SLFN13 Back

schlafen family member 13

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NCBI Description of SLFN13

Community Annotation of SLFN13 Add / Edit SLFN13: Annotations

No community annotations yet for SLFN13.
Sort mutations by: Tumor type  Mutation type  Position  
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Figure notes


• "Mouse over" a mutation to see details.
• Missense green saturation indicates evolutionary conservation of the mutated positions.
• Red hashes in protein strip are splice sites.
• Blue-white-red bars are log2 copy ratio distributions (–1 to +1) from Zack et al. (2013).


Legend

SLFN13 is highly significantly mutated in
(none)
SLFN13 is significantly mutated in
(none)
SLFN13 is near significance in
(none)

Click on a tumor type to see its full list of significant genes.

Data details


Mutation list for SLFN13