name , trait , alternate_id
8558554CV20260single nucleotide variantNM_001463.4(FRZB):c.598C>T (p.Arg200Trp)FRZB-related disorder [RCV003964795]|Osteoarthritis susceptibility 1 [RCV004576878]risk factor|benign2182838608182838608Human8name , trait , alternate_id
8558554CV20260single nucleotide variantNM_001463.4(FRZB):c.598C>T (p.Arg200Trp)FRZB-related disorder [RCV003964795]|Osteoarthritis susceptibility 1 [RCV004576878]risk factor|benign2182838608182838609Human8name , trait , alternate_id
156152387CV2265906single nucleotide variantNM_001463.4(FRZB):c.367C>T (p.Leu123Phe)not specified [RCV004126759]uncertain significance2182866186182866186Humanname
156072705CV2331532single nucleotide variantNM_001463.4(FRZB):c.791G>A (p.Arg264His)not specified [RCV004182135]uncertain significance2182838415182838415Humanname
156104005CV2352419single nucleotide variantNM_001463.4(FRZB):c.881G>A (p.Arg294His)not specified [RCV004200884]uncertain significance2182834946182834946Humanname
156069428CV2355824single nucleotide variantNM_001463.4(FRZB):c.578A>G (p.Asn193Ser)not specified [RCV004201221]uncertain significance2182842492182842492Humanname
155929250CV2369693single nucleotide variantNM_001463.4(FRZB):c.847G>A (p.Gly283Ser)not specified [RCV004215093]uncertain significance2182837962182837962Humanname
156189463CV2375564single nucleotide variantNM_001463.4(FRZB):c.787G>A (p.Glu263Lys)not specified [RCV004226057]uncertain significance2182838419182838419Humanname
329358808CV2425388single nucleotide variantNM_001463.4(FRZB):c.433G>A (p.Gly145Ser)not specified [RCV004251048]uncertain significance2182866120182866120Humanname
329353792CV2439691single nucleotide variantNM_001463.4(FRZB):c.715A>G (p.Thr239Ala)not specified [RCV004255704]uncertain significance2182838491182838491Humanname
329372514CV2443148single nucleotide variantNM_001463.4(FRZB):c.790C>T (p.Arg264Cys)not specified [RCV004255343]uncertain significance2182838416182838416Humanname
329367839CV2457130single nucleotide variantNM_001463.4(FRZB):c.815G>C (p.Gly272Ala)not specified [RCV004264906]uncertain significance2182837994182837994Humanname
401726545CV2683965single nucleotide variantNM_001463.4(FRZB):c.707A>G (p.Asn236Ser)not specified [RCV004295575]uncertain significance2182838499182838499Humanname
401781996CV2690045single nucleotide variantNM_001463.4(FRZB):c.687C>A (p.Asn229Lys)not specified [RCV004299917]uncertain significance2182838519182838519Humanname
401771744CV2722931single nucleotide variantNM_001463.4(FRZB):c.556A>G (p.Thr186Ala)not specified [RCV004327113]uncertain significance2182842514182842514Humanname
401894566CV2788442single nucleotide variantNM_001463.4(FRZB):c.593T>C (p.Val198Ala)not specified [RCV004354968]uncertain significance2182838613182838613Humanname
405782079CV3261201single nucleotide variantNM_001463.4(FRZB):c.365T>A (p.Ile122Lys)not specified [RCV004386950]uncertain significance2182866188182866188Humanname
405782085CV3261202single nucleotide variantNM_001463.4(FRZB):c.564G>T (p.Lys188Asn)not specified [RCV004386951]uncertain significance2182842506182842506Humanname
407495499CV3443119single nucleotide variantNM_001463.4(FRZB):c.752A>G (p.Asn251Ser)not specified [RCV004621611]uncertain significance2182838454182838454Humanname
597741762CV3677349single nucleotide variantNM_001463.4(FRZB):c.661G>A (p.Glu221Lys)not specified [RCV004921741]uncertain significance2182838545182838545Humanname
597769167CV3677350single nucleotide variantNM_001463.4(FRZB):c.341G>T (p.Arg114Leu)not specified [RCV004928036]uncertain significance2182866212182866212Humanname
597741773CV3677352single nucleotide variantNM_001463.4(FRZB):c.622A>G (p.Thr208Ala)not specified [RCV004921743]uncertain significance2182838584182838584Humanname
597741778CV3677353single nucleotide variantNM_001463.4(FRZB):c.463A>G (p.Thr155Ala)not specified [RCV004921744]uncertain significance2182866090182866090Humanname
597741783CV3677354single nucleotide variantNM_001463.4(FRZB):c.613G>A (p.Glu205Lys)not specified [RCV004921745]uncertain significance2182838593182838593Humanname
597741788CV3677356single nucleotide variantNM_001463.4(FRZB):c.911G>A (p.Ser304Asn)not specified [RCV004921746]uncertain significance2182834916182834916Humanname
598231798CV3966481single nucleotide variantNM_001463.4(FRZB):c.476C>T (p.Ala159Val)not specified [RCV005342474]uncertain significance2182866077182866077Humanname
598231806CV3966483single nucleotide variantNM_001463.4(FRZB):c.694C>T (p.Arg232Trp)not specified [RCV005342476]uncertain significance2182838512182838512Humanname
598231811CV3966485single nucleotide variantNM_001463.4(FRZB):c.878T>C (p.Leu293Pro)not specified [RCV005342477]uncertain significance2182834949182834949Humanname
598231816CV3966486single nucleotide variantNM_001463.4(FRZB):c.895A>G (p.Ser299Gly)not specified [RCV005342478]uncertain significance2182834932182834932Humanname
598231820CV3966487single nucleotide variantNM_001463.4(FRZB):c.807G>T (p.Leu269Phe)not specified [RCV005342479]uncertain significance2182838002182838002Humanname
15189641CV697201single nucleotide variantNM_001463.4(FRZB):c.872T>C (p.Met291Thr)not provided [RCV000954239]benign|likely benign2182834955182834955Humanname