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


3 records found for search term Gng12
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
8582416CV116966single nucleotide variantNM_018841.5(GNG12):c.-76-15224A>GLung cancer [RCV000097487]uncertain significance16779273167792731Humanname
8576035CV110390single nucleotide variantNR_040077.1(GNG12-AS1):n.149+52362T>GLung cancer [RCV000090913]uncertain significance16788479867884798Humanname
405768418CV3262104single nucleotide variantNM_018841.6(GNG12):c.52G>A (p.Val18Met)not specified [RCV004395494]uncertain significance16770763567707635Humanname