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


3 records found for search term Snrpg
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
405731729CV3326299single nucleotide variantNM_003096.4(SNRPG):c.33A>G (p.Lys11=)not specified [RCV004464423]likely benign27028937270289372Humanname
405731737CV3326300single nucleotide variantNM_003096.4(SNRPG):c.76C>G (p.His26Asp)not specified [RCV004464424]uncertain significance27028817270288172Humanname
401760970CV2726600single nucleotide variantNM_003096.4(SNRPG):c.155G>T (p.Gly52Val)not specified [RCV004329087]uncertain significance27028809370288093Humanname