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63 records found for search term Prdm4
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
329360123CV2446601single nucleotide variantNM_012406.4(PRDM4):c.5A>G (p.His2Arg)not specified [RCV004251493]uncertain significance12107760511107760511Humanname
401781882CV2689979single nucleotide variantNM_012406.4(PRDM4):c.154G>C (p.Val52Leu)not specified [RCV004297862]uncertain significance12107754101107754101Humanname
401730694CV2711452single nucleotide variantNM_012406.4(PRDM4):c.267C>G (p.Asn89Lys)not specified [RCV004306777]uncertain significance12107753988107753988Humanname
405660698CV3370146single nucleotide variantNM_012406.4(PRDM4):c.104G>T (p.Gly35Val)not specified [RCV004512831]uncertain significance12107756873107756873Humanname
596946817CV3548649single nucleotide variantNM_012406.4(PRDM4):c.1074A>G (p.Gln358=)not provided [RCV004810477]uncertain significance12107751467107751467Humanname
156128706CV2220069single nucleotide variantNM_012406.4(PRDM4):c.502C>T (p.Arg168Cys)not specified [RCV004093944]uncertain significance12107752039107752039Humanname
156079837CV2258097single nucleotide variantNM_012406.4(PRDM4):c.520G>T (p.Gly174Cys)not specified [RCV004121490]uncertain significance12107752021107752021Humanname
156046211CV2308140single nucleotide variantNM_012406.4(PRDM4):c.853C>G (p.Leu285Val)not specified [RCV004164378]uncertain significance12107751688107751688Humanname
156078341CV2318710single nucleotide variantNM_012406.4(PRDM4):c.840G>A (p.Met280Ile)not specified [RCV004173602]uncertain significance12107751701107751701Humanname
156049126CV2336496single nucleotide variantNM_012406.4(PRDM4):c.833A>G (p.Asn278Ser)not specified [RCV004194706]uncertain significance12107751708107751708Humanname
156180388CV2356085single nucleotide variantNM_012406.4(PRDM4):c.847A>G (p.Ser283Gly)not specified [RCV004203498]uncertain significance12107751694107751694Humanname
329388979CV2448554single nucleotide variantNM_012406.4(PRDM4):c.886A>G (p.Thr296Ala)not specified [RCV004259234]uncertain significance12107751655107751655Humanname
401881955CV2774609single nucleotide variantNM_012406.4(PRDM4):c.727A>C (p.Asn243His)not specified [RCV004350079]uncertain significance12107751814107751814Humanname
401899259CV2783787single nucleotide variantNM_012406.4(PRDM4):c.779A>G (p.Asn260Ser)not specified [RCV004360700]uncertain significance12107751762107751762Humanname
405660731CV3377894single nucleotide variantNM_012406.4(PRDM4):c.620A>G (p.Asp207Gly)not specified [RCV004512841]uncertain significance12107751921107751921Humanname
405660734CV3377895single nucleotide variantNM_012406.4(PRDM4):c.718G>T (p.Val240Leu)not specified [RCV004512842]uncertain significance12107751823107751823Humanname
405660737CV3377896single nucleotide variantNM_012406.4(PRDM4):c.721A>G (p.Ser241Gly)not specified [RCV004512843]uncertain significance12107751820107751820Humanname
405660739CV3377897single nucleotide variantNM_012406.4(PRDM4):c.742G>A (p.Ala248Thr)not specified [RCV004512844]likely benign12107751799107751799Humanname
405660742CV3377898single nucleotide variantNM_012406.4(PRDM4):c.901G>A (p.Val301Met)not specified [RCV004512845]uncertain significance12107751640107751640Humanname
407465074CV3468092single nucleotide variantNM_012406.4(PRDM4):c.343T>C (p.Tyr115His)not specified [RCV004660110]uncertain significance12107752198107752198Humanname
407465083CV3468095single nucleotide variantNM_012406.4(PRDM4):c.998C>T (p.Thr333Ile)not specified [RCV004660112]uncertain significance12107751543107751543Humanname
596946009CV3548172single nucleotide variantNM_012406.4(PRDM4):c.506C>T (p.Ser169Phe)not provided [RCV004809503]likely benign12107752035107752035Humanname
597747840CV3581136single nucleotide variantNM_012406.4(PRDM4):c.458A>C (p.Asn153Thr)not specified [RCV004845942]uncertain significance12107752083107752083Humanname
597747844CV3581137single nucleotide variantNM_012406.4(PRDM4):c.892T>C (p.Ser298Pro)not specified [RCV004845943]uncertain significance12107751649107751649Humanname
597747849CV3581138single nucleotide variantNM_012406.4(PRDM4):c.589G>A (p.Val197Ile)not specified [RCV004845944]uncertain significance12107751952107751952Humanname
598179486CV3908097single nucleotide variantNM_012406.4(PRDM4):c.895G>A (p.Val299Ile)not specified [RCV005264832]uncertain significance12107751646107751646Humanname
598179492CV3908098single nucleotide variantNM_012406.4(PRDM4):c.614C>T (p.Ser205Leu)not specified [RCV005264833]uncertain significance12107751927107751927Humanname
598179498CV3908099single nucleotide variantNM_012406.4(PRDM4):c.856A>G (p.Ser286Gly)not specified [RCV005264834]uncertain significance12107751685107751685Humanname
598179503CV3908100single nucleotide variantNM_012406.4(PRDM4):c.689G>C (p.Arg230Thr)not specified [RCV005264835]uncertain significance12107751852107751852Humanname
8627165CV82309single nucleotide variantNM_012406.3(PRDM4):c.445C>T (p.Pro149Ser)Malignant melanoma [RCV000062388]not provided12107752096107752096Humanname
156329284CV2213806single nucleotide variantNM_012406.4(PRDM4):c.2053C>T (p.Arg685Trp)not specified [RCV004089866]uncertain significance12107739423107739423Humanname
156133553CV2216842single nucleotide variantNM_012406.4(PRDM4):c.1307G>A (p.Arg436Gln)not specified [RCV004083268]uncertain significance12107744631107744631Humanname
156387541CV2221540single nucleotide variantNM_012406.4(PRDM4):c.1753A>G (p.Ser585Gly)not specified [RCV004096807]uncertain significance12107741117107741117Humanname
156340914CV2225715single nucleotide variantNM_012406.4(PRDM4):c.1913A>G (p.Lys638Arg)not specified [RCV004103135]uncertain significance12107740957107740957Humanname
156388228CV2231734single nucleotide variantNM_012406.4(PRDM4):c.1157C>G (p.Ser386Trp)not specified [RCV004098553]uncertain significance12107746394107746394Humanname
156388620CV2231922single nucleotide variantNM_012406.4(PRDM4):c.2309C>T (p.Ser770Leu)not specified [RCV004092994]uncertain significance12107734307107734307Humanname
155972660CV2238832single nucleotide variantNM_012406.4(PRDM4):c.1396A>T (p.Ile466Leu)not specified [RCV004109747]uncertain significance12107743282107743282Humanname
156036360CV2243539single nucleotide variantNM_012406.4(PRDM4):c.1487G>A (p.Arg496Gln)not specified [RCV004112492]uncertain significance12107742343107742343Humanname
329386753CV2428440single nucleotide variantNM_012406.4(PRDM4):c.1014G>C (p.Met338Ile)not specified [RCV004253236]uncertain significance12107751527107751527Humanname
329355009CV2449208single nucleotide variantNM_012406.4(PRDM4):c.2165A>G (p.Asn722Ser)not specified [RCV004264259]uncertain significance12107734451107734451Humanname
329395342CV2458284single nucleotide variantNM_012406.4(PRDM4):c.1589G>A (p.Arg530Gln)not specified [RCV004265931]uncertain significance12107742241107742241Humanname
401780600CV2727466single nucleotide variantNM_012406.4(PRDM4):c.1950G>C (p.Leu650Phe)not specified [RCV004329670]uncertain significance12107739526107739526Humanname
401884381CV2761254single nucleotide variantNM_012406.4(PRDM4):c.1837A>G (p.Met613Val)not specified [RCV004341131]uncertain significance12107741033107741033Humanname
401888913CV2765066single nucleotide variantNM_012406.4(PRDM4):c.1206A>G (p.Ile402Met)not specified [RCV004337183]uncertain significance12107746345107746345Humanname
401878632CV2776838single nucleotide variantNM_012406.4(PRDM4):c.1919A>C (p.His640Pro)not specified [RCV004357979]uncertain significance12107740951107740951Humanname
401887974CV2781806single nucleotide variantNM_012406.4(PRDM4):c.1145G>A (p.Arg382His)not specified [RCV004356762]uncertain significance12107746406107746406Humanname
405660695CV3370145single nucleotide variantNM_012406.4(PRDM4):c.1006G>A (p.Val336Ile)not specified [RCV004512830]uncertain significance12107751535107751535Humanname
405660701CV3377885single nucleotide variantNM_012406.4(PRDM4):c.1214G>A (p.Arg405Lys)not specified [RCV004512832]uncertain significance12107746337107746337Humanname
405660705CV3377886single nucleotide variantNM_012406.4(PRDM4):c.1234A>C (p.Lys412Gln)not specified [RCV004512833]uncertain significance12107746317107746317Humanname
405660708CV3377887single nucleotide variantNM_012406.4(PRDM4):c.1658G>A (p.Cys553Tyr)not specified [RCV004512834]uncertain significance12107741212107741212Humanname
405660711CV3377888single nucleotide variantNM_012406.4(PRDM4):c.1739A>G (p.His580Arg)not specified [RCV004512835]uncertain significance12107741131107741131Humanname
405660719CV3377890single nucleotide variantNM_012406.4(PRDM4):c.1937A>G (p.Tyr646Cys)not specified [RCV004512837]uncertain significance12107739539107739539Humanname
405660722CV3377891single nucleotide variantNM_012406.4(PRDM4):c.2090C>T (p.Thr697Ile)not specified [RCV004512838]uncertain significance12107739386107739386Humanname
405660725CV3377892single nucleotide variantNM_012406.4(PRDM4):c.2372A>T (p.Tyr791Phe)not specified [RCV004512839]uncertain significance12107734244107734244Humanname
407465078CV3468093single nucleotide variantNM_012406.4(PRDM4):c.1406A>G (p.Asn469Ser)not specified [RCV004660111]uncertain significance12107743272107743272Humanname
407530052CV3468094single nucleotide variantNM_012406.4(PRDM4):c.1661A>G (p.Asn554Ser)not specified [RCV004656465]likely benign12107741209107741209Humanname
597748166CV3581139single nucleotide variantNM_012406.4(PRDM4):c.1048C>A (p.Leu350Ile)not specified [RCV004845945]uncertain significance12107751493107751493Humanname
597747857CV3581140single nucleotide variantNM_012406.4(PRDM4):c.1931A>G (p.Lys644Arg)not specified [RCV004845946]uncertain significance12107739545107739545Humanname
597747862CV3581141single nucleotide variantNM_012406.4(PRDM4):c.1306C>T (p.Arg436Trp)not specified [RCV004845947]uncertain significance12107744632107744632Humanname
597747867CV3581142single nucleotide variantNM_012406.4(PRDM4):c.1519G>A (p.Asp507Asn)not specified [RCV004845948]uncertain significance12107742311107742311Humanname
597747873CV3581143single nucleotide variantNM_012406.4(PRDM4):c.1148C>G (p.Ala383Gly)not specified [RCV004845949]uncertain significance12107746403107746403Humanname
597747875CV3581144single nucleotide variantNM_012406.4(PRDM4):c.2330A>T (p.Asp777Val)not specified [RCV004845950]uncertain significance12107734286107734286Humanname
598179482CV3908096single nucleotide variantNM_012406.4(PRDM4):c.1168G>A (p.Glu390Lys)not specified [RCV005264831]uncertain significance12107746383107746383Humanname