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


5 records found for search term Cfl1
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
150471730CV1281056single nucleotide variantNM_005507.3(CFL1):c.198C>T (p.Asp66=)not provided [RCV001713245]benign116585604865856048Humanname
155944273CV2241969single nucleotide variantNM_005507.3(CFL1):c.203A>G (p.Tyr68Cys)not specified [RCV004108920]uncertain significance116585604365856043Humanname
401767529CV2727194single nucleotide variantNM_005507.3(CFL1):c.196G>A (p.Asp66Asn)not specified [RCV004327332]uncertain significance116585605065856050Humanname
8634294CV89514single nucleotide variantNM_005507.2(CFL1):c.296T>G (p.Leu99Arg)Malignant melanoma [RCV000069611]not provided116585595065855950Humanname
407501933CV3425429single nucleotide variantNM_005507.3(CFL1):c.436C>T (p.Arg146Cys)not specified [RCV004607499]uncertain significance116585540165855401Humanname