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44 records found for search term Rassf4
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
15153404CV737488single nucleotide variantNM_032023.4(RASSF4):c.21G>A (p.Pro7=)not provided [RCV000901754]likely benign104497022344970223Humanname
155979550CV2339144single nucleotide variantNM_032023.4(RASSF4):c.13T>A (p.Cys5Ser)not specified [RCV004187184]uncertain significance104497021544970215Humanname
401728254CV2685971single nucleotide variantNM_032023.4(RASSF4):c.20C>T (p.Pro7Leu)not specified [RCV004296989]uncertain significance104497022244970222Humanname
405660251CV3312481single nucleotide variantNM_032023.4(RASSF4):c.32T>C (p.Val11Ala)not specified [RCV004438801]uncertain significance104497023444970234Humanname
156226261CV2215913single nucleotide variantNM_032023.4(RASSF4):c.266G>A (p.Arg89Gln)not specified [RCV004096994]likely benign104498264844982648Humanname
156159816CV2311619single nucleotide variantNM_032023.4(RASSF4):c.203G>A (p.Arg68Gln)not specified [RCV004168720]uncertain significance104498258544982585Humanname
156056664CV2320633single nucleotide variantNM_032023.4(RASSF4):c.223C>T (p.Arg75Trp)not specified [RCV004172247]uncertain significance104498260544982605Humanname
156154565CV2328665single nucleotide variantNM_032023.4(RASSF4):c.185G>A (p.Gly62Glu)not specified [RCV004177908]uncertain significance104498256744982567Humanname
156402499CV2361532single nucleotide variantNM_032023.4(RASSF4):c.214C>G (p.Gln72Glu)not specified [RCV004221166]uncertain significance104498259644982596Humanname
155928680CV2363343single nucleotide variantNM_032023.4(RASSF4):c.194G>A (p.Arg65Gln)not specified [RCV004213886]uncertain significance104498257644982576Humanname
329375846CV2468864single nucleotide variantNM_032023.4(RASSF4):c.289C>T (p.Pro97Ser)not specified [RCV004280167]uncertain significance104498402944984029Humanname
401771543CV2686227single nucleotide variantNM_032023.4(RASSF4):c.213G>A (p.Met71Ile)not specified [RCV004297319]likely benign104498259544982595Humanname
401770169CV2719071single nucleotide variantNM_032023.4(RASSF4):c.133C>T (p.Arg45Cys)not specified [RCV004322647]uncertain significance104497184344971843Humanname
405660248CV3312480single nucleotide variantNM_032023.4(RASSF4):c.224G>A (p.Arg75Gln)not specified [RCV004438800]uncertain significance104498260644982606Humanname
598185307CV3902288single nucleotide variantNM_032023.4(RASSF4):c.287A>T (p.Glu96Val)not specified [RCV005265891]uncertain significance104498402744984027Humanname
15116310CV712369single nucleotide variantNM_032023.4(RASSF4):c.288G>T (p.Glu96Asp)not provided [RCV000962011]benign104498402844984028Humanname
155991208CV2256419single nucleotide variantNM_032023.4(RASSF4):c.584G>A (p.Ser195Asn)not specified [RCV004116852]uncertain significance104498932644989326Humanname
156070249CV2292919single nucleotide variantNM_032023.4(RASSF4):c.362C>T (p.Thr121Ile)not specified [RCV004148415]uncertain significance104498410244984102Humanname
156187762CV2342062single nucleotide variantNM_032023.4(RASSF4):c.669C>G (p.Ile223Met)not specified [RCV004189497]uncertain significance104498970544989705Humanname
156040626CV2342063single nucleotide variantNM_032023.4(RASSF4):c.773T>C (p.Met258Thr)not specified [RCV004189498]uncertain significance104499103544991035Humanname
156146023CV2357904single nucleotide variantNM_032023.4(RASSF4):c.505A>G (p.Ile169Val)not specified [RCV004209693]uncertain significance104498494444984944Humanname
155965540CV2395970single nucleotide variantNM_032023.4(RASSF4):c.790G>A (p.Val264Met)not specified [RCV004237519]uncertain significance104499105244991052Humanname
155930496CV2398432single nucleotide variantNM_032023.4(RASSF4):c.551C>A (p.Ala184Asp)not specified [RCV004237760]uncertain significance104498929344989293Humanname
401737779CV2679976single nucleotide variantNM_032023.4(RASSF4):c.488G>A (p.Arg163Gln)not specified [RCV004284251]uncertain significance104498492744984927Humanname
405660254CV3312482single nucleotide variantNM_032023.4(RASSF4):c.330C>A (p.Ser110Arg)not specified [RCV004438802]uncertain significance104498407044984070Humanname
405660258CV3312483single nucleotide variantNM_032023.4(RASSF4):c.364G>A (p.Asp122Asn)not specified [RCV004438803]uncertain significance104498410444984104Humanname
405660261CV3312484single nucleotide variantNM_032023.4(RASSF4):c.449G>C (p.Arg150Thr)not specified [RCV004438804]uncertain significance104498488844984888Humanname
405660264CV3312485single nucleotide variantNM_032023.4(RASSF4):c.937C>T (p.Arg313Cys)not specified [RCV004438805]uncertain significance104499330044993300Humanname
407467075CV3468649single nucleotide variantNM_032023.4(RASSF4):c.676G>A (p.Glu226Lys)not specified [RCV004660628]uncertain significance104498971244989712Humanname
407500941CV3468651single nucleotide variantNM_032023.4(RASSF4):c.757G>T (p.Ala253Ser)not specified [RCV004669661]uncertain significance104499101944991019Humanname
597707158CV3589351single nucleotide variantNM_032023.4(RASSF4):c.481C>T (p.Arg161Cys)not specified [RCV004860582]uncertain significance104498492044984920Humanname
597784285CV3589352single nucleotide variantNM_032023.4(RASSF4):c.353A>G (p.Glu118Gly)not specified [RCV004854443]uncertain significance104498409344984093Humanname
597707167CV3589353single nucleotide variantNM_032023.4(RASSF4):c.670G>A (p.Val224Ile)not specified [RCV004860583]uncertain significance104498970644989706Humanname
597784289CV3589354single nucleotide variantNM_032023.4(RASSF4):c.779C>T (p.Ala260Val)not specified [RCV004854444]uncertain significance104499104144991041Humanname
597707174CV3589356single nucleotide variantNM_032023.4(RASSF4):c.680C>T (p.Ser227Phe)not specified [RCV004860584]uncertain significance104498971644989716Humanname
597707183CV3589357single nucleotide variantNM_032023.4(RASSF4):c.497G>T (p.Arg166Leu)not specified [RCV004860585]uncertain significance104498493644984936Humanname
597707191CV3589358single nucleotide variantNM_032023.4(RASSF4):c.805G>A (p.Glu269Lys)not specified [RCV004860586]uncertain significance104499106744991067Humanname
598185282CV3902284single nucleotide variantNM_032023.4(RASSF4):c.424G>A (p.Asp142Asn)not specified [RCV005265887]uncertain significance104498486344984863Humanname
598185289CV3902285single nucleotide variantNM_032023.4(RASSF4):c.400C>T (p.Pro134Ser)not specified [RCV005265888]uncertain significance104498483944984839Humanname
598185295CV3902286single nucleotide variantNM_032023.4(RASSF4):c.812C>T (p.Ala271Val)not specified [RCV005265889]uncertain significance104499190944991909Humanname
15118554CV712370single nucleotide variantNM_032023.4(RASSF4):c.469G>A (p.Gly157Ser)not provided [RCV000962401]likely benign104498490844984908Humanname
15165021CV712371single nucleotide variantNM_032023.4(RASSF4):c.474G>C (p.Glu158Asp)not provided [RCV000970861]benign104498491344984913Humanname
15151581CV712372single nucleotide variantNM_032023.4(RASSF4):c.482G>A (p.Arg161His)not provided [RCV000968170]benign104498492144984921Humanname
15192736CV723947single nucleotide variantNM_032023.4(RASSF4):c.463G>A (p.Ala155Thr)not provided [RCV000888745]benign104498490244984902Humanname