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30 records found for search term Klf12
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
8583159CV117719single nucleotide variantNM_007249.4(KLF12):c.33+11669A>CLung cancer [RCV000098240]uncertain significance137398332173983321Humanname
598182267CV3976594single nucleotide variantNM_001400136.1(KLF12):c.26C>T (p.Thr9Ile)not specified [RCV005352706]uncertain significance137399499773994997Humanname
401873346CV2776498single nucleotide variantNM_001400136.1(KLF12):c.89G>T (p.Arg30Ile)not specified [RCV004355601]uncertain significance137394401573944015Humanname
405807516CV3265521single nucleotide variantNM_001400136.1(KLF12):c.53A>G (p.Asn18Ser)not specified [RCV004406592]uncertain significance137394405173944051Humanname
597638997CV3692105single nucleotide variantNM_001400136.1(KLF12):c.65T>C (p.Met22Thr)not specified [RCV004941269]uncertain significance137394403973944039Humanname
401891275CV2774936single nucleotide variantNM_001400136.1(KLF12):c.120A>C (p.Gln40His)not specified [RCV004346343]uncertain significance137394398473943984Humanname
401873100CV2776430single nucleotide variantNM_001400136.1(KLF12):c.190G>A (p.Glu64Lys)not specified [RCV004355551]uncertain significance137384630773846307Humanname
598161062CV3976598single nucleotide variantNM_001400136.1(KLF12):c.140A>T (p.Asn47Ile)not specified [RCV005368362]uncertain significance137384635773846357Humanname
156225085CV2203020single nucleotide variantNM_001400136.1(KLF12):c.944G>A (p.Arg315His)not specified [RCV004069273]uncertain significance137371545173715451Humanname
156131964CV2235280single nucleotide variantNM_001400136.1(KLF12):c.740A>G (p.Asn247Ser)not specified [RCV004107320]uncertain significance137381321873813218Humanname
156186629CV2236241single nucleotide variantNM_001400136.1(KLF12):c.371C>T (p.Ala124Val)not specified [RCV004107943]uncertain significance137384612673846126Humanname
156019231CV2272550single nucleotide variantNM_001400136.1(KLF12):c.497C>G (p.Pro166Arg)not specified [RCV004133447]uncertain significance137384600073846000Humanname
155906930CV2279570single nucleotide variantNM_001400136.1(KLF12):c.688G>A (p.Gly230Ser)not specified [RCV004142074]uncertain significance137381327073813270Humanname
156193770CV2321986single nucleotide variantNM_001400136.1(KLF12):c.356C>T (p.Ser119Phe)not specified [RCV004173744]uncertain significance137384614173846141Humanname
329388203CV2468759single nucleotide variantNM_001400136.1(KLF12):c.922T>C (p.Ser308Pro)not specified [RCV004280079]uncertain significance137371547373715473Humanname
405807510CV3265518single nucleotide variantNM_001400136.1(KLF12):c.364C>T (p.Arg122Cys)not specified [RCV004406589]uncertain significance137384613373846133Humanname
405807512CV3265519single nucleotide variantNM_001400136.1(KLF12):c.418T>A (p.Ser140Thr)not specified [RCV004406590]uncertain significance137384607973846079Humanname
405807514CV3265520single nucleotide variantNM_001400136.1(KLF12):c.424G>A (p.Val142Ile)not specified [RCV004406591]uncertain significance137384607373846073Humanname
405807518CV3265522single nucleotide variantNM_001400136.1(KLF12):c.745A>T (p.Thr249Ser)not specified [RCV004406593]uncertain significance137381321373813213Humanname
405807520CV3265523single nucleotide variantNM_001400136.1(KLF12):c.913C>T (p.Arg305Trp)not specified [RCV004406594]uncertain significance137371548273715482Humanname
597638987CV3692103single nucleotide variantNM_001400136.1(KLF12):c.562G>A (p.Val188Met)not specified [RCV004941267]uncertain significance137384593573845935Humanname
597639001CV3692107single nucleotide variantNM_001400136.1(KLF12):c.628A>G (p.Ile210Val)not specified [RCV004941270]uncertain significance137384586973845869Humanname
597639648CV3692108single nucleotide variantNM_001400136.1(KLF12):c.703C>A (p.Gln235Lys)not specified [RCV004941271]uncertain significance137381325573813255Humanname
597639642CV3692109single nucleotide variantNM_001400136.1(KLF12):c.634G>C (p.Val212Leu)not specified [RCV004941272]uncertain significance137384586373845863Humanname
598182261CV3976593single nucleotide variantNM_001400136.1(KLF12):c.700A>G (p.Arg234Gly)not specified [RCV005352705]uncertain significance137381325873813258Humanname
598161057CV3976595single nucleotide variantNM_001400136.1(KLF12):c.572A>C (p.Gln191Pro)not specified [RCV005368361]uncertain significance137384592573845925Humanname
598182272CV3976596single nucleotide variantNM_001400136.1(KLF12):c.329C>T (p.Pro110Leu)not specified [RCV005352707]uncertain significance137384616873846168Humanname
598182277CV3976597single nucleotide variantNM_001400136.1(KLF12):c.620A>G (p.Asn207Ser)not specified [RCV005352708]uncertain significance137384587773845877Humanname
407501021CV3495562single nucleotide variantNM_001400136.1(KLF12):c.1085A>G (p.Asp362Gly)not provided [RCV004697402]uncertain significance137369561473695614Humanname
597638991CV3692104single nucleotide variantNM_001400136.1(KLF12):c.1138G>A (p.Ala380Thr)not specified [RCV004941268]uncertain significance137369556173695561Humanname