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Pathways
Variants search result for Homo sapiens
(View Results for all Objects and Ontologies)


4 records found for search term Eif1b
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
405718459CV3241941single nucleotide variantNM_005875.3(EIF1B):c.41C>G (p.Ala14Gly)not specified [RCV004377678]uncertain significance34031090240310902Humanname
598178775CV3961287single nucleotide variantNM_005875.3(EIF1B):c.39T>G (p.Phe13Leu)not specified [RCV005332389]uncertain significance34031090040310900Humanname
597664092CV3674355single nucleotide variantNM_005875.3(EIF1B):c.122G>A (p.Arg41Lys)not specified [RCV004912257]uncertain significance34031098340310983Humanname
598178769CV3961286single nucleotide variantNM_005875.3(EIF1B):c.257A>G (p.Gln86Arg)not specified [RCV005332388]uncertain significance34031153140311531Humanname