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


3 records found for search term Psma2
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
401892591CV2782255single nucleotide variantNM_002787.5(PSMA2):c.4G>A (p.Ala2Thr)not specified [RCV004359221]uncertain significance74293215542932155Humanname
15153748CV722526single nucleotide variantNM_002787.5(PSMA2):c.387A>G (p.Pro129=)not provided [RCV000880073]benign74292339442923394Humanname
597749714CV3591988single nucleotide variantNM_002787.5(PSMA2):c.287A>G (p.Gln96Arg)not specified [RCV004846285]uncertain significance74292476242924762Humanname