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Variants search result for Homo sapiens
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9 records found for search term Paip2b
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
155975642CV2235912single nucleotide variantNM_020459.1(PAIP2B):c.32C>T (p.Pro11Leu)not specified [RCV004113802]uncertain significance27120255871202558Humanname
156194904CV2347387single nucleotide variantNM_020459.1(PAIP2B):c.59G>A (p.Gly20Glu)not specified [RCV004207227]uncertain significance27120253171202531Humanname
401729186CV2690093single nucleotide variantNM_020459.1(PAIP2B):c.66T>A (p.Ser22Arg)not specified [RCV004300328]uncertain significance27120252471202524Humanname
405756624CV3367622single nucleotide variantNM_020459.1(PAIP2B):c.28T>C (p.Ser10Pro)not specified [RCV004499942]uncertain significance27120256271202562Humanname
155959861CV2285328single nucleotide variantNM_020459.1(PAIP2B):c.105G>C (p.Met35Ile)not specified [RCV004139204]uncertain significance27120248571202485Humanname
407517616CV3470127single nucleotide variantNM_020459.1(PAIP2B):c.198T>G (p.Asp66Glu)not specified [RCV004650719]uncertain significance27118996271189962Humanname
597696169CV3578449single nucleotide variantNM_020459.1(PAIP2B):c.230G>A (p.Arg77Gln)not specified [RCV004839082]uncertain significance27118993071189930Humanname
597696163CV3578450single nucleotide variantNM_020459.1(PAIP2B):c.109A>T (p.Met37Leu)not specified [RCV004839083]uncertain significance27120248171202481Humanname
598257858CV4005461single nucleotide variantNM_020459.1(PAIP2B):c.114G>T (p.Glu38Asp)not specified [RCV005386139]uncertain significance27120247671202476Humanname