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Variants search result for Homo sapiens
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37 records found for search term Klhl23
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
156273542CV2320193single nucleotide variantNM_144711.6(KLHL23):c.49A>G (p.Thr17Ala)not specified [RCV004169816]likely benign2169735063169735063Humanname
407481496CV3448541single nucleotide variantNM_144711.6(KLHL23):c.70G>A (p.Asp24Asn)not specified [RCV004644112]uncertain significance2169735084169735084Humanname
156296388CV2310406single nucleotide variantNM_144711.6(KLHL23):c.158C>T (p.Ala53Val)not specified [RCV004163447]uncertain significance2169735172169735172Humanname
405813344CV3265807single nucleotide variantNM_144711.6(KLHL23):c.160G>A (p.Val54Ile)not specified [RCV004409356]uncertain significance2169735174169735174Humanname
597640069CV3692368single nucleotide variantNM_144711.6(KLHL23):c.218A>C (p.Lys73Thr)not specified [RCV004941464]uncertain significance2169735232169735232Humanname
597640082CV3692370single nucleotide variantNM_144711.6(KLHL23):c.189G>T (p.Lys63Asn)not specified [RCV004941466]uncertain significance2169735203169735203Humanname
156218321CV2253940single nucleotide variantNM_144711.6(KLHL23):c.887C>T (p.Thr296Ile)not specified [RCV004127615]uncertain significance2169735901169735901Humanname
155929251CV2278032single nucleotide variantNM_144711.6(KLHL23):c.991G>A (p.Asp331Asn)not specified [RCV004141259]uncertain significance2169736005169736005Humanname
155985283CV2345073single nucleotide variantNM_144711.6(KLHL23):c.650A>G (p.Glu217Gly)not specified [RCV004193351]uncertain significance2169735664169735664Humanname
405813346CV3265808single nucleotide variantNM_144711.6(KLHL23):c.556A>G (p.Ile186Val)not specified [RCV004409357]uncertain significance2169735570169735570Humanname
405813348CV3276122single nucleotide variantNM_144711.6(KLHL23):c.727A>G (p.Arg243Gly)not specified [RCV004409358]uncertain significance2169735741169735741Humanname
405813350CV3276123single nucleotide variantNM_144711.6(KLHL23):c.798G>T (p.Glu266Asp)not specified [RCV004409359]uncertain significance2169735812169735812Humanname
407481485CV3448539single nucleotide variantNM_144711.6(KLHL23):c.647T>C (p.Ile216Thr)not specified [RCV004644110]uncertain significance2169735661169735661Humanname
407481500CV3448542single nucleotide variantNM_144711.6(KLHL23):c.431C>G (p.Ser144Cys)not specified [RCV004644113]uncertain significance2169735445169735445Humanname
407481505CV3448544single nucleotide variantNM_144711.6(KLHL23):c.881C>A (p.Pro294His)not specified [RCV004644114]uncertain significance2169735895169735895Humanname
597640062CV3692367single nucleotide variantNM_144711.6(KLHL23):c.314G>T (p.Arg105Ile)not specified [RCV004941463]uncertain significance2169735328169735328Humanname
597640076CV3692369single nucleotide variantNM_144711.6(KLHL23):c.588A>C (p.Lys196Asn)not specified [RCV004941465]uncertain significance2169735602169735602Humanname
598182787CV3987326single nucleotide variantNM_144711.6(KLHL23):c.902A>G (p.Gln301Arg)not specified [RCV005352791]uncertain significance2169735916169735916Humanname
598161542CV3987327single nucleotide variantNM_144711.6(KLHL23):c.301G>A (p.Glu101Lys)not specified [RCV005368455]uncertain significance2169735315169735315Humanname
598161547CV3987332single nucleotide variantNM_144711.6(KLHL23):c.674A>G (p.Tyr225Cys)not specified [RCV005368456]uncertain significance2169735688169735688Humanname
15179995CV707845single nucleotide variantNM_144711.6(KLHL23):c.791A>G (p.His264Arg)not provided [RCV000974044]benign2169735805169735805Humanname
156086243CV2390797single nucleotide variantNM_144711.6(KLHL23):c.1673T>A (p.Val558Asp)not specified [RCV004241080]uncertain significance2169749728169749728Humanname
156263406CV2391699single nucleotide variantNM_144711.6(KLHL23):c.1565C>T (p.Thr522Met)not specified [RCV004241854]uncertain significance2169749620169749620Humanname
329367371CV2427380single nucleotide variantNM_144711.6(KLHL23):c.1457A>C (p.Asn486Thr)not specified [RCV004248236]uncertain significance2169749512169749512Humanname
401883500CV2757945single nucleotide variantNM_144711.6(KLHL23):c.1195A>G (p.Ile399Val)not specified [RCV004337079]uncertain significance2169736209169736209Humanname
401868661CV2767302single nucleotide variantNM_144711.6(KLHL23):c.1504G>A (p.Gly502Ser)not specified [RCV004349470]uncertain significance2169749559169749559Humanname
401862761CV2778997single nucleotide variantNM_144711.6(KLHL23):c.1492A>G (p.Arg498Gly)not specified [RCV004348651]uncertain significance2169749547169749547Humanname
405813337CV3265804single nucleotide variantNM_144711.6(KLHL23):c.1340G>A (p.Ser447Asn)not specified [RCV004409353]uncertain significance2169741511169741511Humanname
405813339CV3265805single nucleotide variantNM_144711.6(KLHL23):c.1459G>C (p.Glu487Gln)not specified [RCV004409354]uncertain significance2169749514169749514Humanname
405813341CV3265806single nucleotide variantNM_144711.6(KLHL23):c.1579A>G (p.Ile527Val)not specified [RCV004409355]uncertain significance2169749634169749634Humanname
407481490CV3448540single nucleotide variantNM_144711.6(KLHL23):c.1405T>A (p.Tyr469Asn)not specified [RCV004644111]uncertain significance2169749460169749460Humanname
407481511CV3448545single nucleotide variantNM_144711.6(KLHL23):c.1333G>A (p.Glu445Lys)not specified [RCV004644115]uncertain significance2169741504169741504Humanname
407481514CV3448546single nucleotide variantNM_144711.6(KLHL23):c.1598A>G (p.Asp533Gly)not specified [RCV004644116]uncertain significance2169749653169749653Humanname
598221122CV3987330single nucleotide variantNM_144711.6(KLHL23):c.1141G>A (p.Ala381Thr)not specified [RCV005360763]uncertain significance2169736155169736155Humanname
598221130CV3987331single nucleotide variantNM_144711.6(KLHL23):c.1396A>C (p.Asn466His)not specified [RCV005360764]uncertain significance2169749451169749451Humanname
598182794CV3987333single nucleotide variantNM_144711.6(KLHL23):c.1100T>G (p.Leu367Trp)not specified [RCV005352792]uncertain significance2169736114169736114Humanname
598221138CV3987334single nucleotide variantNM_144711.6(KLHL23):c.1498G>A (p.Glu500Lys)not specified [RCV005360765]uncertain significance2169749553169749553Humanname