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38 records found for search term Crtam
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
8652632CV129207single nucleotide variantNM_019604.3(CRTAM):c.*269G>ALung cancer [RCV000109694]uncertain significance11122871668122871668Humanname
405675489CV3239101single nucleotide variantNM_019604.4(CRTAM):c.9G>T (p.Trp3Cys)not specified [RCV004369983]uncertain significance11122838555122838555Humanname
405675472CV3239097single nucleotide variantNM_019604.4(CRTAM):c.14T>A (p.Val5Asp)not specified [RCV004369979]uncertain significance11122838560122838560Humanname
407464320CV3429737single nucleotide variantNM_019604.4(CRTAM):c.98C>T (p.Thr33Met)not specified [RCV004613424]uncertain significance11122850119122850119Humanname
15199381CV701632single nucleotide variantNM_019604.4(CRTAM):c.441G>A (p.Lys147=)not provided [RCV000957023]benign11122854037122854037Humanname
15199385CV701634single nucleotide variantNM_019604.4(CRTAM):c.579G>A (p.Thr193=)not provided [RCV000957024]benign11122855783122855783Humanname
15118839CV712669single nucleotide variantNM_019604.4(CRTAM):c.47A>C (p.Glu16Ala)not provided [RCV000962447]benign11122850068122850068Humanname
405675477CV3239098single nucleotide variantNM_019604.4(CRTAM):c.186G>C (p.Glu62Asp)not specified [RCV004369980]uncertain significance11122850207122850207Humanname
407464325CV3429738single nucleotide variantNM_019604.4(CRTAM):c.292T>G (p.Cys98Gly)not specified [RCV004613425]uncertain significance11122851791122851791Humanname
597799638CV3657669single nucleotide variantNM_019604.4(CRTAM):c.155C>A (p.Thr52Asn)not specified [RCV004905325]uncertain significance11122850176122850176Humanname
598259981CV3962981single nucleotide variantNM_019604.4(CRTAM):c.136T>G (p.Ser46Ala)not specified [RCV005324888]likely benign11122850157122850157Humanname
15199378CV701631single nucleotide variantNM_019604.4(CRTAM):c.233C>A (p.Ala78Asp)not provided [RCV000957022]benign11122851732122851732Human1name
15199378CV701631single nucleotide variantNM_019604.4(CRTAM):c.233C>A (p.Ala78Asp)not provided [RCV000957022]benign11122851732122851733Human1name
155974167CV2221006single nucleotide variantNM_019604.4(CRTAM):c.578C>T (p.Thr193Met)not specified [RCV004092690]uncertain significance11122855782122855782Humanname
156090306CV2256498single nucleotide variantNM_019604.4(CRTAM):c.926T>C (p.Ile309Thr)not specified [RCV004118702]uncertain significance11122867517122867517Humanname
156362535CV2265552single nucleotide variantNM_019604.4(CRTAM):c.824A>G (p.Asn275Ser)not specified [RCV004124295]uncertain significance11122867415122867415Humanname
156189478CV2302957single nucleotide variantNM_019604.4(CRTAM):c.830A>G (p.Gln277Arg)not specified [RCV004162834]uncertain significance11122867421122867421Humanname
329387289CV2436363single nucleotide variantNM_019604.4(CRTAM):c.970G>A (p.Glu324Lys)not specified [RCV004251759]uncertain significance11122868018122868018Humanname
329401698CV2461105single nucleotide variantNM_019604.4(CRTAM):c.734T>C (p.Val245Ala)not specified [RCV004265247]uncertain significance11122864636122864636Humanname
401781332CV2681969single nucleotide variantNM_019604.4(CRTAM):c.542G>A (p.Ser181Asn)not specified [RCV004296951]uncertain significance11122855746122855746Humanname
405675482CV3239099single nucleotide variantNM_019604.4(CRTAM):c.307G>A (p.Asp103Asn)not specified [RCV004369981]likely benign11122851806122851806Humanname
405675486CV3239100single nucleotide variantNM_019604.4(CRTAM):c.775G>A (p.Glu259Lys)not specified [RCV004369982]uncertain significance11122864677122864677Humanname
407464329CV3429739single nucleotide variantNM_019604.4(CRTAM):c.543C>A (p.Ser181Arg)not specified [RCV004613426]uncertain significance11122855747122855747Humanname
597799632CV3657666single nucleotide variantNM_019604.4(CRTAM):c.949G>A (p.Val317Met)not specified [RCV004905322]uncertain significance11122867540122867540Humanname
597799640CV3657670single nucleotide variantNM_019604.4(CRTAM):c.577A>G (p.Thr193Ala)not specified [RCV004905326]uncertain significance11122855781122855781Humanname
597799642CV3657671single nucleotide variantNM_019604.4(CRTAM):c.712C>T (p.Pro238Ser)not specified [RCV004905327]uncertain significance11122862523122862523Humanname
597799644CV3657672single nucleotide variantNM_019604.4(CRTAM):c.995G>T (p.Ser332Ile)not specified [RCV004905328]uncertain significance11122868043122868043Humanname
598259953CV3962974single nucleotide variantNM_019604.4(CRTAM):c.611A>G (p.Gln204Arg)not specified [RCV005324882]uncertain significance11122855815122855815Humanname
598160180CV3962976single nucleotide variantNM_019604.4(CRTAM):c.565G>A (p.Gly189Ser)not specified [RCV005328716]likely benign11122855769122855769Humanname
598259962CV3962977single nucleotide variantNM_019604.4(CRTAM):c.428C>T (p.Thr143Ile)not specified [RCV005324884]uncertain significance11122854024122854024Humanname
598259967CV3962978single nucleotide variantNM_019604.4(CRTAM):c.907A>G (p.Ile303Val)not specified [RCV005324885]uncertain significance11122867498122867498Humanname
598259972CV3962979single nucleotide variantNM_019604.4(CRTAM):c.488C>A (p.Ser163Tyr)not specified [RCV005324886]likely benign11122854084122854084Humanname
15102150CV701633single nucleotide variantNM_019604.4(CRTAM):c.518A>G (p.Asp173Gly)not provided [RCV000959237]benign11122855722122855722Humanname
15138922CV712670single nucleotide variantNM_019604.4(CRTAM):c.758C>T (p.Thr253Ile)not provided [RCV000965875]benign11122864660122864660Humanname
329358411CV2425248single nucleotide variantNM_019604.4(CRTAM):c.1079A>G (p.Tyr360Cys)not specified [RCV004250920]uncertain significance11122871296122871296Humanname
329370999CV2431836single nucleotide variantNM_019604.4(CRTAM):c.1126G>A (p.Val376Ile)not specified [RCV004254978]uncertain significance11122871343122871343Humanname
597799634CV3657667single nucleotide variantNM_019604.4(CRTAM):c.1118A>C (p.Lys373Thr)not specified [RCV004905323]uncertain significance11122871335122871335Humanname
598259958CV3962975single nucleotide variantNM_019604.4(CRTAM):c.1055C>T (p.Ser352Phe)not specified [RCV005324883]uncertain significance11122871272122871272Humanname