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Variants search result for Homo sapiens
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25 records found for search term Dbx1
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
407457752CV3430176single nucleotide variantNM_001029865.4(DBX1):c.11C>A (p.Pro4His)not specified [RCV004611277]uncertain significance112016031420160314Humanname
401904237CV2816530single nucleotide variantNM_001029865.4(DBX1):c.735G>A (p.Leu245=)not provided [RCV003394786]likely benign112015651120156511Humanname
405689644CV3246478single nucleotide variantNM_001029865.4(DBX1):c.239C>T (p.Ser80Leu)not specified [RCV004373048]uncertain significance112016008620160086Humanname
597800579CV3651852single nucleotide variantNM_001029865.4(DBX1):c.254C>T (p.Pro85Leu)not specified [RCV004905759]uncertain significance112016007120160071Humanname
597800582CV3651854single nucleotide variantNM_001029865.4(DBX1):c.166C>A (p.Arg56Ser)not specified [RCV004905761]uncertain significance112016015920160159Humanname
156062525CV2203609single nucleotide variantNM_001029865.4(DBX1):c.818C>A (p.Pro273His)not specified [RCV004072797]uncertain significance112015642820156428Humanname
155973158CV2238926single nucleotide variantNM_001029865.4(DBX1):c.350C>T (p.Ser117Phe)not specified [RCV004109828]uncertain significance112015997520159975Humanname
155971606CV2262354single nucleotide variantNM_001029865.4(DBX1):c.734T>G (p.Leu245Arg)not specified [RCV004128541]uncertain significance112015651220156512Humanname
155921915CV2284223single nucleotide variantNM_001029865.4(DBX1):c.919G>C (p.Gly307Arg)not specified [RCV004146590]uncertain significance112015632720156327Humanname
156010799CV2362172single nucleotide variantNM_001029865.4(DBX1):c.812A>G (p.Lys271Arg)not specified [RCV004209972]uncertain significance112015643420156434Humanname
329387564CV2436555single nucleotide variantNM_001029865.4(DBX1):c.827A>C (p.Glu276Ala)not specified [RCV004253712]uncertain significance112015641920156419Humanname
329360208CV2446642single nucleotide variantNM_001029865.4(DBX1):c.406A>T (p.Thr136Ser)not specified [RCV004251530]uncertain significance112015925420159254Humanname
401765086CV2701827single nucleotide variantNM_001029865.4(DBX1):c.737C>G (p.Ser246Cys)not specified [RCV004307795]uncertain significance112015650920156509Humanname
401859380CV2771563single nucleotide variantNM_001029865.4(DBX1):c.766C>T (p.Pro256Ser)not specified [RCV004348587]uncertain significance112015648020156480Humanname
405689649CV3246479single nucleotide variantNM_001029865.4(DBX1):c.511C>A (p.Pro171Thr)not specified [RCV004373049]uncertain significance112015719820157198Humanname
405689653CV3246480single nucleotide variantNM_001029865.4(DBX1):c.931C>A (p.Pro311Thr)not specified [RCV004373050]uncertain significance112015631520156315Humanname
405689659CV3246481single nucleotide variantNM_001029865.4(DBX1):c.940G>A (p.Ala314Thr)not specified [RCV004373051]uncertain significance112015630620156306Humanname
405689664CV3246482single nucleotide variantNM_001029865.4(DBX1):c.973T>C (p.Phe325Leu)not specified [RCV004373052]uncertain significance112015627320156273Humanname
407457754CV3430177single nucleotide variantNM_001029865.4(DBX1):c.379G>C (p.Ala127Pro)not specified [RCV004611278]uncertain significance112015928120159281Humanname
597800581CV3651853single nucleotide variantNM_001029865.4(DBX1):c.409T>G (p.Phe137Val)not specified [RCV004905760]uncertain significance112015925120159251Humanname
597800584CV3651855single nucleotide variantNM_001029865.4(DBX1):c.971A>C (p.Asp324Ala)not specified [RCV004905762]uncertain significance112015627520156275Humanname
598252129CV3963504single nucleotide variantNM_001029865.4(DBX1):c.931C>T (p.Pro311Ser)not specified [RCV005323192]uncertain significance112015631520156315Humanname
598252135CV3963505single nucleotide variantNM_001029865.4(DBX1):c.971A>T (p.Asp324Val)not specified [RCV005323193]uncertain significance112015627520156275Humanname
598252141CV3963506single nucleotide variantNM_001029865.4(DBX1):c.380C>T (p.Ala127Val)not specified [RCV005323194]uncertain significance112015928020159280Humanname
598252146CV3963507single nucleotide variantNM_001029865.4(DBX1):c.632G>T (p.Arg211Leu)not specified [RCV005323195]uncertain significance112015707720157077Humanname