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34 records found for search term Dusp10
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
405734578CV3241209single nucleotide variantNM_007207.6(DUSP10):c.88A>C (p.Ser30Arg)not specified [RCV004379643]uncertain significance1221739657221739657Humanname
156287202CV2288377single nucleotide variantNM_007207.6(DUSP10):c.122G>A (p.Ser41Asn)not specified [RCV004151932]uncertain significance1221739623221739623Humanname
401768911CV2686428single nucleotide variantNM_007207.6(DUSP10):c.295G>T (p.Ala99Ser)not specified [RCV004290589]uncertain significance1221739450221739450Humanname
405734556CV3241206single nucleotide variantNM_007207.6(DUSP10):c.209C>T (p.Ser70Leu)not specified [RCV004379640]uncertain significance1221739536221739536Humanname
407490259CV3431087single nucleotide variantNM_007207.6(DUSP10):c.122G>C (p.Ser41Thr)not specified [RCV004620131]uncertain significance1221739623221739623Humanname
597802321CV3674007single nucleotide variantNM_007207.6(DUSP10):c.140C>T (p.Ala47Val)not specified [RCV004906651]uncertain significance1221739605221739605Humanname
598267027CV3957493single nucleotide variantNM_007207.6(DUSP10):c.206G>A (p.Arg69His)not specified [RCV005326791]uncertain significance1221739539221739539Humanname
156249212CV2199434single nucleotide variantNM_007207.6(DUSP10):c.896G>T (p.Gly299Val)not specified [RCV004070996]uncertain significance1221706382221706382Humanname
156089275CV2241461single nucleotide variantNM_007207.6(DUSP10):c.895G>A (p.Gly299Ser)not specified [RCV004104373]uncertain significance1221706383221706383Humanname
156277993CV2252046single nucleotide variantNM_007207.6(DUSP10):c.338C>T (p.Pro113Leu)not specified [RCV004122081]uncertain significance1221739407221739407Humanname
156275787CV2255708single nucleotide variantNM_007207.6(DUSP10):c.328A>G (p.Thr110Ala)not specified [RCV004120103]uncertain significance1221739417221739417Humanname
156180178CV2258412single nucleotide variantNM_007207.6(DUSP10):c.371C>A (p.Thr124Lys)not specified [RCV004115614]uncertain significance1221739374221739374Humanname
156229219CV2267600single nucleotide variantNM_007207.6(DUSP10):c.589G>A (p.Ala197Thr)not specified [RCV004134161]uncertain significance1221739156221739156Humanname
156365651CV2272153single nucleotide variantNM_007207.6(DUSP10):c.319G>A (p.Gly107Arg)not specified [RCV004124929]uncertain significance1221739426221739426Humanname
329373923CV2452711single nucleotide variantNM_007207.6(DUSP10):c.608G>A (p.Arg203Gln)not specified [RCV004275262]uncertain significance1221739137221739137Humanname
401771192CV2726394single nucleotide variantNM_007207.6(DUSP10):c.503C>T (p.Pro168Leu)not specified [RCV004328609]uncertain significance1221739242221739242Humanname
401862033CV2766561single nucleotide variantNM_007207.6(DUSP10):c.551A>G (p.Asn184Ser)not specified [RCV004347179]uncertain significance1221739194221739194Humanname
405734563CV3241207single nucleotide variantNM_007207.6(DUSP10):c.349A>G (p.Met117Val)not specified [RCV004379641]uncertain significance1221739396221739396Humanname
405734572CV3241208single nucleotide variantNM_007207.6(DUSP10):c.383G>T (p.Ser128Ile)not specified [RCV004379642]uncertain significance1221739362221739362Humanname
405734598CV3241211single nucleotide variantNM_007207.6(DUSP10):c.928C>T (p.Pro310Ser)not specified [RCV004379645]likely benign1221706350221706350Humanname
407490262CV3431088single nucleotide variantNM_007207.6(DUSP10):c.556A>G (p.Ser186Gly)not specified [RCV004620132]uncertain significance1221739189221739189Humanname
597802318CV3674006single nucleotide variantNM_007207.6(DUSP10):c.552C>A (p.Asn184Lys)not specified [RCV004906650]uncertain significance1221739193221739193Humanname
597802322CV3674008single nucleotide variantNM_007207.6(DUSP10):c.305C>A (p.Thr102Asn)not specified [RCV004906652]uncertain significance1221739440221739440Humanname
598267022CV3957492single nucleotide variantNM_007207.6(DUSP10):c.357C>A (p.Asn119Lys)not specified [RCV005326790]uncertain significance1221739388221739388Humanname
156254500CV2284177single nucleotide variantNM_007207.6(DUSP10):c.1090G>A (p.Glu364Lys)not specified [RCV004146554]uncertain significance1221706188221706188Humanname
156010447CV2291020single nucleotide variantNM_007207.6(DUSP10):c.1444G>T (p.Val482Leu)not specified [RCV004151562]uncertain significance1221702417221702417Humanname
155910533CV2303614single nucleotide variantNM_007207.6(DUSP10):c.1184A>C (p.Glu395Ala)not specified [RCV004161698]uncertain significance1221702677221702677Humanname
156261312CV2395619single nucleotide variantNM_007207.6(DUSP10):c.1034G>A (p.Arg345Gln)not specified [RCV004241464]uncertain significance1221706244221706244Humanname
401881078CV2789485single nucleotide variantNM_007207.6(DUSP10):c.1354A>T (p.Met452Leu)not specified [RCV004360103]uncertain significance1221702507221702507Humanname
405734535CV3241203single nucleotide variantNM_007207.6(DUSP10):c.1070A>G (p.His357Arg)not specified [RCV004379637]uncertain significance1221706208221706208Humanname
405734543CV3241204single nucleotide variantNM_007207.6(DUSP10):c.1255G>A (p.Val419Ile)not specified [RCV004379638]uncertain significance1221702606221702606Humanname
405734550CV3241205single nucleotide variantNM_007207.6(DUSP10):c.1283G>A (p.Arg428Gln)not specified [RCV004379639]uncertain significance1221702578221702578Humanname
598267029CV3957494single nucleotide variantNM_007207.6(DUSP10):c.1249A>T (p.Thr417Ser)not specified [RCV005326792]uncertain significance1221702612221702612Humanname
598267033CV3957495single nucleotide variantNM_007207.6(DUSP10):c.1024A>G (p.Thr342Ala)not specified [RCV005326793]uncertain significance1221706254221706254Humanname