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Variants search result for Homo sapiens
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43 records found for search term Zfpl1
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
8634286CV89506single nucleotide variantNM_006782.3(ZFPL1):c.214+63C>TMalignant melanoma [RCV000069603]not provided116508528965085289Humanname
156255987CV2194544single nucleotide variantNM_006782.4(ZFPL1):c.92A>G (p.Asn31Ser)not specified [RCV004081607]uncertain significance116508479065084790Humanname
405669346CV3360353single nucleotide variantNM_006782.4(ZFPL1):c.92A>T (p.Asn31Ile)not specified [RCV004486160]uncertain significance116508479065084790Humanname
155908173CV2387244single nucleotide variantNM_006782.4(ZFPL1):c.161G>A (p.Arg54His)not specified [RCV004238340]uncertain significance116508517365085173Humanname
401751736CV2702871single nucleotide variantNM_006782.4(ZFPL1):c.280G>A (p.Gly94Ser)not specified [RCV004321211]uncertain significance116508648065086480Humanname
405669308CV3360345single nucleotide variantNM_006782.4(ZFPL1):c.190G>C (p.Glu64Gln)not specified [RCV004486152]uncertain significance116508520265085202Humanname
405669313CV3360346single nucleotide variantNM_006782.4(ZFPL1):c.245G>A (p.Arg82His)not specified [RCV004486153]uncertain significance116508644565086445Humanname
407458052CV3490178single nucleotide variantNM_006782.4(ZFPL1):c.155A>G (p.Asn52Ser)not specified [RCV004686557]uncertain significance116508516765085167Humanname
407458065CV3490182single nucleotide variantNM_006782.4(ZFPL1):c.200G>A (p.Arg67His)not specified [RCV004686561]uncertain significance116508521265085212Humanname
597794444CV3628175single nucleotide variantNM_006782.4(ZFPL1):c.269C>T (p.Thr90Met)not specified [RCV004877652]uncertain significance116508646965086469Humanname
597794455CV3628180single nucleotide variantNM_006782.4(ZFPL1):c.263G>A (p.Arg88Gln)not specified [RCV004877656]uncertain significance116508646365086463Humanname
597800241CV3628182single nucleotide variantNM_006782.4(ZFPL1):c.223C>T (p.His75Tyr)not specified [RCV004880138]uncertain significance116508642365086423Humanname
598259698CV3937740single nucleotide variantNM_006782.4(ZFPL1):c.244C>T (p.Arg82Cys)not specified [RCV005300279]uncertain significance116508644465086444Humanname
156374809CV2194852single nucleotide variantNM_006782.4(ZFPL1):c.917G>A (p.Arg306His)not specified [RCV004075386]uncertain significance116508809865088098Humanname
156035325CV2246732single nucleotide variantNM_006782.4(ZFPL1):c.445A>G (p.Asn149Asp)not specified [RCV004112274]uncertain significance116508675665086756Humanname
156212600CV2259972single nucleotide variantNM_006782.4(ZFPL1):c.686A>G (p.Asp229Gly)not specified [RCV004118992]uncertain significance116508737365087373Humanname
156028422CV2278529single nucleotide variantNM_006782.4(ZFPL1):c.323C>G (p.Thr108Ser)not specified [RCV004132964]uncertain significance116508652365086523Humanname
156274002CV2283951single nucleotide variantNM_006782.4(ZFPL1):c.608A>G (p.Asn203Ser)not specified [RCV004144262]likely benign116508705465087054Humanname
156070091CV2316876single nucleotide variantNM_006782.4(ZFPL1):c.548C>A (p.Ala183Asp)not specified [RCV004174402]uncertain significance116508699465086994Humanname
156341045CV2348150single nucleotide variantNM_006782.4(ZFPL1):c.713G>A (p.Arg238Gln)not specified [RCV004197823]uncertain significance116508740065087400Humanname
156343927CV2364193single nucleotide variantNM_006782.4(ZFPL1):c.773C>T (p.Pro258Leu)not specified [RCV004223432]uncertain significance116508795465087954Humanname
156159067CV2398082single nucleotide variantNM_006782.4(ZFPL1):c.386G>A (p.Arg129Gln)not specified [RCV004241669]uncertain significance116508658665086586Humanname
401725240CV2726053single nucleotide variantNM_006782.4(ZFPL1):c.569C>T (p.Pro190Leu)not specified [RCV004324410]uncertain significance116508701565087015Humanname
401874559CV2781047single nucleotide variantNM_006782.4(ZFPL1):c.392G>T (p.Gly131Val)not specified [RCV004358431]uncertain significance116508659265086592Humanname
405669329CV3360349single nucleotide variantNM_006782.4(ZFPL1):c.764G>A (p.Arg255Gln)not specified [RCV004486156]uncertain significance116508794565087945Humanname
405669331CV3360350single nucleotide variantNM_006782.4(ZFPL1):c.790C>T (p.Arg264Trp)not specified [RCV004486157]uncertain significance116508797165087971Humanname
405669338CV3360351single nucleotide variantNM_006782.4(ZFPL1):c.791G>A (p.Arg264Gln)not specified [RCV004486158]uncertain significance116508797265087972Humanname
405669342CV3360352single nucleotide variantNM_006782.4(ZFPL1):c.863G>A (p.Arg288Gln)not specified [RCV004486159]uncertain significance116508804465088044Humanname
407458056CV3490179single nucleotide variantNM_006782.4(ZFPL1):c.646G>A (p.Asp216Asn)not specified [RCV004686558]uncertain significance116508733365087333Humanname
407458058CV3490180single nucleotide variantNM_006782.4(ZFPL1):c.862C>T (p.Arg288Trp)not specified [RCV004686559]uncertain significance116508804365088043Humanname
407458061CV3490181single nucleotide variantNM_006782.4(ZFPL1):c.770G>T (p.Arg257Leu)not specified [RCV004686560]uncertain significance116508795165087951Humanname
597794447CV3628176single nucleotide variantNM_006782.4(ZFPL1):c.710G>A (p.Arg237His)not specified [RCV004877653]uncertain significance116508739765087397Humanname
597726253CV3628177single nucleotide variantNM_006782.4(ZFPL1):c.868G>A (p.Ala290Thr)not specified [RCV004888380]uncertain significance116508804965088049Humanname
597794450CV3628178single nucleotide variantNM_006782.4(ZFPL1):c.575G>A (p.Arg192Gln)not specified [RCV004877654]uncertain significance116508702165087021Humanname
597794453CV3628179single nucleotide variantNM_006782.4(ZFPL1):c.449C>T (p.Thr150Met)not specified [RCV004877655]uncertain significance116508676065086760Humanname
598259694CV3937739single nucleotide variantNM_006782.4(ZFPL1):c.868G>T (p.Ala290Ser)not specified [RCV005300278]uncertain significance116508804965088049Humanname
598259702CV3937741single nucleotide variantNM_006782.4(ZFPL1):c.556C>T (p.Pro186Ser)not specified [RCV005300280]uncertain significance116508700265087002Humanname
598259707CV3937742single nucleotide variantNM_006782.4(ZFPL1):c.769C>G (p.Arg257Gly)not specified [RCV005300281]uncertain significance116508795065087950Humanname
598259712CV3937743single nucleotide variantNM_006782.4(ZFPL1):c.541A>G (p.Ser181Gly)not specified [RCV005300282]uncertain significance116508698765086987Humanname
598259717CV3937744single nucleotide variantNM_006782.4(ZFPL1):c.789G>C (p.Gln263His)not specified [RCV005300283]uncertain significance116508797065087970Humanname
598259722CV3937745single nucleotide variantNM_006782.4(ZFPL1):c.316C>T (p.Pro106Ser)not specified [RCV005300284]uncertain significance116508651665086516Humanname
598159021CV3937747single nucleotide variantNM_006782.4(ZFPL1):c.406C>A (p.Leu136Met)not specified [RCV005306470]uncertain significance116508660665086606Humanname
8634287CV89507single nucleotide variantNM_006782.3(ZFPL1):c.439C>T (p.Pro147Ser)Malignant melanoma [RCV000069604]not provided116508675065086750Humanname