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Variants search result for Homo sapiens
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25 records found for search term Dazap1
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
405689073CV3246396single nucleotide variantNM_018959.4(DAZAP1):c.8A>G (p.Asn3Ser)not specified [RCV004372966]uncertain significance1914077811407781Humanname
15162644CV704777single nucleotide variantNM_018959.4(DAZAP1):c.813T>C (p.Pro271=)not provided [RCV000947892]benign1914303041430304Humanname
156108866CV2313846single nucleotide variantNM_018959.4(DAZAP1):c.109G>A (p.Val37Ile)not specified [RCV004164166]uncertain significance1914182421418242Humanname
401773798CV2702443single nucleotide variantNM_018959.4(DAZAP1):c.101G>C (p.Gly34Ala)not specified [RCV004316956]uncertain significance1914182341418234Humanname
405689039CV3246390single nucleotide variantNM_018959.4(DAZAP1):c.262C>T (p.Arg88Trp)not specified [RCV004372960]uncertain significance1914186901418690Humanname
405689045CV3246391single nucleotide variantNM_018959.4(DAZAP1):c.275C>T (p.Pro92Leu)not specified [RCV004372961]uncertain significance1914187031418703Humanname
407453071CV3430150single nucleotide variantNM_018959.4(DAZAP1):c.286C>T (p.Arg96Trp)not specified [RCV004608818]uncertain significance1914187141418714Humanname
156038959CV2332672single nucleotide variantNM_018959.4(DAZAP1):c.640G>A (p.Ala214Thr)not specified [RCV004189349]uncertain significance1914289351428935Humanname
329379420CV2443400single nucleotide variantNM_018959.4(DAZAP1):c.853G>A (p.Gly285Ser)not specified [RCV004262243]uncertain significance1914303441430344Humanname
401724319CV2714797single nucleotide variantNM_018959.4(DAZAP1):c.992C>T (p.Ala331Val)not specified [RCV004320358]uncertain significance1914326341432634Humanname
405689050CV3246392single nucleotide variantNM_018959.4(DAZAP1):c.299G>C (p.Gly100Ala)not specified [RCV004372962]uncertain significance1914187271418727Humanname
405689056CV3246393single nucleotide variantNM_018959.4(DAZAP1):c.424G>T (p.Val142Leu)not specified [RCV004372963]uncertain significance1914223571422357Humanname
405689063CV3246394single nucleotide variantNM_018959.4(DAZAP1):c.593C>T (p.Pro198Leu)not specified [RCV004372964]uncertain significance1914288881428888Humanname
405689069CV3246395single nucleotide variantNM_018959.4(DAZAP1):c.752C>G (p.Ala251Gly)not specified [RCV004372965]uncertain significance1914302431430243Humanname
407453073CV3430151single nucleotide variantNM_018959.4(DAZAP1):c.826C>G (p.Pro276Ala)not specified [RCV004608819]uncertain significance1914303171430317Humanname
597800465CV3651772single nucleotide variantNM_018959.4(DAZAP1):c.322G>A (p.Asp108Asn)not specified [RCV004905697]uncertain significance1914211661421166Humanname
597800469CV3651774single nucleotide variantNM_018959.4(DAZAP1):c.401A>T (p.Lys134Met)not specified [RCV004905699]uncertain significance1914212451421245Humanname
156380437CV2208166single nucleotide variantNM_018959.4(DAZAP1):c.1141T>C (p.Ser381Pro)not specified [RCV004086843]uncertain significance1914348291434829Humanname
11040205CV224690single nucleotide variantNM_018959.4(DAZAP1):c.1213T>C (p.Tyr405His)Monoclonal B-Cell Lymphocytosis [RCV000208559]uncertain significance1914349011434901Human1name
407453069CV3430149single nucleotide variantNM_018959.4(DAZAP1):c.1162G>A (p.Gly388Ser)not specified [RCV004608817]uncertain significance1914348501434850Humanname
407453075CV3430152single nucleotide variantNM_018959.4(DAZAP1):c.1000A>G (p.Met334Val)not specified [RCV004608820]uncertain significance1914326421432642Humanname
597800471CV3651775single nucleotide variantNM_018959.4(DAZAP1):c.1018G>A (p.Ala340Thr)not specified [RCV004905700]uncertain significance1914326601432660Humanname
597800473CV3651776single nucleotide variantNM_018959.4(DAZAP1):c.1095C>G (p.Asp365Glu)not specified [RCV004905701]uncertain significance1914347831434783Humanname
598251816CV3963444single nucleotide variantNM_018959.4(DAZAP1):c.1159G>A (p.Gly387Ser)not specified [RCV005323134]uncertain significance1914348471434847Humanname
598251822CV3963445single nucleotide variantNM_018959.4(DAZAP1):c.1108C>A (p.Pro370Thr)not specified [RCV005323135]uncertain significance1914347961434796Humanname