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Pathways
Variants search result for All species
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9 records found for search term Eif3e
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
401867195CV2472821single nucleotide variantNM_001568.3(EIF3E):c.25C>T (p.Arg9Cys)not provided [RCV003331518]uncertain significance8108248678108248678Humanname
405719978CV3238591single nucleotide variantNM_001568.3(EIF3E):c.35A>C (p.His12Pro)not specified [RCV004377786]uncertain significance8108248668108248668Humanname
405719151CV3238592single nucleotide variantNM_001568.3(EIF3E):c.56T>G (p.Val19Gly)not specified [RCV004377787]uncertain significance8108248647108248647Humanname
597664306CV3674463single nucleotide variantNM_001568.3(EIF3E):c.944G>A (p.Cys315Tyr)not specified [RCV004912308]uncertain significance8108216419108216419Humanname
597665200CV3674464single nucleotide variantNM_001568.3(EIF3E):c.332G>A (p.Arg111Lys)not specified [RCV004912309]uncertain significance8108236195108236195Humanname
597746622CV3674465single nucleotide variantNM_001568.3(EIF3E):c.835A>G (p.Lys279Glu)not specified [RCV004922731]uncertain significance8108217348108217348Humanname
598179225CV3961371single nucleotide variantNM_001568.3(EIF3E):c.578A>G (p.Lys193Arg)not specified [RCV005332473]uncertain significance8108229089108229089Humanname
598179231CV3961372single nucleotide variantNM_001568.3(EIF3E):c.660T>G (p.Phe220Leu)not specified [RCV005332474]uncertain significance8108228329108228329Humanname
155923674CV2212337single nucleotide variantNM_001568.3(EIF3E):c.1072G>C (p.Asp358His)not specified [RCV004091284]uncertain significance8108203493108203493Humanname