This tab shows an overview of the mutation data [more details]
Gene Name:
FBXW7_ENST00000534231
Mutation Id:
COSM108571
AA Mutation:
p.R266C (Substitution - Missense, position 266, RC)
CDS Mutation:
c.796C>T (Substitution, position 796, CT)
GRCh38:
4:152326137..152326137, view Ensembl Contig
COSMIC Genome Browser:
4:152326137..152326137, view in COSMIC JBrowse
Ever confirmed somatic:
Yes
FATHMM prediction:
Pathogenic (score 0.94)
This tab displays the distribution of mutated samples and tissue types. [more details]
This tab displays a table of muated samples, with tissue, histology and zygosity information. Publication information is also included, where available, with links to PUBMED. [more details]
Sample name Gene name Transcript Primary Tissue Histology Pubmed ID Zygosity Somatic Status Sample Source LOH Resistant Mutation Drugs
This tab displays a table of references for the mutation [more details]
Reference Title Author Year Journal Status COSMIC Pubmed