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


4 records found for search term Fcer1g
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
156386995CV2364909single nucleotide variantNM_004106.2(FCER1G):c.23T>C (p.Leu8Pro)not specified [RCV004221809]uncertain significance1161215344161215344Humanname
597724321CV3675836single nucleotide variantNM_004106.2(FCER1G):c.41A>G (p.Glu14Gly)not specified [RCV004919084]uncertain significance1161215362161215362Humanname
597724341CV3675838single nucleotide variantNM_004106.2(FCER1G):c.94C>A (p.Leu32Met)not specified [RCV004919086]uncertain significance1161218030161218030Humanname
597724330CV3675837single nucleotide variantNM_004106.2(FCER1G):c.149T>C (p.Val50Ala)not specified [RCV004919085]uncertain significance1161218248161218248Humanname