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Schematic diagram of gene variants in ovarian clear cell carcinoma. (A) Illustration of probable somatic variants in genes (rows) across tumors (columns) in cohort 2. Red, splice site SNV; black, truncating SNV; green, missense SNV; blue, inframe indels; yellow, unreported variants. (B) Summary of pathways and gene families (rows) affected by probable somatic variants across tumors (columns) in cohort 2.
