GRCh38 · COSMIC v98


This section shows a summary for the selected study (COSU identifier) or publication (COSP identifier). Studies may have been performed by the Sanger Institute Cancer Genome Project, or imported from the ICGC/TCGA. You can see more information on the help pages.

Renal Followup
Study ID
A follow-up series of 311 clinical renal cell carcinoma (RCC) samples comprised of 246 clear cell RCC plus 65 additional samples of mixed additional histologies including chromophobe and papillary cancers were sequenced to evaluate mutation prevalence in genes of interest identified in the primary renal matched pair gene screen. In total 60 genes were screened for mutations in these 311 samples which is equivalent to 85Mb of tumour DNA.