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8 records found for search term Isy1
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
156146306CV2381775single nucleotide variantNM_020701.4(ISY1):c.419-2191C>Tnot specified [RCV004232224]uncertain significance3129137145129137145Humanname
401755938CV2686165single nucleotide variantNM_020701.4(ISY1):c.419-2186G>Anot specified [RCV004297264]uncertain significance3129137140129137140Humanname
401897807CV2772937single nucleotide variantNM_020701.4(ISY1):c.419-2238G>Cnot specified [RCV004357706]uncertain significance3129137192129137192Humanname
405866872CV2842383single nucleotide variantNM_020701.4(ISY1):c.419-2196T>CEBV-positive nodal T- and NK-cell lymphoma [RCV004557740]likely benign3129137150129137150Humanname
405805284CV3271587single nucleotide variantNM_020701.4(ISY1):c.419-2210G>Anot specified [RCV004405457]uncertain significance3129137164129137164Humanname
598195307CV3979813single nucleotide variantNM_020701.4(ISY1):c.419-2195G>Anot specified [RCV005354971]uncertain significance3129137149129137149Humanname
407480120CV3451515single nucleotide variantNM_020701.4(ISY1):c.587G>C (p.Arg196Pro)not specified [RCV004633292]uncertain significance3129134150129134150Humanname
598170839CV3979814single nucleotide variantNM_001204890.2(ISY1-RAB43):c.908C>A (p.Thr303Asn)not specified [RCV005370438]uncertain significance3129095113129095113Humanname