None from Scientific Research

Open access visualization of None, RUNX1 Mutation, Sequencing Read, Reads Frequency
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RUNX1 mutation is private to Ph53-R. RUNX1 gene is on the minus strand and orange and blue represent G and C bases, respectively. A gray line represents a sequencing read, and a bar at the top represents the number of reads covering each position. Frequencies of reads with the c.445G>C mutation are shown.

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