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Variants search result for Homo sapiens
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7 records found for search term Eif5a2
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
155926858CV2395869single nucleotide variantNM_020390.6(EIF5A2):c.10G>A (p.Glu4Lys)not specified [RCV004237431]uncertain significance3170907797170907797Humanname
156015970CV2299033single nucleotide variantNM_020390.6(EIF5A2):c.170A>G (p.His57Arg)not specified [RCV004158553]uncertain significance3170907089170907089Humanname
401743987CV2688073single nucleotide variantNM_020390.6(EIF5A2):c.107G>A (p.Arg36Gln)not specified [RCV004305136]uncertain significance3170907700170907700Humanname
156232337CV2227675single nucleotide variantNM_020390.6(EIF5A2):c.414G>C (p.Met138Ile)not specified [RCV004094071]uncertain significance3170893408170893408Humanname
155969285CV2244491single nucleotide variantNM_020390.6(EIF5A2):c.445A>G (p.Ile149Val)not specified [RCV004100448]uncertain significance3170893377170893377Humanname
405736974CV3238718single nucleotide variantNM_020390.6(EIF5A2):c.383A>G (p.Asn128Ser)not specified [RCV004379987]uncertain significance3170894311170894311Humanname
407506364CV3438209single nucleotide variantNM_020390.6(EIF5A2):c.397G>C (p.Val133Leu)not specified [RCV004624679]uncertain significance3170894297170894297Humanname