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50 records found for search term Dclk2
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
407458126CV3430318single nucleotide variantNM_001040260.4(DCLK2):c.961+955A>Gnot specified [RCV004611419]uncertain significance4150199058150199058Humanname
598262297CV3963694single nucleotide variantNM_001040260.4(DCLK2):c.961+967A>Gnot specified [RCV005325355]likely benign4150199070150199070Humanname
8579291CV113689single nucleotide variantNM_001040260.3(DCLK2):c.421+3197G>ALung cancer [RCV000094212]uncertain significance4150082645150082645Humanname
401923530CV2820204single nucleotide variantNM_001040260.4(DCLK2):c.63G>C (p.Pro21=)not provided [RCV003435179]likely benign4150079090150079090Humanname
401730327CV2680103single nucleotide variantNM_001040260.4(DCLK2):c.14G>A (p.Arg5Lys)not specified [RCV004286593]uncertain significance4150079041150079041Humanname
401755961CV2686183single nucleotide variantNM_001040260.4(DCLK2):c.44G>C (p.Arg15Pro)not specified [RCV004297280]uncertain significance4150079071150079071Humanname
156262353CV2201087single nucleotide variantNM_001040260.4(DCLK2):c.136C>A (p.Pro46Thr)not specified [RCV004075210]uncertain significance4150079163150079163Humanname
155987769CV2251154single nucleotide variantNM_001040260.4(DCLK2):c.297C>G (p.Phe99Leu)not specified [RCV004115388]uncertain significance4150079324150079324Humanname
401923532CV2820205single nucleotide variantNM_001040260.4(DCLK2):c.2193T>C (p.Pro731=)not provided [RCV003435180]likely benign4150256139150256139Humanname
401944759CV2840518single nucleotide variantNM_001040260.4(DCLK2):c.1302A>G (p.Glu434=)not provided [RCV003457423]likely benign4150232339150232339Humanname
598262309CV3963696single nucleotide variantNM_001040260.4(DCLK2):c.146C>A (p.Ala49Glu)not specified [RCV005325357]uncertain significance4150079173150079173Humanname
8631044CV86200single nucleotide variantNM_001040260.3(DCLK2):c.1869T>C (p.Ser623=)Malignant melanoma [RCV000066291]not provided4150247693150247693Humanname
156040482CV2261298single nucleotide variantNM_001040260.4(DCLK2):c.988T>C (p.Ser330Pro)not specified [RCV004128161]uncertain significance4150203821150203821Humanname
156150202CV2289629single nucleotide variantNM_001040260.4(DCLK2):c.797T>G (p.Phe266Cys)not specified [RCV004148547]uncertain significance4150193178150193178Humanname
156289153CV2309657single nucleotide variantNM_001040260.4(DCLK2):c.718G>A (p.Gly240Arg)not specified [RCV004160802]uncertain significance4150102774150102774Humanname
155968734CV2337873single nucleotide variantNM_001040260.4(DCLK2):c.350C>T (p.Pro117Leu)not specified [RCV004183883]uncertain significance4150079377150079377Humanname
401863187CV2771966single nucleotide variantNM_001040260.4(DCLK2):c.941G>A (p.Arg314His)not specified [RCV004344656]uncertain significance4150198083150198083Humanname
401888153CV2791293single nucleotide variantNM_001040260.4(DCLK2):c.940C>A (p.Arg314Ser)not specified [RCV004356918]uncertain significance4150198082150198082Humanname
405691093CV3246759single nucleotide variantNM_001040260.4(DCLK2):c.300T>G (p.Asp100Glu)not specified [RCV004373329]uncertain significance4150079327150079327Humanname
405691098CV3246760single nucleotide variantNM_001040260.4(DCLK2):c.724G>A (p.Val242Ile)not specified [RCV004373330]uncertain significance4150102780150102780Humanname
405691102CV3246761single nucleotide variantNM_001040260.4(DCLK2):c.805T>C (p.Cys269Arg)not specified [RCV004373331]uncertain significance4150193186150193186Humanname
405691108CV3246762single nucleotide variantNM_001040260.4(DCLK2):c.833A>G (p.Gln278Arg)not specified [RCV004373332]uncertain significance4150193214150193214Humanname
407458127CV3430319single nucleotide variantNM_001040260.4(DCLK2):c.408C>G (p.Asp136Glu)not specified [RCV004611420]uncertain significance4150079435150079435Humanname
598262319CV3963698single nucleotide variantNM_001040260.4(DCLK2):c.458G>T (p.Arg153Leu)not specified [RCV005325359]uncertain significance4150102514150102514Humanname
156374576CV2194655single nucleotide variantNM_001040260.4(DCLK2):c.1531A>G (p.Ile511Val)not specified [RCV004082058]uncertain significance4150232793150232793Humanname
156314263CV2196618single nucleotide variantNM_001040260.4(DCLK2):c.2203G>A (p.Val735Ile)not specified [RCV004073888]uncertain significance4150256149150256149Humanname
155950476CV2267861single nucleotide variantNM_001040260.4(DCLK2):c.1858A>G (p.Ile620Val)not specified [RCV004136158]uncertain significance4150247682150247682Humanname
156303060CV2308181single nucleotide variantNM_001040260.4(DCLK2):c.2294G>A (p.Arg765Gln)not specified [RCV004164687]uncertain significance4150256240150256240Humanname
156137886CV2354488single nucleotide variantNM_001040260.4(DCLK2):c.1502A>G (p.Asn501Ser)not specified [RCV004202475]uncertain significance4150232764150232764Humanname
401719779CV2675680single nucleotide variantNM_001040260.4(DCLK2):c.2068A>G (p.Ile690Val)not specified [RCV004287931]uncertain significance4150249679150249679Humanname
401776075CV2692592single nucleotide variantNM_001040260.4(DCLK2):c.2284C>T (p.Arg762Cys)not specified [RCV004312329]uncertain significance4150256230150256230Humanname
401731176CV2693650single nucleotide variantNM_001040260.4(DCLK2):c.1236A>G (p.Ile412Met)not specified [RCV004297987]likely benign4150221780150221780Humanname
401759008CV2705321single nucleotide variantNM_001040260.4(DCLK2):c.1243T>G (p.Ser415Ala)not specified [RCV004312004]uncertain significance4150224502150224502Humanname
401856782CV2761779single nucleotide variantNM_001040260.4(DCLK2):c.2207C>T (p.Pro736Leu)not specified [RCV004339430]likely benign4150256153150256153Humanname
401899022CV2785953single nucleotide variantNM_001040260.4(DCLK2):c.1816T>G (p.Leu606Val)not specified [RCV004359797]uncertain significance4150247640150247640Humanname
401870750CV2792493single nucleotide variantNM_001040260.4(DCLK2):c.1577A>T (p.Tyr526Phe)not specified [RCV004363229]uncertain significance4150239752150239752Humanname
405691067CV3246755single nucleotide variantNM_001040260.4(DCLK2):c.1042T>C (p.Phe348Leu)not specified [RCV004373325]uncertain significance4150203875150203875Humanname
405691074CV3246756single nucleotide variantNM_001040260.4(DCLK2):c.1261G>T (p.Ala421Ser)not specified [RCV004373326]uncertain significance4150224520150224520Humanname
405691080CV3246757single nucleotide variantNM_001040260.4(DCLK2):c.1451C>T (p.Ser484Leu)not specified [RCV004373327]uncertain significance4150232713150232713Humanname
405691087CV3246758single nucleotide variantNM_001040260.4(DCLK2):c.1970A>G (p.Gln657Arg)not specified [RCV004373328]uncertain significance4150249581150249581Humanname
407458122CV3430317single nucleotide variantNM_001040260.4(DCLK2):c.1096G>A (p.Gly366Ser)not specified [RCV004611418]uncertain significance4150220742150220742Humanname
407458130CV3430320single nucleotide variantNM_001040260.4(DCLK2):c.2018T>G (p.Phe673Cys)not specified [RCV004611421]uncertain significance4150249629150249629Humanname
597800931CV3652113single nucleotide variantNM_001040260.4(DCLK2):c.2263G>A (p.Gly755Ser)not specified [RCV004905971]uncertain significance4150256209150256209Humanname
598262282CV3963691single nucleotide variantNM_001040260.4(DCLK2):c.2027C>T (p.Ala676Val)not specified [RCV005325352]uncertain significance4150249638150249638Humanname
598262286CV3963692single nucleotide variantNM_001040260.4(DCLK2):c.1360A>T (p.Met454Leu)not specified [RCV005325353]uncertain significance4150232397150232397Humanname
598262293CV3963693single nucleotide variantNM_001040260.4(DCLK2):c.1591A>C (p.Lys531Gln)not specified [RCV005325354]uncertain significance4150239766150239766Humanname
598262303CV3963695single nucleotide variantNM_001040260.4(DCLK2):c.1123A>C (p.Ser375Arg)not specified [RCV005325356]uncertain significance4150220769150220769Humanname
598262314CV3963697single nucleotide variantNM_001040260.4(DCLK2):c.1943A>G (p.His648Arg)not specified [RCV005325358]uncertain significance4150248372150248372Humanname
598262325CV3963699single nucleotide variantNM_001040260.4(DCLK2):c.2285G>A (p.Arg762His)not specified [RCV005325360]uncertain significance4150256231150256231Humanname
598262329CV3963700single nucleotide variantNM_001040260.4(DCLK2):c.1081T>C (p.Ser361Pro)not specified [RCV005325361]uncertain significance4150220727150220727Humanname