This tab shows an overview of the mutation data [more details]
Gene Name:
SMARCB1
Mutation Id:
COSM1090
AA Mutation:
p.? ( Unknown )
CDS Mutation:
c.1119-41G>A ( Substitution - intronic )
GRCh37:
Ensembl Contig View22:24176282..24176292
COSMIC Genome Browser:
COSMIC JBrowse 22:24176282..24176292
CDD:
NP_003064.2
Homologene:
2310, click hereto look at the multiple sequence alignment.
Ever confirmed somatic:
No
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
This tab displays a table of protein features [more details]
No protein features could be predicted.
This tab displays a table of pathways affected by the mutation [more details]
SourcePathways
WikiPathwayTNF-alpha/NF-kB Signaling Pathway
This tab displays a table of references for the mutation [more details]
Reference Title Author Year Journal Status COSMIC Pubmed