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Variants search result for Homo sapiens
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45 records found for search term Traf2
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
156050154CV2391148single nucleotide variantNM_021138.4(TRAF2):c.8C>T (p.Ala3Val)not specified [RCV004235124]uncertain significance9136898748136898748Humanname
407521729CV3492494single nucleotide variantNM_021138.4(TRAF2):c.26C>A (p.Pro9His)not specified [RCV004677406]uncertain significance9136898766136898766Humanname
15102391CV723478single nucleotide variantNM_021138.4(TRAF2):c.243C>T (p.Gly81=)not provided [RCV000892470]benign9136899648136899648Humanname
597795983CV3621002single nucleotide variantNM_021138.4(TRAF2):c.52G>A (p.Gly18Ser)not specified [RCV004878354]uncertain significance9136898792136898792Humanname
15118515CV711880single nucleotide variantNM_021138.4(TRAF2):c.924G>T (p.Arg308=)not provided [RCV000962395]benign9136920479136920479Humanname
156180938CV2226017single nucleotide variantNM_021138.4(TRAF2):c.164C>T (p.Ser55Phe)not specified [RCV004105175]uncertain significance9136898904136898904Humanname
401761998CV2699485single nucleotide variantNM_021138.4(TRAF2):c.184C>T (p.Leu62Phe)not specified [RCV004299700]uncertain significance9136898924136898924Humanname
401883376CV2757898single nucleotide variantNM_021138.4(TRAF2):c.244A>C (p.Ile82Leu)not specified [RCV004337037]uncertain significance9136899649136899649Humanname
405775951CV3344072single nucleotide variantNM_021138.4(TRAF2):c.155G>A (p.Arg52Gln)not specified [RCV004471108]uncertain significance9136898895136898895Humanname
597795972CV3620999single nucleotide variantNM_021138.4(TRAF2):c.263G>A (p.Ser88Asn)not specified [RCV004878351]uncertain significance9136899668136899668Humanname
598265869CV3924598single nucleotide variantNM_021138.4(TRAF2):c.118G>A (p.Val40Ile)not specified [RCV005281050]uncertain significance9136898858136898858Humanname
15134422CV711881single nucleotide variantNM_021138.4(TRAF2):c.1083C>T (p.Phe361=)not provided [RCV000965124]benign9136921160136921160Humanname
156137098CV2196232single nucleotide variantNM_021138.4(TRAF2):c.448C>T (p.Arg150Cys)not specified [RCV004073586]uncertain significance9136908151136908151Humanname
155973441CV2224648single nucleotide variantNM_021138.4(TRAF2):c.589A>T (p.Ile197Phe)not specified [RCV004092495]uncertain significance9136909980136909980Humanname
156046397CV2234664single nucleotide variantNM_021138.4(TRAF2):c.298G>T (p.Val100Leu)not specified [RCV004102621]uncertain significance9136900452136900452Humanname
155973785CV2239032single nucleotide variantNM_021138.4(TRAF2):c.682G>A (p.Glu228Lys)not specified [RCV004109910]uncertain significance9136920237136920237Humanname
156074772CV2291337single nucleotide variantNM_021138.4(TRAF2):c.430C>T (p.Arg144Cys)not specified [RCV004162028]uncertain significance9136908133136908133Humanname
156177497CV2317250single nucleotide variantNM_021138.4(TRAF2):c.371G>T (p.Cys124Phe)not specified [RCV004178746]uncertain significance9136908074136908074Humanname
155904533CV2385533single nucleotide variantNM_021138.4(TRAF2):c.791C>T (p.Ala264Val)not specified [RCV004233175]likely benign9136920346136920346Humanname
329398139CV2464270single nucleotide variantNM_021138.4(TRAF2):c.547C>T (p.Pro183Ser)not specified [RCV004276231]uncertain significance9136909938136909938Humanname
401724576CV2714893single nucleotide variantNM_021138.4(TRAF2):c.749C>T (p.Ser250Leu)not specified [RCV004322227]uncertain significance9136920304136920304Humanname
405775957CV3344073single nucleotide variantNM_021138.4(TRAF2):c.654C>G (p.Phe218Leu)not specified [RCV004471109]uncertain significance9136916591136916591Humanname
405775963CV3344074single nucleotide variantNM_021138.4(TRAF2):c.709G>C (p.Val237Leu)not specified [RCV004471110]uncertain significance9136920264136920264Humanname
405775969CV3344075single nucleotide variantNM_021138.4(TRAF2):c.793G>A (p.Gly265Arg)not specified [RCV004471111]uncertain significance9136920348136920348Humanname
407521726CV3492493single nucleotide variantNM_021138.4(TRAF2):c.575G>A (p.Cys192Tyr)not specified [RCV004677405]uncertain significance9136909966136909966Humanname
407461285CV3492496single nucleotide variantNM_021138.4(TRAF2):c.392T>G (p.Leu131Arg)not specified [RCV004687615]uncertain significance9136908095136908095Humanname
407521738CV3492498single nucleotide variantNM_021138.4(TRAF2):c.664G>A (p.Gly222Ser)not specified [RCV004677409]uncertain significance9136916601136916601Humanname
597795966CV3620997single nucleotide variantNM_021138.4(TRAF2):c.923G>A (p.Arg308Gln)not specified [RCV004878349]uncertain significance9136920478136920478Humanname
597795969CV3620998single nucleotide variantNM_021138.4(TRAF2):c.473A>G (p.Glu158Gly)not specified [RCV004878350]uncertain significance9136908176136908176Humanname
597795975CV3621000single nucleotide variantNM_021138.4(TRAF2):c.530C>T (p.Ala177Val)not specified [RCV004878352]uncertain significance9136909921136909921Humanname
597795989CV3621004single nucleotide variantNM_021138.4(TRAF2):c.733G>T (p.Ala245Ser)not specified [RCV004878356]uncertain significance9136920288136920288Humanname
598265862CV3924593single nucleotide variantNM_021138.4(TRAF2):c.853A>G (p.Ile285Val)not specified [RCV005281049]uncertain significance9136920408136920408Humanname
598201583CV3924595single nucleotide variantNM_021138.4(TRAF2):c.836C>T (p.Thr279Met)not specified [RCV005290193]uncertain significance9136920391136920391Humanname
598201587CV3924596single nucleotide variantNM_021138.4(TRAF2):c.629G>A (p.Gly210Asp)not specified [RCV005290194]uncertain significance9136916566136916566Humanname
8633288CV88502single nucleotide variantNM_021138.3(TRAF2):c.310C>T (p.Pro104Ser)Malignant melanoma [RCV000068595]not provided9136900464136900464Humanname
156275322CV2330666single nucleotide variantNM_021138.4(TRAF2):c.1258G>A (p.Ala420Thr)not specified [RCV004185738]uncertain significance9136923971136923971Humanname
156211400CV2370341single nucleotide variantNM_021138.4(TRAF2):c.1351G>A (p.Val451Met)not specified [RCV004213248]uncertain significance9136925746136925746Humanname
156064329CV2375971single nucleotide variantNM_021138.4(TRAF2):c.1115G>A (p.Arg372His)not specified [RCV004218177]uncertain significance9136921192136921192Humanname
329401424CV2460839single nucleotide variantNM_021138.4(TRAF2):c.1453G>A (p.Val485Met)not specified [RCV004271148]uncertain significance9136925848136925848Humanname
329353304CV2469126single nucleotide variantNM_021138.4(TRAF2):c.1460A>G (p.Asp487Gly)not specified [RCV004274355]uncertain significance9136925855136925855Humanname
401884078CV2782341single nucleotide variantNM_021138.4(TRAF2):c.1106T>C (p.Val369Ala)not specified [RCV004365088]uncertain significance9136921183136921183Humanname
407521732CV3492495single nucleotide variantNM_021138.4(TRAF2):c.1336G>A (p.Ala446Thr)not specified [RCV004677407]uncertain significance9136925731136925731Humanname
597795978CV3621001single nucleotide variantNM_021138.4(TRAF2):c.1183T>C (p.Tyr395His)not specified [RCV004878353]uncertain significance9136923896136923896Humanname
598201591CV3924597single nucleotide variantNM_021138.4(TRAF2):c.1453G>C (p.Val485Leu)not specified [RCV005290195]uncertain significance9136925848136925848Humanname
598201595CV3924599single nucleotide variantNM_021138.4(TRAF2):c.1327G>A (p.Val443Met)not specified [RCV005290196]uncertain significance9136925722136925722Humanname