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51 records found for search term Ddx47
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
8653693CV130268single nucleotide variantNM_016355.3(DDX47):c.181+1293C>TLung cancer [RCV000110755]uncertain significance121281551712815517Humanname
155984389CV2247758single nucleotide variantNM_016355.4(DDX47):c.13G>A (p.Glu5Lys)not specified [RCV004121228]uncertain significance121281338012813380Humanname
407458765CV3426628single nucleotide variantNM_016355.4(DDX47):c.20A>G (p.His7Arg)not specified [RCV004611674]uncertain significance121281338712813387Humanname
156245421CV2347237single nucleotide variantNM_016355.4(DDX47):c.44A>C (p.Gln15Pro)not specified [RCV004204706]uncertain significance121281341112813411Humanname
156095827CV2399002single nucleotide variantNM_016355.4(DDX47):c.185G>A (p.Arg62His)not specified [RCV004245306]uncertain significance121282121112821211Humanname
405705502CV3239908single nucleotide variantNM_016355.4(DDX47):c.229G>A (p.Ala77Thr)not specified [RCV004375855]uncertain significance121282125512821255Humanname
597805715CV3662206single nucleotide variantNM_016355.4(DDX47):c.274C>T (p.Arg92Cys)not specified [RCV004908795]uncertain significance121282130012821300Humanname
156228945CV2213132single nucleotide variantNM_016355.4(DDX47):c.904C>T (p.Arg302Cys)not specified [RCV004091669]uncertain significance121282454612824546Humanname
155930207CV2224684single nucleotide variantNM_016355.4(DDX47):c.971G>C (p.Ser324Thr)not specified [RCV004092523]uncertain significance121282461312824613Humanname
156298256CV2251932single nucleotide variantNM_016355.4(DDX47):c.820A>G (p.Asn274Asp)not specified [RCV004119902]uncertain significance121282393912823939Humanname
156070024CV2295781single nucleotide variantNM_016355.4(DDX47):c.304C>T (p.Arg102Trp)not specified [RCV004151707]uncertain significance121282133012821330Humanname
156179667CV2324280single nucleotide variantNM_016355.4(DDX47):c.595C>T (p.Arg199Trp)not specified [RCV004177008]uncertain significance121282269412822694Humanname
156325820CV2335372single nucleotide variantNM_016355.4(DDX47):c.988C>A (p.Pro330Thr)not specified [RCV004186928]uncertain significance121282463012824630Humanname
156108905CV2355436single nucleotide variantNM_016355.4(DDX47):c.894T>A (p.Ser298Arg)not specified [RCV004205290]uncertain significance121282401312824013Humanname
156344896CV2372836single nucleotide variantNM_016355.4(DDX47):c.418G>A (p.Ala140Thr)not specified [RCV004222018]uncertain significance121282170212821702Humanname
156211732CV2378325single nucleotide variantNM_016355.4(DDX47):c.680C>T (p.Ala227Val)not specified [RCV004226352]uncertain significance121282324912823249Humanname
329367573CV2427449single nucleotide variantNM_016355.4(DDX47):c.682G>A (p.Val228Ile)not specified [RCV004248299]uncertain significance121282325112823251Humanname
329361785CV2448020single nucleotide variantNM_016355.4(DDX47):c.475A>G (p.Asn159Asp)not specified [RCV004263253]uncertain significance121282199712821997Humanname
401762637CV2720005single nucleotide variantNM_016355.4(DDX47):c.854A>G (p.Asn285Ser)not specified [RCV004323585]uncertain significance121282397312823973Humanname
405705521CV3239910single nucleotide variantNM_016355.4(DDX47):c.554A>C (p.Glu185Ala)not specified [RCV004375857]uncertain significance121282207612822076Humanname
405705528CV3239911single nucleotide variantNM_016355.4(DDX47):c.622A>G (p.Met208Val)not specified [RCV004375858]uncertain significance121282272112822721Humanname
405705536CV3239912single nucleotide variantNM_016355.4(DDX47):c.829C>G (p.Gln277Glu)not specified [RCV004375859]uncertain significance121282394812823948Humanname
405705544CV3239913single nucleotide variantNM_016355.4(DDX47):c.940C>T (p.Arg314Cys)not specified [RCV004375860]uncertain significance121282458212824582Humanname
405705551CV3239914single nucleotide variantNM_016355.4(DDX47):c.952C>A (p.Leu318Ile)not specified [RCV004375861]uncertain significance121282459412824594Humanname
407458759CV3426626single nucleotide variantNM_016355.4(DDX47):c.634G>A (p.Val212Ile)not specified [RCV004611672]uncertain significance121282320312823203Humanname
407458762CV3426627single nucleotide variantNM_016355.4(DDX47):c.941G>A (p.Arg314His)not specified [RCV004611673]uncertain significance121282458312824583Humanname
597805719CV3662210single nucleotide variantNM_016355.4(DDX47):c.814A>G (p.Thr272Ala)not specified [RCV004908799]uncertain significance121282393312823933Humanname
597805720CV3662211single nucleotide variantNM_016355.4(DDX47):c.992A>G (p.His331Arg)not specified [RCV004908800]uncertain significance121282463412824634Humanname
598222645CV3956356single nucleotide variantNM_016355.4(DDX47):c.596G>A (p.Arg199Gln)not specified [RCV005317949]uncertain significance121282269512822695Humanname
598222652CV3956357single nucleotide variantNM_016355.4(DDX47):c.707A>G (p.Glu236Gly)not specified [RCV005317950]uncertain significance121282327612823276Humanname
155916161CV2197262single nucleotide variantNM_016355.4(DDX47):c.1193T>C (p.Met398Thr)not specified [RCV004079038]uncertain significance121282733212827332Humanname
156151932CV2209317single nucleotide variantNM_016355.4(DDX47):c.1140C>G (p.His380Gln)not specified [RCV004093498]uncertain significance121282727912827279Humanname
155972828CV2238862single nucleotide variantNM_016355.4(DDX47):c.1130G>A (p.Arg377His)not specified [RCV004109774]uncertain significance121282726912827269Humanname
155916266CV2281997single nucleotide variantNM_016355.4(DDX47):c.1174C>G (p.Gln392Glu)not specified [RCV004138757]uncertain significance121282731312827313Humanname
155956968CV2281998single nucleotide variantNM_016355.4(DDX47):c.1219C>G (p.Gln407Glu)not specified [RCV004138758]uncertain significance121282735812827358Humanname
155965872CV2330616single nucleotide variantNM_016355.4(DDX47):c.1339G>A (p.Gly447Arg)not specified [RCV004183211]uncertain significance121282952512829525Humanname
156193129CV2344185single nucleotide variantNM_016355.4(DDX47):c.1010A>G (p.Asn337Ser)not specified [RCV004195781]uncertain significance121282465212824652Humanname
155985568CV2344531single nucleotide variantNM_016355.4(DDX47):c.1090A>G (p.Ile364Val)not provided [RCV004695616]|not specified [RCV004195266]uncertain significance121282605412826054Humanname
401877274CV2764570single nucleotide variantNM_016355.4(DDX47):c.1274G>A (p.Arg425Gln)not specified [RCV004339125]uncertain significance121282946012829460Humanname
405705458CV3239902single nucleotide variantNM_016355.4(DDX47):c.1138C>T (p.His380Tyr)not specified [RCV004375849]uncertain significance121282727712827277Humanname
405705465CV3239903single nucleotide variantNM_016355.4(DDX47):c.1227T>G (p.Phe409Leu)not specified [RCV004375850]uncertain significance121282736612827366Humanname
405705475CV3239904single nucleotide variantNM_016355.4(DDX47):c.1232G>A (p.Arg411Gln)not specified [RCV004375851]uncertain significance121282737112827371Humanname
405705481CV3239905single nucleotide variantNM_016355.4(DDX47):c.1248G>C (p.Glu416Asp)not specified [RCV004375852]uncertain significance121282943412829434Humanname
405705487CV3239906single nucleotide variantNM_016355.4(DDX47):c.1268G>A (p.Arg423His)not specified [RCV004375853]uncertain significance121282945412829454Humanname
405705494CV3239907single nucleotide variantNM_016355.4(DDX47):c.1271C>T (p.Ser424Leu)not specified [RCV004375854]uncertain significance121282945712829457Humanname
407458753CV3426624single nucleotide variantNM_016355.4(DDX47):c.1363C>T (p.Arg455Cys)not specified [RCV004611670]uncertain significance121282954912829549Humanname
407458767CV3426629single nucleotide variantNM_016355.4(DDX47):c.1262A>G (p.Lys421Arg)not specified [RCV004611675]uncertain significance121282944812829448Humanname
597805716CV3662207single nucleotide variantNM_016355.4(DDX47):c.1196T>C (p.Leu399Pro)not specified [RCV004908796]uncertain significance121282733512827335Humanname
597805717CV3662208single nucleotide variantNM_016355.4(DDX47):c.1224G>T (p.Arg408Ser)not specified [RCV004908797]uncertain significance121282736312827363Humanname
597805718CV3662209single nucleotide variantNM_016355.4(DDX47):c.1072G>A (p.Gly358Arg)not specified [RCV004908798]uncertain significance121282603612826036Humanname
40814759CV969994single nucleotide variantNM_016355.4(DDX47):c.1129C>A (p.Arg377Ser)Intellectual disability [RCV001261391]uncertain significance121282726812827268Human2name