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54 records found for search term Ddx20
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
155921408CV2340448single nucleotide variantNM_007204.5(DDX20):c.5C>G (p.Ala2Gly)not specified [RCV004197175]uncertain significance1111755929111755929Humanname
156250561CV2394228single nucleotide variantNM_007204.5(DDX20):c.19G>T (p.Ala7Ser)not specified [RCV004238465]uncertain significance1111755943111755943Humanname
156273429CV2323663single nucleotide variantNM_007204.5(DDX20):c.37G>A (p.Ala13Thr)not specified [RCV004165845]likely benign1111755961111755961Humanname
405704518CV3243672single nucleotide variantNM_007204.5(DDX20):c.35C>T (p.Ala12Val)not specified [RCV004375728]uncertain significance1111755959111755959Humanname
405704529CV3243673single nucleotide variantNM_007204.5(DDX20):c.52A>C (p.Met18Leu)not specified [RCV004375729]uncertain significance1111755976111755976Humanname
598226073CV3894337single nucleotide variantNM_007204.5(DDX20):c.501A>G (p.Gly167=)not provided [RCV005257580]likely benign1111759504111759504Humanname
155995382CV2375813single nucleotide variantNM_007204.5(DDX20):c.182C>T (p.Pro61Leu)not specified [RCV004224396]uncertain significance1111756106111756106Humanname
156194823CV2399200single nucleotide variantNM_007204.5(DDX20):c.181C>T (p.Pro61Ser)not specified [RCV004246628]uncertain significance1111756105111756105Humanname
401859322CV2771531single nucleotide variantNM_007204.5(DDX20):c.252G>C (p.Arg84Ser)not specified [RCV004348561]uncertain significance1111756176111756176Humanname
405704510CV3243671single nucleotide variantNM_007204.5(DDX20):c.272A>T (p.Lys91Met)not specified [RCV004375727]uncertain significance1111756196111756196Humanname
598263251CV3960037single nucleotide variantNM_007204.5(DDX20):c.2370C>T (p.Ala790=)not specified [RCV005325634]likely benign1111766794111766794Humanname
155989171CV2251291single nucleotide variantNM_007204.5(DDX20):c.818T>A (p.Leu273His)not specified [RCV004115504]uncertain significance1111760843111760843Humanname
156093370CV2300216single nucleotide variantNM_007204.5(DDX20):c.341G>C (p.Cys114Ser)not specified [RCV004151401]uncertain significance1111756685111756685Humanname
156346142CV2300443single nucleotide variantNM_007204.5(DDX20):c.376C>G (p.Leu126Val)not specified [RCV004153638]uncertain significance1111756720111756720Humanname
156159572CV2314621single nucleotide variantNM_007204.5(DDX20):c.604C>G (p.Pro202Ala)not specified [RCV004168702]uncertain significance1111760512111760512Humanname
156055818CV2326613single nucleotide variantNM_007204.5(DDX20):c.790G>A (p.Val264Ile)not specified [RCV004183153]uncertain significance1111760815111760815Humanname
401743377CV2687936single nucleotide variantNM_007204.5(DDX20):c.379G>A (p.Glu127Lys)not specified [RCV004305024]uncertain significance1111756723111756723Humanname
401894864CV2781940single nucleotide variantNM_007204.5(DDX20):c.844G>A (p.Val282Ile)not specified [RCV004357177]likely benign1111761007111761007Humanname
405704535CV3243674single nucleotide variantNM_007204.5(DDX20):c.986T>C (p.Leu329Pro)not specified [RCV004375730]uncertain significance1111761249111761249Humanname
407458503CV3426561single nucleotide variantNM_007204.5(DDX20):c.913A>G (p.Ser305Gly)not specified [RCV004611607]uncertain significance1111761076111761076Humanname
597805656CV3662039single nucleotide variantNM_007204.5(DDX20):c.895C>A (p.His299Asn)not specified [RCV004908708]uncertain significance1111761058111761058Humanname
597805657CV3662040single nucleotide variantNM_007204.5(DDX20):c.633T>A (p.Asp211Glu)not specified [RCV004908709]uncertain significance1111760541111760541Humanname
15112733CV718094single nucleotide variantNM_007204.5(DDX20):c.410C>G (p.Ala137Gly)not provided [RCV000894527]likely benign1111759413111759413Humanname
156033219CV2214621single nucleotide variantNM_007204.5(DDX20):c.2377C>T (p.His793Tyr)not specified [RCV004090454]uncertain significance1111766801111766801Humanname
156327751CV2217349single nucleotide variantNM_007204.5(DDX20):c.1813G>C (p.Gly605Arg)not specified [RCV004087785]uncertain significance1111766237111766237Humanname
155988772CV2251246single nucleotide variantNM_007204.5(DDX20):c.1007C>A (p.Ala336Asp)not specified [RCV004115467]uncertain significance1111761270111761270Humanname
156299610CV2326116single nucleotide variantNM_007204.5(DDX20):c.1631A>C (p.Glu544Ala)not specified [RCV004180395]uncertain significance1111766055111766055Humanname
156134273CV2346986single nucleotide variantNM_007204.5(DDX20):c.1043G>A (p.Arg348His)not specified [RCV004202430]uncertain significance1111762276111762276Humanname
156186635CV2377997single nucleotide variantNM_007204.5(DDX20):c.1310C>T (p.Pro437Leu)not specified [RCV004230556]uncertain significance1111763005111763005Humanname
329372946CV2428719single nucleotide variantNM_007204.5(DDX20):c.2371G>A (p.Ala791Thr)not specified [RCV004255509]uncertain significance1111766795111766795Humanname
329380522CV2444434single nucleotide variantNM_007204.5(DDX20):c.1207T>G (p.Phe403Val)not specified [RCV004263172]uncertain significance1111762779111762779Humanname
329382885CV2445638single nucleotide variantNM_007204.5(DDX20):c.1184A>G (p.His395Arg)not specified [RCV004259720]uncertain significance1111762756111762756Humanname
329370431CV2461715single nucleotide variantNM_007204.5(DDX20):c.2004A>C (p.Lys668Asn)not specified [RCV004269867]uncertain significance1111766428111766428Humanname
401751425CV2672448single nucleotide variantNM_007204.5(DDX20):c.1597C>T (p.Pro533Ser)not specified [RCV004285702]uncertain significance1111766021111766021Humanname
401782197CV2686585single nucleotide variantNM_007204.5(DDX20):c.1902A>T (p.Lys634Asn)not specified [RCV004300013]uncertain significance1111766326111766326Humanname
401776583CV2703286single nucleotide variantNM_007204.5(DDX20):c.2461C>T (p.His821Tyr)not specified [RCV004315645]uncertain significance1111766885111766885Humanname
401883864CV2764701single nucleotide variantNM_007204.5(DDX20):c.2221C>T (p.Arg741Trp)not specified [RCV004334818]uncertain significance1111766645111766645Humanname
405704446CV3243663single nucleotide variantNM_007204.5(DDX20):c.1367A>G (p.Lys456Arg)not specified [RCV004375719]uncertain significance1111765791111765791Humanname
405704456CV3243664single nucleotide variantNM_007204.5(DDX20):c.1567G>A (p.Glu523Lys)not specified [RCV004375720]uncertain significance1111765991111765991Humanname
405704462CV3243665single nucleotide variantNM_007204.5(DDX20):c.1673C>T (p.Thr558Ile)not specified [RCV004375721]uncertain significance1111766097111766097Humanname
405704470CV3243666single nucleotide variantNM_007204.5(DDX20):c.1838T>C (p.Ile613Thr)not specified [RCV004375722]uncertain significance1111766262111766262Humanname
405704476CV3243667single nucleotide variantNM_007204.5(DDX20):c.2188A>G (p.Arg730Gly)not specified [RCV004375723]uncertain significance1111766612111766612Humanname
405704483CV3243668single nucleotide variantNM_007204.5(DDX20):c.2299T>C (p.Ser767Pro)not specified [RCV004375724]uncertain significance1111766723111766723Humanname
405704491CV3243669single nucleotide variantNM_007204.5(DDX20):c.2375C>A (p.Ser792Tyr)not specified [RCV004375725]uncertain significance1111766799111766799Humanname
405704502CV3243670single nucleotide variantNM_007204.5(DDX20):c.2461C>A (p.His821Asn)not specified [RCV004375726]uncertain significance1111766885111766885Humanname
597805655CV3662038single nucleotide variantNM_007204.5(DDX20):c.1375G>C (p.Val459Leu)not specified [RCV004908707]uncertain significance1111765799111765799Humanname
598128768CV3886566single nucleotide variantNM_007204.5(DDX20):c.1676A>G (p.Asn559Ser)not provided [RCV005244226]likely benign1111766100111766100Humanname
598263255CV3960039single nucleotide variantNM_007204.5(DDX20):c.2215C>T (p.Pro739Ser)not specified [RCV005325636]uncertain significance1111766639111766639Humanname
598263257CV3960040single nucleotide variantNM_007204.5(DDX20):c.1123G>A (p.Ala375Thr)not specified [RCV005325637]uncertain significance1111762695111762695Humanname
598263259CV3960041single nucleotide variantNM_007204.5(DDX20):c.2320G>A (p.Glu774Lys)not specified [RCV005325638]uncertain significance1111766744111766744Humanname
598263261CV3960042single nucleotide variantNM_007204.5(DDX20):c.1457A>G (p.Gln486Arg)not specified [RCV005325639]uncertain significance1111765881111765881Humanname
15143976CV706572single nucleotide variantNM_007204.5(DDX20):c.1775C>A (p.Ala592Asp)not provided [RCV000966761]benign1111766199111766199Humanname
40818052CV969094single nucleotide variantNM_007204.5(DDX20):c.2237T>C (p.Leu746Ser)Amyotrophic lateral sclerosis [RCV001260197]uncertain significance1111766661111766661Human2name
401928146CV2809073microsatelliteNM_007204.5(DDX20):c.1262TGA[2] (p.Met423del)not provided [RCV003406671]likely benign1111762956111762958Humanname