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Variants search result for Homo sapiens
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39 records found for search term Dusp5
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
598267255CV3957554single nucleotide variantNM_004419.4(DUSP5):c.20A>G (p.Asp7Gly)not specified [RCV005326852]uncertain significance10110498141110498141Humanname
329385146CV2454747single nucleotide variantNM_004419.4(DUSP5):c.88C>T (p.Pro30Ser)not specified [RCV004269979]uncertain significance10110498209110498209Humanname
401907776CV2809610single nucleotide variantNM_004419.4(DUSP5):c.420C>T (p.Cys140=)not provided [RCV003422871]likely benign10110502761110502761Humanname
597802534CV3670222single nucleotide variantNM_004419.4(DUSP5):c.84C>G (p.Cys28Trp)not specified [RCV004906734]uncertain significance10110498205110498205Humanname
15192860CV737339single nucleotide variantNM_004419.4(DUSP5):c.963G>C (p.Thr321=)not provided [RCV000910668]benign10110510234110510234Humanname
156169123CV2197756single nucleotide variantNM_004419.4(DUSP5):c.233A>T (p.Glu78Val)not specified [RCV004074955]uncertain significance10110498354110498354Humanname
155923382CV2251935single nucleotide variantNM_004419.4(DUSP5):c.182C>G (p.Ser61Trp)not specified [RCV004119905]uncertain significance10110498303110498303Humanname
401735815CV2692206single nucleotide variantNM_004419.4(DUSP5):c.139C>T (p.Leu47Phe)not specified [RCV004301902]uncertain significance10110498260110498260Humanname
401761583CV2702400single nucleotide variantNM_004419.4(DUSP5):c.280C>T (p.Arg94Cys)not specified [RCV004316918]uncertain significance10110498401110498401Humanname
401879032CV2754749single nucleotide variantNM_004419.4(DUSP5):c.112A>T (p.Asn38Tyr)not specified [RCV004341237]uncertain significance10110498233110498233Humanname
405735327CV3241299single nucleotide variantNM_004419.4(DUSP5):c.140T>C (p.Leu47Pro)not specified [RCV004379733]uncertain significance10110498261110498261Humanname
405735335CV3241300single nucleotide variantNM_004419.4(DUSP5):c.167G>C (p.Arg56Pro)not specified [RCV004379734]uncertain significance10110498288110498288Humanname
405735341CV3241301single nucleotide variantNM_004419.4(DUSP5):c.204C>A (p.Asp68Glu)not specified [RCV004379735]uncertain significance10110498325110498325Humanname
407476920CV3431137single nucleotide variantNM_004419.4(DUSP5):c.191A>G (p.Tyr64Cys)not specified [RCV004617208]uncertain significance10110498312110498312Humanname
597802529CV3670220single nucleotide variantNM_004419.4(DUSP5):c.118C>T (p.Arg40Cys)not specified [RCV004906732]uncertain significance10110498239110498239Humanname
598267272CV3957558single nucleotide variantNM_004419.4(DUSP5):c.221G>T (p.Arg74Leu)not specified [RCV005326856]uncertain significance10110498342110498342Humanname
598267284CV3957561single nucleotide variantNM_004419.4(DUSP5):c.175G>C (p.Ala59Pro)not specified [RCV005326859]uncertain significance10110498296110498296Humanname
15116535CV712150single nucleotide variantNM_004419.4(DUSP5):c.163G>T (p.Ala55Ser)not provided [RCV000962052]benign10110498284110498284Humanname
151353126CV1326021single nucleotide variantNM_004419.4(DUSP5):c.871G>A (p.Asp291Asn)not provided [RCV001816090]|not specified [RCV004040944]uncertain significance10110510142110510142Humanname
156195126CV2211032single nucleotide variantNM_004419.4(DUSP5):c.817A>C (p.Ile273Leu)not specified [RCV004088218]uncertain significance10110510088110510088Humanname
401773253CV2698148single nucleotide variantNM_004419.4(DUSP5):c.591C>G (p.Cys197Trp)not specified [RCV004302930]uncertain significance10110506997110506997Humanname
401759677CV2698588single nucleotide variantNM_004419.4(DUSP5):c.427G>A (p.Val143Ile)not specified [RCV004299073]uncertain significance10110502768110502768Humanname
405735349CV3241302single nucleotide variantNM_004419.4(DUSP5):c.388G>C (p.Glu130Gln)not specified [RCV004379736]uncertain significance10110502729110502729Humanname
405735359CV3241303single nucleotide variantNM_004419.4(DUSP5):c.854G>A (p.Arg285His)not specified [RCV004379737]uncertain significance10110510125110510125Humanname
407476811CV3431138single nucleotide variantNM_004419.4(DUSP5):c.491C>G (p.Pro164Arg)not specified [RCV004617209]uncertain significance10110502832110502832Humanname
597802521CV3670215single nucleotide variantNM_004419.4(DUSP5):c.421G>T (p.Val141Leu)not specified [RCV004906728]uncertain significance10110502762110502762Humanname
597735284CV3670217single nucleotide variantNM_004419.4(DUSP5):c.479A>G (p.Gln160Arg)not specified [RCV004920443]uncertain significance10110502820110502820Humanname
597802525CV3670218single nucleotide variantNM_004419.4(DUSP5):c.424G>A (p.Asp142Asn)not specified [RCV004906730]uncertain significance10110502765110502765Humanname
597802527CV3670219single nucleotide variantNM_004419.4(DUSP5):c.869T>C (p.Phe290Ser)not specified [RCV004906731]uncertain significance10110510140110510140Humanname
598267260CV3957555single nucleotide variantNM_004419.4(DUSP5):c.443A>G (p.Gln148Arg)not specified [RCV005326853]uncertain significance10110502784110502784Humanname
598267264CV3957556single nucleotide variantNM_004419.4(DUSP5):c.362G>T (p.Arg121Leu)not specified [RCV005326854]uncertain significance10110498483110498483Humanname
598267268CV3957557single nucleotide variantNM_004419.4(DUSP5):c.358C>T (p.Pro120Ser)not specified [RCV005326855]uncertain significance10110498479110498479Humanname
598267276CV3957559single nucleotide variantNM_004419.4(DUSP5):c.622C>G (p.Leu208Val)not specified [RCV005326857]uncertain significance10110507028110507028Humanname
598267280CV3957560single nucleotide variantNM_004419.4(DUSP5):c.919A>T (p.Met307Leu)not specified [RCV005326858]uncertain significance10110510190110510190Humanname
155971030CV2392420single nucleotide variantNM_004419.4(DUSP5):c.1088C>T (p.Pro363Leu)not specified [RCV004244001]uncertain significance10110510359110510359Humanname
401738874CV2676392single nucleotide variantNM_004419.4(DUSP5):c.1076C>T (p.Ser359Leu)not specified [RCV004286414]uncertain significance10110510347110510347Humanname
401740650CV2680447single nucleotide variantNM_004419.4(DUSP5):c.1103C>T (p.Ser368Leu)not specified [RCV004289046]uncertain significance10110510374110510374Humanname
401743170CV2715415single nucleotide variantNM_004419.4(DUSP5):c.1047G>A (p.Met349Ile)not specified [RCV004324734]uncertain significance10110510318110510318Humanname
597802523CV3670216single nucleotide variantNM_004419.4(DUSP5):c.1139C>G (p.Thr380Arg)not specified [RCV004906729]uncertain significance10110510410110510410Humanname