Fig. 1From: Characterization of VHL missense mutations in sporadic clear cell renal cell carcinoma: hotspots, affected binding domains, functional impact on pVHL and therapeutic relevance VHL sequence analysis of 360 ccRCC with frequencies of mutated tumors, total number of VHL mutations (including double mutations) as well as VHL mutation types. Deletions/Insertions were grouped into frameshift and in frame mutations; Point mutations were grouped into silent, nonsense and missense mutationsBack to article page