A Novel RET D898Y Germline Mutation in a Patient with Pheochromocytoma

Figure 3

(a) Sanger sequencing revealed a RET mutation (c.2692G>T, p.Asp898Tyr) (chromosome 10:43120165). (b) Detailed information on the RET c.2692G>T, p.Asp898Tyr mutation generated by variant effect predictor (http://www.ensembl.org/info/docs/tools/vep/index.html).

(a)

(b)