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


7 records found for search term Bag2
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
21069376CV795887single nucleotide variantNM_004282.4(BAG2):c.222C>T (p.Asp74=)not provided [RCV000998639]uncertain significance65718214057182140Humanname
156069264CV2237118single nucleotide variantNM_004282.4(BAG2):c.92G>T (p.Ser31Ile)not specified [RCV004114871]uncertain significance65717278957172789Humanname
597741367CV3631348single nucleotide variantNM_004282.4(BAG2):c.292G>A (p.Val98Ile)not specified [RCV004890736]uncertain significance65718384657183846Humanname
156270758CV2290176single nucleotide variantNM_004282.4(BAG2):c.364A>G (p.Asn122Asp)not specified [RCV004152837]uncertain significance65718391857183918Humanname
156129166CV2358605single nucleotide variantNM_004282.4(BAG2):c.392C>T (p.Ala131Val)not specified [RCV004207482]uncertain significance65718394657183946Humanname
598275322CV3926441single nucleotide variantNM_004282.4(BAG2):c.550T>G (p.Ser184Ala)not specified [RCV005304456]uncertain significance65718410457184104Humanname
598275330CV3926451single nucleotide variantNM_004282.4(BAG2):c.478A>G (p.Ile160Val)not specified [RCV005304464]uncertain significance65718403257184032Humanname