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Variants search result for Homo sapiens
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7 records found for search term Polr2l
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
407481741CV3460994single nucleotide variantNM_021128.5(POLR2L):c.17G>C (p.Arg6Pro)not specified [RCV004664668]uncertain significance11842492842492Humanname
155975349CV2235861single nucleotide variantNM_021128.5(POLR2L):c.94G>A (p.Gly32Arg)not specified [RCV004111973]uncertain significance11842415842415Humanname
156395914CV2325994single nucleotide variantNM_021128.5(POLR2L):c.80C>G (p.Ala27Gly)not specified [RCV004176205]uncertain significance11842429842429Humanname
329352832CV2470581single nucleotide variantNM_021128.5(POLR2L):c.61T>C (p.Tyr21His)not specified [RCV004273582]uncertain significance11842448842448Humanname
329400021CV2440396single nucleotide variantNM_021128.5(POLR2L):c.139C>T (p.Arg47Trp)not specified [RCV004256335]uncertain significance11840437840437Humanname
405667220CV3373570single nucleotide variantNM_021128.5(POLR2L):c.124C>T (p.Arg42Cys)not specified [RCV004514409]uncertain significance11840452840452Humanname
598246244CV3907667single nucleotide variantNM_021128.5(POLR2L):c.158T>G (p.Val53Gly)not specified [RCV005258460]uncertain significance11840418840418Humanname